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Professor Nick Martin

Honorary Professor

School of Psychology
Faculty of Health and Behavioural Sciences

Honorary Professor

Royal Brisbane Clinical Unit
Faculty of Medicine
n.martin1@uq.edu.au

Overview

Qualifications

  • Doctor of Philosophy, University of Birmingham
  • Bachelor (Honours), University of Adelaide

Publications

  • Journal Article: Genome-wide association analyses identify 95 risk loci and provide insights into the neurobiology of post-traumatic stress disorder

    Nievergelt, Caroline M., Maihofer, Adam X., Atkinson, Elizabeth G., Chen, Chia-Yen, Choi, Karmel W., Coleman, Jonathan R. I., Daskalakis, Nikolaos P., Duncan, Laramie E., Polimanti, Renato, Aaronson, Cindy, Amstadter, Ananda B., Andersen, Soren B., Andreassen, Ole A., Arbisi, Paul A., Ashley-Koch, Allison E., Austin, S. Bryn, Avdibegoviç, Esmina, Babić, Dragan, Bacanu, Silviu-Alin, Baker, Dewleen G., Batzler, Anthony, Beckham, Jean C., Belangero, Sintia, Benjet, Corina, Bergner, Carisa, Bierer, Linda M., Biernacka, Joanna M., Bierut, Laura J., Bisson, Jonathan I. ... HUNT All-In Psychiatry (2024). Genome-wide association analyses identify 95 risk loci and provide insights into the neurobiology of post-traumatic stress disorder. Nature Genetics. doi: 10.1038/s41588-024-01707-9

  • Journal Article: Patterns of stressful life events and polygenic scores for five mental disorders and neuroticism among adults with depression

    Crouse, Jacob J., Park, Shin Ho, Byrne, Enda M., Mitchell, Brittany L., Scott, Jan, Medland, Sarah E., Lin, Tian, Wray, Naomi R., Martin, Nicholas G. and Hickie, Ian B. (2024). Patterns of stressful life events and polygenic scores for five mental disorders and neuroticism among adults with depression. Molecular Psychiatry, 1-9. doi: 10.1038/s41380-024-02492-x

  • Journal Article: Genetic control of DNA methylation is largely shared across European and East Asian populations

    Hatton, Alesha A., Cheng, Fei-Fei, Lin, Tian, Shen, Ren-Juan, Chen, Jie, Zheng, Zhili, Qu, Jia, Lyu, Fan, Harris, Sarah E., Cox, Simon R., Jin, Zi-Bing, Martin, Nicholas G., Fan, Dongsheng, Montgomery, Grant W., Yang, Jian, Wray, Naomi R., Marioni, Riccardo E., Visscher, Peter M. and McRae, Allan F. (2024). Genetic control of DNA methylation is largely shared across European and East Asian populations. Nature Communications, 15 (1) 2713, 2713. doi: 10.1038/s41467-024-47005-0

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Grants

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Supervision

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Publications

Book Chapter

  • Establishing a resource for genetic, epidemiological, and biomarker studies: the important role of twin registers

    Odintsova, Veronika, Willemsen, Gonneke, Dolan, Conor V., Hottenga, Jouke-Jan, Martin, Nicholas G., Slagboom, P. Eline, Ordoñana, Juan R. and Boomsma, Dorret I. (2022). Establishing a resource for genetic, epidemiological, and biomarker studies: the important role of twin registers. Twin research for everyone: from biology to health, epigenetics, and psychology. (pp. 163-188) edited by Adam D. Tarnoki, David L. Tarnoki, Jennifer R. Harris and Nancy L. Segal. Amsterdam, Netherlands: Elsevier. doi: 10.1016/B978-0-12-821514-2.00011-8

  • Genetic correlation between cortical gray matter thickness and white matter connections

    Shen, Kaikai, Dore, Vincent, Fripp, Jurgen, Rose, Stephen, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Thompson, Paul M., Wright, Margaret J. and Salvado, Olivier (2018). Genetic correlation between cortical gray matter thickness and white matter connections. Imaging genetics. (pp. 85-100) edited by Adrian Dalca, Kayhan Batmanghelich, Mert Sabuncu and Li Shen. London, United Kingdom: Academic Press. doi: 10.1016/B978-0-12-813968-4.00005-5

  • Direction of causation models

    Gillespie, Nathan A. and Martin, Nicholas G. (2014). Direction of causation models. Wiley StatsRef: Statistics Reference Online. (pp. *-*) Chichester, United Kingdom: John Wiley & Sons. doi: 10.1002/9781118445112.stat06685

  • Multiple stages classification of Alzheimer’s disease based on structural brain networks using generalized low rank approximations (GLRAM)

    Zhan, L., Nie, Z., Ye, J., Wang, Y., Jin, Y., Jahanshad, N., Prasad, G., de Zubicaray, G. I., McMahan, K. L., Martin, N. G., Wright, M. J. and Thompson, P. M. (2014). Multiple stages classification of Alzheimer’s disease based on structural brain networks using generalized low rank approximations (GLRAM). Computational diffusion MRI: MICCAI Workshop, Boston, MA, USA, September 2014. (pp. 35-44) edited by Lauren O'Donnell, Gemma Nedjati-Gilani, Yogesh Rathi, Marco Reisert and Torben Schneider. Cham, Switzerland: Springer International Publishing. doi: 10.1007/978-3-319-11182-7_4

  • Multivariate genetic analysis

    Gillespie, Nathan A. and Martin, Nicholas G. (2014). Multivariate genetic analysis. Wiley StatsRef: statistics reference online. Chichester, United Kingdom: John Wiley & Sons. doi: 10.1002/9781118445112.stat06468

  • Modeling the cultural and biological inheritance of social and political behavior in twins and nuclear families

    Eaves, Lindon J., Hatemi, Peter K., Heath, Andrew C. and Martin, Nicholas G. (2011). Modeling the cultural and biological inheritance of social and political behavior in twins and nuclear families. Man is by nature a political animal: evolution, biology, and politics. (pp. 101-184) edited by Peter K. Hatemi and Rose McDermott. Chicago, IL, United States: University of Chicago Press. doi: 10.7208/chicago/9780226319117.003.0005

  • Genetic and Environmental Influences on Sexual Orientation

    Khytam Dawood, J. Michael Bailey and Nicholas G. Martin (2009). Genetic and Environmental Influences on Sexual Orientation. Handbook of Behavior Genetics. (pp. 269-279) edited by Kim, Yong-Kyu. United Sates: Springer New York. doi: 10.1007/978-0-387-76727-7_19

  • Neuroticism as a genetic marker for mood and anxiety

    Gillespie, N. A. and Martin, N. G. (2006). Neuroticism as a genetic marker for mood and anxiety. Biology of Personality & Individual Differences. (pp. 225-250) edited by T. Canli. New York, U.S.A.: Guilford Press.

  • Genetic covariance between processing speed and IQ

    Luciano, M., Wright, M. J., Smith, G. A., Geffen, G. M., Geffen, L. B. and Martin, N. G. (2003). Genetic covariance between processing speed and IQ. Behavior genetics in the postgenomic era. (pp. 163-182) edited by Robert Plomin, John C. Defries, Ian W. Craig and Peter McGuffin. Washington, DC, USA: APA Books.

  • Gene-environment interactions

    Boomsma, D. I. and Martin, N. G. (2002). Gene-environment interactions. Biological Psychiatry. (pp. 181-187) edited by H. D'haenen, J. A. den Boer and P. Willner. New York: John Wiley & Sons Ltd.

  • Biological and cultural inheritance of stature and attitudes

    Eaves, Lindon J., Heath, A., Martin, Nicholas G., Neale, Michael C., Meyer, J. M., Silberg, J. L., Corey, Linda, Truett, Kimberley and Walters, Ellen (1999). Biological and cultural inheritance of stature and attitudes. Personality and Psychopathology. (pp. 269-308) edited by C. Robert Cloninger. Washington: American Psychiatric Press.

  • Gene-environment interaction and twin studies

    Martin, N. G. (1999). Gene-environment interaction and twin studies. Advances in Twin and Sib-pair Analysis. (pp. 143-150) edited by Tim D. Spector, Harold Snieder and Alex J. MacGregor. London: Greenwich Medical Media Ltd.

  • Genetic and environmental structure of personality

    Heath, A., Madden, P. A., Cloninger, C. R. and Martin, N. G. (1999). Genetic and environmental structure of personality. Personality and Psychopathology. (pp. 343-367) edited by C. Robert Cloninger. Washington, U.S.A.: American Psychiatric Press.

  • Insights into the genetic basis of human dental variation from statistical modelling analyses

    Dempsey, P. J., Townsend, G. C. and Martin, N. G. (1999). Insights into the genetic basis of human dental variation from statistical modelling analyses. Perspectives in Human Biology. (pp. 9-18) edited by Loren Knapp. Nedlands: The University of Western Australia.

Journal Article

  • Genome-wide association analyses identify 95 risk loci and provide insights into the neurobiology of post-traumatic stress disorder

    Nievergelt, Caroline M., Maihofer, Adam X., Atkinson, Elizabeth G., Chen, Chia-Yen, Choi, Karmel W., Coleman, Jonathan R. I., Daskalakis, Nikolaos P., Duncan, Laramie E., Polimanti, Renato, Aaronson, Cindy, Amstadter, Ananda B., Andersen, Soren B., Andreassen, Ole A., Arbisi, Paul A., Ashley-Koch, Allison E., Austin, S. Bryn, Avdibegoviç, Esmina, Babić, Dragan, Bacanu, Silviu-Alin, Baker, Dewleen G., Batzler, Anthony, Beckham, Jean C., Belangero, Sintia, Benjet, Corina, Bergner, Carisa, Bierer, Linda M., Biernacka, Joanna M., Bierut, Laura J., Bisson, Jonathan I. ... HUNT All-In Psychiatry (2024). Genome-wide association analyses identify 95 risk loci and provide insights into the neurobiology of post-traumatic stress disorder. Nature Genetics. doi: 10.1038/s41588-024-01707-9

  • Patterns of stressful life events and polygenic scores for five mental disorders and neuroticism among adults with depression

    Crouse, Jacob J., Park, Shin Ho, Byrne, Enda M., Mitchell, Brittany L., Scott, Jan, Medland, Sarah E., Lin, Tian, Wray, Naomi R., Martin, Nicholas G. and Hickie, Ian B. (2024). Patterns of stressful life events and polygenic scores for five mental disorders and neuroticism among adults with depression. Molecular Psychiatry, 1-9. doi: 10.1038/s41380-024-02492-x

  • Genetic control of DNA methylation is largely shared across European and East Asian populations

    Hatton, Alesha A., Cheng, Fei-Fei, Lin, Tian, Shen, Ren-Juan, Chen, Jie, Zheng, Zhili, Qu, Jia, Lyu, Fan, Harris, Sarah E., Cox, Simon R., Jin, Zi-Bing, Martin, Nicholas G., Fan, Dongsheng, Montgomery, Grant W., Yang, Jian, Wray, Naomi R., Marioni, Riccardo E., Visscher, Peter M. and McRae, Allan F. (2024). Genetic control of DNA methylation is largely shared across European and East Asian populations. Nature Communications, 15 (1) 2713, 2713. doi: 10.1038/s41467-024-47005-0

  • Comprehensive sex-stratified genetic analysis of 28 blood biomarkers and depression reveals a significant association between depression and low levels of total protein in females

    Kiewa, Jacqueline, Meltzer-Brody, Samantha, Milgrom, Jeannette, Guintivano, Jerry, Hickie, Ian B, Whiteman, David C, Olsen, Catherine M, Medland, Sarah E, Martin, Nicholas G, Wray, Naomi R and Byrne, Enda M (2024). Comprehensive sex-stratified genetic analysis of 28 blood biomarkers and depression reveals a significant association between depression and low levels of total protein in females. Complex Psychiatry. doi: 10.1159/000538058

  • Family History of Twinning and Fertility Traits in Nigerian Mothers of Dizygotic Twins

    Hur, Yoon-Mi, Martin, Nick, Oginni, Olakunle, Boomsma, Dorret, Hubers, Nikki and Mbarek, Hamdi (2024). Family History of Twinning and Fertility Traits in Nigerian Mothers of Dizygotic Twins. Twin Research and Human Genetics, 1-6. doi: 10.1017/thg.2024.2

  • Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications

    Sterenborg, Rosalie B. T. M., Steinbrenner, Inga, Li, Yong, Bujnis, Melissa N., Naito, Tatsuhiko, Marouli, Eirini, Galesloot, Tessel E., Babajide, Oladapo, Andreasen, Laura, Astrup, Arne, Åsvold, Bjørn Olav, Bandinelli, Stefania, Beekman, Marian, Beilby, John P., Bork-Jensen, Jette, Boutin, Thibaud, Brody, Jennifer A., Brown, Suzanne J., Brumpton, Ben, Campbell, Purdey J., Cappola, Anne R., Ceresini, Graziano, Chaker, Layal, Chasman, Daniel I., Concas, Maria Pina, Coutinho de Almeida, Rodrigo, Cross, Simone M., Cucca, Francesco, Deary, Ian J. ... Regeneron Genetics Center (2024). Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications. Nature Communications, 15 (1) 888, 888. doi: 10.1038/s41467-024-44701-9

  • X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements

    Scholz, Markus, Horn, Katrin, Pott, Janne, Wuttke, Matthias, Kühnapfel, Andreas, Nasr, M. Kamal, Kirsten, Holger, Li, Yong, Hoppmann, Anselm, Gorski, Mathias, Ghasemi, Sahar, Li, Man, Tin, Adrienne, Chai, Jin-Fang, Cocca, Massimiliano, Wang, Judy, Nutile, Teresa, Akiyama, Masato, Åsvold, Bjørn Olav, Bansal, Nisha, Biggs, Mary L., Boutin, Thibaud, Brenner, Hermann, Brumpton, Ben, Burkhardt, Ralph, Cai, Jianwen, Campbell, Archie, Campbell, Harry, Chalmers, John ... Pattaro, Cristian (2024). X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements. Nature Communications, 15 (1) 586, 586. doi: 10.1038/s41467-024-44709-1

  • Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference

    Meng, Xiangrui, Navoly, Georgina, Giannakopoulou, Olga, Levey, Daniel F., Koller, Dora, Pathak, Gita A., Koen, Nastassja, Lin, Kuang, Adams, Mark J., Rentería, Miguel E., Feng, Yanzhe, Gaziano, J. Michael, Stein, Dan J., Zar, Heather J., Campbell, Megan L., van Heel, David A., Trivedi, Bhavi, Finer, Sarah, McQuillin, Andrew, Bass, Nick, Chundru, V. Kartik, Martin, Hilary C., Huang, Qin Qin, Valkovskaya, Maria, Chu, Chia-Yi, Kanjira, Susan, Kuo, Po-Hsiu, Chen, Hsi-Chung, Tsai, Shih-Jen ... BioBank Japan Project (2024). Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference. Nature Genetics, 56 (2), 222-233. doi: 10.1038/s41588-023-01596-4

  • Evening chronotypes with depression report poorer outcomes of SSRIs: A survey-based study of self-ratings

    Crouse, Jacob J., Park, Shin Ho, Byrne, Enda M., Mitchell, Brittany L., Chan, Karina, Scott, Jan, Medland, Sarah E., Martin, Nicholas G., Wray, Naomi R. and Hickie, Ian B. (2024). Evening chronotypes with depression report poorer outcomes of SSRIs: A survey-based study of self-ratings. Biological Psychiatry. doi: 10.1016/j.biopsych.2023.12.023

  • Genetic and shared environmental factors explain the association between adolescent polysubstance use and high school noncompletion

    Davis, Christal N., Gizer, Ian R., Agrawal, Arpana, Statham, Dixie J., Heath, Andrew C., Martin, Nicholas G. and Slutske, Wendy S. (2024). Genetic and shared environmental factors explain the association between adolescent polysubstance use and high school noncompletion. Psychology of Addictive Behaviors, 38 (1), 114-123. doi: 10.1037/adb0000915

  • Multi-ancestry study of the genetics of problematic alcohol use in over 1 million individuals

    Zhou, Hang, Kember, Rachel L., Deak, Joseph D., Xu, Heng, Toikumo, Sylvanus, Yuan, Kai, Lind, Penelope A., Farajzadeh, Leila, Wang, Lu, Hatoum, Alexander S., Johnson, Jessica, Lee, Hyunjoon, Mallard, Travis T., Xu, Jiayi, Johnston, Keira J. A., Johnson, Emma C., Nielsen, Trine Tollerup, Galimberti, Marco, Dao, Cecilia, Levey, Daniel F., Overstreet, Cassie, Byrne, Enda M., Gillespie, Nathan A., Gordon, Scott, Hickie, Ian B., Whitfield, John B., Xu, Ke, Zhao, Hongyu, Huckins, Laura M. ... Million Veteran Program (2023). Multi-ancestry study of the genetics of problematic alcohol use in over 1 million individuals. Nature Medicine, 29 (12), 1-9. doi: 10.1038/s41591-023-02653-5

  • Genome-wide association study meta-analysis of dizygotic twinning illuminates genetic regulation of female fecundity

    Mbarek, Hamdi, Gordon, Scott D, Duffy, David L, Hubers, Nikki, Mortlock, Sally, Beck, Jeffrey J, Hottenga, Jouke-Jan, Pool, René, Dolan, Conor V, Actkins, Ky’Era V, Gerring, Zachary F, Van Dongen, Jenny, Ehli, Erik A, Iacono, William G, Mcgue, Matt, Chasman, Daniel I, Gallagher, C Scott, Schilit, Samantha L P, Morton, Cynthia C, Paré, Guillaume, Willemsen, Gonneke, Whiteman, David C, Olsen, Catherine M, Derom, Catherine, Vlietinck, Robert, Gudbjartsson, Daniel, Cannon-Albright, Lisa, Krapohl, Eva, Plomin, Robert ... Martin, Nicholas G (2023). Genome-wide association study meta-analysis of dizygotic twinning illuminates genetic regulation of female fecundity. Human Reproduction, 39 (1), 240-257. doi: 10.1093/humrep/dead247

  • Can an online battery match in‐person cognitive testing in predicting age‐related cortical changes

    Thienel, Renate, Borne, Léonie, Faucher, Caroline, Robinson, Gail, Fripp, Jurgen, Giorgio, Joseph, Martin, Nicholas G, Breakspear, Michael and Lupton, Michelle K (2023). Can an online battery match in‐person cognitive testing in predicting age‐related cortical changes. Alzheimer's & Dementia, 19 (S12). doi: 10.1002/alz.074476

  • Meta-Analyses of Genome-Wide Association Studies for Postpartum Depression

    Guintivano, Jerry, Byrne, Enda M., Kiewa, Jacqueline, Yao, Shuyang, Bauer, Anna E., Aberg, Karolina A., Adams, Mark J., Campbell, Archie, Campbell, Megan L., Choi, Karmel W., Corfield, Elizabeth C., Havdahl, Alexandra, Hucks, Donald, Koen, Nastassja, Lu, Yi, Maegbaek, Merete L., Mullaer, Jimmy, Peterson, Roseann E., Raffield, Laura M., Sallis, Hannah M., Sealock, Julia M., Walker, Alicia, Watson, Hunna J., Xiong, Ying, Yang, Jessica M. K., Anney, Richard J. L., Gordon-Smith, Katherine, Hubbard, Leon, Jones, Lisa A. ... Sullivan, Patrick (2023). Meta-Analyses of Genome-Wide Association Studies for Postpartum Depression. American Journal of Psychiatry, 180 (12), 884-895. doi: 10.1176/appi.ajp.20230053

  • Poorer online cognitive performance is associated with genetic risk for Alzheimer’s disease and brain phenotypes in healthy mid‐life and older adults

    Lupton, Michelle K, Gomez, Lina, Mitchell, Brittany L, Adsett, Jessica, García‐Marín, Luis M, Renteria, Miguel E., McAloney, Kerrie, Ceslis, Amelia, Thienel, Renate, Robinson, Gail, Breakspear, Michael and Martin, Nicholas G (2023). Poorer online cognitive performance is associated with genetic risk for Alzheimer’s disease and brain phenotypes in healthy mid‐life and older adults. Alzheimer's & Dementia, 19 (S12). doi: 10.1002/alz.078078

  • Discontinuation of antidepressant treatment: a retrospective cohort study on more than 20,000 participants

    Garcia-Marin, Luis M., Mulcahy, Aoibhe, Byrne, Enda M., Medland, Sarah E., Wray, Naomi R., Chafota, Freddy, Lind, Penelope A., Martin, Nicholas G., Hickie, Ian B., Rentería, Miguel E. and Campos, Adrian I. (2023). Discontinuation of antidepressant treatment: a retrospective cohort study on more than 20,000 participants. Annals of General Psychiatry, 22 (1) 49, 49. doi: 10.1186/s12991-023-00480-z

  • GWAS of Dizygotic Twinning in an Enlarged Australian Sample of Mothers of DZ Twins

    Gordon, Scott D., Duffy, David L., Whiteman, David C., Olsen, Catherine M., McAloney, Kerrie, Adsett, Jessica M., Garden, Natalie A., Cross, Simone M., List-Armitage, Susan E., Brown, Joy, Beck, Jeffrey J., Mbarek, Hamdi, Medland, Sarah E., Montgomery, Grant W. and Martin, Nicholas G. (2023). GWAS of Dizygotic Twinning in an Enlarged Australian Sample of Mothers of DZ Twins. Twin Research and Human Genetics, 26 (6), 1-12. doi: 10.1017/thg.2023.45

  • Counting nevi on the outer arm provides an accurate and feasible alternative to total body nevus count

    Ingold, N., Zhu, G., Duffy, D. L., Mothershaw, A., Martin, N. G., MacGregor, S. and Law, M. H. (2023). Counting nevi on the outer arm provides an accurate and feasible alternative to total body nevus count. Journal of the European Academy of Dermatology and Venereology, 37 (11), e1302-e1304. doi: 10.1111/jdv.19279

  • Preliminary results from the Australian Genetics of Bipolar Disorder Study: A nation-wide cohort

    Lind, Penelope A., Siskind, Dan J., Hickie, Ian B, Colodro-Conde, Lucía, Cross, Simone, Parker, Richard, Martin, Nicholas G. and Medland, Sarah E. (2023). Preliminary results from the Australian Genetics of Bipolar Disorder Study: A nation-wide cohort. Australian and New Zealand Journal of Psychiatry, 57 (11), 1428-1442. doi: 10.1177/00048674231195571

  • Uncovering the complex relationship between balding, testosterone and skin cancers in men

    Ong, Jue-Sheng, Seviiri, Mathias, Dusingize, Jean Claude, Wu, Yeda, Han, Xikun, Shi, Jianxin, Olsen, Catherine M., Neale, Rachel E., Thompson, John F., Saw, Robyn P. M., Shannon, Kerwin F., Mann, Graham J., Martin, Nicholas G., Medland, Sarah E., Gordon, Scott D., Scolyer, Richard A., Long, Georgina V., Iles, Mark M., Landi, Maria Teresa, Whiteman, David C., MacGregor, Stuart and Law, Matthew H. (2023). Uncovering the complex relationship between balding, testosterone and skin cancers in men. Nature Communications, 14 (1) 5962, 1-12. doi: 10.1038/s41467-023-41231-8

  • F34. CHARACTERISING ANTIDEPRESSANT USAGE BASED ON ELECTRONIC PRESCRIPTION RECORDS IN THE AUSTRALIAN GENETICS OF DEPRESSION STUDY

    Mitchell, Brittany, Morosoli, José, Martin, Nicholas G., Lind, Penelope A., Hickie, Ian B., Medland, Sarah E. and Wray, Naomi (2023). F34. CHARACTERISING ANTIDEPRESSANT USAGE BASED ON ELECTRONIC PRESCRIPTION RECORDS IN THE AUSTRALIAN GENETICS OF DEPRESSION STUDY. European Neuropsychopharmacology, 75, S238-S239. doi: 10.1016/j.euroneuro.2023.08.422

  • Genetic determinants of thyroid function in children

    Mulder, Tessa A, Campbell, Purdey J, Taylor, Peter N, Peeters, Robin P, Wilson, Scott G, Medici, Marco, Dayan, Colin, Jaddoe, Vincent V W, Walsh, John P, Martin, Nicholas G, Tiemeier, Henning and Korevaar, Tim I M (2023). Genetic determinants of thyroid function in children. European Journal of Endocrinology, 189 (2), 164-174. doi: 10.1093/ejendo/lvad086

  • The effect of genetic predisposition to Alzheimer’s disease and related traits on recruitment bias in a study of cognitive aging

    Gomez, Lina M., Mitchell, Brittany L., McAloney, Kerrie, Adsett, Jessica, Garden, Natalie, Wood, Madeline, Diaz-Torres, Santiago, Garcia-Marin, Luis M., Breakspear, Michael, Martin, Nicholas G. and Lupton, Michelle K. (2023). The effect of genetic predisposition to Alzheimer’s disease and related traits on recruitment bias in a study of cognitive aging. Twin Research and Human Genetics, 26 (3), 1-6. doi: 10.1017/thg.2023.26

  • GWAs identify DNA variants influencing eyebrow thickness variation in Europeans and across continental populations

    Peng, Fuduan, Xiong, Ziyi, Zhu, Gu, Hysi, Pirro G., Eller, Ryan J., Wu, Sijie, Adhikari, Kaustubh, Chen, Yan, Li, Yi, Gonzalez-José, Rolando, Schüler-Faccini, Lavinia, Bortolini, Maria-Cátira, Acuña-Alonzo, Victor, Canizales-Quinteros, Samuel, Gallo, Carla, Poletti, Giovanni, Bedoya, Gabriel, Rothhammer, Francisco, Uitterlinden, André G., Ikram, M. Arfan, Nijsten, Tamar, Ruiz-Linares, Andrés, Wang, Sijia, Walsh, Susan, Spector, Timothy D., Martin, Nicholas G., Kayser, Manfred and Liu, Fan (2023). GWAs identify DNA variants influencing eyebrow thickness variation in Europeans and across continental populations. Journal of Investigative Dermatology, 143 (7), 1317-1322. doi: 10.1016/j.jid.2022.11.026

  • Rare genetic variants underlie outlying levels of DNA methylation and gene-expression

    Chundru, V. Kartik, Marioni, Riccardo E., Pendergast, James G. D., Lin, Tian, Beveridge, Allan J., Martin, Nicholas G, Montgomery, Grant W., Hume, David A., Deary, Ian J., Visscher, Peter M., Wray, Naomi R. and McRae, Allan F. (2023). Rare genetic variants underlie outlying levels of DNA methylation and gene-expression. Human Molecular Genetics, 32 (11), 1912-1921. doi: 10.1093/hmg/ddad028

  • The association between sleep restlessness and neuroimaging biomarkers of Alzheimer’s Disease in mid‐life to older adults and patients

    Kholghi, Mahnoosh, Fazlollahi, Amir, Lupton, Michelle K, Bourgeat, Pierrick, Zhang, Qing, Martin, Nicholas G, Breakspear, Michael, Fripp, Jurgen and PISA (Prospective Imaging Study of Aging: Genes, Brain and Behaviour) (2023). The association between sleep restlessness and neuroimaging biomarkers of Alzheimer’s Disease in mid‐life to older adults and patients. Alzheimer's & Dementia, 19 (S2). doi: 10.1002/alz.062017

  • Author Correction: The power of genetic diversity in genome-wide association studies of lipids

    Graham, Sarah E., Clarke, Shoa L., Wu, Kuan-Han H., Kanoni, Stavroula, Zajac, Greg J. M., Ramdas, Shweta, Surakka, Ida, Ntalla, Ioanna, Vedantam, Sailaja, Winkler, Thomas W., Locke, Adam E., Marouli, Eirini, Hwang, Mi Yeong, Han, Sohee, Narita, Akira, Choudhury, Ananyo, Bentley, Amy R., Ekoru, Kenneth, Verma, Anurag, Trivedi, Bhavi, Martin, Hilary C., Hunt, Karen A., Hui, Qin, Klarin, Derek, Zhu, Xiang, Thorleifsson, Gudmar, Helgadottir, Anna, Gudbjartsson, Daniel F., Holm, Hilma ... Global Lipids Genetics Consortium (2023). Author Correction: The power of genetic diversity in genome-wide association studies of lipids. Nature, 618 (7965), E19-E20. doi: 10.1038/s41586-023-06194-2

  • Associations between cannabis use, polygenic liability for schizophrenia, and cannabis-related experiences in a sample of cannabis users

    Johnson, Emma C., Colbert, Sarah M.C., Jeffries, Paul W., Tillman, Rebecca, Bigdeli, Tim B., Karcher, Nicole R., Chan, Grace, Kuperman, Samuel, Meyers, Jacquelyn L., Nurnberger, John I., Plawecki, Martin H., Degenhardt, Louisa, Martin, Nicholas G., Kamarajan, Chella, Schuckit, Marc A., Murray, Robin M., Dick, Danielle M., Edenberg, Howard J., D’Souza, Deepak Cyril, Di Forti, Marta, Porjesz, Bernice, Nelson, Elliot C. and Agrawal, Arpana (2023). Associations between cannabis use, polygenic liability for schizophrenia, and cannabis-related experiences in a sample of cannabis users. Schizophrenia Bulletin, 49 (3), 778-787. doi: 10.1093/schbul/sbac196

  • Specificity in genetic and environmental risk for prescription opioid misuse and heroin use

    Dash, Genevieve F., Gizer, Ian R., Martin, Nicholas G. and Slutske, Wendy S. (2023). Specificity in genetic and environmental risk for prescription opioid misuse and heroin use. Psychological Medicine, 107 (2), 6828-6837. doi: 10.1017/s003329172300034x

  • The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions

    Rahmioglu, Nilufer, Mortlock, Sally, Ghiasi, Marzieh, Møller, Peter L., Stefansdottir, Lilja, Galarneau, Geneviève, Turman, Constance, Danning, Rebecca, Law, Matthew H., Sapkota, Yadav, Christofidou, Paraskevi, Skarp, Sini, Giri, Ayush, Banasik, Karina, Krassowski, Michal, Lepamets, Maarja, Marciniak, Błażej, Nõukas, Margit, Perro, Danielle, Sliz, Eeva, Sobalska-Kwapis, Marta, Thorleifsson, Gudmar, Topbas-Selcuki, Nura F., Vitonis, Allison, Westergaard, David, Arnadottir, Ragnheidur, Burgdorf, Kristoffer S., Campbell, Archie, Cheuk, Cecilia S. K. ... The 23andMe Research Team (2023). The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions. Nature Genetics, 55 (3), 423-436. doi: 10.1038/s41588-023-01323-z

  • Discovery of genomic loci associated with sleep apnoea risk through multi-trait GWAS analysis with snoring

    Campos, Adrian I., Ingold, Nathan, Huang, Yunru, Mitchell, Brittany L., Kho, Pik-Fang, Han, Xikun, García-Marín, Luis M., Ong, Jue-Sheng, 23andMe Research Team, Law, Matthew H., Yokoyama, Jennifer S., Martin, Nicholas G., Dong, Xianjun, Cuellar-Partida, Gabriel, MacGregor, Stuart, Aslibekyan, Stella and Rentería, Miguel E. (2023). Discovery of genomic loci associated with sleep apnoea risk through multi-trait GWAS analysis with snoring. Sleep, 46 (3) zsac308, 1-14. doi: 10.1093/sleep/zsac308

  • Genetic risk score for intracranial aneurysms: prediction of subarachnoid hemorrhage and role in clinical heterogeneity

    Bakker, Mark K., Kanning, Jos P., Abraham, Gad, Martinsen, Amy E., Winsvold, Bendik S., Zwart, John-Anker, Bourcier, Romain, Sawada, Tomonobu, Koido, Masaru, Kamatani, Yoichiro, Morel, Sandrine, Amouyel, Philippe, Debette, Stéphanie, Bijlenga, Philippe, Berrandou, Takiy, Ganesh, Santhi K., Bouatia-Naji, Nabila, Jones, Gregory, Bown, Matthew, Rinkel, Gabriel J.E., Veldink, Jan H., Ruigrok, Ynte M., Hege Aamodt, Anne, Heidi Skogholt, Anne, Brumpton, Ben M., Willer, Cristen J., Sandset, Else C., Kristoffersen, Espen S., Ellekjær, Hanne ... International Stroke Genetics Consortium (ISGC) Intracranial Aneurysm Working Group (2023). Genetic risk score for intracranial aneurysms: prediction of subarachnoid hemorrhage and role in clinical heterogeneity. Stroke, 54 (3), 810-818. doi: 10.1161/STROKEAHA.122.040715

  • Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexia

    Doust, Catherine, Fontanillas, Pierre, Eising, Else, Gordon, Scott D., Wang, Zhengjun, Alagöz, Gökberk, Molz, Barbara, Aslibekyan, Stella, Auton, Adam, Babalola, Elizabeth, Bell, Robert K., Bielenberg, Jessica, Bryc, Katarzyna, Bullis, Emily, Coker, Daniella, Partida, Gabriel Cuellar, Dhamija, Devika, Das, Sayantan, Elson, Sarah L., Filshtein, Teresa, Fletez-Brant, Kipper, Freyman, Will, Gandhi, Pooja M., Heilbron, Karl, Hicks, Barry, Hinds, David A., Jewett, Ethan M., Jiang, Yunxuan, Kukar, Katelyn ... Quantitative Trait Working Group of the GenLang Consortium (2023). Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexia. Nature Genetics, 55 (3), 520-520. doi: 10.1038/s41588-023-01336-8

  • Epigenome-wide association study reveals CpG sites associated with thyroid function and regulatory effects on KLF9

    Weihs, Antoine, Chaker, Layal, Martin, Tiphaine Christiane, Braun, Kim V.E., Campbell, Purdey J, Cox, Simon R, Fornage, Myriam, Gieger, Christian, Grabe, Hans J, Grallert, Harald, Harris, Sarah E, Kühnel, Brigitte, Marioni, Riccardo E, Martin, Nicholas G, McCartney, Daniel L, McRae, Allan F, Meisinger, Christa, Meurs, Joyce van, Nano, Jana, Nauck, Matthias, Peters, Annette, Prokisch, Holger, Roden, Michael, Selvin, Elizabeth, Beekman, Marian, van Heemst, Diana, Slagboom, Eline P, Swenson, Brenton R, Tin, Adrienne ... Teumer, Alexander (2023). Epigenome-wide association study reveals CpG sites associated with thyroid function and regulatory effects on KLF9. Thyroid (ja), 301-311. doi: 10.1089/thy.2022.0373

  • Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus

    Mathieson, Iain, Day, Felix R., Barban, Nicola, Tropf, Felix C., Brazel, David M., van Heemst, Diana, Vaez, Ahmad, van Zuydam, Natalie, Bitarello, Bárbara D., Gardner, Eugene J., Akimova, Evelina T., Azad, Ajuna, Bergmann, Sven, Bielak, Lawrence F., Boomsma, Dorret I., Bosak, Kristina, Brumat, Marco, Buring, Julie E., Cesarini, David, Chasman, Daniel I., Chavarro, Jorge E., Cocca, Massimiliano, Concas, Maria Pina, Davey Smith, George, Davies, Gail, Deary, Ian J., Esko, Tõnu, Faul, Jessica D., Franco, Oscar ... Perry, John R. B. (2023). Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus. Nature Human Behaviour, 7 (5), 790-801. doi: 10.1038/s41562-023-01528-6

  • Smoking remains associated with education after controlling for social background and genetic factors in a study of 18 twin cohorts

    Silventoinen, Karri, Piirtola, Maarit, Jelenkovic, Aline, Sund, Reijo, Tarnoki, Adam D., Tarnoki, David L., Medda, Emanuela, Nisticò, Lorenza, Toccaceli, Virgilia, Honda, Chika, Inui, Fujio, Tomizawa, Rie, Watanabe, Mikio, Sakai, Norio, Gatz, Margaret, Butler, David A., Lee, Jooyeon, Lee, Soo Ji, Sung, Joohon, Franz, Carol E., Kremen, William S., Lyons, Michael J., Derom, Catherine A., Vlietinck, Robert F., Loos, Ruth J. F., Tynelius, Per, Rasmussen, Finn, Martin, Nicholas G., Medland, Sarah E. ... Kaprio, Jaakko (2022). Smoking remains associated with education after controlling for social background and genetic factors in a study of 18 twin cohorts. Scientific Reports, 12 (1) 13148, 1-9. doi: 10.1038/s41598-022-17536-x

  • Phenotypic and genetic factors associated with donation of DNA and consent to record linkage for prescription history in the Australian Genetics of Depression Study

    Gomez, Lina, Díaz-Torres, Santiago, Colodro-Conde, Lucía, Garcia-Marin, Luis M., Yap, Chloe X., Byrne, Enda M., Yengo, Loic, Lind, Penelope A., Wray, Naomi R., Medland, Sarah E., Hickie, Ian B., Lupton, Michelle K., Rentería, Miguel E., Martin, Nicholas G. and Campos, Adrian I. (2022). Phenotypic and genetic factors associated with donation of DNA and consent to record linkage for prescription history in the Australian Genetics of Depression Study. European Archives of Psychiatry and Clinical Neuroscience, 273 (6), 1359-1368. doi: 10.1007/s00406-022-01527-0

  • Discovery of 42 genome-wide significant loci associated with dyslexia

    Doust, Catherine, Fontanillas, Pierre, Eising, Else, Gordon, Scott D., Wang, Zhengjun, Alagöz, Gökberk, Molz, Barbara, Aslibekyan, Stella, Auton, Adam, Babalola, Elizabeth, Bell, Robert K., Bielenberg, Jessica, Bryc, Katarzyna, Bullis, Emily, Coker, Daniella, Partida, Gabriel Cuellar, Dhamija, Devika, Das, Sayantan, Elson, Sarah L., Filshtein, Teresa, Fletez-Brant, Kipper, Freyman, Will, Gandhi, Pooja M., Heilbron, Karl, Hicks, Barry, Hinds, David A., Jewett, Ethan M., Jiang, Yunxuan, Kukar, Katelyn ... Quantitative Trait Working Group of the GenLang Consortium (2022). Discovery of 42 genome-wide significant loci associated with dyslexia. Nature Genetics, 54 (11), 1621-1629. doi: 10.1038/s41588-022-01192-y

  • Uncovering the genetic architecture of broad antisocial behavior through a genome-wide association study meta-analysis

    Tielbeek, Jorim J., Uffelmann, Emil, Williams, Benjamin S., Colodro-Conde, Lucía, Gagnon, Éloi, Mallard, Travis T., Levitt, Brandt E., Jansen, Philip R., Johansson, Ada, Sallis, Hannah M., Pistis, Giorgio, Saunders, Gretchen R. B., Allegrini, Andrea G., Rimfeld, Kaili, Konte, Bettina, Klein, Marieke, Hartmann, Annette M., Salvatore, Jessica E., Nolte, Ilja M., Demontis, Ditte, Malmberg, Anni L. K., Burt, S. Alexandra, Savage, Jeanne E., Sugden, Karen, Poulton, Richie, Harris, Kathleen Mullan, Vrieze, Scott, McGue, Matt, Iacono, William G. ... Spit for Science Working Group (2022). Uncovering the genetic architecture of broad antisocial behavior through a genome-wide association study meta-analysis. Molecular Psychiatry, 27 (11), 4453-4463. doi: 10.1038/s41380-022-01793-3

  • Educational attainment polygenic scores: examining evidence for gene–environment interplay with adolescent alcohol, tobacco and cannabis use

    Davis, Christal N., Gizer, Ian R., Colodro-Conde, Lucía, Statham, Dixie J., Martin, Nicholas G. and Slutske, Wendy S. (2022). Educational attainment polygenic scores: examining evidence for gene–environment interplay with adolescent alcohol, tobacco and cannabis use. Twin Research and Human Genetics, 25 (4-5), 187-195. doi: 10.1017/thg.2022.33

  • Common genetic variation and age of onset of anorexia nervosa

    Watson, Hunna J., Thornton, Laura M., Yilmaz, Zeynep, Baker, Jessica H., Coleman, Jonathan R.I., Adan, Roger A.H., Alfredsson, Lars, Andreassen, Ole A., Ask, Helga, Berrettini, Wade H., Boehnke, Michael, Boehm, Ilka, Boni, Claudette, Buehren, Katharina, Bulant, Josef, Burghardt, Roland, Chang, Xiao, Cichon, Sven, Cone, Roger D., Courtet, Philippe, Crow, Scott, Crowley, James J., Danner, Unna N., de Zwaan, Martina, Dedoussis, George, DeSocio, Janiece E., Dick, Danielle M., Dikeos, Dimitris, Dina, Christian ... Bulik, Cynthia M. (2022). Common genetic variation and age of onset of anorexia nervosa. Biological Psychiatry Global Open Science, 2 (4), 368-378. doi: 10.1016/j.bpsgos.2021.09.001

  • Self-reported impact of developmental stuttering across the lifespan

    Boyce, Jessica O., Jackson, Victoria E., van Reyk, Olivia, Parker, Richard, Vogel, Adam P., Eising, Else, Horton, Sarah E., Gillespie, Nathan A., Scheffer, Ingrid E., Amor, David J., Hildebrand, Michael S., Fisher, Simon E., Martin, Nicholas G., Reilly, Sheena, Bahlo, Melanie and Morgan, Angela T. (2022). Self-reported impact of developmental stuttering across the lifespan. Developmental Medicine and Child Neurology, 64 (10), 1297-1306. doi: 10.1111/dmcn.15211

  • Author correction: Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis

    Gallagher, C. S., Mäkinen, N., Harris, H. R., Rahmioglu, N., Uimari, O., Cook, J. P., Shigesi, N., Ferreira, T., Velez-Edwards, D. R., Edwards, T. L., Mortlock, S., Ruhioglu, Z., Day, F., Becker, C. M., Karhunen, V., Martikainen, H., Järvelin, M.-R., Cantor, R. M., Ridker, P. M., Terry, K. L., Buring, J. E., Gordon, S. D., Medland, S. E., Montgomery, G. W., Nyholt, D. R., Hinds, D. A., Tung, J. Y., Agee, Michelle, Alipanahi, Babak ... the 23andMe Research Team (2022). Author correction: Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis. Nature Communications, 13 (1) 5543, 5543. doi: 10.1038/s41467-022-33222-y

  • Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention

    Wang, Zhe, Emmerich, Andrew, Pillon, Nicolas J., Moore, Tim, Hemerich, Daiane, Cornelis, Marilyn C., Mazzaferro, Eugenia, Broos, Siacia, Ahluwalia, Tarunveer S., Bartz, Traci M., Bentley, Amy R., Bielak, Lawrence F., Chong, Mike, Chu, Audrey Y., Berry, Diane, Dorajoo, Rajkumar, Dueker, Nicole D., Kasbohm, Elisa, Feenstra, Bjarke, Feitosa, Mary F., Gieger, Christian, Graff, Mariaelisa, Hall, Leanne M., Haller, Toomas, Hartwig, Fernando P., Hillis, David A., Huikari, Ville, Heard-Costa, Nancy, Holzapfel, Christina ... Lifelines Cohort Study (2022). Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention. Nature Genetics, 54 (9), 1332-1344. doi: 10.1038/s41588-022-01165-1

  • Phenome-wide screening of the putative causal determinants of depression using genetic data

    Aman, Asma M., García-Marín, Luis M., Thorp, Jackson G., Campos, Adrian I., Cuellar-Partida, Gabriel, Martin, Nicholas G.. and Rentería, Miguel E. (2022). Phenome-wide screening of the putative causal determinants of depression using genetic data. Human Molecular Genetics, 31 (17), 2887-2898. doi: 10.1093/hmg/ddac081

  • Polygenic influences associated with adolescent cognitive skills

    Mitchell, Brittany L., Hansell, Narelle K., McAloney, Kerrie, Martin, Nicholas G., Wright, Margaret J., Renteria, Miguel E. and Grasby, Katrina L. (2022). Polygenic influences associated with adolescent cognitive skills. Intelligence, 94 101680, 1-9. doi: 10.1016/j.intell.2022.101680

  • Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people

    Eising, Else, Mirza-Schreiber, Nazanin, de Zeeuw, Eveline L., Wang, Carol A., Truong, Dongnhu T., Allegrini, Andrea G., Shapland, Chin Yang, Zhu, Gu, Wigg, Karen G., Gerritse, Margot L., Molz, Barbara, Alagöz, Gökberk, Gialluisi, Alessandro, Abbondanza, Filippo, Rimfeld, Kaili, van Donkelaar, Marjolein, Liao, Zhijie, Jansen, Philip R., Andlauer, Till F M, Bates, Timothy C., Bernard, Manon, Blokland, Kirsten, Bonte, Milene, Børglum, Anders D., Bourgeron, Thomas, Brandeis, Daniel, Ceroni, Fabiola, Csépe, Valéria, Dale, Philip S. ... Fisher, Simon E. (2022). Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people. Proceedings of the National Academy of Sciences of the United States of America, 119 (35) e2202764119, 1-12. doi: 10.1073/pnas.2202764119

  • Changing genetic architecture of body mass index from infancy to early adulthood: an individual based pooled analysis of 25 twin cohorts

    Silventoinen, Karri, Li, Weilong, Jelenkovic, Aline, Sund, Reijo, Yokoyama, Yoshie, Aaltonen, Sari, Piirtola, Maarit, Sugawara, Masumi, Tanaka, Mami, Matsumoto, Satoko, Baker, Laura A., Tuvblad, Catherine, Tynelius, Per, Rasmussen, Finn, Craig, Jeffrey M., Saffery, Richard, Willemsen, Gonneke, Bartels, Meike, van Beijsterveldt, Catharina E. M., Martin, Nicholas G., Medland, Sarah E., Montgomery, Grant W., Lichtenstein, Paul, Krueger, Robert F., McGue, Matt, Pahlen, Shandell, Christensen, Kaare, Skytthe, Axel, Kyvik, Kirsten O. ... Kaprio, Jaakko (2022). Changing genetic architecture of body mass index from infancy to early adulthood: an individual based pooled analysis of 25 twin cohorts. International Journal of Obesity, 46 (10), 1901-1909. doi: 10.1038/s41366-022-01202-3

  • Exploring the clinical and genetic associations of adult weight trajectories using electronic health records in a racially diverse biobank: a phenome-wide and polygenic risk study

    Xu, Jiayi, Johnson, Jessica S., Signer, Rebecca, Eating Disorders Working Group of the Psychiatric Genomics Consortium, Birgegård, Andreas, Jordan, Jennifer, Kennedy, Martin A., Landén, Mikael, Maguire, Sarah L., Martin, Nicholas G., Mortensen, Preben Bo, Petersen, Liselotte V., Thornton, Laura M., Bulik, Cynthia M. and Huckins, Laura M. (2022). Exploring the clinical and genetic associations of adult weight trajectories using electronic health records in a racially diverse biobank: a phenome-wide and polygenic risk study. The Lancet Digital Health, 4 (8), e604-e614. doi: 10.1016/S2589-7500(22)00099-1

  • Clinical, demographic, and genetic risk factors of treatment‐attributed suicidality in >10,000 Australian adults taking antidepressants

    Campos, Adrian I., Byrne, Enda M., Iorfino, Frank, Fabbri, Chiara, Hickie, Ian B., Lewis, Cathryn M., Wray, Naomi R., Medland, Sarah E., Rentería, Miguel E. and Martin, Nicholas G. (2022). Clinical, demographic, and genetic risk factors of treatment‐attributed suicidality in >10,000 Australian adults taking antidepressants. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 189 (6), 196-206. doi: 10.1002/ajmg.b.32913

  • Co-inheritance of variation in all-cause mortality and biochemical risk factors

    Whitfield, John B., Colodro-Conde, Lucía, Zhu, Gu, Timmers, Paul R. H. J., Joshi, Peter K., Montgomery, Grant W. and Martin, Nicholas G (2022). Co-inheritance of variation in all-cause mortality and biochemical risk factors. Twin Research and Human Genetics, 25 (3), 1-8. doi: 10.1017/thg.2022.25

  • Genetic specificity of hippocampal subfield volumes, relative to hippocampal formation, identified in 2148 young adult twins and siblings

    Hansell, Narelle K., Strike, Lachlan T., van Eijk, Liza, O'Callaghan, Victoria, Martin, Nicholas G., de Zubicaray, Greig I., Thompson, Paul M., McMahon, Katie L. and Wright, Margaret J. (2022). Genetic specificity of hippocampal subfield volumes, relative to hippocampal formation, identified in 2148 young adult twins and siblings. Twin Research and Human Genetics, 25 (3), 129-139. doi: 10.1017/thg.2022.20

  • Lifetime prevalence and correlates of perinatal depression in a case-cohort study of depression

    Kiewa, Jacqueline, Meltzer-Brody, Samantha, Milgrom, Jeannette, Bennett, Elizabeth, Mackle, Tracey, Guintivano, Jerry, Hickie, Ian B, Colodro-Conde, Lucia, Medland, Sarah E, Martin, Nick, Wray, Naomi and Byrne, Enda (2022). Lifetime prevalence and correlates of perinatal depression in a case-cohort study of depression. BMJ Open, 12 (8) e059300, 1-7. doi: 10.1136/bmjopen-2021-059300

  • Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals

    Winkler, Thomas W., Rasheed, Humaira, Teumer, Alexander, Gorski, Mathias, Rowan, Bryce X., Stanzick, Kira J., Thomas, Laurent F., Tin, Adrienne, Hoppmann, Anselm, Chu, Audrey Y., Tayo, Bamidele, Thio, Chris H. L., Cusi, Daniele, Chai, Jin-Fang, Sieber, Karsten B., Horn, Katrin, Li, Man, Scholz, Markus, Cocca, Massimiliano, Wuttke, Matthias, van der Most, Peter J., Yang, Qiong, Ghasemi, Sahar, Nutile, Teresa, Li, Yong, Pontali, Giulia, Günther, Felix, Dehghan, Abbas, Correa, Adolfo ... VA Million Veteran Program (2022). Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals. Communications Biology, 5 (1) 580, 1-20. doi: 10.1038/s42003-022-03448-z

  • Dynamic networks of psychological symptoms, impairment, substance use, and social support: the evolution of psychopathology among emerging adults

    Crouse, Jacob J., Ho, Nicholas, Scott, Jan, Parker, Richard, Park, Shin Ho, Couvy-Duchesne, Baptiste, Mitchell, Brittany, Byrne, Enda M., Hermens, Daniel F., Medland, Sarah E., Martin, Nicholas G., Gillespie, Nathan A. and Hickie, Ian B. (2022). Dynamic networks of psychological symptoms, impairment, substance use, and social support: the evolution of psychopathology among emerging adults. European Psychiatry, 65 (1) e32, 1-24. doi: 10.1192/j.eurpsy.2022.23

  • The heritability of twinning in seven large historic pedigrees

    Duffy, David L. and Martin, Nicholas G. (2022). The heritability of twinning in seven large historic pedigrees. Twin Research and Human Genetics, 25 (2), 1-4. doi: 10.1017/thg.2022.14

  • Lindon Eaves: a personal memoir

    Martin, Nick (2022). Lindon Eaves: a personal memoir. Twin Research and Human Genetics, 25 (2), 97-100. doi: 10.1017/thg.2022.13

  • Mapping anorexia nervosa genes to clinical phenotypes

    Johnson, Jessica S., Cote, Alanna C., Dobbyn, Amanda, Sloofman, Laura G., Xu, Jiayi, Cotter, Liam, Charney, Alexander W., Birgegård, Andreas, Jordan, Jennifer, Kennedy, Martin, Landén, Mikaél, Maguire, Sarah L., Martin, Nicholas G., Mortensen, Preben Bo, Thornton, Laura M., Bulik, Cynthia M., Huckins, Laura M. and Eating Disorders Working Group of the Psychiatric Genomics Consortium (2022). Mapping anorexia nervosa genes to clinical phenotypes. Psychological Medicine, 53 (6), 1-15. doi: 10.1017/s0033291721004554

  • Childhood maltreatment and disordered gambling in adulthood: Disentangling causal and familial influences

    Dash, Genevieve F., Martin, Nicholas G. and Slutske, Wendy S. (2022). Childhood maltreatment and disordered gambling in adulthood: Disentangling causal and familial influences. Psychological Medicine, 52 (5), 1-10. doi: 10.1017/S0033291720002743

  • Enhancing discovery of genetic variants for PTSD through integration of quantitative phenotypes and trauma exposure information

    Maihofer, Adam X., Choi, Karmel W., Coleman, Jonathan R. I., Daskalakis, Nikolaos P., Denckla, Christy A., Ketema, Elizabeth, Morey, Rajendra A., Polimanti, Renato, Ratanatharathorn, Andrew, Torres, Katy, Wingo, Aliza P., Zai, Clement C., Aiello, Allison E., Almli, Lynn M., Amstadter, Ananda B., Andersen, Soren B., Andreassen, Ole A., Arbisi, Paul A., Ashley-Koch, Allison E., Austin, S. Bryn, Avdibegovic, Esmina, Borglum, Anders D., Babic, Dragan, Bμkvad-Hansen, Marie, Baker, Dewleen G., Beckham, Jean C., Bierut, Laura J., Bisson, Jonathan I., Boks, Marco P. ... Nievergelt, Caroline M. (2022). Enhancing discovery of genetic variants for PTSD through integration of quantitative phenotypes and trauma exposure information. Biological Psychiatry, 91 (7), 626-636. doi: 10.1016/j.biopsych.2021.09.020

  • Perinatal depression is associated with a higher polygenic risk for major depressive disorder than non-perinatal depression

    Kiewa, Jacqueline, Meltzer‐Brody, Samantha, Milgrom, Jeanette, Guintivano, Jerry, Hickie, Ian B., Whiteman, David C., Olsen, Catherine M., Colodro‐Conde, Lucía, Medland, Sarah E., Martin, Nicholas G., Wray, Naomi R. and Byrne, Enda M. (2022). Perinatal depression is associated with a higher polygenic risk for major depressive disorder than non-perinatal depression. Depression and Anxiety, 39 (3), 182-191. doi: 10.1002/da.23232

  • Shared genetic etiology between cortical brain morphology and tobacco, alcohol, and cannabis use

    Rabinowitz, Jill A., Campos, Adrian I., Ong, Jue-Sheng, García-Marín, Luis M., Alcauter, Sarael, Mitchell, Brittany L, Grasby, Katrina L, Cuéllar-Partida, Gabriel, Gillespie, Nathan A, Huhn, Andrew S, Martin, Nicholas G, Thompson, Paul M, Medland, Sarah E, Maher, Brion S and Rentería, Miguel E (2022). Shared genetic etiology between cortical brain morphology and tobacco, alcohol, and cannabis use. Cerebral Cortex, 32 (4), 796-807. doi: 10.1093/cercor/bhab243

  • Financial strain moderates genetic influences on self-rated health: support for diathesis–stress model of gene–environment interplay

    Finkel, Deborah, Zavala, Catalina, Franz, Carol E., Pahlen, Shandell, Gatz, Margaret, Pedersen, Nancy L., Finch, Brian K., Dahl Aslan, Anna, Catts, Vibeke S., Ericsson, Malin, Krueger, Robert F., Martin, Nicholas G., Mohan, Adith, Mosing, Miriam A., Prescott, Carol A. and Whitfield, Keith E. (2022). Financial strain moderates genetic influences on self-rated health: support for diathesis–stress model of gene–environment interplay. Biodemography and Social Biology, 67 (1), 1-13. doi: 10.1080/19485565.2022.2037069

  • Genome-wide association meta-analysis identifies 29 new acne susceptibility loci

    Mitchell, Brittany L., Saklatvala, Jake R., Dand, Nick, Hagenbeek, Fiona A., Li, Xin, Min, Josine L., Thomas, Laurent, Bartels, Meike, Jan Hottenga, Jouke, Lupton, Michelle K., Boomsma, Dorret I., Dong, Xianjun, Hveem, Kristian, Løset, Mari, Martin, Nicholas G., Barker, Jonathan N., Han, Jiali, Smith, Catherine H., Rentería, Miguel E. and Simpson, Michael A. (2022). Genome-wide association meta-analysis identifies 29 new acne susceptibility loci. Nature Communications, 13 (1) 702, 702. doi: 10.1038/s41467-022-28252-5

  • Australian Parkinson’s Genetics Study (APGS): pilot (n=1532)

    Bivol, Svetlana, Mellick, George D., Gratten, Jacob, Parker, Richard, Mulcahy, Aoibhe, Mosley, Philip E., Poortvliet, Peter C., Campos, Adrian I., Mitchell, Brittany L., Garcia-Marin, Luis M., Cross, Simone, Ferguson, Mary, Lind, Penelope A., Loesch, Danuta Z., Visscher, Peter M., Medland, Sarah E., Scherzer, Clemens R., Martin, Nicholas G. and Rentería, Miguel E. (2022). Australian Parkinson’s Genetics Study (APGS): pilot (n=1532). BMJ Open, 12 (2) e052032, e052032. doi: 10.1136/bmjopen-2021-052032

  • Early effects of amyloid-β on structural and vascular brain changes in mid-life cognitively unimpaired individuals

    Fazlollahi, Amir, Xia, Ying, Lupton, Michelle K., Raniga, Parnesh, Bourgeat, Pierrick, Martin, Nick, Dore, Vincent, Rose, Stephen, Salvado, Olivier, Breakspear, Michael and Fripp, Jurgen (2022). Early effects of amyloid-β on structural and vascular brain changes in mid-life cognitively unimpaired individuals. Alzheimer's and dementia : the journal of the Alzheimer's Association, 17, 1-3. doi: 10.1002/alz.052681

  • Impact of CYP2C19 metaboliser status on SSRI response: a retrospective study of 9500 participants of the Australian Genetics of Depression Study

    Campos, Adrian I., Byrne, Enda M., Mitchell, Brittany L., Wray, Naomi R., Lind, Penelope A., Licinio, Julio, Medland, Sarah E., Martin, Nicholas G., Hickie, Ian B. and Rentería, Miguel E. (2022). Impact of CYP2C19 metaboliser status on SSRI response: a retrospective study of 9500 participants of the Australian Genetics of Depression Study. The Pharmacogenomics Journal, 22 (2), 130-135. doi: 10.1038/s41397-022-00267-7

  • Limb development genes underlie variation in human fingerprint patterns

    Li, Jinxi, Glover, James D., Zhang, Haiguo, Peng, Meifang, Tan, Jingze, Mallick, Chandana Basu, Hou, Dan, Yang, Yajun, Wu, Sijie, Liu, Yu, Peng, Qianqian, Zheng, Shijie C., Crosse, Edie I., Medvinsky, Alexander, Anderson, Richard A., Brown, Helen, Yuan, Ziyu, Zhou, Shen, Xu, Yanqing, Kemp, John P., Ho, Yvonne Y.W., Loesch, Danuta Z., Wang, Lizhong, Li, Yingxiang, Tang, Senwei, Wu, Xiaoli, Walters, Robin G., Lin, Kuang, Meng, Ruogu ... Wang, Sijia (2022). Limb development genes underlie variation in human fingerprint patterns. Cell, 185 (1), 95-112.e18. doi: 10.1016/j.cell.2021.12.008

  • An Epidemiologic, Longitudinal, and Discordant-Twin Study of the Association Between Gambling Disorder and Suicidal Behaviors

    Slutske, Wendy S., Davis, Christal N., Lynskey, Michael T., Heath, Andrew C. and Martin, Nicholas G. (2022). An Epidemiologic, Longitudinal, and Discordant-Twin Study of the Association Between Gambling Disorder and Suicidal Behaviors. Clinical Psychological Science, 10 (5), 901-919. doi: 10.1177/21677026211062599

  • The power of genetic diversity in genome-wide association studies of lipids

    Graham, Sarah E., Clarke, Shoa L., Wu, Kuan-Han H., Kanoni, Stavroula, Zajac, Greg J. M., Ramdas, Shweta, Surakka, Ida, Ntalla, Ioanna, Vedantam, Sailaja, Winkler, Thomas W., Locke, Adam E., Marouli, Eirini, Hwang, Mi Yeong, Han, Sohee, Narita, Akira, Choudhury, Ananyo, Bentley, Amy R., Ekoru, Kenneth, Verma, Anurag, Trivedi, Bhavi, Martin, Hilary C., Hunt, Karen A., Hui, Qin, Klarin, Derek, Zhu, Xiang, Thorleifsson, Gudmar, Helgadottir, Anna, Gudbjartsson, Daniel F., Holm, Hilma ... Global Lipids Genetics Consortium* (2021). The power of genetic diversity in genome-wide association studies of lipids. Nature, 600 (7890), 675-679. doi: 10.1038/s41586-021-04064-3

  • Potential genetic overlap between insomnia and sleep symptoms in major depressive disorder: a polygenic risk score analysis

    Melhuish Beaupre, Lindsay M., Tiwari, Arun K., Gonçalves, Vanessa F., Zai, Clement C., Marshe, Victoria S., Lewis, Cathryn M., Martin, Nicholas G., McIntosh, Andrew M., Adams, Mark J., Baune, Bernhard T., Levinson, Doug F., Boomsma, Dorret I., Penninx, Brenda W. J. H., Breen, Gerome, Hamilton, Steve, Awasthi, Swapnil, Ripke, Stephan, Jones, Lisa, Jones, Ian, Byrne, Enda M., Hickie, Ian B., Potash, James P., Shi, Jianxin, Weissman, Myrna M., Milaneschi, Yuri, Shyn, Stanley I., Geus, Eco J. C. de, Willemsen, Gonneke, Brown, Gregory M. and Kennedy, James L. (2021). Potential genetic overlap between insomnia and sleep symptoms in major depressive disorder: a polygenic risk score analysis. Frontiers in Psychiatry, 12 734077, 734077. doi: 10.3389/fpsyt.2021.734077

  • Author Correction: Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder (Nature Communications, (2021), 12, 1, (576), 10.1038/s41467-020-20443-2)

    Demontis, Ditte, Walters, Raymond K., Rajagopal, Veera M., Waldman, Irwin D., Grove, Jakob, Als, Thomas D., Dalsgaard, Søren, Ribasés, Marta, Bybjerg-Grauholm, Jonas, Bækvad-Hansen, Maria, Werge, Thomas, Nordentoft, Merete, Mors, Ole, Mortensen, Preben Bo, Andreassen, Ole A., Arranz, Maria Jesús, Banaschewski, Tobias, Bau, Claiton, Bellgrove, Mark, Biederman, Joseph, Brikell, Isabell, Buitelaar, Jan K., Burton, Christie L., Casas, Miguel, Crosbie, Jennifer, Doyle, Alysa E., Ebstein, Richard P., Elia, Josephine, Elizabeth, Corfield C. ... Børglum, Anders D. (2021). Author Correction: Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder (Nature Communications, (2021), 12, 1, (576), 10.1038/s41467-020-20443-2). Nature Communications, 12 (1) 1166. doi: 10.1038/s41467-021-21566-w

  • Phenome-wide analysis highlights putative causal relationships between self-reported migraine and other complex traits

    García-Marín, Luis M., Campos, Adrián I., Martin, Nicholas G., Cuéllar-Partida, Gabriel and Rentería, Miguel E. (2021). Phenome-wide analysis highlights putative causal relationships between self-reported migraine and other complex traits. Journal of Headache and Pain, 22 (1) 66, 66. doi: 10.1186/s10194-021-01284-w

  • Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder

    Demontis, Ditte, Walters, Raymond K., Rajagopal, Veera M., Waldman, Irwin D., Grove, Jakob, Als, Thomas D., Dalsgaard, Søren, Ribasas, Marta, Bybjerg-Grauholm, Jonas, Bækvad-Hansen, Maria, Werge, Thomas, Nordentoft, Merete, Mors, Ole, Mortensen, Preben Bo, Andreassen, Ole A., Arranz, Maria Jesús, Banaschewski, Tobias, Bau, Claiton, Bellgrove, Mark, Biederman, Joseph, Brikell, Isabell, Buitelaar, Jan K., Burton, Christie L., Casas, Miguel, Crosbie, Jennifer, Doyle, Alysa E., Ebstein, Richard P., Elia, Josephine, Elizabeth, Corfield C. ... ADHD Working Group of the Psychiatric Genomics Consortium (PGC) (2021). Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder. Nature Communications, 12 (1) 576. doi: 10.1038/s41467-020-20443-2

  • The Eating Disorders Genetics Initiative (EDGI): study protocol

    Bulik, Cynthia M., Thornton, Laura M., Parker, Richard, Kennedy, Hannah, Baker, Jessica H., MacDermod, Casey, Guintivano, Jerry, Cleland, Lana, Miller, Allison L., Harper, Lauren, Larsen, Janne T., Yilmaz, Zeynep, Grove, Jakob, Sullivan, Patrick F., Petersen, Liselotte V., Jordan, Jennifer, Kennedy, Martin A. and Martin, Nicholas G. (2021). The Eating Disorders Genetics Initiative (EDGI): study protocol. BMC Psychiatry, 21 (1) 234. doi: 10.1186/s12888-021-03212-3

  • Big Five personality traits and illicit drug use: Specificity in trait–drug associations

    Dash, Genevieve F., Martin, Nicholas G. and Slutske, Wendy S. (2021). Big Five personality traits and illicit drug use: Specificity in trait–drug associations. Psychology of Addictive Behaviors, 37 (2), 318-330. doi: 10.1037/adb0000793

  • Understanding genetic risk factors for common side effects of antidepressant medications

    Campos, Adrian I., Mulcahy, Aoibhe, Thorp, Jackson G., Wray, Naomi R., Byrne, Enda M., Lind, Penelope A., Medland, Sarah E., Martin, Nicholas G., Hickie, Ian B. and Rentería, Miguel E. (2021). Understanding genetic risk factors for common side effects of antidepressant medications. Communications Medicine, 1 (1) 45, 1-10. doi: 10.1038/s43856-021-00046-8

  • Associations between the CADM2 gene, substance use, risky sexual behavior, and self-control: A phenome-wide association study

    Arends, Rachel M., Pasman, Joëlle A., Verweij, Karin J.H., Derks, Eske M., Gordon, Scott D., Hickie, Ian, Thomas, Nathaniel S., Aliev, Fazil, Zietsch, Brendan P., van der Zee, Matthijs D., Mitchell, Brittany L., Martin, Nicholas G., Dick, Danielle M., Gillespie, Nathan A., de Geus, Eco J.C., Boomsma, Dorret I., Schellekens, Arnt F.A. and Vink, Jacqueline M. (2021). Associations between the CADM2 gene, substance use, risky sexual behavior, and self-control: A phenome-wide association study. Addiction Biology, 26 (6) e13015, e13015. doi: 10.1111/adb.13015

  • Genome-wide analysis of thyroid function in Australian adolescents highlights SERPINA7 and NCOA3

    Nolan, James, Campbell, Purdey J, Brown, Suzanne J, Zhu, Gu, Gordon, Scott, Lim, Ee Mun, Joseph, John, Cross, Simone M, Panicker, Vijay, Medland, Sarah E, Melton, Phillip E, Beilin, Lawrence J, Mori, Trevor A, Mullin, Benjamin H, Pennell, Craig E, Wang, Carol A, Dudbridge, Frank, Walsh, John P, Martin, Nicholas G and Wilson, Scott G (2021). Genome-wide analysis of thyroid function in Australian adolescents highlights SERPINA7 and NCOA3. European Journal of Endocrinology, 185 (5), 743-753. doi: 10.1530/EJE-21-0614

  • The Australian Genetics of Depression Study: new risk loci and dissecting heterogeneity between subtypes

    Mitchell, Brittany L., Campos, Adrian I., Whiteman, David C., Olsen, Catherine M., Gordon, Scott D., Walker, Adam J., Dean, Olivia M., Berk, Michael, Hickie, Ian B., Medland, Sarah E., Wray, Naomi R., Martin, Nicholas G. and Byrne, Enda M. (2021). The Australian Genetics of Depression Study: new risk loci and dissecting heterogeneity between subtypes. Biological Psychiatry, 92 (3), 227-235. doi: 10.1016/j.biopsych.2021.10.021

  • Genetic and environmental influences on perceived social support: differences by sex and relationship

    Coventry, William L., Gillespie, Nathan A., Heath, Andrew C. and Martin, Nicholas G. (2021). Genetic and environmental influences on perceived social support: differences by sex and relationship. Twin Research and Human Genetics, 24 (5), 251-263. doi: 10.1017/thg.2021.43

  • Genetic and environmental influences on sleep-wake behaviours in adolescence

    O'Callaghan, Victoria S., Hansell, Narelle K., Guo, Wei, Carpenter, Joanne S., Shou, Haochang, Strike, Lachlan T., Crouse, Jacob J., McAloney, Kerrie, McMahon, Katie L., Byrne, Enda M., Burns, Jane M., Martin, Nicholas G., Hickie, Ian B., Merikangas, Kathleen R. and Wright, Margaret J. (2021). Genetic and environmental influences on sleep-wake behaviours in adolescence. Sleep Advances, 2 (1) zpab018, zpab018. doi: 10.1093/sleepadvances/zpab018

  • Association and genetic overlap between clinical chemistry tests and migraine

    Tanha, Hamzeh M, Martin, Nicholas G, Whitfield, John B, Nyholt, Dale R, Gormley, Padhraig, Anttila, Verneri, Winsvold, Bendik S, Palta, Priit, Esko, Tonu, Pers, Tune H, Farh, Kai-How, Cuenca-Leon, Ester, Muona, Mikko, Furlotte, Nicholas A, Kurth, Tobias, Ingason, Andres, McMahon, George, Ligthart, Lannie, Terwindt, Gisela M, Kallela, Mikko, Freilinger, Tobias M, Ran, Caroline, Gordon, Scott G, Stam, Anine H, Steinberg, Stacy, Borck, Guntram, Koiranen, Markku, Quaye, Lydia, Adams, Hieab H H ... Palotie, Aarno (2021). Association and genetic overlap between clinical chemistry tests and migraine. Cephalalgia, 41 (11-12), 1208-1221. doi: 10.1177/03331024211018131

  • Genetic correlation analysis does not associate male pattern baldness with COVID-19

    Tanha, Hamzeh M., Medland, Sarah, Martin, Nicholas G. and Nyholt, Dale R. (2021). Genetic correlation analysis does not associate male pattern baldness with COVID-19. Journal of the American Academy of Dermatology, 85 (4), 971-973. doi: 10.1016/j.jaad.2021.05.009

  • Genetic meta-analysis of twin birth weight shows high genetic correlation with singleton birth weight

    Beck, Jeffrey J., Pool, René, Van De Weijer, Margot, Chen, Xu, Krapohl, Eva, Gordon, Scott D., Nygaard, Marianne, Debrabant, Birgit, Palviainen, Teemu, Van Der Zee, Matthijs D., Baselmans, Bart, Finnicum, Casey T., Yi, Lu, Lundström, Sebastian, Van Beijsterveldt, Toos, Christiansen, Lene, Heikkilä, Kauko, Kittelsrud, Julie, Loukola, Anu, Ollikainen, Miina, Christensen, Kaare, Martin, Nicholas G., Plomin, Robert, Nivard, Michel, Bartels, Meike, Dolan, Conor, Willemsen, Gonneke, De Geus, Eco, Almqvist, Catarina ... Hottenga, Jouke-Jan (2021). Genetic meta-analysis of twin birth weight shows high genetic correlation with singleton birth weight. Human Molecular Genetics, 30 (19), 1894-1905. doi: 10.1093/hmg/ddab121

  • Identical twins carry a persistent epigenetic signature of early genome programming

    van Dongen, Jenny, Gordon, Scott D., McRae, Allan F., Odintsova, Veronika V., Mbarek, Hamdi, Breeze, Charles E., Sugden, Karen, Lundgren, Sara, Castillo-Fernandez, Juan E., Hannon, Eilis, Moffitt, Terrie E., Hagenbeek, Fiona A., van Beijsterveldt, Catharina E. M., Jan Hottenga, Jouke, Tsai, Pei-Chien, van Dongen, Jenny, Hottenga, Jouke-Jan, McRae, Allan F., Sugden, Karen, Castillo-Fernandez, Juan E., Hannon, Eilis, Moffitt, Terrie E., Hottenga, Jouke-Jan, de Geus, Eco J. C., Spector, Timothy D., Min, Josine L., Hemani, Gibran, Ehli, Erik A., Paul, Franziska ... Genetics of DNA Methylation Consortium (2021). Identical twins carry a persistent epigenetic signature of early genome programming. Nature Communications, 12 (1) 5618, 5618. doi: 10.1038/s41467-021-25583-7

  • Examining sex differences in neurodevelopmental and psychiatric genetic risk in anxiety and depression

    Martin, Joanna, Asjadi, Kimiya, Hubbard, Leon, Kendall, Kimberley, Pardiñas, Antonio F., Jermy, Bradley, Lewis, Cathryn M., Baune, Bernhard T., Boomsma, Dorret I., Hamilton, Steven P., Lucae, Susanne, Magnusson, Patrik K., Martin, Nicholas G., McIntosh, Andrew M., Mehta, Divya, Mors, Ole, Mullins, Niamh, Penninx, Brenda W. J. H., Preisig, Martin, Rietschel, Marcella, Jones, Ian, Walters, James T. R., Rice, Frances, Thapar, Anita, O’Donovan, Michael and Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium (2021). Examining sex differences in neurodevelopmental and psychiatric genetic risk in anxiety and depression. PLoS One, 16 (9) e0248254, e0248254. doi: 10.1371/journal.pone.0248254

  • Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation

    Min, Josine L., Hemani, Gibran, Hannon, Eilis, Dekkers, Koen F., Castillo-Fernandez, Juan, Luijk, René, Carnero-Montoro, Elena, Lawson, Daniel J., Burrows, Kimberley, Suderman, Matthew, Bretherick, Andrew D., Richardson, Tom G., Klughammer, Johanna, Iotchkova, Valentina, Sharp, Gemma, Al Khleifat, Ahmad, Shatunov, Aleksey, Iacoangeli, Alfredo, McArdle, Wendy L., Ho, Karen M., Kumar, Ashish, Söderhäll, Cilla, Soriano-Tárraga, Carolina, Giralt-Steinhauer, Eva, Kazmi, Nabila, Mason, Dan, McRae, Allan F., Corcoran, David L., Sugden, Karen ... BIOS Consortium (2021). Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation. Nature Genetics, 53 (9), 1311-1321. doi: 10.1038/s41588-021-00923-x

  • Neuropeptide S receptor 1 is a nonhormonal treatment target in endometriosis

    Tapmeier, Thomas T., Rahmioglu, Nilufer, Lin, Jianghai, De Leo, Bianca, Obendorf, Maik, Raveendran, Muthuswamy, Fischer, Oliver M., Bafligil, Cemsel, Guo, Manman, Harris, Ronald Alan, Hess-Stumpp, Holger, Laux-Biehlmann, Alexis, Lowy, Ernesto, Lunter, Gerton, Malzahn, Jessica, Martin, Nicholas G., Martinez, Fernando O., Manek, Sanjiv, Mesch, Stefanie, Montgomery, Grant W., Morris, Andrew P., Nagel, Jens, Simmons, Heather A., Brocklebank, Denise, Shang, Catherine, Treloar, Susan, Wells, Graham, Becker, Christian M., Oppermann, Udo ... Zondervan, Krina T. (2021). Neuropeptide S receptor 1 is a nonhormonal treatment target in endometriosis. Science Translational Medicine, 13 (608) eabd6469, 1-12. doi: 10.1126/scitranslmed.abd6469

  • Phantom epistasis between unlinked loci

    Hemani, Gibran, Powell, Joseph E., Wang, Huanwei, Shakhbazov, Konstantin, Westra, Harm-Jan, Esko, Tonu, Henders, Anjali K., McRae, Allan F., Martin, Nicholas G., Metspalu, Andres, Franke, Lude, Montgomery, Grant W., Goddard, Michael E., Gibson, Greg, Yang, Jian and Visscher, Peter M. (2021). Phantom epistasis between unlinked loci. Nature, 596 (7871), E1-E3. doi: 10.1038/s41586-021-03765-z

  • Polygenic risk scores derived from varying definitions of depression and risk of depression

    Mitchell, Brittany L., Thorp, Jackson G., Wu, Yeda, Campos, Adrian I., Nyholt, Dale R., Gordon, Scott D., Whiteman, David C., Olsen, Catherine M., Hickie, Ian B., Martin, Nicholas G., Medland, Sarah E., Wray, Naomi R. and Byrne, Enda M. (2021). Polygenic risk scores derived from varying definitions of depression and risk of depression. JAMA Psychiatry, 78 (10), 1152-1160. doi: 10.1001/jamapsychiatry.2021.1988

  • Genetic insights into biological mechanisms governing human ovarian ageing

    Ruth, Katherine S., Day, Felix R., Hussain, Jazib, Martínez-Marchal, Ana, Aiken, Catherine E., Azad, Ajuna, Thompson, Deborah J., Knoblochova, Lucie, Abe, Hironori, Tarry-Adkins, Jane L., Gonzalez, Javier Martin, Fontanillas, Pierre, Claringbould, Annique, Bakker, Olivier B., Sulem, Patrick, Walters, Robin G., Terao, Chikashi, Turon, Sandra, Horikoshi, Momoko, Lin, Kuang, Onland-Moret, N. Charlotte, Sankar, Aditya, Hertz, Emil Peter Thrane, Timshel, Pascal N., Shukla, Vallari, Borup, Rehannah, Olsen, Kristina W., Aguilera, Paula, Ferrer-Roda, Mònica ... Perry, John R. B. (2021). Genetic insights into biological mechanisms governing human ovarian ageing. Nature, 596 (7872), 393-397. doi: 10.1038/s41586-021-03779-7

  • Genetic susceptibility to pneumonia: a GWAS meta-analysis between the UK Biobank and FinnGen

    Campos, Adrian I., Kho, Pik, Vazquez-Prada, Karla X., García-Marín, Luis M., Martin, Nicholas G., Cuéllar-Partida, Gabriel and Rentería, Miguel E. (2021). Genetic susceptibility to pneumonia: a GWAS meta-analysis between the UK Biobank and FinnGen. Twin Research and Human Genetics, 24 (3), 145-154. doi: 10.1017/thg.2021.27

  • Genetic association study of childhood aggression across raters, instruments, and age

    Ip, Hill F., van der Laan, Camiel M., Krapohl, Eva M. L., Brikell, Isabell, Sánchez-Mora, Cristina, Nolte, Ilja M., St Pourcain, Beate, Bolhuis, Koen, Palviainen, Teemu, Zafarmand, Hadi, Colodro-Conde, Lucía, Gordon, Scott, Zayats, Tetyana, Aliev, Fazil, Jiang, Chang, Wang, Carol A., Saunders, Gretchen, Karhunen, Ville, Hammerschlag, Anke R., Adkins, Daniel E., Border, Richard, Peterson, Roseann E., Prinz, Joseph A., Thiering, Elisabeth, Seppälä, Ilkka, Vilor-Tejedor, Natàlia, Ahluwalia, Tarunveer S., Day, Felix R., Hottenga, Jouke-Jan ... Boomsma, Dorret I. (2021). Genetic association study of childhood aggression across raters, instruments, and age. Translational Psychiatry, 11 (1) 413, 413. doi: 10.1038/s41398-021-01480-x

  • Genetic risk for chronic pain is associated with lower antidepressant effectiveness: converging evidence for a depression subtype

    Campos, Adrián I., Ngo, Trung Thanh, Medland, Sarah E., Wray, Naomi R., Hickie, Ian B., Byrne, Enda M., Martin, Nicholas G. and Rentería, Miguel E. (2021). Genetic risk for chronic pain is associated with lower antidepressant effectiveness: converging evidence for a depression subtype. Australian and New Zealand Journal of Psychiatry, 56 (9) ARTN 00048674211031491, 1-10. doi: 10.1177/00048674211031491

  • Ethnic Identity and Genome Wide Runs of Homozygosity

    Fieder, Martin, Mitchell, Brittany L., Gordon, Scott, Huber, Susanne and Martin, Nicholas G. (2021). Ethnic Identity and Genome Wide Runs of Homozygosity. Behavior Genetics, 51 (4), 405-413. doi: 10.1007/s10519-021-10053-z

  • Using monozygotic twins to dissect common genes in posttraumatic stress disorder and migraine

    Bainomugisa, Charlotte K., Sutherland, Heidi G., Parker, Richard, Mcrae, Allan F., Haupt, Larisa M., Griffiths, Lyn R., Heath, Andrew, Nelson, Elliot C., Wright, Margaret J., Hickie, Ian B., Martin, Nicholas G., Nyholt, Dale R. and Mehta, Divya (2021). Using monozygotic twins to dissect common genes in posttraumatic stress disorder and migraine. Frontiers in Neuroscience, 15 678350, 678350. doi: 10.3389/fnins.2021.678350

  • Early expressions of psychopathology and risk associated with trans-diagnostic transition to mood and psychotic disorders in adolescents and young adults

    Scott, Jan, Crouse, Jacob J., Ho, Nicholas, Iorfino, Frank, Martin, Nicholas, Parker, Richard, McGrath, John, Gillespie, Nathan A., Medland, Sarah and Hickie, Ian B. (2021). Early expressions of psychopathology and risk associated with trans-diagnostic transition to mood and psychotic disorders in adolescents and young adults. PLoS ONE, 16 (6 June) e0252550, 1-17. doi: 10.1371/journal.pone.0252550

  • Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology

    Mullins, Niamh, Forstner, Andreas J., O'Connell, Kevin S., Coombes, Brandon, Coleman, Jonathan R I, Qiao, Zhen, Als, Thomas D., Bigdeli, Tim B., Børte, Sigrid, Bryois, Julien, Charney, Alexander W., Drange, Ole Kristian, Gandal, Michael J., Hagenaars, Saskia P., Ikeda, Masashi, Kamitaki, Nolan, Kim, Minsoo, Krebs, Kristi, Panagiotaropoulou, Georgia, Schilder, Brian M., Sloofman, Laura G., Steinberg, Stacy, Trubetskoy, Vassily, Winsvold, Bendik S., Won, Hong-Hee, Abramova, Liliya, Adorjan, Kristina, Agerbo, Esben, Al Eissa, Mariam ... Andreassen, Ole A. (2021). Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology. Nature genetics, 53 (6), 817-829. doi: 10.1038/s41588-021-00857-4

  • Phenome-wide screening of GWAS data reveals the complex causal architecture of obesity

    García-Marín, Luis M., Campos, Adrián I., Kho, Pik-Fang, Martin, Nicholas G., Cuéllar-Partida, Gabriel and Rentería, Miguel E. (2021). Phenome-wide screening of GWAS data reveals the complex causal architecture of obesity. Human Genetics, 140 (8), 1253-1265. doi: 10.1007/s00439-021-02298-9

  • Correction to: The augmented Classical Twin Design: incorporating genome‐wide identity by descent sharing into twin studies in order to model violations of the equal environments assumption

    Hwang, Liang-Dar, Mitchell, Brittany L., Medland, Sarah E., Martin, Nicholas G., Neale, Michael C. and Evans, David M. (2021). Correction to: The augmented Classical Twin Design: incorporating genome‐wide identity by descent sharing into twin studies in order to model violations of the equal environments assumption. Behavior Genetics, 51 (4), 441-442. doi: 10.1007/s10519-021-10065-9

  • Days out of role and somatic, anxious-depressive, hypo-manic, and psychotic-like symptom dimensions in a community sample of young adults

    Crouse, Jacob J., Ho, Nicholas, Scott, Jan, Martin, Nicholas G., Couvy-Duchesne, Baptiste, Hermens, Daniel F., Parker, Richard, Gillespie, Nathan A., Medland, Sarah E. and Hickie, Ian B. (2021). Days out of role and somatic, anxious-depressive, hypo-manic, and psychotic-like symptom dimensions in a community sample of young adults. Translational Psychiatry, 11 (1) 285, 285. doi: 10.1038/s41398-021-01390-y

  • The association between genetically determined ABO blood types and major depressive disorder

    Garvert, Linda, Baune, Bernhard T, Berger, Klaus, Boomsma, Dorret I, Breen, Gerome, Greinacher, Andreas, Hamilton, Steven P, Levinson, Douglas F, Lewis, Cathryn M, Lucae, Susanne, Magnusson, Patrik K E, Martin, Nicholas G, McIntosh, Andrew M, Mors, Ole, Müller-Myhsok, Bertram, Penninx, Brenda W J H, Perlis, Roy H, Pistis, Giorgio, Potash, James B, Preisig, Martin, Rietschel, Marcella, Shi, Jianxin, Smoller, Jordan W, Tiemeier, Henning, Uher, Rudolf, Völker, Uwe, Völzke, Henry, Weissman, Myrna M, Grabe, Hans J and Van der Auwera, Sandra (2021). The association between genetically determined ABO blood types and major depressive disorder. Psychiatry Research, 299 113837, 113837. doi: 10.1016/j.psychres.2021.113837

  • Typologies of illicit drug use in mid-adulthood: a quasi-longitudinal latent class analysis in a community-based sample of twins

    Dash, Genevieve F., Martin, Nicholas G., Agrawal, Arpana, Lynskey, Michael T. and Slutske, Wendy S. (2021). Typologies of illicit drug use in mid-adulthood: a quasi-longitudinal latent class analysis in a community-based sample of twins. Addiction, 116 (5), 1101-1112. doi: 10.1111/add.15225

  • Epigenome-wide association study of thyroid function traits identifies novel associations of fT3 with KLF9 and DOT1L

    Lafontaine, Nicole, Campbell, Purdey J., Castillo-Fernandez, Juan E., Mullin, Shelby, Lim, Ee Mun, Kendrew, Phillip, Lewer, Michelle, Brown, Suzanne J., Huang, Rae-Chi, Melton, Phillip E., Mori, Trevor A., Beilin, Lawrence J., Dudbridge, Frank, Spector, Tim D., Wright, Margaret J., Martin, Nicholas G., McRae, Allan F., Panicker, Vijay, Zhu, Gu, Walsh, John P., Bell, Jordana T. and Wilson, Scott G. (2021). Epigenome-wide association study of thyroid function traits identifies novel associations of fT3 with KLF9 and DOT1L. The Journal of Clinical Endocrinology and Metabolism, 106 (5), e2191-e2202. doi: 10.1210/clinem/dgaa975

  • Symptom-level modelling unravels the shared genetic architecture of anxiety and depression

    Thorp, Jackson G., Campos, Adrian I., Grotzinger, Andrew D., Gerring, Zachary F., An, Jiyuan, Ong, Jue-Sheng, Wang, Wei, Shringarpure, Suyash, Byrne, Enda M., MacGregor, Stuart, Martin, Nicholas G., Medland, Sarah E., Middeldorp, Christel M. and Derks, Eske M. (2021). Symptom-level modelling unravels the shared genetic architecture of anxiety and depression. Nature Human Behaviour, 5 (10), 1432-1442. doi: 10.1038/s41562-021-01094-9

  • Comorbid chronic pain and depression: shared risk factors and differential antidepressant effectiveness

    Roughan, William H., Campos, Adrián I., García-Marín, Luis M., Cuéllar-Partida, Gabriel, Lupton, Michelle K., Hickie, Ian B., Medland, Sarah E., Wray, Naomi R., Byrne, Enda M., Ngo, Trung Thanh, Martin, Nicholas G. and Rentería, Miguel E. (2021). Comorbid chronic pain and depression: shared risk factors and differential antidepressant effectiveness. Frontiers in Psychiatry, 12 643609, 1-13. doi: 10.3389/fpsyt.2021.643609

  • 'Essential Tremor' Phenotype in FMR1 Premutation/Gray Zone Sibling Series: Exploring Possible Genetic Modifiers

    Loesch, Danuta Z., Duffy, David L., Martin, Nicholas G., Tassone, Flora, Atkinson, Anna and Storey, Elsdon (2021). 'Essential Tremor' Phenotype in FMR1 Premutation/Gray Zone Sibling Series: Exploring Possible Genetic Modifiers. Twin Research and Human Genetics, 24 (2), 95-102. doi: 10.1017/thg.2021.10

  • Brain correlates of suicide attempt in 18,925 participants across 18 international cohorts

    Campos, Adrian I., Thompson, Paul M., Veltman, Dick J., Pozzi, Elena, van Veltzen, Laura S., Jahanshad, Neda, Adams, Mark J., Baune, Bernhard T., Berger, Klaus, Brosch, Katharina, Bülow, Robin, Connolly, Colm G., Dannlowski, Udo, Davey, Christopher G., de Zubicaray, Greig I., Dima, Danai, Erwin-Grabner, Tracy, Evans, Jennifer W., Fu, Cynthia H.Y., Gotlib, Ian H., Goya-Maldonado, Roberto, Grabe, Hans J., Grotegerd, Dominik, Harris, Matthew A., Harrison, Ben J., Hatton, Sean N., Hermesdorf, Marco, Hickie, Ian B., Ho, Tiffany C. ... Rentería, Miguel E. (2021). Brain correlates of suicide attempt in 18,925 participants across 18 international cohorts. Biological Psychiatry, 90 (4), 243-252. doi: 10.1016/j.biopsych.2021.03.015

  • Genome-wide association study in almost 195,000 individuals identifies 50 previously unidentified genetic loci for eye color

    Simcoe, Mark, Valdes, Ana, Liu, Fan, Furlotte, Nicholas A., Evans, David M., Hemani, Gibran, Ring, Susan M., Smith, George Davey, Duffy, David L., Zhu, Gu, Gordon, Scott D., Medland, Sarah E., Vuckovic, Dragana, Girotto, Giorgia, Sala, Cinzia, Catamo, Eulalia, Concas, Maria Pina, Brumat, Marco, Gasparini, Paolo, Toniolo, Daniela, Cocca, Massimiliano, Robino, Antonietta, Yazar, Seyhan, Hewitt, Alex, Wu, Wenting, Kraft, Peter, Hammond, Christopher J., Shi, Yuan, Chen, Yan ... the International Visible Trait Genetics Consortium (2021). Genome-wide association study in almost 195,000 individuals identifies 50 previously unidentified genetic loci for eye color. Science Advances, 7 (11) abd1239, eabd1239. doi: 10.1126/sciadv.abd1239

  • Genome-wide association study of phenotypes measuring progression from first cocaine or opioid use to dependence reveals novel risk genes

    Sherva, Richard, Zhu, Congcong, Wetherill, Leah, Edenberg, Howard J., Johnson, Emma, Degenhardt, Louisa, Agrawal, Arpana, Martin, Nicholas G., Nelson, Elliot, Kranzler, Henry R., Gelernter, Joel and Farrer, Lindsay A. (2021). Genome-wide association study of phenotypes measuring progression from first cocaine or opioid use to dependence reveals novel risk genes. Exploration of Medicine, 2 (1), 60-73. doi: 10.37349/emed.2021.00032

  • Can network analysis of self-reported psychopathology shed light on the core phenomenology of bipolar disorders in adolescents and young adults?

    Scott, Jan, Crouse, Jacob J., Ho, Nicholas, Carpenter, Joanne, Martin, Nicholas, Medland, Sarah, Parker, Richard, Byrne, Enda, Couvy-Duchesne, Baptiste, Mitchell, Brittany, Merikangas, Kathleen, Gillespie, Nathan A. and Hickie, Ian (2021). Can network analysis of self-reported psychopathology shed light on the core phenomenology of bipolar disorders in adolescents and young adults?. Bipolar Disorders, 23 (6), 584-594. doi: 10.1111/bdi.13067

  • Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries

    Gharahkhani, Puya, NEIGHBORHOOD consortium, Jorgenson, Eric, Hysi, Pirro, Khawaja, Anthony P., Pendergrass, Sarah, Han, Xikun, Ong, Jue Sheng, Hewitt, Alex W., Segrè, Ayellet V., Rouhana, John M., Hamel, Andrew R., Igo, Robert P., Choquet, Helene, Qassim, Ayub, Josyula, Navya S., Cooke Bailey, Jessica N., Bonnemaijer, Pieter W. M., Iglesias, Adriana, Siggs, Owen M., Young, Terri L., Vitart, Veronique, Thiadens, Alberta A. H. J., Karjalainen, Juha, Uebe, Steffen, Melles, Ronald B., Nair, K. Saidas, Luben, Robert, Simcoe, Mark ... 23 and Me Research Team (2021). Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries. Nature Communications, 12 (1) 1258, 1-16. doi: 10.1038/s41467-020-20851-4

  • Cortical thickness across the lifespan: Data from 17,075 healthy individuals aged 3-90 years

    Frangou, Sophia, Modabbernia, Amirhossein, Williams, Steven C. R., Papachristou, Efstathios, Doucet, Gaelle E., Agartz, Ingrid, Aghajani, Moji, Akudjedu, Theophilus N., Albajes-Eizagirre, Anton, Alnaes, Dag, Alpert, Kathryn I, Andersson, Micael, Andreasen, Nancy C, Andreassen, Ole A, Asherson, Philip, Banaschewski, Tobias, Bargallo, Nuria, Baumeister, Sarah, Baur-Streubel, Ramona, Bertolino, Alessandro, Bonvino, Aurora, Boomsma, Dorret I, Borgwardt, Stefan, Bourque, Josiane, Brandeis, Daniel, Breier, Alan, Brodaty, Henry, Brouwer, Rachel M, Buitelaar, Jan K ... Dima, Danai (2021). Cortical thickness across the lifespan: Data from 17,075 healthy individuals aged 3-90 years. Human Brain Mapping, 43 (1) hbm.25364, 431-451. doi: 10.1002/hbm.25364

  • The augmented Classical Twin Design: incorporating genome‐wide identity by descent sharing into twin studies in order to model violations of the equal environments assumption

    Hwang, Liang-Dar, Mitchell, Brittany L., Medland, Sarah E., Martin, Nicholas G., Neale, Michael C. and Evans, David M. (2021). The augmented Classical Twin Design: incorporating genome‐wide identity by descent sharing into twin studies in order to model violations of the equal environments assumption. Behavior Genetics, 51 (3), 223-236. doi: 10.1007/s10519-021-10044-0

  • Subcortical volumes across the lifespan: Data from 18,605 healthy individuals aged 3-90 years

    Dima, Danai, Modabbernia, Amirhossein, Papachristou, Efstathios, Doucet, Gaelle E., Agartz, Ingrid, Aghajani, Moji, Akudjedu, Theophilus N., Albajes-Eizagirre, Anton, Alnaes, Dag, Alpert, Kathryn I., Andersson, Micael, Andreasen, Nancy C., Andreassen, Ole A., Asherson, Philip, Banaschewski, Tobias, Bargallo, Nuria, Baumeister, Sarah, Baur-Streubel, Ramona, Bertolino, Alessandro, Bonvino, Aurora, Boomsma, Dorret I., Borgwardt, Stefan, Bourque, Josiane, Brandeis, Daniel, Breier, Alan, Brodaty, Henry, Brouwer, Rachel M., Buitelaar, Jan K., Busatto, Geraldo F. ... Karolinska Schizophrenia Project (KaSP) (2021). Subcortical volumes across the lifespan: Data from 18,605 healthy individuals aged 3-90 years. Human Brain Mapping, 43 (1) hbm.25320, 452-469. doi: 10.1002/hbm.25320

  • 16Up: Outline of a study investigating wellbeing and information and communication technology use in adolescent twins

    Mitchell, Brittany L., Kirk, Katherine M., McAloney, Kerrie, Wright, Margaret J., Davenport, Tracey A., Hermens, Daniel F., Scott, James G., McGrath, John J., Gillespie, Nathan A., Carpenter, Joanne S., O’Callaghan, Victoria S., Medland, Sarah, Christensen, Helen, Martin, Nicholas G., Burns, Jane M. and Hickie, Ian B. (2021). 16Up: Outline of a study investigating wellbeing and information and communication technology use in adolescent twins. Twin Research and Human Genetics, 23 (6), 1-13. doi: 10.1017/thg.2020.83

  • Comparison of Familial, Polygenic and Biochemical Predictors of Mortality

    Whitfield, John B., Colodro-Conde, Lucía, Timmers, Paul R. H. J., Joshi, Peter K., Montgomery, Grant W. and Martin, Nicholas G. (2021). Comparison of Familial, Polygenic and Biochemical Predictors of Mortality. Twin Research and Human Genetics, 23 (6), 307-315. doi: 10.1017/thg.2020.89

  • Are prescription misuse and illicit drug use etiologically distinct? A genetically-informed analysis of opioids and stimulants

    Dash, Genevieve F., Martin, Nicholas G., Agrawal, Arpana, Lynskey, Michael T. and Slutske, Wendy S. (2021). Are prescription misuse and illicit drug use etiologically distinct? A genetically-informed analysis of opioids and stimulants. Psychological Medicine, 52 (14), 3176-3183. doi: 10.1017/S0033291720005267

  • Examining the Vanishing Twin Hypothesis of Neural Tube Defects: Application of an Epigenetic Predictor for Monozygotic Twinning

    Van Dongen, Jenny, Gordon, Scott D., Odintsova, Veronika V., McRae, Allan F., Robinson, Wendy P., Hall, Judith G., Boomsma, Dorret I. and Martin, Nicholas G. (2021). Examining the Vanishing Twin Hypothesis of Neural Tube Defects: Application of an Epigenetic Predictor for Monozygotic Twinning. Twin Research and Human Genetics, 24 (3), 155-159. doi: 10.1017/thg.2021.25

  • Inference of causal relationships between sleep-related traits and 1,527 phenotypes using genetic data

    García-Marín, Luis M., Campos, Adrián I., Martin, Nicholas G., Cuéllar-Partida, Gabriel and Rentería, Miguel E. (2021). Inference of causal relationships between sleep-related traits and 1,527 phenotypes using genetic data. Sleep, 44 (1) zsaa154. doi: 10.1093/sleep/zsaa154

  • Polygenic Risk Scores have high diagnostic capacity in ankylosing spondylitis

    Li, Zhixiu, Wu, Xin, Leo, Paul J., De Guzman, Erika, Akkoc, Nurullah, Breban, Maxime, MacFarlane, Gary J., Mahmoudi, Mahdi, Marzo-Ortega, Helena, Anderson, Lisa K., Wheeler, Lawrie, Chou, Chung-Tei, Harrison, Andrew A., Stebbings, Simon, Jones, Gareth T., Bang, So-Young, Wang, Geng, Jamshidi, Ahmadreza, Farhadi, Elham, Song, Jing, Lin, Li, Li, Mengmeng, Wei, James Cheng-Chung, Martin, Nicholas G., Wright, Margaret J., Lee, MinJae, Wang, Yuqin, Zhan, Jian, Zhang, Jin-San ... Brown, Matthew A (2021). Polygenic Risk Scores have high diagnostic capacity in ankylosing spondylitis. Annals of the Rheumatic Diseases, 80 (9) annrheumdis-2020- 219446, annrheumdis-2020. doi: 10.1136/annrheumdis-2020-219446

  • Ten years of enhancing neuro-imaging genetics through meta-analysis: an overview from the ENIGMA Genetics Working Group

    Medland, Sarah E., Grasby, Katrina L., Jahanshad, Neda, Painter, Jodie N., Colodro-Conde, Lucía, Bralten, Janita, Hibar, Derrek P., Lind, Penelope A., Pizzagalli, Fabrizio, Thomopoulos, Sophia I., Stein, Jason L., Franke, Barbara, Martin, Nicholas G. and Thompson, Paul M. (2020). Ten years of enhancing neuro-imaging genetics through meta-analysis: an overview from the ENIGMA Genetics Working Group. Human Brain Mapping, 43 (1), 292-299. doi: 10.1002/hbm.25311

  • A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine

    Guo, Yanjun, Rist, Pamela M., Daghlas, Iyas, Giulianini, Franco, Gormley, Padhraig, Anttila, Verneri, Winsvold, Bendik S., Palta, Priit, Esko, Tonu, Pers, Tune H., Farh, Kai-How, Cuenca-Leon, Ester, Muona, Mikko, Furlotte, Nicholas A., Kurth, Tobias, Ingason, Andres, McMahon, George, Ligthart, Lannie, Terwindt, Gisela M., Kallela, Mikko, Freilinger, Tobias M., Ran, Caroline, Gordon, Scott G., Stam, Anine H., Steinberg, Stacy, Borck, Guntram, Koiranen, Markku, Quaye, Lydia, Adams, Hieab H. H. ... Chasman, Daniel I. (2020). A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine. Nature Communications, 11 (1) 3368. doi: 10.1038/s41467-020-17002-0

  • A prospective cohort study of prodromal Alzheimer’s disease: Prospective Imaging Study of Ageing: genes, brain and behaviour (PISA)

    Lupton, Michelle K., Robinson, Gail A., Adam, Robert J, Rose, Stephen, Byrne, Gerard J., Salvado, Olivier, Pachana, Nancy A., Almeida, Osvaldo P., McAloney, Kerrie, Gordon, Scott D., Raniga, Parnesh, Fazlollahi, Amir, Xia, Ying, Ceslis, Amelia, Sonkusare, Saurabh, Zhang, Qing, Kholghi, Mahnoosh, Karunanithi, Mohan, Mosley, Philip E., Lv, Jinglei, Borne, Léonie, Adsett, Jessica, Garden, Natalie, Fripp, Jurgen, Martin, Nicholas G., Guo, Christine C. and Breakspear, Michael (2020). A prospective cohort study of prodromal Alzheimer’s disease: Prospective Imaging Study of Ageing: genes, brain and behaviour (PISA). NeuroImage: Clinical, 29 102527, 102527. doi: 10.1016/j.nicl.2020.102527

  • Genetic and environmental variation in educational attainment: an individual-based analysis of 28 twin cohorts

    Silventoinen, Karri, Jelenkovic, Aline, Sund, Reijo, Latvala, Antti, Honda, Chika, Inui, Fujio, Tomizawa, Rie, Watanabe, Mikio, Sakai, Norio, Rebato, Esther, Busjahn, Andreas, Tyler, Jessica, Hopper, John L., Ordoñana, Juan R., Sánchez-Romera, Juan F., Colodro-Conde, Lucia, Calais-Ferreira, Lucas, Oliveira, Vinicius C., Ferreira, Paulo H., Medda, Emanuela, Nisticò, Lorenza, Toccaceli, Virgilia, Derom, Catherine A., Vlietinck, Robert F., Loos, Ruth J. F., Siribaddana, Sisira H., Hotopf, Matthew, Sumathipala, Athula, Rijsdijk, Fruhling ... Kaprio, Jaakko (2020). Genetic and environmental variation in educational attainment: an individual-based analysis of 28 twin cohorts. Scientific Reports, 10 (1) 12681, 12681. doi: 10.1038/s41598-020-69526-6

  • Pessimism is associated with greater all-cause and cardiovascular mortality, but optimism is not protective

    Whitfield, John B., Zhu, Gu, Landers, J. George and Martin, Nicholas G. (2020). Pessimism is associated with greater all-cause and cardiovascular mortality, but optimism is not protective. Scientific Reports, 10 (1) 12609, 1-7. doi: 10.1038/s41598-020-69388-y

  • The genetic architecture of sporadic and multiple consecutive miscarriage

    Laisk, Triin, Soares, Ana Luiza G., Ferreira, Teresa, Painter, Jodie N., Censin, Jenny C., Laber, Samantha, Bacelis, Jonas, Chen, Chia-Yen, Lepamets, Maarja, Lin, Kuang, Liu, Siyang, Millwood, Iona Y., Ramu, Avinash, Southcombe, Jennifer, Andersen, Marianne S., Yang, Ling, Becker, Christian M., Børglum, Anders D., Gordon, Scott D., Bybjerg-Grauholm, Jonas, Helgeland, Øyvind, Hougaard, David M., Jin, Xin, Johansson, Stefan, Juodakis, Julius, Kartsonaki, Christiana, Kukushkina, Viktorija, Lind, Penelope A., Metspalu, Andres ... Lindgren, Cecilia M. (2020). The genetic architecture of sporadic and multiple consecutive miscarriage. Nature Communications, 11 (1) 5980, 1-12. doi: 10.1038/s41467-020-19742-5

  • High-throughput phenotyping of soybean maturity using time series UAV imagery and convolutional neural networks

    Trevisan, Rodrigo, Pérez, Osvaldo, Schmitz, Nathan, Diers, Brian and Martin, Nicolas (2020). High-throughput phenotyping of soybean maturity using time series UAV imagery and convolutional neural networks. Remote Sensing, 12 (21) 3617, 1-19. doi: 10.3390/rs12213617

  • The role of locus of control in adulthood outcomes: Evidence from Australian twins

    Xue, Sen, Kidd, Michael P., Le, Anh.T., Kirk, Kathy and Martin, Nicholas G. (2020). The role of locus of control in adulthood outcomes: Evidence from Australian twins. Journal of Economic Behavior and Organization, 179, 566-588. doi: 10.1016/j.jebo.2020.09.018

  • Comparison of genome-wide association scans for quantitative and observational measures of human hair curvature

    Ho, Yvonne Y. W., Mina-Vargas, Angela, Zhu, Gu, Brims, Mark, Mcnevin, Dennis, Montgomery, Grant W., Martin, Nicholas G., Medland, Sarah E. and Painter, Jodie N. (2020). Comparison of genome-wide association scans for quantitative and observational measures of human hair curvature. Twin Research and Human Genetics, 23 (5), 271-277. doi: 10.1017/thg.2020.78

  • Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci

    Erzurumluoglu, A. Mesut, Liu, Mengzhen, Jackson, Victoria E., Barnes, Daniel R., Datta, Gargi, Melbourne, Carl A., Young, Robin, Batini, Chiara, Surendran, Praveen, Jiang, Tao, Adnan, Sheikh Daud, Afaq, Saima, Agrawal, Arpana, Altmaier, Elisabeth, Antoniou, Antonis C., Asselbergs, Folkert W., Baumbach, Clemens, Bierut, Laura, Bertelsen, Sarah, Boehnke, Michael, Bots, Michiel L., Brazel, David M, Chambers, John C., Chang-Claude, Jenny, Chen, Chu, Corley, Janie, Chou, Yi-Ling, David, Sean P., de Boer, Rudolf A. ... CHD Exome+ consortium (2020). Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci. Molecular Psychiatry, 25 (10), 2392-2409. doi: 10.1038/s41380-018-0313-0

  • Sex differences in the relative influence of marital status and parenthood on alcohol use disorder symptoms: a multilevel discordant twin design

    Dash, Genevieve F., Martin, Nicholas G., Lynskey, Michael T. and Slutske, Wendy S. (2020). Sex differences in the relative influence of marital status and parenthood on alcohol use disorder symptoms: a multilevel discordant twin design. Journal of Abnormal Psychology, 129 (7), 737-747. doi: 10.1037/abn0000611

  • Genome-wide association study identifies 48 common genetic variants associated with handedness

    Cuellar-Partida, Gabriel, Tung, Joyce Y., Eriksson, Nicholas, Albrecht, Eva, Aliev, Fazil, Andreassen, Ole A., Barroso, Inês, Beckmann, Jacques S., Boks, Marco P., Boomsma, Dorret I., Boyd, Heather A., Breteler, Monique M. B., Campbell, Harry, Chasman, Daniel I., Cherkas, Lynn F., Davies, Gail, de Geus, Eco J. C., Deary, Ian J., Deloukas, Panos, Dick, Danielle M., Duffy, David L., Eriksson, Johan G., Esko, Tõnu, Feenstra, Bjarke, Geller, Frank, Gieger, Christian, Giegling, Ina, Gordon, Scott D., Han, Jiali ... Medland, Sarah E. (2020). Genome-wide association study identifies 48 common genetic variants associated with handedness. Nature Human Behaviour, 5 (1), 59-70. doi: 10.1038/s41562-020-00956-y

  • The reliability and heritability of cortical folds and their genetic correlations across hemispheres

    Pizzagalli, Fabrizio, Auzias, Guillaume, Yang, Qifan, Mathias, Samuel R., Faskowitz, Joshua, Boyd, Joshua D., Amini, Armand, Rivière, Denis, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Mangin, Jean-François, Glahn, David C., Blangero, John, Wright, Margaret J., Thompson, Paul M., Kochunov, Peter and Jahanshad, Neda (2020). The reliability and heritability of cortical folds and their genetic correlations across hemispheres. Communications Biology, 3 (1) 510, 510. doi: 10.1038/s42003-020-01163-1

  • Genetic and environmental causes of individual differences in borderline personality disorder features and loneliness are partially shared

    Schermer, Julie Aitken, Colodro-Conde, Lucía, Grasby, Katrina L., Hickie, Ian B., Burns, Jane, Ligthart, Lannie, Willemsen, Gonneke, Trull, Timothy J., Martin, Nicholas G. and Boomsma, Dorret I. (2020). Genetic and environmental causes of individual differences in borderline personality disorder features and loneliness are partially shared. Twin Research and Human Genetics, 23 (4), 214-220. doi: 10.1017/thg.2020.62

  • Septic shock: a genomewide association study and polygenic risk score analysis

    D'Urso, Shannon, Rajbhandari, Dorrilyn, Peach, Elizabeth, De Guzman, Erika, Li, Qiang, Medland, Sarah E., Gordon, Scott D., Martin, Nicholas G., Ligthart, Symen, Brown, Matthew A., Powell, Joseph, McArthur, Colin, Rhodes, Andrew, Meyer, Jason, Finfer, Simon, Myburgh, John, Blumenthal, Antje, Cohen, Jeremy, Venkatesh, Balasubramanian, Cuellar-Partida, Gabriel and Evans, David M. (2020). Septic shock: a genomewide association study and polygenic risk score analysis. Twin Research and Human Genetics, 23 (4), 204-213. doi: 10.1017/thg.2020.60

  • Genetic comorbidity between major depression and cardio‐metabolic traits, stratified by age at onset of major depression

    Hagenaars, Saskia P., Coleman, Jonathan R. I., Choi, Shing Wan, Gaspar, Héléna, Adams, Mark J., Howard, David M., Hodgson, Karen, Traylor, Matthew, Air, Tracy M., Andlauer, Till F. M., Arolt, Volker, Baune, Bernhard T., Binder, Elisabeth B., Blackwood, Douglas H. R., Boomsma, Dorret I., Campbell, Archie, Cearns, Micah, Czamara, Darina, Dannlowski, Udo, Domschke, Katharina, de Geus, Eco J. C., Hamilton, Steven P., Hayward, Caroline, Hickie, Ian B., Hottenga, Jouke Jan, Ising, Marcus, Jones, Ian, Jones, Lisa, Kutalik, Zoltan ... Lewis, Cathryn M. (2020). Genetic comorbidity between major depression and cardio‐metabolic traits, stratified by age at onset of major depression. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 183 (6) ajmg.b.32807, 309-330. doi: 10.1002/ajmg.b.32807

  • Genetic aetiology of self-harm ideation and behaviour

    Campos, Adrian I., Verweij, Karin J. H., Statham, Dixie J., Madden, Pamela A. F., Maciejewski, Dominique F., Davis, Katrina A. S., John, Ann, Hotopf, Matthew, Heath, Andrew C., Martin, Nicholas G. and Rentería, Miguel E. (2020). Genetic aetiology of self-harm ideation and behaviour. Scientific Reports, 10 (1) 9713, 9713. doi: 10.1038/s41598-020-66737-9

  • Cohort profile: the Australian genetics of depression study

    Byrne, Enda M., Kirk, Katherine M., Medland, Sarah E., McGrath, John J., Colodro-Conde, Lucia, Parker, Richard, Cross, Simone, Sullivan, Lenore, Statham, Dixie J., Levinson, Douglas F., Licinio, Julio, Wray, Naomi R, Hickie, Ian B. and Martin, Nicholas G. (2020). Cohort profile: the Australian genetics of depression study. BMJ Open, 10 (5) e032580, e032580. doi: 10.1136/bmjopen-2019-032580

  • Single cell transcriptomics reveals opioid usage evokes widespread suppression of antiviral gene program

    Karagiannis, Tanya T., Cleary, John P., Gok, Busra, Henderson, Andrew J., Martin, Nicholas G., Yajima, Masanao, Nelson, Elliot C. and Cheng, Christine S. (2020). Single cell transcriptomics reveals opioid usage evokes widespread suppression of antiviral gene program. Nature Communications, 11 (1) 2611, 2611. doi: 10.1038/s41467-020-16159-y

  • Educational attainment polygenic scores are associated with cortical total surface area and regions important for language and memory

    Mitchell, Brittany L., Cuéllar-Partida, Gabriel, Grasby, Katrina L., Campos, Adrian I., Strike, Lachlan T., Hwang, Liang-Dar, Okbay, Aysu, Thompson, Paul M., Medland, Sarah E., Martin, Nicholas G., Wright, Margaret J. and Rentería, Miguel E. (2020). Educational attainment polygenic scores are associated with cortical total surface area and regions important for language and memory. NeuroImage, 212 116691, 116691. doi: 10.1016/j.neuroimage.2020.116691

  • Investigating the genetic and causal relationship between initiation or use of alcohol, caffeine, cannabis and nicotine

    Chang, Lun-Hsien, Ong, Jue-Sheng, An, Jiyuan, Verweij, Karin J.H., Vink, Jacqueline M., Pasman, Joëlle, Liu, Mengzhen, MacGregor, Stuart, Cornelis, Marilyn C., Martin, Nicholas G. and Derks, Eske M. (2020). Investigating the genetic and causal relationship between initiation or use of alcohol, caffeine, cannabis and nicotine. Drug and Alcohol Dependence, 210 107966, 107966. doi: 10.1016/j.drugalcdep.2020.107966

  • Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility

    Landi, Maria Teresa, GenoMEL Consortium, Bishop, D. Timothy, MacGregor, Stuart, Machiela, Mitchell J., Stratigos, Alexander J., Ghiorzo, Paola, Brossard, Myriam, Calista, Donato, Choi, Jiyeon, Fargnoli, Maria Concetta, Zhang, Tongwu, Rodolfo, Monica, Trower, Adam J., Menin, Chiara, Martinez, Jacobo, Hadjisavvas, Andreas, Song, Lei, Stefanaki, Irene, Scolyer, Richard, Yang, Rose, Goldstein, Alisa M., Potrony, Miriam, Kypreou, Katerina P., Pastorino, Lorenza, Queirolo, Paola, Pellegrini, Cristina, Cattaneo, Laura, Zawistowski, Matthew ... MelaNostrum Consortium (2020). Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility. Nature Genetics, 52 (5), 494-504. doi: 10.1038/s41588-020-0611-8

  • Genome-wide association study identifies 143 loci associated with 25 hydroxyvitamin D concentration

    Revez, Joana A., Lin, Tian, Qiao, Zhen, Xue, Angli, Holtz, Yan, Zhu, Zhihong, Zeng, Jian, Wang, Huanwei, Sidorenko, Julia, Kemper, Kathryn E., Vinkhuyzen, Anna A. E., Frater, Julanne, Eyles, Darryl, Burne, Thomas H. J., Mitchell, Brittany, Martin, Nicholas G., Zhu, Gu, Visscher, Peter M., Yang, Jian, Wray, Naomi R. and McGrath, John J. (2020). Genome-wide association study identifies 143 loci associated with 25 hydroxyvitamin D concentration. Nature Communications, 11 (1) 1647, 1-12. doi: 10.1038/s41467-020-15421-7

  • Changes in thyroid function across adolescence: a longitudinal study

    Campbell, Purdey J., Brown, Suzanne J., Kendrew, Phillip, Lewer, Michelle, Lim, Ee Mun, Joseph, John, Cross, Simone M., Wright, Margaret J., Martin, Nicholas G., Wilson, Scott G. and Walsh, John P. (2020). Changes in thyroid function across adolescence: a longitudinal study. The Journal of Clinical Endocrinology and Metabolism, 105 (4), e1162-e1170. doi: 10.1210/clinem/dgz331

  • Minimal phenotyping yields genome-wide association signals of low specificity for major depression

    Cai, Na, Revez, Joana A., Adams, Mark J., Andlauer, Till F. M., Breen, Gerome, Byrne, Enda M., Clarke, Toni-Kim, Forstner, Andreas J., Grabe, Hans J., Hamilton, Steven P., Levinson, Douglas F., Lewis, Cathryn M., Lewis, Glyn, Martin, Nicholas G., Milaneschi, Yuri, Mors, Ole, Müller-Myhsok, Bertram, Penninx, Brenda W. J. H., Perlis, Roy H., Pistis, Giorgio, Potash, James B., Preisig, Martin, Shi, Jianxin, Smoller, Jordan W., Streit, Fabien, Tiemeier, Henning, Uher, Rudolf, Van der Auwera, Sandra, Viktorin, Alexander ... Flint, Jonathan (2020). Minimal phenotyping yields genome-wide association signals of low specificity for major depression. Nature Genetics, 52 (4), 437-447. doi: 10.1038/s41588-020-0594-5

  • The genetic architecture of the human cerebral cortex

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  • Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error

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  • Author Correction: Understanding the role of bitter taste perception in coffee, tea and alcohol consumption through Mendelian randomization

    Ong, Jue-Sheng, Hwang, Liang-Dar, Zhong, Victor W., An, Jiyuan, Gharahkhani, Puya, Breslin, Paul A. S., Wright, Margaret J., Lawlor, Deborah A., Whitfield, John, MacGregor, Stuart, Martin, Nicholas G. and Corneli, Marilyn C. (2020). Author Correction: Understanding the role of bitter taste perception in coffee, tea and alcohol consumption through Mendelian randomization. Scientific Reports, 10 (1) 4778, 4778. doi: 10.1038/s41598-020-60488-3

  • Genome-wide association meta-analysis of nicotine metabolism and cigarette consumption measures in smokers of European descent

    Buchwald, Jadwiga, Chenoweth, Meghan J., Palviainen, Teemu, Zhu, Gu, Benner, Christian, Gordon, Scott, Korhonen, Tellervo, Ripatti, Samuli, Madden, Pamela A. F., Lehtimäki, Terho, Raitakari, Olli T., Salomaa, Veikko, Rose, Richard J., George, Tony P., Lerman, Caryn, Pirinen, Matti, Martin, Nicholas G., Kaprio, Jaakko, Loukola, Anu and Tyndale, Rachel F. (2020). Genome-wide association meta-analysis of nicotine metabolism and cigarette consumption measures in smokers of European descent. Molecular Psychiatry, 26 (6), 2212-2223. doi: 10.1038/s41380-020-0702-z

  • Genome-wide association analysis in humans links nucleotide metabolism to Leukocyte Telomere Length

    Li, Chen, Stoma, Svetlana, Lotta, Luca A., Warner, Sophie, Albrecht, Eva, Allione, Alessandra, Arp, Pascal P., Broer, Linda, Buxton, Jessica L., Da Silva Couto Alves, Alexessander, Deelen, Joris, Fedko, Iryna O., Gordon, Scott D., Jiang, Tao, Karlsson, Robert, Kerrison, Nicola, Loe, Taylor K., Mangino, Massimo, Milaneschi, Yuri, Miraglio, Benjamin, Pervjakova, Natalia, Russo, Alessia, Surakka, Ida, van der Spek, Ashley, Verhoeven, Josine E., Amin, Najaf, Beekman, Marian, Blakemore, Alexandra I., Canzian, Federico ... Codd, Veryan (2020). Genome-wide association analysis in humans links nucleotide metabolism to Leukocyte Telomere Length. American Journal of Human Genetics, 106 (3), 389-404. doi: 10.1016/j.ajhg.2020.02.006

  • Atomic spectrometry update: Review of advances in the analysis of clinical and biological materials, foods and beverages

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  • Leveraging genome-wide data to investigate differences between opioid use vs. opioid dependence in 41,176 individuals from the Psychiatric Genomics Consortium

    Polimanti, Renato, Walters, Raymond K., Johnson, Emma C., McClintick, Jeanette N., Adkins, Amy E., Adkins, Daniel E., Bacanu, Silviu-Alin, Bierut, Laura J., Bigdeli, Tim B., Brown, Sandra, Bucholz, Kathleen K., Copeland, William E., Costello, E. Jane, Degenhardt, Louisa, Farrer, Lindsay A, Foroud, Tatiana M., Fox, Louis, Goate, Alison M., Grucza, Richard, Hack, Laura M., Hancock, Dana B., Hartz, Sarah M., Heath, Andrew C., Hewitt, John K., Hopfer, Christian J., Johnson, Eric O., Kendler, Kenneth S., Kranzler, Henry R., Krauter, Kenneth ... Gelernter, Joel (2020). Leveraging genome-wide data to investigate differences between opioid use vs. opioid dependence in 41,176 individuals from the Psychiatric Genomics Consortium. Molecular Psychiatry, 25 (8), 1673-1687. doi: 10.1038/s41380-020-0677-9

  • Insights into the aetiology of snoring from observational and genetic investigations in the UK Biobank

    Campos, Adrián I., García-Marín, Luis M., Byrne, Enda M., Martin, Nicholas G., Cuéllar-Partida, Gabriel and Rentería, Miguel E. (2020). Insights into the aetiology of snoring from observational and genetic investigations in the UK Biobank. Nature Communications, 11 (1) 817, 817. doi: 10.1038/s41467-020-14625-1

  • Genes determining nevus count and dermoscopic appearance in Australian melanoma cases and controls

    Duffy, David L., Jagirdar, Kasturee, Lee, Katie J., McWhirter, Seamus R., McMeniman, Erin K., De’Ambrosis, Brian, Pflugfelder, Annette, Rayner, Jenna E., Whiteman, David C., Brown, Matthew A., Martin, N.G., Smithers, B.M., Schaider, Helmut, Soyer, H. Peter and Sturm, Richard A. (2020). Genes determining nevus count and dermoscopic appearance in Australian melanoma cases and controls. Journal of Investigative Dermatology, 140 (2), 498-501.e17. doi: 10.1016/j.jid.2019.05.032

  • High-intensity drinking in adult Australian twins

    Dash, Genevieve F., Davis, Christal N., Martin, Nicholas G., Statham, Dixie J., Lynskey, Michael T. and Slutske, Wendy S. (2020). High-intensity drinking in adult Australian twins. Alcoholism: Clinical and Experimental Research, 44 (2), 522-531. doi: 10.1111/acer.14262

  • The Association of Dyslexia and Developmental Speech and Language Disorder Candidate Genes with Reading and Language Abilities in Adults

    Doust, Catherine, Gordon, Scott D., Garden, Natalie, Fisher, Simon E., Martin, Nicholas G., Bates, Timothy C. and Luciano, Michelle (2020). The Association of Dyslexia and Developmental Speech and Language Disorder Candidate Genes with Reading and Language Abilities in Adults. Twin Research and Human Genetics, 23 (1), 23-32. doi: 10.1017/thg.2020.7

  • Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression

    Craig, Jamie E., Han, Xikun, Qassim, Ayub, Hassall, Mark, Cooke Bailey, Jessica N., Kinzy, Tyler G., Khawaja, Anthony P., An, Jiyuan, Marshall, Henry, Gharahkhani, Puya, Igo, Robert P., Graham, Stuart L., Healey, Paul R., Ong, Jue-Sheng, Zhou, Tiger, Siggs, Owen, Law, Matthew H., Souzeau, Emmanuelle, Ridge, Bronwyn, Hysi, Pirro G., Burdon, Kathryn P., Mills, Richard A., Landers, John, Ruddle, Jonathan B., Agar, Ashish, Galanopoulos, Anna, White, Andrew J. R., Willoughby, Colin E., Andrew, Nicholas H. ... MacGregor, Stuart (2020). Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression. Nature Genetics, 52 (2), 160-166. doi: 10.1038/s41588-019-0556-y

  • Genome-wide association study of opioid cessation

    Cox, Jiayi W., Sherva, Richard M., Lunetta, Kathryn L., Johnson, Emma C., Martin, Nicholas G., Degenhardt, Louisa, Agrawal, Arpana, Nelson, Elliot C., Kranzler, Henry R., Gelernter, Joel and Farrer, Lindsay A. (2020). Genome-wide association study of opioid cessation. Journal of Clinical Medicine, 9 (1) 180, 180. doi: 10.3390/jcm9010180

  • Blood and plasma titanium levels associated with well-functioning hip implants

    Swiatkowska, Ilona, Martin, Nicholas G., Henckel, Johann, Apthorp, Hugh, Hamshere, Jane and Hart, Alister J. (2020). Blood and plasma titanium levels associated with well-functioning hip implants. Journal of Trace Elements in Medicine and Biology, 57, 9-17. doi: 10.1016/j.jtemb.2019.09.005

  • Exploring the genetic relationship between hearing impairment and Alzheimer's disease

    Mitchell, Brittany L., Thorp, Jackson G., Evans, David M., Nyholt, Dale R., Martin, Nicholas G. and Lupton, Michelle K. (2020). Exploring the genetic relationship between hearing impairment and Alzheimer's disease. Alzheimer's and Dementia: Diagnosis, Assessment and Disease Monitoring, 12 (1) e12108, 1-10. doi: 10.1002/dad2.12108

  • Prevalence of self-reported subthreshold phenotypes of major mental disorders and their association with functional impairment, treatment and full-threshold syndromes in a community-residing cohort of young adults

    Scott, Jan, Martin, Nicholas G., Parker, Richard, Couvy-Duchesne, Baptiste, Medland, Sarah E. and Hickie, Ian (2020). Prevalence of self-reported subthreshold phenotypes of major mental disorders and their association with functional impairment, treatment and full-threshold syndromes in a community-residing cohort of young adults. Early Intervention in Psychiatry, 15 (2) eip.12942, 306-313. doi: 10.1111/eip.12942

  • Shared genetic risk between eating disorder- and substance-use-related phenotypes: evidence from genome-wide association studies

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  • Genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders

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  • Epigenome-wide meta-analysis of blood DNA methylation and its association with subcortical volumes: findings from the ENIGMA Epigenetics Working Group

    Jia, Tianye, Chu, Congying, Liu, Yun, van Dongen, Jenny, Papastergios, Evangelos, Armstrong, Nicola J., Bastin, Mark E., Carrillo-Roa, Tania, den Braber, Anouk, Harris, Mathew, Jansen, Rick, Liu, Jingyu, Luciano, Michelle, Ori, Anil P. S., Roiz Santiañez, Roberto, Ruggeri, Barbara, Sarkisyan, Daniil, Shin, Jean, Sungeun, Kim, Tordesillas Gutiérrez, Diana, van’t Ent, Dennis, Ames, David, Artiges, Eric, Bakalkin, Georgy, Banaschewski, Tobias, Bokde, Arun L. W., Brodaty, Henry, Bromberg, Uli, Brouwer, Rachel ... Desrivières, Sylvane (2019). Epigenome-wide meta-analysis of blood DNA methylation and its association with subcortical volumes: findings from the ENIGMA Epigenetics Working Group. Molecular Psychiatry, 26 (8), 1-12. doi: 10.1038/s41380-019-0605-z

  • Associations between polygenic risk for tobacco and alcohol use and liability to tobacco and alcohol use, and psychiatric disorders in an independent sample of 13,999 Australian adults

    Chang, Lun-Hsien, Whitfield, John B., Liu, Mengzhen, Medland, Sarah E., Hickie, Ian B., Martin, Nicholas G., Verhulst, Brad, Heath, Andrew C., Madden, Pamela A., Statham, Dixie J., Gillespie, Nathan A. and GSCAN Consortium (2019). Associations between polygenic risk for tobacco and alcohol use and liability to tobacco and alcohol use, and psychiatric disorders in an independent sample of 13,999 Australian adults. Drug and Alcohol Dependence, 205 107704, 107704. doi: 10.1016/j.drugalcdep.2019.107704

  • Identifying subtypes of cannabis users based on simultaneous polysubstance use

    Davis, Christal N., Slutske, Wendy S., Martin, Nicholas G., Agrawal, Arpana and Lynskey, Michael T. (2019). Identifying subtypes of cannabis users based on simultaneous polysubstance use. Drug and Alcohol Dependence, 205 107696, 1-7. doi: 10.1016/j.drugalcdep.2019.107696

  • Shared and specific genetic risk factors for lifetime major depression, depressive symptoms and neuroticism in three population-based twin samples

    Kendler, Kenneth S., Gardner, Charles O., Neale, Michael C., Aggen, Steve, Heath, Andrew, Colodro-Conde, Lucía, Couvyduchesne, Baptiste, Byrne, Enda M., Martin, Nicholas G. and Gillespie, Nathan A. (2019). Shared and specific genetic risk factors for lifetime major depression, depressive symptoms and neuroticism in three population-based twin samples. Psychological Medicine, 49 (16), 2745-2753. doi: 10.1017/S003329171800377X

  • The CODATwins Project: the current status and recent findings of COllaborative Project of Development of Anthropometrical Measures in Twins

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  • The Nigerian Twin and Sibling Registry: An Update

    Hur, Yoon-Mi, Jeong, Hoe-Uk, Kang, Man Chull, Ajose, Frances, Kim, Jong Woo, Beck, Jeffrey J., Hottenga, Jouke-Jan, Mbarek, Hamdi, Finnicum, Casey T., Ehli, Erik A., Martin, Nicholas G., De Geus, Eco J., Boomsma, Dorret I., Davies, Gareth E. and Bates, Timothy (2019). The Nigerian Twin and Sibling Registry: An Update. Twin Research and Human Genetics, 22 (6), 637-640. doi: 10.1017/thg.2019.110

  • Novel genetic loci affecting facial shape variation in humans

    Xiong, Ziyi, Dankova, Gabriela, Howe, Laurence J., Lee, Myoung Keun, Hysi, Pirro G., de Jong, Markus A., Zhu, Gu, Adhikari, Kaustubh, Li, Dan, Li, Yi, Pan, Bo, Feingold, Eleanor, Marazita, Mary L., Shaffer, John R., McAloney, Kerrie, Xu, Shu-Hua, Jin, Li, Wang, Sijia, de Vrij, Femke Ms, Lendemeijer, Bas, Richmond, Stephen, Zhurov, Alexei, Lewis, Sarah, Sharp, Gemma C., Paternoster, Lavinia, Thompson, Holly, Gonzalez-Jose, Rolando, Bortolini, Maria Catira, Canizales-Quinteros, Samuel ... Kayser, Manfred (2019). Novel genetic loci affecting facial shape variation in humans. eLife, 8 e49898. doi: 10.7554/eLife.49898

  • The Relationship Between Adolescents’ Personality and Neurasthenia: A Comparison of Australian and Chinese

    Ye, Lin, Zhu, Gu, Martin, Nick and Liu, Yangyang (2019). The Relationship Between Adolescents’ Personality and Neurasthenia: A Comparison of Australian and Chinese. Journal of Early Adolescence, 39 (9), 1337-1342. doi: 10.1177/0272431618824710

  • Associations of autozygosity with a broad range of human phenotypes

    Clark, David W., Okada, Yukinori, Moore, Kristjan H. S., Mason, Dan, Pirastu, Nicola, Gandin, Ilaria, Mattsson, Hannele, Barnes, Catriona L. K., Lin, Kuang, Zhao, Jing Hua, Deelen, Patrick, Rohde, Rebecca, Schurmann, Claudia, Guo, Xiuqing, Giulianini, Franco, Zhang, Weihua, Medina-Gomez, Carolina, Karlsson, Robert, Bao, Yanchun, Bartz, Traci M., Baumbach, Clemens, Biino, Ginevra, Bixley, Matthew J., Brumat, Marco, Chai, Jin-Fang, Corre, Tanguy, Cousminer, Diana L., Dekker, Annelot M., Eccles, David A. ... Wilson, James F. (2019). Associations of autozygosity with a broad range of human phenotypes. Nature Communications, 10 (1) 4957, 4957. doi: 10.1038/s41467-019-12283-6

  • Association of copy number variation of the 15q11.2 BP1-BP2 region with cortical and subcortical morphology and cognition

    Van Der Meer, Dennis, Sønderby, Ida E., Kaufmann, Tobias, Walters, G. Bragi, Abdellaoui, Abdel, Ames, David, Amunts, Katrin, Andersson, Micael, Armstrong, Nicola J., Bernard, Manon, Blackburn, Nicholas B., Blangero, John, Boomsma, Dorret I., Brodaty, Henry, Brouwer, Rachel M., Bülow, Robin, Cahn, Wiepke, Calhoun, Vince D., Caspers, Svenja, Cavalleri, Gianpiero L., Ching, Christopher R. K., Cichon, Sven, Ciufolini, Simone, Corvin, Aiden, Crespo-Facorro, Benedicto, Curran, Joanne E., Dalvie, Shareefa, Dazzan, Paola, De Geus, Eco J. C. ... Andreassen, Ole A. (2019). Association of copy number variation of the 15q11.2 BP1-BP2 region with cortical and subcortical morphology and cognition. JAMA Psychiatry, 77 (4), 1-11. doi: 10.1001/jamapsychiatry.2019.3779

  • Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis

    Gallagher, C. S., Mäkinen, N., Harris, H. R., Rahmioglu, N., Uimari, O., Cook, J. P., Shigesi, N., Ferreira, T., Velez-Edwards, D. R., Edwards, T. L., Mortlock, S., Ruhioglu, Z., Day, F., Becker, C. M., Karhunen, V., Martikainen, H., Järvelin, M.-R., Cantor, R. M., Ridker, P. M., Terry, K. L., Buring, J. E., Gordon, S. D., Medland, S. E., Montgomery, G. W., Nyholt, D. R., Hinds, D. A., Tung, J. Y., Perry, J. R. B., Lind, P. A. ... Morton, C. C. (2019). Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis. Nature Communications, 10 (1) 4857, 4857. doi: 10.1038/s41467-019-12536-4

  • Genetic architecture of subcortical brain structures in 38,851 individuals

    Satizabal, Claudia L., Adams, Hieab H. H., Hibar, Derrek P., White, Charles C., Knol, Maria J., Stein, Jason L., Scholz, Markus, Sargurupremraj, Muralidharan, Jahanshad, Neda, Roshchupkin, Gennady V., Smith, Albert V., Bis, Joshua C., Jian, Xueqiu, Luciano, Michelle, Hofer, Edith, Teumer, Alexander, van der Lee, Sven J., Yang, Jingyun, Yanek, Lisa R., Lee, Tom V., Li, Shuo, Hu, Yanhui, Koh, Jia Yu, Eicher, John D., Desrivières, Sylvane, Arias-Vasquez, Alejandro, Chauhan, Ganesh, Athanasiu, Lavinia, Rentería, Miguel E. ... Ikram, M. Arfan (2019). Genetic architecture of subcortical brain structures in 38,851 individuals. Nature Genetics, 51 (11), 1624-1636. doi: 10.1038/s41588-019-0511-y

  • International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci

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  • Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels

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  • White matter disturbances in major depressive disorder: a coordinated analysis across 20 international cohorts in the ENIGMA MDD working group

    van Velzen, Laura S., Kelly, Sinead, Isaev, Dmitry, Aleman, Andre, Aftanas, Lyubomir I., Bauer, Jochen, Baune, Bernhard T., Brak, Ivan V., Carballedo, Angela, Connolly, Colm G., Couvy-Duchesne, Baptiste, Cullen, Kathryn R., Danilenko, Konstantin V., Dannlowski, Udo, Enneking, Verena, Filimonova, Elena, Förster, Katharina, Frodl, Thomas, Gotlib, Ian H., Groenewold, Nynke A., Grotegerd, Dominik, Harris, Mathew A., Hatton, Sean N., Hawkins, Emma L., Hickie, Ian B., Ho, Tiffany C., Jansen, Andreas, Kircher, Tilo, Klimes-Dougan, Bonnie ... Schmaal, Lianne (2019). White matter disturbances in major depressive disorder: a coordinated analysis across 20 international cohorts in the ENIGMA MDD working group. Molecular Psychiatry, 25 (7), 1511-1525. doi: 10.1038/s41380-019-0477-2

  • Metabolomics reveals a link between homocysteine and lipid metabolism and leukocyte telomere length: the ENGAGE consortium

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  • Classical human leukocyte antigen alleles and C4 haplotypes are not significantly associated With depression

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  • A behavior genetic analysis of the relationship between humor styles and depression

    Kfrerer, Marisa L., Martin, Nicholas G. and Schermer, Julie Aitken (2019). A behavior genetic analysis of the relationship between humor styles and depression. Humor, 32 (3), 417-431. doi: 10.1515/humor-2017-0098

  • Genetic Similarity Assessment of Twin-Family Populations by Custom-Designed Genotyping Array

    Beck, Jeffrey J., Hottenga, Jouke-Jan, Mbarek, Hamdi, Finnicum, Casey T., Ehli, Erik A., Hur, Yoon-Mi, Martin, Nicholas G., De Geus, Eco J.C., Boomsma, Dorret I. and Davies, Gareth E. (2019). Genetic Similarity Assessment of Twin-Family Populations by Custom-Designed Genotyping Array. Twin Research and Human Genetics, 22 (4), 210-219. doi: 10.1017/thg.2019.41

  • New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disorders

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  • Genetic and environmental risk factors in the non-medical use of over-the-counter or prescribed analgesics, and their relationship to major classes of licit and illicit substance use and misuse in a population-based sample of young adult twins

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  • Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa

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  • Genetic and environmental influences on gambling disorder liability: A replication and combined analysis of two twin studies

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  • Genome-Wide Association Studies Identify Multiple Genetic Loci Influencing Eyebrow Color Variation in Europeans

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  • Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection

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  • Author Correction: GWAS of lifetime cannabis use reveals new risk loci, genetic overlap with psychiatric traits, and a causal effect of schizophrenia liability

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  • Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use

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  • Genetic Epidemiology of Liability for Alcohol-Induced Blacking and Passing Out

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  • New insight into human sweet taste: a genome-wide association study of the perception and intake of sweet substances

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  • A catalog of genetic loci associated with kidney function from analyses of a million individuals

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  • Multi-site meta-analysis of morphometry

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  • Associations between brain structure and perceived intensity of sweet and bitter tastes

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  • Author correction: Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function

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  • Blood titanium level as a biomarker of orthopaedic implant wear

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  • Evidence of causal effect of major depression on alcohol dependence: Findings from the psychiatric genomics consortium

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  • Genome-wide association study identifies 30 loci associated with bipolar disorder

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  • Genetic structure of IQ, phonemic decoding skill, and academic achievement

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  • Homogenizing estimates of heritability among SOLAR-Eclipse, OpenMx, APACE, and FPHI software packages in neuroimaging data

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  • Genome wide analysis for mouth ulcers identifies associations at immune regulatory loci

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  • Atomic Spectrometry Update: Review of adVances in the analysis of clinical and biological materials, foods and beverages

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  • Biomarker and genomic risk factors for liver function test abnormality in hazardous drinkers

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  • A behavior genetic analysis of personality and loneliness

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  • Association between polygenic risk for tobacco or alcohol consumption and liability to licit and illicit substance use in young Australian adults

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  • Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use

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  • Common genetic contributions to high-risk trauma exposure and self-injurious thoughts and behaviors

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  • Quantifying between-cohort and between-sex genetic heterogeneity in major depressive disorder

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  • Social competence in parents increases children's educational attainment: Replicable genetically-mediated effects of parenting revealed by non-transmitted DNA

    Bates, Timothy C., Maher, Brion S., Colodro-Conde, Lucía, Medland, Sarah E., McAloney, Kerrie, Wright, Margaret J., Hansell, Narelle K., Okbay, Aysu, Kendler, Kenneth S., Martin, Nicholas G. and Gillespie, Nathan A. (2019). Social competence in parents increases children's educational attainment: Replicable genetically-mediated effects of parenting revealed by non-transmitted DNA. Twin Research and Human Genetics, 22 (01), 1-3. doi: 10.1017/thg.2018.75

  • Publisher correction: Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways

    Duffy, David L., Zhu, Gu, Li, Xin, Sanna, Marianna, Iles, Mark M., Jacobs, Leonie C., Evans, David M., Yazar, Seyhan, Beesley, Jonathan, Law, Matthew H., Kraft, Peter, Visconti, Alessia, Taylor, John C., Liu, Fan, Wright, Margaret J., Henders, Anjali K., Bowdler, Lisa, Glass, Dan, Ikram, M. Arfan, Uitterlinden, André G., Madden, Pamela A., Heath, Andrew C., Nelson, Elliot C., Green, Adele C., Chanock, Stephen, Barrett, Jennifer H., Brown, Matthew A., Hayward, Nicholas K., MacGregor, Stuart ... Martin, Nicholas G. (2019). Publisher correction: Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways. Nature Communications, 10 (1) 299, 299. doi: 10.1038/s41467-018-08078-w

  • Author correction: Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases

    Iglesias, Adriana I., Mishra, Aniket, Vitart, Veronique, Bykhovskaya, Yelena, Höhn, René, Springelkamp, Henriët, Cuellar-Partida, Gabriel, Gharahkhani, Puya, Bailey, Jessica N. Cooke, Willoughby, Colin E., Li, Xiaohui, Yazar, Seyhan, Nag, Abhishek, Khawaja, Anthony P., Polašek, Ozren, Siscovick, David, Mitchell, Paul, Tham, Yih Chung, Haines, Jonathan L., Kearns, Lisa S., Hayward, Caroline, Shi, Yuan, van Leeuwen, Elisabeth M., Taylor, Kent D., Bonnemaijer, Pieter, Rotter, Jerome I., Martin, Nicholas G., Zeller, Tanja, Mills, Richard A. ... MacGregor, Stuart (2019). Author correction: Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases. Nature Communications, 10 (1) 155, 155. doi: 10.1038/s41467-018-07819-1

  • Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies

    Morris, Andrew P., Le, Thu H., Wu, Haojia, Akbarov, Artur, van der Most, Peter J., Hemani, Gibran, Smith, George Davey, Mahajan, Anubha, Gaulton, Kyle J., Nadkarni, Girish N., Valladares-Salgado, Adan, Wacher-Rodarte, Niels, Mychaleckyj, Josyf C., Dueker, Nicole D., Guo, Xiuqing, Hai, Yang, Haessler, Jeffrey, Kamatani, Yoichiro, Stilp, Adrienne M., Zhu, Gu, Cook, James P., Ärnlöv, Johan, Blanton, Susan H., de Borst, Martin H., Bottinger, Erwin P., Buchanan, Thomas A., Cechova, Sylvia, Charchar, Fadi J., Chu, Pei-Lun ... Franceschini, Nora (2019). Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies. Nature Communications, 10 (1) 29, 29. doi: 10.1038/s41467-018-07867-7

  • Big Five Personality Traits and Alcohol, Nicotine, Cannabis, and Gambling Disorder Comorbidity

    Dash, Genevieve F., Slutske, Wendy S., Martin, Nicholas G., Statham, Dixie J., Agrawal, Arpana and Lynskey, Michael T. (2019). Big Five Personality Traits and Alcohol, Nicotine, Cannabis, and Gambling Disorder Comorbidity. Psychology of Addictive Behaviors, 33 (4), 420-429. doi: 10.1037/adb0000468

  • Comparing the Potential Causal Influence of Two Indicators of Early Alcohol Use on Later Alcohol Use Disorder Symptoms

    Davis, Christal N., Slutske, Wendy S., Piasecki, Thomas M., Martin, Nicholas G. and Lynskey, Michael T. (2019). Comparing the Potential Causal Influence of Two Indicators of Early Alcohol Use on Later Alcohol Use Disorder Symptoms. Journal of Abnormal Psychology, 129 (3), 256-265. doi: 10.1037/abn0000474

  • Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder

    Demontis, Ditte, Walters, Raymond K., Martin, Joanna, Mattheisen, Manuel, Als, Thomas D., Agerbo, Esben, Baldursson, Gísli, Belliveau, Rich, Bybjerg-Grauholm, Jonas, Bækvad-Hansen, Marie, Cerrato, Felecia, Chambert, Kimberly, Churchhouse, Claire, Dumont, Ashley, Eriksson, Nicholas, Gandal, Michael, Goldstein, Jacqueline I., Grasby, Katrina L., Grove, Jakob, Gudmundsson, Olafur O., Hansen, Christine S., Hauberg, Mads Engel, Hollegaard, Mads V., Howrigan, Daniel P., Huang, Hailiang, Maller, Julian B., Martin, Alicia R., Martin, Nicholas G., Moran, Jennifer ... Kemp, John P. (2019). Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder. Nature Genetics, 51 (1), 63-75. doi: 10.1038/s41588-018-0269-7

  • Half the genetic variance in vitamin D concentration is shared with skin colour and sun exposure genes

    Mitchell, Brittany L., Zhu, Gu, Medland, Sarah E., Renteria, Miguel. E., Eyles, Darryl W., Grasby, Katrina L., McGrath, John J. and Martin, Nicholas G. (2019). Half the genetic variance in vitamin D concentration is shared with skin colour and sun exposure genes. Behavior Genetics, 49 (4), 386-398. doi: 10.1007/s10519-019-09954-x

  • In vivo biocompatibility and immunogenicity of metal-phenolic gelation

    Björnmalm, Mattias, Wong, Lok Man, Wojciechowski, Jonathan P., Penders, Jelle, Horgan, Conor C., Booth, Marsilea A., Martin, Nicholas G., Sattler, Susanne and Stevens, Molly M. (2019). In vivo biocompatibility and immunogenicity of metal-phenolic gelation. Chemical Science, 10 (43), 10179-10194. doi: 10.1039/c9sc03325d

  • Twenty-Five and Up (25Up) Study: A New Wave of the Brisbane Longitudinal Twin Study

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  • Antibody response to common human viruses is shaped by genetic factors

    Hayward, Tanisha A., Zhu, Gu, Warrington, Nicole M., Wong, Yide, Ryan, Rachael Y.M., Murray, Abella M., Haigh, Oscar, Martin, Nicholas G., Miles, John J. and Evans, David M. (2018). Antibody response to common human viruses is shaped by genetic factors. Journal of Allergy and Clinical Immunology, 143 (4), 1640-1643. doi: 10.1016/j.jaci.2018.11.039

  • Identification of 55,000 replicated DNA methylation QTL

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  • Getting to the genetic and environmental roots of educational inequality

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  • PPD ACT: an app-based genetic study of postpartum depression

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  • Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders

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  • A fast method for estimating statistical power of multivariate GWAS in real case scenarios: examples from the field of imaging genetics

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  • Understanding the role of bitter taste perception in coffee, tea and alcohol consumption through Mendelian randomization

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  • Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways

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  • Genome analyses of >200,000 individuals identify 58 loci for chronic inflammation and highlight pathways that link inflammation and complex disorders

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  • Genome-wide association meta-analysis of age at first cannabis use

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  • The Anorexia Nervosa Genetics Initiative (ANGI): overview and methods

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  • Towards broadening Forensic DNA Phenotyping beyond pigmentation: Improving the prediction of head hair shape from DNA

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  • Common genetic variants contribute to risk of rare severe neurodevelopmental disorders

    Niemi, Mari E. K., Martin, Hilary C., Rice, Daniel L., Gallone, Giuseppe, Gordon, Scott, Kelemen, Martin, McAloney, Kerrie, McRae, Jeremy, Radford, Elizabeth J., Yu, Sui, Gecz, Jozef, Martin, Nicholas G., Wright, Caroline F., Fitzpatrick, David R., Firth, Helen V., Hurles, Matthew E. and Barrett, Jeffrey C. (2018). Common genetic variants contribute to risk of rare severe neurodevelopmental disorders. Nature, 562 (7726), 268-271. doi: 10.1038/s41586-018-0566-4

  • Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder

    de Jong, Simone, Abdalla Diniz, Mateus Jose, Saloma, Andiara, Gadelha, Ary, Santoro, Marcos L., Ota, Vanessa K., Noto, Cristiano, Curtis, Charlesg, Newhouse, Stephen J., Patel, Hamel, Hall, Lynsey S., O'Reilly, Paul F., Belangero, Sintia, Bressan, Rodrigo A., Breen, Gerome, Wray, Naomi R., Ripke, Stephan, Mattheisen, Manuel, Trzaskowski, Maciej, Byrne, Enda M., Abdellaoui, Abdel, Adams, Mark J., Agerbo, Esben, Air, Tracy M., Andlauer, Till F. M., Bacanu, Silviu-Alin, Baekvad-Hansen, Marie, Beekman, Aartjan T. F., Bigdeli, Tim B. ... Major Depressive Disorder and Bipolar Disorder Working Groups of the Psychiatric Genomics Consortium (2018). Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder. Communications Biology, 1 (163) 163. doi: 10.1038/s42003-018-0155-y

  • Bivariate genome-wide association analysis strengthens the role of bitter receptor clusters on chromosomes 7 and 12 in human bitter taste

    Hwang, Liang-Dar, Gharahkhani, Puya, Breslin, Paul A. S., Gordon, Scott D., Zhu, Gu, Martin, Nicholas G., Reed, Danielle R. and Wright, Margaret J. (2018). Bivariate genome-wide association analysis strengthens the role of bitter receptor clusters on chromosomes 7 and 12 in human bitter taste. BMC Genomics, 19 (678) 678, 678. doi: 10.1186/s12864-018-5058-2

  • Are there distinct cognitive types?

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  • Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma

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  • The genetic relationship between psychological distress, somatic distress, affective disorders, and substance use in young Australian adults: a multivariate twin study

    Chang, Lun-Hsien, Couvy-Duchesne, Baptiste, Medland, Sarah E., Gillespie, Nathan A., Hickie, Ian B., Parker, Richard and Martin, Nicholas G. (2018). The genetic relationship between psychological distress, somatic distress, affective disorders, and substance use in young Australian adults: a multivariate twin study. Twin Research and Human Genetics, 21 (5), 347-360. doi: 10.1017/thg.2018.33

  • Association of current and former smoking with body mass index: a study of smoking discordant twin pairs from 21 twin cohorts

    Piirtola, Maarit, Jelenkovic, Aline, Latvala, Antti, Sund, Reijo, Honda, Chika, Inui, Fujio, Watanabe, Mikio, Tomizawa, Rie, Iwatani, Yoshinori, Ordoñana, Juan R., Sánchez-Romera, Juan F., Colodro-Conde, Lucia, Tarnoki, Adam D., Tarnoki, David L., Martin, Nicholas G., Montgomery, Grant W., Medland, Sarah E., Rasmussen, Finn, Tynelius, Per, Tan, Qihua, Zhang, Dongfeng, Pang, Zengchang, Rebato, Esther, Stazi, Maria A., Fagnani, Corrado, Brescianini, Sonia, Busjahn, Andreas, Harris, Jennifer R., Brandt, Ingunn ... Silventoinen, Karri (2018). Association of current and former smoking with body mass index: a study of smoking discordant twin pairs from 21 twin cohorts. PLoS One, 13 (7) e0200140, e0200140. doi: 10.1371/journal.pone.0200140

  • A multivariate behavior genetic investigation of dual-systems models of alcohol involvement

    Ellingson, Jarrod M., Slutske, Wendy S., Vergés, Alvaro, Littlefield, Andrew K., Statham, Dixie J. and Martin, Nicholas G. (2018). A multivariate behavior genetic investigation of dual-systems models of alcohol involvement. Journal of Studies on Alcohol and Drugs, 79 (4), 617-626. doi: 10.15288/JSAD.2018.79.617

  • The relationship between personality and somatic and psychological distress: a comparison of Chinese and Australian adolescents

    Liu, Yangyang, Gillespie, Nathan A., Ye, Lin, Zhu, Gu, Duffy, David L. and Martin, Nicholas G. (2018). The relationship between personality and somatic and psychological distress: a comparison of Chinese and Australian adolescents. Behavior Genetics, 48 (4), 315-322. doi: 10.1007/s10519-018-9905-3

  • Genome-wide association analysis links multiple psychiatric liability genes to oscillatory brain activity

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  • Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence

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  • Cross-cultural comparison of genetic and cultural transmission of smoking initiation using an extended twin kinship model

    Maes, Hermine H., Morley, Kate, Neale, Michael C., Kendler, Kenneth S., Heath, Andrew C., Eaves, Lindon J. and Martin, Nicholas G. (2018). Cross-cultural comparison of genetic and cultural transmission of smoking initiation using an extended twin kinship model. Twin Research and Human Genetics, 21 (3), 179-190. doi: 10.1017/thg.2018.22

  • Establishing a twin register: an invaluable resource for (behavior) genetic, epidemiological, biomarker, and ‘omics’ studies

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  • Extended twin study of alcohol use in Virginia and Australia

    Verhulst, Brad, Neale, Michael C., Eaves, Lindon J., Medland, Sarah E., Heath, Andrew C., Martin, Nicholas G. and Maes, Hermine H. (2018). Extended twin study of alcohol use in Virginia and Australia. Twin Research and Human Genetics, 21 (3), 163-178. doi: 10.1017/thg.2018.21

  • Genome-wide survey of parent-of-origin effects on DNA methylation identifies candidate imprinted loci in humans

    Cuellar Partida, Gabriel, Laurin, Charles, Ring, Susan M., Gaunt, Tom R., McRae, Allan, Visscher, Peter M., Montgomery, Grant W., Martin, Nicholas G., Hemani, Gibran, Suderman, Matthew, Relton, Caroline L., Davey Smith, George and Evans, David M. (2018). Genome-wide survey of parent-of-origin effects on DNA methylation identifies candidate imprinted loci in humans. Human Molecular Genetics, 27 (16), 2927-2939. doi: 10.1093/hmg/ddy206

  • Childhood aggression and the co-occurrence of behavioural and emotional problems: results across ages 3-16 years from multiple raters in six cohorts in the EU-ACTION project

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  • Genome-wide association study in 176,678 Europeans reveals genetic loci for tanning response to sun exposure

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  • Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

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  • Testing associations between cannabis use and subcortical volumes in two large population-based samples

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  • Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability

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  • Genome-wide association study identifies nine novel loci for 2D:4D finger ratio, a putative retrospective biomarker of testosterone exposure in utero

    Warrington, Nicole M., Shevroja, Enisa, Hemani, Gibran, Hysi, Pirro G., Jiang, Yunxuan, Auton, Adam, Boer, Cindy G., Mangino, Massimo, Wang, Carol A., Kemp, John P., McMahon, George, Medina-Gomez, Carolina, Hickey, Martha, Trajanoska, Katerina, Wolke, Dieter, Ikram, Arfan M., 23 and Me Research Team, Montgomery, Grant W., Felix, Janine F., Wright, Margaret J., Mackey, David A., Jaddoe, Vincent W., Martin, Nicholas G., Tung, Joyce Y., Davey Smith, George, Pennell, Craig E., Spector, Tim D., van Meurs, Joyce, Rivadeneira, Fernando ... Evans, David M. (2018). Genome-wide association study identifies nine novel loci for 2D:4D finger ratio, a putative retrospective biomarker of testosterone exposure in utero. Human Molecular Genetics, 27 (11), 2025-2038. doi: 10.1093/hmg/ddy121

  • Genetic overlap between endometriosis and endometrial cancer: evidence from cross-disease genetic correlation and GWAS meta-analyses

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  • Nineteen and Up study (19Up): Understanding pathways to mental health disorders in young Australian twins

    Couvy-Duchesne, Baptiste, O'Callaghan, Victoria, Parker, Richard, Mills, Natalie, Kirk, Katherine M., Scott, Jan, Vinkhuyzen, Anna., Hermens, Daniel F., Lind, Penelope A., Davenport, Tracey A., Burns, Jane M., Connell, Melissa, Zietsch, Brendan P., Scott, James, Wright, Margaret J., Medland, Sarah E., McGrath, John, Martin, Nicholas G., Hickie, Ian B. and Gillespie, Nathan A. (2018). Nineteen and Up study (19Up): Understanding pathways to mental health disorders in young Australian twins. BMJ Open, 8 (3) e018959, 1-13. doi: 10.1136/bmjopen-2017-018959

  • The Nature of Nurture: Using a Virtual-Parent Design to Test Parenting Effects on Children's Educational Attainment in Genotyped Families

    Bates, Timothy C., Maher, Brion S., Medland, Sarah E., McAloney, Kerrie, Wright, Margaret J., Hansell, Narelle K., Kendler, Kenneth S., Martin, Nicholas G. and Gillespie, Nathan A. (2018). The Nature of Nurture: Using a Virtual-Parent Design to Test Parenting Effects on Children's Educational Attainment in Genotyped Families. Twin Research and Human Genetics, 21 (2), 73-83. doi: 10.1017/thg.2018.11

  • Integrative analysis of omics summary data reveals putative mechanisms underlying complex traits

    Wu, Yang, Zeng, Jian, Zhang, Futao, Zhu, Zhihong, Qi, Ting, Zheng, Zhili, Lloyd-Jones, Luke R., Marioni, Riccardo E., Martin, Nicholas G., Montgomery, Grant W., Deary, Ian J., Wray, Naomi R., Visscher, Peter M., McRae, Allan F. and Yang, Jian (2018). Integrative analysis of omics summary data reveals putative mechanisms underlying complex traits. Nature Communications, 9 (918) 918, 918. doi: 10.1038/s41467-018-03371-0

  • Atomic spectrometry update: review of advances in the analysis of clinical and biological materials, foods and beverages

    Taylor, Andrew, Barlow, Nicola, Day, Martin P., Hill, Sarah, Martin, Nicholas and Patriarca, Marina (2018). Atomic spectrometry update: review of advances in the analysis of clinical and biological materials, foods and beverages. Journal of Analytical Atomic Spectrometry, 33 (3), 338-382. doi: 10.1039/c8ja90005a

  • Endogenous cortisol in keratinized matrices: systematic determination of baseline cortisol levels in hair and the influence of sex, age and hair color

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  • Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder

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  • Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection

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  • Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma

    Gharahkhani, Puya, Burdon, Kathryn P., Cooke Bailey, Jessica N, Hewitt, Alex W., Law, Matthew H., Pasquale, Louis R., Kang, Jae H., Haines, Jonathan L., Souzeau, Emmanuelle, Zhou, Tiger, Siggs, Owen M., Landers, John, Awadalla, Mona, Sharma, Shiwani, Mills, Richard A., Ridge, Bronwyn, Lynn, David, Casson, Robert, Graham, Stuart L., Goldberg, Ivan, White, Andrew, Healey, Paul R., Grigg, John, Lawlor, Mitchell, Mitchell, Paul, Ruddle, Jonathan, Coote, Michael, Walland, Mark, Best, Stephen ... NEIGHBORHOOD consortium (2018). Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma. Scientific reports, 8 (1) 3124, 3124. doi: 10.1038/s41598-018-20435-9

  • Meta-analysis of genome-wide association studies identifies 8 novel loci involved in shape variation of human head hair

    Liu, Fan, Chen, Yan, Zhu, Gu, Hysi, Pirro G., Wu, Sijie, Adhikari, Kaustubh, Breslin, Krystal, Pośpiech, Ewelina, Hamer, Merel A., Peng, Fuduan, Muralidharan, Charanya, Acuna-Alonzo, Victor, Canizales-Quinteros, Samuel, Bedoya, Gabriel, Gallo, Carla, Poletti, Giovanni, Rothhammer, Francisco, Bortolini, Maria Catira, Gonzalez-Jose, Rolando, Zeng, Changqing, Xu, Shuhua, Jin, Li, Uitterlinden, André G., Arfan Ikram, M., van Duijn, Cornelia M., Nijsten, Tamar, Walsh, Susan, Branicki, Wojciech, Wang, Sijia ... Kayser, Manfred (2018). Meta-analysis of genome-wide association studies identifies 8 novel loci involved in shape variation of human head hair. Human Molecular Genetics, 27 (3), 559-575. doi: 10.1093/hmg/ddx416

  • Personality types: a twin study

    Loehlin, John C. and Martin, Nicholas G. (2018). Personality types: a twin study. Personality and Individual Differences, 122, 99-103. doi: 10.1016/j.paid.2017.10.012

  • The protocadherin 17 gene affects cognition, personality, amygdala structure and function, synapse development and risk of major mood disorders

    Chang, H., Hoshina, N., Zhang, C., Ma, Y., Cao, H., Wang, Y., Wu, D. D., Bergen, S. E., Landén, M., Hultman, C. M., Preisig, M., Kutalik, Z., Castelao, E., Grigoroiu-Serbanescu, M., Forstner, A. J., Strohmaier, J., Hecker, J., Schulze, T. G., Müller-Myhsok, B., Reif, A., Mitchell, P. B., Martin, N. G., Schofield, P. R., Cichon, S., Nöthen, M. M., Walter, H., Erk, S., Heinz, A., Amin, N. ... MooDS Bipolar Consortium (2018). The protocadherin 17 gene affects cognition, personality, amygdala structure and function, synapse development and risk of major mood disorders. Molecular Psychiatry, 23 (2), 400-412. doi: 10.1038/mp.2016.231

  • A polymorphism in the OPRM1 3'-untranslated region is associated with methadone efficacy in treating opioid dependence

    Crist, R. C., Doyle, G. A., Nelson, E. C., Degenhardt, L., Martin, N. G., Montgomery, G. W., Saxon, A. J., Ling, W. and Berrettini, W. H. (2018). A polymorphism in the OPRM1 3'-untranslated region is associated with methadone efficacy in treating opioid dependence. The Pharmacogenomics Journal, 18 (1), 173-179. doi: 10.1038/tpj.2016.89

  • Accuracy of inferred APOE genotypes for a range of genotyping arrays and imputation reference panels

    Lupton, Michelle K., Medland, Sarah E., Gordon, Scott D., Goncalves, Tabatha, MacGregor, Stuart, Mackey, David A., Young, Terri L., Duffy, David L., Visscher, Peter M., Wray, Naomi R., Nyholt, Dale R., Bain, Lisa, Ferreira, Manuel A., Henders, Anjali K., Wallace, Leanne, Montgomery, Grant W., Wright, Margaret J. and Martin, Nicholas G. (2018). Accuracy of inferred APOE genotypes for a range of genotyping arrays and imputation reference panels. Journal of Alzheimer's Disease, 64 (1), 49-54. doi: 10.3233/JAD-171104

  • Effects of high alcohol intake, alcohol-related symptoms and smoking on mortality

    Whitfield, John B., Heath, Andrew C., Madden, Pamela A. F., Landers, J. George and Martin, Nicholas G. (2018). Effects of high alcohol intake, alcohol-related symptoms and smoking on mortality. Addiction, 113 (1), 158-166. doi: 10.1111/add.14008

  • Lingual Gyrus Surface Area Is Associated with Anxiety-Depression Severity in Young Adults: A Genetic Clustering Approach

    Couvy-Duchesne, Baptiste, Strike, Lachlan T., de Zubicaray, Greig I., McMahon, Katie L., Thompson, Paul M., Hickie, Ian B., Martin, Nicholas G. and Wright, Margaret J. (2018). Lingual Gyrus Surface Area Is Associated with Anxiety-Depression Severity in Young Adults: A Genetic Clustering Approach. eNeuro, 5 (1) e0153-17.2017, 1-14. doi: 10.1523/ENEURO.0153-17.2017

  • Pathways to depression by age 16 years: Examining trajectories for self-reported psychological and somatic phenotypes across adolescence

    Scott, Jan, Davenport, Tracey A., Parker, Richard, Hermens, Daniel F., Lind, Penelope A., Medland, Sarah E., Wright, Margaret J., Martin, Nicholas G., Gillespie, Nathan A. and Hickie, Ian B. (2017). Pathways to depression by age 16 years: Examining trajectories for self-reported psychological and somatic phenotypes across adolescence. Journal of Affective Disorders, 230, 1-6. doi: 10.1016/j.jad.2017.12.007

  • Common variants at 2q11.2, 8q21.3, and 11q13.2 are associated with major mood disorders

    Xiao, Xiao, Wang, Lu, Wang, Chuang, Yuan, Ti-Fei, Zhou, Dongsheng, Zheng, Fanfan, Li, Lingyi, Grigoroiu-Serbanescu, Maria, Ikeda, Masashi, Iwata, Nakao, Takahashi, Atsushi, Kamatani, Yoichiro, Kubo, Michiaki, Preisig, Martin, Kutalik, Zoltán, Castelao, Enrique, Pistis, Giorgio, Amin, Najaf, Van Duijn, Cornelia M., Forstner, Andreas J., Strohmaier, Jana, Hecker, Julian, Schulze, Thomas G., Müller-Myhsok, Bertram, Reif, Andreas, Mitchell, Philip B., Martin, Nicholas G., Schofield, Peter R., Cichon, Sven ... MooDS Bipolar Consortium (2017). Common variants at 2q11.2, 8q21.3, and 11q13.2 are associated with major mood disorders. Translational Psychiatry, 7 (12) 1273. doi: 10.1038/s41398-017-0019-0

  • Genome-wide association studies of a broad spectrum of antisocial behavior

    Tielbeek, Jorim J., Johansson, Ada, Polderman, Tinca J.C., Rautiainen, Marja-Riitta, Jansen, Philip, Taylor, Michelle, Tong, Xiaoran, Lu, Qing, Burt, Alexandra S., Tiemeier, Henning, Viding, Essi, Plomin, Robert, Martin, Nicholas G., Heath, Andrew C., Madden, Pamela A.F., Montgomery, Grant, Beaver, Kevin M., Waldman, Irwin, Gelernter, Joel, Kranzler, Henry R., Farrer, Lindsay A., Perry, John R.B., Munafò, Marcus, LoParo, Devon, Paunio, Tiina, Tiihonen, Jari, Mous, Sabine E., Pappa, Irene, De Leeuw, Christiaan ... Broad Antisocial Behavior Consortium (2017). Genome-wide association studies of a broad spectrum of antisocial behavior. JAMA Psychiatry, 74 (12), 1242-1250. doi: 10.1001/jamapsychiatry.2017.3069

  • Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity

    Joshi, Peter K., Pirastu, Nicola, Kentistou, Katherine A., Fischer, Krista, Hofer, Edith, Schraut, Katharina E., Clark, David W., Nutile, Teresa, Barnes, Catriona L. K., Timmers, Paul R. H. J., Shen, Xia, Gandin, Ilaria, McDaid, Aaron F., Hansen, Thomas Folkmann, Gordon, Scott D., Giulianini, Franco, Boutin, Thibaud S., Abdellaoui, Abdel, Zhao, Wei, Medina-Gomez, Carolina, Bartz, Traci M., Trompet, Stella, Lange, Leslie A., Raffield, Laura, Van Der Spek, Ashley, Galesloot, Tessel E., Proitsi, Petroula, Yanek, Lisa R., Bielak, Lawrence F. ... Wilson, James F. (2017). Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity. Nature Communications, 8 (1) 910, 910. doi: 10.1038/s41467-017-00934-5

  • Heritability and GWAS analyses of acne in australian adolescent twins

    Mina-Vargas, Angela, Colodro-Conde, Lucía, Grasby, Katrina, Zhu, Gu, Gordon, Scott, Medland, Sarah E. and Martin, Nicholas G. (2017). Heritability and GWAS analyses of acne in australian adolescent twins. Twin Research and Human Genetics, 20 (6), 541-549. doi: 10.1017/thg.2017.58

  • Assessment of moderate coffee consumption and risk of epithelial ovarian cancer: a Mendelian randomization study

    Ong, Jue-Sheng, Hwang, Liang-Dar, Cuellar-Partida, Gabriel, Martin, Nicholas G., Chenevix-Trench, Georgia, Quinn, Michael C. J., Cornelis, Marilyn C., Gharahkhani, Puya, Webb, Penelope M., MacGregor, Stuart and Ovarian Cancer Association Consortium (2017). Assessment of moderate coffee consumption and risk of epithelial ovarian cancer: a Mendelian randomization study. International Journal of Epidemiology, 47 (2), 450-459. doi: 10.1093/ije/dyx236

  • Genome-wide association study identifies a novel locus for cannabis dependence

    Agrawal, A., Chou, Y.- L., Carey, C. E., Baranger, D. A. A., Zhang, B., Sherva, R., Wetherill, L., Kapoor, M., Wang, J.-.C., Bertelsen, S., Anokhin, A. P., Hesselbrock, V., Kramer, J., Lynskey, M. T., Meyers, J. L., Nurnberger, J. I., Rice, J. P., Tischfield, J., Bierut, L. J., Degenhardt, L., Farrer, L. A., Gelernter, J., Hariri, A. R., Heath, A. C., Kranzler, H. R., Madden, P. A. F., Martin, N. G., Montgomery, G. W., Porjesz, B. ... Nelson, E. C. (2017). Genome-wide association study identifies a novel locus for cannabis dependence. Molecular Psychiatry, 23 (5), 1293-1302. doi: 10.1038/mp.2017.200

  • Genome-wide compound heterozygote analysis highlights alleles associated with adult height in Europeans

    Zhong, Kaiyin, Zhu, Gu, Jing, Xiaoxi, Hendriks, A. Emile J., Drop, Sten L. S., Ikram, M. Arfan, Gordon, Scott, Zeng, Changqing, Uitterlinden, Andre G., Martin, Nicholas G., Liu, Fan and Kayser, Manfred (2017). Genome-wide compound heterozygote analysis highlights alleles associated with adult height in Europeans. Human Genetics, 136 (11-12), 1407-1417. doi: 10.1007/s00439-017-1842-3

  • Investigating the relationship between iron and depression

    Mills, Natalie T., Maier, Robert, Whitfield, John B., Wright, Margaret J., Colodro-Conde, Lucia, Byrne, Enda M., Scott, James G., Byrne, Gerard J., Hansell, Narelle K., Vinkhuyzen, Anna A. E., CouvyDuchesne, Baptiste, Montgomery, Grant W., Henders, Anjali K., Martin, Nicholas G., Wray, Naomi R. and Benyamin, Beben (2017). Investigating the relationship between iron and depression. Journal of Psychiatric Research, 94, 148-155. doi: 10.1016/j.jpsychires.2017.07.006

  • Lonely people tend to make fun of themselves: A behavior genetic analysis of humor styles and loneliness

    Schermer, Julie Aitken, Martin, Rod A., Vernon, Philip A., Martin, Nicholas G., Conde, Lucia Colodro, Statham, Dixie and Lynskey, Michael T. (2017). Lonely people tend to make fun of themselves: A behavior genetic analysis of humor styles and loneliness. Personality and Individual Differences, 117, 71-73. doi: 10.1016/j.paid.2017.05.042

  • Education in twins and their parents across birth cohorts over 100 years: an individual-level pooled analysis of 42-twin cohorts

    Silventoinen, Karri, Jelenkovic, Aline, Latvala, Antti, Sund, Reijo, Yokoyama, Yoshie, Ullemar, Vilhelmina, Almqvist, Catarina, Derom, Catherine A., Vlietinck, Robert F., Loos, Ruth J. F., Kandler, Christian, Honda, Chika, Inui, Fujio, Iwatani, Yoshinori, Watanabe, Mikio, Rebato, Esther, Stazi, Maria A., Fagnani, Corrado, Brescianini, Sonia, Hur, Yoon-Mi, Jeong, Hoe-Uk, Cutler, Tessa L., Hopper, John L., Busjahn, Andreas, Saudino, Kimberly J., Ji, Fuling, Ning, Feng, Pang, Zengchang, Rose, Richard J. ... Kaprio, Jaakko (2017). Education in twins and their parents across birth cohorts over 100 years: an individual-level pooled analysis of 42-twin cohorts. Twin Research and Human Genetics, 20 (5), 395-405. doi: 10.1017/thg.2017.49

  • Human subcortical brain asymmetries in 15,847 people worldwide reveal effects of age and sex

    Guadalupe, Tulio, Mathias, Samuel R., vanErp, Theo G. M., Whelan, Christopher D., Zwiers, Marcel P., Abe, Yoshinari, Abramovic, Lucija, Agartz, Ingrid, Andreassen, Ole A., Arias-Vásquez, Alejandro, Aribisala, Benjamin S., Armstrong, Nicola J., Arolt, Volker, Artiges, Eric, Ayesa-Arriola, Rosa, Baboyan, Vatche G., Banaschewski, Tobias, Barker, Gareth, Bastin, Mark E., Baune, Bernhard T., Blangero, John, Bokde, Arun L.W., Boedhoe, Premika S.W., Bose, Anushree, Brem, Silvia, Brodaty, Henry, Bromberg, Uli, Brooks, Samantha, Büchel, Christian ... Francks, Clyde (2017). Human subcortical brain asymmetries in 15,847 people worldwide reveal effects of age and sex. Brain Imaging and Behavior, 11 (5), 1497-1514. doi: 10.1007/s11682-016-9629-z

  • CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits

    Macé, Aurélien, Tuke, Marcus A., Deelen, Patrick, Kristiansson, Kati, Mattsson, Hannele, Nõukas, Margit, Sapkota, Yadav, Schick, Ursula, Porcu, Eleonora, Rüeger, Sina, McDaid, Aaron F., Porteous, David, Winkler, Thomas W., Salvi, Erika, Shrine, Nick, Liu, Xueping, Ang, Wei Q., Zhang, Weihua, Feitosa, Mary F., Venturini, Cristina, Van Der Most, Peter J., Rosengren, Anders, Wood, Andrew R., Beaumont, Robin N., Jones, Samuel E., Ruth, Katherine S., Yaghootkar, Hanieh, Tyrrell, Jessica, Havulinna, Aki S. ... Kutalik, Zoltán (2017). CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits. Nature Communications, 8 (1) 744, 744. doi: 10.1038/s41467-017-00556-x

  • Hidden heritability due to heterogeneity across seven populations

    Tropf, Felix C., Lee, S Hong, Verweij, Renske M., Stulp, Gert, van der Most, Peter J., de Vlaming, Ronald, Bakshi, Andrew, Briley, Daniel A., Rahal, Charles, Hellpap, Robert, Nyman, Anastasia, Esko, Tõnu, Metspalu, Andres, Medland, Sarah E., Martin, Nicholas G., Barban, Nicola, Snieder, Harold, Robinson, Matthew R. and Mills, Melinda C. (2017). Hidden heritability due to heterogeneity across seven populations. Nature Human Behaviour, 1 (10), 757-765. doi: 10.1038/s41562-017-0195-1

  • Assessing the accuracy of perceptions of intelligence based on heritable facial features

    Lee, Anthony J., Hibbs, Courtney, Wright, Margaret J., Martin, Nicholas G., Keller, Matthew C. and Zietsch, Brendan P. (2017). Assessing the accuracy of perceptions of intelligence based on heritable facial features. Intelligence, 64, 1-8. doi: 10.1016/j.intell.2017.06.002

  • Genome-Wide Association shows that pigmentation genes play a role in skin aging

    Law, Matthew H., Medland, Sarah E., Zhu, Gu, Yazar, Seyhan, Vinuela, Ana, Wallace, Leanne, Shekar, Sri Niranjan, Duffy, David L., Bataille, Veronique, Glass, Dan, Spector, Tim D., Wood, Diane, MuTHER Consortium, Gordon, Scott D., Barbour, Julie M., Henders, Anjali K., Hewitt, Alex W., Montgomery, Grant W., Sturm, Richard A., Mackey, David A., Green, Adele C., Martin, Nicholas G. and MacGregor, Stuart (2017). Genome-Wide Association shows that pigmentation genes play a role in skin aging. Journal of Investigative Dermatology, 137 (9), 1887-1894. doi: 10.1016/j.jid.2017.04.026

  • Identification of a bipolar disorder vulnerable gene CHDH at 3p21.1

    Chang, Hong, Li, Lingyi, Peng, Tao, Grigoroiu-Serbanescu, Maria, Bergen, Sarah E., Landén, Mikael, Hultman, Christina M., Forstner, Andreas J., Strohmaier, Jana, Hecker, Julian, Schulze, Thomas G., Müller-Myhsok, Bertram, Reif, Andreas, Mitchell, Philip B., Martin, Nicholas G., Cichon, Sven, Nöthen, Markus M., Jamain, Stéphane, Leboyer, Marion, Bellivier, Frank, Etain, Bruno, Kahn, Jean-Pierre, Henry, Chantal, Rietschel, Marcella, Backlund, Lena, Frisén, Louise, Lavebratt, Catharina, Schalling, Martin, Ösby, Urban ... MooDS Consortium (2017). Identification of a bipolar disorder vulnerable gene CHDH at 3p21.1. Molecular Neurobiology, 54 (7), 5166-5176. doi: 10.1007/s12035-016-0041-x

  • Major depressive disorder, suicidal thoughts and behaviours, and cannabis involvement in discordant twins: a retrospective cohort study

    Agrawal, Arpana, Nelson, Elliot C., Bucholz, Kathleen K., Tillman, Rebecca, Grucza, Richard A., Statham, Dixie J., Madden, Pamela A. F., Martin, Nicholas G., Heath, Andrew C. and Lynskey, Michael T. (2017). Major depressive disorder, suicidal thoughts and behaviours, and cannabis involvement in discordant twins: a retrospective cohort study. The Lancet Psychiatry, 4 (9), 706-714. doi: 10.1016/S2215-0366(17)30280-8

  • Differences in genetic and environmental variation in adult BMI by sex, age, time period, and region: an individual-based pooled analysis of 40 twin cohorts

    Silventoinen, Karri, Jelenkovic, Aline, Sund, Reijo, Yokoyama, Yoshie, Hur, Yoon-Mi, Cozen, Wendy, Hwang, Amie E., Mack, Thomas M., Honda, Chika, Inui, Fujio, Iwatani, Yoshinori, Watanabe, Mikio, Tomizawa, Rie, Pietilainen, Kirsi H., Rissanen, Aila, Siribaddana, Sisira H., Hotopf, Matthew, Sumathipala, Athula, Rijsdijk, Fruhling, Tan, Qihua, Zhang, Dongfeng, Pang, Zengchang, Piirtola, Maarit, Aaltonen, Sari, Oncel, Sevgi Y., Aliev, Fazil, Rebato, Esther, Hjelmborg, Jacob B., Christensen, Kaare ... Kaprio, Jaakko (2017). Differences in genetic and environmental variation in adult BMI by sex, age, time period, and region: an individual-based pooled analysis of 40 twin cohorts. American Journal of Clinical Nutrition, 106 (2), 457-466. doi: 10.3945/ajcn.117.153643

  • From alcohol initiation to tolerance to problems: Discordant twin modeling of a developmental process

    Deutsch, Arielle R., Slutske, Wendy S., Lynskey, Michael T., Bucholz, Kathleen K., Madden, Pamela A. F., Heath, Andrew C. and Martin, Nicholas G. (2017). From alcohol initiation to tolerance to problems: Discordant twin modeling of a developmental process. Development and Psychopathology, 29 (3), 845-861. doi: 10.1017/S0954579416000523

  • Neuroticism and the Overlap between Autistic and ADHD Traits: Findings from a Population Sample of Young Adult Australian Twins

    Park, Shin-Ho, Guastella, Adam J., Lynskey, Michael, Agrawal, Arpana, Constantino, John N., Medland, Sarah E., Song, Yun Ju C., Martin, Nicholas G. and Colodro-Conde, Lucía (2017). Neuroticism and the Overlap between Autistic and ADHD Traits: Findings from a Population Sample of Young Adult Australian Twins. Twin Research and Human Genetics, 20 (4), 319-329. doi: 10.1017/thg.2017.38

  • Validation and psychometric properties of the Somatic and Psychological HEalth REport (SPHERE) in a young Australian-based population sample using non-parametric item response theory

    Couvy-Duchesne, Baptiste, Davenport, Tracey A., Martin, Nicholas G., Wright, Margaret J. and Hickie, Ian B. (2017). Validation and psychometric properties of the Somatic and Psychological HEalth REport (SPHERE) in a young Australian-based population sample using non-parametric item response theory. BMC Psychiatry, 17 (1) 279, 279. doi: 10.1186/s12888-017-1420-1

  • Facial trustworthiness is associated with heritable aspects of face shape

    Lee, Anthony J., Wright, Margaret J., Martin, Nicholas G., Keller, Matthew C. and Zietsch, Brendan P. (2017). Facial trustworthiness is associated with heritable aspects of face shape. Adaptive Human Behavior and Physiology, 3 (4), 351-364. doi: 10.1007/s40750-017-0073-0

  • Common variants of T-cells contribute differently to phenotypic variation in sarcoidosis

    Rivera, Natalia V., Hagemann-Jensen, Michael, Ferreira, Manuel A. R., Kullberg, Susanna, Eklund, Anders, Martin, Nicholas G., Padyukov, Leonid and Grunewald, Johan (2017). Common variants of T-cells contribute differently to phenotypic variation in sarcoidosis. Scientific Reports, 7 (1) 5623. doi: 10.1038/s41598-017-05754-7

  • A direct test of the diathesis–stress model for depression

    Colodro-Conde, L., Couvy-Duchesne, B., Zhu, G., Coventry, W. L., Byrne, E. M., Gordon, S., Wright, M. J., Montgomery, G. W., Madden, P. A. F., Ripke, S., Eaves, L. J., Heath, A. C., Wray, N. R., Medland, S. E. and Martin, N. G. (2017). A direct test of the diathesis–stress model for depression. Molecular Psychiatry, 23 (7), 1590-1596. doi: 10.1038/mp.2017.130

  • No genetic overlap between circulating iron levels and Alzheimer's disease

    Lupton, Michelle K., Benyamin, Beben, Proitsi, Petroula, Nyholt, Dale R., Ferreira, Manuel A., Montgomery, Grant W., Heath, Andrew C., Madden, Pamela A., Medland, Sarah E., Gordon, Scott D., Lovestone, Simon, Tsolaki, Magda, Kloszewska, Iwona, Soininen, Hilkka, Mecocci, Patrizia, Vellas, Bruno, Powell, John F., Bush, Ashley I., Wright, Margaret J., Martin, Nicholas G. and Whitfield, John B. (2017). No genetic overlap between circulating iron levels and Alzheimer's disease. Journal of Alzheimers Disease, 59 (1), 85-99. doi: 10.3233/JAD-170027

  • Cannabis and Depression: A Twin Model Approach to Co-morbidity

    Smolkina, M., Morley, K. I., Rijsdijk, F., Agrawal, A., Bergin, J. E., Nelson, E. C., Statham, D., Martin, N. G. and Lynskey, M. T. (2017). Cannabis and Depression: A Twin Model Approach to Co-morbidity. Behavior Genetics, 47 (4), 394-404. doi: 10.1007/s10519-017-9848-0

  • Single Nucleotide Polymorphisms Associated with Reading Ability Show Connection to Socio-Economic Outcomes

    Luciano, Michelle, Hagenaars, Saskia P. , Cox, Simon R. , Hill, William David , Davies, Gail , Harris, Sarah E. , Deary, Ian J. , Evans, David M. , Martin, Nicholas G. , Wright, Margaret J.  and Bates, Timothy C.  (2017). Single Nucleotide Polymorphisms Associated with Reading Ability Show Connection to Socio-Economic Outcomes. Behavior Genetics, 47 (5), 469-479. doi: 10.1007/s10519-017-9859-x

  • Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia.

    Witt, S. H., Streit, F., Jungkunz, M., Frank, J., Awasthi, S., Reinbold, C. S., Treutlein, J., Degenhardt, F., Forstner, A. J., Heilmann-Heimbach, S., Dietl, L., Schwarze, C. E., Schendel, D., Strohmaier, J., Abdellaoui, A., Adolfsson, R., Air, T. M., Akil, H., Alda, M., Alliey-Rodriguez, N., Andreassen, O. A., Babadjanova, G., Bass, N. J., Bauer, M., Baune, B. T., Bellivier, F., Bergen, S., Bethell, A., Biernacka, J. M. ... Rietschel, M. (2017). Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia.. Translational psychiatry, 7 (6), e1155-e1155. doi: 10.1038/tp.2017.115

  • Genetic influences on individual differences in longitudinal changes in global and subcortical brain volumes: results of the ENIGMA plasticity working group

    Brouwer, Rachel M., Panizzon, Matthew S., Glahn, David C., Hibar, David P., Hua, Xue, Jahanshad, Neda, Abramovic, Lucija, de Zubicaray, Greig I., Franz, Carol E., Hansell, Narelle K., Hickie, Ian B., Koenis, Marinka M. G., Martin, Nicholas G., Mather, Karen A., McMahon, Katie L., Schnack, Hugo G., Strike, Lachlan T., Swagerman, Suzanne C., Thalamuthu, Anbupalam, Wen, Wei, Gilmore, John H., Gogtay, Nitin, Kahn, Rene S., Sachdev, Perminder S., Wright, Margaret J., Boomsma, Dorret I., Kremen, William S., Thompson, Paul M. and Hulshoff Pol, Hilleke E. (2017). Genetic influences on individual differences in longitudinal changes in global and subcortical brain volumes: results of the ENIGMA plasticity working group. Human Brain Mapping, 8 (9), 4444-4458. doi: 10.1002/hbm.23672

  • Familiality and heritability of fatigue in an Australian twin sample

    Corfield, Elizabeth C., Martin, Nicholas G. and Nyholt, Dale R. (2017). Familiality and heritability of fatigue in an Australian twin sample. Twin Research and Human Genetics, 20 (3), 208-215. doi: 10.1017/thg.2017.22

  • The Anorexia Nervosa Genetics Initiative: study description and sample characteristics of the Australian and New Zealand arm

    Kirk, Katherine M., Martin, Felicity C., Mao, Amy, Parker, Richard, Maguire, Sarah, Thornton, Laura M., Zhu, Gu, McAloney, Kerrie, Freeman, Jeremy L., Hay, Phillipa, Madden, Sloane, Morgan, Christine, Russell, Janice, Sawyer, Susan M., Hughes, Elizabeth K., Fairweather-Schmidt, A. Kate, Fursland, Anthea, McCormack, Julie, Wagg, Fiona, Jordan, Jennifer, Kennedy, Martin A., Ward, Warren, Wade, Tracey D., Bulik, Cynthia M. and Martin, Nicholas G. (2017). The Anorexia Nervosa Genetics Initiative: study description and sample characteristics of the Australian and New Zealand arm. Australian and New Zealand Journal of Psychiatry, 51 (6), 583-594. doi: 10.1177/0004867417700731

  • Meta-analysis identifies five novel loci associated with endometriosis highlighting key genes involved in hormone metabolism

    Sapkota, Yadav, Steinthorsdottir, Valgerdur, Morris, Andrew P., Fassbender, Amelie, Rahmioglu, Nilufer, De Vivo, Immaculata, Buring, Julie E., Zhang, Futao, Edwards, Todd L., Jones, Sarah, Dorien, O., Peterse, Danielle, Rexrode, Kathryn M., Ridker, Paul M., Schork, Andrew J., MacGregor, Stuart, Martin, Nicholas G., Becker, Christian M., Adachi, Sosuke, Yoshihara, Kosuke, Enomoto, Takayuki, Takahashi, Atsushi, Kamatani, Yoichiro, Matsuda, Koichi, Kubo, Michiaki, Thorleifsson, Gudmar, Geirsson, Reynir T., Thorsteinsdottir, Unnur, Wallace, Leanne M. ... Nyholt, Dale R. (2017). Meta-analysis identifies five novel loci associated with endometriosis highlighting key genes involved in hormone metabolism. Nature Communications, 8 (1) 15539, 15539. doi: 10.1038/ncomms15539

  • A continuum of genetic liability for minor and major depression

    Corfield, E. C., Yang, Y., Martin, N. G. and Nyholt, D. R. (2017). A continuum of genetic liability for minor and major depression. Translational Psychiatry, 7 (5) e1131, e1131-e1131. doi: 10.1038/tp.2017.99

  • Significant locus and metabolic genetic correlations revealed in genome-wide association study of anorexia nervosa

    Duncan, Laramie, Yilmaz, Zeynep, Gaspar, Helena, Walters, Raymond, Goldstein, Jackie, Anttila, Verneri, Bulik-Sullivan, Brendan, Ripke, Stephan, Thornton, Laura, Hinney, Anke, Daly, Mark, Sullivan, Patrick F., Zeggini, Eleftheria, Breen, Gerome, Bulik, Cynthia M., Duncan, Laramie, Yilmaz, Zeynep, Gaspar, Héléna, Walters, Raymond, Goldstein, Jackie, Anttila, Verneri, Bulik-Sullivan, Brendan, Ripke, Stephan, Adan, Roger, Alfredsson, Lars, Ando, Tetsuya, Andreassen, Ole, Aschauer, Harald, Baker, Jessica ... Eating Disorders Working Group of the Psychiatric Genomics Consortium (2017). Significant locus and metabolic genetic correlations revealed in genome-wide association study of anorexia nervosa. American Journal of Psychiatry, 174 (9), 850-858. doi: 10.1176/appi.ajp.2017.16121402

  • Association between telomere length and risk of cancer and non-neoplastic diseases a Mendelian randomization study

    Haycock, Philip C., Burgess, Stephen, Nounu, Aayah, Zheng, Jie, Okoli, George N., Bowden, Jack, Wade, Kaitlin Hazel, Timpson, Nicholas J., Evans, David M., Willeit, Peter, Aviv, Abraham, Gaunt, Tomr., Hemani, Gibran, Mangino, Massimo, Ellis, Hayley Patricia, Kurian, Kathreena M., Pooley, Karen A., Eeles, Rosalind A., Lee, Jeffrey E., Fang, Shenying, Chen, Wei V., Law, Matthew H., Bowdler, Lisa M., Iles, Mark M., Yang, Qiong, Worrall, Bradford B., Markus, Hugh Stephen, Hung, Rayjean J., Amos, Chris I. ... Smith, George Davey (2017). Association between telomere length and risk of cancer and non-neoplastic diseases a Mendelian randomization study. JAMA Oncology, 3 (5), 636-651. doi: 10.1001/jamaoncol.2016.5945

  • Subcortical brain structure and suicidal behaviour in major depressive disorder: a meta-analysis from the ENIGMA-MDD working group

    Renteria, M. E., Schmaal, L., Hibar, D. P., Couvy-Duchesne, B., Strike, L. T., Mills, N. T., de Zubicaray, G. I., McMahon, K. L., Medland, S. E., Gillespie, N. A., Hatton, S. N., Lagopoulos, J., Veltman, D. J., van der Wee, N., van Erp, T. G. M., Wittfeld, K., Grabe, H. J., Block, A., Hegenscheid, K., Voelzke, H., Veer, I. M., Walter, H., Schnell, K., Schramm, E., Normann, C., Schoepf, D., Konrad, C., Zurowski, B., Godlewska, B. R. ... Hickie, I. B. (2017). Subcortical brain structure and suicidal behaviour in major depressive disorder: a meta-analysis from the ENIGMA-MDD working group. Translational Psychiatry, 7 (5) e1116, e1116-e1116. doi: 10.1038/tp.2017.84

  • Does the sex of one’s co-twin affect height and BMI in adulthood? A study of dizygotic adult twins from 31 cohorts

    Bogl, Leonie H., Jelenkovic, Aline, Vuoksimaa, Eero, Ahrenfeldt, Linda, Pietiläinen, Kirsi H., Stazi, Maria A., Fagnani, Corrado, D’Ippolito, Cristina, Hur, Yoon-Mi, Jeong, Hoe-Uk, Silberg, Judy L., Eaves, Lindon J., Maes, Hermine H., Bayasgalan, Gombojav, Narandalai, Danshiitsoodol, Cutler, Tessa L., Kandler, Christian, Jang, Kerry L., Christensen, Kaare, Skytthe, Axel, Kyvik, Kirsten O., Cozen, Wendy, Hwang, Amie E., Mack, Thomas M., Derom, Catherine A., Vlietinck, Robert F., Nelson, Tracy L., Whitfield, Keith E., Corley, Robin P. ... Kaprio, Jaakko (2017). Does the sex of one’s co-twin affect height and BMI in adulthood? A study of dizygotic adult twins from 31 cohorts. Biology of Sex Differences, 8 (1) 14. doi: 10.1186/s13293-017-0134-x

  • Genome-wide physical activity interactions in adiposity ― a meta-analysis of 200,452 adults

    Graff, Mariaelisa, Scott, Robert A., Justice, Anne E., Young, Kristin L., Feitosa, Mary F., Barata, Llilda, Winkler, Thomas W., Chu, Audrey Y., Mahajan, Anubha, Hadley, David, Xue, Luting, Workalemahu, Tsegaselassie, Heard-Costa, Nancy L., den Hoed, Marcel, Ahluwalia, Tarunveer S., Qi, Qibin, Ngwa, Julius S., Renström, Frida, Quaye, Lydia, Eicher, John D., Hayes, James E., Cornelis, Marilyn, Kutalik, Zoltan, Lim, Elise, Luan, Jian’an, Huffman, Jennifer E., Zhang, Weihua, Zhao, Wei, Griffin, Paula J. ... Kilpeläinen, Tuomas O. (2017). Genome-wide physical activity interactions in adiposity ― a meta-analysis of 200,452 adults. PLoS Genetics, 13 (4) e1006528, e1006528. doi: 10.1371/journal.pgen.1006528

  • Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits

    Justice, Anne E., Winkler, Thomas W., Feitosa, Mary F., Graff, Misa, Fisher, Virginia A., Young, Kristin, Barata, Llilda, Deng, Xuan, Czajkowski, Jacek, Hadley, David, Ngwa, Julius S., Ahluwalia, Tarunveer S., Chu, Audrey Y., Heard-Costa, Nancy L., Lim, Elise, Perez, Jeremiah, Eicher, John D., Kutalik, Zolta'n, Xue, Luting, Mahajan, Anubha, Renström, Frida, Wu, Joseph, Qi, Qibin, Ahmad, Shafqat, Alfred, Tamuno, Amin, Najaf, Bielak, Lawrence F., Bonnefond, Amelie, Bragg, Jennifer ... Cupples, L. Adrienne (2017). Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. Nature Communications, 8 (1) 14977, 14977. doi: 10.1038/ncomms14977

  • Short telomere length is associated with impaired cognitive performance in European ancestry cohorts

    Hagg, S., Zhan, Y., Karlsson, R., Gerritsen, L., Ploner, A., van der Lee, S. J., Broer, L., Deelen, J., Marioni, R. E., Wong, A., Lundquist, A., Zhu, G., Hansell, N. K., Sillanpaa, E., Fedko, I. O., Amin, N. A., Beekman, M., de Craen, A. J. M., Degerman, S., Harris, S. E., Kan, K-J, Martin-Ruiz, C. M., Montgomery, G. W., Adolfsson, A. N., Reynolds, C. A., Samani, N. J., Suchiman, H. E. D., Viljanen, A., von Zglinicki, T. ... Pedersen, N. L. (2017). Short telomere length is associated with impaired cognitive performance in European ancestry cohorts. Translational Psychiatry, 7 (4) e1100, 983-992. doi: 10.1038/tp.2017.73

  • Collaborative meta-analysis finds no evidence of a strong interaction between stress and 5-HTTLPR genotype contributing to the development of depression

    Culverhouse, R. C., Saccone, N. L., Horton, A. C., Ma, Y., Anstey, K. J., Banaschewski, T., Burmeister, M., Cohen-Woods, S., Etain, B., Fisher, H. L., Goldman, N., Guillaume, S., Horwood, J., Juhasz, G., Lester, K. J., Mandelli, L., Middeldorp, C. M., Olie, E., Villafuerte, S., Air, T. M., Araya, R., Bowes, L., Burns, R., Byrne, E. M., Coffey, C., Coventry, W. L., Gawronski, K. A. B., Glei, D., Hatzimanolis, A. ... Bierut, L. J. (2017). Collaborative meta-analysis finds no evidence of a strong interaction between stress and 5-HTTLPR genotype contributing to the development of depression. Molecular Psychiatry, 23 (1), 133-142. doi: 10.1038/mp.2017.44

  • Gene-based analysis of regulatory variants identifies 4 putative novel asthma risk genes related to nucleotide synthesis and signaling

    Ferreira, Manuel A. R., Jansen, Rick, Willemsen, Gonneke, Penninx, Brenda, Bain, Lisa M., Vicente, Cristina T., Revez, Joana A., Matheson, Melanie C., Hui, Jennie, Tung, Joyce Y., Baltic, Svetlana, Le Souef, Peter, Montgomery, Grant W., Martin, Nicholas G., Robertson, Colin F., James, Alan, Thompson, Philip J., Boomsma, Dorret I., Hopper, John L., Hinds, David A., Werder, Rhiannon B., Phipps, Simon and and the Australian Asthma Genetics Consortium Collaborators (2017). Gene-based analysis of regulatory variants identifies 4 putative novel asthma risk genes related to nucleotide synthesis and signaling. Journal of Allergy and Clinical Immunology, 139 (4), 1148-1157. doi: 10.1016/j.jaci.2016.07.017

  • Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk

    Day, Felix R., Thompson, Deborah J., Helgason, Hannes, Chasman, Daniel I., Finucane, Hilary, Sulem, Patrick, Ruth, Katherine S., Whalen, Sean, Sarkar, Abhishek K., Albrecht, Eva, Altmaier, Elisabeth, Amini, Marzyeh, Barbieri, Caterina M., Boutin, Thibaud, Campbell, Archie, Demerath, Ellen, Giri, Ayush, He, Chunyan, Hottenga, Jouke J., Karlsson, Robert, Kolcic, Ivana, Loh, Po-Ru, Lunetta, Kathryn L., Mangino, Massimo, Marco, Brumat, McMahon, George, Medland, Sarah E., Nolte, Ilja M., Noordam, Raymond ... Perry, John R. B. (2017). Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk. Nature Genetics, 49 (6), 834-841. doi: 10.1038/ng.3841

  • Intuitive ethics and political orientations: testing moral foundations as a theory of political ideology

    Smith, Kevin B., Alford, John R., Hibbing, John R., Martin, Nicholas G. and Hatemi, Peter K. (2017). Intuitive ethics and political orientations: testing moral foundations as a theory of political ideology. American Journal of Political Science, 61 (2), 424-437. doi: 10.1111/ajps.12255

  • Genetic effects influencing risk for major depressive disorder in China and Europe

    Bigdeli, T. B., Ripke, S., Peterson, R. E., Trzaskowski, M., Bacanu, S-A, Abdellaoui, A., Andlauer, T. F. M., Beekman, A. T. F., Berger, K., Blackwood, D. H. R., Boomsma, D. I., Breen, G., Buttenschon, H. N., Byrne, E. M., Cichon, S., Clarke, T-K, Couvy-Duchesne, B., Craddock, N., de Geus, E. J. C., Degenhardt, F., Dunn, E. C., Edwards, A. C., Fanous, A. H., Forstner, A. J., Frank, J., Gill, M., Gordon, S. D., Grabe, H. J., Hamilton, S. P. ... Kendler, K. S. (2017). Genetic effects influencing risk for major depressive disorder in China and Europe. Translational Psychiatry, 7 (3) e1074, e1074-e1074. doi: 10.1038/tp.2016.292

  • Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness

    Heilmann-Heimbach, Stefanie, Herold, Christine, Hochfeld, Lara M., Hillmer, Axel M., Nyholt, Dale R., Hecker, Julian, Javed, Asif, Chew, Elaine G. Y., Pechlivanis, Sonali, Drichel, Dmitriy, Heng, Xiu Ting, Del Rosario, Ricardo C.-H., Fier, Heide L., Paus, Ralf, Rueedi, Rico, Galesloot, Tessel E., Moebus, Susanne, Anhalt, Thomas, Prabhakar, Shyam, Li, Rui, Kanoni, Stavroula, Papanikolaou, George, Kutalik, Zoltán, Deloukas, Panos, Philpott, Michael P., Waeber, Gérard, Spector, Tim D., Vollenweider, Peter, Kiemeney, Lambertus A. L. M. ... Nöthen, Markus M. (2017). Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness. Nature Communications, 8 (1) 14694, 14694. doi: 10.1038/ncomms14694

  • GSTP1 does not modify MC1R effects on melanoma risk

    Daley, G. M., Duffy, D. L., Pflugfelder, A., Jagirdar, K., Lee, K. J., Yong, X. L., Eigentler, T. K., Weide, B., Smithers, B. M., Martin, N. G., Garbe, C., Soyer, H. P. and Sturm, R. A. (2017). GSTP1 does not modify MC1R effects on melanoma risk. Experimental Dermatology, 26 (8), 730-733. doi: 10.1111/exd.13114

  • Identification of shared risk loci and pathways for bipolar disorder and schizophrenia

    Forstner, Andreas J., Hecker, Julian, Hofmann, Andrea, Maaser, Anna, Reinbold, Céline S., Mühleisen, Thomas W., Leber, Markus, Strohmaier, Jana, Degenhardt, Franziska, Treutlein, Jens, Mattheisen, Manuel, Schumacher, Johannes, Streit, Fabian, Meier, Sandra, Herms, Stefan, Hoffmann, Per, Lacour, André, Witt, Stephanie H., Reif, Andreas, Müller-Myhsok, Bertram, Lucae, Susanne, Maier, Wolfgang, Schwarz, Markus, Vedder, Helmut, Kammerer-Ciernioch, Jutta, Pfennig, Andrea, Bauer, Michael, Hautzinger, Martin, Moebus, Susanne ... Nöthen, Markus M. (2017). Identification of shared risk loci and pathways for bipolar disorder and schizophrenia. PLoS ONE, 12 (2) e0171595, e0171595. doi: 10.1371/journal.pone.0171595

  • Novel genetic loci associated with hippocampal volume

    Hibar, Derrek P., Adams, Hieab H. H., Jahanshad, Neda, Chauhan, Ganesh, Stein, Jason L., Hofer, Edith, Renteria, Miguel E., Bis, Joshua C., Arias-Vasquez, Alejandro, Ikram, M. Kamran, Desrivieres, Sylvane, Vernooij, Meike W., Abramovic, Lucija, Alhusaini, Saud, Amin, Najaf, Andersson, Micael, Arfanakis, Konstantinos, Aribisala, Benjamin S., Armstrong, Nicola J., Athanasiu, Lavinia, Axelsson, Tomas, Beecham, Ashley H., Beiser, Alexa, Bernard, Manon, Blanton, Susan H., Bohlken, Marc M., Boks, Marco P., Bralten, Janita, Brickman, Adam M. ... Ikram, M. Arfan (2017). Novel genetic loci associated with hippocampal volume. Nature Communications, 8 (1) 13624, 13624. doi: 10.1038/ncomms13624

  • Sensation seeking and impulsive traits as personality endophenotypes for antisocial behavior: evidence from two independent samples

    Mann, Frank D., Engelhardt, Laura, Briley, Daniel A., Grotzinger, Andrew D., Patterson, Megan W., Tackett, Jennifer L., Strathan, Dixie B., Heath, Andrew, Lynskey, Michael, Slutske, Wendy, Martin, Nicholas G., Tucker-Drob, Elliot M. and Harden, K. Paige (2017). Sensation seeking and impulsive traits as personality endophenotypes for antisocial behavior: evidence from two independent samples. Personality and Individual Differences, 105, 30-39. doi: 10.1016/j.paid.2016.09.018

  • Genetic analysis of hyperemesis gravidarum reveals association with intracellular calcium release channel (RYR2)

    Fejzo, Marlena Schoenberg, Myhre, Ronny, Colodro-Conde, Lucía, MacGibbon, Kimber W, Sinsheimer, Janet S., Reddy, M. V. Prasad Linga, Pajukanta, Paivi, Nyholt, Dale R., Wright, Margaret J., Martin, Nicholas G., Engel, Stephanie M., Medland, Sarah E., Magnus, Per and Mullin, Patrick M. (2017). Genetic analysis of hyperemesis gravidarum reveals association with intracellular calcium release channel (RYR2). Molecular and Cellular Endocrinology, 439 (C), 308-316. doi: 10.1016/j.mce.2016.09.017

  • Identification of novel loci affecting circulating chromogranins and related peptides

    Benyamin, Beben, Maihofer, Adam X., Schork, Andrew J., Hamilton, Bruce A., Rao, Fangwen, Schmid-Schonbein, Geert W., Zhang, Kuixing, Mahata, Manjula, Stridsberg, Mats, Schork, Nicholas J., Biswas, Nilima, Hook, Vivian Y., Wei, Zhiyun, Montgomery, Grant W., Martin, Nicholas G., Nievergelt, Caroline M., Whitfield, John B. and O'Connor, Daniel T. (2017). Identification of novel loci affecting circulating chromogranins and related peptides. Human Molecular Genetics, 26 (1), 233-242. doi: 10.1093/hmg/ddw380

  • Genome-wide regional heritability mapping identifies a locus within the TOX2 gene associated with major depressive disorder

    Zeng, Yanni, Navarro, Pau, Shirali, Masoud, Howard, David M., Adams, Mark J., Hall, Lynsey S., Clarke, Toni-Kim, Thomson, Pippa A., Smith, Blair H., Murray, Alison, Padmanabhan, Sandosh, Hayward, Caroline, Boutin, Thibaud, MacIntyre, Donald J., Lewis, Cathryn M., Wray, Naomi R., Mehta, Divya, Penninx, Brenda W. J. H., Milaneschi, Yuri, Baune, Bernhard T., Air, Tracy, Hottenga, Jouke-Jan, Mbarek, Hamdi, Castelao, Enrique, Pistis, Giorgio, Schulze, Thomas G., Streit, Fabian, Forstner, Andreas J., Byrne, Enda M. ... McIntosh, Andrew M. (2016). Genome-wide regional heritability mapping identifies a locus within the TOX2 gene associated with major depressive disorder. Biological Psychiatry, 82 (5), 312-321. doi: 10.1016/j.biopsych.2016.12.012

  • Heritability of the shape of subcortical brain structures in the general population

    Roshchupkin, Gennady V., Gutman, Boris A., Vernooij, Meike W., Jahanshad, Neda, Martin, Nicholas G., Hofman, Albert, McMahon, Katie L., van der Lee, Sven J., Van Duijn, Cornelia M., de Zubicaray, Greig I., Uitterlinden, Andre´ G., Wright, Margaret J., Niessen, Wiro J., Thompson, Paul M., Ikram, M. Arfan and Adams, Hieab H.H. (2016). Heritability of the shape of subcortical brain structures in the general population. Nature Communications, 7 (1) 13738, 1-8. doi: 10.1038/ncomms13738

  • Convergent lines of evidence support LRP8 as a susceptibility gene for psychosis

    Li, Ming, Huang, Liang, Grigoroiu-Serbanescu, Maria, Bergen, Sarah E., Landén, Mikael, Hultman, Christina M., Forstner, Andreas J., Strohmaier, Jana, Hecker, Julian, Schulze, Thomas G., Müller-Myhsok, Bertram, Reif, Andreas, Mitchell, Philip B., Martin, Nicholas G., Cichon, Sven, Nöthen, Markus M., Alkelai, Anna, Lerer, Bernard, Jamain, Stéphane, Leboyer, Marion, Bellivier, Frank, Etain, Bruno, Kahn, Jean-Pierre, Henry, Chantal, Rietschel, Marcella, MooDS Consortium, and The Swedish Bipolar Study Group, (2016). Convergent lines of evidence support LRP8 as a susceptibility gene for psychosis. Molecular Neurobiology, 53 (10), 6608-6619. doi: 10.1007/s12035-015-9559-6

  • Hans J. Eysenck and Raymond B. Cattell on intelligence and personality

    Boyle, Gregory J., Stankov, Lazar, Martin, Nicholas G., Petrides, K. V., Eysenck, Michael W. and Ortet, Generos (2016). Hans J. Eysenck and Raymond B. Cattell on intelligence and personality. Personality and Individual Differences, 103, 40-47. doi: 10.1016/j.paid.2016.04.029

  • Partitioning heritability analysis reveals a shared genetic basis of brain anatomy and schizophrenia

    Lee, P. H., Baker, J. T., Holmes, A. J., Jahanshad, N., Ge, T., Jung, J. -Y., Cruz, Y., Manoach, D. S., Hibar, D. P., Faskowitz, J., McMahon, K. L., De Zubicaray, G. I., Martin, N. H., Wright, M. J., Ongur, D., Buckner, R., Roffman, J., Thompson, P. M. and Smoller, J. W. (2016). Partitioning heritability analysis reveals a shared genetic basis of brain anatomy and schizophrenia. Molecular Psychiatry, 21 (12), 1680-1689. doi: 10.1038/mp.2016.164

  • Shared genetic factors in the co-occurrence of depression and fatigue

    Corfield, Elizabeth C., Martin, Nicholas G. and Nyholt, Dale R. (2016). Shared genetic factors in the co-occurrence of depression and fatigue. Twin Research and Human Genetics, 19 (6), 610-618. doi: 10.1017/thg.2016.79

  • Cannabis involvement and nonsuicidal self-injury: A discordant twin approach

    Few, Lauren R., Grant, Julia D., Nelson, Elliot C., Trull, Timothy J., Grucza, Richard A., Bucholz, Kathleen K., Verweij, Karin J. H., Martin, Nicholas G., Statham, Dixie J., Madden, Pamela A. F., Heath, Andrew C., Lynskey, Michael T. and Agrawal, Arpana (2016). Cannabis involvement and nonsuicidal self-injury: A discordant twin approach. Journal of Studies on Alcohol and Drugs, 77 (6), 873-880. doi: 10.15288/jsad.2016.77.873

  • Co-occurrence and symptomatology of fatigue and depression

    Corfield, Elizabeth C., Martin, Nicholas G. and Nyholt, Dale R. (2016). Co-occurrence and symptomatology of fatigue and depression. Comprehensive Psychiatry, 71, 1-10. doi: 10.1016/j.comppsych.2016.08.004

  • Genetic and environmental contributions to cognitive structure in Australian twins: a reappraisal

    Loehlin, John C., Hansell, Narelle K., Wright, Margaret J. and Martin, Nicholas G. (2016). Genetic and environmental contributions to cognitive structure in Australian twins: a reappraisal. Intelligence, 59, 24-31. doi: 10.1016/j.intell.2016.05.007

  • Genetic loci for Epstein-Barr virus nuclear antigen-1 are associated with risk of multiple sclerosis

    Zhou, Yuan, Zhu, Gu, Charlesworth, Jac C., Simpson, Steve, Rubicz, Rohina, Göring, Harald H.H., Patsopoulos, Nikolaos A., Laverty, Caroline, Wu, Feitong, Henders, Anjali, Ellis, Jonathan J., Van Der Mei, Ingrid, Montgomery, Grant W., Blangero, John, Curran, Joanne E., Johnson, Matthew P., Martin, Nicholas G., Nyholt, Dale R. and Taylor, Bruce V. (2016). Genetic loci for Epstein-Barr virus nuclear antigen-1 are associated with risk of multiple sclerosis. Multiple Sclerosis, 22 (13), 1655-1664. doi: 10.1177/1352458515626598

  • Is the association between sweet and bitter perception due to genetic variation?

    Hwang, Liang-Dar, Breslin, Paul A. S., Reed, Danielle R., Zhu, Gu, Martin, Nicholas G. and Wright, Margaret J. (2016). Is the association between sweet and bitter perception due to genetic variation?. Chemical Senses, 41 (9), 737-744. doi: 10.1093/chemse/bjw083

  • Variation in latent classes of adult attention–deficit hyperactivity disorder by sex and environmental adversity

    Ebejer, Jane L., Medland, Sarah E., van der Werf, Julius, Lynskey, Michael, Martin, Nicholas G. and Duffy, David L. (2016). Variation in latent classes of adult attention–deficit hyperactivity disorder by sex and environmental adversity. Journal of Attention Disorders, 20 (11), 934-945. doi: 10.1177/1087054713506261

  • Evidence for mitochondrial genetic control of autosomal gene expression

    Kassam, Irfahan, Qi, Tuan, Lloyd-Jones, Luke, Holloway, Alexander, Bonder, Marc Jan, Henders, Anjali K., Martin, Nicholas G., Powell, Joseph E., Franke, Lude, Montgomery, Grant W., Visscher, Peter M. and McRae, Allan F. (2016). Evidence for mitochondrial genetic control of autosomal gene expression. Human Molecular Genetics, 25 (24), 5332-5338. doi: 10.1093/hmg/ddw347

  • Novel genetic loci underlying human intracranial volume identified through genome-wide association

    Adams, Hieab H. H., Hibar, Derrek P., Chouraki, Vincent, Stein, Jason L., Nyquist, Paul A., Renteria, Miguel E., Trompet, Stella, Arias-Vasquez, Alejandro, Seshadri, Sudha, Desrivieres, Sylvane, Beecham, Ashley H., Jahanshad, Neda, Wittfeld, Katharina, Van der Lee, Sven J., Abramovic, Lucija, Alhusaini, Saud, Amin, Najaf, Andersson, Micael, Arfanakis, Konstantinos, Aribisala, Benjamin S., Armstrong, Nicola J., Athanasiu, Lavinia, Axelsson, Tomas, Beiser, Alexa, Bernard, Manon, Bis, Joshua C., Blanken, Laura M. E., Blanton, SusanH., Bohlken, Marc M. ... Thompson, Paul M. (2016). Novel genetic loci underlying human intracranial volume identified through genome-wide association. Nature Neuroscience, 19 (12), 1569-1582. doi: 10.1038/nn.4398

  • A genome-wide association meta-analysis of attention-deficit/hyperactivity disorder symptoms in population-based pediatric cohorts

    Middeldorp, Christel M., Hammerschlag, Anke R., Ouwens, Klaasjan G., Groen-Blokhuis, Maria M., St Pourcain, Beate, Greven, Corina U., Pappa, Irene, Tiesler, Carla M. T., Ang, Wei, Nolte, Ilja M., Vilor-Tejedor, Natalia, Bacelis, Jonas, Ebejer, Jane L., Zhao, Huiying, Davies, Gareth E., Ehli, Erik A., Evans, David M., Fedko, Iryna O., Guxens, Monica, Hottenga, Jouke-Jan, Hudziak, James J., Jugessur, Astanand, Kemp, John P., Krapohl, Eva, Martin, Nicholas G., Murcia, Mario, Myhre, Ronny, Ormel, Johan, Ring, Susan M. ... Boomsma, Dorret I. (2016). A genome-wide association meta-analysis of attention-deficit/hyperactivity disorder symptoms in population-based pediatric cohorts. Journal of the American Academy of Child and Adolescent Psychiatry, 55 (10), 896-905.e6. doi: 10.1016/j.jaac.2016.05.025

  • Age at first use and later substance use disorder: shared genetic and environmental pathways for nicotine, alcohol, and cannabis

    Richmond-Rakerd, Leah S., Slutske, Wendy S., Lynskey, Michael T., Agrawal, Arpana, Madden, Pamela A. F., Bucholz, Kathleen K., Heath, Andrew C., Statham, Dixie J. and Martin, Nicholas G. (2016). Age at first use and later substance use disorder: shared genetic and environmental pathways for nicotine, alcohol, and cannabis. Journal of Abnormal Psychology, 125 (7), 946-959. doi: 10.1037/abn0000191

  • Genetic variants in RBFOX3 are associated with sleep latency

    Amin, Najaf, Allebrandt, Karla V., van der Spek, Ashley, Müller-Myhsok, Bertram, Hek, Karin, Teder-Laving, Maris, Hayward, Caroline, Esko, Tõnu, van Mill, Josine G., Mbarek, Hamdi, Watson, Nathaniel F., Melville, Scott A., Del Greco, Fabiola M., Byrne, Enda M., Oole, Edwin, Kolcic, Ivana, Chen, Ting-hsu, Evans, Daniel S., Coresh, Josef, Vogelzangs, Nicole, Karjalainen, Juha, Willemsen, Gonneke, Gharib, Sina A., Zgaga, Lina, Mihailov, Evelin, Stone, Katie L., Campbell, Harry, Brouwer, Rutger W. W., Demirkan, Ayse ... van Duijn, Cornelia M. (2016). Genetic variants in RBFOX3 are associated with sleep latency. European Journal of Human Genetics, 24 (10), 1488-1495. doi: 10.1038/ejhg.2016.31

  • Hair cortisol and its association with psychological risk factors for psychiatric disorders: a pilot study in adolescent twins

    Rietschel, Liz, Streit, Fabian, Zhu, Gu, McAloney, Kerrie, Kirschbaum, Clemens, Frank, Josef, Hansell, Narelle K., Wright, Margaret J., McGrath, John J., Witt, Stephanie H., Rietschel, Marcella and Martin, Nicholas G. (2016). Hair cortisol and its association with psychological risk factors for psychiatric disorders: a pilot study in adolescent twins. Twin Research and Human Genetics, 19 (5), 438-446. doi: 10.1017/thg.2016.50

  • Meta-analysis of genome-wide association studies of anxiety disorders

    Otowa, T., Hek, K., Lee, M., Byrne, E. M., Mirza, S. S., Nivard, M. G., Bigdeli, T., Aggen, S. H., Adkins, D., Wolen, A., Fanous, A., Keller, M. C., Castelao, E., Kutalik, Z., Der Auwera, S. V., Homuth, G., Nauck, M., Teumer, A., Milaneschi, Y., Hottenga, J. -J., Direk, N., Hofman, A., Uitterlinden, A., Mulder, C. L., Henders, A. K., Medland, S. E., Gordon, S., Heath, A. C., Madden, P. A. F. ... Hettema, J. M. (2016). Meta-analysis of genome-wide association studies of anxiety disorders. Molecular Psychiatry, 21 (10), 1391-1399. doi: 10.1038/mp.2015.197

  • Most of the genetic covariation between major depressive and alcohol use disorders is explained by trait measures of negative emotionality and behavioral control

    Ellingson, J. M., Richmond-Rakerd, L. S., Statham, D. J., Martin, N. G. and Slutske, W. S. (2016). Most of the genetic covariation between major depressive and alcohol use disorders is explained by trait measures of negative emotionality and behavioral control. Psychological Medicine, 46 (14), 2919-2930. doi: 10.1017/S0033291716001525

  • Sweet taste perception is associated with body mass index at the phenotypic and genotypic level

    Hwang, Liang-Dar, Cuellar-Partida, Gabriel, Ong, Jue-Sheng, Breslin, Paul A. S., Reed, Danielle R., Macgregor, Stuart, Gharahkhani, Puya, Martin, Nicholas G. and Renteria, Miguel E. (2016). Sweet taste perception is associated with body mass index at the phenotypic and genotypic level. Twin Research and Human Genetics, 19 (5), 465-471. doi: 10.1017/thg.2016.60

  • Genome-wide association study of working memory brain activation

    Blokland, Gabriella A. M., Wallace, Angus K., Hansell, Narelle K., Thompson, Paul M., Hickie, Ian B., Montgomery, Grant W., Martin, Nicholas G., McMahon, Katie L., de Zubicaray, Greig I. and Wright, Margaret J. (2016). Genome-wide association study of working memory brain activation. International Journal of Psychophysiology, 115, 98-111. doi: 10.1016/j.ijpsycho.2016.09.010

  • The association of genetic predisposition to depressive symptoms with non-suicidal and suicidal self-injuries

    Maciejewski, Dominique F., Renteria, Miguel E., Abdellaoui, Abdel, Medland, Sarah E., Few, Lauren R., Gordon, Scott D., Madden, Pamela A. F., Montgomery, Grant, Trull, Timothy J., Heath, Andrew C., Statham, Dixie J., Martin, Nicholas G., Zietsch, Brendan P. and Verweij, Karin J. H. (2016). The association of genetic predisposition to depressive symptoms with non-suicidal and suicidal self-injuries. Behavior Genetics, 47 (1), 1-8. doi: 10.1007/s10519-016-9809-z

  • The role of genes and environment in degree of partner self-similarity

    Sherlock, James M., Verweij, Karin J. H., Murphy, Sean C., Heath, Andrew C., Martin, Nicholas G. and Zietsch, Brendan P. (2016). The role of genes and environment in degree of partner self-similarity. Behavior Genetics, 47 (1), 1-11. doi: 10.1007/s10519-016-9808-0

  • Trans-ethnic fine mapping highlights kidney-function genes linked to salt sensitivity

    Mahajan, Anubha, Rodan, Aylin R., Le, Thu H., Gaulton, Kyle J., Haessler, Jeffrey, Stilp, Adrienne M., Kamatani, Yoichiro, Zhu, Gu, Sofer, Tamar, Puri, Sanjana, Schellinger, Jeffrey N., Chu, Pei-Lun, Cechova, Sylvia, van Zuydam, Natalie, Arnlov, Johan, Flessner, Michael F., Giedraitis, Vilmantas, Heath, Andrew C., Kubo, Michiaki, Larsson, Anders, Lindgren, Cecilia M., Madden, Pamela A.F., Montgomery, Grant W., Papanicolaou, George J., Reiner, Alex P., Sundström, Johan, Thornton, Timothy A., Lind, Lars, Ingelsson, Erik ... Franceschini, Nora (2016). Trans-ethnic fine mapping highlights kidney-function genes linked to salt sensitivity. American Journal of Human Genetics, 99 (3), 636-646. doi: 10.1016/j.ajhg.2016.07.012

  • An analysis of two genome-wide association meta-analyses identifies a new locus for broad depression phenotype

    Direk, Nese, Williams, Stephanie, Smith, Jennifer A., Ripke, Stephan, Air, Tracy, Amare, Azmeraw T., Amin, Najaf, Baune, Bernhard T., Bennett, David A., Blackwood, Douglas H. R., Boomsma, Dorret, Breen, Gerome, Buttenschon, Henriette N., Byrne, Enda M., Borglum, Anders D., Castelao, Enrique, Cichon, Sven, Clarke, Toni-Kim, Cornelis, Marilyn C., Dannlowski, Udo, De Jager, Philip L., Demirkan, Ayse, Domenici, Enrico, van Duijn, Cornelia M., Dunn, Erin C., Eriksson, Johan G., Esko, Tonu, Faul, Jessica D., Ferrucci, Luigi ... Sullivan, Patrick F. (2016). An analysis of two genome-wide association meta-analyses identifies a new locus for broad depression phenotype. Biological Psychiatry, 82 (5), 322-329. doi: 10.1016/j.biopsych.2016.11.013

  • Familial aggregation of migraine and depression: insights from a large Australian twin sample

    Yang, Yuanhao, Zhao, Huiying, Heath, Andrew C., Madden, Pamela A. F., Martin, Nicholas G. and Nyholt, Dale R. (2016). Familial aggregation of migraine and depression: insights from a large Australian twin sample. Twin Research and Human Genetics, 19 (4), 312-321. doi: 10.1017/thg.2016.43

  • Genetic and environmental effects on body mass index from infancy to the onset of adulthood: an individual-based pooled analysis of 45 twin cohorts participating in the COllaborative project of Development of Anthropometrical measures in Twins (CODATwins) study

    Silventoinen, Karri, Jelenkovic, Aline, Sund, Reijo, Hur, Yoon-Mi, Yokoyama, Yoshie, Honda, Chika, Hjelmborg, Jacob B., Moller, Soren, Ooki, Syuichi, Aaltonen, Sari, Ji, Fuling, Ning, Feng, Pang, Zengchang, Rebato, Esther, Busjahn, Andreas, Kandler, Christian, Saudino, Kimberly J., Jang, Kerry L., Cozen, Wendy, Hwang, Amie E., MacK, Thomas M., Gao, Wenjing, Yu, Canqing, Li, Liming, Corley, Robin P., Huibregtse, Brooke M., Christensen, Kaare, Skytthe, Axel, Kyvik, Kirsten O. ... Kaprio, Jaakko (2016). Genetic and environmental effects on body mass index from infancy to the onset of adulthood: an individual-based pooled analysis of 45 twin cohorts participating in the COllaborative project of Development of Anthropometrical measures in Twins (CODATwins) study. American Journal of Clinical Nutrition, 104 (2), 371-379. doi: 10.3945/ajcn.116.130252

  • Genome-wide association study of pathological gambling

    Lang, M., Leménager, T., Streit, F., Fauth-Bühler, M., Frank, J., Juraeva, D., Witt, S. H., Degenhardt, F., Hofmann, A., Heilmann-Heimbach, S., Kiefer, F., Brors, B., Grabe, H. J., John, U., Bischof, A., Bischof, G., Völker, U., Homuth, G., Beutel, M., Lind, P. A., Medland, S. E., Slutske, W. S., Martin, N. G., Völzke, H., Nöthen, M. M., Meyer, C., Rumpf, H. J., Wurst, F. M., Rietschel, M. and Mann, K. F. (2016). Genome-wide association study of pathological gambling. European Psychiatry, 36, 38-46. doi: 10.1016/j.eurpsy.2016.04.001

  • Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

    Gormley, Padhraig, Anttila, Verneri, Winsvold, Bendik S., Palta, Priit, Esko, Tonu, Pers, Tune H., Farh, Kai-How, Cuenca-Leon, Ester, Muona, Mikko, Furlotte, Nicholas A., Kurth, Tobias, Ingason, Andres, McMahon, George, Ligthart, Lannie, Terwindt, Gisela M., Kallela, Mikko, Freilinger, Tobias M., Ran, Caroline, Gordon, Scott G., Stam, Anine H., Steinberg, Stacy, Borck, Guntram, Koiranen, Markku, Quaye, Lydia, Adams, Hieab H. H., Lehtimäki, Terho, Sarin, Antti-Pekka, Wedenoja, Juho, Hinds, David A. ... Palotie, Aarno (2016). Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. Nature Genetics, 48 (8), 856-866. doi: 10.1038/ng.3598

  • Shared genetic factors underlie migraine and depression

    Yang, Yuanhao, Zhao, Huiying, Heath, Andrew C., Madden, Pamela A. F., Martin, Nicholas G. and Nyholt, Dale R. (2016). Shared genetic factors underlie migraine and depression. Twin Research and Human Genetics, 19 (4), 341-350. doi: 10.1017/thg.2016.46

  • Variation and heritability in hair diameter and curvature in an Australian twin sample

    Ho, Yvonne Y. W., Brims, Mark, McNevin, Dennis, Spector, Timothy D., Martin, Nicholas G. and Medland, Sarah E. (2016). Variation and heritability in hair diameter and curvature in an Australian twin sample. Twin Research and Human Genetics, 19 (4), 351-358. doi: 10.1017/thg.2016.45

  • Identification of STOML2 as a putative novel asthma risk gene associated with IL6R

    Revez, J. A., Matheson, M. C., Hui, J., Baltic, S., James, A., Upham, J. W., Dharmage, S., Thompson, P. J., Martin, N. G., Hopper, J. L. and Ferreira, M. A. R. (2016). Identification of STOML2 as a putative novel asthma risk gene associated with IL6R. Allergy, 71 (7), 1020-1030. doi: 10.1111/all.12869

  • Genetic and environmental influences on height from infancy to early adulthood: An individual-based pooled analysis of 45 twin cohorts

    Jelenkovic, Aline, Sund, Reijo, Hur, Yoon-Mi, Yokoyama, Yoshie, Hjelmborg, Jacob V. B., Miller, Soren, Honda, Chika, Magnusson, Patrik K. E., Pedersen, Nancy L., Ooki, Syuichi, Aaltonen, Sari, Stazi, Maria A., Fagnani, Corrado, D'Ippolito, Cristina, Freitas, Duarte L., Maia, Jose Antonio, Ji, Fuling, Ning, Feng, Pang, Zengchang, Rebato, Esther, Busjahn, Andreas, Kandler, Christian, Saudino, Kimberly J., Jang, Kerry L., Cozen, Wendy, Hwang, Amie E., Mack, Thomas M., Gao, Wenjing, Yu, Canqing ... Silventoinen, Karri (2016). Genetic and environmental influences on height from infancy to early adulthood: An individual-based pooled analysis of 45 twin cohorts. Scientific Reports, 6 (1) 28496. doi: 10.1038/srep28496

  • Five endometrial cancer risk loci identified through genome-wide association analysis

    Cheng, Timothy H. T., Thompson, Deborah J., O'Mara, Tracy A., Painter, Jodie N., Glubb, Dylan M., Flach, Susanne, Lewis, Annabelle, French, Juliet D., Freeman-Mills, Luke, Church, David, Gorman, Maggie, Martin, Lynn, Hodgson, Shirley, Webb, Penelope M., Attia, John, Holliday, Elizabeth G., McEvoy, Mark, Scott, Rodney J., Henders, Anjali K., Martin, Nicholas G., Montgomery, Grant W., Nyholt, Dale R., Ahmed, Shahana, Healey, Catherine S., Shah, Mitul, Dennis, Joe, Fasching, Peter A., Beckmann, Matthias W., Hein, Alexander ... Spurdle, Amanda B. (2016). Five endometrial cancer risk loci identified through genome-wide association analysis. Nature Genetics, 48 (6), 667-674. doi: 10.1038/ng.3562

  • Gene-based pleiotropy across migraine with aura and migraine without aura patient groups

    Zhao, Huiying, Eising, Else, De Vries, Boukje, Vijfhuizen, Lisanne S., Anttila, Verneri, Winsvold, Bendik S., Kurth, Tobias, Stefansson, Hreinn, Kallela, Mikko, Malik, Rainer, Stam, Anine H., Arfan Ikram, M., Ligthart, Lannie, Freilinger, Tobias, Alexander, Michael, Müller-Myhsok, Bertram, Schreiber, Stefan, Meitinger, Thomas, Aromas, Arpo, Eriksson, Johan G., Boomsma, Dorret I., Van Duijn, Cornelia M., Zwart, John-Anker, Quaye, Lydia, Kubisch, Christian, Dichgans, Martin, Wessman, Maija, Stefansson, Kari, Chasman, Daniel I. ... Nyholt, Dale R. (2016). Gene-based pleiotropy across migraine with aura and migraine without aura patient groups. Cephalalgia, 36 (7), 648-657. doi: 10.1177/0333102415591497

  • Genome-wide analysis of over 106000 individuals identifies 9 neuroticism-associated loci

    Smith, D. J., Escott-Price, V., Davies, G., Bailey, M. E. S., Colodro-Conde, L., Ward, J., Vedernikov, A., Marioni, R., Cullen, B., Lyall, D., Hagenaars, S. P., Liewald, D. C. M., Luciano, M., Gale, C. R., Ritchie, S. J., Hayward, C., Nicholl, B., Bulik-Sullivan, B., Adams, M., Couvy-Duchesne, B., Graham, N., Mackay, D., Evans, J., Smith, B. H., Porteous, D. J., Medland, S. E., Martin, N. G., Holmans, P., McIntosh, A. M. ... O'Donovan, M. C. (2016). Genome-wide analysis of over 106000 individuals identifies 9 neuroticism-associated loci. Molecular Psychiatry, 21 (6), 749-757. doi: 10.1038/mp.2016.49

  • Heritability and genetic correlation between the cerebral cortex and associated white matter connections

    Shen, Kai-Kai, Dore, Vincent, Rose, Stephen, Fripp, Jurgen, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Thompson, Paul M., Wright, Margaret J. and Salvado, Olivier (2016). Heritability and genetic correlation between the cerebral cortex and associated white matter connections. Human Brain Mapping, 37 (6), 2331-2347. doi: 10.1002/hbm.23177

  • International genome-wide association study consortium identifies novel loci associated with blood pressure in children and adolescents

    Parmar, Priyakumari Ganesh, Taal, H. Rob, Timpson, Nicholas J., Thiering, Elisabeth, Lehtimaki, Terho, Marinelli, Marcella, Lind, Penelope A., Howe, Laura D., Verwoert, Germaine, Aalto, Ville, Uitterlinden, Andre G., Briollais, Laurent, Evans, Dave M., Wright, Margie J., Newnham, John P., Whitfield, John B., Lyytikainen, Leo-Pekka, Rivadeneira, Fernando, Boomsma, Dorrett I., Viikari, Jorma, Gillman, Matthew W., St Pourcain, Beate, Hottenga, Jouke-Jan, Montgomery, Grant W., Hofman, Albert, Kahonen, Mika, Martin, Nicholas G., Tobin, Martin D., Raitakari, Ollie ... Palmer, Lyle J. (2016). International genome-wide association study consortium identifies novel loci associated with blood pressure in children and adolescents. Circulation: Cardiovascular Genetics, 9 (3), 266-278. doi: 10.1161/CIRCGENETICS.115.001190

  • Identification of common genetic variants influencing spontaneous dizygotic twinning and female fertility

    Mbarek, Hamdi, Steinberg, Stacy, Nyholt, Dale R., Gordon, Scott D., Miller, Michael B., McRae, Allan F, Hottenga, Jouke Jan, Day, Felix R., Willemsen, Gonneke, de Geus, Eco J., Davies, Gareth E, Martin, Hilary C, Penninx, Brenda W, Jansen, Rick, McAloney, Kerrie, Vink, Jacqueline M., Kaprio, Jaakko, Plomin, Robert, Spector, Tim D., Magnusson, Patrik K., Reversade, Bruno, Harris, R. Alan, Aagaard, Kjersti, Kristjansson, Ragnar P., Olafsson, Isleifur, Eyjolfsson, Gudmundur Ingi, Sigurdardottir, Olof, Iacono, William G., Lambalk, Cornelis B ... Boomsman, Dorret I. (2016). Identification of common genetic variants influencing spontaneous dizygotic twinning and female fertility. American Journal of Human Genetics, 98 (5), 898-908. doi: 10.1016/j.ajhg.2016.03.008

  • Chorionicity and heritability estimates from twin studies: the prenatal environment of twins and their resemblance across a large number of traits

    van Beijsterveldt, C. E.M., Overbeek, L. I.H., Rozendaal, L., McMaster, M. T.B., Glasner, T. J., Bartels, M., Vink, J. M., Martin, N. G., Dolan, C. V. and Boomsma, D. I. (2016). Chorionicity and heritability estimates from twin studies: the prenatal environment of twins and their resemblance across a large number of traits. Behavior Genetics, 46 (3), 304-314. doi: 10.1007/s10519-015-9745-3

  • Increased incidence of bladder cancer, lymphoid leukaemia, and myeloma in a cohort of Queensland melanoma families

    Read, Jazlyn, Symmons, Judith, Palmer, Jane M., Montgomery, Grant W., Martin, Nicholas G. and Hayward, Nicholas K. (2016). Increased incidence of bladder cancer, lymphoid leukaemia, and myeloma in a cohort of Queensland melanoma families. Familial Cancer, 15 (4), 651-663. doi: 10.1007/s10689-016-9907-3

  • Shared genetic control of expression and methylation in peripheral blood

    Shakhbazov, Konstantin, Powell, Joseph E., Hemani, Gibran, Henders, Anjali K., Martin, Nicholas G., Visscher, Peter M., Montgomery, Grant W. and McRae, Allan F. (2016). Shared genetic control of expression and methylation in peripheral blood. BMC Genomics, 17 (1) 278, 278. doi: 10.1186/s12864-016-2498-4

  • Common genetic variants influence whorls in fingerprint patterns

    Ho, Yvonne Y. W., Evans, David M., Montgomery, Grant W., Henders, Anjali K., Kemp, John P., Timpson, Nicholas J., Pourcain, Beate St., Heath, Andrew C., Madden, Pamela A. F., Loesch, Danuta Z., McNevin, Dennis, Daniel, Runa, Davey-Smith, George, Martin, Nicholas G. and Medland, Sarah E. (2016). Common genetic variants influence whorls in fingerprint patterns. Journal of Investigative Dermatology, 136 (4), 859-862. doi: 10.1016/j.jid.2015.10.062

  • The effect of increased genetic risk for Alzheimer's disease on hippocampal and amygdala volume

    Lupton, Michelle K., Strike, Lachlan, Hansell, Narelle K., Wen, Wei, Mather, Karen A., Armstrong, Nicola J., Thalamuthu, Anbupalam, McMahon, Katie L., de Zubicaray, Greig I., Assareh, Amelia A., Simmons, Andrew, Proitsi, Petroula, Powell, John F., Montgomery, Grant W., Hibar, Derrek P., Westman, Eric, Tsolaki, Magda, Kloszewska, Iwona, Soininen, Hilkka, Mecocci, Patrizia, Velas, Bruno, Lovestone, Simon, Brodaty, Henry, Ames, David, Trollor, Julian N., Martin, Nicholas G., Thompson, Paul M., Sachdev, Perminder S. and Wright, Margaret J. (2016). The effect of increased genetic risk for Alzheimer's disease on hippocampal and amygdala volume. Neurobiology of Aging, 40, 68-77. doi: 10.1016/j.neurobiolaging.2015.12.023

  • Twin's Birth-Order Differences in Height and Body Mass Index From Birth to Old Age: A Pooled Study of 26 Twin Cohorts Participating in the CODATwins Project

    Yokoyama, Yoshie, Jelenkovic, Aline, Sund, Reijo, Sung, Joohon, Hopper, John L., Ooki, Syuichi, Heikkila, Kauko, Aaltonen, Sari, Tarnoki, Adam D., Tarnoki, David L., Willemsen, Gonneke, Bartels, Meike, van Beijsterveldt, Toos C. E. M., Saudino, Kimberly J., Cutler, Tessa L., Nelson, Tracy L., Whitfield, Keith E., Wardle, Jane, Llewellyn, Clare H., Fisher, Abigail, He, Mingguang, Ding, Xiaohu, Bjerregaard-Andersen, Morten, Beck-Nielsen, Henning, Sodemann, Morten, Song, Yun-Mi, Yang, Sarah, Lee, Kayoung, Jeong, Hoe-Uk ... Silventoinen, Karri (2016). Twin's Birth-Order Differences in Height and Body Mass Index From Birth to Old Age: A Pooled Study of 26 Twin Cohorts Participating in the CODATwins Project. Twin Research and Human Genetics, 19 (2), 112-124. doi: 10.1017/thg.2016.11

  • Genome-wide polygenic scores for age at onset of alcohol dependence and association with alcohol-related measures

    Kapoor, M., Chou, Y-L, Edenberg, H. J., Foroud, T., Martin, N. G., Madden, P A F, Wang, J. C., Bertelsen, S., Wetherill, L., Brooks, A., Chan, G., Hesselbrock, V., Kuperman, S., Medland, S. E., Montgomery, G., Tischfield, J., Whitfield, J. B., Bierut, L. J., Heath, A. C., Bucholz, K. K., Goate, A. M. and Agrawal, A. (2016). Genome-wide polygenic scores for age at onset of alcohol dependence and association with alcohol-related measures. Translational Psychiatry, 6 (3) e761, e761-e761. doi: 10.1038/tp.2016.27

  • Cortical abnormalities in adults and adolescents with major depression based on brain scans from 20 cohorts worldwide in the ENIGMA Major Depressive Disorder Working Group

    Schmaal, L., Hibar, D. P., Samann, P. G., Hall, G. B., Baune, B. T., Jahanshad, N., Cheung, J. W., van Erp, T. G. M., Bos, D., Ikram, M. A., Vernooij, M. W., Niessen, W. J., Tiemeier, H., Hofman, A., Wittfeld, K., Grabe, H. J., Janowitz, D., Bulow, R., Selonke, M., Volzke, H., Grotegerd, D., Dannlowski, U., Arolt, V., Opel, N., Heindel, W., Kugel, H., Hoehn, D., Czisch, M., Couvy-Duchesne, B. ... Veltman, D. J. (2016). Cortical abnormalities in adults and adolescents with major depression based on brain scans from 20 cohorts worldwide in the ENIGMA Major Depressive Disorder Working Group. Molecular Psychiatry, 22 (6), 900-909. doi: 10.1038/mp.2016.60

  • Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts

    Schwantes-An, Tae-Hwi, Zhang, Juan, Chen, Li-Shiun, Hartz, Sarah M., Culverhouse, Robert C., Chen, Xiangning, Coon, Hilary, Frank, Josef, Kamens, Helen M., Konte, Bettina, Kovanen, Leena, Latvala, Antti, Legrand, Lisa N., Maher, Brion S., Melroy, Whitney E., Nelson, Elliot C., Reid, Mark W., Robinson, Jason D., Shen, Pei-Hong, Yang, Bao-Zhu, Andrews, Judy A., Aveyard, Paul, Beltcheva, Olga, Brown, Sandra A., Cannon, Dale S., Cichon, Sven, Corley, Robin P., Dahmen, Norbert, Degenhardt, Louisa ... Saccone, Nancy L. (2016). Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts. Behavior Genetics, 46 (2), 151-169. doi: 10.1007/s10519-015-9737-3

  • Common polygenic risk for autism spectrum disorder (ASD) is associated with cognitive ability in the general population

    Clarke, T-K, Lupton, M. K., Fernandez-Pujals, A. M., Starr, J., Davies, G., Cox, S., Pattie, A., Liewald, D. C., Hall, L. S., MacIntyre, D. J., Smith, B. H., Hocking, L. J., Padmanabhan, S., Thomson, P. A., Hayward, C., Hansell, N. K., Montgomery, G. W., Medland, S. E., Martin, N. G., Wright, M. J., Porteous, D. J., Deary, I. J. and McIntosh, A. M. (2016). Common polygenic risk for autism spectrum disorder (ASD) is associated with cognitive ability in the general population. Molecular Psychiatry, 21 (3), 419-425. doi: 10.1038/mp.2015.12

  • Genome-wide association study of lifetime cannabis use based on a large meta-analytic sample of 32 330 subjects from the International Cannabis Consortium

    Stringer, S., Minică, C. C., Verweij, K. J. H., Mbarek, H., Bernard, M., Derringer, J., van Eijk, K. R., Isen, J. D., Loukola, A., Maciejewsk, D. F., Mihailov, E., van der Most, P. J., Sánchez-Mora, C., Roos, L., Sherva, R., Walters, R., Ware, J. J., Abdellaoui, A., Bigdeli, T. B., Branje, S. J. T., Brown, S. A., Bruinenberg, M., Casas, M., Esko, T., Garcia-Martinez, I., Gordon, S. D., Harris, J. M., Hartman, C. A., Henders, A. K. ... Vink, J. M. (2016). Genome-wide association study of lifetime cannabis use based on a large meta-analytic sample of 32 330 subjects from the International Cannabis Consortium. Translational Psychiatry, 6 (3) e769, e769-e769. doi: 10.1038/tp.2016.36

  • Onset of opportunity to use cannabis and progression from opportunity to dependence: are influences consistent across transitions?

    Hines, Lindsey A., Morley, Katherine I., Strang, John, Agrawal, Arpana, Nelson, Elliot C., Statham, Dixie, Martin, Nicholas G. and Lynskey, Michael T. (2016). Onset of opportunity to use cannabis and progression from opportunity to dependence: are influences consistent across transitions?. Drug and Alcohol Dependence, 160, 57-64. doi: 10.1016/j.drugalcdep.2015.12.032

  • CYP19A1 fine-mapping and Mendelian randomization: estradiol is causal for endometrial cancer

    Thompson, Deborah J., O'Mara, Tracy A., Glubb, Dylan M., Painter, Jodie N., Cheng, Timothy, Folkerd, Elizabeth, Doody, Deborah, Dennis, Joe, Webb, Penelope M., Gorman, Maggie, Martin, Lynn, Hodgson, Shirley, Michailidou, Kyriaki, Tyrer, Jonathan P., Maranian, Mel J., Hall, Per, Czene, Kamila, Darabi, Hatef, Li, Jingmei, Fasching, Peter A., Hein, Alexander, Beckmann, Matthias W., Ekici, Arif B., Doerk, Thilo, Hillemanns, Peter, Duerst, Matthias, Runnebaum, Ingo, Zhao, Hui, Depreeuw, Jeroen ... Spurdle, Amanda B. (2016). CYP19A1 fine-mapping and Mendelian randomization: estradiol is causal for endometrial cancer. Endocrine-Related Cancer, 23 (2), 77-91. doi: 10.1530/ERC-15-0386

  • Heritability of naevus patterns in an adult twin cohort from the Brisbane Twin Registry: A cross-sectional study

    Lee, S., Duffy, D.L., Mcclenahan, P., Lee, K. J., McEniery, E., Burke, B., Jagirdar, K., Martin, N.G., Sturm, R.A., Soyer, H.P. and Schaider, H. (2016). Heritability of naevus patterns in an adult twin cohort from the Brisbane Twin Registry: A cross-sectional study. British Journal of Dermatology, 174 (2), 356-363. doi: 10.1111/bjd.14291

  • Impact of a cis-associated gene expression SNP on chromosome 20q11.22 on bipolar disorder susceptibility, hippocampal structure and cognitive performance

    Li, Ming, Luo, Xiong-Jian, Landén, Mikael, Bergen, Sarah E., Hultman, Christina M., Li, Xiao, Zhang, Wen, Yao, Yong-Gang, Zhang, Chen, Liu, Jiewei, Mattheisen, Manuel, Cichon, Sven, Mühleisen, Thomas W., Degenhardt, Franziska A., Nöthen, Markus M., Schulze, Thomas G., Grigoroiu-Serbanescu, Maria, Li, Hao, Fuller, Chris K., Chen, Chunhui, Dong, Qi, Chen, Chuansheng, Jamain, Stéphane, Leboyer, Marion, Bellivier, Frank, Etain, Bruno, Kahn, Jean-Pierre, Henry, Chantal, Preisig, Martin ... The Swedish Bipolar Study Group (2016). Impact of a cis-associated gene expression SNP on chromosome 20q11.22 on bipolar disorder susceptibility, hippocampal structure and cognitive performance. British Journal of Psychiatry, 208 (2), 128-137. doi: 10.1192/bjp.bp.114.156976

  • The Genetic and Environmental Contributions to Internet Use and Associations with Psychopathology: A Twin Study

    Long, Elizabeth C., Verhulst, Brad, Neale, Michael C., Lind, Penelope A., Hickie, Ian B., Martin, Nicholas G. and Gillespie, Nathan A. (2016). The Genetic and Environmental Contributions to Internet Use and Associations with Psychopathology: A Twin Study. Twin Research and Human Genetics, 19 (1), 1-9. doi: 10.1017/thg.2015.91

  • The association between childhood maltreatment, psychopathology, and adult sexual victimization in men and women: results from three independent samples

    Werner, K. B., McCutcheon, V. V., Challa, M., Agrawal, A., Lynskey, M. T., Conroy, E., Statham, D. J., Madden, P. A.F., Henders, A. K., Todorov, A. A., Heath, A. C., Degenhardt, L., Martin, N. G., Bucholz, K. K. and Nelson, E. C. (2016). The association between childhood maltreatment, psychopathology, and adult sexual victimization in men and women: results from three independent samples. Psychological Medicine, 46 (3), 563-573. doi: 10.1017/S0033291715002056

  • The variance shared across forms of childhood trauma is strongly associated with liability for psychiatric and substance use disorders

    Kristjansson, Sean, Mccutcheon, Vivia V., Agrawal, Arpana, Lynskey, Michael T., Conroy, Elizabeth, Statham, Dixie J., Madden, Pamela A. F., Henders, Anjali K., Todorov, Alexandre A., Bucholz, Kathleen K., Degenhardt, Louisa, Martin, Nicholas G., Heath, Andrew C. and Nelson, Elliot C. (2016). The variance shared across forms of childhood trauma is strongly associated with liability for psychiatric and substance use disorders. Brain and Behavior, 6 (2), 1-11. doi: 10.1002/brb3.432

  • A metabolic study of Huntington's disease

    Nambron, Rajasree, Silajdžić, Edina, Kalliolia, Eirini, Ottolenghi, Chris, Hindmarsh, Peter, Hill, Nathan R., Costelloe, Seán J., Martin, Nicholas G., Positano, Vincenzo, Watt, Hilary C., Frost, Chris, Björkqvist, Maria and Warner, Thomas T. (2016). A metabolic study of Huntington's disease. PLoS ONE, 11 (1) e0146480, e0146480. doi: 10.1371/journal.pone.0146480

  • Head motion and inattention/hyperactivity share common genetic influences: Implications for fMRI studies of ADHD

    Couvy-Duchesne, Baptiste, Ebejer, Jane L., Gillespie, Nathan A., Duffy, David L., Hickie, Ian B., Thompson, Paul M., Martin, Nicholas G., de Zubicaray, Greig I., McMahon, Katie L., Medland, Sarah E. and Wright, Margaret J. (2016). Head motion and inattention/hyperactivity share common genetic influences: Implications for fMRI studies of ADHD. PLoS One, 11 (1) e0146271, 1-19. doi: 10.1371/journal.pone.0146271

  • Examining non-syndromic autosomal recessive intellectual disability (NS-ARID) genes for an enriched association with intelligence differences

    Hill, W. D., Davies, G., Liewald, D. C., Payton, A., McNeil, C. J., Whalley, L. J., Horan, M., Ollier, W., Starr, J. M., Pendleton, N., Hansel, N. K., Montgomery, G. W., Medland, S. E., Martin, N. G., Wright, M. J., Bates, T. C. and Deary, I. J. (2016). Examining non-syndromic autosomal recessive intellectual disability (NS-ARID) genes for an enriched association with intelligence differences. Intelligence, 54, 80-89. doi: 10.1016/j.intell.2015.11.005

  • Facial averageness and genetic quality: Testing heritability, genetic correlation with attractiveness, and the paternal age effect

    Lee, Anthony J., Mitchem, Dorian G., Wright, Margaret J., Martin, Nicholas G., Keller, Matthew C. and Zietsch, Brendan P. (2016). Facial averageness and genetic quality: Testing heritability, genetic correlation with attractiveness, and the paternal age effect. Evolution and Human Behavior, 37 (1), 61-66. doi: 10.1016/j.evolhumbehav.2015.08.003

  • Genes influence the amplitude and timing of brain hemodynamic responses

    Shan, Zuyao Y., Vinkhuyzen, Anna A. E., Thompson, Paul M., McMahon, Katie L., Blokland, Gabriella A.M., de Zubicaray, Greig I., Calhoun, Vince, Martin, Nicholas G., Visscher, Peter M., Wright, Margaret J. and Reutens, David C. (2016). Genes influence the amplitude and timing of brain hemodynamic responses. NeuroImage, 124 (Part A), 663-671. doi: 10.1016/j.neuroimage.2015.09.016

  • Subcortical brain alterations in major depressive disorder: findings from the ENIGMA Major Depressive Disorder working group

    Schmaal, L., Veltman, D. J., van Erp, T. G. M., Sämann, P. G., Frodl, T., Jahanshad, N., Loehrer, E., Tiemeier, H., Hofman, A., Niessen, W. J., Vernooij, M. W., Ikram, M. A., Wittfeld, K., Grabe, H. J., Block, A., Hegenscheid, K., Völzke, H., Hoehn, D., Czisch, M., Lagopoulos, J., Hatton, S. N., Hickie, I. B., Goya-Maldonado, R., Krämer, B., Gruber, O., Couvy-Duchesne, B., Rentería, M. E., Strike, L. T., Mills, N. T. ... Hibar, D. P. (2016). Subcortical brain alterations in major depressive disorder: findings from the ENIGMA Major Depressive Disorder working group. Molecular Psychiatry, 21 (6), 806-812. doi: 10.1038/mp.2015.69

  • Trait-based assessment of borderline personality disorder using the NEO five-factor inventory: phenotypic and genetic support

    Few, Lauren R., Miller, Joshua D., Grant, Julia D., Maples, Jessica, Trull, Timothy J., Nelson, Elliot C., Oltmanns, Thomas F., Martin, Nicholas G., Lynskey, Michael T. and Agrawal, Arpana (2016). Trait-based assessment of borderline personality disorder using the NEO five-factor inventory: phenotypic and genetic support. Psychological Assessment, 28 (1), 39-50. doi: 10.1037/pas0000142

  • Sharing a placenta is associated with a greater similarity in DNA methylation in monochorionic versus dichorionic twin pars in blood at age 14

    Bui, Masato, Benyamin, Beben, Shah, Sonia, Henders, Anjali K., Martin, Nicholas G., Montgomery, Grant W. and McRae, Allan F. (2015). Sharing a placenta is associated with a greater similarity in DNA methylation in monochorionic versus dichorionic twin pars in blood at age 14. Twin Research and Human Genetics, 18 (6), 680-685. doi: 10.1017/thg.2015.87

  • The role of conduct disorder in the relationship between alcohol, nicotine and cannabis use disorders

    Grant, J. D., Lynskey, M. T., Madden, P. A.F., Nelson, E. C., Few, L. R., Bucholz, K. K., Statham, D. J., Martin, N. G., Heath, A. C. and Agrawal, A. (2015). The role of conduct disorder in the relationship between alcohol, nicotine and cannabis use disorders. Psychological Medicine, 45 (16), 3505-3515. doi: 10.1017/S0033291715001518

  • Meta-analysis identifies seven susceptibility loci involved in the atopic March

    Marenholz, Ingo, Esparza-Gordillo, Jorge, Ruschendorf, Franz, Bauerfeind, Anja, Strachan, David P., Spycher, Ben D., Baurecht, Hansjorg, Margaritte-Jeannin, Patricia, Saaf, Annika, Kerkhof, Marjan, Ege, Markus, Baltic, Svetlana, Matheson, Melanie C., Li, Jin, Michel, Sven, Ang, Wei Q., McArdle, Wendy, Arnold, Andreas, Homuth, Georg, Demenais, Florence, Bouzigon, Emmanuelle, Soderhall, Cilla, Pershagen, Goran, De Jongste, Johan C., Postma, Dirkje S., Braun-Fahrlander, Charlotte, Horak, Elisabeth, Ogorodova, Ludmila M., Puzyrev, Valery P. ... Lee, Young Ae (2015). Meta-analysis identifies seven susceptibility loci involved in the atopic March. Nature Communications, 6 (1) 8804, 8804.1-8804.8. doi: 10.1038/ncomms9804

  • Heritability of the network architecture of intrinsic brain functional connectivity

    Sinclair, Benjamin, Hansell, Narelle K., Blokland, Gabriella A. M., Martin, Nicholas G., Thompson, Paul M., Breakspear, Michael, de Zubicaray, Greig I., Wright, Margret J. and McMahon, Katie L. (2015). Heritability of the network architecture of intrinsic brain functional connectivity. NeuroImage, 121, 243-252. doi: 10.1016/j.neuroimage.2015.07.048

  • Monoacylglycerol lipase (MGLL) polymorphism rs604300 interacts with childhood adversity to predict cannabis dependence symptoms and amygdala habituation: Evidence from an endocannabinoid system-level analysis

    Carey, Caitlin E., Agrawal, Arpana, Zhang, Bo, Conley, Emily D., Degenhardt, Louisa, Heath, Andrew C., Li, Daofeng, Lynskey, Michael T., Martin, Nicholas G., Montgomery, Grant W., Wang, Ting, Bierut, Laura J., Hariri, Ahmad R., Nelson, Elliot C. and Bogdan, Ryan (2015). Monoacylglycerol lipase (MGLL) polymorphism rs604300 interacts with childhood adversity to predict cannabis dependence symptoms and amygdala habituation: Evidence from an endocannabinoid system-level analysis. Journal of Abnormal Psychology, 124 (4), 860-877. doi: 10.1037/abn0000079

  • Intelligence: Shared genetic basis between Mendelian disorders and a polygenic trait

    Franic, Sanja, Groen-Blokhuis, Maria M., Dolan, Conor V., Kattenberg, Mathijs V., Pool, Rene, Xiao, Xiangjun, Scheet, Paul A., Ehli, Erik A., Davies, Gareth E., van der Sluis, Sophie, Abdellaoui, Abdel, Hansell, Narelle K., Martin, Nicholas G., Hudziak, James J., van Beijsterveldt, Catherina E. M., Swagerman, Suzanne C., Pol, Hilleke E. Hulshoff, de Geus, Eco J. C., Bartels, Meike, Ropers, H. Hilger, Hottenga, Jouke-Jan and Boomsma, Dorret I. (2015). Intelligence: Shared genetic basis between Mendelian disorders and a polygenic trait. European Journal of Human Genetics, 23 (10), 1378-1383. doi: 10.1038/ejhg.2015.3

  • A 24-hour study of the Hypothalamo-pituitary axes in Huntington's disease

    Kalliolia, Eirini, Silajdžic, Edina, Nambron, Rajasree, Costelloe, Seán J., Martin, Nicholas G., Hill, Nathan R., Frost, Chris, Watt, Hilary C., Hindmarsh, Peter, Björkqvist, Maria and Warner, Thomas T. (2015). A 24-hour study of the Hypothalamo-pituitary axes in Huntington's disease. PLoS ONE, 10 (10) e0138848, e0138848. doi: 10.1371/journal.pone.0138848

  • Cis-expression quantitative trait loci mapping reveals replicable associations with heroin addiction in OPRM1

    Hancock, Dana B., Levy, Joshua L., Gaddis, Nathan C., Glasheen, Cristie, Saccone, Nancy L., Page, Grier P., Hulse, Gary K., Wildenauer, Dieter, Kelty, Erin A., Schwab, Sibylle G., Degenhardt, Louisa, Martin, Nicholas G., Montgomery, Grant W., Attia, John, Holliday, Elizabeth G., McEvoy, Mark, Scott, Rodney J., Bierut, Laura J., Nelson, Elliot C., Kral, Alex H. and Johnson, Eric O. (2015). Cis-expression quantitative trait loci mapping reveals replicable associations with heroin addiction in OPRM1. Biological Psychiatry, 78 (7), 474-484. doi: 10.1016/j.biopsych.2015.01.003

  • The influence of age and sex on genetic associations with adult body size and shape: a large-scale genome-wide interaction study

    Winkler, Thomas W., Justice, Anne E., Graff, Mariaelisa, Barata, Llilda, Feitosa, Mary F., Chu, Su, Czajkowski, Jacek, Esko, Tonu, Fall, Tove, Kilpelainen, Tuomas O., Lu, Yingchang, Magi, Reedik, Mihailov, Evelin, Pers, Tune H., Rueeger, Sina, Teumer, Alexander, Ehret, Georg B., Ferreira, Teresa, Heard-Costa, Nancy L., Karjalainen, Juha, Lagou, Vasiliki, Mahajan, Anubha, Neinast, Michael D., Prokopenko, Inga, Simino, Jeannette, Teslovich, Tanya M., Jansen, Rick, Westra, Harm-Jan, White, Charles C. ... Loos, Ruth J. F. (2015). The influence of age and sex on genetic associations with adult body size and shape: a large-scale genome-wide interaction study. PL o S Genetics, 11 (10) e1005378, 1-42. doi: 10.1371/journal.pgen.1005378

  • Zygosity differences in height and body mass index of twins from infancy to old age: a study of the CODATwins project

    Jelenkovic, Aline, Yokoyama, Yoshie, Sund, Reijo, Honda, Chika, Bogl, Leonie H., Aaltonen, Sari, Ji, Fuling, Ning, Feng, Pang, Zengchang, Ordonana, Juan R., Sanchez-Romera, Juan F., Colodro-Conde, Lucia, Burt, S. Alexandra, Klump, Kelly L., Medland, Sarah E., Montgomery, Grant W., Kandler, Christian, McAdams, Tom A., Eley, Thalia C., Gregory, Alice M., Saudino, Kimberly J., Dubois, Lise, Boivin, Michel, Tarnoki, Adam D., Tarnoki, David L., Haworth, Claire M. A., Plomin, Robert, Oncel, Sevgi Y., Aliev, Fazil ... Silventoinen, Karri (2015). Zygosity differences in height and body mass index of twins from infancy to old age: a study of the CODATwins project. Twin Research and Human Genetics, 18 (5), 557-570. doi: 10.1017/thg.2015.57

  • Genome-wide autozygosity is associated with lower general cognitive ability

    Howrigan, D.P., Simonson, M.A., Davies, G., Harris, S.E., Tenesa, A., Starr, J.M., Liewald, D.C., Deary, I.J., McRae, A., Wright, M.J., Montgomery, G.W., Hansell, N., Martin, N.G., Payton, A., Horan, M., Ollier, W.E., Abdellaoui, A., Boomsma, D.I., DeRosse, P., Knowles, E.E.M., Glahn, D.C., Djurovic, S., Melle, I., Andreassen, O.A., Christoforou, A., Steen, V.M., Hellard, S.L., Sundet, K., Reinvang, I. ... Keller, M.C. (2015). Genome-wide autozygosity is associated with lower general cognitive ability. Molecular Psychiatry, 21 (6), 837-843. doi: 10.1038/mp.2015.120

  • Population genetic differentiation of height and body mass index across Europe

    Robinson, Matthew R., Hemani, Gibran, Medina-Gomez, Carolina, Mezzavilla, Massimo, Esko, Tonu, Shakhbazov, Konstantin, Powell, Joseph E., Vinkhuyzen, Anna, Berndt, Sonja I., Gustafsson, Stefan, Justice, Anne E., Kahali, Bratati, Locke, Adam E., Pers, Tune H., Vedantam, Sailaja, Wood, Andrew R., van Rheenen, Wouter, Andreassen, Ole A., Gasparini, Paolo, Metspalu, Andres, van den Berg, Leonard H., Veldink, Jan H., Rivadeneira, Fernando, Werge, Thomas M., Abecasis, Goncalo R., Boomsma, Dorret I., Chasman, Daniel I., de Geus, Eco J. C., Frayling, Timothy M. ... Visscher, Peter M. (2015). Population genetic differentiation of height and body mass index across Europe. Nature Genetics, 47 (11), 1357-1361. doi: 10.1038/ng.3401

  • Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium

    van Den Berg, Stephanie M., de Moor, Marleen H.M., Verweij, Karin J.H., Krueger, Robert F., Luciano, Michelle, Arias Vasquez, Alejandro, Matteson, Lindsay K., Derringer, Jaime, Esko, Tonu, Amin, Najaf, Gordon, Scott D., Hansell, Narelle K., Hart, Amy B., Seppala, Ilkka, Huffman, Jennifer, Konte, Bettina, Lahti, Jari, Lee, Minyoung, Miller, Mike, Nutile, Teresa, Tanaka, Toshiko, Teumer, Alexander, Viktorin, Alexander, Wedenoja, Juho, Abdellaoui, Abdel, Abecasis, Goncalo R., Adkins, Daniel E., Agrawal, Arpana, Allik, Juri ... Boomsma, Dorret I. (2015). Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium. Behavior Genetics, 46 (2), 170-182. doi: 10.1007/s10519-015-9735-5

  • A test of the facultative calibration/reactive heritability model of extraversion

    Haysom, Hannah J., Mitchem, Dorian G., Lee, Anthony J., Wright, Margaret J., Martin, Nicholas G., Keller, Matthew C. and Zietsch, Brendan P. (2015). A test of the facultative calibration/reactive heritability model of extraversion. Evolution and Human Behavior, 36 (5), 414-419. doi: 10.1016/j.evolhumbehav.2015.03.002

  • Does shared genetic risk contribute to the co-occurrence of eating disorders and suicidality?

    Wade, Tracey D., Fairweather-Schmidt, A. Kate, Zhu, Gu and Martin, Nicholas G. (2015). Does shared genetic risk contribute to the co-occurrence of eating disorders and suicidality?. International Journal of Eating Disorders, 48 (6), 684-691. doi: 10.1002/eat.22421

  • Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma

    Law, Matthew H., Bishop, D. Timothy, Lee, Jeffrey E., Brossard, Myriam, Martin, Nicholas G., Moses, Eric K., Song, Fengju, Barrett, Jennifer H., Kumar, Rajiv, Easton, Douglas F., Pharoah, Paul D. P., Swerdlow, Anthony J., Kypreou, Katerina P., Taylor, John C., Harland, Mark, Randerson-Moor, Juliette, Akslen, Lars A., Andresen, Per A., Avril, Marie-Franoise, Azizi, Esther, Scarra, Giovanna Bianchi, Brown, Kevin M., Debniak, Tadeusz, Duffy, David L., Elder, David E., Fang, Shenying, Friedman, Eitan, Galan, Pilar, Ghiorzo, Paola ... Iles, Mark M. (2015). Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma. Nature Genetics, 47 (9), 987-995. doi: 10.1038/ng.3373

  • POLE mutations in families predisposed to cutaneous melanoma

    Aoude, Lauren G., Heitzer, Ellen, Johansson, Peter, Gartside, Michael, Wadt, Karin, Pritchard, Antonia L., Palmer, Jane M., Symmons, Judith, Gerdes, Anne-Marie, Montgomery, Grant W., Martin, Nicholas G., Tomlinson, Ian, Kearsey, Stephen and Hayward, Nicholas K. (2015). POLE mutations in families predisposed to cutaneous melanoma. Familial Cancer, 14 (4), 621-628. doi: 10.1007/s10689-015-9826-8

  • Evidence of CNIH3 involvement in opioid dependence

    Nelson, E. C., Agrawal, A., Heath, A. C., Bogdan, R., Sherva, R., Zhang, B., Al-Hasani, R., Bruchas, M. R., Chou, Y.-L., Demers, C. H., Carey, C. E., Conley, E. D., Fakira, A. K., Farrer, L. A., Goate, A., Gordon, S., Henders, A. K., Hesselbrock, V., Kapoor, M., Lynskey, M. T., Madden, P. A. F., Moron, J. A., Rice, J. P., Saccone, N. L., Schwab, S. G., Shand, F. L., Todorov, A. A., Wallace, L., Wang, T. ... Montgomery, G. W. (2015). Evidence of CNIH3 involvement in opioid dependence. Molecular Psychiatry, 21 (5), 608-614. doi: 10.1038/mp.2015.102

  • The CODATwins project: the cohort description of collaborative project of development of anthropometrical measures in twins to study macro-environmental variation in genetic and environmental effects on anthropometric traits

    Silventoinen, Karri, Jelenkovic, Aline, Sund, Reijo, Honda, Chika, Aaltonen, Sari, Yokoyama, Yoshie, Tarnoki, Adam D., Tarnoki, David L., Ning, Feng, Ji, Fuling, Pang, Zengchang, Ordonana, Juan R., Sanchez-Romera, Juan F., Colodro-Conde, Lucia, Burt, S. Alexandra, Klump, Kelly L., Medland, Sarah E., Montgomery, Grant W., Kandler, Christian, McAdams, Tom A., Eley, Thalia C., Gregory, Alice M., Saudino, Kimberly J., Dubois, Lise, Boivin, Michel, Haworth, Claire M. A., Plomin, Robert, Oncel, Sevgi Y., Aliev, Fazil ... Kaprio, Jaakko (2015). The CODATwins project: the cohort description of collaborative project of development of anthropometrical measures in twins to study macro-environmental variation in genetic and environmental effects on anthropometric traits. Twin Research and Human Genetics, 18 (4), 348-360. doi: 10.1017/thg.2015.29

  • A common genetic influence on human intensity ratings of sugars and high-potency sweeteners

    Hwang, Liang-Dar, Zhu, Gu, Breslin, Paul A. S., Reed, Danielle R., Martin, Nicholas G. and Wright, Margaret J. (2015). A common genetic influence on human intensity ratings of sugars and high-potency sweeteners. Twin Research and Human Genetics, 18 (4), 361-367. doi: 10.1017/thg.2015.42

  • Genetics of skin color variation in Europeans: genome-wide association studies with functional follow-up

    Liu, Fan, Visser, Mijke, Duffy, David L., Hysi, Pirro G., Jacobs, Leonie C., Lao, Oscar, Zhong, Kaiyin, Walsh, Susan, Chaitanya, Lakshmi, Wollstein, Andreas, Zhu, Gu, Montgomery, Grant W., Henders, Anjali K., Mangino, Massimo, Glass, Daniel, Bataille, Veronique, Sturm, Richard A., Rivadeneira, Fernando, Hofman, Albert, van IJcken, Wilfred F. J., Uitterlinden, André G., Palstra, Robert-Jan T. S., Spector, Timothy D., Martin, Nicholas G., Nijsten, Tamar E. C. and Kayser, Manfred (2015). Genetics of skin color variation in Europeans: genome-wide association studies with functional follow-up. Human Genetics, 134 (8), 823-835. doi: 10.1007/s00439-015-1559-0

  • Genetic burden associated with varying degrees of disease severity in endometriosis

    Sapkota, Yadav, Attia, John, Gordon, Scott D., Henders, Anjali K., Holliday, Elizabeth G., Rahmioglu, Nilufer, MacGregor, Stuart, Martin, Nicholas G., McEvoy, Mark, Morris, Andrew P., Scott, Rodney J., Zondervan, Krina T., Montgomery, Grant W. and Nyholt, Dale R. (2015). Genetic burden associated with varying degrees of disease severity in endometriosis. Molecular Human Reproduction, 21 (7), 594-602. doi: 10.1093/molehr/gav021

  • Meta-analysis of genome-wide association studies for neuroticism, and the polygenic association with major depressive disorder

    De Moor, Marleen H.M, Van Den Berg, Stephanie M, Verweij, Karin J.H, Krueger, Robert F, Luciano, Michelle, Arias Vasquez, Alejandro, Matteson, Lindsay K, Derringer, Jaime, Esko, Tonu, Amin, Najaf, Gordon, Scott D, Hansell, Narelle K, Hart, Amy B, Seppala, Ilkka, Huffman, Jennifer E, Konte, Bettina, Lahti, Jari, Lee, Minyoung, Miller, Mike, Nutile, Teresa, Tanaka, Toshiko, Teumer, Alexander, Viktorin, Alexander, Wedenoja, Juho, Abecasis, Goncalo R, Adkins, Daniel E, Agrawal, Arpana, Allik, Juri, Appel, Katja ... Boomsma, Dorret I (2015). Meta-analysis of genome-wide association studies for neuroticism, and the polygenic association with major depressive disorder. JAMA Psychiatry, 72 (7), 642-650. doi: 10.1001/jamapsychiatry.2015.0554

  • WNT10A exonic variant increases the risk of keratoconus by decreasing corneal thickness

    Cuellar-Partida, Gabriel, Springelkamp, Henriet, Lucas, Sionne E. M., Yazar, Seyhan, Hewitt, Alex W., Iglesias, Adriana I., Montgomery, Grant W., Martin, Nicholas G., Pennell, Craig E., van Leeuwen, Elisabeth M., Verhoeven, Virginie J. M., Hofman, Albert, Uitterlinden, Andre G., Ramdas, Wishal D., Wolfs, Roger. C. W., Vingerling, Johannes R., Brown, Matthew A., Mills, Richard A., Craig, Jamie E., Klaver, Caroline C. W., van Duijn, Cornelia M., Burdon, Kathryn P., MacGregor, Stuart and Mackey, David A. (2015). WNT10A exonic variant increases the risk of keratoconus by decreasing corneal thickness. Human Molecular Genetics, 24 (17), 5060-5068. doi: 10.1093/hmg/ddv211

  • Chromogranin A as a predictor of radiological disease progression in neuroendocrine tumours

    Rossi, Roberta Elisa, Garcia-Hernandez, Jorge, Meyer, Tim, Thirlwell, Christina, Watkins, Jennifer, Martin, Nicholas Guy, Caplin, Martyn Evan and Toumpanakis, Christos (2015). Chromogranin A as a predictor of radiological disease progression in neuroendocrine tumours. Annals of Translational Medicine, 3 (9) ARTN 118. doi: 10.3978/j.issn.2305-5839.2015.04.23

  • Is there a genetic correlation between general factors of intelligence and personality?

    Loehlin, John C., Bartels, Meike, Boomsma, Dorret I., Bratko, Denis, Martin, Nicholas G., Nichols, Robert C. and Wright, Margaret J. (2015). Is there a genetic correlation between general factors of intelligence and personality?. Twin Research and Human Genetics, 18 (3), 234-242. doi: 10.1017/thg.2015.28

  • The effect of education on smoking behavior: new evidence from smoking durations of a sample of twins

    Koning, Pierre, Webbink, Dinand and Martin, Nicholas G. (2015). The effect of education on smoking behavior: new evidence from smoking durations of a sample of twins. Empirical Economics, 48 (4), 1479-1497. doi: 10.1007/s00181-014-0842-6

  • The genetic and environmental foundations of political, psychological, social, and economic behaviors: a panel study of twins and families

    Hatemi, Peter K., Smith, Kevin, Alford, John R., Martin, Nicholas G. and Hibbing, John R. (2015). The genetic and environmental foundations of political, psychological, social, and economic behaviors: a panel study of twins and families. Twin Research and Human Genetics, 18 (3), 243-255. doi: 10.1017/thg.2015.13

  • ARHGEF12 influences the risk of glaucoma by increasing intraocular pressure

    Springelkamp, Henriet, Iglesias, Adriana I., Cuellar-Partida, Gabriel, Amin, Najaf, Burdon, Kathryn P., van Leeuwen, Elisabeth M., Gharahkhani, Puya, Mishra, Aniket, van der Lee, Sven J., Hewitt, Alex W., Rivadeneira, Fernando, Viswanathan, Ananth C., Wolfs, Roger C. W., Martin, Nicholas G., Ramdas, Wishal D., van Koolwijk, Leonieke M., Pennell, Craig E., Vingerling, Johannes R., Mountain, Jenny E., Uitterlinden, Andre G., Hofman, Albert, Mitchell, Paul, Lemij, Hans G., Wang, Jie Jin, Klaver, Caroline C. W., Mackey, David A., Craig, Jamie E., van Duijn, Cornelia M. and MacGregor, Stuart (2015). ARHGEF12 influences the risk of glaucoma by increasing intraocular pressure. Human Molecular Genetics, 24 (9), 2689-2699. doi: 10.1093/hmg/ddv027

  • Age- and sex-specific causal effects of adiposity on cardiovascular risk factors

    Fall, Tove, Hagg, Sara, Ploner, Alexander, Maegi, Reedik, Fischer, Krista, Draisma, Harmen H. M., Sarin, Antti-Pekka, Benyamin, Beben, Ladenvall, Claes, Akerlund, Mikael, Kals, Mart, Esko, Tonu, Nelson, Christopher P., Kaakinen, Marika, Huikari, Ville, Mangino, Massimo, Meirhaeghe, Aline, Kristiansson, Kati, Nuotio, Marja-Liisa, Kobl, Michael, Grallert, Harald, Dehghan, Abbas, Kuningas, Maris, de Vries, Paul S., de Bruijn, Renee F. A. G., Willems, Sara M., Heikkila, Kauko, Silventoinen, Karri, Pietilainen, Kirsi H. ... Ingelsson, Erik (2015). Age- and sex-specific causal effects of adiposity on cardiovascular risk factors. Diabetes, 64 (5), 1841-1852. doi: 10.2337/db14-0988

  • Development of a global network of induced pluripotent stem cell haplobanks

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  • Heritability of fractional anisotropy in human white matter: A comparison of Human Connectome Project and ENIGMA-DTI data

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  • No relationship between intelligence and facial attractiveness in a large, genetically informative sample

    Mitchem, Dorian G., Zietsch, Brendan P., Wright, Margaret J., Martin, Nicholas G., Hewitt, John K. and Keller, Matthew C. (2015). No relationship between intelligence and facial attractiveness in a large, genetically informative sample. Evolution and Human Behavior, 36 (3), 240-247. doi: 10.1016/j.evolhumbehav.2014.11.009

  • Retinal microvessels reflect familial vulnerability to psychotic symptoms: A comparison of twins discordant for psychotic symptoms and controls

    Meier, Madeline H., Gillespie, Nathan A., Hansell, Narelle K., Hewitt, Alex W., Hickie, Ian B., Lu, Yi, McGrath, John, MacGregor, Stuart, Medland, Sarah E., Sun, Cong, Wong, Tien Y., Wright, Margaret J., Zhu, Gu, Martin, Nicholas G. and Mackey, David A. (2015). Retinal microvessels reflect familial vulnerability to psychotic symptoms: A comparison of twins discordant for psychotic symptoms and controls. Schizophrenia Research, 164 (1-3), 47-52. doi: 10.1016/j.schres.2015.01.045

  • The relationship between cannabis involvement and suicidal thoughts and behaviors

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  • Common genetic variants influence human subcortical brain structures

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  • Genetic basis of a cognitive complexity metric

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  • Is the adiposity-associated FTO gene variant related to all-cause mortality independent of adiposity? Meta-analysis of data from 169,551 Caucasian adults

    Zimmermann, E., Angquist, L. H., Mirza, S. S., Zhao, J. H., Chasman, D. I., Fischer, K., Qi, Q., Smith, A. V., Thinggaard, M., Jarczok, M. N., Nalls, M. A., Trompet, S., Timpson, N. J., Schmidt, B., Jackson, A. U., Lyytikainen, L. P., Verweij, N., Mueller-Nurasyid, M., Vikstrom, M., Marques-Vidal, P., Wong, A., Meidtner, K., Middelberg, R. P., Strawbridge, R. J., Christiansen, L., Kyvik, K. O., Hamsten, A., Jaaskelainen, T., Tjonneland, A. ... Montgomery, G. W. (2015). Is the adiposity-associated FTO gene variant related to all-cause mortality independent of adiposity? Meta-analysis of data from 169,551 Caucasian adults. Obesity Reviews, 16 (4), 327-340. doi: 10.1111/obr.12263

  • Low birth weight in MZ twins discordant for birth weight is associated with shorter telomere length and lower IQ, but not anxiety/depression in later life

    Strohmaier, Jana, van Dongen, Jenny, Willemsen, Gonneke, Nyholt, Dale R., Zhu, Gu, Codd, Veryan, Novakovic, Boris, Hansell, Narelle, Wright, Margaret J., Rietschel, Liz, Streit, Fabian, Henders, Anjali K., Montgomery, Grant W., Samani, Nilesh J., Gillespie, Nathan A., Hickie, Ian B., Craig, Jeffrey M., Saffery, Richard, Boomsma, Dorret I., Rietschel, Marcella and Martin, Nicholas G. (2015). Low birth weight in MZ twins discordant for birth weight is associated with shorter telomere length and lower IQ, but not anxiety/depression in later life. Twin Research and Human Genetics, 18 (2), 198-209. doi: 10.1017/thg.2015.3

  • Prevalence of germline BAP1, CDKN2A, and CDK4 mutations in an australian population-based sample of cutaneous melanoma cases

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  • Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis (vol 5, 4926, 2014)

    Benyamin, Beben, Esko, Tonu, Ried, Janina S., Radhakrishnan, Aparna, Vermeulen, Sita H., Traglia, Michela, Goegele, Martin, Anderson, Denise, Broer, Linda, Podmore, Clara, Luan, Jianan, Kutalik, Zoltan, Sanna, Serena, van der Meer, Peter, Tanaka, Toshiko, Wang, Fudi, Westra, Harm-Jan, Franke, Lude, Mihailov, Evelin, Milani, Lili, Haelldin, Jonas, Winkelmann, Juliane, Meitinger, Thomas, Thiery, Joachim, Peters, Annette, Waldenberger, Melanie, Rendon, Augusto, Jolley, Jennifer, Sambrook, Jennifer ... Whitfield, John B. (2015). Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis (vol 5, 4926, 2014). Nature Communications, 6 (1) 6542, 1-1. doi: 10.1038/ncomms7542

  • Genome-wide association study of blood lead shows multiple associations near ALAD

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  • Don't it make your brown eyes blue? A comparison of iris colour across latitude in Australian twins

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  • Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk

    Painter J.N., O'Mara T.A., Batra J., Cheng T., Lose F.A., Dennis J., Michailidou K., Tyrer J.P., Ahmed S., Ferguson K., Healey C.S., Kaufmann S., Hillman K.M., Walpole C., Moya L., Pollock P., Jones A., Howarth K., Martin L., Gorman M., Hodgson S., De Polanco M.M.E., Sans M., Carracedo A., Castellvi-Bel S., Rojas-Martinez A., Santos E., Teixeira M.R., Carvajal-Carmona L. ... Spurdle A.B. (2015). Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk. Human Molecular Genetics, 24 (5), 1478-1492. doi: 10.1093/hmg/ddu552

  • Hepascore and hyaluronic acid as markers of fibrosis in liver disease of mixed aetiology

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  • Introduction to the statistical concepts symposium section: Selected review topics to improve our understanding and use of statistics

    Glaz, Barry, Wiersma, Jochum, Hernandez, Jose A., Martin, Nicolas F. and Yeater, Kathleen M. (2015). Introduction to the statistical concepts symposium section: Selected review topics to improve our understanding and use of statistics. Agronomy Journal, 107 (2), 691-691. doi: 10.2134/agronj14.0888

  • A twin study of breastfeeding with a preliminary genome-wide association scan

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  • Heritability of Transforming Growth Factor-β1 and Tumor Necrosis Factor-Receptor Type 1 Expression and Vitamin D Levels in Healthy Adolescent Twins

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  • Large autosomal copy-number differences within unselected monozygotic twin pairs are rare

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  • Nonsense mutations in the shelterin complex genes ACD and TERF2IP in familial melanoma

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  • DNA methylation age of blood predicts all-cause mortality in later life

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  • Association between endometriosis and the interleukin 1A (IL1A) locus

    Sapkota, Yadav, Low, Siew-Kee, Attia, John, Gordon, Scott D., Henders, Anjali K., Holliday, Elizabeth G., MacGregor, Stuart, Martin, Nicholas G., McEvoy, Mark, Morris, Andrew P., Takahashi, Atsushi, Scott, Rodney J., Kubo, Michiaki, Zondervan, Krina T., Montgomery, Grant W. and Nyholt, Dale R. (2015). Association between endometriosis and the interleukin 1A (IL1A) locus. Human Reproduction, 30 (1), 239-248. doi: 10.1093/humrep/deu267

  • Contrast Effects and Sex Influence Maternal and Self-Report Dimensional Measures of Attention-Deficit Hyperactivity Disorder

    Ebejer, J. L., Medland, S. E., van der Werf, J., Wright, M. J., Henders, A. K., Gillespie, N. A., Hickie, I. B., Martin, N. G. and Duffy, D. L. (2015). Contrast Effects and Sex Influence Maternal and Self-Report Dimensional Measures of Attention-Deficit Hyperactivity Disorder. Behavior Genetics, 45 (1), 35-50. doi: 10.1007/s10519-014-9670-x

  • Telescoping and gender differences in the time course of disordered gambling: evidence from a general population sample

    Slutske, Wendy S., Piasecki, Thomas M., Deutsch, Arielle R., Statham, Dixie J. and Martin, Nicholas G. (2015). Telescoping and gender differences in the time course of disordered gambling: evidence from a general population sample. Addiction, 110 (1), 144-151. doi: 10.1111/add.12717

  • The association between speed of transition from initiation to subsequent use of cannabis and later problematic cannabis use, abuse and dependence

    Hines, Lindsey A., Morley, Katherine I., Strang, John, Agrawal, Arpana, Nelson, Elliot C., Statham, Dixie, Martin, Nicholas G. and Lynskey, Michael T. (2015). The association between speed of transition from initiation to subsequent use of cannabis and later problematic cannabis use, abuse and dependence. Addiction, 110 (8), 1311-1320. doi: 10.1111/add.12963

  • Novel loci associated with usual sleep duration: the CHARGE Consortium Genome-Wide Association Study

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  • A meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hip

    Evangelou, Evangelos, Kerkhos, Hanneke J., Styrkarsdottir, Unnur, Ntzani, Evangelia E., Bos, Steffan D., Esko, Tonu, Evans, Daniel S., Metrustry, Sarah, Panoutsopoulou, Kalliope, Ramos, Yolande F. M., Thorleifsson, Gudmar, Tsilides, Konstantinos K., arcOGEN Consortium, Arden, Nigel, Aslam, Nadim, Bellamy, Nicholas, Birrell, Fraser, Blanco, Francisco J., Carr, Andrew, Chapman, Kay, Day-Williams, Aaron G., Deloukas, Panos, Doherty, Michael, Engstrom, Gunnar, Helgadottir, Hafdis T., Hoffman, Albert, Ingvarsson, Thorvaldur, Jonsson, Helgi, Keis, Aime ... Valdes, Anna M. (2014). A meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hip. Annals of the Rheumatic Diseases, 73 (12), 2130-2136. doi: 10.1136/annrheumdis-2012-203114

  • Challenges and opportunities in mass spectrometric analysis of proteins from dried blood spots

    Martin, Nicholas J. and Cooper, Helen J. (2014). Challenges and opportunities in mass spectrometric analysis of proteins from dried blood spots. Expert Review of Proteomics, 11 (6), 685-695. doi: 10.1586/14789450.2014.965158

  • Genetic influences on alcohol-related hangover

    Slutske, Wendy S., Piasecki, Thomas M., Nathanson, Lisa, Statham, Dixie J. and Martin, Nicholas G. (2014). Genetic influences on alcohol-related hangover. Addiction, 109 (12), 2027-2034. doi: 10.1111/add.12699

  • Genetic variation in personality traits explains genetic overlap between borderline personality features and substance use disorders

    Few, Lauren R., Grant, Julia D., Trull, Timothy J., Statham, Dixie J., Martin, Nicholas G., Lynskey, Michael T. and Agrawal, Arpana (2014). Genetic variation in personality traits explains genetic overlap between borderline personality features and substance use disorders. Addiction, 109 (12), 2118-2127. doi: 10.1111/add.12690

  • Personality and gambling involvement: a person-centered approach

    Savage, Jeanne E., Slutske, Wendy S. and Martin, Nicholas G. (2014). Personality and gambling involvement: a person-centered approach. Psychology of Addictive Behaviors, 28 (4), 1198-1211. doi: 10.1037/a0037413

  • Test of a potential causal influence of earlier age of gambling initiation on gambling involvement and disorder: a multilevel discordant twin design

    Slutske, Wendy S., Deutsch, Arielle R., Richmond-Rakerd, Leah S., Chernyavskiy, Pavel, Statham, Dixie J. and Martin, Nicholas G. (2014). Test of a potential causal influence of earlier age of gambling initiation on gambling involvement and disorder: a multilevel discordant twin design. Psychology of Addictive Behaviors, 28 (4), 1177-1189. doi: 10.1037/a0035356

  • The genetic correlation between procrastination and impulsivity

    Loehlin, John C. and Martin, Nicholas G. (2014). The genetic correlation between procrastination and impulsivity. Twin Research and Human Genetics, 17 (6), 512-515. doi: 10.1017/thg.2014.60

  • Obesity gene NEGR1 associated with white matter integrity in healthy young adults

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  • Defining the role of common variation in the genomic and biological architecture of adult human height

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  • Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium

    Li, Qing, Wojciechowski, Robert, Simpson, Claire L., Hysi, Pirro G., Verhoeven, Virginie J. M., Ikram, Mohammad Kamran, Hohn, Rene, Vitart, Veronique, Hewitt, Alex W., Oexle, Konrad, Makela, Kari-Matti, MacGregor, Stuart, Pirastu, Mario, Fan, Qiao, Cheng, Ching-Yu, St Pourcain, Beate, McMahon, George, Kemp, John P., Northstone, Kate, Rahi, Jugnoo S., Cumberland, Phillippa M., Martin, Nicholas G., Sanfilippo, Paul G., Lu, Yi, Wang, Ya Xing, Hayward, Caroline, Polasek, Ozren, Campbell, Harry, Bencic, Goran ... Guggenheim, Jeremy A. (2014). Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium. Human Genetics, 134 (2), 131-146. doi: 10.1007/s00439-014-1500-y

  • Associations between depression and anxiety symptoms and retinal vessel caliber in adolescents and young adults

    Meier, Madeline H., Gillespie, Nathan A., Hansell, Narelle K., Hewitt, Alex W., Hickie, Ian B., Lu, Yi, MacGregor, Stuart, Medland, Sarah E., Sun, Cong, Wong, Tien Y., Wright, Margaret J., Zhu, Gu, Martin, Nicholas G. and Mackey, David A. (2014). Associations between depression and anxiety symptoms and retinal vessel caliber in adolescents and young adults. Psychosomatic Medicine, 76 (9), 732-738. doi: 10.1097/PSY.0000000000000117

  • Genetic and environmental exposures constrain epigenetic drift over the human life course

    Shah, Sonia, McRae, Allan F., Marioni, Riccardo E., Harris, Sarah E., Gibson, Jude, Henders, Anjali K., Redmond, Paul, Cox, Simon R., Pattie, Alison, Corley, Janie, Murphy, Lee, Martin, Nicholas G., Montgomery, Grant W., Starr, John M., Wray, Naomi R., Deary, Ian J. and Visscher, Peter M. (2014). Genetic and environmental exposures constrain epigenetic drift over the human life course. Genome Research, 24 (11), 1725-1733. doi: 10.1101/gr.176933.114

  • Genetic architecture of subcortical brain regions: common and region-specific genetic contributions

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  • Perceived stress has genetic influences distinct from neuroticism and depression

    Rietschel, Liz, Zhu, Gu, Kirschbaum, Clemens, Strohmaier, Jana, Wuest, Stefan, Rietschel, Marcella and Martin, Nicholas G. (2014). Perceived stress has genetic influences distinct from neuroticism and depression. Behavior Genetics, 44 (6), 639-645. doi: 10.1007/s10519-013-9636-4

  • Serum cholesterol and variant in cholesterol-related gene CETP predict white matter microstructure

    Warstadt, Nicholus M., Dennis, Emily L., Jahanshad, Neda, Kohannim, Omid, Nir, Talia M., McMahon, Katie L., de Zubicaray, Greig I., Montgomery, Grant W., Henders, Anjali K., Martin, Nicholas G., Whitfield, John B., Jack, Clifford R. Jr., Bernstein, Matt A., Weiner, Michael W., Toga, Arthur W., Wright, Margaret J., Thompson, Paul M. and for the Alzheimer’s Disease Neuroimaging Initiative (ADNI) (2014). Serum cholesterol and variant in cholesterol-related gene CETP predict white matter microstructure. Neurobiology of Aging, 35 (11), 2504-2513. doi: 10.1016/j.neurobiolaging.2014.05.024

  • Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis

    Benyamin, Beben, Esko, Tonu, Ried, Janina S., Radhakrishnan, Aparna, Vermeulen, Sita H., Traglia, Michela, Goegele, Martin, Anderson, Denise, Broer, Linda, Podmore, Clara, Luan, Jian'an, Kutalik, Zoltan, Sanna, Serena, van der Meer, Peter, Tanaka, Toshiko, Wang, Fudi, Westra, Harm-Jan, Franke, Lude, Mihailov, Evelin, Milani, Lili, Haeldin, Jonas, Winkelmann, Juliane, Meitinger, Thomas, Thiery, Joachim, Peters, Annette, Waldenberger, Melanie, Rendon, Augusto, Jolley, Jennifer, Sambrook, Jennifer ... Whitfield, John B. (2014). Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis. Nature Communications, 5 (1) 5926, 4926.1-4926.10. doi: 10.1038/ncomms5926

  • Investigating brain connectivity heritability in a twin study using diffusion imaging data

    Shen, Kai-Kai, Rose, Stephen, Fripp, Jurgen, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Thompson, Paul M., Wright, Margaret J. and Salvado, Olivier (2014). Investigating brain connectivity heritability in a twin study using diffusion imaging data. Neuroimage, 100, 628-641. doi: 10.1016/j.neuroimage.2014.06.041

  • Another explanation for apparent epistasis: reply

    Hemani, Gibran, Shakhbazov, Konstantin, Westra, Harm-Jan, Esko, Tonu, Henders, Anjali K., McRae, Allan F., Yang, Jian, Gibson, Greg, Martin, Nicholas G., Metspalu, Andres, Franke, Lude, Montgomery, Grant W., Visscher, Peter M. and Powell, Joseph E. (2014). Another explanation for apparent epistasis: reply. Nature, 514 (7520), E5-E6. doi: 10.1038/nature13692

  • Attitudes toward economic risk and occupational choice

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  • Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma

    Hysi, Pirro G., Cheng, Ching-Yu, Springelkamp, Henriet, Macgregor, Stuart, Bailey, Jessica N. Cooke, Wojciechowski, Robert, Vitart, Veronique, Nag, Abhishek, Hewitt, Alex W., Hohn, Rene, Venturini, Cristina, Mirshahi, Alireza, Ramdas, Wishal D., Thorleifsson, Gudmar, Vithana, Eranga, Khor, Chiea-Chuen, Stefansson, Arni B., Liao, Jiemin, Haines, Jonathan L., Amin, Najaf, Wang, Ya Xing, Wild, Philipp S., Ozel, Ayse B., Li, Jun Z., Fleck, Brian W., Zeller, Tanja, Staffieri, Sandra E., Teo, Yik-Ying, Cuellar-Partida, Gabriel ... Aung, Tin (2014). Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma. Nature Genetics, 46 (10), 1126-1130. doi: 10.1038/ng.3087

  • Common genetic variants associated with cognitive performance identified using the proxy-phenotype method

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  • Common genetic variants associated with cognitive performance identified using the proxy-phenotype method (vol 111, pg 13790, 2014)

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  • Human mate selection and addiction: A conceptual critique

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  • Identification of a melanoma susceptibility locus and somatic mutation in TET2

    Song, Fengju, Amos, Christopher I., Lee, Jeffrey E., Lian, Christine G., Fang, Shenying, Liu, Hongliang, MacGregor, Stuart, Iles, Mark M., Law, Matthew H., Lindeman, Neal I., Montgomery, Grant W., Duffy, David L., Cust, Anne E., Jenkins, Mark A., Whiteman, David C., Kefford, Richard F., Giles, Graham G., Armstrong, Bruce K., Aitken, Joanne F., Hopper, John L., Brown, Kevin M., Martin, Nicholas G., Mann, Graham J., Bishop, D. Timothy, Bishop, Julia A. Newton, Kraft, Peter, Qureshi, Abrar A., Kanetsky, Peter A., Hayward, Nicholas K. ... Han, Jiali (2014). Identification of a melanoma susceptibility locus and somatic mutation in TET2. Carcinogenesis, 35 (9) bgu140, 2097-2101. doi: 10.1093/carcin/bgu140

  • Genome-wide interaction analysis reveals replicated epistatic effects on brain structure

    Hibar, Derrek P., Stein, Jason L., Jahanshad, Neda, Kohannim, Omid, Hua, Xue, Toga, Arthur W., McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J., Alzheimer’s Disease Neuroimaging Initiative, Weiner, Michael W. and Thompson, Paul M. (2014). Genome-wide interaction analysis reveals replicated epistatic effects on brain structure. Neurobiology of Aging, 36 (S1), S151-S158. doi: 10.1016/j.neurobiolaging.2014.02.033

  • Variants close to NTRK2 gene are associated with birth weight in female twins

    Metrustry, Sarah J., Edwards, Mark H., Medland, Sarah E., Holloway, John W., Montgomery, Grant W., Martin, Nicholas G., Spector, Tim D., Cooper, Cyrus and Valdes, Ana M. (2014). Variants close to NTRK2 gene are associated with birth weight in female twins. Twin Research and Human Genetics, 17 (4), 254-261. doi: 10.1017/thg.2014.34

  • Applying polygenic risk scores to postpartum depression

    Byrne, Edna M., Carrillo-Roa, Tania, Penninx, Brenda W. J. H., Sallis, Hannah M., Viktorin, Alexander, Chapman, Brett, Henders, Anjali K., Pergadia, Michele L., Heath, Andrew C., Madden, Pamela A. F., Sullivan, Patrick F., Boschloo, Lynn, van Grootheest, Gerard, McMahon, George, Lawlor, Debbie A., Landen, Mikael, Lichtenstein, Paul, Magnusson, Patrik K. E., Evans, David M., Montgomery, Grant W., Boomsma, Dorret I., Martin, Nicholas G., Meltzer-Brody, Samantha and Wray, Naomi R. (2014). Applying polygenic risk scores to postpartum depression. Archives of Women's Mental Health, 17 (6), 519-528. doi: 10.1007/s00737-014-0428-5

  • Multi-site study of additive genetic effects on fractional anisotropy of cerebral white matter: comparing meta and megaanalytical approaches for data pooling

    Kochunov, Peter, Jahanshad, Neda, Sprooten, Emma, Nichols, Thomas E., Mandl, René C., Almasy, Laura, Booth, Tom, Brouwer, Rachel M., Curran, Joanne E., de Zubicaray, Greig I., Dimitrova, Rali, Duggirala, Ravi, Fox, Peter T., Hong, L. Elliot, Landman, Bennett A., Lemaitre, Hervé, Lopez, Lorna M., Martin, Nicholas G., McMahon, Katie L., Mitchell, Braxton D., Olvera, Rene L., Peterson, Charles P., Starr, John M., Sussmann, Jessika E., Toga, Arthur W., Wardlaw, Joanna M., Wright, Margaret J., Wright, Susan N., Bastin, Mark E. ... Glahn, David C. (2014). Multi-site study of additive genetic effects on fractional anisotropy of cerebral white matter: comparing meta and megaanalytical approaches for data pooling. Neuroimage, 95, 136-150. doi: 10.1016/j.neuroimage.2014.03.033

  • Harmonization of neuroticism and extraversion phenotypes across inventories and cohorts in the Genetics of Personality Consortium: an application of item response theory

    van den Berg, Stephanie M., de Moor, Marleen H. M., McGue, Matt, Pettersson, Erik, Terracciano, Antonio, Verweij, Karin J. H., Amin, Najaf, Derringer, Jaime, Esko, Tonu, van Grootheest, Gerard, Hansell, Narelle K., Huffman, Jennifer, Konte, Bettina, Lahti, Jari, Luciano, Michelle, Matteson, Lindsay K., Viktorin, Alexander, Wouda, Jasper, Agrawal, Arpana, Allik, Jueri, Bierut, Laura, Broms, Ulla, Campbell, Harry, Smith, George Davey, Eriksson, Johan G., Ferrucci, Luigi, Franke, Barbera, Fox, Jean-Paul, de Geus, Eco J. C. ... Boomsma, Dorret I. (2014). Harmonization of neuroticism and extraversion phenotypes across inventories and cohorts in the Genetics of Personality Consortium: an application of item response theory. Behavior Genetics, 44 (4), 295-313. doi: 10.1007/s10519-014-9654-x

  • PTSD risk associated with a functional DRD2 polymorphism in heroin-dependent cases and controls is limited to amphetamine-dependent individuals

    Nelson, Elliot C., Heath, Andrew C., Lynskey, Michael T., Agrawal, Arpana, Henders, Anjali K., Bowdler, Lisa M., Todorov, Alexandre A., Madden, Pamela A. F., Moore, Elizabeth, Degenhardt, Louisa, Martin, Nicholas G. and Montgomery, Grant W. (2014). PTSD risk associated with a functional DRD2 polymorphism in heroin-dependent cases and controls is limited to amphetamine-dependent individuals. Addiction Biology, 19 (4), 700-707. doi: 10.1111/adb.12062

  • Assessment of PALB2 as a candidate melanoma susceptibility gene

    Aoude, Lauren G., Xu, Mai, Zhao, Zhen Zhen, Kovacs, Michael, Palmer, Jane M., Johansson, Peter, Symmons, Judith, Trent, Jeffrey M., Martin, Nicholas G., Montgomery, Grant W., Brown, Kevin M. and Hayward, Nicholas K. (2014). Assessment of PALB2 as a candidate melanoma susceptibility gene. PLoS One, 9 (6) e100683, e100683.1-e100683.7. doi: 10.1371/journal.pone.0100683

  • Molecular analysis of common polymorphisms within the human Tyrosinase locus and genetic association with pigmentation traits

    Jagirdar, Kasturee, Smit, Darren J., Ainger, Stephen A., Lee, Katie J., Brown, Darren L., Chapman, Brett, Zhao, Zhen Zhen, Montgomery, Grant W., Martin, Nicholas G., Stow, Jennifer L., Duffy, David L. and Sturm, Richard A. (2014). Molecular analysis of common polymorphisms within the human Tyrosinase locus and genetic association with pigmentation traits. Pigment Cell and Melanoma Research, 27 (4), 552-564. doi: 10.1111/pcmr.12253

  • Overlapping genetic and environmental influences on nonsuicidal self-injury and suicidal ideation different outcomes, same etiology?

    Maciejewski, Dominique F., Creemers, Hanneke E., Lynskey, Michael T., Madden, Pamela A. F., Heath, Andrew C., Statham, Dixie J., Martin, Nicholas G. and Verweij, Karin J. H. (2014). Overlapping genetic and environmental influences on nonsuicidal self-injury and suicidal ideation different outcomes, same etiology?. Jama Psychiatry, 71 (6), 699-705. doi: 10.1001/jamapsychiatry.2014.89

  • The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data

    Thompson, Paul M., Stein, Jason L., Medland, Sarah E., Hibar, Derrek P., Arias Vasquez, Alejandro, Renteria, Miguel E., Toro, Roberto, Jahanshad, Neda, Schumann, Gunter, Franke, Barbara, Wright, Margaret J., Martin, Nicholas G., Agartz, Ingrid, Alda, Martin, Alhusaini, Saud, Almasy, Laura, Almeida, Jorge, Alpert, Kathryn, Andreasen, Nancy C., Andreassen, Ole A., Apostolova, Liana G., Appel, Katja, Armstrong, Nicola J., Aribisala, Benjamin, Bastin, Mark E., Bauer, Michael, Bearden, Carrie E., Bergmann, Ørjan, Binder, Elisabeth B. ... Saguenay Youth Study (SYS) Group (2014). The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data. Brain Imaging and Behavior, 8 (2), 153-182. doi: 10.1007/s11682-013-9269-5

  • Contribution of genetic variation to transgenerational inheritance of DNA methylation

    McRae, Allan F., Powell, Joseph E., Henders, Anjali K., Bowdler, Lisa, Hemani, Gibran, Shah, Sonia, Painter, Jodie N., Martin, Nicholas G., Visscher, Peter M. and Montgomery, Grant W. (2014). Contribution of genetic variation to transgenerational inheritance of DNA methylation. Genome Biology, 15 (5), 1-10. doi: 10.1186/gb-2014-15-5-r73

  • Genetic influences on political ideologies: Twin analyses of 19 measures of political ideologies from five democracies and genome-wide findings from three populations

    Hatemi, Peter K., Medland, Sarah E., Klemmensen, Robert, Oskarsson, Sven, Littvay, Levente, Dawes, Christopher T., Verhulst, Brad, McDermott, Rose, Norgaard, Asbjorn Sonne, Klofstad, Casey A., Christensen, Kaare, Johannesson, Magnus, Magnusson, Patrik K. E., Eaves, Lindon J. and Martin, Nicholas G. (2014). Genetic influences on political ideologies: Twin analyses of 19 measures of political ideologies from five democracies and genome-wide findings from three populations. Behavior Genetics, 44 (3), 282-294. doi: 10.1007/s10519-014-9648-8

  • Genome-wide association study identifies 25 known breast cancer susceptibility loci as risk factors for triple-negative breast cancer

    Purrington, Kristen S., Slager, Susan, Eccles, Diana, Yannoukakos, Drakoulis, Fasching, Peter A., Miron, Penelope, Carpenter, Jane, Chang-Claude, Jenny, Martin, Nicholas G., Montgomery, Grant W., Kristensen, Vessela, Anton-Culver, Hoda, Goodfellow, Paul, Tapper, William J., Rafiq, Sajjad, Gerty, Susan M., Durcan, Lorraine, Konstantopoulou, Irene, Fostira, Florentia, Vratimos, Athanassios, Apostolou, Paraskevi, Konstanta, Irene, Kotoula, Vassiliki, Lakis, Sotiris, Dimopoulos, Meletios A., Skarlos, Dimosthenis, Pectasides, Dimitrios, Fountzilas, George, Beckmann, Matthias W. ... Couch, Fergus J. (2014). Genome-wide association study identifies 25 known breast cancer susceptibility loci as risk factors for triple-negative breast cancer. Carcinogenesis, 35 (5), 1012-1019. doi: 10.1093/carcin/bgt404

  • Lindon eaves: The astonishing decade

    Martin, Nick (2014). Lindon eaves: The astonishing decade. Behavior Genetics, 44 (3), 193-197. doi: 10.1007/s10519-013-9613-y

  • Hypermethylation in the ZBTB20 gene is associated with major depressive disorder

    Davies, Matthew N., Krause, Lutz, Bell, Jordana T., Gao, Fei, Ward, Kirsten J., Wu, Honglong, Lu, Hanlin, Liu, Yuan, Tsai, Pei-Chein, Collier, David A., Murphy, Therese, Dempster, Emma, Mill, Jonathan, UK Brain Expression Consortium, Battle, Alexis, Mostafavi, Sara, Zhu, Xiaowei, Henders, Anjali, Byrne, Enda, Wray, Naomi R., Martin, Nicholas G., Spector, Tim D. and Wang, Jun (2014). Hypermethylation in the ZBTB20 gene is associated with major depressive disorder. Genome Biology, 15 (4) R56, R56.1-R56.12. doi: 10.1186/gb-2014-15-4-r56

  • A commonly carried genetic variant in the delta opioid receptor gene, OPRD1, is associated with smaller regional brain volumes: replication in elderly and young populations

    Roussotte, Florence F., Jahanshad, Neda, Hibar, Derrek P., Sowell, Elizabeth R., Kohannim, Omid, Barysheva, Marina, Hansell, Narelle K., McMahon, Katie L., de Zubicaray, Greig I., Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J., Toga, Arthur W., Jack Jr, Clifford R., Weiner, Michael W., Thompson, Paul M. and ADNI (2014). A commonly carried genetic variant in the delta opioid receptor gene, OPRD1, is associated with smaller regional brain volumes: replication in elderly and young populations. Human Brain Mapping, 35 (4), 1226-1236. doi: 10.1002/hbm.22247

  • Comparing factor, class, and mixture models of cannabis initiation and DSM cannabis use disorder criteria, including craving, in the Brisbane longitudinal twin study

    Kubarych, Thomas S., Kendler, Kenneth S., Aggen, Steven H., Estabrook, Ryne, Edwards, Alexis C., Clark, Shaunna L., Martin, Nicholas G., Hickie, Ian B., Neale, Michael C. and Gillespie, Nathan A. (2014). Comparing factor, class, and mixture models of cannabis initiation and DSM cannabis use disorder criteria, including craving, in the Brisbane longitudinal twin study. Twin Research and Human Genetics, 17 (2), 89-98. doi: 10.1017/thg.2014.9

  • Development of insula connectivity between ages 12 and 30 revealed by high angular resolution diffusion imaging

    Dennis, Emily L., Jahanshad, Neda, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Hickie, Ian B., Toga, Arthur W., Wright, Margaret J. and Thompson, Paul M. (2014). Development of insula connectivity between ages 12 and 30 revealed by high angular resolution diffusion imaging. Human Brain Mapping, 35 (4), 1790-1800. doi: 10.1002/hbm.22292

  • Hepatitis C testing and status among opioid substitution treatment clients in New South Wales

    Shand, Fiona L., Day, Carolyn, Rawlinson, William, Degenhardt, Louisa, Martin, Nicholas G. and Nelson, Elliot C. (2014). Hepatitis C testing and status among opioid substitution treatment clients in New South Wales. Australian and New Zealand Journal of Public Health, 38 (2), 160-164. doi: 10.1111/1753-6405.12173

  • Sex differences in magical ideation: A community-based twin study

    Karcher, Nicole R., Slutske, Wendy S., Kerns, John G., Piasecki, Thomas M. and Martin, Nicholas G. (2014). Sex differences in magical ideation: A community-based twin study. Personality Disorders-Theory Research and Treatment, 5 (2), 212-219. doi: 10.1037/per0000040

  • Sleep spindles and rapid eye movement sleep as predictors of next morning cognitive performance in healthy middle-aged and older participants

    Lafortune, Marjolaine, Gagnon, Jean-Francois, Martin, Nicolas, Latreille, Veronique, Dube, Jonathan, Bouchard, Maude, Bastien, Celyne and Carrier, Julie (2014). Sleep spindles and rapid eye movement sleep as predictors of next morning cognitive performance in healthy middle-aged and older participants. Journal of Sleep Research, 23 (2), 159-167. doi: 10.1111/jsr.12108

  • Telomere length in circulating leukocytes is associated with lung function and disease

    Albrecht, Eva, Sillanpaa, Elina, Karrasch, Stefan, Alves, Alexessander Couto, Codd, Veryan, Hovatta, Iiris, Buxton, Jessica L., Nelson, Christopher P., Broer, Linda, Hagg, Sara, Mangino, Massimo, Willemsen, Gonneke, Surakka, Ida, Ferreira, Manuel A. R., Amin, Najaf, Oostra, Ben A., Backmand, Hell M., Peltonen, Markku, Sarna, Seppo, Rantanen, Taina, Sipila, Sarianna, Korhonen, Tellervo, Madden, Pamela A. F., Gieger, Christian, Jorres, Rudolf A., Heinrich, Joachim, Behr, Juergen, Huber, Rudolf M., Peters, Annette ... Schulz, Holger (2014). Telomere length in circulating leukocytes is associated with lung function and disease. European Respiratory Journal, 43 (4), 983-992. doi: 10.1183/09031936.00046213

  • Genome-wide association study reveals two new risk loci for bipolar disorder

    Muehleisen, Thomas W., Leber, Markus, Schulze, Thomas G., Strohmaier, Jana, Degenhardt, Franziska, Treutlein, Jens, Mattheisen, Manuel, Forstner, Andreas J., Schumacher, Johannes, Breuer, Rene, Meier, Sandra, Herms, Stefan, Hoffmann, Per, Lacour, Andre, Witt, Stephanie H., Reif, Andreas, Mueller-Myhsok, Bertram, Lucae, Susanne, Maier, Wolfgang, Schwarz, Markus, Vedder, Helmut, Kammerer-Ciernioch, Jutta, Pfennig, Andrea, Bauer, Michael, Hautzinger, Martin, Moebus, Susanne, Priebe, Lutz, Czerski, Piotr M., Hauser, Joanna ... Cichon, Sven (2014). Genome-wide association study reveals two new risk loci for bipolar disorder. Nature Communications, 5 (3339) 3339, 1-8. doi: 10.1038/ncomms4339

  • ADHD symptoms, autistic traits, and substance use and misuse in adult Australian twins

    De Alwis, Duneesha, Agrawal, Arpana, Reiersen, Angela M., Constantino, John N., Henders, Anjali, Martin, Nicholas G. and Lynskey, Michael T. (2014). ADHD symptoms, autistic traits, and substance use and misuse in adult Australian twins. Journal of Studies On Alcohol and Drugs, 75 (2), 211-221. doi: 10.15288/jsad.2014.75.211

  • Comparison of total cortisol, free cortisol, and surrogate markers of free cortisol in diagnosis of adrenal insufficiency in patients with stable cirrhosis

    Fede, Giuseppe, Spadaro, Luisa, Tomaselli, Tania, Privitera, Graziella, Scicali, Roberto, Vasianopoulou, Panayota, Thalassinos, Evangelos, Martin, Nicholas, Thomas, Michael, Purrello, Francesco and Burroughs, Andrew Kenneth (2014). Comparison of total cortisol, free cortisol, and surrogate markers of free cortisol in diagnosis of adrenal insufficiency in patients with stable cirrhosis. Clinical Gastroenterology and Hepatology, 12 (3), 504-512. doi: 10.1016/j.cgh.2013.08.028

  • Genetic and environmental influences on the ages of drinking and gambling initiation: evidence for distinct aetiologies and sex differences

    Richmond-Rakerd, Leah S., Slutske, Wendy S., Heath, Andrew C. and Martin, Nicholas G. (2014). Genetic and environmental influences on the ages of drinking and gambling initiation: evidence for distinct aetiologies and sex differences. Addiction, 109 (2), 323-331. doi: 10.1111/add.12310

  • Genetic effects on the cerebellar role in working memory: same brain, different genes?

    Blokland, Gabriëlla A. M., McMahon, Katie L., Thompson, Paul M., Hickie, Ian B., Martin, Nicholas G., de Zubicaray, Greig I. and Wright, Margaret J. (2014). Genetic effects on the cerebellar role in working memory: same brain, different genes?. NeuroImage, 86, 392-403. doi: 10.1016/j.neuroimage.2013.10.006

  • Genetic risk score analysis indicates migraine with and without comorbid depression are genetically different disorders

    Ligthart, Lannie, Hottenga, Jouke-Jan, Lewis, Cathryn M., Farmer, Anne E., Craig, Ian W., Breen, Gerome, Willemsen, Gonneke, Vink, Jacqueline M., Middeldorp, Christel M., Byrne, Enda M., Heath, Andrew C., Madden, Pamela A. F., Pergadia, Michele L., Montgomery, Grant W., Martin, Nicholas G., Penninx, Brenda W. J. H., McGuffin, Peter, Boomsma, Dorret I. and Nyholt, Dale R. (2014). Genetic risk score analysis indicates migraine with and without comorbid depression are genetically different disorders. Human Genetics, 133 (2), 173-186. doi: 10.1007/s00439-013-1370-8

  • Modeling of the hemodynamic responses in block design fMRI studies

    Shan, Zuyao Y., Wright, Margaret J., Thompson, Paul M., McMahon, Katie L., Blokland, Gabriella G. A. M., de Zubicaray, Greig I., Martin, Nicholas G., Vinkhuyzen, Anna A. E. and Reutens, David C. (2014). Modeling of the hemodynamic responses in block design fMRI studies. Journal of Cerebral Blood Flow and Metabolism, 34 (2), 316-324. doi: 10.1038/jcbfm.2013.200

  • Multi-site genetic analysis of diffusion images and voxelwise heritability analysis: A pilot project of the ENIGMA-DTI working group (vol 81, pg 455, 2013)

    Jahanshad, Neda, Kochunov, Peter V., Sprooten, Emma, Mandl, Rene C., Nichols, Thomas E., Almasy, Laura, Blangero, John, Brouwer, Rachel M., Curran, Joanne E., de Zubicaray, Greig I., Duggirala, Ravi, Fox, Peter T., Hong, L. Elliot, Landman, Bennett A., Martin, Nicholas G., McMahon, Katie L., Medland, Sarah E., Mitchell, Braxton D., Olvera, Rene L., Peterson, Charles P., Starr, John M., Sussmann, Jessika E., Toga, Arthur W., Wardlaw, Joanna M., Wright, Margaret J., Pol, Hilleke E. Hulshoff, Bastin, Mark E., McIntosh, Andrew M., Deary, Ian J. ... Glahn, David C. (2014). Multi-site genetic analysis of diffusion images and voxelwise heritability analysis: A pilot project of the ENIGMA-DTI working group (vol 81, pg 455, 2013). Neuroimage, 90, 470-471. doi: 10.1016/j.neuroimage.2013.12.053

  • Human cognitive ability is influenced by genetic variation in components of postsynaptic signalling complexes assembled by NMDA receptors and MAGUK proteins

    Hill, W. D., Davies, G., Van De Lagemaat, L. N., Christoforou, A., Marioni, R. E., Fernandes, C. P. D., Liewald, D. C., Croning, M. D. R., Payton, A., Craig, L. C. A., Whalley, L. J., Horan, M., Ollier, W., Hansell, N. K., Wright, M. J., Martin, N. G., Montgomery, G. W., Steen, V. M., Le Hellard, S., Espeseth, T., Lundervold, A. J., Reinvang, I., Starr, J. M., Pendleton, N., Grant, S. G. N., Bates, T. C. and Deary, I. J. (2014). Human cognitive ability is influenced by genetic variation in components of postsynaptic signalling complexes assembled by NMDA receptors and MAGUK proteins. Translational Psychiatry, 4 (1) e341, 1-8. doi: 10.1038/tp.2013.114

  • DNA modification study of major depressive disorder: beyond locus-by-locus comparisons

    Oh, Gabriel, Wang, Sun-Chong, Pal, Mrinal, Chen, Zheng Fei, Khare, Tarang, Tochigi, Mamoru, Ng, Catherine, Yang, Yeqing A., Kwan, Andrew, Kaminsky, Zachary A., Mill, Jonathan, Gunasinghe, Cerisse, Tackett, Jennifer L., Gottesman, Irving I., Willemsen, Gonneke, de Geus, Eco J. C., Vink, Jacqueline M., Slagboom, P. Eline, Wray, Naomi R., Heath, Andrew C., Montgomery, Grant W., Turecki, Gustavo, Martin, Nicholas G., Boomsma, Dorret I., McGuffin, Peter, Kustra, Rafal and Petronis, Art (2014). DNA modification study of major depressive disorder: beyond locus-by-locus comparisons. Biological Psychiatry, 77 (3), 246-255. doi: 10.1016/j.biopsych.2014.06.016

  • Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility

    Li, M., Luo, X-j, Rietschel, M., Lewis, C. M., Mattheisen, M., Mueller-Myhsok, B., Jamain, S., Leboyer, M., Landen, M., Thompson, P. M., Cichon, S., Noethen, M. M., Schulze, T. G., Sullivan, P. F., Bergen, S. E., Donohoe, G., Morris, D. W., Hargreaves, A., Gill, M., Corvin, A., Hultman, C., Toga, A. W., Shi, L., Lin, Q., Shi, H., Gan, L., Meyer-Lindenberg, A., Czamara, D., Henry, C. ... Su, B. (2014). Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility. Molecular Psychiatry, 19 (4), 452-461. doi: 10.1038/mp.2013.37

  • Association of OPRD1 polymorphisms with heroin dependence in a large case-control series

    Nelson, Elliot C., Lynskey, Michael T., Heath, Andrew C., Wray, Naomi, Agrawal, Arpana, Shand, Fiona L., Henders, Anjali K., Wallace, Leanne, Todorov, Alexandre A., Schrage, Andrew J., Madden, Pamela A. F., Degenhardt, Louisa, Martin, Nicholas G. and Montgomery, Grant W. (2014). Association of OPRD1 polymorphisms with heroin dependence in a large case-control series. Addiction Biology, 19 (1), 111-121. doi: 10.1111/j.1369-1600.2012.00445.x

  • Automatic clustering and population analysis of white matter tracts using maximum density paths

    Prasad, Gautam, Joshi, Shantanu H., Jahanshad, Neda, Villalon-Reina, Julio, Aganj, Iman, Lenglet, Christophe, Guillermo Sapiro, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J., Toga, Arthur W. and Thompson, Paul M. (2014). Automatic clustering and population analysis of white matter tracts using maximum density paths. NeuroImage, 97, 284-295. doi: 10.1016/j.neuroimage.2014.04.033

  • Common variant at 16p11.2 conferring risk of psychosis

    Steinberg, S., de Jong, S., Mattheisen, M., Costas, J., Demontis, D., Jamain, S., Pietilainen, O. P. H., Lin, K., Papiol, S., Huttenlocher, J., Sigurdsson, E., Vassos, E., Giegling, I., Breuer, R., Fraser, G., Walker, N., Melle, I., Djurovic, S., Agartz, I., Tuulio-Henriksson, A., Suvisaari, J., Lonnqvist, J., Paunio, T., Olsen, L., Hansen, T., Ingason, A., Pirinen, M., Strengman, E., Hougaard, D. M. ... Stefansson, K. (2014). Common variant at 16p11.2 conferring risk of psychosis. Molecular Psychiatry, 19 (1), 108-114. doi: 10.1038/mp.2012.157

  • Common variants in the CYP2C19 gene are associated with susceptibility to endometriosis

    Painter, Jodie N., Nyholt, Dale R, Krause, Lutz, Zhao, Zhen Z., Chapman, Brett, Zhang, Christine, Medland, Sarah, Martin, Nicholas G., Kennedy, Stephen, Treloar, Susan, Zondervan, Krina and Montgomery, Grant W. (2014). Common variants in the CYP2C19 gene are associated with susceptibility to endometriosis. Fertility and Sterility, 102 (2), 496-502.e5. doi: 10.1016/j.fertnstert.2014.04.015

  • Genetic factors that increase male facial masculinity decrease facial attractiveness of female relatives

    Lee, Anthony J., Mitchem, Dorian G., Wright, Margaret J., Martin, Nicholas G., Keller, Matthew C. and Zietsch, Brendan P. (2014). Genetic factors that increase male facial masculinity decrease facial attractiveness of female relatives. Psychological Science, 25 (2), 476-484. doi: 10.1177/0956797613510724

  • Genetic predisposition to schizophrenia associated with increased use of cannabis

    Power, R. A., Verweij, K. J. H., Zuhair, M., Montgomery, G. W., Henders, A. K., Heath, A. C., Madden, P. A. F., Medland, S. E., Wray, N. R. and Martin, N. G. (2014). Genetic predisposition to schizophrenia associated with increased use of cannabis. Molecular Psychiatry, 19 (11), 1201-1204. doi: 10.1038/mp.2014.51

  • Genome-wide association study on detailed profiles of smoking behavior and nicotine dependence in a twin sample

    Loukola, A., Wedenoja, J., Keskitalo-Vuokko, K., Broms, U., Korhonen, T., Ripatti, S., Sarin, A-P, Pitkaniemi, J., He, L., Happola, A., Heikkila, K., Chou, Y-L, Pergadia, M. L., Heath, A. C., Montgomery, G. W., Martin, N. G., Madden, P. A. F. and Kaprio, J. (2014). Genome-wide association study on detailed profiles of smoking behavior and nicotine dependence in a twin sample. Molecular Psychiatry, 19 (5), 615-624. doi: 10.1038/mp.2013.72

  • Heritability of head motion during resting state functional MRI in 462 healthy twins

    Couvy-Duchesne, Baptiste, Blokland, Gabriëlla A.M., Hickie, Ian B., Thompson, Paul M., Martin, Nicholas G., de Zubicaray, Greig I., McMahon, Katie L. and Wright, Margaret J. (2014). Heritability of head motion during resting state functional MRI in 462 healthy twins. Neuroimage, 102 (2), 424-434. doi: 10.1016/j.neuroimage.2014.08.010

  • Novel Approach Identifies SNPs in SLC2A10 and KCNK9 with Evidence for Parent-of-Origin Effect on Body Mass Index

    Hoggart, C. J., Venturini, G., Mangino, M., Gomez, F., Ascari, G., Zhao, J.H., Teumer, A., Winkler, T. W., Tsernikova, N., Luan, J., Mihailov, E., Ehret, G. B., Zhang, W., Lamparter, D., Esko, T., Mace, A., Rueger, S., Bochud, P.-Y., Barcella, M., Dauvilliers, Y., Benyamin, B., Evans, D. M., Hayward, C., Lopez, M. F., Franke, L., Russo, A., Heid, I. M., Salvi, E., Vendantam, S. ... Kutalik Z. (2014). Novel Approach Identifies SNPs in SLC2A10 and KCNK9 with Evidence for Parent-of-Origin Effect on Body Mass Index. PLoS Genetics, 10 (7) e1004508, 1-12. doi: 10.1371/journal.pgen.1004508

  • POT1 loss-of-function variants predispose to familial melanoma

    Robles-Espinoza, Carla Daniela, Harland, Mark, Ramsay, Andrew J, Aoude, Lauren G, Quesada, Víctor, Ding, Zhihao, Pooley, Karen A, Pritchard, Antonia L, Tiffen, Jessamy C, Petljak, Mia, Palmer, Jane M, Symmons, Judith, Johansson, Peter, Stark, Mitchell S., Gartside, Michael G, Snowden, Helen, Montgomery, Grant W, Martin, Nicholas G, Liu, Jimmy Z, Choi, Jiyeon, Makowski, Matthew, Brown, Kevin M, Dunning, Alison M, Keane, Thomas M, Lopez-Otin, Carlos, Gruis, Nelleke A, Hayward, Nicholas K, Bishop, D Timothy, Newton-Bishop, Julia A and Adams, David J (2014). POT1 loss-of-function variants predispose to familial melanoma. Nature Genetics, 46 (5), 478-481. doi: 10.1038/ng.2947

  • Parental separation and early substance involvement: results from children of alcoholic and cannabis dependent twins

    Waldron, Mary, Grant, Julia D., Bucholz, Kathleen K., Lynskey, Michael T., Slutske, Wendy S., Glowinski, Anne L., Henders, Anjali, Statham, Dixie J., Martin, Nicholas G. and Heath, Andrew C. (2014). Parental separation and early substance involvement: results from children of alcoholic and cannabis dependent twins. Drug and Alcohol Dependence, 134 (1), 78-84. doi: 10.1016/j.drugalcdep.2013.09.010

  • Sexual orientation, prejudice, and segregation

    Plug, Erik, Webbink, Dinand and Martin, Nick (2014). Sexual orientation, prejudice, and segregation. Journal of Labor Economics, 32 (1), 123-159. doi: 10.1086/673315

  • Substance use and sexual intercourse onsets in adolescence: A genetically informative discordant twin design

    Deutsch, Arielle R., Slutske, Wendy S., Heath, Andrew C., Madden, Pamela A. F. and Martin, Nicholas G. (2014). Substance use and sexual intercourse onsets in adolescence: A genetically informative discordant twin design. Journal of Adolescent Health, 54 (1), 114-116. doi: 10.1016/j.jadohealth.2013.07.013

  • Testing the role of circadian genes in conferring risk for psychiatric disorders

    Byrne, Enda M., Heath, Andrew C., Madden, Pamela A. F., Pergadia, Michele L., Hickie, Ian B., Montgomery, Grant W., Martin, Nicholas G. and Wray, Naomi R. (2014). Testing the role of circadian genes in conferring risk for psychiatric disorders. American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 165 (3), 254-260. doi: 10.1002/ajmg.b.32230

  • Genome-wide association analysis identifies 11 risk variants associated with the asthma with hay fever phenotype

    Ferreira, Manuel A. R., Matheson, Melanie C., Tang, Clara S., Granell, Raquel, Ang, Wei., Hui, Jennie, Kiefer, Amy K., Duffy, David L., Baltic, Svetlana, Danoy, Patrick, Bui, Minh, Price, Loren, Sly, Peter D., Eriksson, Nicholas, Madden, Pamela A., Abraham, Michael J. A., Holt, Patrick G., Heath, p Andrew C., Hunter, Michael, Musk, Bill, Robertson, Colin F., Le Souef, Peter, Montgomery, Grant W., Henderson, A. John, Tung, Joyce Y., Dharmage, Shyamali C., Brown, Matthew A., James, Alan, Thompson, Philip J. ... Australian Asthma Genetics Consortium Collaborators (2013). Genome-wide association analysis identifies 11 risk variants associated with the asthma with hay fever phenotype. Journal of Allergy And Clinical Immunology, 133 (6), 1564-1571. doi: 10.1016/j.jaci.2013.10.030

  • Distinct loci in the CHRNA5/CHRNA3/CHRNB4 gene cluster are associated with onset of regular smoking

    Stephens, Sarah H., Hartz, Sarah M., Hoft, Nicole R., Saccone, Nancy L., Corley, Robin C., Hewitt, John K., Hopfer, Christian J., Breslau, Naomi, Coon, Hilary, Chen, Xiangning, Ducci, Francesca, Dueker, Nicole, Franceschini, Nora, Frank, Josef, Han, Younghun, Hansel, Nadia N., Jiang, Chenhui, Korhonen, Tellervo, Lind, Penelope A., Liu, Jason, Lyytikaeinen, Leo-Pekka, Michel, Martha, Shaffer, John R., Short, Susan E., Sun, Juzhong, Teumer, Alexander, Thompson, John R., Vogelzangs, Nicole, Vink, Jacqueline M. ... Ehringer, Marissa A. (2013). Distinct loci in the CHRNA5/CHRNA3/CHRNB4 gene cluster are associated with onset of regular smoking. Genetic Epidemiology, 37 (8), 846-859. doi: 10.1002/gepi.21760

  • Germline variants and advanced colorectal adenomas: adenoma prevention with celecoxib trial genome-wide association study

    Wang, Jiping, Carvajal-Carmona, Luis G., Chu, Jen-Hwa, Zauber, Ann G., Kubo, Michikai, Matsuda, Koichi, Dunlop, Malcolm, Houlston, Richard S., Sieber, Oliver, Lipton, Lara, Gibbs, Peter, Martin, Nicholas G., Montgomery, Grant W., Young, Joanne, Baird, Paul N., Ratain, Mark J., Nakamura, Yusuke, Weiss, Scott T., Tomlinson, Ian and Bertagnolli, Monica M. (2013). Germline variants and advanced colorectal adenomas: adenoma prevention with celecoxib trial genome-wide association study. Clinical Cancer Research, 19 (23), 6430-6437. doi: 10.1158/1078-0432.CCR-13-0550

  • Is the relationship between early-onset cannabis use and educational attainment causal or due to common liability?

    Verweij, Karin J. H., Huizink, Anja C., Agrawal, Arpana, Martin, Nicholas G. and Lynskey, Michael T. (2013). Is the relationship between early-onset cannabis use and educational attainment causal or due to common liability?. Drug and Alcohol Dependence, 133 (2), 580-586. doi: 10.1016/j.drugalcdep.2013.07.034

  • Relation between variants in the neurotrophin receptor gene, NTRK3, and white matter integrity in healthy young adults

    Braskie, Meredith N., Kohannim, Omid, Jahanshad, Neda, Chiang, Ming-Chang, Barysheva, Marina, Toga, Arthur W., Ringman, John M., Montgomery, Grant W., McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2013). Relation between variants in the neurotrophin receptor gene, NTRK3, and white matter integrity in healthy young adults. Neuroimage, 82, 146-153. doi: 10.1016/j.neuroimage.2013.05.095

  • Estimating the sex-specific effects of genes on facial attractiveness and sexual dimorphism

    Mitchem, Dorian G., Purkey, Alicia M., Grebe, Nicholas M., Carey, Gregory, Garver-Apgar, Christine E., Bates, Timothy C., Arden, Rosalind, Hewitt, John K., Medland, Sarah E., Martin, Nicholas G., Zietsch, Brendan P. and Keller, Matthew C. (2013). Estimating the sex-specific effects of genes on facial attractiveness and sexual dimorphism. Behavior Genetics, 44 (3), 270-281. doi: 10.1007/s10519-013-9627-5

  • A genome-wide association study of alcohol-dependence symptom counts in extended pedigrees identifies C15orf53

    Wang, J-C, Foroud, T., Hinrichs, A. L., Le, N. X. H., Bertelsen, S., Budde, J. P., Harari, O., Koller, D. L., Wetherill, L., Agrawal, A., Almasy, L., Brooks, A. I., Bucholz, K., Dick, D., Hesselbrock, V., Johnson, E. O., Kang, S., Kapoor, M., Kramer, J., Kuperman, S., Madden, P. A. F., Manz, N., Martin, N. G., McClintick, J. N., Montgomery, G. W., Nurnberger, J. I., Rangaswamy, M., Rice, J., Schuckit, M. ... Goate, A. M. (2013). A genome-wide association study of alcohol-dependence symptom counts in extended pedigrees identifies C15orf53. Molecular Psychiatry, 18 (11), 1218-1224. doi: 10.1038/mp.2012.143

  • Are bottom-up and top-down traits in dual-systems models of risky behavior genetically distinct?

    Ellingson, Jarrod M., Verges, Alvaro, Littlefield, Andrew K., Martin, Nicholas G. and Slutske, Wendy S. (2013). Are bottom-up and top-down traits in dual-systems models of risky behavior genetically distinct?. Behavior Genetics, 43 (6), 480-490. doi: 10.1007/s10519-013-9615-9

  • Common variants associated with plasma triglycerides and risk for coronary artery disease

    Do, Ron, Willer, Cristen J., Schmidt, Ellen M., Sengupta, Sebanti, Gao, Chi, Peloso, Gina M., Gustafsson, Stefan, Kanoni, Stavroula, Ganna, Andrea, Chen, Jin, Buchkovich, Martin L., Mora, Samia, Beckmann, Jacques S., Bragg-Gresham, Jennifer L., Chang, Hsing-Yi, Demirkan, Ayse, Den Hertog, Heleen M., Donnelly, Louise A., Ehret, Georg B., Esko, Tonu, Feitosa, Mary F., Ferreira, Teresa, Fischer, Krista, Fontanillas, Pierre, Fraser, Ross M., Freitag, Daniel F., Gurdasani, Deepti, Heikkila, Kauko, Hyppoenen, Elina ... Kathiresan, Sekar (2013). Common variants associated with plasma triglycerides and risk for coronary artery disease. Nature Genetics, 45 (11), 1345-1352. doi: 10.1038/ng.2795

  • Discovery and refinement of loci associated with lipid levels

    Willer C.J., Schmidt E.M., Sengupta S., Peloso G.M., Gustafsson S., Kanoni S., Ganna A., Chen J., Buchkovich M.L., Mora S., Beckmann J.S., Bragg-Gresham J.L., Chang H.-Y., Demirkan A., Den Hertog H.M., Do R., Donnelly L.A., Ehret G.B., Esko T., Feitosa M.F., Ferreira T., Fischer K., Fontanillas P., Fraser R.M., Freitag D.F., Gurdasani D., Heikkila K., Hypponen E., Isaacs A. ... Abecasis G.R. (2013). Discovery and refinement of loci associated with lipid levels. Nature Genetics, 45 (11), 1274-1285. doi: 10.1038/ng.2797

  • Genetic and environmental contributions to sleep-wake behavior in 12-year-old twins

    Sletten, Tracey L., Rajaratnam, Shantha M. W., Wright, Margaret J., Zhu, Gu, Naismith, Sharon, Martin, Nicholas G. and Hickie, Ian (2013). Genetic and environmental contributions to sleep-wake behavior in 12-year-old twins. Sleep, 36 (11), 1715-1722. doi: 10.5665/sleep.3136

  • Inference of the Genetic Architecture Underlying BMI and Height with the Use of 20,240 Sibling Pairs

    Hemani, Gibran, Yang, Jian, Vinkhuyzen, Anna, Powell, Joseph E., Willemsen, Gonneke, Hottenga, Jouke-Jan, Abdellaoui, Abdel, Mangino, Massimo, Valdes, Ana M., Medland, Sarah E., Madden, Pamela A., Heath, Andrew C., Henders, Anjali K., Nyholt, Dale R., de Geus, Eco J. C., Magnusson, Patrik K. E., Ingelsson, Erik, Montgomery, Grant W., Spector, Timothy D., Boomsma, Dorret I., Pedersen, Nancy L., Martin, Nicholas G. and Visscher, Peter M. (2013). Inference of the Genetic Architecture Underlying BMI and Height with the Use of 20,240 Sibling Pairs. American Journal of Human Genetics, 93 (5), 865-875. doi: 10.1016/j.ajhg.2013.10.005

  • Personality and occupational markers of 'solid citizenship' are associated with having fewer children

    Perkins, Adam M., Cserjesi, Renata, Ettinger, Ulrich, Kumari, Veena, Martin, Nicholas G. and Arden, Rosalind (2013). Personality and occupational markers of 'solid citizenship' are associated with having fewer children. Personality and Individual Differences, 55 (8), 871-876. doi: 10.1016/j.paid.2013.07.011

  • Toward the development of a global induced pluripotent stem cell library

    Turner, Marc, Leslie, Stephen, Martin, Nicholas G., Peschanski, Marc, Rao, Mahendra, Taylor, Craig J., Trounson, Alan, Turner, David, Yamanaka, Shinya and Wilmut, Ian (2013). Toward the development of a global induced pluripotent stem cell library. Cell Stem Cell, 13 (4), 382-384. doi: 10.1016/j.stem.2013.08.003

  • A new regulatory variant in the interleukin-6 receptor gene associates with asthma risk

    Revez, J. A., Bain, L., Chapman, B., Powell, J. E., Jansen, R., Duffy, D. L., Tung, J. Y., AAGC Collaborators, Penninx, B. W., Visscher, P. M., De Geus, E. J. C., Boomsma, D. I., Hinds, D. A., Martin, N. G., Montgomery, G. W., Ferreira, M. A. R., Danoy, Patrick and Brown, Matthew A. (2013). A new regulatory variant in the interleukin-6 receptor gene associates with asthma risk. Genes and Immunity, 14 (7), 441-446. doi: 10.1038/gene.2013.38

  • A twin study of alcohol dependence, binge eating, and compensatory behaviors

    Munn-Chernoff, Melissa A., Duncan, Alexis E., Grant, Julia D., Wade, Tracey D., Agrawal, Arpana, Bucholz, Kathleen K., Madden, Pamela A. F., Martin, Nicholas G. and Heath, Andrew C. (2013). A twin study of alcohol dependence, binge eating, and compensatory behaviors. Journal of Studies On Alcohol and Drugs, 74 (5), 664-673. doi: 10.15288/jsad.2013.74.664

  • Causal influence of age at first drink on alcohol involvement in adulthood and its moderation by familial context

    Deutsch, Arielle R., Slutske, Wendy S., Richmond-Rakerd, Leah S., Chernyavskiy, Pavel, Heath, Andrew C. and Martin, Nicholas G. (2013). Causal influence of age at first drink on alcohol involvement in adulthood and its moderation by familial context. Journal of Studies On Alcohol and Drugs, 74 (5), 703-713. doi: 10.15288/jsad.2013.74.703

  • Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

    Lee, S. Hong, Ripke, Stephan, Neale, Benjamin M., Faraone, Stephen V., Purcell, Shaun M., Perlis, Roy H., Mowry, Bryan J., Thapar, Anita, Goddard, Michael E., Witte, John S., Absher, Devin, Agartz, Ingrid, Akil, Huda, Amin, Farooq, Andreassen, Ole A., Anjorin, Adebayo, Anney, Richard, Anttila, Verneri, Arking, Dan E., Asherson, Philip, Azevedo, Maria H., Backlund, Lena, Badner, Judith A., Bailey, Anthony J., Banaschewski, Tobias, Barchas, Jack D., Barnes, Michael R., Barrett, Thomas B., Bass, Nicholas ... Wray, Naomi R. (2013). Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nature Genetics, 45 (9), 984-995. doi: 10.1038/ng.2711

  • Genetic variants associated with disordered eating

    Wade, Tracey D., Gordon, Scott, Medland, Sarah, Bulik, Cynthia M., Heath, Andrew C., Montgomery, Grant W. and Martin, Nicholas G. (2013). Genetic variants associated with disordered eating. International Journal of Eating Disorders, 46 (6), 594-608. doi: 10.1002/eat.22133

  • A genetic perspective on the proposed inclusion of cannabis withdrawal in DSM-5

    Verweij, K. J. H., Agrawal, A., Nat, N. O., Creemers, H. E., Huizink, A. C., Martin, N. G. and Lynskey, M. T. (2013). A genetic perspective on the proposed inclusion of cannabis withdrawal in DSM-5. Psychological Medicine, 43 (8), 1713-1722. doi: 10.1017/S0033291712002735

  • Association of adiposity genetic variants with menarche timing in 92,105 women of European descent

    Fernández-Rhodes, Lindsay, Demerath, Ellen W., Cousminer, Diana L., Tao, Ran, Dreyfus, Jill G., Esko, Tõnu, Smith, Albert V., Gudnason, Vilmundur, Harris, Tamara B., Launer, Lenore, McArdle, Patrick F., Yerges-Armstrong, Laura M., Elks, Cathy E., Strachan, David P., Kutalik, Zoltán, Vollenweider, Peter, Feenstra, Bjarke, Boyd, Heather A., Metspalu, Andres, Mihailov, Evelin, Broer, Linda, Zillikens, M. Carola, Oostra, Ben, van Duijn, Cornelia M., Lunetta, Kathryn L., Perry, John R. B., Murray, Anna, Koller, Daniel L., Lai, Dongbing ... Franceschini, Nora (2013). Association of adiposity genetic variants with menarche timing in 92,105 women of European descent. American Journal of Epidemiology, 178 (3), 451-460. doi: 10.1093/aje/kws473

  • GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association

    Rentería, Miguel E., Coolen, Marcel W., Statham, Aaron L., Choi, R. Seong Min, Qu, Wenjia, Campbell, Megan J., Smith, Sara, Henders, Anjali K., Montgomery, Grant W., Clark, Susan J., Martin, Nicholas G. and Medland, Sarah E. (2013). GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association. Twin Research and Human Genetics, 16 (4), 767-781. doi: 10.1017/thg.2013.30

  • Meta-analysis of genome-wide association studies identifies ten loci influencing allergic sensitization

    Bønnelykke, Klaus, Matheson, Melanie C., Pers, Tune H., Granell, Raquel, Strachan, David P., Alves, Alexessander Couto, Linneberg, Allan, Curtin, John A., Warrington, Nicole M., Standl, Marie, Kerkhof, Marjan, Jonsdottir, Ingileif, Bukvic, Blazenka K., Kaakinen, Marika, Sleimann, Patrick, Thorleifsson, Gudmar, Thorsteinsdottir, Unnur, Schramm, Katharina, Baltic, Svetlana, Kreiner-Møller, Eskil, Simpson, Angela, St Pourcain, Beate, Coin, Lachlan, Hui, Jennie, Walters, Eugene H., Tiesler, Carla M. T., Duffy, David L., Jones, Graham, Ring, Susan M. ... Brown, Matthew A. (2013). Meta-analysis of genome-wide association studies identifies ten loci influencing allergic sensitization. Nature Genetics, 45 (8), 902-906. doi: 10.1038/ng.2694

  • The nature and nurture of high IQ: an extended sensitive period for intellectual development

    Brant, Angela M., Munakata, Yuko, Boomsma, Dorret I., DeFries, John C., Haworth, Claire M. A., Keller, Matthew C., Martin, Nicholas G., McGue, Matthew, Petrill, Stephen A., Plomin, Robert, Wadsworth, Sally J., Wright, Margaret J. and Hewitt, John K. (2013). The nature and nurture of high IQ: an extended sensitive period for intellectual development. Psychological Science, 24 (8), 1487-1495. doi: 10.1177/0956797612473119

  • No genetic support for a contribution of prostaglandins to the aetiology of androgenetic alopecia

    Heilmann, S., Nyholt, D. R., Brockschmidt, F. F., Hillmer, A. M., Herold, C., Becker, T., Martin, N. G. and Noethen, M. M. (2013). No genetic support for a contribution of prostaglandins to the aetiology of androgenetic alopecia. British Journal of Dermatology, 169 (1), 222-224. doi: 10.1111/bjd.12292

  • Scrutiny of the CHRNA5-CHRNA3-CHRNB4 smoking behavior locus reveals a novel association with alcohol use in a Finnish population based study

    Haefors, Jenni, Loukola, Anu, Pitkaeemi, Janne, Broms, Ulla, Maennistoe, Satu, Salomaa, Veikko, Helioevaara, Markku, Lehtimaeki, Terho, Raitakari, Olli, Madden, Pamela A. F., Heath, Andrew C., Montgomery, Grant W., Martin, Nicholas G., Korhonen, Tellervo and Kaprio, Jaakko (2013). Scrutiny of the CHRNA5-CHRNA3-CHRNB4 smoking behavior locus reveals a novel association with alcohol use in a Finnish population based study. International Journal of Molecular Epidemiology and Genetics, 4 (2), 109-119.

  • The role of adiposity in cardiometabolic traits: a Mendelian randomization analysis

    Fall, Tove, Hägg, Sara, Maegi, Reedik, Ploner, Alexander, Fischer, Krista, Horikoshi, Momoko, Sarin, Antti-Pekka, Thorleifsson, Gudmar, Ladenvall, Claes, Kals, Mart, Kuningas, Maris, Draisma, Harmen H. M., Ried, Janina S., van Zuydam, Natalie R., Huikari, Ville, Mangino, Massimo, Sonestedt, Emily, Benyamin, Beben, Nelson, Christopher P., Rivera, Natalia V., Kristiansson, Kati, Shen, Huei-yi, Havulinna, Aki S., Dehghan, Abbas, Donnelly, Louise A., Kaakinen, Marika, Nuotio, Marja-Liisa, Robertson, Neil, de Bruijn, Renee F. A. G. ... Prokopenko, Inga (2013). The role of adiposity in cardiometabolic traits: a Mendelian randomization analysis. PLoS Medicine, 10 (6) e1001474, e1001474.1-e1001474.15. doi: 10.1371/journal.pmed.1001474

  • Genetic Loci for Retinal Arteriolar Microcirculation

    Sim X., Jensen R.A., Ikram M.K., Cotch M.F., Li X., MacGregor S., Xie J., Smith A.V., Boerwinkle E., Mitchell P., Klein R., Klein B.E.K., Glazer N.L., Lumley T., McKnight B., Psaty B.M., de Jong P.T.V.M., Hofman A., Rivadeneira F., Uitterlinden A.G., van Duijn C.M., Aspelund T., Eiriksdottir G., Harris T.B., Jonasson F., Launer L.J., Attia J., Baird P.N., Harrap S. ... Wong T.Y. (2013). Genetic Loci for Retinal Arteriolar Microcirculation. PLoS ONE, 8 (6) e65804, e65804.1-e65804.12. doi: 10.1371/journal.pone.0065804

  • Androgenetic alopecia: identification of four genetic risk loci and evidence for the contribution of WNT signaling to its etiology

    Heilmann, Stefanie, Kiefer, Amy K., Fricker, Nadine, Drichel, Dmitriy, Hillmer, Axel M., Herold, Christine, Tung, Joyce Y., Eriksson, Nicholas, Redler, Silke, Betz, Regina C., Li, Rui, Karason, Ari, Nyholt, Dale R., Song, Kijoung, Vermeulen, Sita H., Kanoni, Stavroula, Dedoussis, George, Martin, Nicholas G., Kiemeney, Lambertus A., Mooser, Vincent, Stefansson, Kari, Richards, J. Brent, Becker, Tim, Brockschmidt, Felix F., Hinds, David A. and Noethen, Markus M. (2013). Androgenetic alopecia: identification of four genetic risk loci and evidence for the contribution of WNT signaling to its etiology. Journal of Investigative Dermatology, 133 (6), 1489-1496. doi: 10.1038/jid.2013.43

  • Effects of sibship size and composition on younger brothers' and sisters' alcohol use initiation: findings from an Australian twin sample

    Richmond-Rakerd, Leah S., Slutske, Wendy S., Heath, Andrew C. and Martin, Nicholas G. (2013). Effects of sibship size and composition on younger brothers' and sisters' alcohol use initiation: findings from an Australian twin sample. Alcoholism-Clinical and Experimental Research, 37 (6), 1016-1024. doi: 10.1111/acer.12052

  • GWAS of 126,559 individuals identifies genetic variants associated with educational attainment

    Rietveld, Cornelius A., Medland, Sarah E., Derringer, Jaime, Yang, Jian, Esko, Tonu, Martin, Nicolas W., Westra, Harm-Jan, Shakhbazov, Konstantin, Abdellaoui, Abdel, Agrawal, Arpana, Albrecht, Eva, Alizadeh, Behrooz Z., Amin, Najaf, Bamard, John, Baumeister, Sebastian E., Benke, Kelly S., Bielak, Lawrence F., Boatman, Jeffrey A., Boyle, Patricia A., Davies, Gail, De Leeuw, Christiaan, Eklund, Niina, Evans, Daniel S., Ferhmann, Rudolf, Fischer, Krista, Gieger, Christian, Gjessing, Hakon K., Haegg, Sara, Harris, Jennifer R. ... Koellinger, Philipp D. (2013). GWAS of 126,559 individuals identifies genetic variants associated with educational attainment. Science, 340 (6139), 1467-1471. doi: 10.1126/science.1235488

  • Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders

    den Hoed, Marcel, Eijgelsheim, Mark, Esko, Tonu, Brundel, Bianca J. J. M., Peal, David S., Evans, David M., Nolte, Ilja M., Segre, Ayellet V., Holm, Hilma, Handsaker, Robert E., Westra, Harm-Jan, Johnson, Toby, Isaacs, Aaron, Yang, Jian, Lundby, Alicia, Zhao, Jing Hua, Kim, Young Jin, Go, Min Jin, Almgren, Peter, Bochud, Murielle, Boucher, Gabrielle, Cornelis, Marilyn C., Gudbjartsson, Daniel, Hadley, David, van der Harst, Pim, Hayward, Caroline, den Heijer, Martin, Igl, Wilmar, Jackson, Anne U. ... Loos, Ruth J. F. (2013). Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders. Nature Genetics, 45 (6), 621-634. doi: 10.1038/ng.2610

  • Monozygotic twins affected with major depressive disorder have greater variance in methylation than their unaffected co-twin

    Byrne, E. M., Carrillo-Roa, T., Henders, A. K., Bowdler, L., McRae, A. F., Heath, A. C., Martin, N. G., Montgomery, G. W., Krause, L. and Wray, N. R. (2013). Monozygotic twins affected with major depressive disorder have greater variance in methylation than their unaffected co-twin. Translational Psychiatry, 3 (6) e269, e269.1-e269.6. doi: 10.1038/tp.2013.45

  • Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits

    Randall, Joshua C., Winkler, Thomas W., Kutalik, Zoltan, Berndt, Sonja I., Jackson, Anne U., Monda, Keri L., Kilpelaeinen, Tuomas O., Esko, Tonu, Maegi, Reedik, Li, Shengxu, Workalemahu, Tsegaselassie, Feitosa, Mary F., Croteau-Chonka, Damien C., Day, Felix R., Fall, Tove, Ferreira, Teresa, Gustafsson, Stefan, Locke, Adam E., Mathieson, Iain, Scherag, Andre, Vedantam, Sailaja, Wood, Andrew R., Liang, Liming, Steinthorsdottir, Valgerdur, Thorleifsson, Gudmar, Dermitzakis, Emmanouil T., Dimas, Antigone S., Karpe, Fredrik, Min, Josine L. ... MAGIC Investigators (2013). Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits. Plos Genetics, 9 (6) e1003500, e1003500.1-e1003500.19. doi: 10.1371/journal.pgen.1003500

  • The general factor of personality and humor styles

    Schermer, Julie Aitken, Martin, Rod A., Martin, Nicholas G., Lynskey, Michael and Vernon, Philip A. (2013). The general factor of personality and humor styles. Personality and Individual Differences, 54 (8), 890-893. doi: 10.1016/j.paid.2012.12.026

  • A genome-wide association study of sleep habits and insomnia

    Byrne, Enda M., Gehrman, Philip R., Medland, Sarah E., Nyholt, Dale R., Heath, Andrew C., Madden, Pamela A. F., Hickie, Ian B., Van Duijn, Cornelia M., Henders, Anjali K., Montgomery, Grant W., Martin, Nicholas G., Wray, Naomi R. and The Chronogen Consortium (2013). A genome-wide association study of sleep habits and insomnia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 162 (5), 439-451. doi: 10.1002/ajmg.b.32168

  • Genome-wide association study identifies loci affecting blood copper, selenium and zinc.

    Evans, David M., Zhu, Gu, Dy, Veronica, Heath, Andrew C., Madden, Pamela A. F., Kemp, John P., McMahon, George, St Pourcain, Beate, Timpson, Nicholas J., Golding, Jean, Lawlor, Debbie A., Steer, Colin, Montgomery, Grant W., Martin, Nicholas G, Smith, George Davey and Whitfield, John B. (2013). Genome-wide association study identifies loci affecting blood copper, selenium and zinc.. Human Molecular Genetics, 22 (19), 3998-4006. doi: 10.1093/hmg/ddt239

  • Congruence of additive and non-additive effects on gene expression estimated from pedigree and SNP data

    Powell, Joseph E., Henders, Anjali K., McRae, Allan F., Kim, Jinhee, Hemani, Gibran, Martin, Nicholas G., Dermitzakis, Emmanouil T., Gibson, Greg, Montgomery, Grant W. and Visscher, Peter M. (2013). Congruence of additive and non-additive effects on gene expression estimated from pedigree and SNP data. PLoS Genetics, 9 (5) e1003502, e1003502.1-e1003502.10. doi: 10.1371/journal.pgen.1003502

  • Correction: Maintenance of variation in human personality: testing evolutionary models by estimating heritability due to common causal variants and investigating the effect of distant inbreeding (vol 66, pg 3238, 2012)

    Verweij, K. J. H., Yang, J., Lahti, J., Veijola, J., Hintsanen, M., Pulkki-Raback, L., Heinonen, K., Pouta, A., Pesonen, A. -K., Widen, E., Taanila, A., Isohanni, M., Miettunen, J., Palotie, A., Penke, L., Service, S. K., Heath, A. C., Montgomery, G. W., Raitakari, O., Kaehoenen, M., Viikari, J., Raeikkoenen, K., Eriksson, J. G., Keltikangas-Jaervinen, L., Lehtimaeki, T., Martin, N. G., Jaervelin, M. -R., Visscher, P. M., Keller, M. C. and Zietsch, B. P. (2013). Correction: Maintenance of variation in human personality: testing evolutionary models by estimating heritability due to common causal variants and investigating the effect of distant inbreeding (vol 66, pg 3238, 2012). Evolution, 67 (5), 1537-1537. doi: 10.1111/evo.12095

  • First all-in-one diagnostic tool for DNA intelligence: genome-wide inference of biogeographic ancestry, appearance, relatedness, and sex with the Identitas v1 Forensic Chip

    Keating, Brendan, Bansal, Aruna T., Walsh, Susan, Millman, Jonathan, Newman, Jonathan, Kidd, Kenneth, Budowle, Bruce, Eisenberg, Arthur, Donfack, Joseph, Gasparini, Paolo, Budimlija, Zoran, Henders, Anjali K., Chandrupatla, Hareesh, Duffy, David L., Gordon, Scott D., Hysi, Pirro, Liu, Fan, Medland, Sarah E., Rubin, Laurence, Martin, Nicholas G., Spector, Timothy D. and Kayser, Manfred (2013). First all-in-one diagnostic tool for DNA intelligence: genome-wide inference of biogeographic ancestry, appearance, relatedness, and sex with the Identitas v1 Forensic Chip. International Journal of Legal Medicine, 127 (3), 559-572. doi: 10.1007/s00414-012-0788-1

  • Genome-wide association study of a quantitative disordered gambling trait

    Lind, Penelope A., Zhu, Gu, Montgomery, Grant W., Madden, Pamela A. F., Heath, Andrew C., Martin, Nicholas G. and Slutske, Wendy S. (2013). Genome-wide association study of a quantitative disordered gambling trait. Addiction Biology, 18 (3), 511-522. doi: 10.1111/j.1369-1600.2012.00463.x

  • Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

    Berndt, Sonja I., Gustafsson, Stefan, Maegi, Reedik, Ganna, Andrea, Wheeler, Eleanor, Feitosa, Mary F., Justice, Anne E., Monda, Keri L., Croteau-Chonka, Damien C., Day, Felix R., Esko, Tonu, Fall, Tove, Ferreira, Teresa, Gentilini, Davide, Jackson, Anne U., Luan, Jian'an, Randall, Joshua C., Vedantam, Sailaja, Willer, Cristen J., Winkler, Thomas W., Wood, Andrew R., Workalemahu, Tsegaselassie, Hu, Yi-Juan, Lee, Sang Hong, Liang, Liming, Lin, Dan-Yu, Min, Josine L., Neale, Benjamin M., Thorleifsson, Gudmar ... Ingelsson, Erik (2013). Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. Nature Genetics, 45 (5), 501-U69. doi: 10.1038/ng.2606

  • Genotype by environment interactions in cognitive ability: a survey of 14 studies from four countries covering four age groups

    Molenaar, Dylan, van der Sluis, Sophie, Boomsma, Dorret I., Haworth, Claire M. A., Hewitt, John K., Martin, Nicholas G., Plomin, Robert, Wright, Margaret J. and Dolan, Conor V. (2013). Genotype by environment interactions in cognitive ability: a survey of 14 studies from four countries covering four age groups. Behavior Genetics, 43 (3), 208-219. doi: 10.1007/s10519-012-9581-7

  • Investigating the influence of prenatal androgen exposure and sibling effects on alcohol use and alcohol use disorder in females from opposite-sex twin pairs

    Ellingson, Jarrod M., Slutske, Wendy S., Richmond-Rakerd, Leah S. and Martin, Nicholas G. (2013). Investigating the influence of prenatal androgen exposure and sibling effects on alcohol use and alcohol use disorder in females from opposite-sex twin pairs. Alcoholism-Clinical and Experimental Research, 37 (5), 868-876. doi: 10.1111/acer.12035

  • No association between general cognitive ability and rare copy number variation

    McRae, Allan F., Wright, Margaret J., Hansell, Narelle K., Montgomery, Grant W. and Martin, Nicholas G. (2013). No association between general cognitive ability and rare copy number variation. Behavior Genetics, 43 (3), 202-207. doi: 10.1007/s10519-013-9587-9

  • A mega-analysis of genome-wide association studies for major depressive disorder

    Major Depressive Disorder Working Group of the Psychiatric GWAS Consortium, Wray, Naomi, Byrne, Enda M., Martin, Nicholas G., Gordon, Scott D., Henders, Anjali K., Montgomery, Grant M., Nyholt, Dale R. and Middeldorp, Christel M. (2013). A mega-analysis of genome-wide association studies for major depressive disorder. Molecular Psychiatry, 18 (4), 497-511. doi: 10.1038/mp.2012.21

  • General and supplementary factors of personality in genetic and environmental correlation matrices

    Loehlin, John C. and Martin, Nicholas G. (2013). General and supplementary factors of personality in genetic and environmental correlation matrices. Personality and Individual Differences, 54 (6), 761-766. doi: 10.1016/j.paid.2012.12.014

  • Metabolic and biochemical effects of low-to-moderate alcohol consumption

    Whitfield, John B., Heath, Andrew C., Madden, Pamela A. F., Pergadia, Michele L., Montgomery, Grant W. and Martin, Nicholas G. (2013). Metabolic and biochemical effects of low-to-moderate alcohol consumption. Alcoholism: Clinical and Experimental Research, 37 (4), 575-586. doi: 10.1111/acer.12015

  • Shared genetic vulnerability for disordered gambling and alcohol use disorder in men and women: evidence from a national community-based Australian twin study

    Slutske, Wendy S., Ellingson, Jarrod M., Richmond-Rakerd, Leah S., Zhu, Gu and Martin, Nicholas G. (2013). Shared genetic vulnerability for disordered gambling and alcohol use disorder in men and women: evidence from a national community-based Australian twin study. Twin Research and Human Genetics, 16 (2), 525-534. doi: 10.1017/thg.2013.11

  • The effect of schooling on problem drinking: evidence from Australian twins

    Zubanov, N., Webbink, H. D. and Martin, N. G. (2013). The effect of schooling on problem drinking: evidence from Australian twins. Applied Economics, 45 (12), 1583-1599. doi: 10.1080/00036846.2011.631897

  • The genetic correlation between height and IQ: shared genes or assortative mating?

    Keller, Matthew C., Garver-Apgar, Christine E., Wright, Margaret J., Martin, Nicholas G., Corley, Robin P., Stallings, Michael C., Hewitt, John K. and Zietsch, Brendan P. (2013). The genetic correlation between height and IQ: shared genes or assortative mating?. PLoS Genetics, 9 (4) e1003451, e1003451.1-e1003451.10. doi: 10.1371/journal.pgen.1003451

  • Genome-wide scan of healthy human connectome discovers SPON1 gene variant influencing dementia severity

    Jahanshad, Neda, Rajagopalan, Priya, Hua, Xue, Hibar, Derrek P., Nir, Talia M., Toga, Arthur W., Jack, Jr, Clifford R., Saykin, Andrew J., Green, Robert C., Weiner, Michael W., Medland, Sarah E., Montgomery, Grant W., Hansell, Narelle K., McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J., Thompson, Paul M. and The Alzheimer’s Disease Neuroimaging Initiative (2013). Genome-wide scan of healthy human connectome discovers SPON1 gene variant influencing dementia severity. Proceedings of the National Academy of Sciences of the United States of America, 110 (12), 4768-4773. doi: 10.1073/pnas.1216206110

  • Correction: Genome-wide association studies of asthma in population-based cohorts confirm known and suggested loci and identify an additional association near HLA (PLoS ONE)

    Ramasamy, Adaikalavan, Kuokkanen, Mikko, Vedantam, Sailaja, Gajdos, Zofia K., Alves, Alexessander Couto, Lyon, Helen N., Ferreira, Manuel A. R., Strachan, David P., Zhao, Jing Hua, Abramson, Michael J., Brown, Matthew A., Coin, Lachlan, Dharmage, Shyamali C., Duffy, David L., Haahtela, Tari, Heath, Andrew C., Janson, Christer, Kähönen, Mika, Khaw, Kay-Tee, Laitinen, Jaana, Souef, Peter Le, Lehtimäki, Terho, Madden, Pamela A. F., Marks, Guy B., Martin, Nicholas G., Matheson, Melanie C., Palmer, Cameron D., Palotie, Aarno, Pouta, Anneli ... Hirschhorn, Joel N. (2013). Correction: Genome-wide association studies of asthma in population-based cohorts confirm known and suggested loci and identify an additional association near HLA (PLoS ONE). PLoS ONE, 8 (3), 1-1. doi: 10.1371/annotation/9630862b-4676-4b82-9869-8d8fbb2a2e65

  • ANKK1, TTC12, and NCAM1 polymorphisms and heroin dependence: importance of considering drug exposure

    Nelson, Elliot C., Lynskey, Michael T., Heath, Andrew C., Wray, Naomi, Agrawal, Arpana, Shand, Fiona L., Henders, Anjali K., Wallace, Leanne, Todorov, Alexandre A., Schrage, Andrew J., Saccone, Nancy L., Madden, Pamela A. F., Degenhardt, Louisa, Martin, Nicholas G. and Montgomery, Grant W. (2013). ANKK1, TTC12, and NCAM1 polymorphisms and heroin dependence: importance of considering drug exposure. JAMA Psychiatry, 70 (3), 325-333. doi: 10.1001/jamapsychiatry.2013.282

  • Do early experiences with cannabis vary in cigarette smokers?

    Agrawal, Arpana, Madden, Pamela A. F., Martin, Nicholas G. and Lynskey, Michael T. (2013). Do early experiences with cannabis vary in cigarette smokers?. Drug and Alcohol Dependence, 128 (3), 255-259. doi: 10.1016/j.drugalcdep.2012.09.002

  • Examining the association of NRXN3 SNPs with borderline personality disorder phenotypes in heroin dependent cases and socio-economically disadvantaged controls

    Panagopoulos, Vassilis N., Trull, Timothy J., Glowinski, Anne L., Lynskey, Michael T., Heath, Andrew C., Agrawal, Arpana, Henders, Anjali K., Wallace, Leanne, Todorov, Alexandre A., Madden, Pamela A. F., Moore, Elizabeth, Degenhardt, Louisa, Martin, Nicholas G., Montgomery, Grant W. and Nelson, Elliot C. (2013). Examining the association of NRXN3 SNPs with borderline personality disorder phenotypes in heroin dependent cases and socio-economically disadvantaged controls. Drug and Alcohol Dependence, 128 (3), 187-193. doi: 10.1016/j.drugalcdep.2012.11.011

  • A study of changes in genetic and environmental influences on weight and shape concern across adolescence

    Wade, Tracey D., Hansell, Narelle K., Crosby, Ross D., Bryant-Waugh, Rachel, Treasure, Janet, Nixon, Reginald, Byrne, Susan and Martin, Nicholas G. (2013). A study of changes in genetic and environmental influences on weight and shape concern across adolescence. Journal of Abnormal Psychology, 122 (1), 119-130. doi: 10.1037/a0030290

  • Genetic overlap between personality and risk for disordered gambling: evidence from a national community-based Australian twin study

    Slutske, Wendy S., Cho, Seung Bin, Piasecki, Thomas M. and Martin, Nicholas G. (2013). Genetic overlap between personality and risk for disordered gambling: evidence from a national community-based Australian twin study. Journal of Abnormal Psychology, 122 (1), 250-255. doi: 10.1037/a0029999

  • Genome-wide association analyses identify 18 new loci associated with serum urate concentrations

    Koettgen, Anna, Albrecht, Eva, Teumer, Alexander, Vitart, Veronique, Krumsiek, Jan, Hundertmark, Claudia, Pistis, Giorgio, Ruggiero, Daniela, O'Seaghdha, Conall M., Haller, Toomas, Yang, Qiong, Tanaka, Toshiko, Johnson, Andrew D., Kutalik, Zoltan, Smith, Albert V., Shi, Julia, Struchalin, Maksim, Middelberg, Rita P. S., Brown, Morris J., Gaffo, Angelo L., Pirastu, Nicola, Li, Guo, Hayward, Caroline, Zemunik, Tatijana, Huffman, Jennifer, Yengo, Loic, Zhao, Jing Hua, Demirkan, Ayse, Feitosa, Mary F. ... Gieger, Christian (2013). Genome-wide association analyses identify 18 new loci associated with serum urate concentrations. Nature Genetics, 45 (2), 145-154. doi: 10.1038/ng.2500

  • Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus

    Lu, Yi, Vitart, Veronique, Burdon, Kathryn P., Khor, Chiea Chuen, Bykhovskaya, Yelena, Mirshahi, Alireza, Hewitt, Alex W., Koehn, Demelza, Hysi, Pirro G., Ramdas, Wishal D., Zeller, Tanja, Vithana, Eranga N., Cornes, Belinda K., Tay, Wan-Ting, Tai, E. Shyong, Cheng, Ching-Yu, Liu, Jianjun, Foo, Jia-Nee, Saw, Seang Mei, Thorleifsson, Gudmar, Stefansson, Kari, Dimasi, David P., Mills, Richard A., Mountain, Jenny, Ang, Wei, Hoehn, Rene, Verhoeven, Virginie J. M., Grus, Franz, Wolfs, Roger ... Wong, Tien Y. (2013). Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus. Nature Genetics, 45 (2), 155-163. doi: 10.1038/ng.2506

  • Topography of age-related changes in sleep spindles

    Martin, Nicolas, Lafortune, Marjolaine, Godbout, Jonathan, Barakat, Marc, Robillard, Rebecca, Poirier, Gaetan, Bastien, Celyne and Carrier, Julie (2013). Topography of age-related changes in sleep spindles. Neurobiology of Aging, 34 (2), 468-476. doi: 10.1016/j.neurobiolaging.2012.05.020

  • Why are criminals less educated than non-criminals? Evidence from a cohort of young Australian twins

    Webbink, Dinand, Koning, Pierre, Vujić, Sunčica and Martin, Nicholas G. (2013). Why are criminals less educated than non-criminals? Evidence from a cohort of young Australian twins. Journal of Law Economics & Organization, 29 (1), 115-144. doi: 10.1093/jleo/ews014

  • A genome-wide association study for reading and language abilities in two population cohorts

    Luciano, M., Evans, D. M., Hansell, N. K., Medland, S. E., Montgomery, G. W., Martin, N. G., Wright, M. J. and Bates, T. C. (2013). A genome-wide association study for reading and language abilities in two population cohorts. Genes, Brain and Behavior, 12 (6), 645-652. doi: 10.1111/gbb.12053

  • A variant in FTO shows association with melanoma risk not due to BMI

    Iles M.M., Law M.H., Stacey S.N., Han J., Fang S., Pfeiffer R., Harland M., MacGregor S., Taylor J.C., Aben K.K., Akslen L.A., Avril M.-F., Azizi E., Bakker B., Benediktsdottir K.R., Bergman W., Scarra G.B., Brown K.M., Calista D., Chaudru V., Fargnoli M.C., Cust A.E., Demenais F., De Waal A.C., Debniak T., Elder D.E., Friedman E., Galan P., Ghiorzo P. ... Barrett J.H. (2013). A variant in FTO shows association with melanoma risk not due to BMI. Nature Genetics, 45 (4), 428-432. doi: 10.1038/ng.2571

  • Efficacy and safety of deferasirox at low and high iron burdens: results from the EPIC magnetic resonance imaging substudy

    Porter, J. B., Elalfy, M. S., Taher, A. T., Aydinok, Y., Chan, L. L., Lee, S. H., Sutcharitchan, P., Habr, D., Martin, N. and El-Beshlawy, A. (2013). Efficacy and safety of deferasirox at low and high iron burdens: results from the EPIC magnetic resonance imaging substudy. Annals of Hematology, 92 (2), 211-219. doi: 10.1007/s00277-012-1588-x

  • Genetic and nongenetic variation revealed for the principal components of human gene expression

    Goldinger, Anita, Henders, Anjali K., McRae, Allan F., Martin, Nicholas G., Gibson, Greg, Montgomery, Grant W., Visscher, Peter M. and Powell, Joseph E. (2013). Genetic and nongenetic variation revealed for the principal components of human gene expression. Genetics, 195 (3), 1117-1128. doi: 10.1534/genetics.113.153221

  • Genome-wide association identifies genetic variants associated with lentiform nucleus volume in N = 1345 young and elderly subjects

    Hibar, Derrek P., Stein, Jason L., Ryles, April B., Kohannim, Omid, Jahanshad, Neda, Medland, Sarah E., Hansell, Narelle K., McMahon, Katie L., de Zubicaray, Greig I., Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J., Saykin, Andrew J., Jack, lifford R., Weiner, Michael W., Toga, Arthur W. and Thompson, Paul M. (2013). Genome-wide association identifies genetic variants associated with lentiform nucleus volume in N = 1345 young and elderly subjects. Brain Imaging and Behavior, 7 (2), 102-115. doi: 10.1007/s11682-012-9199-7

  • Genome-wide association studies identify four ER negative-specific breast cancer risk loci

    Garcia-Closas M., Couch F.J., Lindstrom S., Michailidou K., Schmidt M.K., Brook M.N., Orr N., Rhie S.K., Riboli E., Feigelson H.S., Le Marchand L., Buring J.E., Eccles D., Miron P., Fasching P.A., Brauch H., Chang-Claude J., Carpenter J., Godwin A.K., Nevanlinna H., Giles G.G., Cox A., Hopper J.L., Bolla M.K., Wang Q., Dennis J., Dicks E., Howat W.J., Schoof N. ... Kraft P. (2013). Genome-wide association studies identify four ER negative-specific breast cancer risk loci. Nature Genetics, 45 (4), 392-398. doi: 10.1038/ng.2561

  • Genome-wide association study of inattention and hyperactivity-impulsivity measured as quantitative traits

    Ebejer, Jane L., Duffy, David L., van der Werf, Julius, Wright, Margaret J., Montgomery, Grant, Gillespie, Nathan A., Hickie, Ian B., Martin, Nicholas G. and Medland, Sarah E. (2013). Genome-wide association study of inattention and hyperactivity-impulsivity measured as quantitative traits. Twin Research and Human Genetics, 16 (2), 560-574. doi: 10.1017/thg.2013.12

  • Genome-wide meta-analysis identifies new susceptibility loci for migraine

    Anttila, Verneri, Winsvold, Bendik S., Gormley, Padhraig, Kurth, tobias, Bettella, Francesco, McMahon, george, Kallela, mikko, Malik, Rainer, De Vries, Boukje, Terwindt, Gisela, Medland, Sarah E., Todt, Unda, McArdle, Wendy L., Quaye, Lydia, Koiranen, Markku, Ikram, M. Arfan, Lehtimaki, Terho, Stam, Anine H., Ligthart, Lannie, Wedenoja, Juho, Dunham, Ian, Neale, Benjamin M., Palta, Priit, Hamalainen, Eija, Schurks, Markus, Rose, Lynda M., Buring, Julie E., Ridker, Paul M., Steinberg, Stacy ... Palotie, Aarno (2013). Genome-wide meta-analysis identifies new susceptibility loci for migraine. Nature Genetics, 45 (8), 912-917. doi: 10.1038/ng.2676

  • Identification of seven loci affecting mean telomere length and their association with disease

    Codd, Veryan, Nelson, Christopher P., Albrecht, Eva, Mangino, Massimo, Deelen, Joris, Buxton, Jessica L., Hottenga, Jouke Jan, Fischer, Krista, Esko, Tonu, Surakka, Ida, Broer, Linda, Nyholt, Dale R., Leach, Irene Mateo, Salo, Perttu, Hagg, Sara, Matthews, Mary K., Palmen, Jutta, Norata, Giuseppe D., O'Reilly, Paul F., Saleheen, Danish, Amin, Najaf, Balmforth, Anthony J., Beekman, Marian, de Boer, Rudolf A., Bohringer, Stefan, Braund, Peter S., Burton, Paul R., de Craen, Anton J. M., Denniff, Matthew ... Samani, Nilesh J. (2013). Identification of seven loci affecting mean telomere length and their association with disease. Nature Genetics, 45 (4), 422-427. doi: 10.1038/ng.2528

  • Meta-analysis of telomere length in 19 713 subjects reveals high heritability, stronger maternal inheritance and a paternal age effect

    Broer, Linda, Codd, Veryan, Nyholt, Dale R., Deelen, Joris, Mangino, Massimo, Willemsen, Gonneke, Albrecht, Eva, Amin, Najaf, Beekman, Marian, de Geus, Eco J. C., Henders, Anjali, Nelson, Christopher P., Steves, Claire J., Wright, Margie J., de Craen, Anton J. M., Isaacs, Aaron, Matthews, Mary, Moayyeri, Alireza, Montgomery, Grant W., Oostra, Ben A., Vink, Jacqueline M., Spector, Tim D., Slagboom, P. Eline, Martin, Nicholas G., Samani, Nilesh J., van Duijn, Cornelia M. and Boomsma, Dorret I. (2013). Meta-analysis of telomere length in 19 713 subjects reveals high heritability, stronger maternal inheritance and a paternal age effect. European Journal of Human Genetics, 21 (10), 1163-1168. doi: 10.1038/ejhg.2012.303

  • Mining the Human Phenome Using Allelic Scores That Index Biological Intermediates

    Evans, David M., Brion, Marie Jo A., Paternoster, Lavinia, Kemp, John P., McMahon, George, Munafo, Marcus, Whitfield, John B., Medland, Sarah E., Montgomery, Grant W., The GIANT consortium, The CRP consortium, The TAG Consortium, Timpson, Nicholas J., St. Pourcain, Beate, Lawlor, Debbie A., Martin, Nicholas G., Dehghan, Abbas, Hirschhorn, Joel and Davey Smith, George (2013). Mining the Human Phenome Using Allelic Scores That Index Biological Intermediates. PLoS Genetics, 9 (10) e1003919, e1003919.1-e1003919.15. doi: 10.1371/journal.pgen.1003919

  • Multi-site genetic analysis of diffusion images and voxelwise heritability analysis: a pilot project of the ENIGMA–DTI working group

    Jahanshad, Neda, Kochunov, Peter V., Sprooten, Emma, Mandl, René C., Nichols, Thomas E., Almassy, Laura, Blangero, John, Brouwer, Rachel M., Curran, Joanne E., de Zubicaray, Greig I., Duggirala, Ravi, Fox, Peter T., Hong, L. Elliot, Landman, Bennett A., Martin, Nicholas G., McMahon, Katie L., Medland, Sarah E., Mitchell, Braxton D., Olvera, Rene L., Peterson, Charles P., Starr, John M., Sussmann, Jessika E., Toga, Arthur W., Wardlaw, Joanna M., Wright, Margaret J., Hulshoff Pol, Hilleke E., Bastind, Mark E., McIntosh, Andrew M., Deary, Ian J. ... Glahn, David C. (2013). Multi-site genetic analysis of diffusion images and voxelwise heritability analysis: a pilot project of the ENIGMA–DTI working group. NeuroImage, 81, 455-469. doi: 10.1016/j.neuroimage.2013.04.061

  • Refining genome-wide linkage intervals using a meta-analysis of genome-wide association studies identifies loci influencing personality dimensions

    Amin, Najaf, Hottenga, Jouke-Jan, Hansell, Narelle K., Janssens, A. Cecile J. W., de Moor, Marleen H. M., Madden, Pamela A. F., Zorkoltseva, Irina V., Penninx, Brenda W., Terracciano, Antonio, Uda, Manuela, Tanaka, Toshiko, Esko, Tonu, Realo, Anu, Ferrucci, Luigi, Luciano, Michelle, Davies, Gail, Metspalu, Andres, Abecasis, Goncalo R., Deary, Ian J., Raikkonen, Katri, Bierut, Laura J., Costa, Paul T., Saviouk, Viatcheslav, Zhu, Gu, Kirichenko, Anatoly V., Isaacs, Aaron, Aulchenko, Yurii S., Willemsen, Gonneke, Heath, Andrew C. ... van Duijn, Cornelia M. (2013). Refining genome-wide linkage intervals using a meta-analysis of genome-wide association studies identifies loci influencing personality dimensions. European Journal of Human Genetics, 21 (8), 876-882. doi: 10.1038/ejhg.2012.263

  • The Brisbane Longitudinal Twin Study: pathways to cannabis use, abuse, and dependence project - current status, preliminary results, and future directions

    Gillespie, Nathan A., Henders, Anjali K., Davenport, Tracy A., Hermens, Daniel F., Wright, Margie J., Martin, Nicholas G. and Hickie, Ian B. (2013). The Brisbane Longitudinal Twin Study: pathways to cannabis use, abuse, and dependence project - current status, preliminary results, and future directions. Twin Research and Human Genetics, 16 (1), 21-33. doi: 10.1017/thg.2012.111

  • A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11

    Siddiq, Afshan, Couch, Fergus J., Chen, Gary K., Lindstrom, Sara, Eccles, Diana, Millikan, Robert C., Michailidou, Kyriaki, Stram, Daniel O., Beckmann, Lars, Rhie, Suhn Kyong, Ambrosone, Christine B., Aittomaki, Kristiina, Amiano, Pilar, Apicella, Carmel, Baglietto, Laura, Bandera, Elisa V., Beckmann, Matthias W., Berg, Christine D., Bernstein, Leslie, Blomqvist, Carl, Brauch, Hiltrud, Brinton, Louise, Bui, Quang M., Buring, Julie E., Buys, Saundra S., Campa, Daniele, Carpenter, Jane E., Chasman, Daniel I., Chang-Claude, Jenny ... Vachon, Celine M. (2012). A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11. Human Molecular Genetics, 21 (24), 5373-5384. doi: 10.1093/hmg/dds381

  • Pathway analysis of smoking quantity in multiple GWAS identifies cholinergic and sensory pathways

    Harari, Oscar, Wang, Jen-Chyong, Bucholz, Kathleen, Edenberg, Howard J., Heath, Andrew, Martin, Nicholas G., Pergadia, Michele L., Montgomery, Grant, Schrage, Andrew, Bierut, Laura J., Madden, Pamela F. and Goate, Alison M. (2012). Pathway analysis of smoking quantity in multiple GWAS identifies cholinergic and sensory pathways. Plos One, 7 (12) e50913, e50913. doi: 10.1371/journal.pone.0050913

  • Association between in vivo alcohol metabolism and genetic variation in pathways that metabolize the carbon skeleton of ethanol and NADH reoxidation in the Alcohol Challenge Twin Study

    Lind, Penelope A., Macgregor, Stuart, Heath, Andrew C., Madden, Pamela A. F., Montgomery, Grant W., Martin, Nicholas G. and Whitfield, John B. (2012). Association between in vivo alcohol metabolism and genetic variation in pathways that metabolize the carbon skeleton of ethanol and NADH reoxidation in the Alcohol Challenge Twin Study. Alcoholism: Clinical and Experimental Research, 36 (12), 2074-2085. doi: 10.1111/j.1530-0277.2012.01829.x

  • Genome-wide association meta-analysis identifies new endometriosis risk loci

    Nyholt, Dale R., Low, Siew-Kee, Anderson, Carl A., Painter, Jodie N., Uno, Satoko, Morris, Andrew P., MacGregor, Stuart, Gordon, Scott D., Henders, Anjali K., Martin, Nicholas G., Attia, John, Holliday, Elizabeth G., McEvoy, Mark, Scott, Rodney J., Kennedy, Stephen H., Treloar, Susan A., Missmer, Stacey A., Adachi, Sosuke, Tanaka, Kenichi, Nakamura, Yusuke, Zondervan, Krina T., Zembutsu, Hitoshi and Montgomery, Grant W. (2012). Genome-wide association meta-analysis identifies new endometriosis risk loci. Nature Genetics, 44 (12), 1355-1359. doi: 10.1038/ng.2445

  • Liberal neutrality and charitable purposes

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  • Meta-analysis and brain imaging data support the involvement of VRK2 (rs2312147) in schizophrenia susceptibility

    Li, Ming, Wang, Yi, Zheng, Xue-bin, Ikeda, Masashi, Iwata, Nakao, Luo, Xiong-jian, Chong, Siow-Ann, Lee, Jimmy, Rietschel, Marcella, Zhang, Fengyu, Mueller-Myhsok, Bertram, Cichon, Sven, Weinberger, Daniel R., Mattheisen, Manuel, Schulze, Thomas G., Martin, Nicholas G., Mitchell, Philip B., Schofield, Peter R., Liu, Jian-jun and Su, Bing (2012). Meta-analysis and brain imaging data support the involvement of VRK2 (rs2312147) in schizophrenia susceptibility. Schizophrenia Research, 142 (1-3), 200-205. doi: 10.1016/j.schres.2012.10.008

  • Modeling the direction of causation between cross-sectional measures of disrupted sleep, anxiety and depression in a sample of male and female Australian twins

    Gillespie, Nathan A., Gehrman, Philip, Byrne, Enda M., Kendler, Kenneth S., Heath, Andrew C. and Martin, Nicholas G. (2012). Modeling the direction of causation between cross-sectional measures of disrupted sleep, anxiety and depression in a sample of male and female Australian twins. Journal of Sleep Research, 21 (6), 675-683. doi: 10.1111/j.1365-2869.2012.01026.x

  • Offspring ADHD as a risk factor for parental marital problems: controls for genetic and environmental confounds

    Schermerhorn, Alice C., D'Onofrio, Brian M., Slutske, Wendy S., Emery, Robert E., Turkheimer, Eric, Harden, K. Paige, Heath, Andrew C. and Martin, Nicholas G. (2012). Offspring ADHD as a risk factor for parental marital problems: controls for genetic and environmental confounds. Twin Research and Human Genetics, 15 (6), 700-713. doi: 10.1017/thg.2012.55

  • Seventy-five genetic loci influencing the human red blood cell

    van der Harst, Pim, Zhang, Weihua, Leach, Irene Mateo, Rendon, Augusto, Verweij, Niek, Sehmi, Joban, Paul, Dirk S., Elling, Ulrich, Allayee, Hooman, Li, Xinzhong, Radhakrishnan, Aparna, Tan, Sian-Tsung, Voss, Katrin, Weichenberger, Christian X., Albers, Cornelis A., Al-Hussani, Abtehale, Asselbergs, Folkert W., Ciullo, Marina, Danjou, Fabrice, Dina, Christian, Esko, Tonu, Evans, David M., Franke, Lude, Goegele, Martin, Hartiala, Jaana, Hersch, Micha, Holm, Hilma, Hottenga, Jouke-Jan, Kanoni, Stavroula ... Chambers, John C. (2012). Seventy-five genetic loci influencing the human red blood cell. Nature, 492 (7429), 369-375. doi: 10.1038/nature11677

  • Neuropeptide Y (NPY): Genetic Variation in the Human Promoter Alters Glucocorticoid Signaling, Yielding Increased NPY Secretion and Stress Responses (vol 60, pg 1678, 2012)

    Zhang, K., Rao, F., Miramontes-Gonzalez, J. P., Hightower, C. M., Vaught, B., Chen, Y., Greenwood, T. A., Schork, A. J., Wang, L., Mahata, M., Stridsberg, M., Khandrika, S., Biswas, N., Fung, M. M., Waalen, J., Middelberg, R. P., Heath, A. C., Montgomery, G. W., Martin, N. G., Whitfield, J. B., Baker, D. G., Schork, N. J., Nievergelt, C. M. and O'Connor, D. T. (2012). Neuropeptide Y (NPY): Genetic Variation in the Human Promoter Alters Glucocorticoid Signaling, Yielding Increased NPY Secretion and Stress Responses (vol 60, pg 1678, 2012). Journal of the American College of Cardiology, 60 (21), 2261-2261. doi: 10.1016/j.jacc.2012.10.002

  • Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci

    Asselbergs, Folkert W., Guo, Yiran, van Iperen, Erik P. A., Sivapalaratnam, Suthesh, Tragante, Vinicius, Lanktree, Matthew B., Lange, Leslie A., Almoguera, Berta, Appelman, Yolande E., Barnard, John, Baumert, Jens, Beitelshees, Amber L., Bhangale, Tushar R., Chen, Yii-Der Ida, Gaunt, Tom R., Gong, Yan, Hopewell, Jemma C., Johnson, Toby, Kleber, Marcus E., Langaee, Taimour Y., Li, Mingyao, Li, Yun R., Liu, Kiang, McDonough, Caitrin W., Meijs, Matthijs El., Middelberg, Rita P. S., Musunuru, Kiran, Nelson, Christopher P., O'Connell, Jeffery R. ... Drenos, Fotios (2012). Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. American Journal of Human Genetics, 91 (5), 823-838. doi: 10.1016/j.ajhg.2012.08.032

  • Environmental influences predominate in remission from alcohol use disorder in young adult twins

    McCutcheon, V. V., Grant, J. D., Heath, A. C., Bucholz, K. K., Sartor, C. E., Nelson, E. C., Madden, P. A. F. and Martin, N. G. (2012). Environmental influences predominate in remission from alcohol use disorder in young adult twins. Psychological Medicine, 42 (11), 2421-2431. doi: 10.1017/S003329171200044X

  • Erratum: The genetics of addiction - a translational perspective (Translational Psychiatry (2012) 2 (e140) DOI: 10.1038/tp.2012.54)

    Agrawal, A., Verweij, K. J. H., Gillespie, N. A., Heath, A. C., Lessov-Schlaggar, C. N., Martin, N. G., Nelson, E. C., Slutske, W. S., Whitfield, J. B. and Lynskey, M. T. (2012). Erratum: The genetics of addiction - a translational perspective (Translational Psychiatry (2012) 2 (e140) DOI: 10.1038/tp.2012.54). Translational Psychiatry, 2 (11) e193, e193-e193. doi: 10.1038/tp.2012.129

  • Genetic and environmental transmission of body mass index fluctuation

    Bergin, Jocilyn E., Neale, Michael C., Eaves, Lindon J., Martin, Nicholas G., Heath, Andrew C. and Maes, Hermine H. (2012). Genetic and environmental transmission of body mass index fluctuation. Behavior Genetics, 42 (6), 867-874. doi: 10.1007/s10519-012-9567-5

  • Genome-wide meta-analysis of common variant differences between men and women

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  • Multi-locus genome-wide association analysis supports the role of glutamatergic synaptic transmission in the etiology of major depressive disorder

    Lee, P. H., Perlis, R. H., Jung, J-Y, Byrne, E. M., Rueckert, E., Siburian, R., Haddad, S., Mayerfeld, C. E., Heath, A. C., Pergadia, M. L., Madden, P. A. F., Boomsma, D. I., Penninx, B. W., Sklar, P., Martin, N. G., Wray, N. R., Purcell, S. M. and Smoller, J. W. (2012). Multi-locus genome-wide association analysis supports the role of glutamatergic synaptic transmission in the etiology of major depressive disorder. Translational Psychiatry, 2 (11) e184, e184.1-e184.9. doi: 10.1038/tp.2012.95

  • The genetics of addiction - a translational perspective

    Agrawal, A., Verweij, K. J. H., Gillespie, N. A., Heath, A. C., Lessov-Schlaggar, C. N., Martin, N. G., Nelson, E. C., Slutske, W. S., Whitfield, J. B. and Lynskey, M. T. (2012). The genetics of addiction - a translational perspective. Translational Psychiatry, 2 e140. doi: 10.1038/tp.2012.54

  • Neuropeptide Y (NPY): genetic variation in the human promoter alters glucocorticoid signaling, yielding increased NPY secretion and stress responses

    Zhang, Kuixing, Rao, Fangwen, Miramontes-Gonzalez, Jose Pablo, Hightower, C. Makena, Vaught, Brian, Chen, Yuhong, Greenwood, Tiffany A., Schork, Andrew J., Wang, Lei, Mahata, Manjula, Stridsberg, Mats, Khandrika, Srikrishna, Biswas, Nilima, Fung, Maple M., Waalen, Jill, Middelberg, Rita P., Heath, Andrew C., Montgomery, Grant W., Martin, Nicholas G., Whitfield, John B., Baker, Dewleen G., Schork, Nicholas J., Nievergelt, Caroline M. and O'Connor, Daniel T. (2012). Neuropeptide Y (NPY): genetic variation in the human promoter alters glucocorticoid signaling, yielding increased NPY secretion and stress responses. Journal of the American College of Cardiology, 60 (17), 1678-1689. doi: 10.1016/j.jacc.2012.06.042

  • Attention deficit hyperactivity disorder in Australian adults: prevalence, persistence, conduct problems and disadvantage

    Ebejer, Jane L., Medland, Sarah E., van der Werf, Julius, Gondro, Cedric, Henders, Anjali K., Lynskey, Michael, Martin, Nicholas G. and Duffy, David L. (2012). Attention deficit hyperactivity disorder in Australian adults: prevalence, persistence, conduct problems and disadvantage. Plos One, 7 (10) e47404, e47404. doi: 10.1371/journal.pone.0047404

  • Genome-wide linkage and association analyses implicate FASN in predisposition to uterine leiomyomata

    Eggert, Stacey L., Huyck, Karen L., Somasundaram, Priya, Kavalla, Raghava, Stewart, Elizabeth A., Lu, Ake T., Painter, Jodie N., Montgomery, Grant W., Medland, Sarah E., Nyholt, Dale R., Treloar, Susan A., Zondervan, Krina T., Heath, Andrew C., Madden, Pamela A. F., Rose, Lynda, Buring, Julie E., Ridker, Paul M., Chasman, Daniel I., Martin, Nicholas G., Cantor, Rita M. and Morton, Cynthia C. (2012). Genome-wide linkage and association analyses implicate FASN in predisposition to uterine leiomyomata. American Journal of Human Genetics, 91 (4), 621-628. doi: 10.1016/j.ajhg.2012.08.009

  • A behavioral genetic study of humor styles in an Australian sample

    Baughman, H. M., Giammarco, E. A., Veselka, Livia, Schermer, Julie A., Martin, Nicholas G., Lynskey, Michael and Vernon, Phillip A. (2012). A behavioral genetic study of humor styles in an Australian sample. win Research and Human Genetics, 15 (5), 663-667. doi: 10.1017/thg.2012.23

  • A genome-wide association study of monozygotic twin-pairs suggests a locus related to variability of serum high-density lipoprotein cholesterol

    Surakka, Ida, Whitfield, John B., Perola, Markus, Visscher, Peter M., Montgomery, Grant W., Falchi, Mario, Willemsen, Gonneke, de Geus, Eco J. C., Magnusson, Patrik K. E., Christensen, Kaare, Sorensen, Thorild I. A., Pietilainen, Kirsi H., Rantanen, Taina, Silander, Kaisa, Widen, Elisabeth, Muilu, Juhu, Rahman, Iffat, Liljedahl, Ulrika, Syvanen, Ann-Christine, Palotie, Aarno, Kaprio, Jaakko, Kyvik, Kirsten O., Pedersen, Nancy L., Boomsma, Dorret I., Spector, Tim, Martin, Nicolas G., Ripatti, Samuli and Peltonen, Leena (2012). A genome-wide association study of monozygotic twin-pairs suggests a locus related to variability of serum high-density lipoprotein cholesterol. Twin Research and Human Genetics, 15 (6), 691-699. doi: 10.1017/thg.2012.63

  • An Australian twin study of cannabis and other illicit drug use and misuse, and other psychopathology

    Lynskey, Michael T., Agrawal, Arpana, Henders, Anjali, Nelson, Elliot C., Madden, Pamela A. F. and Martin, Nicholas G. (2012). An Australian twin study of cannabis and other illicit drug use and misuse, and other psychopathology. Twin Research and Human Genetics, 15 (5), 631-641. doi: 10.1017/thg.2012.41

  • Genetic variants near PDGFRA are associated with corneal curvature in Australians

    Mishra, Aniket, Yazar, Seyhan, Hewitt, Alex W., Mountain, Jenny A., Ang, Wei, Pennell, Craig E., Martin, Nicholas G., Montgomery, Grant W., Hammond, Christopher J., Young, Terri L., Macgregor, Stuart and Mackey, David A. (2012). Genetic variants near PDGFRA are associated with corneal curvature in Australians. Investigative Ophthalmology and Visual Science, 53 (11), 7131-7136. doi: 10.1167/iovs.12-10489

  • Heritability of strabismus: genetic influence is specific to eso-deviation and independent of refractive error

    Sanfilippo, Paul G., Hammond, Christopher J., Staffieri, Sandra E., Kearns, Lisa S., Liew, S. H. Melissa, Barbour, Julie M., Hewitt, Alex W., Ge, Dongliang, Snieder, Harold, MacKinnon, Jane R., Brown, Shayne A., Lorenz, Birgit, Spector, Tim D., Martin, Nicholas G., Wilmer, Jeremy B. and Mackeymo, David A. (2012). Heritability of strabismus: genetic influence is specific to eso-deviation and independent of refractive error. Twin Research and Human Genetics, 15 (5), 624-630. doi: 10.1017/thg.2012.22

  • Maintenance of genetic variation in human personality: testing evolutionary models by estimating heritability due to common causal variants and investigating the effect of distant inbreeding

    Verweij, Karin J. H., Yang, Jian, Lahti, Jari, Veijola, Juha, Hintsanen, Mirka, Pulkki-Raback, Laura, Heinonen, Kati, Pouta, Anneli, Pesonen, Anu-Katriina, Widen, Elisabeth, Taanila, Anja, Isohanni, Matti, Miettunen, Jouko, Palotie, Aarno, Penke, Lars, Service, Susan K., Heath, Andrew C., Montgomery, Grant W., Raitakari, Olli, Kahonen, Mika, Viikari, Jorma, Raikkonen, Katri, Eriksson, Johan G., Keltikangas-Jarvinen, Liisa, Lehtimaki, Terho, Martin, Nicholas G., Jarvelin, Marjo-Riitta, Visscher, Peter M., Keller, Matthew C. and Zietsch, Brendan P. (2012). Maintenance of genetic variation in human personality: testing evolutionary models by estimating heritability due to common causal variants and investigating the effect of distant inbreeding. Evolution, 66 (10), 3238-3251. doi: 10.1111/j.1558-5646.2012.01679.x

  • Unraveling the genetic etiology of adult antisocial behavior: a genome-wide association study

    Tielbeek, Jorim J., Medland, Sarah E., Benyamin, Beben, Byrne, Enda M., Heath, Andrew C., Madden, Pamela A. F., Martin, Nicholas G., Wray, Naomi R. and Verweij, Karin J. H. (2012). Unraveling the genetic etiology of adult antisocial behavior: a genome-wide association study. PLoS One, 7 (10) e45086, e1005378-e1005378. doi: 10.1371/journal.pone.0045086

  • FTO genotype is associated with phenotypic variability of body mass index

    Yang, Jian, Loos, Ruth J., Powell, Joseph E., Medland, Sarah E, Speliotes, Elizabeth K., Chasman, Daniel I., Rose, Lynda M., Thorleifsson, Gudmar, Steinthorsdottir, Valgerdur, Magi, Reedik, Waite, Lindsay, Vernon Smith, Albert, Yerges-Armstrong, Laura M., Monda, Keri L., Hadley, David, Mahajan, Anubha, Li, Guo, Kapur, Karen, Vitart, Veronique, Huffman, Jennifer E., Wang, Sophie R., Palmer, Cameron, Esko, To˜nu, Fischer, Krista, Hua Zhao, Jing, Demirkan, Ayse, Isaacs, Aaron, Feitosa, Mary F., Luan, Jian’an ... Visscher, Peter (2012). FTO genotype is associated with phenotypic variability of body mass index. Nature, 490 (7419), 267-272. doi: 10.1038/nature11401

  • A Genome-Wide Association Study Identifies Five Loci Influencing Facial Morphology in Europeans

    Liu, Fan, van der Lijn, Fedde, Schurmann, Claudia, Zhu, Gu, Chakravarty, M. Mallar, Hysi, Pirro G., Wollstein, Andreas, Lao, Oscar, de Bruijne, Marleen, Ikram, M. Arfan, van der Lugt, Aad, Rivadeneira, Fernando, Uitterlinden, Andre G., Hofman, Albert, Niessen, Wiro J., Homuth, Georg, de Zubicaray, Greig, McMahon, Katie L., Thompson, Paul M., Daboul, Amro, Puls, Ralf, Hegenscheid, Katrin, Bevan, Liisa, Pausova, Zdenka, Medland, Sarah E., Montgomery, Grant W., Wright, Margaret J., Wicking, Carol A., Boehringer, Stefan ... Kayser, Manfred for the International Visible Trait Genetics (VisiGen) Consortium (2012). A Genome-Wide Association Study Identifies Five Loci Influencing Facial Morphology in Europeans. PLoS Genetics, 8 (9) e1002932, e1002932.1-e1002932.13. doi: 10.1371/journal.pgen.1002932

  • Genetic and environmental influences on analogical and categorical verbal and spatial reasoning in 12-year old twins

    Mosing, Miriam A., Mellanby, Jane, Martin, Nicholas G. and Wright, Margaret J. (2012). Genetic and environmental influences on analogical and categorical verbal and spatial reasoning in 12-year old twins. Behavior Genetics, 42 (5), 722-731. doi: 10.1007/s10519-012-9540-3

  • Genome-Wide Association Studies of Asthma in Population-Based Cohorts Confirm Known and Suggested Loci and Identify an Additional Association near HLA

    Ramasamy, Adaikalavan, Kuokkanen, Mikko, Vedantam, Sailaja, Gajdos, Zofia K., Alves, Alexessander Couto, Lyon, Helen N., Ferreira, Manuel A. R., Strachan, David P., Zhao, Jing Hua, Abramson, Michael J., Brown, Matthew A., Coin, Lachlan, Dharmage, Shyamali C., Duffy, David L., Haahtela, Tari, Heath, Andrew C., Janson, Christer, Kahonen, Mika, Khaw, Kay-Tee, Laitinen, Jaana, Le Souef, Peter, Lehtimaki, Terho, Madden, Pamela A. F., Marks, Guy B., Martin, Nicholas G., Matheson, Melanie C., Palmer, Cameron D., Palotie, Aarno, Pouta, Anneli ... Hirschhorn, Joel N. (2012). Genome-Wide Association Studies of Asthma in Population-Based Cohorts Confirm Known and Suggested Loci and Identify an Additional Association near HLA. PLoS One, 7 (9 Article No. e44008) e44008, e44008-1-e44008-10. doi: 10.1371/journal.pone.0044008

  • Genome-wide association uncovers shared genetic effects among personality traits and mood states

    Luciano, Michelle, Huffman, Jennifer E., Arias-Vasquez, Alejandro, Vinkhuyzen, Anna A. E., Middeldorp, Christel M., Giegling, Ina, Payton, Antony, Davies, Gail, Zgaga, Lina, Janzing, Joost, Ke, Xiayi, Galesloot, Tessel, Hartmann, Annette M., Ollier, William, Tenesa, Albert, Hayward, Caroline, Verhagen, Maaike, Montgomery, Grant W., Hottenga, Jouke-Jan, Konte, Bettina, Starr, John M., Vitart, Veronique, Vos, Pieter E., Madden, Pamela A. F., Willemsen, Gonneke, Konnerth, Heike, Horan, Michael A., Porteous, David J., Campbell, Harry ... Deary, Ian J. (2012). Genome-wide association uncovers shared genetic effects among personality traits and mood states. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 159B (6), 684-695. doi: 10.1002/ajmg.b.32072

  • How a common variant in the growth factor receptor gene, NTRK1, affects white matter

    Braskie, Meredith N., Jahanshad, Neda, Toga, Arthur W., McMahon, Katie L, de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2012). How a common variant in the growth factor receptor gene, NTRK1, affects white matter. BioArchitecture, 2 (5), 1-4. doi: 10.4161/bioa.22190

  • Substantial genetic overlap between schizotypy and neuroticism: a twin study

    Macare, Christine, Bates, Timothy C., Heath, Andrew C., Martin, Nicholas G. and Ettinger, Ulrich (2012). Substantial genetic overlap between schizotypy and neuroticism: a twin study. Behavior Genetics, 42 (5), 732-742. doi: 10.1007/s10519-012-9558-6

  • The continuing value of twin studies in the omics era

    van Dongen, Jenny, Slagboom, P. Eline, Draisma, Harmen H. M., Martin, Nicholas G. and Boomsma, Dorret I. (2012). The continuing value of twin studies in the omics era. Nature Reviews Genetics, 13 (9), 640-653. doi: 10.1038/nrg3243

  • Commentary: discussion of 'The history of twins, as a criterion of the relative powers of nature And nurture' by Francis Galton (1875)

    Martin, Nicholas G. (2012). Commentary: discussion of 'The history of twins, as a criterion of the relative powers of nature And nurture' by Francis Galton (1875). International Journal of Epidemiology, 41 (4) dys110, 917-919. doi: 10.1093/ije/dys110

  • Reduced slow-wave rebound during daytime recovery sleep in middle-aged subjects

    Lafortune, Marjolaine, Gagnon, Jean-Francois, Latreille, Veronique, Vandewalle, Gilles, Martin, Nicolas, Filipini, Daniel, Doyon, Julien and Carrier, Julie (2012). Reduced slow-wave rebound during daytime recovery sleep in middle-aged subjects. Plos One, 7 (8) e43224, e43224. doi: 10.1371/journal.pone.0043224

  • Discovery and replication of gene influences on brain structure using LASSO regression

    Kohannim, Omid, Hibar, Derrek P., Stein, Jason L., Jahanshad, Neda, Hua, Xue, Rajagopalan, Priya, Toga, Arthur W., Jack Jr., Clifford R., Weiner, Michael W., de Zubicaray, Greig I., McMahon, Katie L., Hansell, Narelle K., Martin, Nicholas G., Margaret J. Wright, Thompson, Paul M. and The Alzheimer’s Disease Neuroimaging Initiative (2012). Discovery and replication of gene influences on brain structure using LASSO regression. Frontiers in Neuroscience, 6 (AUG) Article 115, 115.1-115.13. doi: 10.3389/fnins.2012.00115

  • Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers

    Hartz, Sarah M., Short, Susan E., Saccone, Nancy L., Culverhouse, Robert, Chen, LiShiun, Schwantes-An, Tae-Hwi, Coon, Hilary, Han, Younghun, Stephens, Sarah H., Sun, Juzhong, Chen, Xiangning, Ducci, Francesca, Dueker, Nicole, Franceschini, Nora, Frank, Josef, Geller, Frank, Guobjartsson, Daniel, Hansel, Nadia N., Jiang, Chenhui, Keskitalo-Vuokko, Kaisu, Liu, Zhen, Lyytikainen, Leo-Pekka, Michel, Martha, Rawal, Rajesh, Hum, Sc, Rosenberger, Albert, Scheet, Paul, Shaffer, John R., Teumer, Alexander ... Bierut, Laura J. (2012). Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers. Archives of General Psychiatry, 69 (8), 854-861. doi: 10.1001/archgenpsychiatry.2012.124

  • The effect of childhood conduct disorder on human capital

    Webbink, Dinand, Vujić, Sunčica, Koning, Pierre and Martin, Nicholas G. (2012). The effect of childhood conduct disorder on human capital. Health Economics, 21 (8), 928-945. doi: 10.1002/hec.1767

  • The genetic aetiology of cannabis use initiation: a meta-analysis of genome-wide association studies and a SNP-based heritability estimation

    Verweij, Karin J. H., Vinkhuyzen, Anna A. E., Benyamin, Beben, Lynskey, Michael T., Quaye, Lydia, Agrawal, Arpana, Gordon, Scott D., Montgomery, Grant W., Madden, Pamela A. F., Heath, Andrew C., Spector, Andrew C., Martin, Nicholas G. and Medland, Sarah E. (2012). The genetic aetiology of cannabis use initiation: a meta-analysis of genome-wide association studies and a SNP-based heritability estimation. Addiction Biology, 18 (5), 846-850. doi: 10.1111/j.1369-1600.2012.00478.x

  • A genome-wide association study of caffeine-related sleep disturbance: confirmation of a role for a common variant in the adenosine receptor

    Byrne, Enda M., Johnson, Julie, McRae, Allan F., Nyholt, Dale R., Medland, Sarah E., Gehrman, Philip R., Heath, Andrew C., Madden, Pamela A. F., Montgomery, Grant W., Chenevix-Trench, Georgia and Martin, Nicholas G. (2012). A genome-wide association study of caffeine-related sleep disturbance: confirmation of a role for a common variant in the adenosine receptor. Sleep, 35 (7), 967-975. doi: 10.5665/sleep.1962

  • Cannabinoid receptor genotype moderation of the effects of childhood physical abuse on anhedonia and depression

    Agrawal, Arpana, Nelson, Elliot C., Littlefield, Andrew K., Bucholz, Kathleen K., Degenhardt, Louisa, Henders, Anjali K., Madden, Pamela A. F., Martin, Nicholas G., Montgomery, Grant W., Pergadia, Michele L., Sher, Kenneth J., Heath, Andrew C. and Lynskey, Michael T. (2012). Cannabinoid receptor genotype moderation of the effects of childhood physical abuse on anhedonia and depression. Archives of General Psychiatry, 69 (7), 732-740. doi: 10.1001/archgenpsychiatry.2011.2273

  • Evidence of inbreeding depression on human height

    McQuillan, Ruth, Eklund, Niina, Pirastu, Nicola, Kuningas, Maris, McEvoy, Brian P., Esko, Tonu, Corre, Tanguy, Davies, Gail, Kaakinen, Marika, Lyytikainen, Leo-Pekka, Kristiansson, Kati, Havulinna, Aki S., Gogele, Martin, Vitart, Veronique, Tenesa, Albert, Aulchenko, Yurii, Hayward, Caroline, Johansson, Asa, Boban, Mladen, Ulivi, Sheila, Robino, Antonietta, Boraska, Vesna, Igl, Wilmar, Wild, Sarah H., Zgaga, Lina, Amin, Najaf, Theodoratou, Evropi, Polasek, Ozren, Girotto, Giorgia ... Wilson, James F. (2012). Evidence of inbreeding depression on human height. Plos Genetics, 8 (7) e1002655, e1002655. doi: 10.1371/journal.pgen.1002655

  • Genetic influences on four measures of executive functions and their covariation with general cognitive ability: The Older Australian Twins Study

    Lee, Teresa, Mosing, Miriam A., Henry, Julie D., Trollor, Julian N., Ames, David, Martin, Nicholas G., Wright, Margaret J., Sachdev, Perminder S. and OATS Research Team (2012). Genetic influences on four measures of executive functions and their covariation with general cognitive ability: The Older Australian Twins Study. Behavior Genetics, 42 (4), 528-538. doi: 10.1007/s10519-012-9526-1

  • Use of a predictive model derived from in vivo endophenotype measurements to demonstrate associations with a complex locus, CYP2A6

    Bloom, A. Joseph, Harari, Oscar, Martinez, Maribel, Madden, Pamela A. F., Martin, Nicholas G., Montgomery, Grant W., Rice, John P., Murphy, Sharon E., Bierut, Laura J. and Goate, Alison (2012). Use of a predictive model derived from in vivo endophenotype measurements to demonstrate associations with a complex locus, CYP2A6. Human Molecular Genetics, 21 (13) dds114, 3050-3062. doi: 10.1093/hmg/dds114

  • Gene network effects on brain microstructure and intellectual performance identified in 472 twins

    Chiang, Ming-Chang, Barysheva, Marina, McMahon, Katie L., de Zubicaray, Greig I., Johnson, Kori, Montgomery, Grant W., Martin, Nicholas G., Toga, Arthur W., Wright, Margaret J., Shapshak, Paul and Thompson, Paul M. (2012). Gene network effects on brain microstructure and intellectual performance identified in 472 twins. Journal of Neuroscience, 32 (25), 8732-8745. doi: 10.1523/JNEUROSCI.5993-11.2012

  • Alzheimer's disease risk gene, GAB2, is associated with regional brain volume differences in 755 young healthy twins

    Hibar, Derrek P., Jahanshad, Neda, Stein, Jason L., Kohannim, Omid, Toga, Arthur W., Medland, Sarah E., Hansell, Narelle K., McMahon, Katie L., de Zubicaray, Greig I., Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2012). Alzheimer's disease risk gene, GAB2, is associated with regional brain volume differences in 755 young healthy twins. Twin Research and Human Genetics, 15 (3), 286-295. doi: 10.1017/thg.2012.15

  • Six novel susceptibility loci for early-onset androgenetic alopecia and their unexpected association with common diseases

    Li, Rui, Brockschmidt, Felix F., Kiefer, Amy K., Stefansson, Hreinn, Nyholt, Dale R., Song, Kijoung, Vermeulen, Sita H., Kanoni, Stavroula, Glass, Daniel, Medland, Sarah E., Dimitriou, Maria, Waterworth, Dawn, Tung, Joyce Y., Geller, Frank, Heilmann, Stefanie, Hillmer, Axel M., Bataille, Veronique, Eigelshoven, Sibylle, Hanneken, Sandra, Moebus, Susanne, Herold, Christine, den Heijer, Martin, Montgomery, Grant W., Deloukas, Panos, Eriksson, Nicholas, Heath, Andrew C., Becker, Tim, Sulem, Patrick, Mangino, Massimo ... Richards, J. Brent (2012). Six novel susceptibility loci for early-onset androgenetic alopecia and their unexpected association with common diseases. PLoS Genetics, 8 (5) e1002746, 222-224. doi: 10.1371/journal.pgen.1002746

  • Common SNPs explain some of the variation in the personality dimensions of neuroticism and extraversion (vol 2, e125, 2012)

    Vinkhuyzen, A. A. E., Pedersen, N. L., Yang, J., Lee, S. H., Magnusson, P. K. E., Iacono, W. G., McGue, M., Madden, P. A. F., Heath, A. C., Luciano, M., Payton, A., Horan, M., Ollier, W., Pendleton, N., Deary, I. J., Montgomery, G. W., Martin, N. G., Visscher, P. M. and Wray, N. R. (2012). Common SNPs explain some of the variation in the personality dimensions of neuroticism and extraversion (vol 2, e125, 2012). Translational Psychiatry, 2 (5) e125, e125-e125. doi: 10.1038/tp.2012.49

  • A genome-wide meta-analysis of association studies of Cloninger's Temperament Scales

    Service, S. K., Verweij, K. J. H., Lahti, J., Congdon, E., Ekelund, J., Hintsanen, M., Raikkonen, K., Lehtimaki, T., Kahonen, M., Widen, E., Taanila, A., Veijola, J., Heath, A. C., Madden, P. A. F., Montgomery, G. W., Sabatti, C., Jarvelin, M-R, Palotie, A., Raitakari, O., Viikari, J., Martin, N. G., Eriksson, J. G., Keltikangas-Jarvinen, L., Wray, N. R. and Freimer, N. B. (2012). A genome-wide meta-analysis of association studies of Cloninger's Temperament Scales. Translational Psychiatry, 2 (5) e116, e116-e116. doi: 10.1038/tp.2012.37

  • Common variants at 12q14 and 12q24 are associated with hippocampal volume

    Bis, Joshua C., DeCarli, Charles, Smith, Albert Vernon, van der Lijn, Fedde, Crivello, Fabrice, Fornage, Myriam, Debette, Stephanie, Shulman, Joshua M., Schmidt, Helena, Srikanth, Velandai, Schuur, Maaike, Yu, Lei, Choi, Seung-Hoan, Sigurdsson, Sigurdur, Verhaaren, Benjamin F. J., DeStefano, Anita L., Lambert, Jean-Charles, Jack, Clifford R., Struchalin, Maksim, Stankovich, Jim, Ibrahim-Verbaas, Carla A., Fleischman, Debta, Zijdenbos, Alex, den Heijer, Tom, Mazoyer, Bernard, Coker, Laura H., Enzinger, Christian, Danoy, Patrick, Amin, Najaf ... Cohorts Heart Aging Res Genomic Ep (2012). Common variants at 12q14 and 12q24 are associated with hippocampal volume. Nature Genetics, 44 (5), 545-551. doi: 10.1038/ng.2237

  • No association of candidate genes with cannabis use in a large sample of Australian twin families

    Verweij, Karin J. H., Zietsch, Brendan P., Liu, Jimmy Z., Medland, Sarah E., Lynskey, Michael T., Madden, Pamela A. F., Agrawal, Arpana, Montgomery, Grant W., Heath, Andrew C. and Martin, Nicholas G. (2012). No association of candidate genes with cannabis use in a large sample of Australian twin families. Addiction Biology, 17 (3), 687-690. doi: 10.1111/j.1369-1600.2011.00320.x

  • Relationship of a variant in the NTRK1 gene to white matter microstructure in young adults

    Braskie, Meredith N., Jahanshad, Neda, Stein, Jason L., Barysheva, Marina, Johnson, Kori, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J., Ringman, John M., Toga, Arthur W. and Thompson, Paul M. (2012). Relationship of a variant in the NTRK1 gene to white matter microstructure in young adults. The Journal of Neuroscience, 32 (17), 5964-5972. doi: 10.1523/JNEUROSCI.5561-11.2012

  • Evidence of differential allelic effects between adolescents and adults for plasma high-density lipoprotein

    Middelberg, Rita P. S., Heath, Andrew C., Madden, Pamela A. F., Montgomery, Grant W., Martin, Nicholas G. and Whitfield, John B. (2012). Evidence of differential allelic effects between adolescents and adults for plasma high-density lipoprotein. PLoS ONE, 7 (4) e35605, e35605. doi: 10.1371/journal.pone.0035605

  • Meta-analyses of genome-wide linkage scans of anxiety-related phenotypes

    Webb, Bradley T., Guo, An-Yuan, Maher, Brion S., Zhao, Zhongming, van den Oord, Edwin J., Kendler, Kenneth S., Riley, Brien P., Gillespie, Nathan A., Prescott, Carol A., Middeldorp, Christel M., Willemsen, Gonneke, de Geus, Eco J. C., Hottenga, Jouke-Jan, Boomsma, Dorret I., Slagboom, Eline P., Wray, Naomi R., Montgomery, Grant W., Martin, Nicholas G., Wright, Margie J., Heath, Andrew C., Madden, Pamela A., Gelernter, Joel, Knowles, James A., Hamilton, Steven P., Weissman, Myrna M., Fyer, Abby J., Huezo-Diaz, Patricia, McGuffin, Peter, Farmer, Anne ... Hettema, John M. (2012). Meta-analyses of genome-wide linkage scans of anxiety-related phenotypes. European Journal of Human Genetics, 20 (10), 1078-1084. doi: 10.1038/ejhg.2012.47

  • Brain structure in healthy adults is related to serum transferrin and the H63D polymorphism in the HFE gene

    Jahanshad, Neda, Kohannim, Omid, Hibar, Derrek P., Stein, Jason L., McMahon, Katie L., de Zubicaray, Greig I., Medland, Sarah E., Montgomery, Grant W., Whitfield, John B., Martin, Nicholas G., Wright, Margaret J., Toga, Arthur W. and Thompson, Paul M. (2012). Brain structure in healthy adults is related to serum transferrin and the H63D polymorphism in the HFE gene. Proceedings of the National Academy of Sciences of USA, 109 (14), E851-E859. doi: 10.1073/pnas.1105543109

  • Altered structural brain connectivity in healthy carriers of the autism risk gene, CNTNAP2

    Dennis, Emily L., Jahanshad, Neda, Rudie, Jeffrey D., Brown, Jesse A., Johnson, Kori, McMahon, Katie L., de Zubicaray, Greig I., Montgomery, Grant, Martin, Nicholas G., Wright, Margaret J., Bookheimer, Susan Y., Dapretto, Mirella, Toga, Arthur W. and Thompson, Paul M. (2012). Altered structural brain connectivity in healthy carriers of the autism risk gene, CNTNAP2. Brain Connectivity, 1 (6), 447-460. doi: 10.1089/brain.2011.0064

  • Common SNPs explain some of the variation in the personality dimensions of neuroticism and extraversion

    Vinkhuyzen, A. A. E., Pedersen, N. L., Yang, J., Lee, S. H., Magnusson, P. K. E., Iacono, W. G., McGue, M., Madden, P. A. F., Heath, A. C., Luciano, M., Payton, A., Horan, M., Ollier, W., Pendleton, N., Deary, I. J., Montgomery, G. W., Martin, N. G., Visscher, P. M. and Wray, N. R. (2012). Common SNPs explain some of the variation in the personality dimensions of neuroticism and extraversion. Translational Psychiatry, 2 (e102) 201227, e102-e102. doi: 10.1038/tp.2012.27

  • Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits

    Yang, Jian, Ferreira, Teresa, Morris, Andrew P., Medland, Sarah E., Madden, Pamela A. F., Heath, Andrew C., Martin, Nicholas G., Montgomery, Grant W., Weedon, Michael N., Loos, Ruth J., Frayling, Timothy M., McCarthy, Mark I., Hirschhorn, Joel N., Goddard, Michael E., Visscher, Peter M., Genetic Invest ANthropometric Trai and DIAbet Genetics Replication Meta-A (2012). Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits. Nature Genetics, 44 (4), 369-375. doi: 10.1038/ng.2213

  • The Brisbane systems genetics study: genetical genomics meets complex trait genetics

    Powell, Joseph E., Henders, Anjali K., McRae, Allan F., Caracella, Anthony, Smith, Sara, Wright, Margaret J., Whitfield, John B., Dermitzakis, Emmanouil T., Martin, Nicholas G., Visscher, Peter M. and Montgomery, Grant W. (2012). The Brisbane systems genetics study: genetical genomics meets complex trait genetics. PLoS One, 7 (4) e35430, e35430.1-e35430.9. doi: 10.1371/journal.pone.0035430

  • Genetic Influences on Four Measures of Executive Functions and Their Covariation with General Cognitive Ability: The Older Australian Twins Study (vol 42, pg 528, 2012)

    Lee, Teresa, Mosing, Miriam A., Henry, Julie D., Trollor, Julian N., Ames, David, Martin, Nicholas G., Wright, Margaret J. and Sachdev, Perminder S. (2012). Genetic Influences on Four Measures of Executive Functions and Their Covariation with General Cognitive Ability: The Older Australian Twins Study (vol 42, pg 528, 2012). Behavior Genetics, 42 (4), 539-540. doi: 10.1007/s10519-012-9536-z

  • Common heritable contributions to low-risk trauma, high-risk trauma, posttraumatic stress disorder, and major depression

    Sartor, Carolyn E., Grant, Julia D., Lynskey, Michael T., McCutcheon, Vivia V., Waldron, Mary, Statham, Dixie J., Bucholz, Kathleen K., Madden, Pamela A. F., Heath, Andrew C., Martin, Nicholas G. and Nelson, Elliot C. (2012). Common heritable contributions to low-risk trauma, high-risk trauma, posttraumatic stress disorder, and major depression. Archives of General Psychiatry, 69 (3), 293-299. doi: 10.1001/archgenpsychiatry.2011.1385

  • Do shared etiological factors contribute to the relationship between sexual orientation and depression?

    Zietsch, B. P., Verweij, K. J. H., Heath, A. C., Madden, P. A. F., Martin, N. G., Nelson, E. C. and Lynskey, M. T. (2012). Do shared etiological factors contribute to the relationship between sexual orientation and depression?. Psychological Medicine, 42 (3), 521-532. doi: 10.1017/S0033291711001577

  • Genetic control of gene expression in whole blood and lymphoblastoid cell lines is largely independent

    Powell, Joseph E., Henders, Anjali K., McRae, Allan F., Wright, Margaret J., Martin, Nicholas G., Dermitzakis, Emmanouil T., Montgomery, Grant W. and Visscher, Peter M. (2012). Genetic control of gene expression in whole blood and lymphoblastoid cell lines is largely independent. Genome Research, 22 (3), 456-466. doi: 10.1101/gr.126540.111

  • Longevity candidate genes and their association with personality traits in the elderly

    Luciano, Michelle, Lopez, Lorna M., de Moor, Marleen H. M., Harris, Sarah E., Davies, Gail, Nutile, Teresa, Krueger, Robert F., Esko, Tonu, Schlessinger, David, Toshiko, Tanaka, Derringer, Jaime L., Realo, Anu, Hansell, Narelle K., Pergadia, Michele L., Pesonen, Anu-Katriina, Sanna, Serena, Terracciano, Antonio, Madden, Pamela A. F., Penninx, Brenda, Spinhoven, Philip, Hartman, Catherina A., Oostra, Ben A., Janssens, A. Cecile J. W., Eriksson, Johan G., Starr, John M., Cannas, Alessandra, Ferrucci, Luigi, Metspalu, Andres, Wright, Margeret J. ... Deary, Ian J. (2012). Longevity candidate genes and their association with personality traits in the elderly. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 159 B (2), 192-200. doi: 10.1002/ajmg.b.32013

  • The different effects of gender and sex on vote choice

    Hatemi, Peter K., McDermott, Rose, Bailey, J. Michael and Martin, Nicholas G. (2012). The different effects of gender and sex on vote choice. Political Research Quarterly, 65 (1), 76-92. doi: 10.1177/1065912910391475

  • Hierarchical topological network analysis of anatomical human brain connectivity and differences related to sex and kinship

    Duarte-Carvajalino, Julio M., Jahanshad, Neda, Lenglet, Christophe, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J., Thompson, Paul M. and Sapiro, Guillermo (2012). Hierarchical topological network analysis of anatomical human brain connectivity and differences related to sex and kinship. NeuroImage, 59 (4), 3784-3804. doi: 10.1016/j.neuroimage.2011.10.096

  • Refinement of the associations between risk of colorectal cancer and polymorphisms on chromosomes 1q41 and 12q13.13

    Spain, Sarah L., Carvajal-Carmona, Luis G., Howarth, Kimberley M., Jones, Angela M., Su, Zhan, Cazier, Jean-Baptiste, Williams, Jennet, Aaltonen, Lauri A., Pharoah, Paul, Kerr, David J., Cheadle, Jeremy, Li, Li, Casey, Graham, Vodicka, Pavel, Sieber, Oliver, Lipton, Lara, Gibbs, Peter, Martin, Nicholas G., Montgomery, Grant W., Young, Joanne, Baird, Paul N., Morreau, Hans, van Wezel, Tom, Ruiz-Ponte, Clara, Fernandez-Rozadilla, Ceres, Carracedo, Angel, Castells, Antoni, Castellvi-Bel, Sergi, Dunlop, Malcolm ... Tomlinson, Ian P. M. (2012). Refinement of the associations between risk of colorectal cancer and polymorphisms on chromosomes 1q41 and 12q13.13. Human Molecular Genetics, 21 (4) ddr523, 934-946. doi: 10.1093/hmg/ddr523

  • Genetic and environmental contributions to weight, height, and BMI from birth to 19 years of age: An international study of over 12,000 twin pairs

    Dubois, Lise, Kyvik, Kirsten Ohm, Girard, Manon, Tatone-Tokuda, Fabiola, Perusse, Daniel, Hjelmborg, Jacob, Skytthe, Axel, Rasmussen, Finn, Wright, Margaret J., Lichtenstein, Paul and Martin, Nicholas G. (2012). Genetic and environmental contributions to weight, height, and BMI from birth to 19 years of age: An international study of over 12,000 twin pairs. PLoS ONE, 7 (2) e30153, e30153. doi: 10.1371/journal.pone.0030153

  • Meta-analysis combining new and existing data sets confirms that the TERT-CLPTM1L locus influences melanoma risk

    Law, Matthew H., Montgomery, Grant W., Brown, Kevin M., Martin, Nicholas G., Mann, Graham J., Hayward, Nicholas K., MacGregor, Stuart and Q-MEGA and AMFS Investigators (2012). Meta-analysis combining new and existing data sets confirms that the TERT-CLPTM1L locus influences melanoma risk. Journal of Investigative Dermatology, 132 (2), 485-487. doi: 10.1038/jid.2011.322

  • The effects of a single nucleotide polymorphism in SLCO1B1 on the pharmacodynamics of pravastatin

    Martin, Nicholas G., Li, Ka Wah, Murray, Heather, Putt, Wendy, Packard, Chris J. and Humphries, Steve E. (2012). The effects of a single nucleotide polymorphism in SLCO1B1 on the pharmacodynamics of pravastatin. British Journal of Clinical Pharmacology, 73 (2), 303-306. doi: 10.1111/j.1365-2125.2011.04090.x

  • A genome-wide study on the perception of the odorants androstenone and galaxolide

    Knaapila, Antti, Zhu, Gu, Medland, Sarah E., Wysocki, Charles J., Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J. and Reed, Danielle R. (2012). A genome-wide study on the perception of the odorants androstenone and galaxolide. Chemical Senses, 37 (6), 541-552. doi: 10.1093/chemse/bjs008

  • Development of brain structural connectivity between ages 12 and 30: a 4-tesla diffusion imaging study in 439 adolescents and adults

    Dennis, Emily L., Jahanshad, Neda, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Hickie, Ian B., Toga, Arthur W., Wright, Margaret J. and Thompson, Paul M. (2012). Development of brain structural connectivity between ages 12 and 30: a 4-tesla diffusion imaging study in 439 adolescents and adults. NeuroImage, 64 (1), 671-684. doi: 10.1016/j.neuroimage.2012.09.004

  • Genetic co-morbidity between neuroticism, anxiety/depression and somatic distress in a population sample of adolescent and young adult twins

    Hansell, N. K., Wright, M. J., Medland, S. E., Davenprot, T. A., Wray, N. R., Martin, N. G. and Hickie, I. B. (2012). Genetic co-morbidity between neuroticism, anxiety/depression and somatic distress in a population sample of adolescent and young adult twins. Psychological Medicine, 42 (6), 1249-1260. doi: 10.1017/S0033291711002431

  • Genetic influences on five measures of processing speed and their covariation with general cognitive ability in the elderly: The older Australian twins study

    Lee, Teresa, Mosing, Miriam A., Henry, Julie D., Trollor, Julian N., Lammel, Andrea, Ames, David, Martin, Nicholas G., Wright, Margaret J. and Sachdev, Perminder S. (2012). Genetic influences on five measures of processing speed and their covariation with general cognitive ability in the elderly: The older Australian twins study. Behavior Genetics, 42 (1), 96-106. doi: 10.1007/s10519-011-9474-1

  • Genetic influences on life span and its relationship to personality: A 16-year follow-up study of a sample of aging twins

    Mosing, Miriam A., Medland, Sarah E., McRae, Allan, Landers, Joseph George, Wright, Margaret J. and Martin, Nicholas G. (2012). Genetic influences on life span and its relationship to personality: A 16-year follow-up study of a sample of aging twins. Psychosomatic Medicine, 74 (1), 16-22. doi: 10.1097/PSY.0b013e3182385784

  • Genetic variation within a metabolic motif in the chromogranin A promoter: Pleiotropic influence on cardiometabolic risk traits in twins

    Rao, Fangwen, Chiron, Stephane, Wei, Zhiyun, Fung, Maple M., Chen, Yuqing, Wen, Gen, Khandrika, Srikrishna, Ziegler, Michael G., Benyamin, Beben, Montgomery, Grant, Whitfield, John B., Martin, Nicholas G., Waalen, Jill, Hamiltoni, Bruce A., Mahata, Sushil K. and O'Connor, Daniel T. (2012). Genetic variation within a metabolic motif in the chromogranin A promoter: Pleiotropic influence on cardiometabolic risk traits in twins. American Journal of Hypertension, 25 (1), 29-40. doi: 10.1038/ajh.2011.163

  • Genome-wide association study of major depressive disorder: New results, meta-analysis, and lessons learned

    Wray, N. R., Pergadia, M. L., Blackwood, D. H. R., Penninx, B. W. J. H., Gordon, S. D., Nyholt, D. R., Ripke, S., MacIntyre, D. J., McGhee, K. A., MacLean, A. W., Smit, J. H., Hottenga, J. J., Willemsen, G., Middeldorp, C. M., De Geus, E. J. C., Lewis, C. M., McGuffin, P., Hickie, I. B., Van Den Oord, E. J. C. G., Liu, J. Z., MacGregor, S., McEvoy, B. P., Byrne, E. M., Medland, S. E., Statham, D. J., Henders, A. K., Heath, A. C., Montgomery, G. W., Martin, N. G. ... Sullivan, P. F. (2012). Genome-wide association study of major depressive disorder: New results, meta-analysis, and lessons learned. Molecular Psychiatry, 17 (1), 36-48. doi: 10.1038/mp.2010.109

  • Health-related quality of life, treatment satisfaction, adherence and persistence in beta-thalassemia and myelodysplastic syndrome patients with iron overload receiving deferasirox: Results from the EPIC clinical trial

    Porter, John, Bowden, Donald K., Economou, Marina, Troncy, Jacques, Ganser, Arnold, Habr, Dany, Martin, Nicolas, Gater, Adam, Rofail, Diana, Abetz-Webb, Linda, Lau, Helen and Cappellini, Maria Domenica (2012). Health-related quality of life, treatment satisfaction, adherence and persistence in beta-thalassemia and myelodysplastic syndrome patients with iron overload receiving deferasirox: Results from the EPIC clinical trial. Anemia, 2012 297641, 1-10. doi: 10.1155/2012/297641

  • Is CAG sequence length in the androgen receptor gene correlated with finger-length ratio?

    Loehlin, John C., Medland, Sarah E. and Martin, Nicholas G. (2012). Is CAG sequence length in the androgen receptor gene correlated with finger-length ratio?. Personality and Individual Differences, 52 (2), 224-227. doi: 10.1016/j.paid.2011.09.009

  • Loci affecting gamma-glutamyl transferase in adults and adolescents show age x SNP interaction and cardiometabolic disease associations

    Middelberg, Rita P., Benyamin, Beben, de Moor, Marleen H. M., Warrington, Nicole M., Gordon, Scott, Henders, Anjali K., Medland, Sarah E., Nyholt, Dale R., de Geus, Eco J. C., Hottenga, Jouke J., Willemsen, Gonneke, Beilin, Lawrence J., Mori, Trevor A., Wright, Margaret J., Heath, Andrew C., Madden, Pamela A. F., Boomsma, Dorret I., Pennell, Craig E., Montgomery, Grant W., Martin, Nicholas G. and Whitfield, John B. (2012). Loci affecting gamma-glutamyl transferase in adults and adolescents show age x SNP interaction and cardiometabolic disease associations. Human Molecular Genetics, 21 (2) ddr478, 446-455. doi: 10.1093/hmg/ddr478

  • Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways

    Stolk L., Perry J.R.B., Chasman D.I., He C., Mangino M., Sulem P., Barbalic M., Broer L., Byrne E.M., Ernst F., Esko T., Franceschini N., Gudbjartsson D.F., Hottenga J.-J., Kraft P., McArdle P.F., Porcu E., Shin S.-Y., Smith A.V., Van Wingerden S., Zhai G., Zhuang W.V., Albrecht E., Alizadeh B.Z., Aspelund T., Bandinelli S., Lauc L.B., Beckmann J.S., Boban M. ... Lunetta K.L. (2012). Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways. Nature Genetics, 44 (3), 260-268. doi: 10.1038/ng.1051

  • Meta-analysis of genome-wide association studies for personality

    de Moor, M. H. M., Costa, P. T., Terracciano, A., Krueger, R. F., de Geus, E. J. C., Toshiko, T., Penninx, B. W. J. H., Esko, T., Madden, P. A. F., Derringer, J., Amin, N., Willemsen, G., Hottenga, J.-J., Distel, M. A., Uda, M., Sanna, S., Spinhoven, P., Hartman, C. A., Sullivan, P., Realo, A., Allik, J., Heath, A. C., Pergadia, M. L., Agrawal, A., Lin, P., Grucza, R., Nutile, T., Ciullo, M., Rujescu, D. ... Boomsma, D. I. (2012). Meta-analysis of genome-wide association studies for personality. Molecular Psychiatry, 17 (3), 337-349. doi: 10.1038/mp.2010.128

  • Predicting white matter integrity from multiple common genetic variants

    Kohannim, Omid, Jahanshad, Neda, Braskie, Meredith N., Stein, Jason L., Chiang, Ming-Chang, Reese. April H., Hibar, Derrek P., Toga, Arthur W., McMahon, Katie L., de Zubicaray, Greig I., Medland, Sarah E., Montgomery, Grant W., Martin, Nicholas G., Wright. Margaret J. and Thompson, Paul M. (2012). Predicting white matter integrity from multiple common genetic variants. Neuropsychopharmacology, 37 (9), 2012-2019. doi: 10.1038/npp.2012.49

  • The heritability and genetic correlates of mobile phone use: a twin study of consumer behavior

    Miller, Geoffrey, Zhu, Gu, Wright, Margaret J., Hansell, Narelle K. and Martin, Nicholas G. (2012). The heritability and genetic correlates of mobile phone use: a twin study of consumer behavior. Twin Research and Human Genetics, 15 (1), 97-106. doi: 10.1375/twin.15.1.97

  • A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma

    Yokoyama, Satoru, Woods, Susan L., Boyle, Glen M., Aoude, Lauren G., MacGregor, Stuart, Zismann, Victoria, Gartside, Michael, Cust, Anne E., Haq, Rizwan, Harland, Mark, Taylor, John C., Duffy, David L., Holohan, Kelly, Dutton-Regester, Ken, Palmer, Jane M., Bonazzi, Vanessa, Stark, Mitchell S., Symmons, Judith, Law, Matthew H., Schmidt, Christopher, Lanagan, Cathy, O'Connor, Linda, Holland, Elizabeth A., Schmid, Helen, Maskiell, Judith A., Jetann, Jodie, Ferguson, Megan, Jenkins, Mark A., Kefford, Richard F. ... Brown, Kevin M. (2011). A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma. Nature, 480 (7375), 99-103. doi: 10.1038/nature10630

  • Genome-wide association study identifies novel loci predisposing to cutaneous melanoma

    Amos, Christopher I., Wang, Li-E, Lee, Jeffrey E., Gershenwald, Jeffrey E., Chen, Wei V., Fang, Shenying, Kosoy, Roman, Zhang, Mingfeng, Qureshi, Abrar A., Vattathil, Selina, Schacherer, Christopher W., Gardner, Julie M., Wang, Yuling, Bishop, D. Tim, Barrett, Jennifer H., MacGregor, Stuart, Hayward, Nicholas K., Martin, Nicholas G., Duffy, David L., Mann, Graham J., Cust, Anne, Hopper, John, Brown, Kevin M., Grimm, Elizabeth A., Xu, Yaji, Han, Younghun, Jing, Kaiyan, McHugh, Caitlin, Laurie, Cathy C. ... Wei, Qingyi (2011). Genome-wide association study identifies novel loci predisposing to cutaneous melanoma. Human Molecular Genetics, 20 (24) ddr415, 5012-5023. doi: 10.1093/hmg/ddr415

  • New gene functions in megakaryopoiesis and platelet formation

    Gieger, Christian, Radhakrishnan, Aparna, Cvejic, Ana, Tang, Weihong, Porcu, Eleonora, Pistis, Giorgio, Serbanovic-Canic, Jovana, Elling, Ulrich, Goodall, Alison H., Labrune, Yann, Lopez, Lorna M., Magi, Reedik, Meacham, Stuart, Okada, Yukinori, Pirastu, Nicola, Sorice, Rossella, Teumer, Alexander, Voss, Katrin, Zhang, Weihua, Ramirez-Solis, Ramiro, Bis, Joshua C., Ellinghaus, David, Gogele, Martin, Hottenga, Jouke-Jan, Langenberg, Claudia, Kovacs, Peter, O'Reilly, Paul F., Shin, So-Youn, Esko, Tonu ... Soranzo, Nicole (2011). New gene functions in megakaryopoiesis and platelet formation. Nature, 480 (7376), 201-208. doi: 10.1038/nature10659

  • The value of twin studies: a response to Slate magazine

    Segal, Nancy L., Turkheimer, Eric, Gottesman, Irving I., Gatz, Margaret and Martin, Nicholas G. (2011). The value of twin studies: a response to Slate magazine. Twin Research and Human Genetics, 14 (6), 593-597. doi: 10.1375/twin.14.6.593

  • GWAS of butyrylcholinesterase activity identifies four novel loci, independent effects within BCHE and secondary associations with metabolic risk factors

    Benyamin, Beben, Middelberg, Rita P., Lind, Penelope A., Valle, Anne M., Gordon, Scott, Nyholt, Dale R., Medland, Sarah E., Henders, Anjali K., Heath, Andrew C., Madden, Pamela A. F., Visscher, Peter M., O'Connor, Daniel T., Montgomery, Grant W., Martin, Nicholas G. and Whitfield, John B. (2011). GWAS of butyrylcholinesterase activity identifies four novel loci, independent effects within BCHE and secondary associations with metabolic risk factors. Human Molecular Genetics, 20 (22) ddr375, 4504-4514. doi: 10.1093/hmg/ddr375

  • Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3

    MacGregor, Stuart, Montgomery, Grant W., Liu, Jimmy Z., Zhao, Zhen Zhen, Henders, Anjali K., Stark, Mitchell, Schmid, Helen, Holland, Elizabeth A., Duffy, David L., Zhang, Mingfeng, Painter, Jodie N., Nyholt, Dale R., Maskiell, Judith A., Jetann, Jodie, Ferguson, Megan, Cust, Anne E., Jenkins, Mark A., Whiteman, David C., Olsson, Hakan, Puig, Susana, Bianchi-Scarra, Giovanna, Hansson, Johan, Demenais, Florence, Landi, Maria Teresa, Debniak, Tadeusz, Mackie, Rona, Azizi, Esther, Bressac-de Paillerets, Brigitte, Goldstein, Alisa M. ... Hayward, Nicholas K. (2011). Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3. Nature Genetics, 43 (11), 1114-1118. doi: 10.1038/ng.958

  • What does a general factor of personality look like in unshared environmental variance?

    Loehlin, John C. and Martin, Nicholas G. (2011). What does a general factor of personality look like in unshared environmental variance?. Personality and Individual Differences, 51 (7), 862-865. doi: 10.1016/j.paid.2011.07.021

  • Meta-analysis of genome-wide association studies identifies common variants in CTNNA2 associated with excitement-seeking

    Terracciano, A., Esko, T., Sutin, A. R., de Moor, M. H. M., Meirelles, O., Zhu, G., Tanaka, T., Giegling, I., Nutile, T., Realo, A., Allik, J., Hansell, N. K., Wright, M. J., Montgomery, G. W., Willemsen, G., Hottenga, J-J, Friedl, M., Ruggiero, D., Sorice, R., Sanna, S., Cannas, A., Raikkonen, K., Widen, E., Palotie, A., Eriksson, J. G., Cucca, F., Krueger, R. F., Lahti, J., Luciano, M. ... Uda, M. (2011). Meta-analysis of genome-wide association studies identifies common variants in CTNNA2 associated with excitement-seeking. Translational Psychiatry, 1 (10) e49, e49-e49. doi: 10.1038/tp.2011.42

  • Impact of the genome on the epigenome is manifested in DNA methylation patterns of imprinted regions in monozygotic and dizygotic twins

    Coolen, Marcel W., Statham, Aaron L., Qu, Wenjia, Campbell, Megan J., Henders, Anjali K., Montgomery, Grant W., Martin, Nick G. and Clark, Susan J. (2011). Impact of the genome on the epigenome is manifested in DNA methylation patterns of imprinted regions in monozygotic and dizygotic twins. PLoS ONE, 6 (10) e25590, 1-12. doi: 10.1371/journal.pone.0025590

  • A genome-wide screen for interactions reveals a new locus on 4p15 modifying the effect of waist-to-hip ratio on total cholesterol

    Surakka, Ida, Isaacs, Aaron, Karssen, Lennart C., Laurila, Pirkka-Pekka P., Middelberg, Rita P. S., Tikkanen, Emmi, Ried, Janina S., Lamina, Claudia, Mangino, Massimo, Igl, Wilmar, Hottenga, Jouke-Jan, Lagou, Vasiliki, van der Harst, Pim, Leach, Irene Mateo, Esko, Tonu, Kutalik, Zoltan, Wainwright, Nicholas W., Struchalin, Maksim V., Sarin, Antti-Pekka, Kangas, Antti J., Viikari, Jorma S., Perola, Markus, Rantanen, Taina, Petersen, Ann-Kristin, Soininen, Pasi, Johansson, Asa, Soranzo, Nicole, Heath, Andrew C., Papamarkou, Theodore ... Ripatti, Samuli (2011). A genome-wide screen for interactions reveals a new locus on 4p15 modifying the effect of waist-to-hip ratio on total cholesterol. PLoS Genetics, 7 (10) e1002333, e1002333. doi: 10.1371/journal.pgen.1002333

  • Cognitive functioning in older twins: The older Australian twins study

    Sachdev, Perminder S., Lee, Teresa, Lammel, Andrea, Crawford, John, Trollor, Julian N., Wright, Margaret J., Brodaty, Henry, Ames, David, Martin, Nicholas G. and OATS Research Team (2011). Cognitive functioning in older twins: The older Australian twins study. Australasian Journal on Ageing, 30 (Supp. 2), 17-23. doi: 10.1111/j.1741-6612.2011.00534.x

  • Common breast cancer susceptibility loci are associated with triple-negative breast cancer

    Stevens, Kristen N., Vachon, Celine M., Lee, Adam M., Slager, Susan, Lesnick, Timothy, Olswold, Curtis, Fasching, Peter A., Miron, Penelope, Eccles, Diana, Carpenter, Jane E., Godwin, Andrew K., Ambrosone, Christine, Winqvist, Robert, Brauch, Hiltrud, Schmidt, Marjanka K., Cox, Angela, Cross, Simon S., Sawyer, Elinor, Hartmann, Arndt, Beckmann, Matthias W., Schulz-Wendtland, Ruediger, Ekici, Arif B., Tapper, William J., Gerty, Susan M., Durcan, Lorraine, Graham, Nikki, Hein, Rebecca, Nickels, Stephan, Flesch-Janys, Dieter ... Couch, Fergus J. (2011). Common breast cancer susceptibility loci are associated with triple-negative breast cancer. Cancer Research, 71 (19), 6240-6249. doi: 10.1158/0008-5472.CAN-11-1266

  • Polymorphisms in nevus-associated genes MTAP, PLA2G6, and IRF4 and the risk of invasive cutaneous melanoma

    Kvaskoff, Marina, Whiteman, David C., Zhao, Zhen Z., Montgomery, Grant W., Martin, Nicholas G., Hayward, Nicholas K. and Duffy, David L. (2011). Polymorphisms in nevus-associated genes MTAP, PLA2G6, and IRF4 and the risk of invasive cutaneous melanoma. Twin Research and Human Genetics, 14 (5), 422-432. doi: 10.1375/twin.14.5.422

  • Variation in BMPR1B, TGFRB1 and BMPR2 and control of dizygotic twinning

    Luong, Hein T. T., Chaplin, Justin, McRae, Allan F., Medland, Sarah E., Willemsen, Gonneke, Nyholt, Dale R., Henders, Anjali K., Hoekstra, Chantal, Duffy, David L., Martin, Nicholas G., Boomsma, Dorret I., Montgomery, Grant W. and Painter, Jodie N. (2011). Variation in BMPR1B, TGFRB1 and BMPR2 and control of dizygotic twinning. Twin Research and Human Genetics, 14 (5), 408-416. doi: 10.1375/twin.14.5.408

  • Genetic variants in LPL, OASL and TOMM40/APOE-C1-C2-C4 genes are associated with multiple cardiovascular-related traits

    Middelberg, Rita P. S., Ferreira, Manuel A. R., Henders, Anjali K., Heath, Andrew C., Madden, Pamela A. F., Montgomery, Grant W., Martin, Nicholas G. and Whitfield, John B. (2011). Genetic variants in LPL, OASL and TOMM40/APOE-C1-C2-C4 genes are associated with multiple cardiovascular-related traits. BMC Medical Genetics, 12 (123) 123, 1-9. doi: 10.1186/1471-2350-12-123

  • A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications

    Heath, Andrew C., Whitfield, John B., Martin, Nicholas G., Pergadia, Michele L., Goate, Alison M., Lind, Penelope A., McEvoy, Brian P., Schrage, Andrew J., Grant, Julia D., Chou, Yi-Ling, Zhu, Rachel, Henders, Anjali K., Medland, Sarah E., Gordon, Scott D., Nelson, Elliot C., Agrawal, Arpana, Nyholt, Dale R., Bucholz, Kathleen K., Madden, Pamela A. F. and Montgomery, Grant W. (2011). A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications. Biological Psychiatry, 70 (6), 513-518. doi: 10.1016/j.biopsych.2011.02.028

  • Discovery and replication of dopamine-related gene effects on caudate volume in young and elderly populations (N=1198) using genome-wide search

    Stein, J. L., Hibar, D. P., Madsen, S. K., Khamis, M, McMahon, K. L., de Zubicaray, G. I., Hansell, N. K., Montgomery, G. W., Martin, N. G., Wright, M. J., Saykin, A. J., Jack Jr, C. R., Weiner. M. W., Toga. A. W., Thompson, P. M. and The Alzheimer’s Disease Neuroimaging Initiative (2011). Discovery and replication of dopamine-related gene effects on caudate volume in young and elderly populations (N=1198) using genome-wide search. Molecular Psychiatry, 16 (9), 927-937. doi: 10.1038/mp.2011.32

  • Genome-wide association study identifies two loci strongly affecting transferrin glycosylation

    Kutalik, Zoltan, Benyamin, Beben, Bergmann, Sven, Mooser, Vincent, Waeber, Gerard, Montgomery, Grant W., Martin, Nicholas G., Madden, Pamela A. F., Heath, Andrew C., Beckmann, Jacques S., Vollenweider, Peter, Marques-Vidal, Pedro and Whitfield, John B. (2011). Genome-wide association study identifies two loci strongly affecting transferrin glycosylation. Human Molecular Genetics, 20 (18) ddr272, 3710-3717. doi: 10.1093/hmg/ddr272

  • Identification of IL6R and chromosome 11q13.5 as risk loci for asthma

    Ferreira, Manuel A. R., Matheson, Melanie C., Duffy, David L., Marks, Guy B., Hui, Jennie, Le Souef, Peter, Danoy, Patrick, Baltic, Svetlana, Nyholt, Dale R., Jenkins, Mark, Hayden, Catherine, Willemsen, Gonneke, Ang, Wei, Kuokkanen, Mikko, Beilby, John, Cheah, Faang, de Geus, Eco J.C., Ramasamy, Adaikalavan, Vedantam, Sailaka, Salomaa, Veikko, Madden, Pamela A., Heath, Andrew C., Hopper, John L., Visscher, Peter M., Musk, Bill, Leeder, Stephen R., Jarvelin, Marjo-Riitta, Pennell, Craig, Boomsma, Dorret I. ... Wright, Margaret J. (2011). Identification of IL6R and chromosome 11q13.5 as risk loci for asthma. Lancet, 378 (9795), 1006-1014. doi: 10.1016/S0140-6736(11)60874-X

  • Genome-wide association reveals dopamine-related genetic effects on caudate volume

    Stein, J. L., Hibar, D. P., Madsen, S. K., Khamis, M., McMahon, K. L., De Zubicaray, G. I., Hansell, N. K., Montgomery, G. W., Martin, N. G., Wright, M. J., Saykin, A. J., Jack, C. R., Weiner, M. W., Toga, A. W. and Thompson, P. M. (2011). Genome-wide association reveals dopamine-related genetic effects on caudate volume. Molecular Psychiatry, 16 (9), 881-881. doi: 10.1038/mp.2011.98

  • Attitudes towards economic risk and the gender pay gap

    Le, Anh T., Miller, Paul W., Slutske, Wendy S. and Martin, Nicholas G. (2011). Attitudes towards economic risk and the gender pay gap. Labour Economics, 18 (4), 555-561. doi: 10.1016/j.labeco.2010.12.007

  • Disordered gambling as defined by the diagnostic and statistical manual of mental disorders and the South Oaks Gambling Screen: evidence for a common etiologic structure

    Slutske, Wendy S., Zhu, Gu, Meier, Madeline H. and Martin, Nicholas G. (2011). Disordered gambling as defined by the diagnostic and statistical manual of mental disorders and the South Oaks Gambling Screen: evidence for a common etiologic structure. Journal of Abnormal Psychology, 120 (3), 743-751. doi: 10.1037/a0022879

  • Female orgasm rates are largely independent of other traits: Implications for "female orgasmic disorder" and evolutionary theories of orgasm

    Zietsch, Brendan P., Miller, Geoffrey F., Bailey, J. Michael and Martin, Nicholas G. (2011). Female orgasm rates are largely independent of other traits: Implications for "female orgasmic disorder" and evolutionary theories of orgasm. Journal of Sexual Medicine, 8 (8), 2305-2316. doi: 10.1111/j.1743-6109.2011.02300.x

  • GWAS findings for human iris patterns: Associations with variants in genes that influence normal neuronal pattern development

    Larsson, Mats, Duffy, David L., Zhu, Gu, Liu, Jimmy Z., Macgregor, Stuart, McRae, Allan F., Wright, Margaret J., Sturm, Richard A., Mackey, David A., Montgomery, Grant W., Martin, Nicholas G. and Medland, Sarah E. (2011). GWAS findings for human iris patterns: Associations with variants in genes that influence normal neuronal pattern development. American Journal of Human Genetics, 89 (2), 334-343. doi: 10.1016/j.ajhg.2011.07.011

  • Genome-wide association analysis of coffee drinking suggests association with CYP1A1/CYP1A2 and NRCAM

    Amin, N., Byrne, E., Johnson, J., Chenevix-Trench, G., Walter, S., Nolte, I. M., kConFab Investigators, Vink, J.M., Rawal, R., Mangino, M., Teumer, A., Keers, J. C., Verwoert, G., Baumeister, S., Biffar, R., Petersmann, A., Dahmen, N., Doering, A., Isaacs, A., Broer, L., Wray, N. R., Montgomery, G. W., Levy, D., Psaty, B. M., Gudnason, V., Chakravarti, A., Sulem, P., Gudbjartsson, D. F., Kiemeney, L. A. ... van Duijn, C. M. (2011). Genome-wide association analysis of coffee drinking suggests association with CYP1A1/CYP1A2 and NRCAM. Molecular Psychiatry, 17 (11), 1116-1129. doi: 10.1038/mp.2011.101

  • LPAR1 and ITGA4 Regulate Peripheral Blood Monocyte Counts

    Maugeri, Narelle, Powell, Joseph E., 't Hoen, Peter A. C., de Geus, Eco J. C., Willemsen, Gonneke, Kattenberg, Mathijs, Henders, Anjali K., Wallace, Leanne, Penninx, Brenda, Hottenga, Jouke-Jan, Medland, Sarah E., Saviouk, Viatcheslav, Martin, Nicholas G., Visscher, Peter M., van Ommen, Gert-Jan B., Frazer, Ian H., Boomsma, Dorret I., Montgomery, Grant W. and Ferreira, Manuel A. R (2011). LPAR1 and ITGA4 Regulate Peripheral Blood Monocyte Counts. Human Mutation, 32 (8), 873-876. doi: 10.1002/humu.21536

  • Risk for suicidal thoughts and behavior after childhood sexual abuse in women and men

    Bedi, Saaniya, Nelson, Elliot C., Lynskey, Michael T., McCutcheon, Vivia V., Heath, Andrew C., Madden, Pamela A. F. and Martin, Nicholas G. (2011). Risk for suicidal thoughts and behavior after childhood sexual abuse in women and men. Suicide and Life-Threatening Behavior, 41 (4), 406-415. doi: 10.1111/j.1943-278X.2011.00040.x

  • Heritability of working memory brain activation

    Blokland, Gabriella A. M., McMahon, Katie L., Thompson, Paul M., Martin, Nicholas G., de Zubicaray, Greig I. and Wright, Margaret J. (2011). Heritability of working memory brain activation. Journal of Neuroscience, 31 (30), 10882-10890. doi: 10.1523/JNEUROSCI.5334-10.2011

  • Genetic architecture of circulating lipid levels

    Demirkan, Ayse, Amin, Najaf, Isaacs, Aaron, Jarvelin, Marjo-Riitta, Whitfield, John B., Wichmann, Heinz-Erich, Kyvik, Kirsten Ohm, Rudan, Igor, Gieger, Christian, Hicks, Andrew A., Johansson, Asa, Hottenga, Jouke-Jan, Smith, Johannes J., Wild, Sarah H., Pedersen, Nancy L., Willemsen, Gonneke, Mangino, Massimo, Hayward, Caroline, Uitterlinden, Andre G., Hofman, Albert, Witteman, Jacqueline, Montgomery, Grant W., Pietilainen, Kirsi H., Rantanen, Taina, Kaprio, Jaakko, Doering, Angela, Pramstaller, Peter P., Gyllensten, Ulf, de Geus, Eco J. C. ... van Duijn, Cornelia M. (2011). Genetic architecture of circulating lipid levels. European Journal of Human Genetics, 19 (7), 813-819. doi: 10.1038/ejhg.2011.21

  • Genomic inflation factors under polygenic inheritance

    Yang, Jian, Weedon, Michael N., Purcell, Shaun, Lettre, Guillaume, Estrada, Karol, Willer, Cristen J., Smith, Albert V., Ingelsson, Erik, O'Connell, Jeffrey R., Mangino, Massimo, Maegi, Reedik, Madden, Pamela A., Heath, Andrew C., Nyholt, Dale R., Martin, Nicholas G., Montgomery, Grant W., Frayling, Timothy M., Hirschhorn, Joel N., McCarthy, Mark I., Goddard, Michael E. and Visscher, Peter M. (2011). Genomic inflation factors under polygenic inheritance. European Journal of Human Genetics, 19 (7), 807-812. doi: 10.1038/ejhg.2011.39

  • Ophthalmic phenotypes and the representativeness of twin data for the general population

    Sanfilippo, Paul G., Medland, Sarah E., Hewitt, Alex W., Kearns, Lisa S., Ruddle, Jonathan B., Sun, Cong, Hammond, Christopher J., Young, Terri L., Martin, Nicholas G. and Mackey, David A. (2011). Ophthalmic phenotypes and the representativeness of twin data for the general population. Investigative Ophthalmology & Visual Science, 52 (8), 5565-5572. doi: 10.1167/iovs.11-7258

  • Parental depression and offspring psychopathology: a Children of Twins study

    Singh, A. L., D'Onofrio, B. M., Slutske, W. S., Turkheimer, E., Emery, R. E., Harden, K. P., Heath, A. C., Madden, P. A. F., Statham, D. J. and Martin, N. G. (2011). Parental depression and offspring psychopathology: a Children of Twins study. Psychological Medicine, 41 (7), 1385-1395. doi: 10.1017/S0033291710002059

  • Performance of a third-generation TSH-receptor antibody in a UK clinic

    Theodoraki, A., Jones, G., Parker, J., Woolman, E., Martin, N., Perera, S., Thomas, M., Bunn, C., Khoo, B., Bouloux, P. M. and Vanderpump, M. P. J. (2011). Performance of a third-generation TSH-receptor antibody in a UK clinic. Clinical Endocrinology, 75 (1), 127-133. doi: 10.1111/j.1365-2265.2011.04022.x

  • Sensation seeking in females from opposite-versus same-sex twin pairs: hormone transfer or sibling imitation?

    Slutske, Wendy S., Bascom, Elise N., Meier, Madeline H., Medland, Sarah E. and Martin, Nicholas G. (2011). Sensation seeking in females from opposite-versus same-sex twin pairs: hormone transfer or sibling imitation?. Behavior Genetics, 41 (4), 533-542. doi: 10.1007/s10519-010-9416-3

  • Educational Attainment: A Genome Wide Association Study in 9538 Australians

    Martin, Nicolas W., Medland, Sarah E., Verweij, Karin J. H., Lee, S. Hong, Nyholt, Dale R., Madden, Pamela A., Heath, Andrew C., Montgomery, Grant W., Wright, Margaret J. and Martin, Nicholas G. (2011). Educational Attainment: A Genome Wide Association Study in 9538 Australians. PLoS One, 6 (6) e20128, e20128.1-e20128.8. doi: 10.1371/journal.pone.0020128

  • Genetics of insomnia

    Gehrman, Philip R., Byrne, Enda, Gillespie, Nathan and Martin, Nicholas G. (2011). Genetics of insomnia. Sleep Medicine Clinics, 6 (2), 191-202. doi: 10.1016/j.jsmc.2011.03.003

  • Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1

    Burdon, Kathryn P., Macgregor, Stuart, Hewitt, Alex W., Sharma, Shiwani, Chidlow, Glyn, Mills, Richard A., Danoy, Patrick, Casson, Robert, Viswanathan, Ananth C., Liu, Jimmy Z., Landers, John, Henders, Anjali K., Wood, John, Souzeau, Emmanuelle, Crawford, April, Leo, Paul, Wang, Jie Jin, Rochtchina, Elena, Nyholt, Dale R., Martin, Nicholas G., Montgomery, Grant W., Mitchell, Paul, Brown, Matthew A., Mackey, David A. and Craig, Jamie E. (2011). Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1. Nature Genetics, 43 (6), 574-578. doi: 10.1038/ng.824

  • High-density fine-mapping of a chromosome 10q26 linkage peak suggests association between endometriosis and variants close to CYP2C19

    Painter, Jodie N., Nyholt, Dale R., Morris, Andrew, Zhao, Zhen Z., Henders, Anjali K., Lambert, Ann, Wallace, Leanne, Martin, Nicholas G., Kennedy, Stephen H., Treloar, Susan A., Zondervan, Krina T. and Montgomery, Grant W. (2011). High-density fine-mapping of a chromosome 10q26 linkage peak suggests association between endometriosis and variants close to CYP2C19. Fertility and Sterility, 95 (7), 2236-2240. doi: 10.1016/j.fertnstert.2011.03.062

  • Revisiting the effect of marital support on depressive symptoms in mothers and fathers: a genetically informed study

    Beam, Christopher R., Horn, Erin E., Hunt, Stacy Karagis, Emery, Robert E., Turkheimer, Eric and Martin, Nick (2011). Revisiting the effect of marital support on depressive symptoms in mothers and fathers: a genetically informed study. Journal of Family Psychology, 25 (3), 336-344. doi: 10.1037/a0023758

  • SNP sets and reading ability: testing confirmation of a 10-SNP set in a population sample

    Luciano, Michelle, Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J. and Bates, Timothy C. (2011). SNP sets and reading ability: testing confirmation of a 10-SNP set in a population sample. Twin Research and Human Genetics, 14 (3), 228-232. doi: 10.1375/twin.14.3.228

  • Transferrin saturation and mortality

    Benyamin, Beben, Montgomery, Grant W., Martin, Nicholas G. and Whitfield, John B. (2011). Transferrin saturation and mortality. Clinical Chemistry, 57 (6), 921-923. doi: 10.1373/clinchem.2011.162784

  • Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption (vol 108, pg 7119, 2011)

    Schumann, Gunter, Coin, Lachlan J., Lourdusamy, Anbarasu, Charoen, Pimphen, Berger, Karen H., Stacey, David, Desrivieres, Sylvane, Aliev, Fazil A., Khan, Anokhi A., Amin, Najaf, Aulchenko, Yurii S., Bakalkin, Georgy, Bakker, Stephan J., Balkau, Beverley, Beulens, Joline W., Bilbao, Ainhoa, de Boer, Rudolf A., Beury, Delphine, Bots, Michiel L., Breetvelt, Elemi J., Cauchi, Stephane, Cavalcanti-Proenca, Christine, Chambers, John C., Clarke, Toni-Kim, Dahmen, Norbert, de Geus, Eco J., Dick, Danielle, Ducci, Francesca, Easton, Alanna ... Elliott, Paul (2011). Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption (vol 108, pg 7119, 2011). Proceedings of the National Academy of Sciences of the United States of America, 108 (22), 9316-9316. doi: 10.1073/pnas.1106917108

  • Common Alzheimer's disease risk variant within the CLU gene affects white matter microstructure in young adults

    Braskie, Meredith N., Jahanshad, Neda, Stein, Jason L., Barysheva, Marina, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J., Ringman, John M., Toga, Arthur W. and Thompson, Paul M. (2011). Common Alzheimer's disease risk variant within the CLU gene affects white matter microstructure in young adults. The Journal of Neuroscience, 31 (18), 6764-6770. doi: 10.1523/JNEUROSCI.5794-10.2011

  • Sex differences in the genetic and environmental influences on childhood conduct disorder and adult antisocial behavior

    Meier, Madeline H., Slutske, Wendy S., Heath, Andrew C. and Martin, Nicholas G. (2011). Sex differences in the genetic and environmental influences on childhood conduct disorder and adult antisocial behavior. Journal of Abnormal Psychology, 120 (2), 377-388. doi: 10.1037/a0022303

  • Variation in human mate choice: Simultaneously investigating heritability, parental influence, sexual imprinting, and assortative mating

    Zietsch, Brendan P., Verweij, Karin J. H., Heath, Andrew C. and Martin, Nicholas G. (2011). Variation in human mate choice: Simultaneously investigating heritability, parental influence, sexual imprinting, and assortative mating. The American Naturalist, 177 (5), 605-616. doi: 10.1086/659629

  • Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption

    Schumann, Gunter, Coin, Lachlan J., Lourdusamy, Anbarasu, Charoen, Pimphen, Berger, Karen H., Stacey, David, Desrivieres, Sylvane, Aliev, Fazil A., Khan, Anokhi A., Amin, Najaf, Aulchenko, Yurii S., Bakalkin, Georgy, Bakker, Stephan J., Balkau, Beverley, Beulens, Joline W., Bilbao, Ainhoa, de Boer, Rudolf A., Beury, Delphine, Bots, Michiel L., Breetvelt, Elemi J., Cauchi, Stéphane, Cavalcanti-Proenca, Christine, Chambers, John C., Clarke, Toni-Kim, Dahmen, Norbert, de Geus, Eco J., Dick, Danielle, Ducci, Francesca, Easton, Alanna ... Elliott, Paul (2011). Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption. Proceedings of the National Academy of Sciences of the United States of America, 108 (17), 7119-7124. doi: 10.1073/pnas.1017288108

  • Alcoholic marriage: later start, sooner end

    Waldron, Mary, Heath, Andrew C., Lynskey, Michael T., Bucholz, Kathleen K., Madden, Pamela A. F. and Martin, Nicholas G. (2011). Alcoholic marriage: later start, sooner end. Alcoholism: Clinical and Experimental Research, 35 (4), 632-642. doi: 10.1111/j.1530-0277.2010.01381.x

  • Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in Australia

    Ferreira, Manuel A. R., McRae, Allan F., Medland, Sarah E., Nyholt, Dale R., Gordon, Scott D., Wright, Margaret J., Henders, Anjali K., Madden, Pamela A., Visscher, Peter M., Wray, Naomi R., Heath, Andrew C., Montgomery, Grant W., Duffy, David L. and Martin, Nicholas G. (2011). Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in Australia. European Journal of Human Genetics, 19 (4), 458-464. doi: 10.1038/ejhg.2010.191

  • Corrigendum to: "The general factor of personality: questions and elaborations" [J. Res. Pers. 45 (2011) 44-49]

    Loehlin, John C. and Martin, Nicholas G. (2011). Corrigendum to: "The general factor of personality: questions and elaborations" [J. Res. Pers. 45 (2011) 44-49]. Journal of Research in Personality, 45 (2), 258-258. doi: 10.1016/j.jrp.2011.02.010

  • Does teenage childbearing reduce investment in human capital?

    Webbink, Dinand, Martin, Nicholas G. and Visscher, Peter M. (2011). Does teenage childbearing reduce investment in human capital?. Journal of Population Economics, 24 (2), 701-730. doi: 10.1007/s00148-009-0270-7

  • Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis

    Painter, Jodie N., Anderson, Carl A., Nyholt, Dale R., Macgregor, Stuart, Lin, Jianghai, Lee, Sang Hong, Lambert, Ann, Zhao, Zhen Z., Roseman, Fenella, Guo, Qun, Gordon, Scott D., Wallace, Leanne, Henders, Anjali K., Visscher, Peter M., Kraft, Peter, Martin, Nicholas G., Morris, Andrew P., Treloar, Susan A., Kennedy, Stephen H., Missmer, Stacey A., Montgomery, Grant W. and Zondervan, Krina T. (2011). Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis. Obstetrical and Gynecological Survey, 66 (4), 214-216. doi: 10.1097/OGX.0b013e318210cea1

  • The politics of mate choice

    Alford, John R., Hatemi, Peter K., Hibbing, John R., Martin, Nicholas G. and Eaves, Lindon J. (2011). The politics of mate choice. The Journal of Politics, 73 (2), 362-379. doi: 10.1017/S0022381611000016

  • Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder

    Cichon, Sven, Muehleisen, Thomas W., Degenhardt, Franziska A., Mattheisen, Manuel, Miro, Xavier, Strohmaier, Jana, Steffens, Michael, Meesters, Christian, Herms, Stefan, Weingarten, Moritz, Priebe, Lutz, Haenisch, Britta, Aexander, Michael, Vollmer, Jennifer, Breuer, Rene, Schmael, Christine, Tessmann, Peter, Moebus, Susanne, Wichmann, H. -Erich, Schreiber, Stefan, Mueller-Myhsok, Bertram, Lucae, Susanne, Jamain, Stephane, Leboyer, Marion, Bellivier, Frank, Etain, Bruno, Henry, Chantal, Kahn, Jean-Pierre, Heath, Simon ... Noethen, Markus M. (2011). Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder. American Journal of Human Genetics, 88 (3), 372-381. doi: 10.1016/j.ajhg.2011.01.017

  • Genome-wide association analysis identifies variants associated with nonalcoholic fatty liver disease that have distinct effects on metabolic traits

    Speliotes, Elizabeth K., Yerges-Armstrong, Laura M., Wu, Jun, Hernaez, Ruben, Kim, Lauren J., Palmer, Cameron D., Gudnason, Vilmundur, Eiriksdottir, Gudny, Garcia, Melissa E., Launer, Lenore J., Nalls, Michael A., Clark, Jeanne M., Mitchell, Braxton D., Shuldiner, Alan R., Butler, Johannah L., Tomas, Marta, Hoffmann, Udo, Hwang, Shih-Jen, Massaro, Joseph M., O'Donnell, Christopher J., Sahani, Dushyant V., Salomaa, Veikko, Schadt, Eric E., Schwartz, Stephen M., Siscovick, David S., NASH CRN, GIANT Consortium, MAGIC Investigators, Voight, Benjamin F. ... Coin, Lachlan (2011). Genome-wide association analysis identifies variants associated with nonalcoholic fatty liver disease that have distinct effects on metabolic traits. PLoS Genetics, 7 (3) e1001324, e1001324.1-e1001324.14. doi: 10.1371/journal.pgen.1001324

  • BDNF gene effects on brain circuitry replicated in 455 twins

    Chiang, M. C., Barysheva, M., Toga, A. W., Medland, S. E., Hansel, N. K., James, M. R., McMahon, K. L., de Zubicaray, G. I., Martin, N. G., Wright, M. J. and Thompson, P. M. (2011). BDNF gene effects on brain circuitry replicated in 455 twins. NeuroImage, 55 (2), 448-454. doi: 10.1016/j.neuroimage.2010.12.053

  • Whole genome association scan for genetic polymorphisms influencing information processing speed

    Luciano, Michelle, Hansell, Narelle K., Lahti, Jari, Davies, Gail, Medland, Sarah E., Raikkonen, Katri, Tenesa, Albert, Widen, Elisabeth, McGhee, Kevin A., Palotie, Aarno, Liewald, David, Porteous, David J., Starr, John M., Montgomery, Grant W., Martin, Nicholas G., Eriksson, Johan G., Wright, Margaret J. and Deary, Ian J. (2011). Whole genome association scan for genetic polymorphisms influencing information processing speed. Biological Psychology, 86 (3), 193-202. doi: 10.1016/j.biopsycho.2010.11.008

  • Genome-wide Association Study Identifies Genetic Variation in Neurocan as a Susceptibility Factor for Bipolar Disorder (vol 88, pg 372, 2011)

    Cichon, Sven, Muehleisen, Thomas W., Degenhardt, Franziska A., Mattheisen, Manuel, Miro, Xavier, Strohmaier, Jana, Steffens, Michael, Meesters, Christian, Herms, Stefan, Weingarten, Moritz, Priebe, Lutz, Haenisch, Britta, Alexander, Michael, Vollmer, Jennifer, Breuer, Rene, Schmael, Christine, Tessmann, Peter, Moebus, Susanne, Wichmann, H. -Erich, Schreiber, Stefan, Mueller-Myhsok, Bertram, Lucae, Susanne, Jamain, Stephane, Leboyer, Marion, Bellivier, Frank, Etain, Bruno, Henry, Chantal, Kahn, Jean-Pierre, Heath, Simon ... Noethen, Markus M. (2011). Genome-wide Association Study Identifies Genetic Variation in Neurocan as a Susceptibility Factor for Bipolar Disorder (vol 88, pg 372, 2011). American Journal of Human Genetics, 88 (3), 396-396. doi: 10.1016/j.ajhg.2011.03.001

  • The contribution of genes to cortical thickness and volume

    Joshi, A.A., Lepore, N., Joshi, S.H., Lee, A.D., Barysheva, M., Stein, J.L., McMahon, K.L., Johnson, K., de Zubicaray, G.I., Martin, N.G., Wright, M.J., Toga, A.W. and Thompson, P.M. (2011). The contribution of genes to cortical thickness and volume. NeuroReport, 22 (3), 101-105. doi: 10.1097/WNR.0b013e3283424c84

  • Fast and slow spindle involvement in the consolidation of a new motor sequence

    Barakat, M., Doyon, J., Debas, K., Vandewalle, G., Morin, A., Poirier, G., Martin, N., Lafortune, M., Karni, A., Ungerleider, L. G., Benali, H. and Carrier, J. (2011). Fast and slow spindle involvement in the consolidation of a new motor sequence. Behavioural Brain Research, 217 (1), 117-121. doi: 10.1016/j.bbr.2010.10.019

  • Genetics of white matter development: A DTI study of 705 twins and their siblings aged 12 to 29

    Chiang, MC, McMahon, KL, de Zubicaray, GI, Martin, NG, Hickie, I, Toga, AW, Wright, MJ and Thompson, PM (2011). Genetics of white matter development: A DTI study of 705 twins and their siblings aged 12 to 29. NeuroImage, 54 (3), 2308-2317. doi: 10.1016/j.neuroimage.2010.10.015

  • Nevi, family history, and fair skin increase the risk of second primary melanoma

    Siskind, Victor, Hughes, Maria Celia B., Palmer, Jane M., Symmons, Judith M., Aitken, Joanne F., Martin, Nicholas G., Hayward, Nicholas K. and Whiteman, David C. (2011). Nevi, family history, and fair skin increase the risk of second primary melanoma. The Journal of Investigative Dermatology, 131 (2), 461-467. doi: 10.1038/jid.2010.298

  • Psychiatric and genetic studies of binocular rivalry: an endophenotype for bipolar disorder?

    Ngo, Trung T., Mitchell, Philip B., Martin, Nicholas G. and Miller, Steven M. (2011). Psychiatric and genetic studies of binocular rivalry: an endophenotype for bipolar disorder?. Acta Neuropsychiatrica, 23 (1), 37-42. doi: 10.1111/j.1601-5215.2010.00510.x

  • Sexual orientation and psychiatric vulnerability: A twin study of neuroticism and psychoticism

    Zietsch, Brendan P., Verweij, Karin J. H., Bailey, J. Michael, Wright, Margaret J. and Martin, Nicholas G. (2011). Sexual orientation and psychiatric vulnerability: A twin study of neuroticism and psychoticism. Archives of Sexual Behavior, 40 (1), 133-142. doi: 10.1007/s10508-009-9508-4

  • Sleep slow wave changes during the middle years of life

    Carrier, Julie, Viens, Isabelle, Poirier, Gaétan , Robillard, Rébecca , Lafortune, Marjolaine, Vandewalle, Gilles, Martin, Nicolas, Barakat, Marc, Paquet, Jean and Filipini, Daniel (2011). Sleep slow wave changes during the middle years of life. European Journal of Neuroscience, 33 (4), 758-766. doi: 10.1111/j.1460-9568.2010.07543.x

  • The general factor of personality: questions and elaborations

    Loehlin, John C. and Martin, Nicholas G. (2011). The general factor of personality: questions and elaborations. Journal of Research in Personality, 45 (1), 44-49. doi: 10.1016/j.jrp.2010.11.008

  • The relationship between retinal arteriolar and venular calibers is genetically mediated, and each is associated with risk of cardiovascular disease

    Fahy, Samantha J., Sun, Cong, Zhu, Gu, Healey, Paul R., Spector, Tim D., Martin, Nicolas G., Mitchell, Paul, Wong, Tien Y., Mackey, David A., Hammond, Christopher J. and Andrew, Toby (2011). The relationship between retinal arteriolar and venular calibers is genetically mediated, and each is associated with risk of cardiovascular disease. Investigative Ophthalmology & Visual Science, 52 (2), 975-981. doi: 10.1167/iovs.10-5927

  • Variance components models for physical activity with age as modifier: a comparative twin study in seven countries

    Vink, Jacqueline M., Boomsma, Dorret I., Medland, Sarah E., de Moor, Marleen H. M., Stubbe, Janine H., Cornes, Belinda K., Martin, Nicholas G., Skytthea, Axel, Kyvik, Kirsten O., Rose, Richard J., Kujala, Urho M., Kaprio, Jaakko, Harris, Jennifer R., Pedersen, Nancy L., Cherkas, Lynn, Spector, Tim D. and de Geus, Eco J. C. (2011). Variance components models for physical activity with age as modifier: a comparative twin study in seven countries. Twin Research and Human Genetics, 14 (1), 25-34. doi: 10.1375/twin.14.1.25

  • A 3p26-3p25 genetic linkage finding for DSM-IV major depression in heavy smoking families

    Pergadia, Michele L., Glowinski, Anne L., Wray, Naomi, Agrawal, Arpana, Saccone, Scott F., Loukola, Anu, Broms, Ulla, Koronen, Tellervo, Penninx, Brenda W. J. H., Grant, Julia D., Nelson, Elliot C., Henders, Anjali K., Schrage, Andrew J., Chou, Yi-Ling, Keskitalo-Vuokko, Kaisu, Zhu, Qin, Gordon, Scott D., Vink, Jacqueline M., de Geus, Eco J. C., MacGregor, Stuart, Liu, Jimmy Z., Willemsen, Gonneke, Medland, Sarah E., Boomsma, Dorret I., Montgomery, Grant W., Rice, John P., Goate, Alison M., Heath, Andrew, C, Martin, Nicholas G. and Madden, Pamela A. F. (2011). A 3p26-3p25 genetic linkage finding for DSM-IV major depression in heavy smoking families. American Journal Psychiatry, 168 (8), 848-852. doi: 10.1176/appi.ajp.2011.10091319

  • A genome-wide analysis of liberal and conservative political attitudes

    Hatemi, Peter K., Gillespie, Nathan A., Eaves, Lindon J., Maher, Brion S., Webb, Bradley T., Heath, Andrew C., Medland, Sarah E., Smyth, David C., Beeby, Harry N., Gordon, Scott D., Montgomery, Grant W., Zhu, Ghu, Byrne, Enda M. and Martin, Nicholas G. (2011). A genome-wide analysis of liberal and conservative political attitudes. Journal of Politics, 73 (1), 271-285. doi: 10.1017/S0022381610001015

  • Cognitive function in adolescence: Testing for interactions between breast-feeding and FADS2 polymorphisms

    Martin, Nicolas W., Benyamin, Beben, Hansell, Narelle K., Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J. and Bates, Timothy C. (2011). Cognitive function in adolescence: Testing for interactions between breast-feeding and FADS2 polymorphisms. Journal of the American Academy of Child and Adolescent Psychiatry, 50 (1), 55-62.e4. doi: 10.1016/j.jaac.2010.10.010

  • Genetic variance in a component of the language acquisition device: ROBO1 polymorphisms associated with phonological buffer deficits

    Bates, Timothy C., Luciano, Michelle, Medland, Sarah E., Montgomery, Grant W., Wright, Margaret J. and Martin, Nicholas G. (2011). Genetic variance in a component of the language acquisition device: ROBO1 polymorphisms associated with phonological buffer deficits. Behavior Genetics, 41 (1), 50-57. doi: 10.1007/s10519-010-9402-9

  • Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis

    Painter, JN, Anderson, CA, Nyholt, DR, Macgregor, S, Lin, JH, Lee, SH, Lambert, A, Zhao, ZZ, Roseman, F, Guo, Q, Gordon, SD, Wallace, L, Henders, AK, Visscher, PM, Kraft, P, Martin, NG, Morris, AP, Treloar, SA, Kennedy, SH, Missmer, SA, Montgomery, GW and Zondervan, KT (2011). Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis. Nature Genetics, 43 (1), 51-54. doi: 10.1038/ng.731

  • Genome-wide association study identifies three new melanoma susceptibility loci

    Barrett, Jennifer H., Iles, Mark M., Harland, Mark, Taylor, John C., Aitken, Joanne F., Andresen, Per Arne, Akslen, Lars A., Armstrong, Bruce K., Avril, Marie-Francoise, Azizi, Esther, Bakker, Bert, Bergman, Wilma, Bianchi-Scarrà, Giovanna, Bressac-de Paillerets, Brigitte, Calista, Donato, Cannon-Albright, Lisa A., Corda, Eve, Cust, Anne E., Dębniak, Tadeusz, Duffy, David, Dunning, Alison M., Easton, Douglas F., Friedman, Eitan, Galan, Pilar, Ghiorzo, Paola, Giles, Graham G., Hansson, Johan, Hocevar, Marko, Höiom, Veronica ... Bishop, D. Timothy (2011). Genome-wide association study identifies three new melanoma susceptibility loci. Nature Genetics, 43 (11), 1108-1113. doi: 10.1038/ng.959

  • Identification of tag haplotypes for 5HTTLPR for different genome-wide SNP platforms

    Vinkhuyzen, A. A. E., Dumenil, T., Ryan, L., Gordon, S. D., Henders, A. K., Madden, P. A. F., Heath, A. C., Montgomery, G. W., Martin, N. G. and Wray, N. R. (2011). Identification of tag haplotypes for 5HTTLPR for different genome-wide SNP platforms. Molecular Psychiatry, 16 (11), 1073-1075. doi: 10.1038/mp.2011.68

  • The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: evidence from a large collaborative study totaling 4,963 subjects

    Rizzi, Thais S., Arias-Vasquez, Alejandro, Rommelse, Nanda, Kuntsi, Jonna, Anney, Richard, Asherson, Philip, Buitelaar, Jan, Banaschewski, Tobias, Ebstein, Richard, Ruano, Dina, van der Sluis, Sophie, Markunas, Christina A., Garrett, Melanie E., Ashley-Koch, Allison E., Kollins, Scott H., Anastopoulos, Arthur D., Hansell, Narelle K., Wright, Margaret J., Montgomery, Grant W., Martin, Nicholas G., Harris, Sarah E., Davies, Gail, Tenesa, Albert, Porteous, David J., Starr, John M., Deary, Ian J., St. Pourcain, Beate, Smith, George Davey, Timpson, Nicholas J. ... Posthuma, Danielle (2011). The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: evidence from a large collaborative study totaling 4,963 subjects. American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 156 (2), 145-157. doi: 10.1002/ajmg.b.31149

  • The genetic association between personality and major depression or bipolar disorder. A polygenic score analysis using genome-wide association data

    Middeldorp, C. M., de Moor, M. H. M., McGrath, L. M., Gordon, S. D., Blackwood, D. H., Costa, P. T., Terracciano, A., Krueger, R. F., de Geus, E. J. C., Nyholt, D. R., Tanaka, T., Esko, T., Madden, P. A. F., Derringer, J., Amin, N., Willemsen, G., Hottenga, J-J., Distel, M. A., Uda, M., Sanna, S., Spinhoven, P., Hartman, C. A, Ripke, S., Sullivan, P. F., Realo, A., Allik, J., Heath, A. C., Pergadia, M. L., Agrawal, A. ... Boomsma, D. I. (2011). The genetic association between personality and major depression or bipolar disorder. A polygenic score analysis using genome-wide association data. Translational Psychiatry, 1 (10) e50, e50.1-e50.8. doi: 10.1038/tp.2011.45

  • Undue influence of weight and shape: Is it distinct from body dissatisfaction and concern about weight and shape?

    Wade, T. D., Zhu, G. and Martin, N. G. (2011). Undue influence of weight and shape: Is it distinct from body dissatisfaction and concern about weight and shape?. Psychological Medicine, 41 (4), 819-828. doi: 10.1017/S0033291710001066

  • Associations of birth weight with ocular biometry, refraction, and glaucomatous endophenotypes: The Australian twins eye study

    Sun, Cong, Ponsonby, Anne-Louise, Brown, Shayne A., Kearns, Lisa S., Mackinnon, Jane R., Barbour, Julie M., Ruddle, Jonathan B., Wright, Margaret J., Martin, Nicholas G., Dwyer, Terence and Mackey, David A. (2010). Associations of birth weight with ocular biometry, refraction, and glaucomatous endophenotypes: The Australian twins eye study. American Journal of Ophthalmology, 150 (6), 909-916. doi: 10.1016/j.ajo.2010.06.028

  • Dyslexia and DYX1C1: Deficits in reading and spelling associated with a missense mutation

    Bates, T. C., Lind, P. A., Luciano, M., Montgomery, G. W., Martin, N. G. and Wright, M. J. (2010). Dyslexia and DYX1C1: Deficits in reading and spelling associated with a missense mutation. Molecular Psychiatry, 15 (12), 1190-1196. doi: 10.1038/mp.2009.120

  • Pathological gambling recovery in the absence of abstinence

    Slutske, Wendy S., Piasecki, Thomas M., Blaszczynski, Alex and Martin, Nicholas G. (2010). Pathological gambling recovery in the absence of abstinence. Addiction, 105 (12), 2169-2175. doi: 10.1111/j.1360-0443.2010.03080.x

  • Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies

    Elks, C. E., Perry, J. R. B., Sulem, P., Chasman, D. I., Franceschini, N., He, C. Y., Lunetta, K. L., Visser, J. A., Byrne, E. M., Cousminer, D. L., Gudbjartsson, D. F., Esko, T., Feenstra, B., Hottenga, J. J., Koller, D. L., Kutalik, Z., Lin, P., Mangino, M., Marongiu, M., McArdle, P. F., Smith, A. V., Stolk, L., Van Wingerden, S. H., Zhao, J. H., Albrecht, E., Corre, T., Ingelsson, E., Hayward, C., Magnusson, P. K. E. ... GIANT Consortium (2010). Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. Nature Genetics, 42 (12), 1077-1085. doi: 10.1038/ng.714

  • Which patient will feel down, which will be happy? The need to study the genetic disposition of emotional states

    Sprangers, Mirjam A. G., Bartels, Meike, Veenhoven, Ruut, Baas, Frank, Martin, Nicholas G., Mosing, Miriam, Movsas, Benjamin, Ropka, Mary E., Shinozaki, Gen, Swaab, Dick and The GENEQOL Consortium (2010). Which patient will feel down, which will be happy? The need to study the genetic disposition of emotional states. Quality of Life Research, 19 (10), 1429-1437. doi: 10.1007/s11136-010-9652-2

  • Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index

    Elizabeth K Speliotes, Cristen J Willer, Sonja I Berndt, Keri L Monda, Gudmar Thorleifsson, Anne U Jackson, Hana Lango Allen, Cecilia M Lindgren, Jian'an Luan, Reedik Magi, Joshua C Randall, Sailaja Vedantam, Thomas W Winkler, Lu Qi, Tsegaselassie Workalemahu, Iris M Heid, Valgerdur Steinthorsdottir, Heather M Stringham, Michael N Weedon, Eleanor Wheeler, Andrew R Wood, Teresa Ferreira, Robert J Weyant, Ayellet V Segre, Karol Estrada, Liming Liang, James Nemesh, Ju-Hyun Park, Stefan Gustafsson ... Ruth J F Loos (2010). Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index. Nature Genetics, 42 (11), 937-948. doi: 10.1038/ng.686

  • The heritability of general cognitive ability increases linearly from childhood to young adulthood

    Haworth, Cma, Wright, MJ, Luciano, M, Martin, NG, de Geus, EJC, van Beijsterveldt, CEM, Bartels, M, Posthuma, D, Boomsma, DI, Davis, OSP, Kovas, Y, Corley, RP, DeFries, JC, Hewitt, JK, Olson, RK, Rhea, SA, Wadsworth, SJ, Iacono, WG, McGue, M, Thompson, LA, Hart, SA, Petrill, SA, Lubinski, D and Plomin, R (2010). The heritability of general cognitive ability increases linearly from childhood to young adulthood. Molecular Psychiatry, 15 (11), 1112-1120. doi: 10.1038/mp.2009.55

  • The perception of quinine taste intensity is associated with common genetic variants in a bitter receptor cluster on chromosome 12

    Reed, Danielle R., Zhu, Gu, Breslin, Paul A. S., Duke, Fujiko F., Henders, Anjali K., Campbell, Megan J., Montgomery, Grant W., Medland, Sarah E., Martin, Nicholas G. and Wright, Margaret J. (2010). The perception of quinine taste intensity is associated with common genetic variants in a bitter receptor cluster on chromosome 12. Human Molecular Genetics, 19 (21) ddq324, 4278-4285. doi: 10.1093/hmg/ddq324

  • Hundreds of variants clustered in genomic loci and biological pathways affect human height

    Allen, Hana Lango, Estrada, Karol, Lettre, Guillaume, Berndt, Sonja I., Weedon, Michael N., Rivadeneira, Fernando, Willer, Cristen J., Jackson, Anne U., Vedantam, Sailaja, Raychaudhuri, Soumya, Nyholt, Dale, Martin, Nicholas G., Montgomery, Grant W. and Visscher, Peter M. (2010). Hundreds of variants clustered in genomic loci and biological pathways affect human height. Nature, 467 (7317), 832-838. doi: 10.1038/nature09410

  • A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25

    Hysi, Pirro G., Young, Terri L., Mackey, David A., Andrew, Toby, Fernandez-Medarde, Alberto, Solouki, Abbas M., Hewitt, Alex W., Macgregor, Stuart, Vingerling, Johannes R., Li, Yi-Ju, Ikram, M. Kamran, Fai, Lee Yiu, Sham, Pak C., Manyes, Lara, Porteros, Angel, Lopes, Margarida C., Carbonaro, Francis, Fahy, Samantha J., Martin, Nicholas G., van Diujn, Cornelia M., Spector, Timothy D., Rahi, Jugnoo S., Santos, Eugenio, Klaver, Caroline C. W. and Hammond, Christopher J. (2010). A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25. Nature Genetics, 42 (10), 902-905. doi: 10.1038/ng.664

  • A genome-wide association study of Cloninger’s temperament scales: Implications for the evolutionary genetics of personality

    Verweij, Kjh, Zietsch, BP, Medland, SE, Gordon, SD, Benyamin, B, Nyholt, DR, McEvoy, BP, Sullivan, PF, Heath, AC, Madden, PAF, Henders, AK, Montgomery, GW, Martin, NG and Wray, NR (2010). A genome-wide association study of Cloninger’s temperament scales: Implications for the evolutionary genetics of personality. Biological Psychology, 85 (2), 306-317. doi: 10.1016/j.biopsycho.2010.07.018

  • A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor–negative breast cancer in the general population

    Antoniou, Antonis C., Wang, Xianshu, Fredericksen, Zachary S., McGuffog, Lesley, Tarrell, Robert, Sinilnikova, Olga M., Healey, Sue, Morrison, Jonathan, Kartsonaki,Christiana, Lesnick, Timothy, Ghoussaini, Maya, Barrowdale, Daniel, Peock, Susan, Cook, Margaret, Oliver, Clare, Frost, Debra, Eccles, Diana, Evans, D. Gareth, Eeles, Ros, Izatt, Louise, Chu, Carol, Douglas, Fiona, Paterson, Joan, Stoppa-Lyonnet, Dominique, Houdayer, Claude, Mazoyer, Sylvie, Giraud, Sophie, Lasset, Christine, Remenieras, Audrey ... Lakhani, Sunil (2010). A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor–negative breast cancer in the general population. Nature Genetics, 42 (10), 885-892. doi: 10.1038/ng.669

  • Body mass index and breast size in women: Same or different genes?

    Wade, Tracey D., Zhu, Gu and Martin, Nicholas G. (2010). Body mass index and breast size in women: Same or different genes?. Twin Research and Human Genetics, 13 (5), 450-454. doi: 10.1375/twin.13.5.450

  • Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma

    Thorleifsson, Gudmar, Walters, G. Bragi, Hewitt, Alex W., Masson, Gisli, Helgason, Agnar, DeWan, Andrew, Sigurdsson, Asgeir, Jonasdottir, Adalbjorg, Gudjonsson, Sigurjon A., Magnusson, Kristinn P., Stefansson, Hreinn, Lam, Dennis S. C., Tam, Pancy O. S., Gudmundsdottir, Gudrun J., Southgate, Laura, Burdon, Kathryn P., Gottfredsdottir, Maria Soffia, Aldred, Micheala A., Mitchell, Paul, St Clair, David, Collier, David A., Tang, Nelson, Sveinsson, Orn, Macgregor, Stuart, Martin, Nicholas G., Cree, Angela J., Gibson, Jane, MacLeod, Alex, Jacob, Aby ... Stefansson, Kari (2010). Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma. Nature Genetics, 42 (10), 906-910. doi: 10.1038/ng.661

  • Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo

    Ikram, M. Kamran, Sim, Xueling, Jensen, Richard A., Cotch, Mary Frances, Hewitt, Alex W., Ikram, M. Arfan, Wang, Jie Jin, Klein, Ronald, Klein, Barbara E. K., Breteler, Monique M. B., Cheung, Ning, Liew, Gerald, Mitchell, Paul, Uitterlinden, Andrew G., Rivadeneira, Fernando, Hofman, Albert, de Jong, Paulus T. V. M., van Kuijn, Cornelia M., Kao, Linda, Cheng, Ching-Yu, Smith, Albert Vernon, Glazer, Nicole L., Lumley, Thomas, McKnight, Barbara, Psaty, Bruce M., Jonasson, Fridbert, Eiriksdottir, Gudny, Aspelund, Thor, Global BPgen Consortium ... Wong, Tien Y. (2010). Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo. PLoS Genetics, 6 (10) e1001184, 1-12. doi: 10.1371/journal.pgen.1001184

  • Stringent programming of DNA methylation in humans

    Aung, Hnin T., Harrison, Dion K., Findlay, Ian, Mattick, John S., Martin, Nicholas G. and Carroll, Bernard J. (2010). Stringent programming of DNA methylation in humans. Twin Research and Human Genetics, 13 (5), 405-411. doi: 10.1375/twin.13.5.405

  • The nature of the relationship between personality traits and political attitudes

    Verhulst, Brad, Hatemi, Peter K. and Martin, Nicholas G. (2010). The nature of the relationship between personality traits and political attitudes. Personality and Individual Differences, 49 (4), 306-316. doi: 10.1016/j.paid.2009.11.013

  • Biological, clinical and population relevance of 95 loci for blood lipids

    Teslovich, Tanya M., Musunuru, Kiran, Smith, Albert V., Edmondson, Andrew C., Stylianou, Ioannis M., Koseki, Masahiro, Pirruccello, James P., Ripatti, Samuli, Chasman, Daniel I., Willer, Cristen J., Johansen, Christopher T., Fouchier, Sigrid W., Isaacs, Aaron, Peloso, Gina M., Barbalic, Maja, Ricketts, Sally L., Bis, Joshua C., Aulchenko, Yurii S., Thorleifsson, Gudmar, Feitosa, Mary F., Chambers, John, Orho-Melander, Marju, Melander, Olle, Johnson, Toby, Li, Xiaohui, Guo, Xiuqing, Li, Mingyao, Cho, Yoon Shin, Go, Min Jin ... Kathiresan, Sekar (2010). Biological, clinical and population relevance of 95 loci for blood lipids. Nature, 466 (7307), 707-713. doi: 10.1038/nature09270

  • A genome-wide association study of self-rated health

    Mosing, Miriam A., Verweij, Karin J. H., Medland, Sarah E., Painter, Jodie, Gordon, Scott D., Heath, Andrew C., Madden, Pamela A., Montgomery, Grant W. and Martin, Nicholas G. (2010). A genome-wide association study of self-rated health. Twin Research and Human Genetics, 13 (4), 398-403. doi: 10.1375/twin.13.4.398

  • Are attitudes towards economic risk heritable? Analyses using the Australian twin study of gambling

    Le, Anh T., Miller, Paul W., Slutske, Wendy S. and Martin, Nicholas G. (2010). Are attitudes towards economic risk heritable? Analyses using the Australian twin study of gambling. Twin Research And Human Genetics, 13 (4), 330-339. doi: 10.1375/twin.13.4.330

  • Genetic covariance structure of the four main features of borderline personality disorder

    Distel, Marijn A., Willemsen, Gonneke, Ligthart, Lannie, Derom, Catherine A., Martin, Nicholas G., Neale, Michael C., Trull, Timothy J. and Boomsma, Dorret I. (2010). Genetic covariance structure of the four main features of borderline personality disorder. Journal of Personality Disorders, 24 (4), 427-444. doi: 10.1521/pedi.2010.24.4.427

  • Genetic influences on brain asymmetry: A DTI study of 374 twins and siblings

    Jahanshad, Neda, Lee, Agatha D., Barysheva, Marina, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J., Toga, Arthur W. and Thompson, Paul M. (2010). Genetic influences on brain asymmetry: A DTI study of 374 twins and siblings. NeuroImage, 52 (2), 455-469. doi: 10.1016/j.neuroimage.2010.04.236

  • Heritability of head size in Dutch and Australian twin families at ages 0-50 years

    Smit, Dirk J. A., Luciano, Michelle, Bartels, Meike, van Beijsterveldt, Catharine E. M., Wright, Margaret J., Hansell, Narelle K., Brunner, Han G., Estourgie-van Burk, G. Frederiek, de Geus, Eco J. C., Martin, Nicholas G. and Boomsma, Dorret I. (2010). Heritability of head size in Dutch and Australian twin families at ages 0-50 years. Twin Research And Human Genetics, 13 (4), 370-380. doi: 10.1375/twin.13.4.370

  • Imaging genomics

    Thompson, Paul M., Martin, Nicholas G. and Wright, Margaret J. (2010). Imaging genomics. Current Opinion in Neurology, 23 (4), 368-373. doi: 10.1097/WCO.0b013e32833b764c

  • Major depression and the metabolic syndrome

    Foley, Debra L., Morley, Katherine I., Madden, Pamela A. F., Heath, Andrew C., Whitfield, John B. and Martin, Nicholas G. (2010). Major depression and the metabolic syndrome. Twin Research and Human Genetics, 13 (4), 347-358. doi: 10.1375/twin.13.4.347

  • Multiple independent loci at chromosome 15q25.1 affect smoking quantity: A meta-analysis and comparison with lung cancer and COPD

    Saccone, Nancy L., Culverhouse, Robert C., Schwantes-An, Tae-Hwi, Cannon, Dale S., Chen, Xiangning, Cichon, Sven, Giegling, Ina, Han, Shizhong, Han, Younghun, Keskitalo-Vuokko, Kaisu, Kong, Xiangyang, Landi, Maria Teresa, Ma, Jennie Z., Short, Susan E., Stephens, Sarah H., Stevens, Victoria L., Sun, Lingwei, Wang, Yufei, Wenzlaff, Angela S., Aggen, Steven H., Breslau, Naomi, Broderick, Peter, Chatterjee, Nilanjan, Chen, Jingchun, Heath, Andrew C., Heliovaara, Markku, Hoft, Nicole R., Hunter, David J., Jensen, Majken K. ... Bierut, Laura J. (2010). Multiple independent loci at chromosome 15q25.1 affect smoking quantity: A meta-analysis and comparison with lung cancer and COPD. PLoS Genetics, 6 (8) ARTN e1001053, 1-16. doi: 10.1371/journal.pgen.1001053

  • Nicotine withdrawal symptoms in adolescent and adult twins

    Pergadia, Michele L., Agrawal, Arpana, Heath, Andrew C., Martin, Nicholas G., Bucholz, Kathleen K. and Madden, Pamela A. F. (2010). Nicotine withdrawal symptoms in adolescent and adult twins. Twin Research And Human Genetics, 13 (4), 359-369. doi: 10.1375/twin.13.4.359

  • Sex differences in the genetic architecture of optimism and health and their interrelation: A study of Australian and Swedish twins

    Mosing, Miriam A., Pedersen, Nancy L., Martin, Nicholas G. and Wright, Margaret J. (2010). Sex differences in the genetic architecture of optimism and health and their interrelation: A study of Australian and Swedish twins. Twin Research And Human Genetics, 13 (4), 322-329. doi: 10.1375/twin.13.4.322

  • The family history method in disordered gambling research: A comparison of reports obtained from discordant twin pairs

    Slutske, Wendy S., Piasecki, Thomas M., Ellingson, Jarrod M. and Martin, Nicholas G. (2010). The family history method in disordered gambling research: A comparison of reports obtained from discordant twin pairs. Twin Research and Human Genetics, 13 (4), 340-346. doi: 10.1375/twin.13.4.340

  • A versatile gene-based test for genome-wide association studies

    Liu, Jimmy Z., McRae, Allan F., Nyholt, Dale R., Medland, Sarah E., Wray, Naomi R., Brown, Kevin M., AMFS Investigators, Hayward, Nicholas K., Montgomery, Grant W., Visscher, Peter M., Martin, Nicholas G. and Macgregor, Stuart (2010). A versatile gene-based test for genome-wide association studies. American Journal of Human Genetics, 87 (1), 139-145. doi: 10.1016/j.ajhg.2010.06.009

  • Common SNPs explain a large proportion of the heritability for human height

    Yang, Jian, Benyamin, Beben, McEvoy, Brian P., Gordon, Scott, Henders, Anjali K., Nyholt, Dale R., Madden, Pamela A., Heath, Andrew C., Martin, Nicholas G., Montgomery, Grant W., Goddard, Michael E. and Visscher, Peter M. (2010). Common SNPs explain a large proportion of the heritability for human height. Nature Genetics, 42 (7), 565-569. doi: 10.1038/ng.608

  • Genome-wide association identifies ATOH7 as a major gene determining human optic disc size

    Macgregor, Stuart, Hewitt, Alex W., Hysi, Pirro G., Ruddle, Jonathan B., Medland, Sarah E., Henders, Anjali K., Gordon, Scott D., Andrew, Toby, McEvoy, Brian, Sanfilippo, Paul G., Carbonaro, Francis, Tah, Vikas, Li, Yi Ju, Bennett, Sonya L., Craig, Jamie E., Montgomery, Grant W., Tran-Viet, Khanh-Nhat, Brown, Nadean L., Spector, Timothy D., Martin, Nicholas G., Young, Terri L., Hammond, Christopher J. and Mackey, David A. (2010). Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. Human Molecular Genetics, 19 (13) ddq144, 2716-2724. doi: 10.1093/hmg/ddq144

  • IRF4 variants have age-specific effects on nevus count and predispose to melanoma

    Duffy, David L., Iles, Mark M., Glass, Dan, Zhu, Gu, Barrett, Jennifer H., Hoiom, Veronica, Zhao, Zhen Z., Sturm, Richard A., Soranzo, Nicole, Hammond, Chris, Kvaskoff, Marina, Whiteman, David C., Mangino, Massimo, Hansson, Johan, Newton-Bishop, Julia A., Bataille, Veronique, Hayward, Nicholas K., Martin, Nicholas G., Bishop, D. Timothy, Spector, Timothy D. and Montgomery, Grant W. (2010). IRF4 variants have age-specific effects on nevus count and predispose to melanoma. American Journal of Human Genetics, 87 (1), 6-16. doi: 10.1016/j.ajhg.2010.05.017

  • Not by twins alone: Using the extended family design to investigate genetic influence on political beliefs

    Hatemi, Peter K., Hibbing, John R., Medland, Sarah E., Keller, Matthew C., Alford, John R., Smith, Kevin B., Martin, Nicholas G. and Eaves, Lindon J. (2010). Not by twins alone: Using the extended family design to investigate genetic influence on political beliefs. American Journal of Political Science, 54 (3), 798-814. doi: 10.1111/j.1540-5907.2010.00461.x

  • A genetic basis for social trust?

    Sturgis, Patrick, Read, Sanna, Hatemi, Peter K., Zhu, Gu, Trull, Tim, Wright, Margaret J. and Martin, Nicholas G. (2010). A genetic basis for social trust?. Political Behavior, 32 (2), 205-230. doi: 10.1007/s11109-009-9101-5

  • A genome wide linkage scan for dizygotic twinning in 525 families of mothers of dizygotic twins

    Painter, Jodie N., Willemsen, Gonneke, Nyholt, Dale, Hoekstra, Chantal, Duffy, David L., Henders, Anjali K., Wallace, Leanne, Healey, Sue, Cannon-Albright, Lisa A., Skolnick, Mark, Martin, Nicholas G., Boomsma, Dorret I. and Montgomery, Grant W. (2010). A genome wide linkage scan for dizygotic twinning in 525 families of mothers of dizygotic twins. Human Reproduction, 25 (6), 1569-1580. doi: 10.1093/humrep/deq084

  • Dyslexia and DCDC2: Normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample

    Lind, Penelope A., Luciano, Michelle, Wright, Margaret J., Montgomery, Grant W., Martin, Nicholas G. and Bates, Timothy C. (2010). Dyslexia and DCDC2: Normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample. European Journal of Human Genetics, 18 (6), 668-673. doi: 10.1038/ejhg.2009.237

  • Genetic and environmental influences on disordered gambling in men and women

    Slutske, Wendy S., Zhu, Gu, Meier, Madeline H. and Martin, Nicholas G. (2010). Genetic and environmental influences on disordered gambling in men and women. Archives of General Psychiatry, 67 (6), 624-630. doi: 10.1001/archgenpsychiatry.2010.51

  • Genetic effects on toxic and essential elements in humans: Arsenic, cadmium, copper, lead, mercury, selenium, and zinc in erythrocytes

    Whitfield, John B., Dy, Veronica, McQuilty, Robert, Zhu, Gu, Heath, Andrew C., Montgomery, Grant W. and Martin, Nicholas G. (2010). Genetic effects on toxic and essential elements in humans: Arsenic, cadmium, copper, lead, mercury, selenium, and zinc in erythrocytes. Environmental Health Perspectives, 118 (6), 776-782. doi: 10.1289/ehp.0901541

  • The reliability and validity of the family history method for assessing pathological gambling and gambling involvement

    Ellingson, Jarrod M., Slutske, Wendy S. and Martin, Nicholas G. (2010). The reliability and validity of the family history method for assessing pathological gambling and gambling involvement. Psychology of Addictive Behaviors, 24 (2), 292-299. doi: 10.1037/a0018126

  • Common genetic variants near the brittle cornea syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness

    Lu, Yi, Dimasi, David P., Hysi, Pirro G., Hewitt, Alex W., Burdon, Kathryn P., Toh, Tze'Yo, Ruddle, Jonathan B., Li, Yi Ju, Mitchell, Paul, Healey, Paul R., Montgomery, Grant W., Hansell, Narelle, Spector, Timothy D., Martin, Nicholas G., Young, Terri L., Hammond. Christopher J., Macgregor, Stuart, Craig, Jamie E. and Mackey, David A. (2010). Common genetic variants near the brittle cornea syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness. PLoS Genetics, 6 (5), e1000947.1-e1000947.10. doi: 10.1371/journal.pgen.1000947

  • Digital quantification of human eye color highlights genetic association of three new loci

    Liu, Fan, Wollstein, Andreas, Hysi, Pirro G., Ankra-Badu, Georgina A., Spector, Timothy D., Park, Daniel, Zhu, Gu, Larsson, Mats, Duffy, David L., Montgomery, Grant W., Mackey, David A., Walsh, Susan, Lao, Oscar, Hofman, Albert, Rivadeneira, Fernando, Vingerling, Johannes R., Uitterlinden, Andrew G., Martin, Nicholas G., Hammond, Christopher J. and Kayser, Manfred (2010). Digital quantification of human eye color highlights genetic association of three new loci. PLoS Genetics, 6 (5), e1000934-1-e1000934-15. doi: 10.1371/journal.pgen.1000934

  • Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior

    Thorgeirsson, Thorgeir E., Gudbjartsson, Daniel F., Surakka, Ida, Vink, Jacqueline M., Amin, Najaf, Geller, Frank, Sulem, Patrick, Rafnar, Thorunn, Esko, Tōnu, Walter, Stefan, Gieger, Christian, Rawal, Rajesh, Mangino, Massimo, Prokopenko, Inga, Mägi, Reedik, Keskitalo, Kaisu, Gudjonsdottir, Iris H., Gretarsdottir, Solveig, Stefansson, Hreinn, Thompson, John R., Aulchenko, Yurii S., Nelis, Mari, Aben, Katja K., den Heijer, Martin, Dirksen, Asger, Ashraf, Haseem, Soranzo, Nicole, Valdes, Ana M., Steves, Claire ... Stefansson, Kari (2010). Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior. Nature Genetics, 42 (5), 448-454. doi: 10.1038/ng.573

  • A variant in LIN28B is Associated with 2D:4D finger-length ratio, a putative retrospective biomarker of prenatal testosterone exposure

    Medland, Sarah E., Zayats,Tetyana, Glaser, Beate, Nyholt, Dale R., Gordon,Scott D., Wright, Margaret J., Montgomery, Grant W., Campbell, Megan J., Henders, Anjali K., Timpson, Nicholas J., Peltonen, Leena, Wolke, Dieter, Ring, Susan M., Deloukas, Panos, Martin, Nicholas G., Smith, George Davey and Evans, David M. (2010). A variant in LIN28B is Associated with 2D:4D finger-length ratio, a putative retrospective biomarker of prenatal testosterone exposure. American Journal of Human Genetics, 86 (4), 519-525. doi: 10.1016/j.ajhg.2010.02.017

  • A Family Study of Adult Twins with and without a History of Childhood Abuse: Stability of Retrospective Reports of Maltreatment and Associated Family Measures

    Nelson, Elliot C., Lynskey, Michael T., Heath, Andrew C., Madden, Pamela A. F. and Martin, Nicholas G. (2010). A Family Study of Adult Twins with and without a History of Childhood Abuse: Stability of Retrospective Reports of Maltreatment and Associated Family Measures. Twin Research and Human Genetics, 13 (2), 121-130. doi: 10.1375/twin.13.2.121

  • Genome-wide association study of height and body mass index in Australian twin families

    Liu, Jimmy Z., Medland, Sarah E., Wright, Margaret J., Henders, Anjali K., Heath, Andrew C., Madden, Pamela A. F., Duncan, Alexis, Montgomery, Grant W., Martin, Nicholas G. and McRae, Allan F. (2010). Genome-wide association study of height and body mass index in Australian twin families. Twin Research And Human Genetics, 13 (2), 179-193. doi: 10.1375/twin.13.2.179

  • Characterization of the methylation patterns of MS4A2 in atopic cases and controls

    M. A. R. Ferreira, N. A. Oates, J. van Vliet, Z. Z. Zhao, M. Ehrich, N. G. Martin, G. W. Montgomery, E. Whitelaw and D. L. Duffy (2010). Characterization of the methylation patterns of MS4A2 in atopic cases and controls. ALLERGY, 65 (3), 333-337. doi: 10.1111/j.1398-9995.2009.02135.x

  • Common genetic contributions to alcohol and cannabis use and dependence symptomatology

    Sartor, Carolyn E., Grant, Julia D., Bucholz, Kathleen K., Madden, Pamela A. F., Heath, Andrew C., Agrawal, Arpana, Whitfield, John B., Statham, Dixie J., Martin, Nicholas G. and Lynkey, Michael T. (2010). Common genetic contributions to alcohol and cannabis use and dependence symptomatology. Alcoholism: Clinical and Experimental Research, 34 (3), 545-554. doi: 10.1111/j.1530-0277.2009.01120.x

  • Genetic and environmental influences on cannabis use initiation and problematic use: A meta-analysis of twin studies

    Verweij, Karin J. H., Zietsch, Brendan P., Lynskey, Michael T., Medland, Sarah E., Neale, Michael C., Martin, Nicholas G., Boomsma, Dorret I. and Vink, Jacqueline M. (2010). Genetic and environmental influences on cannabis use initiation and problematic use: A meta-analysis of twin studies. Addiction, 105 (3), 417-430. doi: 10.1111/j.1360-0443.2009.02831.x

  • A genomewide association study of nicotine and alcohol dependence in Australian and Dutch populations

    Lind, Penelope A., Macgregor, Stuart, Vink, Jacqueline M., Pergadia, Michele L., Hansell, Narelle K., de Moor, Marleen H. M., Smit, August B., Hottenga, Jouke-Jan, Richter, Melinda M., Heath, Andrew C., Martin, Nicholas G., Willemsen, Gonneke, de Geus, Eco J. C., Vogelzangs,Nicole, Penninx, Brenda W., Whitfield, John B., Montgomery, Grant W., Boomsma, Dorret I. and Madden, Pamela A. F. (2010). A genomewide association study of nicotine and alcohol dependence in Australian and Dutch populations. Twin Research And Human Genetics, 13 (1), 10-29. doi: 10.1375/twin.13.1.10

  • Clustering of trauma and associations with single and co-occurring depression and panic attack over twenty years

    McCutcheon, Vivia V., Heath, Andrew C., Nelson, Elliot C., Bucholz, Kathleen K., Madden, Pamela A. F. and Martin, Nicholas G. (2010). Clustering of trauma and associations with single and co-occurring depression and panic attack over twenty years. Twin Research And Human Genetics, 13 (1), 57-65. doi: 10.1375/twin.13.1.57

  • Genetic contribution to individual variation in binocular rivalry rate

    Miller, Steven M., Hansell, Narelle K., Ngo, Trung T., Liu, Guang B., Pettigrew, John D., Martin, Nicholas G. and Wright, Margaret J. (2010). Genetic contribution to individual variation in binocular rivalry rate. Proceedings of the National Academy of Sciences of the United States of America, 107 (6), 2664-2668. doi: 10.1073/pnas.0912149107

  • Multiple pigmentation gene polymorphisms account for a substantial proportion of risk of cutaneous malignant melanoma

    Duffy, David L., Zhao, Zhen Z., Sturm, Richard A., Hayward, Nicholas K., Martin, Nicholas G. and Montgomery, Grant W. (2010). Multiple pigmentation gene polymorphisms account for a substantial proportion of risk of cutaneous malignant melanoma. Journal of Investigative Dermatology, 130 (2), 520-528. doi: 10.1038/jid.2009.258

  • Quantitative trait loci for CD4:CD8 lymphocyte ratio are associated with risk of type 1 diabetes and HIV-1 immune control

    Ferreira, Mar, Mangino, M, Brumme, CJ, Zhao, ZZ, Medland, SE, Wright, MJ, Nyholt, DR, Gordon, S, Campbell, M, McEvoy, BP, Henders, A, Evans, DM, Lanchbury, JS, Pereyra, F, Walker, BD, Haas, DW, Soranzo, N, Spector, TD, de Bakker, PIW, Frazer, IH, Montgomery, GW, Martin, NG and Int HIV Controllers Study (2010). Quantitative trait loci for CD4:CD8 lymphocyte ratio are associated with risk of type 1 diabetes and HIV-1 immune control. American Journal of Human Genetics, 86 (1), 88-92. doi: 10.1016/j.ajhg.2009.12.008

  • Does education reduce the probability of being overweight?

    Webbink, Dinand, Martin, Nicholas G. and Visscher, Peter M. (2010). Does education reduce the probability of being overweight?. Journal of Health Economics, 29 (1), 29-38. doi: 10.1016/j.jhealeco.2009.11.013

  • Genetic and Environmental Influences on Sexual Orientation

    Dawood, Khytam, Bailey, J. Michael and Martin, Nicholas G. (2010). Genetic and Environmental Influences on Sexual Orientation. Handbook of Behavior Genetics, 269-279. doi: 10.1007/978-0-387-76727-7_19

  • Genetic and environmental influences on risky sexual behaviour and its relationship with personality

    Zietsch, B. P., Verweij, K. J. H., Bailey, J. M., Wright, M. J. and Martin, N. G. (2010). Genetic and environmental influences on risky sexual behaviour and its relationship with personality. Behavior Genetics, 40 (1), 12-21. doi: 10.1007/s10519-009-9300-1

  • H2 haplotype at chromosome 17q21.31 protects against childhood sexual abuse-associated risk for alcohol consumption and dependence

    Nelson, Elliot C., Agrawal, Arpana, Pergadia, Michele L., Wang, Jen C., Whitfield, John B., Saccone, F. Scott, Kern, Jason, Grant, Julia D., Schrage, Andrew J., Rice, John P., Montgomery, Grant W., Heath, Andrew C, Goate, Alison M., Martin, Nicholas G. and Madden, Pamela A. F. (2010). H2 haplotype at chromosome 17q21.31 protects against childhood sexual abuse-associated risk for alcohol consumption and dependence. Addiction Biology, 15 (1), 1-11. doi: 10.1111/j.1369-1600.2009.00181.x

  • Linkage analysis of alcohol dependence symptoms in the community

    Hansell, Narelle K., Agrawal, Arpana, Whitfield, John B., Morley, Katherine I., Gordon, Scott D., Lind, Penelope A., Pergadia, Michele L., Montgomery, Grant W., Madden, Pamela A. F., Todd, Richard D., Heath, Andrew C. and Martin, Nicholas G. (2010). Linkage analysis of alcohol dependence symptoms in the community. Alcoholism: Clinical and Experimental Research, 34 (1), 158-163. doi: 10.1111/j.1530-0277.2009.01077.x

  • Meta-analysis of 20 genome-wide linkage studies evidenced new regions linked to asthma and atopy

    Bouzigon, Emmanuelle, Forabosco, Paola, Koppelman, Gerard H., Cookson, William O. C. M., Dizier, Marie-Helene, Duffy, David L., Evans, David M., Ferreira, Manuel A. R., Kere, Juha, Laitinen, Tarja, Malerba, Giovanni, Meyers, Deborah A., Moffatt, Miriam, Martin, Nicholas G, Ng, Mandy Y., Pignatti, Pier Franco, Wjst, Mathias, Kauffmann, Francine, Demenais, Florence and Lewis, Cathryn M. (2010). Meta-analysis of 20 genome-wide linkage studies evidenced new regions linked to asthma and atopy. European Journal of Human Genetics, 18 (6), 700-706. doi: 10.1038/ejhg.2009.224

  • The Five-Factor Model of Personality and Borderline Personality Disorder: A Genetic Analysis of Comorbidity

    Marijn A. Distel, Timothy J. Trull, Gonneke Willemsen, Jacqueline M. Vink, Catherine A. Derom, Michael Lynskey, Nicholas G. Martin and Dorret I. Boomsm (2009). The Five-Factor Model of Personality and Borderline Personality Disorder: A Genetic Analysis of Comorbidity. BIOLOGICAL PSYCHIATRY, 66 (12), 1131-1138. doi: 10.1016/j.biopsych.2009.07.017

  • A comprehensive neuropsychiatric study of elderly twins: The Older Australian Twins Study

    Sachdev, Perminder S., Lammel, Andrea, Trollor, Julian N., Lee, Teresa, Wright, Margaret J., Ames, David, Wen, Wei, Martin, Nicholas G., Brodaty, Henry, Schofield, Peter R. and OATS Research Team (2009). A comprehensive neuropsychiatric study of elderly twins: The Older Australian Twins Study. Twin Research and Human Genetics, 12 (6), 573-582. doi: 10.1375/twin.12.6.573

  • Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans

    Medland, S, Nyholt, D, Painter, JN, McEnvoy, BP, Allan McRae, Zhu, G, Gordon, SD, Ferreira, MAR, Wright, MJ, Henders, AK, Campbell MJ, Duffy, D, Hansell, N K, Macgregor, S, Slutske, WS, Heath, AC, Montgomery, GW and Martin, NG (2009). Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans. American Journal of Human Genetics, 85 (5), 750-755. doi: 10.1016/j.ajhg.2009.10.009

  • Do 5HTTLPR and stress interact in risk for depression and suicidality? Item response analyses of a large sample

    William L. Coventry, Michael R. James, Lindon J. Eaves, Scott D. Gordon, Nathan A. Gillespie, Leanne Ryan, Andrew C. Heath, Grant W. Montgomery, Nicholas G. Martin and Naomi R. Wray (2009). Do 5HTTLPR and stress interact in risk for depression and suicidality? Item response analyses of a large sample. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 153b (3), 757-765. doi: 10.1002/ajmg.b.31044

  • Common variants in TMPRSS6 are associated with iron status and erythrocyte volume

    Benyamin, B, Ferreira, MAR, Willemsen, G, Gordon, S, Middelberg, RPS, McEvoy, BP, Hottenga, JJ, Henders, AK, Campbell, MJ, Wallace, L, Frazer, IH, Heath, AC, de Geus, EJC, Nyholt, DR, Visscher, PM, Penninx, BW, Boomsma, DI, Martin, NG, Montgomery, GW and Whitfield, JB (2009). Common variants in TMPRSS6 are associated with iron status and erythrocyte volume. Nature Genetics, 41 (11), 1173-1175. doi: 10.1038/ng.456

  • Genetic and environmental influences on optimism and its relationship to mental and self-rated health: A study of aging twins

    Mosing, Miriam A., Zietsch, Brendan P., Shekar, Sri N., Wright, Margaret J. and Martin, Nicholas G. (2009). Genetic and environmental influences on optimism and its relationship to mental and self-rated health: A study of aging twins. Behavior Genetics, 39 (6), 597-604. doi: 10.1007/s10519-009-9287-7

  • Sequence Variants in Three Loci Influence Monocyte Counts and Erythrocyte Volume

    Ferreira, MAR, Hottenga, JJ, Warrington, NM, Medland, SE, Willemsen, G, Lawrence, RW, Gordon, S, de Geus, EJC, Henders, AK, Smit, JH, Campbell, MJ, Wallace, L, Evans, DM, Wright, MJ, Nyholt, DR, James, AL, Beilby, JP, Penninx, BW, Palmer, LJ, Frazer, IH, Montgomery, GW, Martin, NG and Boomsma, DI (2009). Sequence Variants in Three Loci Influence Monocyte Counts and Erythrocyte Volume. AMERICAN JOURNAL OF HUMAN GENETICS, 85 (5), 745-749. doi: 10.1016/j.ajhg.2009.10.005

  • Alcohol consumption indices of genetic risk for alcohol dependence

    Julia D. Grant, Arpana Agrawal, Kathleen K. Bucholz, Pamela A.F. Madden, Michele L. Pergadia, Elliot C. Nelson, Michael T. Lynskey, Richard D. Todd, Alexandre A. Todorov, Narelle K. Hansell, John B. Whitfield, Nicholas G. Martin and Andrew C. Heath (2009). Alcohol consumption indices of genetic risk for alcohol dependence. Biological Psychiatry, 66 (8), 795-800. doi: 10.1016/j.biopsych.2009.05.018

  • Association and interaction analyses of eight genes under asthma linkage peaks

    Ferreira, M. A. R., Zhao, Z. Z., Thomsen, S. F., James, M., Evans, D. M., Postmus, P. E., Kyvik, K. O., Backer, V., Boomsma, D. I., Martin, N. G., Montgomery, G. W. and Duffy, D. L. (2009). Association and interaction analyses of eight genes under asthma linkage peaks. Allergy, 64 (11), 1623-1628. doi: 10.1111/j.1398-9995.2009.02091.x

  • Estimating the Heritability of Hair Curliness in Twins of European Ancestry

    Sarah E. Medland, Gu Zhu and Nicholas G. Martin (2009). Estimating the Heritability of Hair Curliness in Twins of European Ancestry. Twin Research and Human Genetics, 12 (5), 514-518. doi: 10.1375/twin.12.5.514

  • Parental Alcoholism and Offspring Behavior Problems: Findings in Australian Children of Twins

    Mary Waldron, Nicholas G. Martin and Andrew C. Heath (2009). Parental Alcoholism and Offspring Behavior Problems: Findings in Australian Children of Twins. Twin Research and Human Genetics, 12 (5), 433-440. doi: 10.1375/twin.12.5.433

  • Quantitative Genetic Analysis of the Retinal Vascular Caliber: The Australian Twins Eye Study

    Sun, Cong, Zhu, Gu, Wong, Tien Y, Hewitt, Alex W, Ruddle, Jonathan B, Hodgson, Lauren, Montgomery, Grant W, Young, Terri L, Hammond, Christopher J, Craig, Jamie E, Martin, Nicholas G, He, Mingguang and Mackey, David A. (2009). Quantitative Genetic Analysis of the Retinal Vascular Caliber: The Australian Twins Eye Study. Hypertension, 54 (4), 788-795. doi: 10.1161/HYPERTENSIONAHA.109.132902

  • Sex Differences in the Rates of Recovery, Treatment-Seeking, and Natural Recovery in Pathological Gambling: Results From an Australian Community-Based Twin Survey

    Wendy S. Slutske, Alex Blaszczynski and Nicholas G. Martin (2009). Sex Differences in the Rates of Recovery, Treatment-Seeking, and Natural Recovery in Pathological Gambling: Results From an Australian Community-Based Twin Survey. Twin Research and Human Genetics, 12 (5), 425-432. doi: 10.1375/twin.12.5.425

  • Twins Eye Study in Tasmania (TEST): Rationale and Methodology to Recruit and Examine Twins

    David A. Mackey, Jane R. MacKinnon, Shayne A. Brown, Lisa S. Kearns, Jonathan B. Ruddle, Paul G. Sanfilippo, Cong Sun, Christopher J. Hammond, Terri L. Young, Nicholas G. Martin and Alex W. Hewitt (2009). Twins Eye Study in Tasmania (TEST): Rationale and Methodology to Recruit and Examine Twins. Twin Research and Human Genetics, 12 (5), 441-454. doi: 10.1375/twin.12.5.441

  • Evidence for an Interaction Between Age at First Drink and Genetic Influences on DSM-IV Alcohol Dependence Symptoms

    Arpana Agrawal, Carolyn E. Sartor, Michael T. Lynskey, Julia D. Grant, Michele L. Pergadia, Richard Grucza, Kathleen K. Bucholz, Elliot C. Nelson, Pamela A. F. Madden, Nicholas G. Martin and Andrew C. Heath (2009). Evidence for an Interaction Between Age at First Drink and Genetic Influences on DSM-IV Alcohol Dependence Symptoms. Alcoholism: Clinical and Experimental Research, 33 (12), 2047-2056. doi: 10.1111/j.1530-0277.2009.01044.x

  • Family-based mitochondrial association study of traits related to type 2 diabetes and the metabolic syndrome in adolescents

    E. M. Byrne, A. F. McRae, D. L. Duffy, Z. Z. Zhao, N. G. Martin, J. B. Whitfield, P. M. Visscher and G. W. Montgomery (2009). Family-based mitochondrial association study of traits related to type 2 diabetes and the metabolic syndrome in adolescents. Diabetologia, 52 (11), 2359-2368. doi: 10.1007/s00125-009-1510-9

  • A Population-Based Study of Australian Twins with Melanoma Suggests a Strong Genetic Contribution to Liability

    Shekar, SN, Duffy, DL, Youl, P, Baxter, AJ, Kvaskoff, M, Whiteman, DC, Green, AC, Hughes, MC, Hayward, NK, Coates, M and Martin, NG (2009). A Population-Based Study of Australian Twins with Melanoma Suggests a Strong Genetic Contribution to Liability. Journal of Investigative Dermatology, 129 (9), 2211-2219. doi: 10.1038/jid.2009.48

  • Accurate, Large-Scale Genotyping of 5HTTLPR and Flanking Single Nucleotide Polymorphisms in an Association Study of Depression, Anxiety, and Personality Measures

    Naomi R. Wray, Michael R. James, Scott D. Gordon, Troy Dumenil, Leanne Ryan, William L. Coventry, Dixie J. Statham, Michele L. Pergadia, Pamela A.F. Madden, Andrew C. Heath, Grant W. Montgomery and Nicholas G. Martin (2009). Accurate, Large-Scale Genotyping of 5HTTLPR and Flanking Single Nucleotide Polymorphisms in an Association Study of Depression, Anxiety, and Personality Measures. Biological Psychiatry, 66 (5), 468-476. doi: 10.1016/j.biopsych.2009.04.030

  • Association Study of Common Mitochondrial Variants and Cognitive Ability

    Byrne, EM, McRae, AF, Duffy, DL, Zhao, ZZ, Martin, NG, Wright, MJ, Montgomery, GW and Visscher, PM (2009). Association Study of Common Mitochondrial Variants and Cognitive Ability. BEHAVIOR GENETICS, 39 (5), 504-512. doi: 10.1007/s10519-009-9276-x

  • Is There a "Party" in Your Genes?

    Hatemi, Peter K., Alford, John R., Hibbing, John R., Martin, Nicholas G. and Eaves, Lindon J. (2009). Is There a "Party" in Your Genes?. Political Research Quarterly, 62 (3), 584-600. doi: 10.1177/1065912908327606

  • Multicenter dizygotic twin cohort study confirms two linkage susceptibility loci for body mass index at 3q29 and 7q36 and identifies three further potential novel loci

    J Kettunen, M Perola, N G Martin, B K Cornes, S G Wilson, G W Montgomery, B Benyamin, J R Harris, D Boomsma, G Willemsen, J-J Hottenga, P E Slagboom, K Christensen, K O Kyvik, T I A Sørensen, N L Pedersen, P K E Magnusson, T Andrew, T D Spector, E Widen, K Silventoinen, J Kaprio, A Palotie and L Peltonen (2009). Multicenter dizygotic twin cohort study confirms two linkage susceptibility loci for body mass index at 3q29 and 7q36 and identifies three further potential novel loci. International Journal of Obesity, 33 (11), 1235-1242. doi: 10.1038/ijo.2009.168

  • Smoking and Illicit Drug Use Associations With Early Versus Delayed Reproduction: Findings in a Young Adult Cohort of Australian Twins

    Mary Waldron, , , ,, ,, Andrew C. Heath, Michael T. Lynskey, Elliot C. Nelson, Kathleen K. Bucholz, Pamela A.F. Madden and Nicholas G. Martin (2009). Smoking and Illicit Drug Use Associations With Early Versus Delayed Reproduction: Findings in a Young Adult Cohort of Australian Twins. Journal of Studies on Alcohol and Drugs, 70 (5), 786-796. doi: 10.15288/jsad.2009.70.786

  • Timing of first alcohol use and alcohol dependence: evidence of common genetic influences

    Carolyn E. Sartor, Michael T. Lynskey, Kathleen K. Bucholz, Pamela A. F. Madden, Nicholas G. Martin and Andrew C. Heath (2009). Timing of first alcohol use and alcohol dependence: evidence of common genetic influences. Addiction, 104 (9), 1512-1518. doi: 10.1111/j.1360-0443.2009.02648.x

  • Non-pathological paternal isodisomy of chromosome 2 detected from a genome-wide SNP scan.

    Matthew C. Keller, Allan F. McRae, Julie M. McGaughran, Peter M. Visscher, Nicholas G. Martin and Grant W. Montgomery (2009). Non-pathological paternal isodisomy of chromosome 2 detected from a genome-wide SNP scan.. American Journal of Medical Genetics. Part A, 149A (8), 1823-1826. doi: 10.1002/ajmg.a.32973

  • Genome-wide association study identifies three loci associated with melanoma risk

    Bishop, DT, Demenais, F, Iles, MM, Harland, M, Taylor, JC, Corda, E, Randerson-Moor, J, Aitken, JF, Avril, MF, Azizi, E, Bakker, B, Bianchi-Scarra, G, Bressac-de Paillerets, B, Calista, D, Cannon-Albright, LA, Chin-A-Woeng, T, Debniak, T, Galore-Haskel, G, Ghiorzo, P, Gut, I, Hansson, J, Hocevar, M, Hoiom, V, Hopper, JL, Ingvar, C, Kanetsky, PA, Kefford, RF, Landi, MT, Lang, J ... Bishop, JAN (2009). Genome-wide association study identifies three loci associated with melanoma risk. Nature Genetics, 41 (8), 920-925. doi: 10.1038/ng.411

  • Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi

    Falchi, M, Bataille, V, Hayward, NK, Duffy, DL, Bishop, JAN, Pastinen, T, Cervino, A, Zhao, ZZ, Deloukas, P, Soranzo, N, Elder, DE, Barrett, JH, Martin, NG, Bishop, DT, Montgomery, GW and Spector, TD (2009). Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi. Nature Genetics, 41 (8), 915-919. doi: 10.1038/ng.410

  • A Twin Study of the Genetics of High Cognitive Ability Selected from 11,000 Twin Pairs in Six Studies from Four Countries

    Claire M. A. Haworth, Margaret J. Wright, Nicolas W. Martin, Nicholas G. Martin, Dorret I. Boomsma, Meike Bartels, Danielle Posthuma, Oliver S. P. Davis, Angela M. Brant, Robin P. Corley, John K. Hewitt, William G. Iacono, Matthew McGue, Lee A. Thompson, Sara A. Hart, Stephen A. Petrill, David Lubinski and Robert Plomin (2009). A Twin Study of the Genetics of High Cognitive Ability Selected from 11,000 Twin Pairs in Six Studies from Four Countries. Behavior Genetics, 39 (4), 359-370. doi: 10.1007/s10519-009-9262-3

  • Genetic and Environmental Transmission of Political Attitudes Over a Life Time

    Hatemi, Peter K., Funk, Carolyn L., Medland, Sarah E., Maes, Hermine M., Silberg, Judy L., Martin, Nicholas G. and Eaves, Lindon J. (2009). Genetic and Environmental Transmission of Political Attitudes Over a Life Time. Journal of Politics, 71 (3), 1141-1156. doi: 10.1017/S0022381609090938

  • Genetic covariation between the author recognition test and reading and verbal abilities: What can we learn from the analysis of high performance?

    Martin, Nicolas W., Hansell, Narelle K., Wainwright, Mark A., Shekar, Sri N., Medland, Sarah E., Bates, Timothy C., Burt, Jennifer S., Martin, Nicholas G. and Wright, Margaret J. (2009). Genetic covariation between the author recognition test and reading and verbal abilities: What can we learn from the analysis of high performance?. Behavior Genetics, 39 (4), 417-426. doi: 10.1007/s10519-009-9275-y

  • Genetic variation in female BMI increases with number of children born but failure to replicate association between GN beta 3 variants and increased BMI in parous females

    Cornes, Belinda K., Medland, Sarah E., Lind, Penelope A., Nyholt, Dale R., Montgomery, Grant W. and Martin, Nicholas G. (2009). Genetic variation in female BMI increases with number of children born but failure to replicate association between GN beta 3 variants and increased BMI in parous females. Twin Research and Human Genetics, 12 (3), 276-285. doi: 10.1375/twin.12.3.276

  • The Establishment of the GENEQOL Consortium to Investigate the Genetic Disposition of Patient-Reported Quality-of-Life Outcomes

    Sprangers, Mirjam A. G., Sloan, Jeff A., Veenhoven, Ruut, Cleeland, Charles S., Halyard, Michele Y., Abertnethy, Amy R., Baas, Frank, Barsevick, Andrea M., Bartels, Meike, Boomsma, Dorret I., Chauhan, Cynthia, Dueck, Amylou C., Frost, Marlene H., Hall, Per, Klepstad, Pal, Martin, Nicholas G., Miaskowski, Christine, Mosing, Miriam, Movsas, Benjamin, Van Noorden, Cornelis J. F., Patrick, Donald L., Pedersen, Nancy L., Ropka, Mary E., Shi, Quiling, Shinozaki, Gen, Singh, Jasvinder A., Yang, Ping and Zwinderman, Ailko H. (2009). The Establishment of the GENEQOL Consortium to Investigate the Genetic Disposition of Patient-Reported Quality-of-Life Outcomes. Twin Research and Human Genetics, 12 (3), 301-311. doi: 10.1375/twin.12.3.301

  • No Association Between Cholinergic Muscarinic Receptor 2 (CHRM2) Genetic Variation and Cognitive Abilities in Three Independent Samples

    Penelope A. Lind, Michelle Luciano, Michael A. Horan, Riccardo E. Marioni, Margaret J. Wright, Timothy C. Bates, Patrick Rabbitt, Sarah E. Harris, Yvonne Davidson, Ian J. Deary, Linda Gibbons, Andrew Pickles, William Ollier, Neil Pendleton, Jackie F. Price, Antony Payton and Nicholas G. Martin (2009). No Association Between Cholinergic Muscarinic Receptor 2 (CHRM2) Genetic Variation and Cognitive Abilities in Three Independent Samples. Behavior Genetics, 39 (5), 513-523. doi: 10.1007/s10519-009-9274-z

  • Geographical structure and differential natural selection among North European populations

    Brian P. McEvoy, Grant W. Montgomery, Allan F. McRae, Samuli Ripatti, Markus Perola, Tim D. Spector, Lynn Cherkas, Kourosh R. Ahmadi, Dorret Boomsma, Gonneke Willemsen, Jouke J. Hottenga, Nancy L. Pedersen, Patrik K.E. Magnusson, Kirsten Ohm Kyvik, Kaare Christensen, Jaakko Kaprio, Kauko Heikkilä, Aarno Palotie, Elisabeth Widen, Juha Muilu, Ann-Christine Syvänen, Ulrika Liljedahl, Orla Hardiman, Simon Cronin, Leena Peltonen, Nicholas G. Martin and Peter M. Visscher (2009). Geographical structure and differential natural selection among North European populations. Genome Research, 19 (5), 804-814. doi: 10.1101/gr.083394.108

  • Bayesian latent trait modeling of migraine symptom data

    Carla Chia Ming Chen, Jonathan M. Keith, Dale R. Nyholt, Nicholas G. Martin and Kerrie L. Mengersen (2009). Bayesian latent trait modeling of migraine symptom data. Human Genetics, 126 (2), 277-288. doi: 10.1007/s00439-009-0671-4

  • Familial Resemblance of Borderline Personality Disorder Features: Genetic or Cultural Transmission?

    Marijn A. Distel, Irene Rebollo-Mesa, Gonneke Willemsen, Catherine A. Derom, Timothy J. Trull, Nicholas G. Martin and Dorret I. Boomsma (2009). Familial Resemblance of Borderline Personality Disorder Features: Genetic or Cultural Transmission?. PLoS One, 4 (4) e5334, e5334. doi: 10.1371/journal.pone.0005334

  • Heritability and Linkage Analysis of Appendicitis Utilizing Age at Onset

    Christopher Oldmeadow, Kerrie Mengersen, Nicholas Martin and David L. Duffy (2009). Heritability and Linkage Analysis of Appendicitis Utilizing Age at Onset. Twin Research and Human Genetics, 12 (2), 150-157. doi: 10.1375/twin.12.2.150

  • Polymorphisms in the syntaxin 17 gene are not associated with human cutaneous malignant melanoma

    Zhao, ZZ, Duffy, DL, Thomas, SA, Martin, NG, Hayward, NK and Montgomery, GW (2009). Polymorphisms in the syntaxin 17 gene are not associated with human cutaneous malignant melanoma. Melanoma Research, 19 (2), 80-85. doi: 10.1097/CMR.0b013e328322fc45

  • Relative Finger Lengths, Sex Differences, and Psychological Traits

    Loehlin, JC, Medland, SE and Martin, NG (2009). Relative Finger Lengths, Sex Differences, and Psychological Traits. Archives of Sexual Behavior, 38 (2), 298-305. doi: 10.1007/s10508-007-9303-z

  • Linkage and heritability analysis of migraine symptom groupings: A comparison of three different clustering methods on twin data

    Chen, Carla C. M., Mengersen, Kerrie L., Keith, Jonathan M., Martin, Nicholas G. and Nyholt, Dale R. (2009). Linkage and heritability analysis of migraine symptom groupings: A comparison of three different clustering methods on twin data. Human Genetics, 125 (5-6), 591-604. doi: 10.1007/s00439-009-0652-7

  • Genome-wide Association Study of Smoking Initiation and Current Smoking

    Jacqueline M. Vink1, August B. Smit, Eco J.C. de Geus, Patrick Sullivan, Gonneke Willemsen, Jouke-Jan Hottenga, Johannes H. Smit, Witte J. Hoogendijk, Frans G. Zitman, Leena Peltonen, Jaakko Kaprio, Nancy L. Pedersen, Patrik K. Magnusson, Tim D. Spector, Kirsten Ohm Kyvik, Katherine I. Morley, Andrew C. Heath, Nicholas G. Martin, Rudi G.J. Westendorp, P. Eline Slagboom, Henning Tiemeier, Albert Hofman, Andre G. Uitterlinden, Yurii S. Aulchenko, Najaf Amin, Cornelia van Duijn, Brenda W. Penninx and Dorret I. Boomsma (2009). Genome-wide Association Study of Smoking Initiation and Current Smoking. American Journal of Human Genetics, 84 (3), 367-379. doi: 10.1016/j.ajhg.2009.02.001

  • The Role of Harsh Discipline in Explaining Sex Differences in Conduct Disorder: a Study of Opposite-Sex Twin Pairs

    Madeline H. Meier, Wendy S. Slutske, Andrew C. Heath and Nicholas G. Martin (2009). The Role of Harsh Discipline in Explaining Sex Differences in Conduct Disorder: a Study of Opposite-Sex Twin Pairs. Journal of Abnormal Child Psychology, 37 (5), 653-664. doi: 10.1007/s10802-009-9309-1

  • Further evidence for an association between the gamma-aminobutyric acid receptor A, subunit 4 genes on chromosome 4 and Fagerstrom test for nicotine dependence

    Agrawal, Arpana, Pergadia, Michele L., Balasubramanian, Sumitra, Saccone, Scott F., Hinrichs, Anthony L., Saccone, Nancy L., Breslau, Naomi, Johnson, Eric O., Hatsukami, Dorothy, Martin, Nicholas G., Montgomery, Grant W., Goate, Alison M., Rice, John P., Bierut, Laura J. and Madden, Pamela A.F. (2009). Further evidence for an association between the gamma-aminobutyric acid receptor A, subunit 4 genes on chromosome 4 and Fagerstrom test for nicotine dependence. Addiction, 104 (3), 471-477. doi: 10.1111/j.1360-0443.2008.02445.x

  • Association of childhood trauma exposure and GABRA2 polymorphisms with risk of posttraumatic stress disorder in adults

    Nelson, E. C., Agrawal, A., Pergadia, M. L., Lynskey, M. T., Todorov, A. A., Wang, J. C., Todd, R. D., Martin, N. G., Heath, A. C., Goate, A. M., Montgomery, G. W. and Madden, P. A. F. (2009). Association of childhood trauma exposure and GABRA2 polymorphisms with risk of posttraumatic stress disorder in adults. Molecular Psychiatry, 14 (3), 234-235. doi: 10.1038/mp.2008.81

  • Variation in the dysbindin gene and normal cognitive function in three independent population samples

    M. Luciano, F. Miyajima, P. A. Lind, T. C. Bates, M. Horan, S. E. Harris, M. J. Wright, W. E. Ollier, C. Hayward, N. Pendleton, A. J. Gow, P. M. Visscher, J. M. Starr, I. J. Deary, N. G. Martin and A. Payton (2009). Variation in the dysbindin gene and normal cognitive function in three independent population samples. Genes, Brain and Behavior, 8 (2), 218-227. doi: 10.1111/j.1601-183X.2008.00462.x

  • An examination of the overlap between genetic and environmental risk factors for intentional weight loss and overeating

    Tracey D. Wade, Susan A. Treloar, Andrew C. Heath and Nicholas G. Martin (2009). An examination of the overlap between genetic and environmental risk factors for intentional weight loss and overeating. International Journal of Eating Disorders, 42 (6), 492-497. doi: 10.1002/eat.20668

  • ADH single nucleotide polymorphism associations with alcohol metabolism in vivo

    Andrew J. Birley, Michael R. James, Peter A. Dickson, Grant W. Montgomery, Andrew C. Heath, Nicholas G. Martin and John B. Whitfield (2009). ADH single nucleotide polymorphism associations with alcohol metabolism in vivo. Human Molecular Genetics, 18 (8), 1533-1542. doi: 10.1093/hmg/ddp060

  • Associations of ADH and ALDH2 gene variation with self report alcohol reactions, consumption and dependence: an integrated analysis

    Stuart Macgregor, Penelope A. Lind, Kathleen K. Bucholz, Narelle K. Hansell, Pamela A.F. Madden, Melinda M. Richter, Grant W. Montgomery, Nicholas G. Martin, Andrew C. Heath and John B. Whitfield (2009). Associations of ADH and ALDH2 gene variation with self report alcohol reactions, consumption and dependence: an integrated analysis. Human Molecular Genetics, 18 (3), 580-593. doi: 10.1093/hmg/ddn372

  • Common genetic influences underlie comorbidity of migraine and endometriosis

    Nyholt, Dale R., Gillespie, Nathan G., Merikangas, Kathleen R., Treloar, Susan A., Martin, Nicholas G. and Montgomery, Grant W. (2009). Common genetic influences underlie comorbidity of migraine and endometriosis. Genetic Epidemiology, 33 (2), 105-113. doi: 10.1002/gepi.20361

  • Flexible Mx Specification of Various Extended Twin Kinship Designs

    Hermine H. Maes, Michael C. Neale, Sarah E. Medland, Matthew C. Keller, Nicholas G. Martin, Andrew C. Heath and Lindon J. Eaves (2009). Flexible Mx Specification of Various Extended Twin Kinship Designs. Twin Research and Human Genetics, 12 (1), 26-34. doi: 10.1375/twin.12.1.26

  • Shared aetiology of risky sexual behaviour and adolescent misconduct : Genetic and environmental influences

    Verweij, K. J. H., Zietsch, B. P., Bailey, J. M. and Martin, N. G. (2009). Shared aetiology of risky sexual behaviour and adolescent misconduct : Genetic and environmental influences. Genes, Brain And Behavior, 8 (1), 107-113. doi: 10.1111/j.1601-183X.2008.00456.x

  • The Australian twin study of gambling (OZ-GAM): Rationale, sample description, predictors of participation, and a first look at sources of individual differences in gambling involvement

    Wendy S. Slutske, Madeline H. Meier, Gu Zhu, Dixie J. Statham, Alex Blaszczynski and Nicholas G. Martin (2009). The Australian twin study of gambling (OZ-GAM): Rationale, sample description, predictors of participation, and a first look at sources of individual differences in gambling involvement. Twin Research and Human Genetics, 12 (1), 63-78. doi: 10.1375/twin.12.1.63

  • Genetic linkage findings for DSM-IV nicotine withdrawal in two populations

    Michele L. Pergadia, Arpana Agrawal, Anu Loukola, Grant W. Montgomery, Ulla Broms, Scott F. Saccone, Jen C. Wang, Alexandre A. Todorov, Kauko Heikkilä, Dixie J. Statham, Anjali K. Henders, Megan J. Campbell, John P. Rice, Richard D. Todd, Andrew C. Heath, Alison M. Goate, Leena Peltonen, Jaakko Kaprio, Nicholas G. Martin and Pamela A.F. Madden (2009). Genetic linkage findings for DSM-IV nicotine withdrawal in two populations. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 150b (7), 950-959. doi: 10.1002/ajmg.b.30924

  • Can We Identify Genes For Alcohol Consumption In Samples Ascertained For Heterogeneous Purposes?

    Narelle K. Hansell, Arpana Agrawal, John B. Whitfield, Katherine I. Morley, Scott D. Gordon, Penelope A. Lind, Michele L. Pergadia, Grant W. Montgomery, Pamela A. F. Madden, Richard D. Todd, Andrew C. Heath and Nicholas G. Martin (2009). Can We Identify Genes For Alcohol Consumption In Samples Ascertained For Heterogeneous Purposes?. Alcoholism: Clinical and Experimental Research, 33 (4), 729-739. doi: 10.1111/j.1530-0277.2008.00890.x

  • DNA methylation profiles in monozygotic and dizygotic twins

    Zachary A Kaminsky, Thomas Tang, Sun-Chong Wang, Carolyn Ptak, Gabriel H T Oh, Albert H C Wong, Laura A Feldcamp, Carl Virtanen, Jonas Halfvarson, Curt Tysk, Allan F McRae, Peter M Visscher, Grant W Montgomery, Irving I Gottesman, Nicholas G Martin and Art Petronis (2009). DNA methylation profiles in monozygotic and dizygotic twins. Nature Genetics, 41 (2), 240-245. doi: 10.1038/ng.286

  • Variants in TF and HFE Explain 40% of Genetic Variation in Serum-Transferrin Levels

    Beben Benyamin, Allan F. McRae, Gu Zhu, Scott Gordon, Anjali K. Henders, Aarno Palotie, Leena Peltonen, Nicholas G. Martin, Grant W. Montgomery, John B. Whitfield and Peter M. Visscher (2009). Variants in TF and HFE Explain 40% of Genetic Variation in Serum-Transferrin Levels. American Journal of Human Genetics, 84 (1), 60-65. doi: 10.1016/j.ajhg.2008.11.011

  • Accumulation of trauma over time and risk for depression in a twin sample

    V. V. McCutcheon, A. C. Heath, E. C. Nelson, K. K. Bucholz, P. A. F. Madden and N. G. Martin (2009). Accumulation of trauma over time and risk for depression in a twin sample. Psychological Medicine, 39 (3), 431-441. doi: 10.1017/S0033291708003759

  • Genetic influences on handedness: Data from 25,732 Australian and Dutch twin families

    Medland, Sarah E., Duffy, David L., Wright, Margaret J., Geffen, Gina M., Hay, David A., Levy, Florence, Van-Beijsterveldt, Catherina E.M., Willemsen, Gonneke, Townsend, Grant C., White, Vicki, Hewitt, Alex W., Mackey, David A., Bailey, J. Michael, Slutske, Wendy S., Nyholt, Dale R., Treloar, Susan A., Martin, Nicholas G. and Boomsma, Dorret I. (2009). Genetic influences on handedness: Data from 25,732 Australian and Dutch twin families. Neuropsychologia, 47 (2), 330-337. doi: 10.1016/j.neuropsychologia.2008.09.005

  • Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo

    Sullivan, P. F., de Geus, E. J. C., Willemsen, G., James, M. R., Smit, J. H., Zandbelt, T., Martin, N. G., Wray, N. R., Boomsma, D. I. and Penninx, B. W. J. H. (2009). Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo. Molecular Psychiatry, 14 (4), 359-375. doi: 10.1038/mp.2008.125

  • Genomewide Association Studies: History, Rationale, and Prospects for Psychiatric Disorders

    Psychiatric GWAS Consortium Coordinating Committee, Martin, N., Wray, N., Mowry, B. and Holliday, E. (2009). Genomewide Association Studies: History, Rationale, and Prospects for Psychiatric Disorders. American Journal of Psychiatry, 166 (5), 540-556. doi: 10.1176/appi.ajp.2008.08091354

  • Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts

    Yurii S Aulchenko, Samuli Ripatti, Ida Lindqvist, Dorret Boomsma, Iris M Heid, Peter P Pramstaller, Brenda W J H Penninx, A Cecile J W Janssens, James F Wilson, Tim Spector, Nicholas G Martin, Nancy L Pedersen, Kirsten Ohm Kyvik, Jaakko Kaprio, Albert Hofman, Nelson B Freimer, Marjo-Riitta Jarvelin, Ulf Gyllensten, Harry Campbell, Igor Rudan, Åsa Johansson, Fabio Marroni, Caroline Hayward, Veronique Vitart, Inger Jonasson, Cristian Pattaro, Alan Wright, Nick Hastie, Irene Pichler ... Jouke-Jan Hottenga (2009). Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. Nature Genetics, 41 (1), 47-55. doi: 10.1038/ng.269

  • Replication of the association of common rs9939609 variant of FTO with increased BMI in an Australian adult twin population but no evidence for gene by environment (G × E) interaction

    Cornes, B., Lind, P. A., Medland, S. E., Montgomery, G. W ., Nyholt, D. R. and Martin, N. G . (2009). Replication of the association of common rs9939609 variant of FTO with increased BMI in an Australian adult twin population but no evidence for gene by environment (G × E) interaction. International Journal of Obesity, 33 (1), 75-79. doi: 10.1038/ijo.2008.223

  • Autosomal linkage analysis for cannabis use behaviors in Australian adults

    Agrawal, Arpana, Morley, Katherine I., Hansell, Narelle K., Pergadia, Michele L., Montgomery, Grant W., Statham, Dixie J., Todd, Richard D., Madden, Pamela A. F., Heath, Andrew C., Whitfield, John, Martin, Nicholas G. and Lynskey, Michael T. (2008). Autosomal linkage analysis for cannabis use behaviors in Australian adults. Drug and Alcohol Dependence, 98 (3), 185-190. doi: 10.1016/j.drugalcdep.2008.05.009

  • Evidence for shared genetic influences on self-reported ADHD and autistic symptoms in young adult Australian twins

    Reiersen, Angela M., Constantino, John N., Grimmer, Marisa, Martin, Nicholas G. and Todd, Richard D. (2008). Evidence for shared genetic influences on self-reported ADHD and autistic symptoms in young adult Australian twins. Twin Research and Human Genetics, 11 (6), 579-585. doi: 10.1375/twin.11.6.579

  • Linkage and Association Analyses of Longitudinally Measured Lipid Phenotypes in Adolescence

    Middelberg, Rita P., Gordon, Scott D., Zhu, Gu, McRae, Allan, Montgomery, Grant W., Martin, Nicholas G. and Whitfield, John B. (2008). Linkage and Association Analyses of Longitudinally Measured Lipid Phenotypes in Adolescence. Twin Research and Human Genetics, 11 (6), 603-620. doi: 10.1375/twin.11.6.603

  • Meeting the challenges of neuroimaging genetics

    De Zubicaray, Greig I., Chiang, Ming-Chang, McMahon, Katie L., Shattuck, David W., Toga, Arthur W., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2008). Meeting the challenges of neuroimaging genetics. Brian Imaging and Behavior, 2 (4), 258-263. doi: 10.1007/s11682-008-9029-0

  • A high-density association screen of 155 ion transport genes for involvement with common migraine

    Nyholt, Dale R., LaForge, K. Steven, Kallela, Mikko, Alakurtti, Kirsi, Anttila, Verneri, Farkkila, Markus, Hamalainen, Eija, Kaprio, Jaakko, Kaunisto, Mari A., Heath, Andrew C., Montgomery, Grant W., Goebel, Hartmut, Todt, Unda, Ferrari, Michel D., Launer, Lenore J., Frants, Rune R., Terwindt, Gisela M., de Vries, Boukje, Verschuren, W. M. Monique, Brand, Jan, Freilinger, Tobias, Pfaffenrath, Volker, Straube, Andreas, Ballinger, Dennis G., Zhan, Yiping, Daly, Mark J., Cox, David R., Dichgans, Martin, van den Maagdenberg, Arn M. J. M. ... Palotie, Aarno (2008). A high-density association screen of 155 ion transport genes for involvement with common migraine. Human Molecular Genetics, 17 (21), 3318-3331. doi: 10.1093/hmg/ddn227

  • Alcohol Dependence and Reproductive Onset: Findings in Two Australian Twin Cohorts

    Waldron, Mary, Heath, Andrew C., Bucholz, Kathleen K., Madden, Pamela A. F. and Martin, Nicholas G. (2008). Alcohol Dependence and Reproductive Onset: Findings in Two Australian Twin Cohorts. Alcoholism-Clinical and Experimental Research, 32 (11), 1865-1874. doi: 10.1111/j.1530-0277.2008.00771.x

  • Early cannabis use and DSM-IV nicotine dependence: A twin study

    Agrawal, Arpana, Lynskey, Michael T., Pergadia, Michele L., Bucholz, Kathleen K., Heath, Andrew C., Martin, Nicholas G. and Madden, Pamela A. F. (2008). Early cannabis use and DSM-IV nicotine dependence: A twin study. Addiction, 103 (11), 1896-1904. doi: 10.1111/j.1360-0443.2008.02354.x

  • Genetic factors predisposing to homosexuality may increase mating success in heterosexuals

    Zietsch, Brendan P., Morley, Katherine I., Shekar, Sri N., Verweij, Karin J. H., Keller, Matthew C., Macgregor, Stuart, Wright, Margaret J., Bailey, J. Michael and Martin, Nicholas G. (2008). Genetic factors predisposing to homosexuality may increase mating success in heterosexuals. Evolution and Human Behavior, 29 (6), 424-433. doi: 10.1016/j.evolhumbehav.2009.07.002

  • Recently-derived variants of brain-size genes ASPM, MCPH1, CDK5RAP and BRCA1 not associated with general cognition, reading or language

    Bates, Timothy C., Luciano, Michelle, Lind, Penelope A., Wright, Margaret J., Montgomery, Grant W. and Martin, Nicholas G. (2008). Recently-derived variants of brain-size genes ASPM, MCPH1, CDK5RAP and BRCA1 not associated with general cognition, reading or language. Intelligence, 36 (6), 689-693. doi: 10.1016/j.intell.2008.04.001

  • Susceptibility variants for male-pattern baldness on chromosome 20p11

    Hillmer, Axel M., Brockschmidt, Felix F., Hanneken, Sandra, Eigelshoven, Sibylle, Steffens, Michael, Flaquer, Antonia, Herms, Stefan, Becker, Tim, Kortuem, Anne-Katrin, Nyholt, Dale R., Zhao, Zhen Zhen, Montgomery, Grant W., Martin, Nicholas G., Muehleisen, Thomas W., Alblas, Margrieta A., Moebus, Susanne, Joeckel, Karl-Heinz, Broecker-Preuss, Martina, Erbel, Raimund, Reinartz, Roman, Betz, Regina C., Cichon, Sven, Propping, Peter, Baur, Max P., Wienker, Thomas F., Kruse, Roland and Noethen, Markus M. (2008). Susceptibility variants for male-pattern baldness on chromosome 20p11. Nature Genetics, 40 (11), 1279-1281. doi: 10.1038/ng.228

  • The use of common mitochondrial variants to detect and characterise population structure in the Australian population: Implications for genome-wide association studies

    Byrne, Enda M., Mcrae, Allan F., Zhao, Zhen-Zhen, Martin, Nicholas G., Montgomery, Grant W. and Visscher, Peter M. (2008). The use of common mitochondrial variants to detect and characterise population structure in the Australian population: Implications for genome-wide association studies. European Journal of Human Genetics, 16 (11), 1396-1403. doi: 10.1038/ejhg.2008.117

  • A genome-wide linkage scan for age at menarche in three populations of European descent

    Anderson, Carl A., Zhu, Gu, Falchi, Mario, van den Berg, Stéphanie M., Treloar, Susan A., Spector, Timothy D., Martin, Nicholas G., Boomsma, Dorret I., Visscher, Peter M. and Montgomery, Grant W. (2008). A genome-wide linkage scan for age at menarche in three populations of European descent. Journal of Clinical Endocrinology and Metabolism., 93 (10), 3965-3970. doi: 10.1210/jc.2007-2568

  • Genetic influences on the difference in variability of height, weight and body mass index between Caucasian and East Asian adolescent twins

    Hur, Y-M, Kaprio, J., Iacono, W. G., Boomsma, D. I., McGgue, M., Silventoinen, K., Martin, N. G., Luciano, M., Visscher, P. M., Rose, R. J., He, M., Ando, J., Ooki, S., Nonaka, K., Lin, C. C. H., Lajunen, H. R., Cornes, B. K., Bartels, M., van Beijsterveldt, C. E. M., Cherny, S. S. and Mitchell, K. (2008). Genetic influences on the difference in variability of height, weight and body mass index between Caucasian and East Asian adolescent twins. International Journal of Obesity, 32 (10), 1455-1467. doi: 10.1038/ijo.2008.144

  • Phenotypic, Genetic, and Environmental Properties of the Portrait Values Questionnaire

    Schermer, Julie Aitken, Feather, N. T., Zhu, Gu and Martin, Nicholas G. (2008). Phenotypic, Genetic, and Environmental Properties of the Portrait Values Questionnaire. Twin Research and Human Genetics, 11 (5), 531-537. doi: 10.1375/twin.11.5.531

  • Shared and unique risk factors between lifetime purging and objective binge eating: A twin study

    Wade, T. D., Treloar, S. and Martin, N. G. (2008). Shared and unique risk factors between lifetime purging and objective binge eating: A twin study. Psychological Medicine, 38 (10), 1455-1464. doi: 10.1017/S0033291708002791

  • The role of GABRA2 in alcohol dependence, smoking, and illicit drug use in an Australian population sample

    Lind, Penelope A., Macgregor, Stuart, Agrawal, Arpana, Montgomery, Grant W., Heath, Andrew C., Martin, Nicholas G. and Whitfield, John B. (2008). The role of GABRA2 in alcohol dependence, smoking, and illicit drug use in an Australian population sample. Alcoholism: Clinical and Experimental Research, 32 (10), 1721-1731. doi: 10.1111/j.1530-0277.2008.00768.x

  • Variation in bone morphogenetic protein 15 is not associated with spontaneous human dizygotic twinning

    Zhao, Zhen Zhen, Painter, Jodie N., Palmer, James S., Webb, Penelope M., Hayward, Nicholas K., Whiteman, David C., Boomsma, Dorret I., Martin, Nicholas G., Duffy, David L. and Montgomery, Grant W. (2008). Variation in bone morphogenetic protein 15 is not associated with spontaneous human dizygotic twinning. Human Reproduction, 23 (10), 2372-2379. doi: 10.1093/humrep/den268

  • Vitamin D receptor gene polymorphisms have negligible effect on human height

    Macgregor, Stuart, Hottenga, Jouke-Jan, Lind, Penelope A., Suchiman, H. Eka D., Willemsen, Gonneke, Slagboom, P. Eline, Montgomery, Grant W., Martin, Nicholas G., Visscher, Peter M. and Boomsma, Dorret I. (2008). Vitamin D receptor gene polymorphisms have negligible effect on human height. Twin Research and Human Genetics, 11 (5), 488-494. doi: 10.1375/twin.11.5.488

  • Evaluation of HapMap data in six populations of European descent

    Lundmark, Per E., Liljedahl, Ulrika, Boomsma, Dorret I., Mannila, Heikki, Martin, Nicholas G., Palotie, Aarno, Peltonen, Leena, Perola, Markus, Spector, Tim D. and Syvanen, Ann-Christine (2008). Evaluation of HapMap data in six populations of European descent. European Journal of Human Genetics, 16 (9), 1142-1150. doi: 10.1038/ejhg.2008.77

  • Heritability of borderline personality disorder features is similar across three countries

    Distel, M. A., Trull, T. J., Derom, C. A., Thiery, E. W., Grimmer, M. A., Martin, N. G., Willemsen, G. and Boomsma, D. I. (2008). Heritability of borderline personality disorder features is similar across three countries. Psychological Medicine, 38 (9), 1219-1229. doi: 10.1017/S0033291707002024

  • Homocysteine, folates, and the eye

    Wright, A. D., Martin, N. and Dodson, P. M. (2008). Homocysteine, folates, and the eye. Eye, 22 (8), 989-993. doi: 10.1038/sj.eye.6703061

  • Investigation of the relationship between smoking and appendicitis in Australian twins

    Oldmeadow, Chris, Wood, Ian, Mengersen, Kerrie, Visscher, Peter M., Martin, Nicholas G. and Duffy, David L. (2008). Investigation of the relationship between smoking and appendicitis in Australian twins. Annals of Epidemiology, 18 (8), 631-636. doi: 10.1016/j.annepidem.2008.04.004

  • Searching for an environmental effect of parental alcoholism on offspring alcohol use disorder: A genetically informed study of children of alcoholics

    Slutske, Wendy S., D'Onofrio, Brian M., Turkheimer, Eric, Emery, Robert E., Harden, K. Paige, Heath, Andrew C. and Martin, Nicholas G. (2008). Searching for an environmental effect of parental alcoholism on offspring alcohol use disorder: A genetically informed study of children of alcoholics. Journal of Abnormal Psychology, 117 (3), 534-551. doi: 10.1037/a0012907

  • Welcome - Human genetics society of Australasia

    Martin, Nick (2008). Welcome - Human genetics society of Australasia. Twin Research and Human Genetics, 11 (4), III-III. doi: 10.1375/twin.11.4.iii

  • Heritability and genome-wide linkage in US and Australian twins identify novel genomic regions controlling chromogranin A

    O'Connor, Daniel T., Zhu, Gu, Rao, Fangwen, Taupenot, Laurent, Fung, Maple M., Das, Madhusudan, Mahata, Sushil K., Mahata, Manjula, Wang, Lei, Zhang, Kuixing, Greenwood, Tiffany A., Shih, Pei-an Betty, Cockburn, Myles G, Ziegler, Michael G., Stridsberg, Mats, Martin, Nicholas G. and Whitfield, John B. (2008). Heritability and genome-wide linkage in US and Australian twins identify novel genomic regions controlling chromogranin A. Circulation, 118 (3), 247-257. doi: 10.1161/CIRCULATIONAHA.107.709105

  • Suggestive linkage on chromosome 2, 8, and 17 for lifetime major depression

    Middeldorp, CM, Sullivan, PF, Wray, NR, Hottenga, JJ, de Geus, EJC, van den Berg, M, Montgomery, GW, Coventry, WL, Statham, DJ, Andrews, G, Slagboom, PE, Boomsma, DI and Martin, NG (2008). Suggestive linkage on chromosome 2, 8, and 17 for lifetime major depression. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 150B (3), 352-358. doi: 10.1002/ajmg.b.30817

  • Common sequence variants on 20q11.22 confer melanoma susceptibility

    Brown, K. M., MacGregor, S., Montgomery, G. W., Craig, D. W., Zhao, Z. Z., Iyadurai, K., Henders, A. K., Homer, N., Campbell, M. J., Stark, M., Thomas, S., Schmid, H., Maskiell, J. A., Jetann, J., Ferguson, M., Stephan, D. A., Cust, A. E., Whiteman, D. C., Green, A., Olsson, H., Puig, S., Ghiorzo, P., Hansson, J., Demenais, F., Goldstein, A. M., Gruis, N. A., Elder, D. E., Newton Bishop, J., Kefford, R. F. ... Hayward, N. (2008). Common sequence variants on 20q11.22 confer melanoma susceptibility. Nature Genetics, 40 (7), 838-840. doi: 10.1038/ng.163

  • Does teenage childbearing increase smoking, drinking and body size?

    Webbink, Dinand, Martin, Nicholas G. and Visscher, Peter M. (2008). Does teenage childbearing increase smoking, drinking and body size?. Journal of Health Economics, 27 (4), 888-903. doi: 10.1016/j.jhealeco.2008.02.005

  • Measuring carbohydrate-deficient transferrin by direct immunoassay: factors affecting diagnostic sensitivity for excessive alcohol intake

    Whitfield, John B., Day, Veronica, Madden, Pamela A. F., Heath, Andrew C., Martin, Nicholas G. and Montgomery, Grant W. (2008). Measuring carbohydrate-deficient transferrin by direct immunoassay: factors affecting diagnostic sensitivity for excessive alcohol intake. Clinical Chemistry, 54 (7), 1158-1165. doi: 10.1373/clinchem.2007.101733

  • An autosomal linkage scan for cannabis use disorders in the nicotine addiction genetics project

    Agrawal, Arpana, Pergadia, Michele. L., Saccone, Scott F., Lynskey, Michael T., Wang, Jen C., Martin, Nicholas G., Statham, Dixie, Henders, Anjali, Campbell, Megan, Garcia, Robertino, Broms, Ulla, Todd, Richard D., Goate, Alison M., Rice, John, Kaprio, Jaakko, Heath, Andrew C., Montgomery, Grant W. and Madden, Pamela A. F. (2008). An autosomal linkage scan for cannabis use disorders in the nicotine addiction genetics project. Archives of General Psychiatry, 65 (6), 713-722. doi: 10.1001/archpsyc.65.6.713

  • Gamma-aminobutyric acid receptor genes and nicotine dependence: Evidence for association from a case-control study

    Agrawal, Arpana, Pergadia, Michele L., Saccone, Scott F., Hinrichs, Anthony L., Lessov-Schlaggar, Christina N., Saccone, Nancy L., Neuman, Rosalind J., Breslau, Naomi, Johnson, Eric, Hatsukami, Dorothy, Montgomery, Grant W., Heath, Andrew C., Martin, Nicholas G., Goate, Alison M., Rice, John P., Bierut, Laura J. and Madden, Pamela A. F. (2008). Gamma-aminobutyric acid receptor genes and nicotine dependence: Evidence for association from a case-control study. Addiction, 103 (6), 1027-1038. doi: 10.1111/j.1360-0443.2008.02236.x

  • Genetic Dissection of Myopia Evidence for Linkage of Ocular Axial Length to Chromosome 5q

    Zhu, Gu, Hewitt, Alex W., Ruddle, Jonathan B., Kearns, Lisa S., Brown, Shayne A., Mackinnon, Jane R., Chen, Christine Y., Hammond, Christopher J., Craig, Jamie E., Montgomery, Grant W., Martin, Nicholas G. and Mackey, David A. (2008). Genetic Dissection of Myopia Evidence for Linkage of Ocular Axial Length to Chromosome 5q. Ophthalmology, 115 (6), 1053-1057. doi: 10.1016/j.ophtha.2007.08.013

  • Genetic covariation among facets of openness to experience and general cognitive ability

    Wainwright, Mark A., Wright, Margaret J., Luciano, Michelle, Geffen, Gina M. and Martin, Nicholas G. (2008). Genetic covariation among facets of openness to experience and general cognitive ability. Twin Research and Human Genetics, 11 (3), 275-286. doi: 10.1375/twin.11.3.275

  • Long-term stability and heritability of telephone interview measures of alcohol consumption and dependence

    Hansell, Narelle K., Agrawal, Arpana, Whitfield, John B., Morley, Katherine I., Zhu, Gu, Lind, Penelope A., Pergadia, Michele L., Madden, Pamela A., Todd, Richard D., Heath, Andrew C. and Martin, Nicholas G. (2008). Long-term stability and heritability of telephone interview measures of alcohol consumption and dependence. Twin Research and Human Genetics, 11 (3), 287-305. doi: 10.1375/twin.11.3.287

  • Consistently replicating locus linked to migraine on 10q22-q23

    Anttila, Verneri, Nyholt, Dale R., Kallela, Mikko, Artto, Ville, Vepsalainen, Salli, Jakkula, Eveliina, Wennerstrom, Annika, Tikka-Kleemola, Paeivi, Kaunisto, Mari A., Hamalainen, Eija, Widen, Elisabeth, Terwilliger, Joseph, Merikangas, Kathleen, Montgomery, Grant W., Martin, Nicholas G., Daly, Mark, Kaprio, Jaakko, Peltonen, Leena, Farkkila, Markus, Wessman, Maija and Palotie, Aarno (2008). Consistently replicating locus linked to migraine on 10q22-q23. American Journal of Human Genetics, 82 (5), 1051-1063. doi: 10.1016/j.ajhg.2008.03.003

  • A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation

    Han, J., Kraft, P., Nan, H., Guo, Q., Chen, C., Qureshi, A., Hankinson, S.E., Hu, F.B., Duffy, D., Zhao, Z.Z., Martin, N. G., Montgomery, G., Hayward, N., Thomas, G., Hoover, R.N., Chanock, S. and Hunter, D.J. (2008). A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation. Plos Genetics, 4 (5) e1000074, e1000074. doi: 10.1371/journal.pgen.1000074

  • Genetic and environmental influences on individual differences in attidues toward homosexuality: An Australian twin study

    Verweji, Karin J. H., Shekar, Sri N., Zietsch, Brendan P., Eaves, Lindon J., Bailey, J. Michael, Boomsma, Dorret I. and Martin, Nicholas G. (2008). Genetic and environmental influences on individual differences in attidues toward homosexuality: An Australian twin study. Behavior Genetics, 38 (3), 257-265. doi: 10.1007/s10519-008-9200-9

  • Spectrophotometric methods for quantifying pigmentation in human hair - influence of MC1R genotype and environment

    Shekar, Sri N., Duffy, David L., Frudakis, Tony, Montgomery, Grant W., James, Michael R., Sturm, Richard A. and Martin, Nicholas G. (2008). Spectrophotometric methods for quantifying pigmentation in human hair - influence of MC1R genotype and environment. Photochemistry and Photobiology, 84 (3), 719-726. doi: 10.1111/j.1751-1097.2007.00237.x

  • Correlates of cigarette smoking during pregnancy and its genetic and environmental overlap with nicotine dependence

    Agrawal, Arpana, Knopik, Valerie S., Pergadia, Michele L., Waldron, Mary, Bucholz, Kathleen K., Martin, Nicholas G., Heath, Andrew C. and Madden, Pamela A. F. (2008). Correlates of cigarette smoking during pregnancy and its genetic and environmental overlap with nicotine dependence. Nicotine and Tobacco Research, 10 (4), 567-578. doi: 10.1080/14622200801978672

  • Effects of GABRA2 variation on physiological, psychomotor and subjective responses in the Alcohol Challenge Twin Study

    Lind, Penelope A., MacGregor, Stuart, Montgomery, Grant W., Heath, Andrew C., Martin, Nicholas G. and Whitfield, John B. (2008). Effects of GABRA2 variation on physiological, psychomotor and subjective responses in the Alcohol Challenge Twin Study. Twin Research and Human Genetics, 11 (2), 174-182. doi: 10.1375/twin.11.2.174

  • No effects of prenatal hormone transfer on digit ratio in a large sample of same- and opposite-sex dizygotic twins

    Medland, Sarah E., Loehlin, John C. and Martin, Nicholas G. (2008). No effects of prenatal hormone transfer on digit ratio in a large sample of same- and opposite-sex dizygotic twins. Personality and Individual Differences, 44 (5), 1225-1234. doi: 10.1016/j.paid.2007.11.017

  • Within-family outliers: segregating alleles or environmental effects? A linkage analysis of height from 5815 sibling pairs

    Benyamin, Beben, Perola, Markus, Cornes, Belinda K., Madden, Pamela A. F., Palotie, Aarno, Nyholt, Dale R., Montgomery, Grant W., Peltonen, Leena, Martin, Nicholas G. and Visscher, Peter M. (2008). Within-family outliers: segregating alleles or environmental effects? A linkage analysis of height from 5815 sibling pairs. European Journal of Human Genetics, 16 (4), 516-524. doi: 10.1038/sj.ejhg.5201992

  • Linkage and association analysis of spectrophotometrically quantified hair color in Australian adolescents: The effects of OCA2 and HERC2

    Shekar, Sri N., Duffy, David L., Frudakis, Tony, Sturm, Richard A., Zhao, Zhen Z., Montgomery, Grant W. and Martin, Nicholas G. (2008). Linkage and association analysis of spectrophotometrically quantified hair color in Australian adolescents: The effects of OCA2 and HERC2. Journal of Investigative Dermatology, 128 (12), 2807-2814. doi: 10.1038/jid.2008.147

  • Genetic and environmental contributions to perceived intensity and pleasantness of androstenone odor: an international twin study

    Knaapila, Antti, Tuorila, Hely, Silventoinen, Karri, Wright, Margaret J., Kyvik, Kirsten O., Cherkas, Lynn F., Keskitalo, Kaisu, Hansen, Jonathan, Martin, Nicholas G., Spector, Tim D., Kaprio, Jaakko and Perola, Markus (2008). Genetic and environmental contributions to perceived intensity and pleasantness of androstenone odor: an international twin study. Chemosensory Perception, 1 (1), 34-42. doi: 10.1007/s12078-007-9005-x

  • A single SNP in an evolutionary conserved region within intron 86 of the HERC2 gene determines human blue-brown eye colour

    Sturm, Richard A., Duffy, David L., Zhao, Zhen Zhen, Leite, Fabio P.N., Stark, Mitchell S., Hayward, Nicholas K., Martin, Nicholas G. and Montgomery, Grant W. (2008). A single SNP in an evolutionary conserved region within intron 86 of the HERC2 gene determines human blue-brown eye colour. The American Journal of Human Genetics, 82 (2), 424-431. doi: 10.1016/j.ajhg.2007.11.005

  • A study of diabetes mellitus within a large sample of Australian twins

    Condon, Julianne, Shaw, Joanne E., Luciano, Michelle, Kyvik, Kirsten O., Martin, Nicholas G. and Duffy, David L. (2008). A study of diabetes mellitus within a large sample of Australian twins. Twin Research and Human Genetics, 11 (1), 28-40. doi: 10.1375/twin.11.1.28

  • A genome-wide scan for Eysenckian personality dimensions in adolescent twin sibships: Psychoticism, Extraversion, Neuroticism, and Lie

    Gillespie, Nathan A., Zhu, Gu, Evans, David M., Medland, Sarah E., Wright, Margie J. and Martin, Nick G. (2008). A genome-wide scan for Eysenckian personality dimensions in adolescent twin sibships: Psychoticism, Extraversion, Neuroticism, and Lie. Journal of Personality, 76 (6), 1415-1445. doi: 10.1111/j.1467-6494.2008.00527.x

  • A whole genome association study of neuroticism using DNA pooling

    Shifman, S., Bhomra, A., Smiley, S., Wray, N. R., James, M. R., Martin, N. G., Hettema, J. M., An, S. S., Neale, M. C., van den Oord, E. J., Kendler, K. S., Chen, X., Boomsma, D. I., Middeldorp, C. M., Hottenga, J. J., Slagboom, P. E. and Flint, J. (2008). A whole genome association study of neuroticism using DNA pooling. Molecular Psychiatry, 13 (3), 302-312. doi: 10.1038/sj.mp.4002048

  • Association of the gastric alcohol dehydrogenase gene Adh7 with variation in alcohol metabolism

    Birley, Andrew J., James, Michael R., Dickson, Peter A., Montgomery, Grant W., Heath, Andrew C., Whitfield, John B. and Martin, Nicholas G. (2008). Association of the gastric alcohol dehydrogenase gene Adh7 with variation in alcohol metabolism. Human Molecular Genetics, 17 (2), 179-189. doi: 10.1093/hmg/ddm295

  • Association study of candidate variants from brain-derived neurotrophic factor and dystrobrevin-binding protein 1 with neuroticism, anxiety, and depression

    Wray, Naomi R., James, Michael R., Handoko, Herlina Y., Dumenil, Troy, Lind, Penelope A., Montgomery, Grant W. and Martin, Nicholas G. (2008). Association study of candidate variants from brain-derived neurotrophic factor and dystrobrevin-binding protein 1 with neuroticism, anxiety, and depression. Psychiatric Genetics, 18 (5), 219-225. doi: 10.1097/YPG.0b013e3283050aee

  • Association study of candidate variants of COMT with neuroticism, anxiety and depression

    Wray, Naomi, James, Michael R., Dumenil, Troy, Handoko, Herlina Y., Lind, Penelope A., Montgomery, Grant W. and Martin, Nicholas G. (2008). Association study of candidate variants of COMT with neuroticism, anxiety and depression. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 147B (7), 1314-1318. doi: 10.1002/ajmg.b.30744

  • Childhood sexual abuse moderates genetic influences on age at first consensual sexual intercourse in women

    Waldron, Mary, Heath, Andrew C., Turkheimer, Eric N., Emery, Robert E., Nelson, Elliot, Bucholz, Kathleen K., Madden, Pamela A. F. and Martin, Nicholas G. (2008). Childhood sexual abuse moderates genetic influences on age at first consensual sexual intercourse in women. Behavior Genetics, 38 (1), 1-10. doi: 10.1007/s10519-007-9176-x

  • Dizygotic twinning

    Hoekstra, Chantal, Zhao, Zhen Zhen, Lambalk, Cornelius B., Willemsen, Gonneke, Martin, Nicholas G., Boomsma, Dorret I. and Montgomery, Grant W. (2008). Dizygotic twinning. Human Reproduction Update, 14 (1), 37-47. doi: 10.1093/humupd/dmm036

  • Genome-wide linkage analysis of multiple measures of neuroticism of 2 large cohorts from Australia and the Netherlands

    Wray, Naomi R., Middeldorp, Christel M., Birley, Andrew J., Gordon, Scott D., Sullivan, Patrick F., Visscher, Peter M., Nyholt, Dale R, Willemsen, Gonneke, de Geus, Eco J.C., Slagboom, P. Eline, Montgomery, Grant W., Martin, Nicholas G. and Boomsma, Dorret I. (2008). Genome-wide linkage analysis of multiple measures of neuroticism of 2 large cohorts from Australia and the Netherlands. Archives of General Psychiatry, 65 (6), 649-658. doi: 10.1001/archpsyc.65.6.649

  • Linkage of nicotine dependence and smoking behavior on 10q, 7q and 11p in twins with homogeneous genetic background

    Loukola, A., Broms, U., Maunu, H., Widen, E., Heikkila, K., Siivola, M., Salo, A., Pergadia, M. L., Nyman, E., Sammalisto, S., Perola, M., Agrawal, A., Heath, A. C., Martin, N. G., Madden, P. A., Peltonen, L. and Kaprio, J. (2008). Linkage of nicotine dependence and smoking behavior on 10q, 7q and 11p in twins with homogeneous genetic background. The Pharmacogenomics Journal, 8 (3), 209-219. doi: 10.1038/sj.tpj.6500464

  • QTLs identified for P3 amplitude in a non-clinical sample: Importance of neurodevelopmental and neurotransmitter genes

    Wright, Margaret J., Luciano, Michelle, Hansell, Narelle K., Montgomery, Grant W., Geffen, Gina M. and Martin, Nicholas (2008). QTLs identified for P3 amplitude in a non-clinical sample: Importance of neurodevelopmental and neurotransmitter genes. Biological Psychiatry, 63 (9), 864-873. doi: 10.1016/j.biopsych.2007.09.002

  • Quantifying the heritability of task-related brain activation and performance during the N-back working memory task: a twin fMRI study

    Blokland, Gabriella A.M., McMahon, Katie L., Hoffman, Jan, Zhu, Gu, Meredith, Matthew, Martin, Nicholas G., Thompson, Paul M., De Zubicaray, Greig I. and Wright, Margaret J. (2008). Quantifying the heritability of task-related brain activation and performance during the N-back working memory task: a twin fMRI study. Biological Psychology, 79 (1), 70-79. doi: 10.1016/j.biopsycho.2008.03.006

  • Shared temperament risk factors for anorexia nervosa: a twin study

    Wade, T. D., Tiggemann, M., Bulik, C. M., Fairburn, C. G., Wray, N. R. and Martin, N. G. (2008). Shared temperament risk factors for anorexia nervosa: a twin study. Psychosomatic Medicine, 70 (2), 239-244. doi: 10.1097/PSY.0b013e31815c40f1

  • Testing replication of a 5-SNP set for general cognitive ability in six population samples

    Luciano, Michelle, Lind, Penelope A., Deary, Ian J., Payton, Antony, Posthuma, Danielle, Butcher, Lee M., Bochdanovits, Zoltan, Whalley, Lawrence J., Visscher, Peter M., Harris, Sarah E., Polderman, Tinca J. C., Davis, Oliver S. P., Wright, Margaret J., Starr, John M., de Geus, Eco J. C., Bates, Timothy C., Montgomery, Grant W., Boomsma, Dorret I., Martin, Nicholas G. and Plomin, Robert (2008). Testing replication of a 5-SNP set for general cognitive ability in six population samples. European Journal of Human Genetics, 16 (11), 1388-1395. doi: 10.1038/ejhg.2008.100

  • The Queensland study of melanoma:Environmental and genetic associations (Q_MEGA): study design, baseline characteristics, and repeatability of phenotype and sun exposure measures

    Baxter, A.J., Hughes, M.C., Kvaskoff, M, Siskind, V., Shekar, S., Aitken, J. F., Green, A. C., Duffy, D., Hayward, N., Martin, N. G. and Whiteman, D. C. (2008). The Queensland study of melanoma:Environmental and genetic associations (Q_MEGA): study design, baseline characteristics, and repeatability of phenotype and sun exposure measures. Twin Research and Human Genetics, 11 (2), 183-196. doi: 10.1375/twin.11.2.183

  • A comparison of early family life events amongst monozygotic twin women with lifetime anorexia nervosa, bulimia nervosa, or major depression

    Wade, T. D., Gillespie, N. and Martin, N. G. (2007). A comparison of early family life events amongst monozygotic twin women with lifetime anorexia nervosa, bulimia nervosa, or major depression. International Journal of Eating Disorders, 40 (8), 679-686. doi: 10.1002/eat.20461

  • Genome partitioning of genetic variation for height from 11,214 sibling pairs

    Visscher, Peter M., Macgregor, Stuart, Benyamin, Beben, Zhu, Gu, Gordon, Scott, Medland, Sarah, Hill, William G., Hottenga, Jouke-Jan, Willemsen, Gonneke, Boomsma, Dorret I., Liu, Yao-Zhong, Deng, Hong-Wen, Montgomery, Grant W. and Martin, Nicholas G. (2007). Genome partitioning of genetic variation for height from 11,214 sibling pairs. American Journal of Human Genetics, 81 (5), 1104-1110. doi: 10.1086/522934

  • A haplotype spanning KIAA0319 and TTRAP is associated with normal variation in reading and spelling ability

    Luciano, Michelle, Lind, Penelope A., Duffy, David L., Castles, Anne, Wright, Margaret J., Montgomery, Grant W., Martin, Nicholas G. and Bates, Timothy C. (2007). A haplotype spanning KIAA0319 and TTRAP is associated with normal variation in reading and spelling ability. Biological Psychiatry, 62 (7), 811-817. doi: 10.1016/j.biopsych.2007.03.007

  • A longitudinal genetic study of uric Acid and liver enzymes in adolescent twins

    Middelberg, Rita P. S., Medland, Sarah E., Martin, Nicholas G. and Whitfield, John B. (2007). A longitudinal genetic study of uric Acid and liver enzymes in adolescent twins. Twin Research and Human Genetics, 10 (5), 757-764. doi: 10.1375/twin.10.5.757

  • Gene-interleaving patterns of synteny in the Saccharomyces cerevisiae genome: Are they proof of an ancient genome duplication event?

    Martin, Nicolas, Ruedi, Elizabeth A., LeDuc, Richard, Sun, Feng-Jie and Caetano-Anollés, Gustavo (2007). Gene-interleaving patterns of synteny in the Saccharomyces cerevisiae genome: Are they proof of an ancient genome duplication event?. Biology Direct, 2 (1) 23. doi: 10.1186/1745-6150-2-23

  • Sex differences in genetic variation in weight: a longitudinal study of body mass index in adolescent twins

    Cornes, B. K., Zhu, G. and Martin, N. G. (2007). Sex differences in genetic variation in weight: a longitudinal study of body mass index in adolescent twins. Behavior Genetics, 37 (5), 648-660. doi: 10.1007/s10519-007-9165-0

  • Estimation of variance components for age at menarche in twin families

    Anderson, Carl A., Duffy, David L., Martin, Nicholas G. and Visscher, Peter M. (2007). Estimation of variance components for age at menarche in twin families. Behavior Genetics, 37 (5), 668-677. doi: 10.1007/s10519-007-9163-2

  • A genetically informed study of the intergenerational transmission of marital instability

    D'Onofrio, Brian M., Turkheimer, Eric, Emery, Robert E., Harden, K. Paige, Slutske, Wendy S., Heath, Andrew C., Madden, Pamela A. F. and Martin, Nicholas G. (2007). A genetically informed study of the intergenerational transmission of marital instability. Journal of Marriage and Family, 69 (3), 793-809. doi: 10.1111/j.1741-3737.2007.00406.x

  • Linkage analysis of a model quantitative trait in humans: Finger ridge count shows significant multivariate linkage to 5q14.1

    Medland, Sarah E., Loesch, Danuta Z., Mdzewski, Bogdan, Zhu, Gu, Montgomery, Grant W. and Martin, Nicholas G. (2007). Linkage analysis of a model quantitative trait in humans: Finger ridge count shows significant multivariate linkage to 5q14.1. PLoS Genetics, 3 (9), 1736-1744. doi: 10.1371/journal.pgen.0030165

  • LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia

    Francks, C., Maegawa, S., Lauren, J., Abrahams, B. S., Velayos-Baeza, A., Medland, S. E., Colella, S., Groszer, M., McAuley, E. Z., Caffrey, T. M., Timmusk, T., Pruunsild, P., Koppel, I., Lind, P. A., Matsumoto-Itaba, N., Nicod, J., Xiong, L., Joober, R., Enard, W., Krinsky, B., Nanba, E., Richardson, A. J., Riley, B. P., Martin, N. G., Strittmatter, S. M., Moller, H. J., Rujescu, D., St Clair, D., Muglia, P. and Roos, J. L. (2007). LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia. Molecular Psychiatry, 12 (12), 1129-1139. doi: 10.1038/sj.mp.4002053

  • Intergenerational transmission of childhood conduct problems: a children of twins study

    D'Onofrio, Brian M., Slutske, Wendy S., Turkheimer, Eric, Emery, Robert E., Harden, K. Paige, Heath, Andrew C., Madden, Pamela A. F. and Martin, Nicholas G. (2007). Intergenerational transmission of childhood conduct problems: a children of twins study. Archives of General Psychiatry, 64 (7), 820-829. doi: 10.1001/archpsyc.64.7.820

  • Evidence of genetic effects on blood lead concentration

    Whitfield, John B., Dy, Veronica, McQuilty, Robert, Zhu, Gu, Montgomery, Grant W., Ferreira, Manuel A. R., Duffy, David L., Neale, Michael C., Heijmans, Bas T., Heath, Andrew C. and Martin, Nicholas G. (2007). Evidence of genetic effects on blood lead concentration. Environmental Health Perspectives, 115 (8), 1224-1230. doi: 10.1289/ehp.8847

  • Variants in EMX2 and PTEN do not contribute to risk of endometriosis

    Treloar, S. A., Zhao, Z. Z., Le, L., Zondervan, K. T., Martin, N. G., Kennedy, S., Nyholt, D. R. and Montgomery, G. W. (2007). Variants in EMX2 and PTEN do not contribute to risk of endometriosis. Molecular Human Reproduction, 13 (8), 587-594. doi: 10.1093/molehr/gam023

  • Combined genome scans for body stature in 6,602 European twins: Evidence for common Caucasian loci

    Perola, Markus, Sammalisto, Sampo, Hiekkalinna, Tero, Martin, Nick G., Visscher, Peter M., Montgomery, Grant W., Benyamin, Beben, Harris, Jennifer R., Boomsma, Dorret, Willemsen, Gonneke, Hottenga, Jouke-Jan, Christensen, Karre, Kyvik, Kirsten Ohm, Sorensen, Thorkild I., Pedersen, Nancy L., Magnusson, Patrik K., Spector, Tim D., Widen, Elisabeth, Silventoinen, Karri, Kaprio, Jaakko, Palotie, Aarno, Peltonen, Leena and GenomEUtwin Project (2007). Combined genome scans for body stature in 6,602 European twins: Evidence for common Caucasian loci. PLoS Genetics, 3 (6), 1019-1028. doi: 10.1371/journal.pgen.0030097

  • Heritability of NEO PI-R extraversion facets and their relationship with IQ

    Pincombe, Jennifer L., Luciano, Michelle, Martin, Nicholas G. and Wright, Margaret J. (2007). Heritability of NEO PI-R extraversion facets and their relationship with IQ. Twin Research and Human Genetics, 10 (3), 462-469. doi: 10.1375/twin.10.3.462

  • Cohort Trends in Prevalence and Spousal Concordance for Smoking

    Kuo, P. H., Wood, P., Morley, K. I., Madden, P., Martin, N. G. and Heath, A. C. (2007). Cohort Trends in Prevalence and Spousal Concordance for Smoking. Drug & Alcohol Dependence, 88 (2-3), 122-129. doi: 10.1016/j.drugalcdep.2006.09.021

  • Common and specific genetic influences on EEG power bands delta, theta, alpha, and beta

    Zietsch, Brendan P., Hansen, Jonathan L., Hansell, Narelle K, Geffen, Gina M., Martin, Nicholas G. and Wright, Margaret J. (2007). Common and specific genetic influences on EEG power bands delta, theta, alpha, and beta. Biological Psychology, 75 (2), 154-164. doi: 10.1016/j.biopsycho.2007.01.004

  • Spousal concordance for alcohol dependence: evidence for assortative mating or spousal interaction effects?

    Grant, J. D., Heath, A. C., Bucholz, K. K., Madden, P. A., Agrawal, A., Statham, D. J. and Martin, N. G. (2007). Spousal concordance for alcohol dependence: evidence for assortative mating or spousal interaction effects?. Alcoholism: Clinical & Experimental Research, 31 (5), 717-728. doi: 10.1111/j.1530-0277.2007.00356.x

  • The Genetics of Voting: an Australian Twin Study

    Hatemi, P. K., Medland, S. E., Morley, K. I., Heath, A. C. and Martin, N. G. (2007). The Genetics of Voting: an Australian Twin Study. Behavior Genetics, 37 (3) 435, 435-448. doi: 10.1007/s10519-006-9138-8

  • Effect of the BDNF V166M polymorphism on working memory in healthy adolescents

    Hansell, N. K., James, M. R., Duffy, D. L., Birley, A. J., Luciano, M., Geffen, G. M., Wright, M. J., Montgomery, G. W. and Martin, N. G. (2007). Effect of the BDNF V166M polymorphism on working memory in healthy adolescents. Genes, Brain and Behavior, 6 (3), 260-268. doi: 10.1111/j.1601-183X.2006.00254.x

  • Height and 2D : 4D within and between ethnic groups: Reply to Hurd and van Anders (2007)

    Loehlin, John C., McFadden, Dennis, Medland, Sarah E. and Martin, Nicholas G. (2007). Height and 2D : 4D within and between ethnic groups: Reply to Hurd and van Anders (2007). Archives of Sexual Behavior, 36 (2), 143-143. doi: 10.1007/s10508-006-9153-0

  • Anxiety and comorbid measures associated with PLXNA2

    Wray, Naomi R., James, Michael R., Mah, Steven P., Nelson, Matthew, Andrews, Gavin, Sullivan, Patrick F., Montgomery, Grant W., Birley, Andrew J., Braun, Andreas and Martin, Nicholas G. (2007). Anxiety and comorbid measures associated with PLXNA2. Archives of General Psychiatry, 64 (3), 318-326. doi: 10.1001/archpsyc.64.3.318

  • A longitudinal genetic study of plasma lipids in adolescent twins

    Middelberg, Rita P. S., Martin, Nicholas G. and Whitfield, John B. (2007). A longitudinal genetic study of plasma lipids in adolescent twins. Twin Research & Human Genetics, 10 (1), 127-135. doi: 10.1375/twin.10.1.127

  • Prevalence of premature ovarian failure in monozygotic and dizygotic twins

    Gosden, R. G., Treloar, S. A., Martin, N. G., Cherkas, L. F., Spector, T. D., Faddy, M. J. and Silber, S. J. (2007). Prevalence of premature ovarian failure in monozygotic and dizygotic twins. Human Reproduction, 22 (2), 610-615. doi: 10.1093/humrep/del382

  • Replicated effects of sex and genotype on gene expression in human lymphoblastoid cell lines

    McRae, A. F., Matigian, N. A., Vadlamudi, L., Mulley, J. C., Mowry, B., Martin, N. G., Berkovic, S. F., Hayward, N. K. and Visscher, P. M. (2007). Replicated effects of sex and genotype on gene expression in human lymphoblastoid cell lines. Human Molecular Genetics, 16 (4), 364-373. doi: 10.1093/hmg/ddl456

  • Replication of reported linkages for dyslexia and spelling and suggestive evidence for novel regions on chromosomes 4 and 17

    Bates, Timothy C., Luciano, Michelle, Castles, Anne, Coltheart, Max, Wright, Margaret J. and Martin, Nicholas G. (2007). Replication of reported linkages for dyslexia and spelling and suggestive evidence for novel regions on chromosomes 4 and 17. European Journal of Human Genetics, 15 (2), 194-203. doi: 10.1038/sj.ejhg.5201739

  • The ongoing adaptive evolution of ASPM and microcephalin is not explained by increased intelligence

    Mekel-Bobrov, Nitzan, Posthuma, Danielle, Gilbert, Sandra L., Lind, Penelope, Gosso, M. Florencia, Luciano, Michelle, Harris, Sarah E., Bates, Timothy C., Polderman, Tinca J., Whalley, Lawrence J., Fox, Helen, Starr, John M., Evans, Patrick D., Montgomery, Grant W., Fernandes, Croydon, Heutink, Peter, Martin, Nicholas G., Boomsma, Dorret I., Deary, Ian J., Wright, Margaret J., de Geus, Eco J. and Lahn, Bruce T. (2007). The ongoing adaptive evolution of ASPM and microcephalin is not explained by increased intelligence. Human Molecular Genetics, 16 (6), 600-608. doi: 10.1093/hmg/ddl487

  • "No thanks, it keeps me awake". The genetics of coffee-attributed sleep disturbance

    Luciano, M., Ghu, Z., Kirk, K. M., Gordon, S. D., Heath, A. C., Montgomery, G. W. and Martin, N. G. (2007). "No thanks, it keeps me awake". The genetics of coffee-attributed sleep disturbance. Sleep, 30 (10), 1378-1386. doi: 10.1093/sleep/30.10.1378

  • A behavior genetic investigation of adolescent motherhood and offspring mental health problems

    Harden, K. P., Lynch, S. K., Turkheimer, E., Emery, R. E., D'Onofrio, B. M., Slutske, W. S., Waldron, M. D., Statham, D. J. and Martin, N. G. (2007). A behavior genetic investigation of adolescent motherhood and offspring mental health problems. Journal of Abnormal Psychology, 116 (4), 667-683. doi: 10.1037/0021-843X.116.4.667

  • A genome-wide scan for naevus count: Linkage to CDKN2A and to other chromosome regions

    Zhu, Gu, Montgomery, Grant W., James, Michael R., Trent, Jeff M., Hayward, Nicholas K., Martin, Nicholas G. and Duffy, David L. (2007). A genome-wide scan for naevus count: Linkage to CDKN2A and to other chromosome regions. European Journal of Human Genetics, 15 (1), 94-102. doi: 10.1038/sj.ejhg.5201729

  • A three-single-nucleotide polymorphism haplotype in intron 1 of OCA2 explains most human eye-color variation

    Duffy, D. L., Montgomery, G. W., Chen, W., Zhao, Z. Z., Le, L., James, M. R., Hayward, N. K., Martin, N. G. and Sturm, R. A. (2007). A three-single-nucleotide polymorphism haplotype in intron 1 of OCA2 explains most human eye-color variation. American Journal of Human Genetics, 80 (2), 241-252. doi: 10.1086/510885

  • Age at first sexual intercourse and teenage pregnancy in Australian female twins

    Waldron, M., Heath, A. C., Turkheimer, E., Emery, R., Bucholz, K. K., Madden, P. A. and Martin, N. G. (2007). Age at first sexual intercourse and teenage pregnancy in Australian female twins. Twin Research & Human Genetics, 10 (3), 440-449. doi: 10.1375/twin.10.3.440

  • Cholinergic nicotinic receptor genes implicated in a nicotine dependence association study targeting 348 candidate genes with 3713 SNPs

    Saccone, S. F., Hinrichs, A. L., Saccone, N. L., Chase, G. A., Konvicka, K., Madden, P. A., Breslau, N., Johnson, E. O., Hatsukami, D., Pomerleau, O., Swan, G. E., Goate, A. M., Rutter, J., Bertelsen, S., Fox, L., Fugman, D., Martin, N. G., Montgomery, G. W., Wang, J. C., Ballinger, D. G., Rice, J. P. and Bierut, L. J. (2007). Cholinergic nicotinic receptor genes implicated in a nicotine dependence association study targeting 348 candidate genes with 3713 SNPs. Human Molecular Genetics, 16 (1), 36-49. doi: 10.1093/hmg/ddl438

  • Contrasting models of genetic co-morbidity for cannabis and other illicit drugs in adult Australian twins

    Agrawal, A., Lynskey, M. T., Bucholz, K. K., Martin, N. G., Madden, P. A. and Heath, A. C. (2007). Contrasting models of genetic co-morbidity for cannabis and other illicit drugs in adult Australian twins. Psychological Medicine, 37 (1), 49-60. doi: 10.1017/S0033291706009287

  • Effects of SCA1, MJD, and DPRLA triplet repeat polymorphisms on cognitive phenotypes in a normal population of adolescent twins

    Luciano, M, Hine, E., Wright, M. J., Duffy, D. L., MacMillan, J. and Martins, N. G. (2007). Effects of SCA1, MJD, and DPRLA triplet repeat polymorphisms on cognitive phenotypes in a normal population of adolescent twins. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 144B (1), 95-100. doi: 10.1002/ajmg.b.30413

  • Exploring the inter-relationship of smoking age-at-onset, cigarette consumption and smoking persistence: Genes or environment?

    Morley, K. I., Lynskey, M. T., Madden, P. A., Treloar, S. A., Heath, A. C. and Martin, N. G. (2007). Exploring the inter-relationship of smoking age-at-onset, cigarette consumption and smoking persistence: Genes or environment?. Psychological Medicine, 37 (9), 1357-1367. doi: 10.1017/S0033291707000748

  • Genetic and phenotypic stability of measures of neuroticism over 22 years

    Wray, N. R., Birley, A. J., Sullivan, P. F., Visscher, P. M. and Martin, N. G. (2007). Genetic and phenotypic stability of measures of neuroticism over 22 years. Twin Research & Human Genetics, 10 (5), 695-702. doi: 10.1375/twin.10.5.695

  • Genetic linkage to chromosome 22q12 for a heavy-smoking quantitative trait in two independent samples

    Saccone, Scott F., Pergadia, Michele L., Loukola, Anu, Broms, Ula, Montgomery, Grant W., Wang, Jen C., Agrawal, Arpana, Dick, Danielle M., Heath, Andrew C., Todorov, Alexandre A., Maunu, Heidi, Heikkila, Kauko, Morley, Katherine I., Rice, John P., Todd, Richard D., Kaprio, Jaakko, Peltonen, Leena, Martin, Nicholas G., Goate, Alison M. and Madden, Pamela A. (2007). Genetic linkage to chromosome 22q12 for a heavy-smoking quantitative trait in two independent samples. American Journal of Human Genetics, 80 (5), 856-866. doi: 10.1086/513703

  • Genome-wide scan for blood pressure in Australian and Dutch subjects suggests linkage at 5P, 14Q, and 17P

    Hottenga, Jouke-Jan, Whitfield, John B., Posthuma, Danielle, Willemsen, Gonneke, de Geus, Eco J. C., Martin, Nicholas G. and Boomsma, Dorret I. (2007). Genome-wide scan for blood pressure in Australian and Dutch subjects suggests linkage at 5P, 14Q, and 17P. Hypertension, 49 (4), 832-838. doi: 10.1161/01.HYP.0000260092.93964.ed

  • Genomewide scans of red cell indices suggest linkage on chromosome 6q23

    Iliadou, A., Evans, D. M., Zhu, G., Duffy, D. L., Frazer, I. H., Montgomery, G. W. and Martin, N. G. (2007). Genomewide scans of red cell indices suggest linkage on chromosome 6q23. Journal of Medical Genetics, 44 (1), 24-30. doi: 10.1136/jmg.2006.043521

  • Marital conflict and conduct problems in Children of Twins

    Harden, K. P., Turkheimer, E., Emery, R. E., D'Onofrio, B. M., Slutske, W. S., Heath, A. C. and Martin, N. G. (2007). Marital conflict and conduct problems in Children of Twins. Child Development, 78 (1), 1-18. doi: 10.1111/j.1467-8624.2007.00982.x

  • Novel genes identified in a high-density genome wide association study for nicotine dependence

    Bierut, L. J., Madden, P. A., Breslau, N., Johnson, E. O., Hatsukami, D., Pomerleau, O. F., Swan, G. E., Rutter, J., Bertelsen, S., Fox, L., Fugman, D., Goate, A. M., Hinrichs, A. L., Konvicka, K., Martin, N. G., Montgomery, G. W., Saccone, N. L., Saccone, S. F., Wang, J. C., Chase, G. A., Rice, J. P. and Ballinger, D. G. (2007). Novel genes identified in a high-density genome wide association study for nicotine dependence. Human Molecular Genetics, 16 (1), 24-35. doi: 10.1093/hmg/ddl441

  • Ridgecounter: A program for obtaining semi-automated finger ridge counts

    Medland, S. E., Park, D. A., Loesch, D. Z. and Martin, N. G. (2007). Ridgecounter: A program for obtaining semi-automated finger ridge counts. Annals of Human Biology, 34 (4), 504-517. doi: 10.1080/03014460701431896

  • Significant evidence of one or more susceptibility loci for endometriosis with near-Mendelian inheritance on chromosome 7p13-15

    Zondervan, K. T., Treloar, S. A., Lin, J., Weeks, D. E., Nyholt, D. R., Mangion, J., MacKay, I. J., Cardon, L. R., Martin, N. G., Kennedy, S. H. and Montgomery, G. W. (2007). Significant evidence of one or more susceptibility loci for endometriosis with near-Mendelian inheritance on chromosome 7p13-15. Human Reproduction, 22 (3), 717-728. doi: 10.1093/humrep/del446

  • Stimulant use and symptoms of abuse/dependence: epidemiology and associations with cannabis use--a twin study

    Lynskey, Michael T., Grant, Julia D., Li, Lia, Nelson, Elliot C., Bucholz, Kathleen K., Madden, Pamela A. F., Statham, Dixie, Martin, Nicholas G. and Heath, Andrew C. (2007). Stimulant use and symptoms of abuse/dependence: epidemiology and associations with cannabis use--a twin study. Drug & Alcohol Dependence, 86 (2-3), 147-153. doi: 10.1016/j.drugalcdep.2006.05.023

  • Genetic Influences on Exercise Participation in 37.051 Twin Pairs from Seven Countries

    Stubbe, Janine H., Boomsma, Dorret I., Vink, Jacqueline M., Cornes, Belinda K., Martin, Nicholas G., Skytthe, Axel, Kyvik, Kirsten O., Rose, Richard J., Kujala, Urho M., Harris, Jennifer R., Pedersen, Nancy L., Hunkin, Janice, Spector, Tin D. and De Geus, Eco J. C. (2006). Genetic Influences on Exercise Participation in 37.051 Twin Pairs from Seven Countries. PLoS ONE, 1 (1) e22, e22. doi: 10.1371/journal.pone.0000022

  • Use of latent profile analysis to identify eating disorder phenotypes in an adult Australian twin cohort

    Wade, Tracey D., Crosby, Ross D. and Martin, Nicholas G. (2006). Use of latent profile analysis to identify eating disorder phenotypes in an adult Australian twin cohort. Archives of General Psychiatry, 63 (12), 1377-1384. doi: 10.1001/archpsyc.63.12.1377

  • Genetic and Cultural Transmission of Smoking Initiation: An Extended Twin Kinship Model

    Maes, Hermine H., Neale, Michael C., Kendler, Kenneth S., Martin, Nicholas G., Heath, Andrew C. and Eaves, Lindon J. (2006). Genetic and Cultural Transmission of Smoking Initiation: An Extended Twin Kinship Model. Behavior Genetics, 36 (6), 795-808. doi: 10.1007/s10519-006-9085-4

  • Childhood sexual abuse and risks for licit and illicit drug-related outcomes: a twin study

    Nelson, Elliot C., Heath, Andrew C., Lynskey, Michael T., Bucholz, Kathleen K., Madden, Pamela A. F., Statham, Dixie J. and Martin, Nicholas G. (2006). Childhood sexual abuse and risks for licit and illicit drug-related outcomes: a twin study. Psychological Medicine, 36 (10), 1473-1483. doi: 10.1017/S0033291706008397

  • A simple method to localise pleiotropic susceptibility loci using univariate linkage analyses of correlated traits

    Ferreira, Manuel A. R., Visscher, Peter M., Martin, Nicholas G. and Duffy, David L. (2006). A simple method to localise pleiotropic susceptibility loci using univariate linkage analyses of correlated traits. European Journal of Human Genetics, 14 (8), 953-962. doi: 10.1038/sj.ejhg.5201646

  • Genetic variation of individual alpha frequency (IAF) and alpha power in a large adolescent twin sample

    Smit, Christine M., Wright, Margaret J., Hansell, Narelle K., Geffen, Gina M. and Martin, Nicholas G. (2006). Genetic variation of individual alpha frequency (IAF) and alpha power in a large adolescent twin sample. International Journal of Psychophysiology, 61 (2), 235-243. doi: 10.1016/j.ijpsycho.2005.10.004

  • Increased DNA Methylation at the AXIN1 Gene in a Monozygotic Twin from a Pair Discordant for a Caudal Duplication Anomaly

    Oates, N. A., van Vliet, J., Duffy, D. L., Kroes, H. Y., Martin, N. G., Boomsma, D. I., Campbell, M., Coulthard, M. G., Whitelaw, E. and Chong, S. (2006). Increased DNA Methylation at the AXIN1 Gene in a Monozygotic Twin from a Pair Discordant for a Caudal Duplication Anomaly. American Journal of Human Genetics, 79 (1), 155-162. doi: 10.1086/505031

  • Duration of cannabis use - a novel phenotype?

    Lynskey, Michael T., Grant, Julia D., Nelson, Elliot C., Bucholz, Kathleen K., Madden, Pamela A. F., Statham, Dixie J., Martin, Nicholas G. and Heath, Andrew C. (2006). Duration of cannabis use - a novel phenotype?. Addictive Behaviors, 31 (6), 984-994. doi: 10.1016/j.addbeh.2006.03.048

  • Heritability and genetic covariation of sensitivity to PROP, SOA, quinine HCl, and caffeine

    Hansen, Jonathan L., Reed, Danielle R., Wright, Margaret J., Martin, Nicholas G. and Breslin, Paul. A. S. (2006). Heritability and genetic covariation of sensitivity to PROP, SOA, quinine HCl, and caffeine. Chemical Senses, 31 (3), 403-413. doi: 10.1093/chemse/bjj044

  • The heritability of conscientiousness facets and their relationship to IQ and academic achievement

    Luciano, Michelle, Wainwright, Mark A., Wright, Margaret J. and Martin, Nicholas G. (2006). The heritability of conscientiousness facets and their relationship to IQ and academic achievement. Personality and Individual Differences, 40 (6), 1189-1199. doi: 10.1016/j.paid.2005.10.013

  • Assumption-free estimation of heritability from genome-wide identity-by-descent sharing between full siblings

    Visscher, Peter M., Medland, Sarah E., Ferreira, Manuel A. R., Morley, Katherine I., Zhu, Gu, Cornes, Belinda K., Montgomery, Grant W. and Martin, Nicholas G. (2006). Assumption-free estimation of heritability from genome-wide identity-by-descent sharing between full siblings. Plos Genetics, 2 (3), 316-325. doi: 10.1371/journal.pgen.0020041

  • Cognitive modelling and the behaviour genetics of reading

    Castles, Anne, Bates, Timothy, Coltheart, Max, Luciano, Michelle and Martin, Nicholas G. (2006). Cognitive modelling and the behaviour genetics of reading. Journal of Research In Reading, 29 (1), 92-103. doi: 10.1111/j.1467-9817.2006.00294.x

  • Handedness in twins: Joint analysis of data from 35 samples

    Medland, Sarah E., Duffy, David L., Wright, Margaret J., Geffen, Gina M. and Martin, Nicholas G. (2006). Handedness in twins: Joint analysis of data from 35 samples. Twin Research and Human Genetics, 9 (1), 46-53. doi: 10.1375/183242706776402885

  • A Transdiagnostic Approach to Understanding Eating Disorders

    Wade, Tracey D., Bergin, Jacqueline L., Martin, Nicholas G., Gillespie, Nathan A. and Fairburn, Christopher G. (2006). A Transdiagnostic Approach to Understanding Eating Disorders. Journal of Nervous And Mental Disease, 194 (7), 510-517. doi: 10.1097/01.nmd.0000225067.42191.b0

  • A genetically informed study of the association between harsh punishment and offspring behavioral problems

    Lynch, Stacy K., Turkheimer, Eric, D'Onofrio, Brian M., Mendle, Jane, Emery, Robert E., Slutske, Wendy S. and Martin, Nicholas G. (2006). A genetically informed study of the association between harsh punishment and offspring behavioral problems. Journal of Family Psychology, 20 (2), 190-198. doi: 10.1037/0893-3200.20.2.190

  • A genetically informed study of the processes underlying the association between parental marital instability and offspring adjustment

    Donofrio, Brian M., Turkheimer, Eric, Emery, Robert E., Slutske, Wendy S., Heath, Andrew C., Madden, Pamela A. and Martin, Nicholas G. (2006). A genetically informed study of the processes underlying the association between parental marital instability and offspring adjustment. Developmental Psychology, 42 (3), 486-499. doi: 10.1037/0012-1649.42.3.486

  • A genome scan for epidermal skin pattern in adolescent twins reveals suggestive linkage on 12p13.31

    Shekar, Sri Niranjan, Duffy, David L., Montgomery, Grant W. and Martin, Nicholas G. (2006). A genome scan for epidermal skin pattern in adolescent twins reveals suggestive linkage on 12p13.31. Journal of Investigative Dermatology, 126 (2), 277-282. doi: 10.1038/sj.jid.5700067

  • A linkage study of academic skills defined by the Queensland Core Skills Test

    Wainwright, Mark A., Wright, Margaret J., Luciano, Michelle, Montgomery, Grant W., Geffen, Gina M. and Martin, Nicholas G. (2006). A linkage study of academic skills defined by the Queensland Core Skills Test. Behavior Genetics, 36 (1), 56-64. doi: 10.1007/s10519-005-9013-z

  • A possible smoking susceptibility locus on chromosome 11p12: Evidence from sex-limitation linkage analyses in a sample of Australian twin families

    Morley, Katherine I., Medland, Sarah E., Ferreira, Manuel A. R., Lynskey, Michael T., Montgomery, Grant W., Heath, Andrew C., Madden, Pamela A. F. and Martin, Nicholas G. (2006). A possible smoking susceptibility locus on chromosome 11p12: Evidence from sex-limitation linkage analyses in a sample of Australian twin families. Behavior Genetics, 36 (1), 87-99. doi: 10.1007/s10519-005-9004-0

  • Assortative Mating for Cigarette Smoking and for Alcohol Consumption in Female Australian Twins and their Spouses

    Agrawal, Arpana, Heath, Andrew C., Grant, Julia D., Pergadia, Michele L., Statham, Dixie J., Bucholz, Kathleen K., Martin, Nicholas G. and Madden, Pamela A. F. (2006). Assortative Mating for Cigarette Smoking and for Alcohol Consumption in Female Australian Twins and their Spouses. Behavior Genetics, 36 (4), 553-566. doi: 10.1007/s10519-006-9081-8

  • Bias, precision and heritability of self-reported and clinically measured height in Australian twins

    Macgregor, Stuart, Cornes, Belinda K., Martin, Nicholas G. and Visscher, Peter M. (2006). Bias, precision and heritability of self-reported and clinically measured height in Australian twins. Human Genetics, 120 (4), 571-580. doi: 10.1007/s00439-006-0240-z

  • Butyrylcholinesterase: Association with the metabolic syndrome and identification of 2 gene loci affecting activity

    Valle, Anne, OConnor, Daniel T., Taylor, Palmer, Zhu, Gu, Montgomery, Grant W., Slagboom, P. Eline, Martin, Nicholas G. and Whitfield, John B. (2006). Butyrylcholinesterase: Association with the metabolic syndrome and identification of 2 gene loci affecting activity. Clinical Chemistry, 52 (6), 1014-1020. doi: 10.1373/clinchem.2005.065052

  • Effects of Variation at the ALDH2 Locus on Alcohol Metabolism, Sensitivity, Consumption, and Dependence in Europeans

    Dickson, Peter A., James, Michael R., Heath, Andrew C., Montgomery, Grant W., Martin, Nicholas G., Whitfield, John B. and Birley, Andrew J. (2006). Effects of Variation at the ALDH2 Locus on Alcohol Metabolism, Sensitivity, Consumption, and Dependence in Europeans. Alcoholism - Clinical And Experimental Research, 30 (7), 1093-1100. doi: 10.1111/j.1530-0277.2006.00128.x

  • Empirical Evaluation of the Genetic Similarity of Samples From Twin Registries in Australia and the Netherlands Using 359 STRP Markers

    Sullivan, Patrick F., Montgomery, Grant W., Hottenga, Jouke J., Wray, Naomi R., Boomsma, Dorret I. and Martin, Nicholas G. (2006). Empirical Evaluation of the Genetic Similarity of Samples From Twin Registries in Australia and the Netherlands Using 359 STRP Markers. Twin Research And Human Genetics, 9 (4), 600-602. doi: 10.1375/183242706778025026

  • Family structure and age at menarche: A children-of-twins approach

    Mendle, Jane, Turkheimer, Eric, D'Onofrio, Brian M., Lynch, Stacy K., Emery, Robert E., Slutske, Wendy S. and Martin, Nicholas G. (2006). Family structure and age at menarche: A children-of-twins approach. Developmental Psychology, 42 (3), 533-542. doi: 10.1037/0012-1649.42.3.533

  • Genetic analyses of DSM-IV nicotine withdrawal in adult twins

    Pergadia, Michele L., Heath, Andrew C., Martin, Nicholas G. and Madden, Pamela A. F. (2006). Genetic analyses of DSM-IV nicotine withdrawal in adult twins. Psychological Medicine, 36 (7), 963-972. doi: 10.1017/S0033291706007495

  • Genetic and environmental influences on extreme personality dispositions in adolescent female twins

    Pergadia, Michele L., Madden, Pamela A. F., Lessov, Christina N., Todorov, Alexandre A., Bucholz, Kathleen K., Martin, Nicholas G. and Heath, Andrew C. (2006). Genetic and environmental influences on extreme personality dispositions in adolescent female twins. Journal of Child Psychology And Psychiatry, 47 (9), 902-909. doi: 10.1111/j.1469-7610.2005.01568.x

  • Genome-wide linkage scan for loci influencing plasma triglycerides

    Middelberg, Rita P., Martin, Nicholas G., Montgomery, Grant W. and Whitfield, John B. (2006). Genome-wide linkage scan for loci influencing plasma triglycerides. Clinica Chimica Acta, 374 (1-2), 87-92. doi: 10.1016/j.cca.2006.05.033

  • Genome-wide scan of IQ finds significant linkage to a quantitative trait locus on 2q

    Luciano, M., Wright, M. J., Duffy, D. L., Wainwright, M. A., Zhu, G., Evans, D. M., Geffen, G. M., Montgomery, G. W. and Martin, N. G. (2006). Genome-wide scan of IQ finds significant linkage to a quantitative trait locus on 2q. Behavior Genetics, 36 (1), 45-55. doi: 10.1007/s10519-005-9003-1

  • HLA and Genomewide Allele Sharing in Dizygotic Twins

    Montgomery, Grant W., Zhu, Gu, Hottenga, Jouke J., Duffy, David L., Heath, Andrew C., Boomsma, Dorret I., Martin, Nicholas G. and Visscher, Peter M. (2006). HLA and Genomewide Allele Sharing in Dizygotic Twins. American Journal of Human Genetics, 79 (6), 1052-1058. doi: 10.1086/510136

  • Heritability and Stability of Resting Blood Pressure in Australian Twins

    Hottenga, Jouke-Jan, Whitfield, John B., de Geus, Eco J. C., Boomsma, Dorret I. and Martin, Nicholas G. (2006). Heritability and Stability of Resting Blood Pressure in Australian Twins. Twin Research And Human Genetics, 9 (2), 205-209. doi: 10.1375/183242706776382455

  • Heritability and nineteen-year stability of long and short EPQ-R Neuroticism scales

    Birley, Andrew J., Gillespie, Nathan A., Heath, Andrew C., Sullivan, Patrick F., Boomsma, Dorret I. and Martin, Nicholas G. (2006). Heritability and nineteen-year stability of long and short EPQ-R Neuroticism scales. Personality And Individual Differences, 40 (4), 737-747. doi: 10.1016/j.paid.2005.09.005

  • KRAS variation and risk of endometriosis

    Zhao, Z. Z., Nyholt, D. R., Le, L., Martin, N. G., James, M. R., Treloar, S. A. and Montgomery, G. W. (2006). KRAS variation and risk of endometriosis. Molecular Human Reproduction, 12 (11), 671-676. doi: 10.1093/molehr/gal078

  • Linkage analyses of event-related potential slow wave phenotypes recorded in a working memory task

    Hansell, N. K., Medland, S. E., Ferreira, A. R., Geffen, G. M., Zhu, G., Montgomery, G. W., Duffy, D. L., Wright, M.J. and Martin, N. G. (2006). Linkage analyses of event-related potential slow wave phenotypes recorded in a working memory task. Behavior Genetics, 36 (1), 29-44. doi: 10.1007/s10519-005-9002-2

  • Longitudinal Genetic Analysis of Plasma Lipids

    Middelberg, Rita P., Martin, Nicholas G. and Whitfield, John B. (2006). Longitudinal Genetic Analysis of Plasma Lipids. Twin Research And Human Genetics, 9 (4), 550-557. doi: 10.1375/183242706778024946

  • Maternal alcohol use disorder and offspring ADHD: disentangling genetic and environmental effects using a children-of-twins design

    Knopik, Valerie S., Heath, Andrew C., Jacob, Theodore, Slutske, Wendy S., Bucholz, Kathleen K., Madden, Pamela A. F., Waldron, Mary and Martin, Nicholas G. (2006). Maternal alcohol use disorder and offspring ADHD: disentangling genetic and environmental effects using a children-of-twins design. Psychological Medicine, 36 (10), 1461-1471. doi: 10.1017/S0033291706007884

  • Migraine With Aura and Migraine Without Aura Are Not Distinct Entities: Further Evidence From a Large Dutch Population Study

    Ligthart, Lannie, Boomsma, Dorret I., Martin, Nicholas G., Stubbe, Janine H. and Nyholt, Dale R. (2006). Migraine With Aura and Migraine Without Aura Are Not Distinct Entities: Further Evidence From a Large Dutch Population Study. Twin Research And Human Genetics, 9 (1), 54-63. doi: 10.1375/183242706776403019

  • Novel variants in growth differentiation factor 9 in mothers of dizygotic twins

    Palmer, J. S., Zhao, Z. Z., Hoekstra, C., Hayward, N. K., Webb, P. M., Whiteman, D. C., Martin, N. G., Boomsma, D. I., Duffy, D. L. and Montgomery, G. W. (2006). Novel variants in growth differentiation factor 9 in mothers of dizygotic twins. Journal of Clinical Endocrinology And Metabolism, 91 (11), 4713-4716. doi: 10.1210/jc.2006-0970

  • Population differences in finger-length ratios: Ethnicity or latitude?

    Loehlin, John C., McFadden, Dennis, Medland, Sarah E. and Martin, Nicholas G. (2006). Population differences in finger-length ratios: Ethnicity or latitude?. Archives of Sexual Behavior, 35 (6), 739-742. doi: 10.1007/s10508-006-9039-1

  • Rapid screening of 4000 individuals for germ-line variations in the BRAF gene

    James, Michael R., Dumeni, Troy, Stark, Mitchell S., Duffy, David L., Montgomery, Grant W., Martin, Nicholas G. and Hayward, Nicholas K. (2006). Rapid screening of 4000 individuals for germ-line variations in the BRAF gene. Clinical Chemistry, 52 (9), 1675-1678. doi: 10.1373/clinchem.2006.070169

  • Replicated linkage for eye color on 15q using comparative ratings of sibling pairs

    Posthuma, D., Visscher, P. M., Willemsen, G., Zhu, G., Martin, N. G., Slagboom, P. E., de Geus, E. J. C. and Boomsma, D. I. (2006). Replicated linkage for eye color on 15q using comparative ratings of sibling pairs. Behavior Genetics, 36 (1), 12-17. doi: 10.1007/s10519-005-9007-x

  • Sex Differences in Symptoms of Depression in Unrelated Individuals and Opposite-Sex Twin and Sibling Pairs

    Middeldorp, Christel M., Wray, Naomi R., Andrews, Gavin, Martin, Nicholas G. and Boomsma, Dorret I. (2006). Sex Differences in Symptoms of Depression in Unrelated Individuals and Opposite-Sex Twin and Sibling Pairs. Twin Research And Human Genetics, 9 (5), 632-636. doi: 10.1375/183242706778553507

  • Subtypes of Illicit Drug Users: A Latent Class Analysis of Data From an Australian Twin Sample

    Lynskey, Michael T., Agrawal, Arpana, Bucholz, Kathleen K., Nelson, Elliot C., Madden, Pamela A. F., Todorov, Alexandre A., Grant, Julia D., Martin, Nicholas G. and Heath, Andrew C. (2006). Subtypes of Illicit Drug Users: A Latent Class Analysis of Data From an Australian Twin Sample. Twin Research And Human Genetics, 9 (4), 523-530. doi: 10.1375/183242706778024964

  • The implications of simultaneous smoking initiation for inferences about the genetics of smoking behavior from twin data

    Pergadia, Michele L., Heath, Andrew C., Agrawal, Arpana, Bucholz, Kathleen K., Martin, Nicholas G. and Madden, Pamela A. F. (2006). The implications of simultaneous smoking initiation for inferences about the genetics of smoking behavior from twin data. Behavior Genetics, 36 (4), 567-576. doi: 10.1007/s10519-005-9042-7

  • The return to schooling: Estimates from a sample of young Australian twins

    Miller, Paul, Mulvey, Charles and Martin, Nick (2006). The return to schooling: Estimates from a sample of young Australian twins. Labour Economics, 13 (5), 571-587. doi: 10.1016/j.labeco.2004.10.008

  • Variance components analyses of multiple asthma traits in a large sample of Australian families ascertained through a twin proband

    Ferreira, M. A. R., OGorman, L., Souef, P. L., Burton, P. R., Toelle, B. G., Robertson, C. F., Martin, N. G. and Duffy, D. L. (2006). Variance components analyses of multiple asthma traits in a large sample of Australian families ascertained through a twin proband. Allergy, 61 (2), 245-253. doi: 10.1111/j.1398-9995.2005.00954.x

  • ViewPoint and ViewDist: Utilities for rapid graphing of linkage distributions and identification of outliers

    Beeby, Harry N., Medland, Sarah E. and Martin, Nicholas G. (2006). ViewPoint and ViewDist: Utilities for rapid graphing of linkage distributions and identification of outliers. Behavior Genetics, 36 (1), 7-11. doi: 10.1007/s10519-006-9045-z

  • A comparison of twin birthweight data from Australia, the Netherlands, the United States, Japan, and South Korea: Are genetic and environmental variations in birthweight similar in Caucasians and East Asians?

    Hur, YM, Luciano, M, Martin, NG, Boomsma, DI, Iacono, WG, McGue, M, Shin, JS, Jun, JK, Ooki, S, van Beijsterveldt, CEM and Han, JY (2005). A comparison of twin birthweight data from Australia, the Netherlands, the United States, Japan, and South Korea: Are genetic and environmental variations in birthweight similar in Caucasians and East Asians?. Twin Research and Human Genetics, 8 (6), 638-648. doi: 10.1375/twin.8.6.638

  • BRAF Polymorphisms and Risk of Melanocytic Neoplasia

    James, Michael R., Roth, Richard B., Shi, Michael M., Kammerer, Stefan, Nelson, Matthew R., Stark, Mitchell S., Dumenil, Troy, Montgomery, Grant W., Hayward, Nicholas K., Martin, Nicholas G., Braun, Andreas and Duffy, David L. (2005). BRAF Polymorphisms and Risk of Melanocytic Neoplasia. Journal of Investigative Dermatology, 125 (6), 1252-1258. doi: 10.1111/j.0022-202X.2005.23937.x

  • Familial clustering of major depression and anxiety disorders in Australian and Dutch twins and siblings

    Middledorp, Christel M., Birley, Andrew J., Cath, Danielle C., Gillespie, Nathan A., Willemsen, Gonneke, Statham, Dixie J., de Geus, Eco J. C., Andrews, J. Gavin, van Dyck, Richard, Beem, A. Leo, Sullivan, Patrick F., Martin, Nicholas G. and Boomsma, Dorret I. (2005). Familial clustering of major depression and anxiety disorders in Australian and Dutch twins and siblings. Twin Research and Human Genetics, 8 (6), 609-615. doi: 10.1375/183242705774860123

  • Genetic and environmental influences on skin pattern deterioration

    Shekar, Sri Niranjan, Luciano, Michelle, Duffy, David L. and Martin, Nicholas G. (2005). Genetic and environmental influences on skin pattern deterioration. Journal of Investigative Dermatology, 125 (6), 1119-1129. doi: 10.1111/j.0022-202X.2005.23961.x

  • Limitations of DSM-IV operationalizations of alcohol abuse and dependence in a sample of Australian twins

    Lynskey, Michael T., Nelson, Elliot C., Neuman, Rosalind J., Bucholz, Kathleen K., Madden, Pamela A. F., Knopik, Valerie S., Slutske, Wendy, Whitfield, John B., Martin, Nicholas G. and Heath, Andrew C. (2005). Limitations of DSM-IV operationalizations of alcohol abuse and dependence in a sample of Australian twins. Twin Research and Human Genetics, 8 (6), 574-584. doi: 10.1375/183242705774860178

  • Robust estimation of experimentwise P values applied to a genome scan of multiple asthma traits identifies a new region of significant linkage on chromosome 20q13

    Ferreira, MAR, O'Gorman, L, Le Souef, P, Burton, PR, Toelle, BG, Robertson, CF, Visscher, PM, Martin, NG and Duffy, DL (2005). Robust estimation of experimentwise P values applied to a genome scan of multiple asthma traits identifies a new region of significant linkage on chromosome 20q13. American Journal of Human Genetics, 77 (6), 1075-1085. doi: 10.1086/497997

  • Sex-limited genome-wide linkage scan for body mass index in an unselected sample of 933 Australian twin families

    Cornes, BK, Medland, SE, Ferreira, MAR, Morley, KI, Duffy, DL, Heijmans, BT, Montgomery, GW and Martin, NG (2005). Sex-limited genome-wide linkage scan for body mass index in an unselected sample of 933 Australian twin families. Twin Research and Human Genetics, 8 (6), 616-632. doi: 10.1375/183242705774860240

  • A genetically informed study of marital instability and its association with offspring psychopathology

    D'Onofrio, Brian M., Turkheimer, Eric, Emery, Robert E., Slutske, Wendy S., Heath, Andrew C., Madden, Pamela A. and Martin, Nicholas G. (2005). A genetically informed study of marital instability and its association with offspring psychopathology. Journal of Abnormal Psychology, 114 (4), 570-586. doi: 10.1037/0021-843X.114.4.570

  • Correlates of regular cigarette smoking in a population-based sample of Australian twins

    Agrawal, Arpana, Madden, Pamela A. F., Heath, Andrew C., Lynskey, Michael T., Bucholz, Kathleen K. and Martin, Nicholas G. (2005). Correlates of regular cigarette smoking in a population-based sample of Australian twins. Addiction, 100 (11), 1709-1719. doi: 10.1111/j.1360-0443.2005.01217.x

  • Genetic covariation between event-related potential (ERP) and behavioral non-ERP measures of working-memory, processing speed, and IQ

    Hansell, N. K., Wright, M. J., Luciano, M., Geffen, G. M., Geffen, L. B. and Martin, N. G. (2005). Genetic covariation between event-related potential (ERP) and behavioral non-ERP measures of working-memory, processing speed, and IQ. Behavior Genetics, 35 (6), 695-706. doi: 10.1007/s10519-005-6188-2

  • Opposite effects of androgen receptor CAG repeat length on increased risk of left-handedness in males and females

    Medland, Sarah E., Duffy, David L., Spurdle, Amanda B., Wright, Margaret J., Geffen, Gina M., Montgomery, Grant W. and Martin, Nicholas G. (2005). Opposite effects of androgen receptor CAG repeat length on increased risk of left-handedness in males and females. Behavior Genetics, 35 (6), 735-744. doi: 10.1007/s10519-005-6187-3

  • Widespread evidence for non-additive genetic variation in Cloninger's and Eysenck's personality dimensions using a twin plus sibling design

    Keller, MC, Coventry, WL, Heath, AC and Martin, NG (2005). Widespread evidence for non-additive genetic variation in Cloninger's and Eysenck's personality dimensions using a twin plus sibling design. Behavior Genetics, 35 (6), 707-721. doi: 10.1007/s10519-005-6041-7

  • Meta-analysis of four new genome scans for lipid parameters and analysis of positional candidates in positive linkage regions

    Heijmans, BT, Beekman, M, Putter, H, Lakenberg, N, van der Wijk, HJ, Whitfield, JB, Posthuma, D, Pedersen, NL, Martin, NG, Boomsma, DI and Slagboom, PE (2005). Meta-analysis of four new genome scans for lipid parameters and analysis of positional candidates in positive linkage regions. European Journal of Human Genetics, 13 (10), 1143-1153. doi: 10.1038/sj.ejhg.5201466

  • Psychological masculinity-femininity via the gender diagnosticity approach: heritability and consistency across ages and populations

    Loehlin, John C., Jonsson, Erik G., Gustavsson, J. Petter, Stallings, Michael C., Gillespie, Nathan A., Wright, Margaret J. and Martin, Nicholas G. (2005). Psychological masculinity-femininity via the gender diagnosticity approach: heritability and consistency across ages and populations. Journal of Personality, 73 (5), 1295-1320. doi: 10.1111/j.1467-6494.2005.00350.x

  • The genetics of tea and coffee drinking and preference for source of caffeine in a large community sample of Australian twins

    Luciano, Michelle, Kirk, Katherine M., Heath, Andrew C. and Martin, Nicholas G. (2005). The genetics of tea and coffee drinking and preference for source of caffeine in a large community sample of Australian twins. Addiction, 100 (10), 1510-1517. doi: 10.1111/j.1360-0443.2005.01223.x

  • Genomewide significant linkage to migrainous Hheadache on chromosome 5q21

    Nyholt, Dale R., Morley, Katherine I., Ferreira, Manual A. R., Medland, Sarah E., Boomsma, Dorret I., Heath, Andrew C., Merikangas, Kathleen R., Montgomery, Grant W. and Martin, Nicholas G. (2005). Genomewide significant linkage to migrainous Hheadache on chromosome 5q21. American Journal Of Human Genetics, 77 (3), 500-512. doi: 10.1086/444510

  • A genomewide scan for intelligence identifies quantitative trait loci on 2q and 6p

    Posthuma, Danielle, Luciano, Michelle, de Geus, Eco J. C., Wright, Margie J., Slagboom, P. Eline, Montgomery, Grant W., Boomsma, Dorret I. and Martin, Nicholas G. (2005). A genomewide scan for intelligence identifies quantitative trait loci on 2q and 6p. American Journal of Human Genetics, 77 (2), 318-326. doi: 10.1086/432647

  • Evidence of age-dependent genetic influences on plasma total cholesterol

    Middelberg, R, Heath, AC, Martin, NG and Whitfield, JB (2005). Evidence of age-dependent genetic influences on plasma total cholesterol. European Journal of Cardiovascular Prevention & Rehabilitation, 12 (4), 380-386. doi: 10.1097/01.hjr.0000160602.41762.9f

  • Eysenck's Psychoticism and the X-linked androgen receptor gene CAG polymorphism in additional Australian samples

    Loehlin, JC, Medland, SE, Montgomery, GW and Martin, NG (2005). Eysenck's Psychoticism and the X-linked androgen receptor gene CAG polymorphism in additional Australian samples. Personality and Individual Differences, 39 (3), 661-667. doi: 10.1016/j.paid.2005.02.016

  • An analysis of risk factors for cutaneous melanoma by anatomical site (Australia)

    Siskind, Victor, Whiteman, David C., Aitken, Joanne F., Martin, Nicholas G. and Green, Adele C. (2005). An analysis of risk factors for cutaneous melanoma by anatomical site (Australia). Cancer Causes and Control, 16 (3), 193-199. doi: 10.1007/s10552-004-4325-5

  • New concepts for distinguishing the hidden patterns of linkage disequilibrium which underlie association between genotypes and complex phenotypes

    Wicks, Jacqueline, Treloar, Susan A., Martin, Nicholas G and Duffy, David L. (2005). New concepts for distinguishing the hidden patterns of linkage disequilibrium which underlie association between genotypes and complex phenotypes. Twin Research And Human Genetics, 8 (2), 95-100. doi: 10.1375/1832427053738737

  • Birth weight and schooling and earnings: estimates from a sample of twins

    Miller, P, Mulvey, C and Martin, N (2005). Birth weight and schooling and earnings: estimates from a sample of twins. Economics Letters, 86 (3), 387-392. doi: 10.1016/j.econlet.2004.10.002

  • Bladder neck mobility is a heritable trait

    Dietz, H. P., Hansell, N. K., Grace, M. E., Eldridge, A.M., Clarke, B. and Martin, N. G. (2005). Bladder neck mobility is a heritable trait. BJOG: An International Journal of Obstetrics and Gynaecology, 112 (3), 334-339. doi: 10.1111/j.1471-0528.2004.00428.x

  • Multivariate Genetic Analysis of Chronic Pelvic Pain and Associated Phenotypes

    Zondervan, K., Kennedy, S., Cardon, L., Martin, N. G. and Treloar, S. (2005). Multivariate Genetic Analysis of Chronic Pelvic Pain and Associated Phenotypes. Behavior Genetics, 35 (2), 177-188. doi: 10.1007/s10519-004-1017-6

  • Teenage acne is influenced by genetic factors

    Evans, D. M., Kirk, K. M., Nyholt, D. R., Novac, C. and Martin, N. G. (2005). Teenage acne is influenced by genetic factors. British Journal of Dermatology, 152 (3), 579-581. doi: 10.1111/j.1365-2133.2005.06387.x

  • The genetic basis of academic achievement on the Queensland Core Skills Test and its shared genetic variance with IQ

    Wainwright, Mark A., Wright, Margaret J., Geffen, Gina M., Luciano, Michelle and Martin, Nicholas G. (2005). The genetic basis of academic achievement on the Queensland Core Skills Test and its shared genetic variance with IQ. Behavior Genetics, 35 (2), 133-145. doi: 10.1007/s10519-004-1014-9

  • Choice of residential location: Chance, family influences, or genes?

    Whitfield, John B., Zhu, Gu, Heath, Andrew C. and Martin, Nicholas G. (2005). Choice of residential location: Chance, family influences, or genes?. Twin Research and Human Genetics, 8 (1), 22-26. doi: 10.1375/twin.8.1.22

  • Discordant MZ twins with cleft lip and palate: A model for identifying genes in complex traits

    Mansilla, MA, Kimani, J, Mitchell, LE, Christensen, K, Boomsma, DI, Daack-Hirsch, S, Nepomucena, B, Wyszynski, DF, Felix, TM, Martin, NG and Murray, JC (2005). Discordant MZ twins with cleft lip and palate: A model for identifying genes in complex traits. Twin Research and Human Genetics, 8 (1), 39-46. doi: 10.1375/1832427053435373

  • Early childhood behaviours, schooling and labour market outcomes: estimates from a sample of twins

    Le, AT, Miller, PW, Heath, AC and Martin, N (2005). Early childhood behaviours, schooling and labour market outcomes: estimates from a sample of twins. Economics of Education Review, 24 (1), 1-17. doi: 10.1016/j.econedurev.2004.04.004

  • Genetic and environmental influences on the frequency of female orgasm

    Dawood, Khytam, Kirk, Katherine M., Bailey, J. Michael, Andrews, Paul W. and Martin, Nicholas G. (2005). Genetic and environmental influences on the frequency of female orgasm. Twin Research and Human Genetics, 8 (1), 27-33. doi: 10.1375/1832427053435427

  • Association between polymorphisms in the progesterone receptor gene and endometriosis

    Treloar, Susan A., Zhao, Zhen Zhen, Armitage, Trudi, Duffy, David L., Wicks, Jacqueline, O'Connor, Daniel T., Martin, Nicholas G. and Montgomery, Grant W. (2005). Association between polymorphisms in the progesterone receptor gene and endometriosis. Molecular Human Reproduction, 11 (9), 641-647. doi: 10.1093/molehr/gah221

  • Erythrocyte aldehyde dehydrogenase activity: Lack of association with alcohol use and dependence or alcohol reactions in Australian twins

    Hansell, NK, Pang, D, Heath, AC, Martin, NG and Whitfield, JB (2005). Erythrocyte aldehyde dehydrogenase activity: Lack of association with alcohol use and dependence or alcohol reactions in Australian twins. Alcohol and Alcoholism, 40 (5), 343-348. doi: 10.1093/alcalc/agh168

  • Estimation of the rate of SNP genotyping errors from DNA extracted from different tissues

    Montgomery, GW, Campbell, MJ, Dickson, P, Herbert, S, Siemering, K, Ewen-White, KR, Visscher, PM and Martin, NG (2005). Estimation of the rate of SNP genotyping errors from DNA extracted from different tissues. Twin Research and Human Genetics, 8 (4), 346-352. doi: 10.1375/1832427054936673

  • Evaluation of multiple displacement amplification in a 5 cM STR genome-wide scan

    Dickson, PA, Montgomery, GW, Henders, A, Campbell, MJ, Martin, NG and James, MR (2005). Evaluation of multiple displacement amplification in a 5 cM STR genome-wide scan. Nucleic Acids Research, 33 (13), 1-4. doi: 10.1093/nar/gni126

  • Genetic time-series analysis identifies a major QTL for in vivo alcohol metabolism not predicted by in vitro studies of structural protein polymorphism at the ADH1B or ADH1C loci

    Birley, A. J., Whitfield, J. B., Neale, M. C., Duffy, D. L., Heath, A. C., Boomsma, D. I. and Martin, N. G. (2005). Genetic time-series analysis identifies a major QTL for in vivo alcohol metabolism not predicted by in vitro studies of structural protein polymorphism at the ADH1B or ADH1C loci. Behavior Genetics, 35 (5), 509-524. doi: 10.1007/s10519-005-3851-6

  • Genomewide linkage study in 1,176 affected sister pair families identifies a significant susceptibility locus for endometriosis on chromosome 10q26

    Treloar, Susan A., Wicks, Jacqueline, Nyholt, Dale R., Montgomery, Grant W., Bahlo, Melanie, Smith, Vicki, Dawson, Gary, Mackay, Ian J., Weeks, Daniel E., Bennett, Simon T., Carey, Alisoun, Ewen-White, Kelly R., Duffy, David L., O'Connor, Daniel T., Barlow, David H., Martin, Nicholas G. and Kennedy, Stephen H. (2005). Genomewide linkage study in 1,176 affected sister pair families identifies a significant susceptibility locus for endometriosis on chromosome 10q26. American Journal of Human Genetics, 77 (3), 365-376. doi: 10.1086/432960

  • Multivariate genetic analysis of academic skills of the Queensland Core Skills Test and IQ highlight the importance of genetic g

    Wainwright, Mark A., Wright, Margaret J., Luciano, Michelle, Geffen, Gina M. and Martin, Nicholas G. (2005). Multivariate genetic analysis of academic skills of the Queensland Core Skills Test and IQ highlight the importance of genetic g. Twin Research and Human Genetics, 8 (6), 602-608. doi: 10.1375/183242705774860259

  • Perceptual speed does not cause intelligence, and intelligence does not cause perceptual speed

    Luciano, Michelle, Posthuma, Danielle, Wright, Margaret J., de Geus, Eco J. C., Smith, Glen A., Geffen, Gina M., Boomsma, Dorret I. and Martin, Nicholas G. (2005). Perceptual speed does not cause intelligence, and intelligence does not cause perceptual speed. Biological Psychology, 70 (1), 1-8. doi: 10.1016/j.biopsycho.2004.11.011

  • The relationship between stressful life events, the serotonin transporter (5-HTTLPR) genotype and major depression

    Gillespie, NA, Whitfield, JB, Williams, B, Heath, AC and Martin, NG (2005). The relationship between stressful life events, the serotonin transporter (5-HTTLPR) genotype and major depression. Psychological Medicine, 35 (1), 101-111. doi: 10.1017/S0033291704002727

  • A test of the sorting model of education in Australia

    Miller, PW, Mulvey, C and Martin, N (2004). A test of the sorting model of education in Australia. Economics of Education Review, 23 (5), 473-482. doi: 10.1016/j.econedurev.2004.04.003

  • Major Depressive Disorder, Suicidal Ideation, and Suicide Attempt in Twins Discordant for Cannabis Dependence and Early-Onset Cannabis Use

    Lynskey, Michael T., Glowinski, Anne L., Todorov, Alexandr A., Bucholz, Kathleen K., Madden, Pamela A. F., Nelson, Elliot C., Statham, Dixie J., Martin, Nicholas G. and Heath, Andrew C. (2004). Major Depressive Disorder, Suicidal Ideation, and Suicide Attempt in Twins Discordant for Cannabis Dependence and Early-Onset Cannabis Use. Archives of General Psychiatry, 61 (10), 1026-1032. doi: 10.1001/archpsyc.61.10.1026

  • Major quantitative trait locus for eosinophil count is located on chromosome 2q

    Evans, DM, Zhu, G, Duffy, DL, Montgomery, GW, Frazer, IH and Martin, NG (2004). Major quantitative trait locus for eosinophil count is located on chromosome 2q. Journal of Allergy And Clinical Immunology, 114 (4), 826-830. doi: 10.1016/j.jaci.2004.05.060

  • Personality, arousal theory and the relationship to cognitive ability as measured by inspection time and IQ

    Luciano, Michelle, Leisser, Romana, Wright, Margaret J. and Martin, Nicholas G. (2004). Personality, arousal theory and the relationship to cognitive ability as measured by inspection time and IQ. Personality and Individual Differences, 37 (5), 1081-1089. doi: 10.1016/j.paid.2003.11.016

  • Behaviour genetic analyses of reading and spelling: a component processes approach

    Bates, Timothy C., Castles, Anne, Coltheart, Max, Gillespie, Nathan, Wright, Margie and Martin, Nicholas G. (2004). Behaviour genetic analyses of reading and spelling: a component processes approach. Australian Journal of Psychology, 56 (2), 115-126. doi: 10.1080/00049530410001734847

  • Brisbane adolescent twin study: outline of study methods and research projects

    Wright, Margaret J. and Martin, Nicholas G. (2004). Brisbane adolescent twin study: outline of study methods and research projects. Australian Journal of Psychology, 56 (2), 65-78. doi: 10.1080/00049530410001734865

  • Genetic influences on cognitive processes associated with distraction: An event-related potential study of the slow wave

    Hansell, Narelle K., Wright, Margaret J., Geffen, Gina M., Geffen, Laurie B. and Martin, Nicholas G. (2004). Genetic influences on cognitive processes associated with distraction: An event-related potential study of the slow wave. Australian Journal of Psychology, 56 (2), 89-98. doi: 10.1080/0049530410001734856

  • Monozygotic twin pairs discordant for lifetime anorexia nervosa: an exploratory investigation

    Wade, Tracey, Treloar, Susan A., Martin, Nicholas G., Statham, Dixie and Heath, Andrew C. (2004). Monozygotic twin pairs discordant for lifetime anorexia nervosa: an exploratory investigation. Australian Journal of Psychology, 56 (2), 127-132. doi: 10.1080/00049530410001734810

  • Genetic and environmental sources of covariance between reading tests used in neuropsychological assessment and IQ subtests

    Wainwright, Mark, Wright, Margaret J., Geffen, Gina M., Geffen, Laurie B., Luciano, Michelle and Martin, Nicholas G. (2004). Genetic and environmental sources of covariance between reading tests used in neuropsychological assessment and IQ subtests. Behavior Genetics, 34 (4), 365-376. doi: 10.1023/B:BEGE.0000023642.34853.cb

  • Using identity-by-de scent information in affected sib pairs to increase the efficiency of genetic association studies

    Wicks, Jacqueline, Treloar, Susan A. and Martin, Nicholas G. (2004). Using identity-by-de scent information in affected sib pairs to increase the efficiency of genetic association studies. Twin Research, 7 (2), 211-216. doi: 10.1375/136905204323016195

  • Copulas in QTL mapping

    Basrak, Bojan, Klaassen, Chris A. J., Beekman, Marion, Martin, Nicholas G. and Boomsma, Dorret I. (2004). Copulas in QTL mapping. Behavior Genetics, 34 (2), 161-171. doi: 10.1023/B:BEGE.0000013730.63991.ba

  • Genetic Epidemiology of Alcohol-Induced Blackouts

    Nelson, Elliot C., Heath, Andrew C., Bucholz, Kathleen K., Madden, Pamela A. F., Fu, Qiang, Knopik, Valerie, Lynskey, Michael T., Whitfield, John B., Statham, Dixie J. and Martin, Nicholas G. (2004). Genetic Epidemiology of Alcohol-Induced Blackouts. Archives of General Psychiatry, 61 (3), 257-263. doi: 10.1001/archpsyc.61.3.257

  • A deletion mutation in GDF9 in sisters with spontaneous DZ twins

    Montgomery, G. W., Zhao, Z. Z., Marsh, A. J., Mayne, R., Treloar, S. A., James, M., Martin, N. G., Boomsma, D. I. and Duffy, D. L. (2004). A deletion mutation in GDF9 in sisters with spontaneous DZ twins. Twin Research, 7 (6), 548-555. doi: 10.1375/1369052042663823

  • A genetic investigation of the covariation among Inspection Time, Choice Reaction Time, and IQ subtest scores

    Luciano, Michelle, Wright, Margaret J., Geffen, Gina M., Geffen, Laurie B., Smith, Glen A. and Martin, Nicholas G. (2004). A genetic investigation of the covariation among Inspection Time, Choice Reaction Time, and IQ subtest scores. Behavior Genetics, 34 (1), 41-50. doi: 10.1023/B:BEGE.0000009475.35287.9d

  • A genome scan for eye color in 502 twin families: Most variation is due to a QTL on chromosome 15q

    Zhu, G., Evans, D. M., Duffy, D. L., Montgomery, G. W., Medland, S. E., Gillespie, N. A., Ewen, K. R., Jewell, M., Liew, Y. W., Hayward, N. K., Sturm, R. A., Trent, J. M. and Martin, N. G. (2004). A genome scan for eye color in 502 twin families: Most variation is due to a QTL on chromosome 15q. Twin Research, 7 (2), 197-210. doi: 10.1375/136905204323016186

  • A major quantitative trait locus for CD4-CD8 ratio is located on chromosome 11

    Evans, D. M., Zhu, G., Duffy, D. L., Frazer, I. H., Montgomery, G. W. and Martin, N. G. (2004). A major quantitative trait locus for CD4-CD8 ratio is located on chromosome 11. Genes and Immunity, 5 (7), 548-552. doi: 10.1038/sj.gene.6364126

  • Analysis of Melanoma Onset: Assessing Familial Aggregation by Using Estimating Equations and Fitting Variance Components via Bayesian Random Effects Models

    Do, Kim-Anh, Aitken, Joanne F., Green, Adele C and Martin, Nicholas G. (2004). Analysis of Melanoma Onset: Assessing Familial Aggregation by Using Estimating Equations and Fitting Variance Components via Bayesian Random Effects Models. Twin Research, 7 (1), 98-113. doi: 10.1375/13690520460741480

  • CCR5-Delta 32 mutation is strongly associated with primary sclerosing cholangitis

    Eri, R, Jonsson, JR, Pandeya, N, Purdie, DM, Clouston, AD, Martin, N, Duffy, D, Powell, EE, Fawcett, J, Florin, THJ and Radford-Smith, GL (2004). CCR5-Delta 32 mutation is strongly associated with primary sclerosing cholangitis. Genes And Immunity, 5 (6), 444-450. doi: 10.1038/sj.gene.6364113

  • Defining nicotine dependence for genetic research: evidence from Australian twins

    Lessov, Christina N., Martin, Nicholas G., Statham, Dixie J., Todorov, Alexandre A., Slutske, Wendy S., Bucholz, Kathleen K., Heath, Andrew C. and Madden, Pamela A. F. (2004). Defining nicotine dependence for genetic research: evidence from Australian twins. Psychological Medicine, 34 (5), 865-879. doi: 10.1017/S0033291703001582

  • Do the Genetic or Environmental Determinants of Anxiety and Depression Change with Age? A Longitudinal Study of Australian Twins

    Gillespie, Nathan A., Kirk, Katherine M., Evans, David M., Heath, Andrew C., Hickie, Ian B. and Martin, Nicholas G. (2004). Do the Genetic or Environmental Determinants of Anxiety and Depression Change with Age? A Longitudinal Study of Australian Twins. Twin Research, 7 (1), 39-53. doi: 10.1375/13690520460741435

  • Effects of dopamine receptor D4 variation on alcohol and tobacco use and on novelty seeking: Multivariate linkage and association analysis

    Luciano, Michelle, Zhu, Gu, Kirk, K. M., Whitfield, J. B., Butler, R., Heath, A. C., Madden, P. A. F. and Martin, N. G. (2004). Effects of dopamine receptor D4 variation on alcohol and tobacco use and on novelty seeking: Multivariate linkage and association analysis. American Journal of Medical Genetics Part B-neuropsychiatric Genetics, 124B (1), 113-123. doi: 10.1002/ajmg.b.20077

  • Epidermal Growth Factor Gene (EGF) Polymorphism and Risk of Melanocytic Neoplasiay

    James, Michael R., Hayward, Nicholas K., Dumenil, Troy, Montgomery, Grant W., Martin, Nicholas G. and Duffy, David L. (2004). Epidermal Growth Factor Gene (EGF) Polymorphism and Risk of Melanocytic Neoplasiay. Journal of Investigative Dermatology, 123 (4), 760-762. doi: 10.1111/j.0022-202X.2004.23305.x

  • Exploring the Etiology of the Association Between Birthweight and IQ in an Adolescent Twin Sample

    Luciano, Michelle, Wright, Margaret J. and Martin, Nicholas G. (2004). Exploring the Etiology of the Association Between Birthweight and IQ in an Adolescent Twin Sample. Twin Research, 7 (1), 62-71. doi: 10.1375/13690520460741453

  • Gender diagnosticity and androgen receptor gene CAG repeat sequence

    Loehlin, John C., Jonsson, Erik G., Gustavsson, J. Petter, Schalling, Martin, Medland, Sarah E., Montgomery, Grant W. and Martin, Nicholas G. (2004). Gender diagnosticity and androgen receptor gene CAG repeat sequence. Twin Research, 7 (5), 456-461. doi: 10.1375/1369052042335359

  • Genetic Simplex Modeling of Eysenck's Dimensions of Personality in a Sample of Young Australian Twins

    Gillespie, Nathan A., Evans, David E., Wright, Margie M. and Martin, Nicholas G. (2004). Genetic Simplex Modeling of Eysenck's Dimensions of Personality in a Sample of Young Australian Twins. Twin Research, 7 (6), 637-648. doi: 10.1375/1369052042663814

  • Genetic covariation of pelvic organ and elbow mobility in twins and their sisters

    Hansell, N. K., Dietz, H. P., Treloar, S. A., Clarke, B. and Martin, N. G. (2004). Genetic covariation of pelvic organ and elbow mobility in twins and their sisters. Twin Research, 7 (3), 254-260. doi: 10.1375/136905204774200532

  • Genetic effects on alcohol dependence risk: re-evaluating the importance of psychiatric and other heritable risk factors

    Knopik, Valerie S., Heath, Andrew C., Madden, Pamela A. F., Bucholz, Kathleen K., Slutske, Wendy S., Nelson, Ellieo C., Statham, Dixie, Whitfield, John B. and Martin, Nicholas G. (2004). Genetic effects on alcohol dependence risk: re-evaluating the importance of psychiatric and other heritable risk factors. Psychological Medicine, 34 (8), 1519-1530. doi: 10.1017/S0033291704002922

  • Interactive effects of MC1R and OCA2 on melanoma risk phenotypes

    Duffy, D. L., Box, N. F., Chen, W., Palmer, J. S., Montgomery, G. W., James, M. R., Hayward, N. K., Martin, N. G. and Sturm, R. A. (2004). Interactive effects of MC1R and OCA2 on melanoma risk phenotypes. Human Molecular Genetics, 13 (4), 447-461. doi: 10.1093/hmg/ddh043

  • Latent class and genetic analysis does not support migraine with aura and migraine without aura as separate entities

    Nyholt, Dale R., Gillespie, Nathan G., Heath, Andrew C., Merikangas, Kathleen R., Duffy, David L. and Martin, Nicholas G. (2004). Latent class and genetic analysis does not support migraine with aura and migraine without aura as separate entities. Genetic Epidemiology, 26 (3), 231-244. doi: 10.1002/gepi.10311

  • Multivariate QTL linkage analysis suggests a QTL for platelet count on chromosome 19q

    Evans, D. M., Zhu, G., Duffy, D. L., Montgomery, G. W., Frazer, IH and Martin, NG (2004). Multivariate QTL linkage analysis suggests a QTL for platelet count on chromosome 19q. European Journal of Human Genetics, 12 (10), 835-842. doi: 10.1038/sj.ejhg.5201248

  • Multivariate genetic analysis of cognitive abilities in an adolescent twin sample

    Luciano, M., Wright, M. J., Geffen, G. M., Geffen, L. B., Smith, G. A. and Martin, N. G. (2004). Multivariate genetic analysis of cognitive abilities in an adolescent twin sample. Australian Journal of Psychology, 56 (2), 79-88. doi: 10.1080/00049530410001734874

  • Perceived social support in a large community sample - Age and sex differences

    Coventry, W. L., Gillespie, N. A., Heath, A. C. and Martin, N. G. (2004). Perceived social support in a large community sample - Age and sex differences. Social Psychiatry And Psychiatric Epidemiology, 39 (8), 625-636. doi: 10.1007/s00127-004-0795-8

  • Quantitative Association Tests of Immune Responses to Antigens of Mycobacterium Tuberculosis: A Study of Twins in West Africa

    Wiart, Amanda, Jepson, Annette, Banya, Winston, Bennett, Steve, Whittle, Hilton, Martin, Nicholas G. and Hill, Adrain V. S. (2004). Quantitative Association Tests of Immune Responses to Antigens of Mycobacterium Tuberculosis: A Study of Twins in West Africa. Twin Research, 7 (6), 578-588. doi: 10.1375/1369052042663887

  • The epidemiology and genetics of smoking initiation and persistence: Crosscultural comparisons of twin study results

    Madden, Pamela A. F., Pedersen, Nancy L., Kaprio, Jaakko, Koskenvuo, Markku J . and Martin, Nicholas G. (2004). The epidemiology and genetics of smoking initiation and persistence: Crosscultural comparisons of twin study results. Twin Research, 7 (1), 82-97. doi: 10.1375/13690520460741471

  • The genetics of alcohol intake and of alcohol dependence

    Whitfield, John B., Zhu, Gu, Madden, Pamela A., Neale, Michael C., Heath, Andrew C. and Martin, Nicholas G. (2004). The genetics of alcohol intake and of alcohol dependence. Alcoholism-clinical And Experimental Research, 28 (8), 1153-1160. doi: 10.1097/01.ALC.0000134221.32773.69

  • Genetic Basis of Male Pattern Baldness [Letter to the editor]

    Nyholt, Dale R., Gillespie, Nathan A., Heath, Andrew C. and Martin, Nicholas G. (2003). Genetic Basis of Male Pattern Baldness [Letter to the editor]. Journal of Investigative Dermatology, 121 (6), 1561-1564. doi: 10.1111/j.1523-1747.2003.12615.x

  • The genetic and environmental relationship between Cloninger's dimensions of temperament and character

    Gillespie, NA, Cloninger, CR, Heath, AC and Martin, NG (2003). The genetic and environmental relationship between Cloninger's dimensions of temperament and character. Personality and Individual Differences, 35 (8), 1931-1946. doi: 10.1016/S0191-8869(03)00042-4

  • A role for the appendix in inflammatory bowel disease? Cut it out

    Edwards, J. E., Florin, T. H., Green, A, Martin, N. G., Newman, B., Pandeya, N., Purdie, D. M., Radford-Smith, G. L. and Watson, M. (2003). A role for the appendix in inflammatory bowel disease? Cut it out. Gastroenterology, 125 (4), 1270-1272. doi: 10.1016/j.gastro.2003.05.002

  • Ocular melanoma is not associated with CDKN2A or MC1R variants - a population-based study

    Vajdic, C, Kricker, A, Duffy, DL, Aitken, JF, Stark, M, ter Huurne, JAC, Martin, NG, Armstrong, BK and Hayward, NK (2003). Ocular melanoma is not associated with CDKN2A or MC1R variants - a population-based study. Melanoma Research, 13 (4), 409-413. doi: 10.1097/01.cmr.0000056244.56735.28

  • Direction of Causation Modeling Between Cross-Sectional Measures of Parenting and Psychological Distress in Female Twins

    Gillespie, Nathan A., Zhu, Gu, Neale, Michael C., Heath, Andrew C. and Martin, Nicholas G. (2003). Direction of Causation Modeling Between Cross-Sectional Measures of Parenting and Psychological Distress in Female Twins. Behavior Genetics, 33 (4), 383-396. doi: 10.1023/A:1025365325016

  • The role of melanocortin-1 receptor polymorphism in skin cancer risk phenotypes

    Sturm, R. A., Duffy, D. L., Box, N. F., Chen, W., Smit, D. J., Brown, D. L., Stow, J. L., Leonard, J. H. and Martin, N. G. (2003). The role of melanocortin-1 receptor polymorphism in skin cancer risk phenotypes. Pigment Cell Research, 16 (3), 266-272. doi: 10.1034/j.1600-0749.2003.00041.x

  • Escalation of Drug Use in Early-Onset Cannabis Users vs Co-twin Controls

    Lynskey, Michael T., Heath, Andrew C., Bucholz, Kathleen K., Slutske, Wendy S., Madden, Pamela A. F., Nelson, Elliot C., Statham, Dixie J. and Martin, Nicholas G. (2003). Escalation of Drug Use in Early-Onset Cannabis Users vs Co-twin Controls. JAMA : The Journal of the American Medical Association, 289 (4), 427-433. doi: 10.1001/jama.289.4.427

  • A genetic two-factor model of the covariation among a subset of Multidimensional Aptitude Battery and Wechsler Adult Intelligence Scale - Revised subtests

    Luciano, M., Wright, M. J., Geffen, G. M., Geffen, L. B., Smith, G. A., Evans, D. M. and Martin, N. G. (2003). A genetic two-factor model of the covariation among a subset of Multidimensional Aptitude Battery and Wechsler Adult Intelligence Scale - Revised subtests. Intelligence, 31 (6), 589-605. doi: 10.1016/S0160-2896(03)00057-6

  • ADH genotype does not modify the effects of alcohol on high-density lipoprotein

    Whitfield, John B., OBrien, Martin E., Nightingale, Brian N., Zhu, Gu, Heath, Andrew C. and Martin, Nicholas G. (2003). ADH genotype does not modify the effects of alcohol on high-density lipoprotein. Alcoholism-clinical And Experimental Research, 27 (3), 509-514. doi: 10.1097/01.ALC.0000057940.57330.70

  • Accuracy of Mothers' Retrospective Reports of Smoking During Pregnancy: Comparison with Twin Sister Informant Ratings

    Heath, Andrew C., Knopik, Valerie S., Madden, Pamela A., Neuman, Rosalind J., Lynskey, Michael J., Slutske, Wendy S., Jacob, Theodore and Martin, Nicholas G. (2003). Accuracy of Mothers' Retrospective Reports of Smoking During Pregnancy: Comparison with Twin Sister Informant Ratings. Twin Research, 6 (4), 297-301. doi: 10.1375/136905203322296656

  • Dizygotic twinning is not associated with methylenetetrahydrofolate reductase haplotypes

    Montgomery, Grant W., Zhao, Zhen Zehn, Morley, Katherine I., Marsh, Anna J., Boomsma, Dorret I., Martin, Nicholas G. and Duffy, David L. (2003). Dizygotic twinning is not associated with methylenetetrahydrofolate reductase haplotypes. Human Reproduction, 18 (11), 2460-2464. doi: 10.1093/humrep/deg441

  • Evidence for a QTL on chromosome 19 influencing LDL cholesterol levels in the general population

    Beekman, Marian, Heijmans, Bastian T., Martin, Nicholas G., Whitfield, John B., Pedersen, Nancy L., DeFaire, Ulf, Snieder, Harold, Lakenberg, Nico, Suchiman, H. Eka D., De Knijff, Peter, Frants, Rune R., van Ommen, Gert Jan B., Kluft, Cornelis, Vogler, George P., Boomsma, Dorret I. and Slagboom, P. Eline (2003). Evidence for a QTL on chromosome 19 influencing LDL cholesterol levels in the general population. European Journal of Human Genetics, 11 (11), 845-850. doi: 10.1038/sj.ejhg.5201053

  • Genetic and Environmental Influences on Migraine: A Twin Study Across Six Countries

    Mulder, Elles J., van Baal, Caroline, Gaistz, David, Kallela, Mikko, Kaprio, Jaakko, Svensson, Dan A., Nyholt, Dale R., Martin, Nicholas G., MacGregor, Alex J., Cherkas, Lynn F., Boomsma, Dorret I. and Palotie, Aarno (2003). Genetic and Environmental Influences on Migraine: A Twin Study Across Six Countries. Twin Research, 6 (5), 422-431. doi: 10.1375/136905203770326420

  • Heritability of adult body height: A comparative study of twin cohorts in eight countries

    Silventoinen, K., Sammalisto, S., Perola, M., Boomsma, D. I., Cornes, B. K., Davis, C., Dunkel, L., deLange, M., Harris, J. R., Hjelmborg, J. V. B., Luciano, M., Martin, N. G., Mortensen, J., Nistico, L. and Pedersen, N. L. (2003). Heritability of adult body height: A comparative study of twin cohorts in eight countries. Twin Research, 6 (5), 399-408. doi: 10.1375/136905203770326402

  • Linkage and Association Analysis of Radiation Damage Repair Genes XRCC3 and XRCC5 with Nevus Density in Adolescent Twins

    Zhu, Gu, Duffy, David L., Turner, David R., Ewen, Kelly R., Montgomery, Grant W. and Martin, Nicholas G. (2003). Linkage and Association Analysis of Radiation Damage Repair Genes XRCC3 and XRCC5 with Nevus Density in Adolescent Twins. Twin Research, 6 (4), 315-321. doi: 10.1375/136905203322296683

  • Localization of a novel melanoma susceptibility locus to 1p22

    Gillanders, Elizabeth, Juo, Suh-Hang Hank, Holland, Elizabeth A., Jones, MaryPat, Nancarrow, Derek, Freas-Lutz, Diana, Sood, Raman, Park, Naeun, Faruque, Mezbah, Markey, Carol, Kefford, Richard F., Palmer, Jane, Bergman, Wilma, Bishop, D. Timothy, Tucker, Margaret A., Bressac-de Paillerets, Brigitte, Hansson, Johan, The Lund Melanoma Study Group, Stark, Mitchell, Gruis, Nelleke, Newton Bishop, Julia, Goldstein, Alisa M., Bailey-Wilson, Joan E., Mann, Graham J., Hayward, Nicholas, Trent, Jeffrey, Martin, Nicholas G. and The Melanoma Genetics Consortium (2003). Localization of a novel melanoma susceptibility locus to 1p22. American Journal of Human Genetics, 73 (2), 301-313. doi: 10.1086/377140

  • Osteoarthritis of the hands, hips and knees in an Australian twin sample - Evidence of association with the aggrecan VNTR polymorphism

    Kirk, K. M., Doege, K. J., Hecht, J., Bellamy, N. and Martin, N. G. (2003). Osteoarthritis of the hands, hips and knees in an Australian twin sample - Evidence of association with the aggrecan VNTR polymorphism. Twin Research, 6 (1), 62-66. doi: 10.1375/136905203762687915

  • Relative importance of female-specific and non-female-specific effects on variation in iron stores between women

    Whitfield, John B., Treloar, Susan, Zhu, Gu, Powell, Lawrie W. and Martin, Nicholas G. (2003). Relative importance of female-specific and non-female-specific effects on variation in iron stores between women. British Journal of Haematology, 120 (5), 860-866. doi: 10.1046/j.1365-2141.2003.04224.x

  • Serum inhibin A and B concentrations during the menstrual cycle in mothers of spontaneous dizygotic twins

    Gilfillan, Christopher P., Montgomery, Grant W., Zhu, Gu, Martin, Nicholas G., Groome, N. P. and Robertson, David M. (2003). Serum inhibin A and B concentrations during the menstrual cycle in mothers of spontaneous dizygotic twins. Twin Research, 6 (1), 27-33. doi: 10.1375/136905203762687870

  • Sex differences in heritability of BMI: A comparative study of results from twin studies in eight countries

    Schousboe, K., Willemsen, G., Kyvik, K. O., Mortensen, J., Boomsma, D. I., Cornes, B. K., Davis, C. J., Fagnani, C., Hjelmborg, J., Kaprio, J., de Lange, M., Luciano, M., Martin, N. G., Pedersen, N. and Pietilainen, K. H. (2003). Sex differences in heritability of BMI: A comparative study of results from twin studies in eight countries. Twin Research, 6 (5), 409-421. doi: 10.1375/136905203770326411

  • Special twin environments, genetic influences and their effects on the handedness of twins and their siblings

    Medland, S. E., Wright, M. J., Geffen, G. M., Hay, D. A., Levy, F., Martin, N. G. and Duffy, D. L. (2003). Special twin environments, genetic influences and their effects on the handedness of twins and their siblings. Twin Research, 6 (2), 119-130. doi: 10.1375/136905203321536245

  • The genetics of coronary heart disease: the contribution of twin studies

    Evans, Alun, van Baal, G. Caroline M., McCarron, Peter, deLange, Marlies, Soerensen, Thorkild I. A., De Geus, Eco J. C., Kyvik, Kirsten, Pedersen, Nancy L., Spector, Tim D., Andrew, Toby, Patterson, Christopher, Whitfield, John B., Zhu, Gu, Martin, Nicholas G., Kaprio, Jaakko and Boomsma, Dorret I. (2003). The genetics of coronary heart disease: the contribution of twin studies. Twin Research, 6 (5), 432-441. doi: 10.1375/136905203770326439

  • Two-locus Linkage Analysis Applied to Putative Quantitative Trait Loci for Lipoprotein(a) Levels

    Beekman, Marian, Heijmans, Bastiaan T., Martin, Nicholas G., Whitfield, John B., Pedersen, Nancy L., DeFaire, Ulf, Snieder, Harold, Lakenberg, Nico, Knijff, Peter, Frants, Rune R., van Ommen, Gert Jan B., Kluft, Cornelis, Vogler, George R., Slagboom, P. Eline and Boomsma, Dorret I. (2003). Two-locus Linkage Analysis Applied to Putative Quantitative Trait Loci for Lipoprotein(a) Levels. Twin Research and Human Genetics, 6 (4), 322-324. doi: 10.1375/136905203322296692

  • Zygosity Diagnosis in the Absence of Genotypic Data: An Approach Using Latent Class Analysis

    Heath, Andrew C., Nyholt, Dale R., Neuman, Rosalind, Madden, Pamela A. F., Bucholz, Kathleen K., Todd, Richard D., Nelson, Elliot C., Montgomery, Grant W. and Martin, Nicholas G. (2003). Zygosity Diagnosis in the Absence of Genotypic Data: An Approach Using Latent Class Analysis. Twin Research and Human Genetics, 6 (1), 22-26. doi: 10.1375/136905203762687861

  • Protective role of appendicectomy on onset and severity of ulcerative colitis and Crohn's disease

    Radford-Smith, GL, Edwards, JE, Purdie, DM, Pandeya, N, Watson, M, Martin, NG, Green, A, Newman, B and Florin, THJ (2002). Protective role of appendicectomy on onset and severity of ulcerative colitis and Crohn's disease. Gut, 51 (6), 808-813. doi: 10.1136/gut.51.6.808

  • Biometrical Genetics

    Evans, David M., Gillespie, N. A. and Martin, N. G. (2002). Biometrical Genetics. Biological Psychology, 61 (1-2), 33-51. doi: 10.1016/S0301-0511(02)00051-0

  • Genetic sources of covariation among P3(00) and online performance variables in a delayed-response working memory task

    Wright, M. J., Luciano, M., Hansell, N. K., Geffen, G. M., Geffen, L. B. and Martin, N. G. (2002). Genetic sources of covariation among P3(00) and online performance variables in a delayed-response working memory task. Biological Psychology, 61 (1-2), 183-202. doi: 10.1016/S0301-0511(02)00058-3

  • Genetic Covariation between Serum {gamma}-Glutamyltransferase Activity and Cardiovascular Risk Factors

    Whitfield, John B., Zhu, Gu, Nestler, John E., Heath, Andrew C. and Martin, Nicholas G. (2002). Genetic Covariation between Serum {gamma}-Glutamyltransferase Activity and Cardiovascular Risk Factors. Clinical Chemistry, 48 (9), 1426-1431. doi: 10.1093/clinchem/48.9.1426

  • Repeated blood pressure measurements in a sample of Swedish twins: heritabilities and associations with polymorphisms in the renin-angiotensin-aldosterone system Iliadou, Anastasia, Lichtenstein, Paul, Morgenstern, Ralf, Forsberg, Lena, Svensson, Richard,

    Iliadou, Anastasi, Lichtenstein, Paul, Morgenstern, Ralf, Forsberg, Lena, Svensson, Richard, de Faire, Ulf, Martin, Nicholas and Pedersen, Nancy (2002). Repeated blood pressure measurements in a sample of Swedish twins: heritabilities and associations with polymorphisms in the renin-angiotensin-aldosterone system Iliadou, Anastasia, Lichtenstein, Paul, Morgenstern, Ralf, Forsberg, Lena, Svensson, Richard,. Journal of Hypertension, 20 (8), 1543-1550. doi: 10.1097/00004872-200208000-00017

  • Association Between Self-reported Childhood Sexual Abuse and Adverse Psychosocial Outcomes: Results From a Twin Study

    Nelson, Elliott C., Heath, Andrew C., Madden, Pamela A. F., Cooper, M. Lynne, Dinwiddie, Stephen H., Bucholz, Kathleen K., Glowinski, Anne, McLaughlin, Tara, Dunne, Michael P., Statham, Dixie J. and Martin, Nicholas G. (2002). Association Between Self-reported Childhood Sexual Abuse and Adverse Psychosocial Outcomes: Results From a Twin Study. Archives of General Psychiatry, 59 (2), 139-145. doi: 10.1001/archpsyc.59.2.139

  • Estimating Two-Stage Models for Genetic Influences on Alcohol, Tobacco or Drug Use Initiation and Dependence Vulnerability in Twin and Family Data

    Heath, Andrew C., Martin, Nicholas G., Lynskey, Michael T., Todorov, Alexandre A. and Madden, Pamela A. F. (2002). Estimating Two-Stage Models for Genetic Influences on Alcohol, Tobacco or Drug Use Initiation and Dependence Vulnerability in Twin and Family Data. Twin Research, 5 (2), 113-124. doi: 10.1375/1369052022983

  • Gene-Environment Interaction Effects on Behavioral Variation and Risk of Complex Disorders: The Example of Alcoholism and Other Psychiatric Disorders

    Heath, Andrew C., Todorov, Alexandre A., Nelson, Elliot C., Madden, Pamela A. F., Bucholz, Kathleen K. and Martin, Nicholas G. (2002). Gene-Environment Interaction Effects on Behavioral Variation and Risk of Complex Disorders: The Example of Alcoholism and Other Psychiatric Disorders. Twin Research, 5 (1), 30-37. doi: 10.1375/1369052022875

  • Genetic and environmental contributions to cannabis dependence in a national young adult twin sample

    Lynskey, M. T., Heath, A. C., Nelson, E. C., Bucholz, K. K., Madden, P. A. F., Slutske, W. S., Statham, D. J. and Martin, N. G. (2002). Genetic and environmental contributions to cannabis dependence in a national young adult twin sample. Psychological Medicine, 32 (2), 195-207. doi: 10.1017/S0033291701005062

  • Genetic and environmental influences on premenstrual symptoms in an Australian twin sample

    Treloar, S. A., Heath, A. C. and Martin, N. G. (2002). Genetic and environmental influences on premenstrual symptoms in an Australian twin sample. Psychological Medicine, 32 (1), 25-38. doi: 10.1017/S0033291701004901

  • Genetics of Serum Dehydroepiandrosterone Sulfate and Its Relationship to Insulin in a Population-Based Cohort of Twin Subjects

    Nestler, John E., Whitfield, John B., Williams, Terre Y., Zhu, Gu, Condon, Juliann, Kirk, Katherine M., Heath, Andrew C., Montgomery, Grant W. and Martin, Nicholas G. (2002). Genetics of Serum Dehydroepiandrosterone Sulfate and Its Relationship to Insulin in a Population-Based Cohort of Twin Subjects. Journal of Clinical Endocrinology And Metabolism, 87 (2), 682-686. doi: 10.1210/jc.87.2.682

  • Heritabilities of Apolipoprotein and Lipid Levels in Three Countries

    Beekman, Marian, Heijmans, Bastiaan T., Martin, Nicholas G., Pedersen, Nancy L., Whitfield, John B., DeFaire, Ulf, van Baal, G. Caroline M., Snieder, Harold, Vogler, George P., Slagboom, P. Eline and Boomsma, Dorret . (2002). Heritabilities of Apolipoprotein and Lipid Levels in Three Countries. Twin Research, 5 (2), 87-97. doi: 10.1375/1369052022956

  • Melanoma in adolescents: A case-control study of risk factors in Queensland, Australia

    Youl, Philippa, Aitken, Joanne, Hayward, Nicholas, Hogg, David, Liu, Ling, Lassam, Norman, Martin, Nicholas and Green, Adele (2002). Melanoma in adolescents: A case-control study of risk factors in Queensland, Australia. International Journal of Cancer, 98 (1), 92-98. doi: 10.1002/ijc.10117

  • Personality and the genetic risk for alcohol dependence

    Slutske, Wendy S., Heath, Andrew C., Madden, Pamela A. F., Bucholz, Kathleen K., Statham, Dixie J. and Martin, Nicholas G. (2002). Personality and the genetic risk for alcohol dependence. Journal of Abnormal Psychology, 111 (1), 124-133. doi: 10.1037//0021-843X.111.1.124

  • Sun exposure and interaction with family history in risk of melanoma, Queensland, Australia

    Siskind, Victor, Aitken, Joanne, Green, Adele and Martin, Nicholas (2002). Sun exposure and interaction with family history in risk of melanoma, Queensland, Australia. International Journal of Cancer, 97 (1), 90-95. doi: 10.1002/ijc.1563

  • The validity and heritability of self-report osteoarthritis in an Australian older twin sample

    Kirk, K. M., Bellamy, N., O'Gorman, L. E., Kuhnert, P. M., Klestov, A., Muirden, K., Tesar, P., Walker, D. and Martin, N. G. (2002). The validity and heritability of self-report osteoarthritis in an Australian older twin sample. Twin Research, 5 (2), 98-106. doi: 10.1375/1369052022965

  • Genetic covariation of neuroticism with monoamine oxidase activity and smoking

    Kirk, Katherine M., Whitfield, John B., Pang, Dona, Heath, Andrew C. and Martin, Nicholas G. (2001). Genetic covariation of neuroticism with monoamine oxidase activity and smoking. American Journal of Medical Genetics, 105 (8), 700-706. doi: 10.1002/ajmg.1555

  • (Book Review) Retrieving the 'eu' from eugenics

    Martin, Nick (2001). (Book Review) Retrieving the 'eu' from eugenics. Nature, 414 (6864), 583-583. doi: 10.1038/414583a

  • Genetic covariance among measures of information processing speed, working memory, and IQ

    Luciano, M., Wright, M. J., Smith, G. A., Geffen, G. M., Geffen, L. B. and Martin, N. G. (2001). Genetic covariance among measures of information processing speed, working memory, and IQ. Behavior Genetics, 31 (6), 581-592. doi: 10.1023/A:1013397428612

  • Genetic influence on ERP slow wave measures of working memory

    Hansell, N. K., Wright, M. J., Geffen, G. M., Geffen, L. B., Smith, G. A. and Martin, N. G. (2001). Genetic influence on ERP slow wave measures of working memory. Behavior Genetics, 31 (6), 603-614. doi: 10.1023/A:1013301629521

  • Genetic influence on the variance in P3 amplitude and latency

    Wright, M. J., Hansell, N. K., Geffen, G. M., Geffen, L. B., Smith, G. A. and Martin, N. G. (2001). Genetic influence on the variance in P3 amplitude and latency. Behavior Genetics, 31 (6), 555-565. doi: 10.1023/A:1013393327704

  • Genetics of brain function and cognition

    Eco, D., Wright, M. J., Martin, N. G. and Boomsa, D. I. (2001). Genetics of brain function and cognition. Behavior Genetics, 31 (6), 498-500. doi: 10.1023/A:1013360909048

  • On the heritability of inspection time and its covariance with IQ: A twin study

    Luciano, M., Smith, G. A., Wright, M. J., Geffen, G. M., Geffen, L. B. and Martin, N. G. (2001). On the heritability of inspection time and its covariance with IQ: A twin study. Intelligence, 29 (6), 443-457. doi: 10.1016/S0160-2896(01)00071-X

  • The genetic and environmental relationship between the interpersonal sensitivity measure (IPSM) and the personality dimensions of Eysenck and Cloninger

    Gillespie, Nathan A., Johnstone, Stuart J., Boyce, Philip, Heath, Andrew C. and Martin, Nicholas G. (2001). The genetic and environmental relationship between the interpersonal sensitivity measure (IPSM) and the personality dimensions of Eysenck and Cloninger. Personality And Individual Differences, 31 (7), 1039-1051. doi: 10.1016/S0191-8869(00)00200-2

  • Relating body mass index to figural stimuli: population-based normative data for Caucasians

    Bulik, C. M., Wade, T. D., Heath, A. C., Martin, N. G., Stunkard, A. J. and Eaves, L. J. (2001). Relating body mass index to figural stimuli: population-based normative data for Caucasians. International Journal of Obesity, 25 (10), 1517-1524. doi: 10.1038/sj.ijo.0801742

  • Mutation analysis of the CDKN2A promoter in Australian melanoma families

    Pollock, Pamela M., Stark, Mitchell S., Palmer, Jane M., Walters, Marilyn K., Aitken, Joanne F., Martin, Nicholas G. and Hayward, Nicholas K. (2001). Mutation analysis of the CDKN2A promoter in Australian melanoma families. Genes Chromosomes and Cancer, 32 (1), 89-94. doi: 10.1002/gcc.1170

  • Variation in Alcohol Pharmacokinetics as a Risk Factor for Alcohol Dependence

    Whitfield, J. B., Zhu, Gu, Duffy, D. L., Birley, A. J., Madden, P. A. F., Heath, A. C. and Martin, N. G. (2001). Variation in Alcohol Pharmacokinetics as a Risk Factor for Alcohol Dependence. Alcoholism-clinical And Experimental Research, 25 (9), 1257-1263. doi: 10.1111/j.1530-0277.2001.tb02345.x

  • Lack of Genetic and Epigenetic Changes in CDKN2A in Melanocytic Nevi [Letter to the editor]

    Welch, John, Millar, Doug, Goldman, Alana, Heenan, Peter, Stark, Mitchell, Eldon, Michael, Clark, Susan, Martin, Nicholas G. and Hayward, Nicholas K. (2001). Lack of Genetic and Epigenetic Changes in CDKN2A in Melanocytic Nevi [Letter to the editor]. Journal of Investigative Dermatology, 117 (2), 383-384. doi: 10.1046/j.0022-202x.2001.01391.x

  • A comparison of family functioning, temperament, and childhood conditions in monozygotic twin pairs discordant for lifetime bulimia nervosa

    Treloar, S. A., Wade, T. D. and Martin, N. G. (2001). A comparison of family functioning, temperament, and childhood conditions in monozygotic twin pairs discordant for lifetime bulimia nervosa. American Journal of Psychiatry, 158 (7), 1155-1157. doi: 10.1176/appi.ajp.158.7.1155

  • Effects of alcohol consumption on indices of iron stores and of iron stores on alcohol intake markers

    Whitfield, John B., Zhu, Gu, Heath, Andrew C., Martin, Nicholas G. and Powell, Lawrie W. (2001). Effects of alcohol consumption on indices of iron stores and of iron stores on alcohol intake markers. Alcoholism: Clinical and Experimental Research, 25 (7), 1037-1045. doi: 10.1097/00000374-200107000-00014

  • Genetic and environmental contributions to educational attainment in Australia

    Miller, Paul, Mulvey, Charles and Martin, Nick (2001). Genetic and environmental contributions to educational attainment in Australia. Economics of Education Review, 20 (3), 211-224. doi: 10.1016/S0272-7757(00)00018-2

  • Age changes in personality traits and their heritabilities during the adult years: evidence from Australian Twin Registry samples

    Loehlin, J. C. and Martin, N. G. (2001). Age changes in personality traits and their heritabilities during the adult years: evidence from Australian Twin Registry samples. Personality and Individual Differences, 30 (7), 1147-1160. doi: 10.1016/S0191-8869(00)00099-4

  • Human twinning is not linked to the region of chromosome 4 syntenic with the sheep twinning gene FecB

    Duffy, David L., Montgomery, Grant W., Hall, Jeff, Mayne, Carol, Healey, Sue C., Brown, Joy, Boomsma, Dorret I. and Martin, Nicholas G. (2001). Human twinning is not linked to the region of chromosome 4 syntenic with the sheep twinning gene FecB. American Journal of Medical Genetics Part A, 100 (3), 182-186. doi: 10.1002/ajmg.1255

  • Mutations in the follicle-stimulating hormone receptor and familial dizygotic twinning

    Montgomery, Grant W., Duffy, David L., Hall, Jeff, Kudo, Masataka, Martin, Nicholas G. and Hsueh, Aaron J. (2001). Mutations in the follicle-stimulating hormone receptor and familial dizygotic twinning. Lancet, 357 (9258), 773-774. doi: 10.1016/S0140-6736(00)04164-7

  • Natural selection and quantitative genetics of life-history traits in Western women: A twin study

    Kirk, K. M., Blomberg, S. P., Duffy, D. L., Heath, A. C., Owens, I. P. and Martin, N. G. (2001). Natural selection and quantitative genetics of life-history traits in Western women: A twin study. Evolution, 55 (2), 423-435. doi: 10.1554/0014-3820(2001)055[0423:NSAQGO]2.0.CO;2

  • Natural selection and quantitative genetics of life-history traits in Western women: a twin study

    Kirk, Katherine M., Blomberg, Simon P., Duffy, David L., Heath, Andrew C., Owens, Ian P. and Martin, Nick G. (2001). Natural selection and quantitative genetics of life-history traits in Western women: a twin study. Evolution, 55 (2), 423-435. doi: 10.1111/j.0014-3820.2001.tb01304.x

  • A twin study of the etiology of prolonged fatigue and immune activation

    Hickie, I. B., Bansal, A. S., Kirk, K. M., Lloyd, A. R. and Martin, N. G. (2001). A twin study of the etiology of prolonged fatigue and immune activation. Twin Research, 4 (2), 94-102. doi: 10.1375/twin.4.2.94

  • An Australian twin study of the genetic basis of preeclampsia and eclampsia

    Treloar, Susan A., Cooper, Desmond W., Brennecke, Shaun P., Grehan, Madonna M. and Martin, Nicholas G. (2001). An Australian twin study of the genetic basis of preeclampsia and eclampsia. American Journal of Obstetrics And Gynecology, 184 (3), 374-381. doi: 10.1067/mob.2001.109400

  • An integrative approach for studying the etiology of alcoholism and other addictions

    Jacob, T., Sher, K. J., Bucholz, K. K., True, W. T., Sirevaag, E. J., Rohrbaugh, J. W., Nelson, E., Neuman, R. J., Todd, R. D., Slutske, W. S., Whitfield, J. B., Kirk, K. M., Martin, N. G., Madden, P. A. F. and Heath, A. C. (2001). An integrative approach for studying the etiology of alcoholism and other addictions. Twin Research, 4 (2), 103-118. doi: 10.1375/twin.4.2.103

  • Developmental genetics of red cell indices during puberty: A longitudinal twin study

    Evans, D. M., Frazer, I. H., Boomsma, D. I. and Martin, N. G. (2001). Developmental genetics of red cell indices during puberty: A longitudinal twin study. International Journal of Human Genetics, 1 (1), 41-53. doi: 10.1080/09723757.2001.11885735

  • Genetic and non-genetic factors affecting birth-weight and adult body mass index

    Whitfield, John B., Treloar, Susan A., Zhu, Gu and Martin, Nicholas G. (2001). Genetic and non-genetic factors affecting birth-weight and adult body mass index. Twin Research, 4 (5), 365-370. doi: 10.1375/twin.4.5.365

  • Genetic influence on the relationship between choice reaction time and IQ: A twin study

    Luciano, M., Smith, G., Wright, M., Geffen, G. M., Geffen, L. B. and Martin, N. G. (2001). Genetic influence on the relationship between choice reaction time and IQ: A twin study. Foreign Psychology, 14, 49-59.

  • Genetics of cognition: Outline of a collaborative twin study

    Wright, M. J., Eco, D., Ando, J, Luciano, M., Posthuma, D., Ono, Y., Hansell, N. K., Van Baal, C., Hiraishi, K., Hasegawa, T., Smith, G., Geffen, G. M., Geffen, L. B., Kanba, S., Miyake, A., Martin, N. G. and Boomsa, D. I. (2001). Genetics of cognition: Outline of a collaborative twin study. Twin Research, 4 (1), 48-56. doi: 10.1375/twin.4.1.48

  • Height discordance in monozygotic females is not attributable to discordant inactivation of X-linked stature determining genes

    Healey, S. C., Kirk, K. M., Hyland, V. J., Munns, C., Henders, A. K., Batch, J. A., Heath, A. C., Martin, N. G. and Glass, I. A. (2001). Height discordance in monozygotic females is not attributable to discordant inactivation of X-linked stature determining genes. Twin Research, 4 (1), 19-24. doi: 10.1375/twin.4.1.19

  • Heritability and gene-environment interactions for melanocytic nevus density examined in a U.K. adolescent twin study

    Wachsmuth, R. C., Gaut, R. M., Barrett, J. H., Saunders, C. L., Randerson-Moor, J. A., Eldridge, A., Martin, N. G., Bishop, T. D. and Newton Bishop, J. A. (2001). Heritability and gene-environment interactions for melanocytic nevus density examined in a U.K. adolescent twin study. Journal of Investigative Dermatology, 117 (2), 348-352. doi: 10.1046/j.0022-202x.2001.01415.x

  • IBD sharing around the PPARG locus is not increased in dizygotic twins or their mothers

    Duffy, David, Montgomery, Grant, Treloar, Susan, Birley, Andrew, Kirk, Katherine, Boomsma, Dorret, Beem, Leo, de Geus, Eco, Slagboom, Eline, Knighton, Joharna, Reed, Peter and Martin, Nicholas (2001). IBD sharing around the PPARG locus is not increased in dizygotic twins or their mothers. Nature Genetics, 28 (4), 315-315. doi: 10.1038/91074

  • Increasing the response rate to a mailed questionnaire by including more stamps on the return envelope: A cotwin control study

    Duffy, D. L. and Martin, N. G. (2001). Increasing the response rate to a mailed questionnaire by including more stamps on the return envelope: A cotwin control study. Twin Research, 4 (2), 71-72. doi: 10.1375/twin.4.2.71

  • MC1R genotype modifies risk of melanoma in families segregating CDKN2A mutations

    Box, N. F., Duffy, D. L., Chen, W., Stark, M., Martin, N. G., Sturm, R. A. and Hayward, N. K. (2001). MC1R genotype modifies risk of melanoma in families segregating CDKN2A mutations. American Journal of Human Genetics, 69 (4), 765-773. doi: 10.1086/323412

  • Phenotypic and genetic analyses of a short measure of psychosis-proneness in a large-scale Australian twin study

    Hay, D., Martin, N. G., Foley, D., Treloar, S. A., Kirk, K. M. and Heath, A. C. (2001). Phenotypic and genetic analyses of a short measure of psychosis-proneness in a large-scale Australian twin study. Twin Research, 4 (1), 30-40. doi: 10.1375/twin.4.1.30

  • Predictors of non-response to a questionnaire survey of a volunteer twin panel: Findings from the Australian 1989 twin cohort

    Heath, A. C., Howells, W., Kirk, K. M., Madden, P. A., Bucholz, K. K., Nelson, E. C., Slutske, W. S., Statham, D. B. and Martin, N. G. (2001). Predictors of non-response to a questionnaire survey of a volunteer twin panel: Findings from the Australian 1989 twin cohort. Twin Research, 4 (2), 73-80. doi: 10.1375/twin.4.2.73

  • The influence of genetic and environmental factors in estimations of current body size, desired body size, and body dissatisfaction

    Wade, Tracey D., Bulik, Cynthia M., Heath, Andrew C., Martin, Nicholas G. and Eaves, Lindon J. (2001). The influence of genetic and environmental factors in estimations of current body size, desired body size, and body dissatisfaction. Twin Research, 4 (4), 260-265. doi: 10.1375/twin.4.4.260

  • Towards a molecular epidemiology of alcohol dependence analysing the interplay of genetic and environmental risk factors

    Heath, A. C., Whitfield, J. B., Madden, P. A., Bucholz, K. K., Dinwiddie, S. H., Slutske, W.S., Bierut, L. J., Statham, D. B. and Martin, N. G. (2001). Towards a molecular epidemiology of alcohol dependence analysing the interplay of genetic and environmental risk factors. British Journal of Psychiatry, 178 (40), S33-S40. doi: 10.1192/bjp.178.40.s33

  • The subtlety of sex-atypicality

    Dunne, M. P., Bailey, J. M., Kirk, K. M. and Martin, N. G. (2000). The subtlety of sex-atypicality. Archives of Sexual Behavior, 29 (6), 549-565. doi: 10.1023/A:1002002420159

  • Childhood sexual abuse and pathogenic parenting in the childhood recollections of adult twin pairs

    McLaughlin, T. L., Heath, A. C., Bucholz, K. K., Madden, P. A. F., Bierut, L. J., Slutske, W. S., Dinwiddie, S., Statham, D. J., Dunne, M. P. and Martin, N. G. (2000). Childhood sexual abuse and pathogenic parenting in the childhood recollections of adult twin pairs. Psychological Medicine, 30 (6), 1293-1302. doi: 10.1017/S0033291799002809

  • A study of the genetic and environmental etiology of stuttering in a selected twin sample

    Felsenfeld, S, Kirk, KM, Zhu, G, Statham, DJ, Neale, MC and Martin, NG (2000). A study of the genetic and environmental etiology of stuttering in a selected twin sample. Behavior Genetics, 30 (5), 359-366. doi: 10.1023/A:1002765620208

  • Dizygotic Twinning Is Not Linked to Variation at the {alpha}-Inhibin Locus on Human Chromosome 2

    Montgomery, Grant W., Duffy, David L., Hall, Jeff, Haddon, Barbara R., Kudo, Masataka, McGee, Elizabeth A., Palmer, James S., Hsueh, Aaron J., Boomsma, Dorrett I. and Martin, Nicholas G. (2000). Dizygotic Twinning Is Not Linked to Variation at the {alpha}-Inhibin Locus on Human Chromosome 2. Journal of Clinical Endocrinology & Metabolism, 85 (9), 3391-3395. doi: 10.1210/jc.85.9.3391

  • Twin study of adolescent genetic susceptibility to mosquito bites using ordinal and comparative rating data

    Kirk, K. M., Eaves, L. J., Meyer, J. M., Saul, A. and Martin, N. G. (2000). Twin study of adolescent genetic susceptibility to mosquito bites using ordinal and comparative rating data. Genetic Epidemiology, 19 (2), 178-190. doi: 10.1002/1098-2272(200009)19:2<178::AID-GEPI5>3.0.CO;2-3

  • Etiology of male sexual orientation in an Australian twin sample

    Bailey, J. M., Kirk, M. and Martin, N. G. (2000). Etiology of male sexual orientation in an Australian twin sample. Psychology, Evolution & Gender, 2 (Dec 3), 301-311. doi: 10.1093/pubmed/fdw069

  • Measurement models for sexual orientation in a community twin sample

    Kirk, KM, Bailey, JM, Dunne, MP and Martin, NG (2000). Measurement models for sexual orientation in a community twin sample. Behavior Genetics, 30 (4), 345-356. doi: 10.1023/A:1026557719181

  • The validity of twin studies

    Evans, David M. and Martin, Nicholas G. (2000). The validity of twin studies. GeneScreen, 1 (2), 77-79. doi: 10.1046/j.1466-9218.2000.00027.x

  • Genetic analysis of the age at menopause by using estimating equations and Bayesian random effects models

    Do, K. A., Broom, B. M., Kuhnert, P., Duffy, D. L., Todorov, A. A., Treloar, S. A. and Martin, N. G. (2000). Genetic analysis of the age at menopause by using estimating equations and Bayesian random effects models. Statistics in Medicine, 19 (9), 1217-1235. doi: 10.1002/(SICI)1097-0258(20000515)19:9<1217::AID-SIM421>3.3.CO;2-H

  • Further Evidence Against the Environmental Transmission of Individual Differences in Neuroticism from a Collaborative Study of 45,850 Twins and Relatives on Two Continents

    Lake, Robert I. E., Eaves, Lindon J., Maes, Hermine M., Heath, Andrew C. and Martin, Nicholas G. (2000). Further Evidence Against the Environmental Transmission of Individual Differences in Neuroticism from a Collaborative Study of 45,850 Twins and Relatives on Two Continents. Behavior Genetics, 30 (3), 223-233. doi: 10.1023/A:1001918408984

  • CYP17 promotor polymorphism and ovarian cancer risk

    Spurdle, Amanda B., Chen, Xiaoqing, Abbazadegan, Mohammed, Martin, Nicholas, Khoo, Soo-Keat, Hurst, Terry, Ward, Bruce, Webb, Penelope M. and Chenevix-Trench, Georgia (2000). CYP17 promotor polymorphism and ovarian cancer risk. International Journal of Cancer, 89 (2), 436-439.

  • Effects of HFE C282Y and H63D Polymorphisms and Polygenic Background on Iron Stores in a Large Community Sample of Twins

    Whitfield, J. B., Cullen, L. M., Jazwinska, E. C., Powell, L. W., Heath, A. C., Zhu, Gu, Duffy, D. L. and Martin, N. G. (2000). Effects of HFE C282Y and H63D Polymorphisms and Polygenic Background on Iron Stores in a Large Community Sample of Twins. American Journal of Human Genetics, 66 (4), 1246-1258. doi: 10.1086/302862

  • Genetic and environmental risk factors shared between disordered eating, psychological and family variables

    Wade, T., Martin, N. G., Tiggemann, M., Abraham, S., Treloar, S. A. and Heath, A. C. (2000). Genetic and environmental risk factors shared between disordered eating, psychological and family variables. Personality & Individual Differences, 28 (4), 729-740. doi: 10.1016/S0191-8869(99)00134-8

  • Monoamine oxidase: associations with alcohol dependence, smoking and other measures of psychopathology

    Whitfield, J. B., Pang, D., Bucholz, K. K., Madden, P. A. F., Heath, A. C., Statham, D. J. and Martin, N. G. (2000). Monoamine oxidase: associations with alcohol dependence, smoking and other measures of psychopathology. Psychological Medicine, 30 (2), 443-454. doi: 10.1017/S0033291799001798

  • Androgen receptor EXON 1 CAG repeat length and risk of ovarian cancer

    Spurdle, A. B., Webb, P. M., Chen, X. D., Martin, N. G., Giles, G. G., Hopper, J. L. and Chenevix-Trench, G. (2000). Androgen receptor EXON 1 CAG repeat length and risk of ovarian cancer. International Journal of Cancer, 87 (5), 637-643. doi: 10.1002/1097-0215(20000901)87:5<637::AID-IJC3>3.0.CO;2-R

  • Anxiety and depression in twin and sib pairs extremely discordant and concordant for neuroticism: Prodromus to a linkage study

    Kirk, Katherine M., Birley, Andrew J., Statham, Dixie J., Haddon, Barbara, Lake, Robert I. E., Andrews, J Gavin and Martin, Nicholas G. (2000). Anxiety and depression in twin and sib pairs extremely discordant and concordant for neuroticism: Prodromus to a linkage study. Twin Research, 3 (4), 299-309. doi: 10.1375/twin.3.4.299

  • Birth weight and age at menopause in Australian female twin pairs: exploration of the fetal origin hypothesis

    Treloar, S. A., Sadrzadeh, S., Do, K. A., Martin, N. G. and Lambalk, C. B. (2000). Birth weight and age at menopause in Australian female twin pairs: exploration of the fetal origin hypothesis. Human Reproduction, 15 (1), 55-59. doi: 10.1093/humrep/15.1.55

  • CYP17 promotor polymorphism and ovarian cancer risk

    Spurdle, Amanda B., Chen, Xiaoqing, Abbazadegan, Mohammed, Martin, Nicholas, Khoo, Soo-Keat, Hurst, Terry, Ward, Bruce, Webb, Penelope M. and Chenevix-Trench, Georgia (2000). CYP17 promotor polymorphism and ovarian cancer risk. International Journal of Cancer, 86 (3), 436-439. doi: 10.1002/(SICI)1097-0215(20000501)86:3<436::AID-IJC21>3.0.CO;2-A

  • Dimensions of psychological masculinity-femininity in adult twins from opposite-sex and same-sex pairs

    Loehlin, John C. and Martin, Nicholas G. (2000). Dimensions of psychological masculinity-femininity in adult twins from opposite-sex and same-sex pairs. Behavior Genetics, 30 (1), 19-28. doi: 10.1023/A:1002082325784

  • Do individual differences in sociosexuality represent genetic or environmentally contingent strategies? Evidence from the Australian twin registry

    Bailey, J. M., Kirk, K. M., Zhu, G., Dunne, M. P. and Martin, N. G. (2000). Do individual differences in sociosexuality represent genetic or environmentally contingent strategies? Evidence from the Australian twin registry. Journal of Personality & Social Psychology, 78 (3), 537-545. doi: 10.1037/0022-3514.78.3.537

  • Early sexual abuse and lifetime psychopathology: a co-twin-control study

    Dinwiddie, S., Heath, A. C., Dunne, M. P., Bucholz, K. K., Madden, P. A. F., Slutske, W. S., Bierut, L. J., Statham, D. B. and Martin, N. G. (2000). Early sexual abuse and lifetime psychopathology: a co-twin-control study. Psychological Medicine, 30 (1), 41-52. doi: 10.1017/S0033291799001373

  • Genetic and environmental influences on sexual orientation and its correlates in an Australian twin sample

    Bailey, J. M., Dunne, M. P. and Martin, N. G. (2000). Genetic and environmental influences on sexual orientation and its correlates in an Australian twin sample. Journal of Personality & Social Psychology, 78 (3), 524-536. doi: 10.1037//0022-3514.78.3.524

  • Genetic influence on the variance in coincidence timing and its covariance with IQ: A twin study

    Wright, Margaret J., Smith, Glen A., Geffen, Gina M., Geffen, Laurie B. and Martin, Nicholas G. (2000). Genetic influence on the variance in coincidence timing and its covariance with IQ: A twin study. Intelligence, 28 (4), 239-250. doi: 10.1016/S0160-2896(99)00036-7

  • Genetic influences on premature parturition in an Australian twin sample

    Treloar, S. A., Macones, G. A., Mitchell, L. A. M. and Martin, N. G. (2000). Genetic influences on premature parturition in an Australian twin sample. Twin Research, 3 (2), 80-82. doi: 10.1375/twin.3.2.80

  • Melanocortin-1 receptor polymorphisms and risk of melanoma: is the association explained solely by pigmentation phenotype?

    Palmer, JS, Duffy, DL, Box, NF, Aitken, JF, O'Gorman, LE, Green, AC, Hayward, NK, Martin, NG and Sturm, RA (2000). Melanocortin-1 receptor polymorphisms and risk of melanoma: is the association explained solely by pigmentation phenotype?. American Journal of Human Genetics, 66 (1), 176-186. doi: 10.1086/302711

  • Shared and unique environmental factors determine the ecology of methanogens in humans and rats

    Florin, T. H. J., Zhu, G., Kirk, K. M. and Martin, N. G. (2000). Shared and unique environmental factors determine the ecology of methanogens in humans and rats. American Journal of Gastroenterology, 95 (10), 2872-2879. doi: 10.1016/S0002-9270(00)01111-4

  • Smoking and the genetic contribution to alcohol-dependence risk

    Madden, PAF, Bucholz, KK, Martin, NG and Heath, AC (2000). Smoking and the genetic contribution to alcohol-dependence risk. Alcohol Research & Health, 24 (4), 209-214.

  • Taxometric analyses of sexual orientation and gender identity

    Gangestad, S. W., Bailey, J. M. and Martin, N. G. (2000). Taxometric analyses of sexual orientation and gender identity. Journal of Personality and Social Psychology, 78 (6), 1109-1121. doi: 10.1037//0022-3514.78.6.1109

  • The effect of apolipoprotein(a)-, apolipoprotein E-, and apolipoprotein A4- polymorphisms on quantitative lipoprotein(a) concentrations

    Boomsma, D. I., Knijff, P., Kaptein, A., Labeur, C., Martin, N. G., Havekes, L. M. and Princen, H. M. (2000). The effect of apolipoprotein(a)-, apolipoprotein E-, and apolipoprotein A4- polymorphisms on quantitative lipoprotein(a) concentrations. Twin Research, 3 (3), 152-158. doi: 10.1375/twin.3.3.152

  • The genetic aetiology of somatic distress

    Gillespie, N. A., Zhu, G., Heath, A. C., Hickie, I. B. and Martin, N. G. (2000). The genetic aetiology of somatic distress. Psychological Medicine, 30 (5), 1051-1061. doi: 10.1017/S0033291799002640

  • Perceptual variation in grading hand, hip and knee radiographs: observations based on an Australian twin registry study of osteoarthritis

    Bellamy, N., Tesar, P., Walker, D., Klestov, A., Muirden, K., Kuhnert, P., Do, K. A., O'Gorman, L. and Martin, N. (1999). Perceptual variation in grading hand, hip and knee radiographs: observations based on an Australian twin registry study of osteoarthritis. Annals of the Rheumatic Diseases, 58 (12), 766-769. doi: 10.1136/ard.58.12.766

  • An assessment of the genetic relationship between alcohol metabolism and alcoholism risk in Australian twins of European ancestry

    Grant, JD, Heath, AC, Madden, PAF, Bucholz, KK, Whitfield, JB and Martin, NG (1999). An assessment of the genetic relationship between alcohol metabolism and alcoholism risk in Australian twins of European ancestry. Behavior Genetics, 29 (6), 463-472. doi: 10.1023/A:1021683106532

  • Melanocytic naevi in eastern Australia: Latitude is important but most variation is within cities

    MacLennan, Robert, Kelly, John W. and Martin, Nicholas G. (1999). Melanocytic naevi in eastern Australia: Latitude is important but most variation is within cities. Australasian Journal of Dermatology, 40 (3), 167-167.

  • The genetics of smoking persistence in men and women: A multicultural study

    Madden, PAF, Heath, AC, Pedersen, NL, Kaprio, J, Koskenvuo, MJ and Martin, NG (1999). The genetics of smoking persistence in men and women: A multicultural study. Behavior Genetics, 29 (6), 423-431. doi: 10.1023/A:1021674804714

  • Somatic distress as a distinct psychological dimension

    Gillespie, N., Kirk, K. M., Heath, A. C., Martin, N. G. and Hickie, I. (1999). Somatic distress as a distinct psychological dimension. Social Psychiatry & Psychiatric Epidemiology, 34 (9), 451-458. doi: 10.1007/s001270050219

  • A major quantitative-trait locus for mole density is linked to the familial melanoma gene CDKN2A: a maximum-likelihood combined linkage and association analysis in twins and their sibs

    Zhu, G, Duffy, DL, Eldridge, A, Grace, M, Mayne, C, O'Gorman, L, Aitken, JF, Neale, MC, Hayward, NK, Green, AC and Martin, NG (1999). A major quantitative-trait locus for mole density is linked to the familial melanoma gene CDKN2A: a maximum-likelihood combined linkage and association analysis in twins and their sibs. American Journal of Human Genetics, 65 (2), 483-492. doi: 10.1086/302494

  • Genetic and environmental causes of variation in basal levels of blood cells

    Evans, David M., Frazer, Ian H. and Martin, Nicholas G. (1999). Genetic and environmental causes of variation in basal levels of blood cells. Twin Research, 2 (4), 250-257. doi: 10.1375/twin.2.4.250

  • Distinguishing population stratification from genuine allelic effects with Mx: association of ADH2 with alcohol consumption

    Neale, M. C., Cherny, S. S., Sham, P. C., Whitfield, J. B., Heath, A. C., Birley, A. J. and Martin, N. G. (1999). Distinguishing population stratification from genuine allelic effects with Mx: association of ADH2 with alcohol consumption. Behavior Genetics, 29 (4), 233-243. doi: 10.1023/A:1021638122693

  • Major depressive disorder in a community-based twin sample: are there different genetic and environmental contributions for men and women

    Bierut, Laura Jean, Heath, Andrew C., Bucholz, Kathleen K., Dinwiddie, Stephen H., Madden, Pamela A. F., Statham, Dixie. J., Dunne, Michael P. and Martin, Nicholas G. (1999). Major depressive disorder in a community-based twin sample: are there different genetic and environmental contributions for men and women. Archives of General Psychiatry, 56 (6), 557-563.

  • Predictors of hysterectomy: an Australian study

    Treloar, Susan A., Do, Kim-Anh, O'Connor, Vivienne M., O'Connor, Daniel T., Yeo, Margaret A. and Martin, Nicholas G. (1999). Predictors of hysterectomy: an Australian study. American Journal of Obstetrics & Gynecology, 180 (4), 945-954. doi: 10.1016/S0002-9378(99)70666-6

  • Fatigue as related to anxiety and depression in a community-based sample of twins aged over 50.

    Kirk, K. M., Hickie, I. B. and Martin, N. G. (1999). Fatigue as related to anxiety and depression in a community-based sample of twins aged over 50.. Social Psychiatry & Psychiatric Epidemiology, 34 (2), 85-90. doi: 10.1007/s001270050116

  • Mendelian segregation of normal CAG trinucleotide repeat alleles at three autosomal loci

    MacMillan, J., Voisey, J., Healey, S. C. and Martin, N. G. (1999). Mendelian segregation of normal CAG trinucleotide repeat alleles at three autosomal loci. Journal of Medical Genetics, 36 (3), 258-259. doi: 10.1136/jmg.36.3.258

  • Perceptual variation in categorizing individual peripheral joints for the presence or absence of osteoarthritis: observations based on an Australian Twin Reigstry study of osteoarthritis

    Bellamy, N., Klestov, A., Muirden, K. D., Kuhnert, P., Do, K. A., O'Gorman, L. and Martin, N. G. (1999). Perceptual variation in categorizing individual peripheral joints for the presence or absence of osteoarthritis: observations based on an Australian Twin Reigstry study of osteoarthritis. Inflammopharmacology, 7 (1), 37-46. doi: 10.1007/s10787-999-0024-x

  • A genetic analysis of the eating and attitudes associated with bulimia nervosa: dealing with the problem of ascertainment in twin studies.

    Wade, T., Neale, M. C., Lake, R. I. and Martin, N. G. (1999). A genetic analysis of the eating and attitudes associated with bulimia nervosa: dealing with the problem of ascertainment in twin studies.. Behavior Genetics, 29 (1), 1-10. doi: 10.1023/A:1021429604095

  • CDKN2A variants in a population-based sample of Queensland families with melanoma

    Aitken, J., Welch, J., Duffy, D., Milligan, A., Green, A., Martin, N. G. and Hayward, N. (1999). CDKN2A variants in a population-based sample of Queensland families with melanoma. Journal of the National Cancer Institute, 91 (5), 446-452. doi: 10.1093/jnci/91.5.446

  • Comparing the biological and cultural inheritance of personality and social attitudes in the Virginia 30,000 study of twins and their relatives

    Eaves, Lindon, Heath, Andrew, Martin, Nicholas, Maes, Hermine, Neale, Michael, Kendler, Kenneth, Kirk, Katherine and Corey, Linda (1999). Comparing the biological and cultural inheritance of personality and social attitudes in the Virginia 30,000 study of twins and their relatives. Twin Research, 2 (2), 62-80. doi: 10.1375/136905299320565933

  • Complex genetic and environmental relationships between psychological distress, fatigue and immune functioning: a twin study

    Hickie, I., Bennett, B., Lloyd, A., Heath, A. and Martin, N. (1999). Complex genetic and environmental relationships between psychological distress, fatigue and immune functioning: a twin study. Psychological Medicine, 29 (2), 269-277. doi: 10.1017/S0033291798007922

  • Frequency of church attendance in Australia and the United States: models of family resemblance

    Kirk, K. M., Maes, H., Neale, M. C., Heath, A., Martin, N. G. and Eaves, L. J. (1999). Frequency of church attendance in Australia and the United States: models of family resemblance. Twin Research, 2 (2), 99-107. doi: 10.1375/twin.2.2.99

  • Genetic and environmental contributions to size, color, shape, and other characteristics of melanocytic naevi in a sample of adolescent twins.

    McGregor, B., Pfitzner, J., Zhu, G., Grace, M., Eldridge, A., Pearson, J., Mayne, C., Aitken, J. F., Green, A. C. and Martin, N. G. (1999). Genetic and environmental contributions to size, color, shape, and other characteristics of melanocytic naevi in a sample of adolescent twins.. Genetic Epidemiology, 16 (1), 40-53. doi: 10.1002/(SICI)1098-2272(1999)16:1<40::AID-GEPI4>3.0.CO;2-1

  • Genetic differences in alcohol sensitivity and the inheritance of alcoholism risk.

    Heath, A., Madden, P. A., Bucholz, K. K., Dinwiddie, S. H., Slutske, W. W., Bierut, L. J., Rohrbaugh, J. W., Statham, D. J., Dunne, M. P., Whitfield, J. B. and Martin, N. G. (1999). Genetic differences in alcohol sensitivity and the inheritance of alcoholism risk.. Psychological Medicine, 29 (5), 1069-1081. doi: 10.1017/S0033291799008909

  • Genetic influences on endometriosis in an Australian twin sample.

    Treloar, S. A., O'Connor, D. T., O'Connor, V. M. and Martin, N. G. (1999). Genetic influences on endometriosis in an Australian twin sample.. Fertility & Sterility, 71 (4), 701-710. doi: 10.1016/S0015-0282(98)00540-8

  • Genetic influences on post-natal depressive symptoms: findings from an Australian twin sample.

    Treloar, S. A., Martin, N. G., Bucholz, K. K., Madden, P. A. and Heath, A. (1999). Genetic influences on post-natal depressive symptoms: findings from an Australian twin sample.. Psychological Medicine, 29 (3), 645-654. doi: 10.1017/S0033291799008387

  • Genetics of early cancer detection behaviours in Australian female twins

    Treloar, S. A., McDonald, C. A. and Martin, N. G. (1999). Genetics of early cancer detection behaviours in Australian female twins. Twin Research, 2 (1), 33-42. doi: 10.1375/twin.2.1.33

  • How accurate is the family history method for assessing siblings' sexual orientation?

    Kirk, Katherine M., Bailey, J. Michael and Martin, Nicholas G. (1999). How accurate is the family history method for assessing siblings' sexual orientation?. Archives of Sexual Behaviour, 28 (2), 129-137. doi: 10.1023/A:1018715821801

  • Number of X-linked androgen receptor gene CAG repeats and femininity in women.

    Loehlin, J. C., Spurdle, A. B., Treloar, S. A. and Martin, N. G. (1999). Number of X-linked androgen receptor gene CAG repeats and femininity in women.. Personality & Individual Differences, 27 (5), 887-899. doi: 10.1016/S0191-8869(99)00038-0

  • Perceptual variation in categorizing individuals according to American College of Rheumatology classification criteria for hand, knee, and hip osteoarthritis (OA): observations based on an Australian Twin Registry study of OA

    Bellamy, N., Klestov, A., Muirden, K., Kuhnert, P., Do, K. A., O'Gorman, L. and Martin, N. (1999). Perceptual variation in categorizing individuals according to American College of Rheumatology classification criteria for hand, knee, and hip osteoarthritis (OA): observations based on an Australian Twin Registry study of OA. Journal of Rheumatology, 26 (12), 2654-2658.

  • Religious attendance and frequency of alcohol use: same genes or same environments: a bivariate extended twin kinship model

    Maes, Hermine H., Neale, Michael C., Martin, Nicholas G., Heath, Andrew C. and Eaves, Lindon J. (1999). Religious attendance and frequency of alcohol use: same genes or same environments: a bivariate extended twin kinship model. Twin Research, 2 (2), 169-179. doi: 10.1375/twin.2.2.169

  • Self-transcendence as a measure of spirituality in a sample of older Australian twins

    Kirk, Katherine M., Eaves, Lindon J. and Martin, Nicholas G. (1999). Self-transcendence as a measure of spirituality in a sample of older Australian twins. Twin Research, 2 (2), 81-87. doi: 10.1375/136905299320565942

  • Some implications of chaos theory for the genetic analysis of human development and variation.

    Eaves, L. J., Kirk, K. M., Martin, N. G. and Russell, R. J. (1999). Some implications of chaos theory for the genetic analysis of human development and variation.. Twin Research, 2 (1), 43-48. doi: 10.1375/twin.2.1.43

  • The structure of genetic and environmental risk factors for three measures of disordered eating

    Wade, T., Martin, N. G., Neale, M. C., Tiggemann, M., Treloar, S. A., Bucholz, K. K., Madden, P. A. F. and Heath, A. C. (1999). The structure of genetic and environmental risk factors for three measures of disordered eating. Psychological Medicine, 29 (4), 925-934. doi: 10.1017/S0033291799008740

  • Unique genetic and environmental determinants of prolonged fatigue: a twin study

    Hickie, I., Kirk, K. and Martin, N. (1999). Unique genetic and environmental determinants of prolonged fatigue: a twin study. Psychological Medicine, 29 (2), 259-268. doi: 10.1017/S0033291798007934

  • Predictive factors of age at menopause in a large Australian twin study

    Do, Kim-Anh, Treloar, Susan A., Pandeya, Nirmala, Purdie, David, Green, Adele C., Heath, Andrew C. and Martin, Nicholas G. (1998). Predictive factors of age at menopause in a large Australian twin study. Human Biology, 70 (6), 1073-1091.

  • Smoking, obesity, and hypertension alter the dose-response curve and test sensitivity of carbohydrate-deficient transferrin as a marker of alcohol intake

    Whitfield, JB, Fletcher, LM, Murphy, TL, Powell, LW, Halliday, J, Heath, AC and Martin, NG (1998). Smoking, obesity, and hypertension alter the dose-response curve and test sensitivity of carbohydrate-deficient transferrin as a marker of alcohol intake. Clinical Chemistry, 44 (12), 2480-2489.

  • Assessing the effects of cooperation bias and attrition in behavioral genetic research using data-weighting

    Heath, AC, Madden, PAF and Martin, NG (1998). Assessing the effects of cooperation bias and attrition in behavioral genetic research using data-weighting. Behavior Genetics, 28 (6), 415-427. doi: 10.1023/A:1021633127604

  • Genetic influences on the age at menopause

    Treloar, SA, Do, KA and Martin, NG (1998). Genetic influences on the age at menopause. Lancet, 352 (9134), 1084-1085. doi: 10.1016/S0140-6736(05)79753-1

  • ADH genotypes and alcohol use and dependence in Europeans

    Whitfield, JB, Nightingale, BN, Bucholz, KK, Madden, PAF, Heath, AC and Martin, NG (1998). ADH genotypes and alcohol use and dependence in Europeans. Alcoholism-Clinical and Experimental Research, 22 (7), 1463-1469. doi: 10.1111/j.1530-0277.1998.tb03936.x

  • The Short Interpersonal Reactions Inventory, Self-regulation and Differentiation scales in an older Australian twin sample

    Kirk, KM and Martin, NG (1998). The Short Interpersonal Reactions Inventory, Self-regulation and Differentiation scales in an older Australian twin sample. Personality and Individual Differences, 25 (3), 591-604. doi: 10.1016/S0191-8869(98)00116-0

  • Genetic and environmental risk factors for the weight and shape concerns characteristic of bulimia nervosa

    Wade, T., Martin, N. G. and Tiggemann, M. (1998). Genetic and environmental risk factors for the weight and shape concerns characteristic of bulimia nervosa. Psychological Medicine, 28 (4), 761-771. doi: 10.1017/S0033291798006989

  • Suicidal behaviour: an epidemiological and genetic study

    Statham, DJ, Heath, AC, Madden, PAF, Bucholz, KK, Bierut, L, Dinwiddie, SH, Slutske, WS, Dunne, MP and Martin, NG (1998). Suicidal behaviour: an epidemiological and genetic study. Psychological Medicine, 28 (4), 839-855. doi: 10.1017/S0033291798006916

  • Dating the origin of the CCR5-Delta 32 AIDS-resistance allele by the coalescence of haplotypes

    Stephens, JC, Reich, DE, Goldstein, DB, Shin, HD, Smith, MW, Carrington, M, Winkler, C, Huttley, GA, Allikmets, R, Schriml, L, Gerrard, B, Malasky, M, Ramos, MD, Morlot, S, Tzetis, M, Oddoux, C, di Giovine, FS, Nasioulas, G, Chandler, D, Aseev, M, Hanson, M, Kalaydjieva, L, Glavac, D, Gasparini, P, Kanavakis, E, Claustres, M, Kambouris, M, Ostrer, H, Duff, G ... Dean, M (1998). Dating the origin of the CCR5-Delta 32 AIDS-resistance allele by the coalescence of haplotypes. American Journal of Human Genetics, 62 (6), 1507-1515. doi: 10.1086/301867

  • Genetic and environmental risk factors for asthma - A cotwin-control study

    Duffy, DL, Mitchell, CA and Martin, NG (1998). Genetic and environmental risk factors for asthma - A cotwin-control study. American Journal of Respiratory and Critical Care Medicine, 157 (3), 840-845. doi: 10.1164/ajrccm.157.3.9702070

  • Longitudinal genetic analysis of menstrual flow, pain, and limitation in a sample of Australian twins

    Treloar, SA, Martin, NG and Heath, AC (1998). Longitudinal genetic analysis of menstrual flow, pain, and limitation in a sample of Australian twins. Behavior Genetics, 28 (2), 107-116. doi: 10.1023/A:1021419907305

  • A comparison of adult female twins from opposite-sex and same-sex pairs on variables related to reproduction

    Loehlin, JC and Martin, NG (1998). A comparison of adult female twins from opposite-sex and same-sex pairs on variables related to reproduction. Behavior Genetics, 28 (1), 21-27. doi: 10.1023/A:1021452630561

  • Complete sequence and polymorphism study of the human TYRP1 gene encoding tyrosinase-related protein 1

    Box, Neil F., Wyeth, Jason R., Mayne, Carol J., O'Gorman, Louise E., Martin, Nicholas G. and Sturm, Richard A (1998). Complete sequence and polymorphism study of the human TYRP1 gene encoding tyrosinase-related protein 1. Mammalian Genome, 9 (1), 50-53. doi: 10.1007/s003359900678

  • A comparison of the Eating Disorder Examination and a general psychiatric schedule

    Wade, T, Tiggemann, M, Martin, N and Heath, A (1997). A comparison of the Eating Disorder Examination and a general psychiatric schedule. Australian and New Zealand Journal of Psychiatry, 31 (6), 852-857. doi: 10.3109/00048679709065511

  • A twin-pronged attack on complex traits

    Martin, N, Boomsma, D and Machin, G (1997). A twin-pronged attack on complex traits. Nature Genetics, 17 (4), 387-392. doi: 10.1038/ng1297-387

  • Smoking and intoxication after alcohol challenge in women and men: Genetic influences

    Madden, PAF, Heath, AC and Martin, NG (1997). Smoking and intoxication after alcohol challenge in women and men: Genetic influences. Alcoholism-Clinical and Experimental Research, 21 (9), 1732-1741. doi: 10.1097/00000374-199712000-00029

  • Genetic and environmental contributions to alcohol dependence risk in a national twin sample: consistency of findings in women and men

    Heath, AC, Bucholz, KK, Madden, PAF, Dinwiddie, SH, Slutske, WS, Bierut, LJ, Statham, DJ, Dunne, MP, Whitfield, JB and Martin, NG (1997). Genetic and environmental contributions to alcohol dependence risk in a national twin sample: consistency of findings in women and men. Psychological Medicine, 27 (6), 1381-1396. doi: 10.1017/S0033291797005643

  • Characterization of melanocyte stimulating hormone receptor variant alleles in twins with red hair

    Box, Neil F., Wyeth, Jason R., O'Gorman, Louise E., Martin, Nicholas G. and Sturm, Richard A. (1997). Characterization of melanocyte stimulating hormone receptor variant alleles in twins with red hair. Human Molecular Genetics, 6 (11), 1891-1897. doi: 10.1093/hmg/6.11.1891

  • What are the causes of individual differences in food consumption and are they modified by personality?

    Yeo, MA, Treloar, SA, Marks, GC, Heath, AC and Martin, NG (1997). What are the causes of individual differences in food consumption and are they modified by personality?. Personality and Individual Differences, 23 (4), 535-542. doi: 10.1016/S0191-8869(97)00094-9

  • Personality and change in the frequency of religious observance

    Dunne, MP, Martin, NG, Pangan, T and Heath, AC (1997). Personality and change in the frequency of religious observance. Personality and Individual Differences, 23 (3), 527-530. doi: 10.1016/S0191-8869(97)80020-7

  • Participation bias in a sexuality survey: Psychological and behavioural characteristics of responders and non-responders

    Dunne, MP, Martin, NG, Bailey, JM, Heath, AC, Bucholz, KK, Madden, PAF and Statham, DJ (1997). Participation bias in a sexuality survey: Psychological and behavioural characteristics of responders and non-responders. International Journal of Epidemiology, 26 (4), 844-854. doi: 10.1093/ije/26.4.844

  • Nicotine withdrawal in women

    Madden, PAF, Bucholz, KK, Dinwiddie, SH, Slutske, WS, Bierut, LJ, Statham, DJ, Dunne, MP, Martin, NG and Heath, AC (1997). Nicotine withdrawal in women. Addiction, 92 (7), 889-902. doi: 10.1046/j.1360-0443.1997.92788911.x

  • Genetic and environmental contributions to variance in age at first sexual intercourse

    Dunne, MP, Martin, NG, Statham, DJ, Slutske, WS, Dinwiddie, SH, Bucholz, KK, Madden, PAF and Heath, AC (1997). Genetic and environmental contributions to variance in age at first sexual intercourse. Psychological Science, 8 (3), 211-216. doi: 10.1111/j.1467-9280.1997.tb00414.x

  • MN blood group affects response of serum LDL cholesterol level to a low fat diet

    Birley, AJ, MacLennan, R, Wahlqvist, M, Gerns, L, Pangan, T and Martin, NG (1997). MN blood group affects response of serum LDL cholesterol level to a low fat diet. Clinical Genetics, 51 (5), 291-295. doi: 10.1111/j.1399-0004.1997.tb02476.x

  • Age changes in the causes of individual differences in conservatism

    Eaves, L, Martin, N, Heath, A, Schieken, R, Meyer, J, Silberg, J, Neale, M and Corey, L (1997). Age changes in the causes of individual differences in conservatism. Behavior Genetics, 27 (2), 121-124. doi: 10.1023/A:1025633307992

  • Family characteristics and the returns to schooling: Evidence on gender differences from a sample of Australian twins

    Miller, P, Mulvey, C and Martin, N (1997). Family characteristics and the returns to schooling: Evidence on gender differences from a sample of Australian twins. Economica, 64 (253), 119-136. doi: 10.1111/1468-0335.00067

  • Genetic effects on variation in red-blood-cell folate in adults: Implications for the familial aggregation of neural tube defects

    Mitchell, LE, Duffy, DL, Duffy, P, Bellingham, G and Martin, NG (1997). Genetic effects on variation in red-blood-cell folate in adults: Implications for the familial aggregation of neural tube defects. American Journal of Human Genetics, 60 (2), 433-438.

  • The consistency of recalled age at first sexual intercourse

    Dunne, MP, Martin, NG, Statham, DJ, Pangan, T, Madden, PA and Heath, AC (1997). The consistency of recalled age at first sexual intercourse. Journal of Biosocial Science, 29 (1), 1-7. doi: 10.1017/S0021932097000011

  • Assessing the prevalence of eating disorders in an Australian twin population

    Wade, T, Heath, AC, Abraham, S, Treloar, SA, Martin, NG and Tiggemann, M (1996). Assessing the prevalence of eating disorders in an Australian twin population. Australian and New Zealand Journal of Psychiatry, 30 (6), 845-851. doi: 10.3109/00048679609065054

  • Accuracy of case-reported family history of melanoma in Queensland, Australia

    Aitken, JF, Youl, P, Green, A, MacLennan, R and Martin, NG (1996). Accuracy of case-reported family history of melanoma in Queensland, Australia. Melanoma Research, 6 (4), 313-317. doi: 10.1097/00008390-199608000-00006

  • Reliability of computer image analysis of pigmented skin lesions of Australian adolescents

    Aitken, Joanne F., Pfitzner, John, Battistutta, Diana, O'Rourke, Peter K., Green, Adèle C. and Martin, Nicholas G. (1996). Reliability of computer image analysis of pigmented skin lesions of Australian adolescents. Cancer, 78 (2), 252-257. doi: 10.1002/(SICI)1097-0142(19960715)78:2<252::AID-CNCR10>3.0.CO;2-V

  • Reliability and reporting biases for perceived parental history of alcohol-related problems: Agreement between twins and differences between discordant pairs

    Slutske, WS, Heath, AC, Madden, PAF, Bucholz, KK, Dinwiddie, SH, Dunne, MP, Statham, DJ and Martin, NG (1996). Reliability and reporting biases for perceived parental history of alcohol-related problems: Agreement between twins and differences between discordant pairs. Journal of Studies On Alcohol, 57 (4), 387-395. doi: 10.15288/jsa.1996.57.387

  • Multiple regression analysis of the occupational status of twins: A comparison of economic and behavioural genetics models

    Miller, P, Mulvey, C and Martin, N (1996). Multiple regression analysis of the occupational status of twins: A comparison of economic and behavioural genetics models. Oxford Bulletin of Economics and Statistics, 58 (2), 227-227.

  • The Queensland Familial Melanoma Project: Study design and characteristics of participants

    Aitken, JF, Green, AC, MacLennan, R and Martin, NG (1996). The Queensland Familial Melanoma Project: Study design and characteristics of participants. Melanoma Research, 6 (2), 155-165. doi: 10.1097/00008390-199604000-00011

  • The control of ovulation in mothers of dizygotic twins

    Gilfillan, CP, Robertson, DM, Burger, HG, Leoni, MA, Hurley, VA and Martin, NG (1996). The control of ovulation in mothers of dizygotic twins. Journal of Clinical Endocrinology & Metabolism, 81 (4), 1557-1562. doi: 10.1210/jc.81.4.1557

  • Genetics of educational attainment in Australian twins: Sex differences and secular changes

    Baker, LA, Treloar, SA, Reynolds, CA, Heath, AC and Martin, NG (1996). Genetics of educational attainment in Australian twins: Sex differences and secular changes. Behavior Genetics, 26 (2), 89-102. doi: 10.1007/BF02359887

  • Social contact, social attitudes, and twin similarity

    Posner, SF, Baker, L, Heath, A and Martin, NG (1996). Social contact, social attitudes, and twin similarity. Behavior Genetics, 26 (2), 123-133. doi: 10.1007/BF02359890

  • Alcohol reactions in subjects of European descent: Effects on alcohol use and on physical and psychomotor responses to alcohol

    Whitfield, JB and Martin, NG (1996). Alcohol reactions in subjects of European descent: Effects on alcohol use and on physical and psychomotor responses to alcohol. Alcoholism-Clinical and Experimental Research, 20 (1), 81-86. doi: 10.1111/j.1530-0277.1996.tb01048.x

  • Seasonal changes in mood and behavior - The role of genetic factors

    Madden, PAF, Heath, AC, Rosenthal, NE and Martin, NG (1996). Seasonal changes in mood and behavior - The role of genetic factors. Archives of General Psychiatry, 53 (1), 47-55. doi: 10.1001/archpsyc.1996.01830010049008

  • Structure of disordered eating in a twin community sample

    Wade, T, Tiggemann, M, Heath, AC, Abraham, S, Treloar, SA and Martin, NG (1996). Structure of disordered eating in a twin community sample. International Journal of Eating Disorders, 19 (1), 63-71. doi: 10.1002/(sici)1098-108x(199601)19:1<63::aid-eat8>3.0.co;2-u

  • Self-report psychiatric symptoms in twins and their nontwin relatives: Are twins different?

    Kendler, KS, Martin, NG, Heath, AC and Eaves, LJ (1995). Self-report psychiatric symptoms in twins and their nontwin relatives: Are twins different?. American Journal of Medical Genetics, 60 (6), 588-591. doi: 10.1002/ajmg.1320600622

  • A TWIN-FAMILY STUDY OF SELF-REPORT SYMPTOMS OF PANIC-PHOBIA AND SOMATIZATION

    KENDLER, KS, WALTERS, EE, TRUETT, KR, HEATH, AC, NEALE, MC, MARTIN, NG and EAVES, LJ (1995). A TWIN-FAMILY STUDY OF SELF-REPORT SYMPTOMS OF PANIC-PHOBIA AND SOMATIZATION. Behavior Genetics, 25 (6), 499-515. doi: 10.1007/BF02327574

  • ALCOHOL SENSITIVITY AND SMOKING HISTORY IN MEN AND WOMEN

    MADDEN, PAF, HEATH, AC, STARMER, GA, WHITFIELD, JB and MARTIN, NG (1995). ALCOHOL SENSITIVITY AND SMOKING HISTORY IN MEN AND WOMEN. Alcoholism-Clinical and Experimental Research, 19 (5), 1111-1120. doi: 10.1111/j.1530-0277.1995.tb01588.x

  • GENETIC COVARIANCE STRUCTURE OF INCISOR CROWN SIZE IN TWINS

    DEMPSEY, PJ, TOWNSEND, GC, MARTIN, NG and NEALE, MC (1995). GENETIC COVARIANCE STRUCTURE OF INCISOR CROWN SIZE IN TWINS. Journal of Dental Research, 74 (7), 1389-1398. doi: 10.1177/00220345950740071101

  • IS ALCOHOL-RELATED FLUSHING A PROTECTIVE FACTOR FOR ALCOHOLISM IN CAUCASIANS

    SLUTSKE, WS, HEATH, AC, MADDEN, PAF, BUCHOLZ, KK, DINWIDDIE, SH, DUNNE, MP, STATHAM, DS, WHITFIELD, JB and MARTIN, NG (1995). IS ALCOHOL-RELATED FLUSHING A PROTECTIVE FACTOR FOR ALCOHOLISM IN CAUCASIANS. Alcoholism-Clinical and Experimental Research, 19 (3), 582-592. doi: 10.1111/j.1530-0277.1995.tb01552.x

  • OSTEOPOROSIS IN RHEUMATOID-ARTHRITIS - A MONOZYGOTIC COTWIN CONTROL STUDY

    SAMBROOK, PN, SPECTOR, TD, SEEMAN, E, BELLAMY, N, BUCHANAN, RRC, DUFFY, DL, MARTIN, NG, PRINCE, R, OWEN, E, SILMAN, AJ and EISMAN, JA (1995). OSTEOPOROSIS IN RHEUMATOID-ARTHRITIS - A MONOZYGOTIC COTWIN CONTROL STUDY. Arthritis and Rheumatism, 38 (6), 806-809. doi: 10.1002/art.1780380614

  • A psychometric evaluation of the Short Interpersonal Reactions Inventory (SIRI) in an Australian twin sample

    Roberts, Leonard J., Duffy, David L. and Martin, Nicholas G. (1995). A psychometric evaluation of the Short Interpersonal Reactions Inventory (SIRI) in an Australian twin sample. Personality and Individual Differences, 18 (3), 307-320. doi: 10.1016/0191-8869(94)00158-O

  • Personality and the inheritance of smoking-behavior - a genetic perspective

    Heath, AC, Madden, PAF, Slutske, WS and Martin, NG (1995). Personality and the inheritance of smoking-behavior - a genetic perspective. Behavior Genetics, 25 (2), 103-117. doi: 10.1007/BF02196921

  • EPQ-R PERSONALITY-CORRELATES OF BULIMIA-NERVOSA IN AN AUSTRALIAN TWIN POPULATION

    WADE, T, TIGGEMANN, M, HEATH, AC, ABRAHAM, S and MARTIN, NG (1995). EPQ-R PERSONALITY-CORRELATES OF BULIMIA-NERVOSA IN AN AUSTRALIAN TWIN POPULATION. Personality and Individual Differences, 18 (2), 283-285. doi: 10.1016/0191-8869(94)00141-E

  • COMPUTER IMAGE-ANALYSIS IN THE DIAGNOSIS OF MELANOMA

    GREEN, A, MARTIN, N, PFITZNER, J, OROURKE, M and KNIGHT, N (1994). COMPUTER IMAGE-ANALYSIS IN THE DIAGNOSIS OF MELANOMA. Journal of the American Academy of Dermatology, 31 (6), 958-964. doi: 10.1016/S0190-9622(94)70264-0

  • HETEROGENEITY OF MELANOMA RISK IN FAMILIES OF MELANOMA PATIENTS

    AITKEN, JF, DUFFY, DL, GREEN, A, YOUL, P, MACLENNAN, R and MARTIN, NG (1994). HETEROGENEITY OF MELANOMA RISK IN FAMILIES OF MELANOMA PATIENTS. American Journal of Epidemiology, 140 (11), 961-973. doi: 10.1093/oxfordjournals.aje.a117203

  • DIZYGOUS TWINNING AND PREMATURE MENOPAUSE IN FRAGILE-X SYNDROME

    TURNER, G, ROBINSON, H, WAKE, S and MARTIN, N (1994). DIZYGOUS TWINNING AND PREMATURE MENOPAUSE IN FRAGILE-X SYNDROME. Lancet, 344 (8935), 1500-1500. doi: 10.1016/S0140-6736(94)90313-1

  • SOURCES OF INDIVIDUAL-DIFFERENCES IN DEPRESSIVE SYMPTOMS - ANALYSIS OF 2 SAMPLES OF TWINS AND THEIR FAMILIES

    KENDLER, KS, WALTERS, EE, TRUETT, KR, HEATH, AC, NEALE, MC, MARTIN, NG and EAVES, LJ (1994). SOURCES OF INDIVIDUAL-DIFFERENCES IN DEPRESSIVE SYMPTOMS - ANALYSIS OF 2 SAMPLES OF TWINS AND THEIR FAMILIES. American Journal of Psychiatry, 151 (11), 1605-1614. doi: 10.1176/ajp.151.11.1605

  • ANALYSIS OF THE P16 GENE (CDKN2) AS A CANDIDATE FOR THE CHROMOSOME 9P MELANOMA SUSCEPTIBILITY LOCUS

    KAMB, A, SHATTUCKEIDENS, D, EELES, R, LIU, Q, GRUIS, NA, DING, W, HUSSEY, C, TRAN, T, MIKI, Y, WEAVERFELDHAUS, J, MCCLURE, M, AITKEN, JF, ANDERSON, DE, BERGMAN, W, FRANTS, R, GOLDGAR, DE, GREEN, A, MACLENNAN, R, MARTIN, NG, MEYER, LJ, YOUL, P, ZONE, JJ, SKOLNICK, MH and CANNONALBRIGHT, LA (1994). ANALYSIS OF THE P16 GENE (CDKN2) AS A CANDIDATE FOR THE CHROMOSOME 9P MELANOMA SUSCEPTIBILITY LOCUS. Nature Genetics, 8 (1), 22-26. doi: 10.1038/ng0994-22

  • NEVOID BASAL-CELL CARCINOMA SYNDROME - REVIEW OF 118 AFFECTED INDIVIDUALS

    SHANLEY, S, RATCLIFFE, J, HOCKEY, A, HAAN, E, OLEY, C, RAVINE, D, MARTIN, N, WICKING, C and CHENEVIXTRENCH, G (1994). NEVOID BASAL-CELL CARCINOMA SYNDROME - REVIEW OF 118 AFFECTED INDIVIDUALS. American Journal of Medical Genetics, 50 (3), 282-290. doi: 10.1002/ajmg.1320500312

  • ALCOHOL-CONSUMPTION AND ALCOHOL PHARMACOKINETICS - INTERACTIONS WITHIN THE NORMAL POPULATION

    WHITFIELD, JB and MARTIN, NG (1994). ALCOHOL-CONSUMPTION AND ALCOHOL PHARMACOKINETICS - INTERACTIONS WITHIN THE NORMAL POPULATION. Alcoholism-Clinical and Experimental Research, 18 (2), 238-243. doi: 10.1111/j.1530-0277.1994.tb00007.x

  • TESTING A MODEL FOR THE GENETIC-STRUCTURE OF PERSONALITY - A COMPARISON OF THE PERSONALITY SYSTEMS OF CLONINGER AND EYSENCK

    HEATH, AC, CLONINGER, CR and MARTIN, NG (1994). TESTING A MODEL FOR THE GENETIC-STRUCTURE OF PERSONALITY - A COMPARISON OF THE PERSONALITY SYSTEMS OF CLONINGER AND EYSENCK. Journal of Personality and Social Psychology, 66 (4), 762-775. doi: 10.1037//0022-3514.66.4.762

  • COMPARABILITY OF NEVUS COUNTS BETWEEN AND WITHIN EXAMINERS, AND COMPARISON WITH COMPUTER IMAGE-ANALYSIS

    AITKEN, JF, GREEN, A, ELDRIDGE, A, GREEN, L, PFITZNER, J, BATTISTUTTA, D and MARTIN, NG (1994). COMPARABILITY OF NEVUS COUNTS BETWEEN AND WITHIN EXAMINERS, AND COMPARISON WITH COMPUTER IMAGE-ANALYSIS. British Journal of Cancer, 69 (3), 487-491. doi: 10.1038/bjc.1994.88

  • SHORTENED VERSIONS OF THE INTERPERSONAL SENSITIVITY MEASURE, PARENTAL BONDING INSTRUMENT AND INTIMATE BOND MEASURE

    TODD, AL, BOYCE, PM, HEATH, AC and MARTIN, NG (1994). SHORTENED VERSIONS OF THE INTERPERSONAL SENSITIVITY MEASURE, PARENTAL BONDING INSTRUMENT AND INTIMATE BOND MEASURE. Personality and Individual Differences, 16 (2), 323-329. doi: 10.1016/0191-8869(94)90169-4

  • A MODEL SYSTEM FOR ANALYSIS OF FAMILY RESEMBLANCE IN EXTENDED KINSHIPS OF TWINS

    TRUETT, KR, EAVES, LJ, WALTERS, EE, HEATH, AC, HEWITT, JK, MEYER, JM, SILBERG, J, NEALE, MC, MARTIN, NG and KENDLER, KS (1994). A MODEL SYSTEM FOR ANALYSIS OF FAMILY RESEMBLANCE IN EXTENDED KINSHIPS OF TWINS. Behavior Genetics, 24 (1), 35-49. doi: 10.1007/BF01067927

  • DIRECTION OF CAUSATION - REPLY TO COMMENTARIES

    NEALE, MC, DUFFY, DL and MARTIN, NG (1994). DIRECTION OF CAUSATION - REPLY TO COMMENTARIES. Genetic Epidemiology, 11 (6), 463-472. doi: 10.1002/gepi.1370110603

  • INFERRING THE DIRECTION OF CAUSATION IN CROSS-SECTIONAL TWIN DATA - THEORETICAL AND EMPIRICAL CONSIDERATIONS

    DUFFY, DL and MARTIN, NG (1994). INFERRING THE DIRECTION OF CAUSATION IN CROSS-SECTIONAL TWIN DATA - THEORETICAL AND EMPIRICAL CONSIDERATIONS. Genetic Epidemiology, 11 (6), 483-502. doi: 10.1002/gepi.1370110606

  • PSORIASIS IN AUSTRALIAN TWINS

    DUFFY, DL, SPELMAN, LS and MARTIN, NG (1993). PSORIASIS IN AUSTRALIAN TWINS. Journal of the American Academy of Dermatology, 29 (3), 428-434. doi: 10.1016/0190-9622(93)70206-9

  • COMPARABILITY OF SURROGATE AND SELF-REPORTED INFORMATION ON MELANOMA RISK-FACTORS

    AITKEN, JF, GREEN, A, MACLENNAN, R, JACKMAN, L and MARTIN, NG (1993). COMPARABILITY OF SURROGATE AND SELF-REPORTED INFORMATION ON MELANOMA RISK-FACTORS. British Journal of Cancer, 67 (5), 1036-1041. doi: 10.1038/bjc.1993.190

  • GENETIC AND ENVIRONMENTAL COVARIANCE OF SERUM-CHOLESTEROL AND BLOOD-PRESSURE IN FEMALE TWINS

    WILLIAMS, PD, PUDDEY, IB, MARTIN, NG and BEILIN, LJ (1993). GENETIC AND ENVIRONMENTAL COVARIANCE OF SERUM-CHOLESTEROL AND BLOOD-PRESSURE IN FEMALE TWINS. Atherosclerosis, 100 (1), 19-31. doi: 10.1016/0021-9150(93)90064-2

  • REPRODUCTIVE HORMONE GENES IN MOTHERS OF SPONTANEOUS DIZYGOTIC TWINS - AN ASSOCIATION STUDY

    CHENEVIXTRENCH, G, HEALEY, S and MARTIN, NG (1993). REPRODUCTIVE HORMONE GENES IN MOTHERS OF SPONTANEOUS DIZYGOTIC TWINS - AN ASSOCIATION STUDY. Human Genetics, 91 (2), 118-120. doi: 10.1007/bf00222710

  • AVERSIVE REACTIONS AND ALCOHOL-USE IN EUROPEANS

    WHITFIELD, JB and MARTIN, NG (1993). AVERSIVE REACTIONS AND ALCOHOL-USE IN EUROPEANS. Alcoholism-Clinical and Experimental Research, 17 (1), 131-134. doi: 10.1111/j.1530-0277.1993.tb00737.x

  • SITE DISTRIBUTION OF CUTANEOUS MELANOMA IN QUEENSLAND

    GREEN, A, MACLENNAN, R, YOUL, P and MARTIN, N (1993). SITE DISTRIBUTION OF CUTANEOUS MELANOMA IN QUEENSLAND. International Journal of Cancer, 53 (2), 232-236. doi: 10.1002/ijc.2910530210

  • GENETIC MODELS FOR THE NATURAL-HISTORY OF SMOKING - EVIDENCE FOR A GENETIC INFLUENCE ON SMOKING PERSISTENCE

    HEATH, AC and MARTIN, NG (1993). GENETIC MODELS FOR THE NATURAL-HISTORY OF SMOKING - EVIDENCE FOR A GENETIC INFLUENCE ON SMOKING PERSISTENCE. Addictive Behaviors, 18 (1), 19-34. doi: 10.1016/0306-4603(93)90005-T

  • CLEFT-LIP WITH OR WITHOUT CLEFT-PALATE - ASSOCIATIONS WITH TRANSFORMING GROWTH FACTOR-ALPHA AND RETINOIC ACID RECEPTOR LOCI

    CHENEVIXTRENCH, G, JONES, K, GREEN, AC, DUFFY, DL and MARTIN, NG (1992). CLEFT-LIP WITH OR WITHOUT CLEFT-PALATE - ASSOCIATIONS WITH TRANSFORMING GROWTH FACTOR-ALPHA AND RETINOIC ACID RECEPTOR LOCI. American Journal of Human Genetics, 51 (6), 1377-1385.

  • INCREASING INCIDENCE OF CUTANEOUS MELANOMA IN QUEENSLAND, AUSTRALIA

    MACLENNAN, R, GREEN, AC, MCLEOD, GRC and MARTIN, NG (1992). INCREASING INCIDENCE OF CUTANEOUS MELANOMA IN QUEENSLAND, AUSTRALIA. Journal of the National Cancer Institute, 84 (18), 1427-1432. doi: 10.1093/jnci/84.18.1427

  • PATHWAYS TO HYSTERECTOMY - INSIGHTS FROM LONGITUDINAL TWIN RESEARCH

    TRELOAR, SA, MARTIN, NG, DENNERSTEIN, L, RAPHAEL, B and HEATH, AC (1992). PATHWAYS TO HYSTERECTOMY - INSIGHTS FROM LONGITUDINAL TWIN RESEARCH. American Journal of Obstetrics and Gynecology, 167 (1), 82-88. doi: 10.1016/S0002-9378(11)91632-9

  • GENETIC-DIFFERENCES IN PSYCHOMOTOR PERFORMANCE DECREMENT AFTER ALCOHOL - A MULTIVARIATE-ANALYSIS

    HEATH, AC and MARTIN, NG (1992). GENETIC-DIFFERENCES IN PSYCHOMOTOR PERFORMANCE DECREMENT AFTER ALCOHOL - A MULTIVARIATE-ANALYSIS. Journal of Studies On Alcohol, 53 (3), 262-271. doi: 10.15288/jsa.1992.53.262

  • PROTEASE INHIBITOR (PI) LOCUS, FERTILITY AND TWINNING

    BOOMSMA, DI, FRANTS, RR, BANK, RA and MARTIN, NG (1992). PROTEASE INHIBITOR (PI) LOCUS, FERTILITY AND TWINNING. Human Genetics, 89 (3), 329-332. doi: 10.1007/BF00220552

  • RHEUMATOID-ARTHRITIS IN TWINS - A STUDY OF ETIOPATHOGENESIS BASED ON THE AUSTRALIAN-TWIN-REGISTRY

    BELLAMY, N, DUFFY, D, MARTIN, N and MATHEWS, J (1992). RHEUMATOID-ARTHRITIS IN TWINS - A STUDY OF ETIOPATHOGENESIS BASED ON THE AUSTRALIAN-TWIN-REGISTRY. Annals of the Rheumatic Diseases, 51 (5), 588-593. doi: 10.1136/ard.51.5.588

  • FITTING GENETIC MODELS TO CARABELLI TRAIT DATA IN SOUTH AUSTRALIAN TWINS

    TOWNSEND, GC and MARTIN, NG (1992). FITTING GENETIC MODELS TO CARABELLI TRAIT DATA IN SOUTH AUSTRALIAN TWINS. Journal of Dental Research, 71 (2), 403-409. doi: 10.1177/00220345920710021001

  • Genetic control of the renal clearance of urate: A study of twins

    Emmerson B.T., Nagel S.L., Duffy D.L. and Martin N.G. (1992). Genetic control of the renal clearance of urate: A study of twins. Annals of the Rheumatic Diseases, 51 (3), 375-377. doi: 10.1136/ard.51.3.375

  • Religion and education as mediators of attitudes - a multivariate-analysis

    Truett, KR, Eaves, LJ, Meyer, JM, Heath, AC and Martin, NG (1992). Religion and education as mediators of attitudes - a multivariate-analysis. Behavior Genetics, 22 (1), 43-62. doi: 10.1007/BF01066792

  • ESTIMATING GENETIC INFLUENCES ON THE AGE-AT-MENARCHE - A SURVIVAL ANALYSIS APPROACH

    MEYER, JM, EAVES, LJ, HEATH, AC and MARTIN, NG (1991). ESTIMATING GENETIC INFLUENCES ON THE AGE-AT-MENARCHE - A SURVIVAL ANALYSIS APPROACH. American Journal of Medical Genetics, 39 (2), 148-154. doi: 10.1002/ajmg.1320390207

  • SEXUAL ORIENTATION, SEXUAL IDENTITY, AND SEX-DIMORPHIC BEHAVIORS IN MALE TWINS

    BUHRICH, N, BAILEY, JM and MARTIN, NG (1991). SEXUAL ORIENTATION, SEXUAL IDENTITY, AND SEX-DIMORPHIC BEHAVIORS IN MALE TWINS. Behavior Genetics, 21 (1), 75-96. doi: 10.1007/BF01067668

  • GENETICS OF ASTHMA AND HAY-FEVER IN AUSTRALIAN TWINS

    DUFFY, DL, MARTIN, NG, BATTISTUTTA, D, HOPPER, JL and MATHEWS, JD (1990). GENETICS OF ASTHMA AND HAY-FEVER IN AUSTRALIAN TWINS. American Review of Respiratory Disease, 142 (6), 1351-1358. doi: 10.1164/ajrccm/142.6_Pt_1.1351

  • FACTOR AND SIMPLEX MODELS FOR REPEATED MEASURES - APPLICATION TO 2 PSYCHOMOTOR MEASURES OF ALCOHOL SENSITIVITY IN TWINS

    BOOMSMA, DI, MARTIN, NG and MOLENAAR, PCM (1989). FACTOR AND SIMPLEX MODELS FOR REPEATED MEASURES - APPLICATION TO 2 PSYCHOMOTOR MEASURES OF ALCOHOL SENSITIVITY IN TWINS. Behavior Genetics, 19 (1), 79-96. doi: 10.1007/BF01065885

  • INTERACTIVE EFFECTS OF GENOTYPE AND SOCIAL-ENVIRONMENT ON ALCOHOL-CONSUMPTION IN FEMALE TWINS

    HEATH, AC, JARDINE, R and MARTIN, NG (1989). INTERACTIVE EFFECTS OF GENOTYPE AND SOCIAL-ENVIRONMENT ON ALCOHOL-CONSUMPTION IN FEMALE TWINS. Journal of Studies On Alcohol, 50 (1), 38-48. doi: 10.15288/jsa.1989.50.38

  • A GENETIC EPIDEMIOLOGIC-STUDY OF SELF-REPORT SUSPICIOUSNESS

    KENDLER, KS, HEATH, A and MARTIN, NG (1987). A GENETIC EPIDEMIOLOGIC-STUDY OF SELF-REPORT SUSPICIOUSNESS. Comprehensive Psychiatry, 28 (3), 187-196. doi: 10.1016/0010-440X(87)90026-5

  • PLASMA-LIPIDS IN TWINS - ENVIRONMENTAL AND GENETIC INFLUENCES

    WHITFIELD, JB and MARTIN, NG (1983). PLASMA-LIPIDS IN TWINS - ENVIRONMENTAL AND GENETIC INFLUENCES. Atherosclerosis, 48 (3), 265-277. doi: 10.1016/0021-9150(83)90044-8

  • BIAS IN THE ESTIMATION OF HERITABILITY FROM TRUNCATED SAMPLES OF TWINS

    MARTIN, NG and WILSON, (1982). BIAS IN THE ESTIMATION OF HERITABILITY FROM TRUNCATED SAMPLES OF TWINS. Behavior Genetics, 12 (4), 467-472. doi: 10.1007/BF01065638

  • GENETIC, ENVIRONMENTAL AND PERSONALITY-FACTORS INFLUENCING AGE OF 1ST SEXUAL INTERCOURSE IN TWINS

    MARTIN, NG, EAVES, LJ and EYSENCK, HJ (1977). GENETIC, ENVIRONMENTAL AND PERSONALITY-FACTORS INFLUENCING AGE OF 1ST SEXUAL INTERCOURSE IN TWINS. Journal of Biosocial Science, 9 (1), 91-97. doi: 10.1017/s0021932000000493

  • INHERITANCE OF SCHOLASTIC ABILITIES IN A SAMPLE OF TWINS .2. GENETIC-ANALYSIS OF EXAMINATION RESULTS

    MARTIN, NG (1975). INHERITANCE OF SCHOLASTIC ABILITIES IN A SAMPLE OF TWINS .2. GENETIC-ANALYSIS OF EXAMINATION RESULTS. Annals of Human Genetics, 39 (OCT), 219-229. doi: 10.1111/j.1469-1809.1975.tb00125.x

Conference Publication

  • Can polygenic Risk Scores Predict Who Will Receive or Respond Better to Electroconvulsive Therapy for Treatment of Major Depressive Disorder?

    Hopkins, Kristen L., Lind, Penelope A., Mitchell, Brittany L., Whiteman, David C., Olsen, Catherine M., Siskind, Dan J., Hickie, Ian B., Martin, Nicholas G. and Medland, Sarah E. (2022). Can polygenic Risk Scores Predict Who Will Receive or Respond Better to Electroconvulsive Therapy for Treatment of Major Depressive Disorder?. 51st Annual Meeting of the Behavior-Genetics-Association (BGA), Los Angeles Ca, Jun 22-25, 2022. NEW YORK: SPRINGER.

  • Challenges to Incorporating Polygenic Risk Scores in Clinical Mental Health Practice

    Medland, Sarah E., Mitchell, Brittany, Campos, Adrian, Whiteman, David C., Olsen, Catherine M., Siskind, Dan J., Hickie, Ian, Lind, Penelope A. and Martin, Nicholas G. (2022). Challenges to Incorporating Polygenic Risk Scores in Clinical Mental Health Practice. 51st Annual Meeting of the Behavior-Genetics-Association (BGA), Los Angeles Ca, Jun 22-25, 2022. NEW YORK: SPRINGER.

  • Genomics Driven Screening for Causal Determinants of Suicide Attempt

    Campos, Adrian I., Garcia-Marin, Luis M., Christensen, Helen, Batterham, Philip J., van Velzen, Laura S., Schmaal, Lianne, Rabinowitz, Jill A., Jahanshad, Neda, Martin, Nicholas G., Cuellar-Partida, Gabriel, Ruderfer, Douglas M., Mullins, Niamh and Renteria, Miguel E. (2022). Genomics Driven Screening for Causal Determinants of Suicide Attempt. SOBP 77th Annual Scientific Meeting, New Orleans, LA United States, 28-30 April 2022. Philadelphia, PA United States: Elsevier.

  • The use of online testing to assess cognitive differences in healthy individuals at high genetic risk of Alzheimer's disease

    Lupton, Michelle K., McAloney, Kerrie, Ceslis, Amelia, Robinson, Gail, Thienel, Renate, Breakspear, Michael and Martin, Nicholas G. (2021). The use of online testing to assess cognitive differences in healthy individuals at high genetic risk of Alzheimer's disease. 2021 Alzheimer's Association International Conference, Denver, CO United States, 26 - 30 July 2021. Hoboken, NJ United States: John Wiley & Sons. doi: 10.1002/alz.055369

  • Symptom-level genetic modelling identifies novel risk loci and unravels the shared genetic architecture of anxiety and depression

    Thorp, Jackson G., Campos, Adrian I., Grotzinger, Andrew D., Gerring, Zachary, An, Jiyuan, Ong, Jue-Sheng, Wang, Wei, Shringarpure, Suyash, Byrne, Enda M., MacGregor, Stuart, Martin, Nicholas G., Medland, Sarah E., Middeldorp, Christel M. and Derks, Eske M. (2020). Symptom-level genetic modelling identifies novel risk loci and unravels the shared genetic architecture of anxiety and depression. 50th Annual Meeting of the Behavior-Genetics-Association (BGA), Electr Network, Jun 26, 2020. NEW YORK: SPRINGER.

  • The relationship between comorbid chronic pain and poorer self-reported antidepressant efficacy is partly mediated by genetics

    Campos, Adrián I., Roughan, William H., García-Marin, Luis M., Cuéllar-Partida, Gabriel, Lupton, Michelle K., Hickie, Ian B., Medland, Sarah E., Wray, Naomi R., Byrne, Enda M., Ngo, Trung T., Martin, Nicholas G. and Rentería, Miguel E. (2020). The relationship between comorbid chronic pain and poorer self-reported antidepressant efficacy is partly mediated by genetics. Virtual 2020 World Congress of Psychiatric Genetics (WCPG), Online, 16–22 October 2020.

  • Anorexia nervosa genome-wide association study identifies eight loci and implicates psychiatric and metabolic origins

    Hubel, C., Watson, H. J., Yilmaz, Z., Landen, M., Martin, N. G., Mortensen, P., Sullivan, P. F., Breen, G. and Bulik, C. M. (2019). Anorexia nervosa genome-wide association study identifies eight loci and implicates psychiatric and metabolic origins. 52nd Conference of the European-Society-of-Human-Genetics (ESHG), Gothenburg Sweden, Jun 15-18, 2019. LONDON: NATURE PUBLISHING GROUP.

  • Replication and discovery of genetic variants influencing human bitter taste perception

    Hwang, Liang-Dar, Gharahkhani, Puya, Zhu, Gu, Gordon, Scott D., Breslin, Paul A. S., Martin, Nicholas G., Reed, Danielle R. and Wright, Margaret J. (2018). Replication and discovery of genetic variants influencing human bitter taste perception. 39th Annual Meeting of the Association for Chemoreception Sciences, Bonita Springs, FL, United States, 26 - 29 April 2017. Oxford, United Kingdom: Oxford University Press. doi: 10.1093/chemse/bjy003

  • A perceptual endophenotype for mental illness: Characterising normal genetic variation in the trait

    Cuéllar-Partida, Gabriel, Ngo, Trung T., Couvy-Duchesne, Baptiste, Rentería, Miguel E., Colodro Conde, Lucia, Gordon, Scott D., Hansell, Narelle K., Medland, Sarah E., Wright, Margaret J. and Martin, Nicholas G. (2017). A perceptual endophenotype for mental illness: Characterising normal genetic variation in the trait. BLiSS 2017 — Brisbane Life Science ECR Symposium, Translational Research Institute, Brisbane, 24 November 2017.

  • GWAS of complementary perceptual endophenotype measures: How do they rate?

    Ngo, Trung T., Cuéllar-Partida, Gabriel, Couvy-Duchesne, Baptiste, Rentería, Miguel E., Colodro Conde, Lucia, Gordon, Scott D., Hansell, Narelle K., Medland, Sarah E., Wright, Margaret J. and Martin, Nicholas G. (2017). GWAS of complementary perceptual endophenotype measures: How do they rate?. Australasian Society for Bipolar & Depressive Disorders (ASBDD) 2017 Conference, Deakin Edge, Melbourne, 15–17 September 2017.

  • Mapping age effects along fiber tracts in young adults

    Dennis, Emily L., Rashid, Faisal, Faskowitz, Josh, Jin, Yan, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Hickie, Ian B., Wright, Margaret J., Jahanshad, Neda and Thompson, Paul M. (2017). Mapping age effects along fiber tracts in young adults. 2017 IEEE 14th International Symposium on Biomedical Imaging (ISBI 2017),, Melbourne, VIC, Australia, 18-21 April 2017. NEW YORK: IEEE. doi: 10.1109/ISBI.2017.7950478

  • Genetic analysis of cortical sulci in 1,009 adults

    Pizzagalli, Fabrizio, Auzias, Guillaume, Kochunov, Peter, Faskowitz, Joshua I., McMahon, Katie L., De Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J., Jahanshad, Neda and Thompson, Paul M. (2016). Genetic analysis of cortical sulci in 1,009 adults. 2016 IEEE 13th International Symposium on Biomedical Imaging: From Nano to Macro, ISBI 2016, Prague, Czech Republic, 13-16 April 2016. Piscataway, NJ, United States: Institute of Electrical and Electronics Engineers. doi: 10.1109/ISBI.2016.7493395

  • Genetic Modeling of Human Intensity Ratings of Four Sweeteners

    Hwang, Liang-Dar, Zhu, Gu, Wright, Margaret J., Martin, Nicholas G., Reed, Danielle R. and Breslin, Paul A. S. (2015). Genetic Modeling of Human Intensity Ratings of Four Sweeteners. 15th Scientific Meeting of the Australasian Association for ChemoSensory Science (AACSS), Brisbane, QLD Australia, 03-05 December 2014. Oxford, United Kingdom: Oxford University Press. doi: 10.1093/chemse/bjv008

  • Genetic analysis of structural brain connectivity using DICCCOL models of diffusion MRI in 522 twins

    Zhu, Dajiang, Zhan, Liang, Faskowitz, Joshua, Daianu, Madelaine, Jahanshad, Neda, De Zubicaray, Greig I., McMahon, Katie L., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2015). Genetic analysis of structural brain connectivity using DICCCOL models of diffusion MRI in 522 twins. IEEE 12th International Symposium on Biomedical Imaging, New York, United States, Apr 16-19, 2015. Piscataway, NJ, United States: IEEE. doi: 10.1109/ISBI.2015.7164080

  • Heritability analysis of surface-based cortical thickness estimation on a large twin cohort

    Shen, Kaikai, Dore, Vincent, Rose, Stephen, Fripp, Jurgen, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Thompson, Paul M., Wright, Margaret J. and Salvado, Olivier (2015). Heritability analysis of surface-based cortical thickness estimation on a large twin cohort. Medical Imaging 2015: Image Processing, Orlando, Florida, United States, Feb 24-26, 2015. Bellingham, WA United States: SPIE. doi: 10.1117/12.2081677

  • Heritability of brain network topology in 853 twins and siblings

    Zhan, L., Jahanshad, N., Faskowitz, J., Zhu, D., Prasad, G., Martin, N. G., de Zubicaray, G. I., McMahon, K. L., Wright, M. J. and Thompson, P. M. (2015). Heritability of brain network topology in 853 twins and siblings. IEEE 12th International Symposium on Biomedical Imaging, New York, United States, Apr 16-19, 2015. Piscataway, NJ, United States: IEEE. doi: 10.1109/ISBI.2015.7163908

  • Combining meta- and mega- analytic approaches for multi-site diffusion imaging based genetic studies: From the ENIGMA-DTI working group

    Jahanshad, Neda, Kochunov, Peter, Nichols, Thomas E., Sprooten, Emma, Mandl, Rene C., Almasy, Laura, Brouwer, Rachel M., Curran, Joanne E., de Zubicaray, Greig I., Dimitrova, Rali, Fox, Peter T., Hong, L. Elliot, Landman, Bennett A., Lemaitre, Herve, Lopez, Lorna, Martin, Nicholas G., McMahon, Katie L., Mitchell, Braxton D., Olvera, Rene L., Peterson, Charles P., Sussmann, Jessika E., Toga, Arthur W., Wardlaw, Joanna M., Wright, Margaret J., Wright, Susan N., Bastin, Mark E., McIntosh, Andrew M., Boomsma, Dorret I., Kahn, Rene S. ... Thompson, Paul M. (2014). Combining meta- and mega- analytic approaches for multi-site diffusion imaging based genetic studies: From the ENIGMA-DTI working group. 11th IEEE International Symposium on Biomedical Imaging (ISBI), Beijing, Peoples Republic of China, 29 April-02 May 2014. Piscataway, NJ., United States: IEEE. doi: 10.1109/ISBI.2014.6868099

  • Identifying candidate gene effects by restricting search space in a multivariate genetic analysis of white matter microstructure

    Warstadt, Nicholus M., Jahanshad, Neda, Dennis, Emily L., Kohannim, Omid, McMahon, Katie L., de Zubicaray, Greig I., Montgomery, Grant W., Henders, Anjali K., Martin, Nicholas G., Whitfield, John B., Wright, Margaret J. and Thompson, Paul M. (2014). Identifying candidate gene effects by restricting search space in a multivariate genetic analysis of white matter microstructure. Biomedical Imaging ISBI, Beijing, China, 29 April - 2 May, 2014. Piscataway, NJ, United States: IEEE. doi: 10.1109/ISBI.2014.6867881

  • Estimating the sex-specific effects of genes on facial attractiveness and sexual dimorphism

    Mitchem, Dorian, Purkey, Alicia, Grebe, Nicholas, Carey, Greg, Garver-Apgar, Christine, Bates, Timothy, Arden, Rosalind, Hewitt, John, Medland, Sarah, Martin, Nick G., Zietsch, Brendan and Keller, Matthew (2013). Estimating the sex-specific effects of genes on facial attractiveness and sexual dimorphism. 43rd Annual Meeting of the Behavior-Genetics-Association, Marseille France, Jun 28-Jul 02, 2013. NEW YORK: SPRINGER.

  • Bivariate genome-wide association study of genetically correlated neuroimaging phenotypes from DTI and MRI through a seemingly unrelated regression model

    Jahanshad, Neda, Bhatt, Priya, Hibar, Derrek P., Villalon, Julio E., Nir, Talia M., Toga, Arthur W., Jack Jr., Clifford R., Bernstein, Matt A. B, Weiner, Michael W., McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2013). Bivariate genome-wide association study of genetically correlated neuroimaging phenotypes from DTI and MRI through a seemingly unrelated regression model. 3rd International Workshop on Multimodal Brain Image Analysis, MBIA 2013, Held in Conjunction with the 16th International Conference on Medical Image Computing and Computer Assisted Intervention, MICCAI 2013, Nagoya, Japan, 22 September 2013. Heidelberg, Germany: Springer. doi: 10.1007/978-3-319-02126-3_19

  • Brain network efficiency and topology depend on the fiber tracking method: 11 tractography algorithms compared in 536 subjects

    Zhan, Liang, Jahanshad, Neda, Jin, Yan, Toga, Arthur W., McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2013). Brain network efficiency and topology depend on the fiber tracking method: 11 tractography algorithms compared in 536 subjects. 2013 IEEE 10th International Symposium on Biomedical Imaging: From Nano to Macro, ISBI 2013, San Francisco, CA, United States, 7-11 April 2013. Piscataway, NJ, United States: IEEE. doi: 10.1109/ISBI.2013.6556679

  • Clarification of varying genetic expression and structure within adolescent monozygotic and dizygotic twins discordant for high and low attention and activity

    Ebejer, Jane, Medland, Sarah, Martin, Nick G., Wright, Margaret, Montgomery, Grant, Powell, Joseph, Visscher, Peter and Duffy, David (2013). Clarification of varying genetic expression and structure within adolescent monozygotic and dizygotic twins discordant for high and low attention and activity. 43rd Annual Meeting of the Behavior-Genetics-Association, Marseille France, 28 June-02 July 2013. New York, NY United States: Springer New York LLC. doi: 10.1007/s10519-013-9623-9

  • Exhaustive search of the SNP-SNP interactome identifies epistatic effects on brain volume in two cohorts

    Hibar, Derrek P., Stein, Jason L., Jahanshad, Neda, Kohannim, Omid, Toga, Arthur W., McMahon, Katie L., de Zubicaray, Greig I., Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J., Weiner, Michael W. and Thompson, Paul M. (2013). Exhaustive search of the SNP-SNP interactome identifies epistatic effects on brain volume in two cohorts. 16th International Conference on Medical Image Computing and Computer Assisted Intervention, MICCAI 2013, Nagoya, Japan, 22-26 September 2013. Berlin, Germany: Springer. doi: 10.1007/978-3-642-40760-4_75

  • Genetic clustering on the hippocampal surface for genome-wide association studies

    Hibar, Derrek P., Medland, Sarah E., Stein, Jason L., Kim, Sungeun, Shen, Li, Saykin, Andrew J., de Zubicaray, Greig I., McMahon, Katie L, Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J., Djurovic, Srdjan, Agartz, Ingrid A., Andreassen, Ole A. and Thompson, Paul M. (2013). Genetic clustering on the hippocampal surface for genome-wide association studies. 16th International Conference on Medical Image Computing and Computer Assisted Intervention, MICCAI 2013, Nagoya, Japan, 22-26 September 2013. Berlin, Germany: Springer. doi: 10.1007/978-3-642-40763-5_85

  • Labeling white matter tracts in hardi by fusing multiple tract atlases with applications to genetics

    Jin, Yan, Shi, Yonggang, Zhan, Liang, de Zubicaray, Greig I., McMahon, Katie L., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2013). Labeling white matter tracts in hardi by fusing multiple tract atlases with applications to genetics. 2013 IEEE 10th International Symposium on Biomedical Imaging: From Nano to Macro, ISBI 2013, San Francisco, CA, United States, 7-11 April 2013. Piscataway, NJ, United States: IEEE. doi: 10.1109/ISBI.2013.6556524

  • Power estimates for voxel-based genetic association studies using diffusion imaging

    Jahanshad, Neda, Kochunov, Peter, Glahn, David C., Blangero, John, Nichols, Thomas E., McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J., Jack, Jr., Clifford R., Bernstein, Matt A., Weiner, Michael W., Toga, Arthur W. and Thompson, Paul M. (2013). Power estimates for voxel-based genetic association studies using diffusion imaging. MMBC 2013: Mathematical Methods for Brain Connectivity. Held in conjunction with MICCAI 2013: The 16th International Conference on Medical Image Computing and Computer Assisted Intervention Workshops, Nagoya, Japan, 22 September, 2013. Cham, Switzerland: Springer International Publishing. doi: 10.1007/978-3-319-02475-2_21

  • Automatic population HARDI white matter tract clustering by label fusion of multiple tract atlases

    Jin, Yan, Shi, Yonggang, Zhan, Liang, Li, Junning, de Zubicaray, Greig I., McMahon, Katie L., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2012). Automatic population HARDI white matter tract clustering by label fusion of multiple tract atlases. Second International Multimodal Brain Image Analysis Workshop (MBIA 2012) in Conjunction with MICCAI 2012, Nice, France, 1 - 5 October 2012. Heidelberg, Germany: Springer. doi: 10.1007/978-3-642-33530-3_12

  • Changes in Anatomical Brain Connectivity Between Ages 12 and 30: A HARDI Study of 484 Adolescents and Adults

    Dennis, Emily L., Jahanshad, Neda, Toga, Arthur W., Johnson, Kori, McMahon, Katie L., de Zubicaray, Greig I., Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2012). Changes in Anatomical Brain Connectivity Between Ages 12 and 30: A HARDI Study of 484 Adolescents and Adults. 9th IEEE International Symposium on Biomedical Imaging, Barcelona, Spain, 2-5 May 2012. Piscataway NJ, United States: IEEE. doi: 10.1109/ISBI.2012.6235695

  • Diffusion imaging protocol effects on genetic associations

    Jahanshad, Neda, Kohannim, Omid, Toga, Arthur W., McMahon, Katie L., de Zubicaray, Greig I., Hansell, Narelle K., Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2012). Diffusion imaging protocol effects on genetic associations. International Symposium on Biomedical Imaging, Barcelona, Spain, 2-5 May 2012. NEW YORK: IEEE. doi: 10.1109/ISBI.2012.6235712

  • Discovery of genes that affect human brain connectivity: a genome-wide analysis of the connectome

    Jahanshad, Neda, Hibar, Derrek, Ryles, April, Toga, Arthur W., McMahon, Katie L., de Zubicaray, Greig I., Hansel, Narelle K., Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2012). Discovery of genes that affect human brain connectivity: a genome-wide analysis of the connectome. 9th International Symposium on Biomedical Imaging, Barcelona, Spain, 2-5 May 2012. Piscataway, NJ, United States: IEEE (Institute for Electrical and Electronic Engineers). doi: 10.1109/ISBI.2012.6235605

  • Genetic contribution to individual variation in binocular rivalry, an endophenotype for bipolar disorder

    Miller, S. M., Hansell, N. K., Ngo, T. T., Liu, G. B., Pettigrew, J. D., Wright, M. J. and Martin, N. G. (2012). Genetic contribution to individual variation in binocular rivalry, an endophenotype for bipolar disorder. 5th Biennial Conference of the International-Society-for-Bipolar-Disorders, Istanbul, Turkey, 14-17 March 2012. Malden, MA, United States: Wiley-Blackwell. doi: 10.1111/j.1399-5618.2012.00981.x

  • Genetic influences on sulcal patterns of the brain

    Joshi, S. H., Joshi, A. A., Gutman, B., Toga, A. W., McMahon, K., de Zubicaray, G., Martin, N., Wright, M. and Thompson, P. M. (2012). Genetic influences on sulcal patterns of the brain. 9th International Symposium on Biomedical Imaging, Barcelona, Spain, 2 - 5 May 2012. Piscataway, NJ, United States: IEEE (Institute for Electrical and Electronic Engineers). doi: 10.1109/ISBI.2012.6235572

  • Left versus right hemisphere differences in brain connectivity: 4-Tesla HARDI tractography in 569 twins

    Daianu, Madelaine, Jahanshad, Neda, Dennis, Emily L., Toga, Arthur W., McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J., Hickie, Ian B. and Thompson, Paul M. (2012). Left versus right hemisphere differences in brain connectivity: 4-Tesla HARDI tractography in 569 twins. 9th IEEE International Symposium on Biomedical Imaging (ISBI) - From Nano to Macro, Barcelona Spain, 2 - 5 May 2012. Piscataway, NJ, United States: IEEE (Institute for Electrical and Electronic Engineers). doi: 10.1109/ISBI.2012.6235601

  • Robust identification of partial-correlation based networks with applications to cortical thickness data

    Wheland, D., Joshi, A., McMahon, K., Hansell, N., Martin, N., Wright, M., Thompson, P., Shattuck, D. and Leahy, R. (2012). Robust identification of partial-correlation based networks with applications to cortical thickness data. 9th IEEE International Symposium on Biomedical Imaging: From Nano to Macro, ISBI 2012, Barcelona, Spain, 2 - 5 May 2012. Piscataway, NJ United States: I E E E. doi: 10.1109/ISBI.2012.6235869

  • Test-retest reliability of graph theory measures of structural brain connectivity

    Dennis, Emily L., Jahanshad, Neda, Toga, Arthur W., McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2012). Test-retest reliability of graph theory measures of structural brain connectivity. 15th International Conference on Medical Image Computing and Computer Assisted Intervention (MICCAI 2012), Nice, France, 1-5 October 2012. Springer: Heidelberg, Germany. doi: 10.1007/978-3-642-33454-2_38

  • Brain segmentation using deformable organisms and error learning

    Prasad, Gautam, Joshi, Anand A., Feng, Albert, Barysheva, Marina, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J., Toga, Arthur W., Terzopoulos, Demetri and Thompson, Paul M. (2011). Brain segmentation using deformable organisms and error learning. 3rd MICCAI Workshop on Mathematical Foundations of Computational Anatomy (MFCA 2011), Toronto, Canada, 22 September 2011. Toronto, Canada: MFCA.

  • Heritability of white matter fiber tract shapes: A HARDI study of 198 twins

    Jin, Yan, Shi, Yonggang, Joshi, Shantanu, Jahanshad, Neda, Zhan, Lian, de Zubicaray, Greig I., McMahon, Katie L., Martin, Nicholas G., Wright, Margaret J., Toga, Arthur W. and Thompson, Paul M. (2011). Heritability of white matter fiber tract shapes: A HARDI study of 198 twins. Multimodal Brain Image Analysis: First International Workshop, MBIA 2011. Held in Conjunction with MICCAI 2011, Toronto, Canada, 18-22 September 2011. Heidelberg, Germany: Springer. doi: 10.1007/978-3-642-24446-9_5

  • Hierarchical clustering of the genetic connectivity matrix reveals the network topology of gene action on brain microstructure: An N=531 twin study

    Chiang, Ming-Chang, Barysheva, Marina, McMahon, Katie L., de Zubicaray, Greig I., Johnson, Kori, Martin, Nicholas G., Toga, Arthur W., Wright, Margaret J. and Thompson, Paul M. (2011). Hierarchical clustering of the genetic connectivity matrix reveals the network topology of gene action on brain microstructure: An N=531 twin study. 2011 IEEE 8th International Symposium on Biomedical Imaging (ISBI 2011), Chicago, United States, 30 March - 2 April 2011. Piscataway, NJ, United States: IEEE. doi: 10.1109/ISBI.2011.5872533

  • Opportunity and Educational Outcomes in Australia

    Le, Anh T., Miller, Paul W., Slutske, Wendy S. and Martin, Nicholas G. (2011). Opportunity and Educational Outcomes in Australia. 39th Australian Conference of Economists, Sydney Australia, 27-29 September 2010. Richmond, VIC., Australia: Wiley-Blackwell Publishing. doi: 10.1111/j.1475-4932.2011.00749.x

  • Sex differences in the human connectome: 4-Tesla High Angular Resolution Diffusion Imaging (HARDI) tractography in 234 young adult twins

    Jahanshad, Neda, Aganj, Iman, Lenglet, Christophe, Joshi, Anand, Jin, Yan, Barysheva, Marina, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright Margaret J., Toga, Arthur W., Sapiro, Guillermo and Thompson, Paul M. (2011). Sex differences in the human connectome: 4-Tesla High Angular Resolution Diffusion Imaging (HARDI) tractography in 234 young adult twins. 2011 IEEE 8th International Symposium on Biomedical Imaging (ISBI 2011), Chicago, United States, 30 March - 2 April 2011. Piscataway, NJ, United States: IEEE. doi: 10.1109/ISBI.2011.5872558

  • White matter tract analysis in 454 adults using maximum density paths

    Prasad, Gautam, Joshi, Shantanu H,, Jahanshad, Neda, Villalon, Julio, Aganj, Iman, Lenglet, Christophe, Sapiro, Guillermo, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J., Toga, Arthur W and Thompson, Paul M. (2011). White matter tract analysis in 454 adults using maximum density paths. CDMRI'11 - Workshop on Computational Diffusion MRI, Toronto, Canada, 22 September 2011.

  • Genome Wide Analysis Identifies Putative Loci Associated With Interpupillary Distance

    Staffieri, S. E., Ruddle, J. B., Hewitt, A. W., Kearns, L. S., Sanfilippo, P. G., MacGregor, S., Martin, N. G., Young, T. L., Hammond, C. J. and Mackey, D. A. (2010). Genome Wide Analysis Identifies Putative Loci Associated With Interpupillary Distance. ROCKVILLE: ASSOC RESEARCH VISION OPHTHALMOLOGY INC.

  • Up to What Age is a Cyclopleged Refraction Required? Results From the Twins Eye Study Tasmania(TEST)

    Kearns, L. S., Hewitt, A. W., Ruddle, J. B., Bigault, O., Staffieri, S. E., Sanfillipo, P., Martin, N. G., Hammond, C. J., Young, T. L. and Mackey, D. A. (2010). Up to What Age is a Cyclopleged Refraction Required? Results From the Twins Eye Study Tasmania(TEST). ROCKVILLE: ASSOC RESEARCH VISION OPHTHALMOLOGY INC.

  • A study of genetic influence on SPHERE (somatic and psychological health report) measures collected in adolescents and young adults

    Hansell, Narelle K., Hickie, Ian B., Davenport, Tracey A., Hadzi-Pavlovic, Dusan, Wray, Naomi R., Martin, Nicholas G. and Wright, Margaret J. (2010). A study of genetic influence on SPHERE (somatic and psychological health report) measures collected in adolescents and young adults. 40th Annual Meeting of Behavior Genetics Association, Pennsylvania, PA, U.S.A., May 2009. New York, NY, U.S.A.: Springer New York LLC. doi: 10.1007/s10519-010-9392-7

  • Ability and heritability: Investigating the continuous effect of IQ score on IQ etiology in multiple samples

    Brant, Angela M., Boomsma, Dorret I., Corley, Robin P., DeFries, John C., Haworth, Clare M. A., Hewitt, John K., Martin, Nicholas G., McGue, Matthew, Petrill, Stephen A., Plomin, Robert, Wadsworth, Sally J. and Wright, Margaret J. (2010). Ability and heritability: Investigating the continuous effect of IQ score on IQ etiology in multiple samples. The 40th Annual Behavior Genetic Association Meeting, Seoul, Korea, 2- 5 June 2010. New York, NY, U.S.A.: Springer New York LLC. doi: 10.1007/s10519-010-9392-7

  • Common variants in the Trichohyalin gene are associated with straight hair in Europeans genetics and genodermatoses

    Medland, S. E., Nyholt, D. R., Painter, J. N., McEvoy, B. P., McRae, A. F., Montgomery, G. W. and Martin, N. G. (2010). Common variants in the Trichohyalin gene are associated with straight hair in Europeans genetics and genodermatoses. 6th World Congress for Hair Research, Cairns, QLD, Australia, 16-19 June 2010. Oxford, United Kingdom: Wiley-Blackwell. doi: 10.1111/j.1600-0625.2010.01097.x

  • Examining the relationship between sexual orientation and depression: overlapping genetic and early environmental influences

    Verweij, Kjh, Zietsch, BP, Lynskey, MT, Heath, AC and Martin, NG (2010). Examining the relationship between sexual orientation and depression: overlapping genetic and early environmental influences. 40th Annual Meeting of Behavior-Genetics-Association, Pennsylvania PA, MAY, 2009.

  • Genes for a component of the language acquisition mechanism: ROBO1 polymorphisms associated with phonological buffer deficits

    Bates, Timothy C., Luciano, Michelle, Montgomery, Grant W., Wright, Margaret J. and Martin, Nicholas G. (2010). Genes for a component of the language acquisition mechanism: ROBO1 polymorphisms associated with phonological buffer deficits. Behavior Genetics Association 40th Annual Meeting, Seoul, Korea, 2-5 June 2010. New York, U.S.A.: Springer New York LLC. doi: 10.1007/s10519-010-9392-7

  • Genetic analysis of high angular resolution diffusion images (HARDI)

    Zhan, Liang, Leow, Alex D., Jahanshad, Neda, Lee, Agatha D., Barysheva, Marina, Toga, Arthur W., McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2010). Genetic analysis of high angular resolution diffusion images (HARDI). MICCAI 2010 Workshop on Computational Diffusion MRI, Beijiing, China, 20-24 September 2010. Berlin, Germany: Springer.

  • Genetic influences on optimism and its relationship to health

    Mosing, MA, Wright, MJ, Pedersen, Nancy L. and Martin, NG (2010). Genetic influences on optimism and its relationship to health. 40th Annual Meeting of Behavior-Genetics-Association, Pennsylvania PA, MAY, 2009.

  • Genomewide association study of quantitative alcohol phenotypes in community-ascertained families

    Martin, N., Madden, P., Pergadia, M., Nelson, E., Bucholz, K., Whitfield, J.B., Montgomery, G. and Heath, G. (2010). Genomewide association study of quantitative alcohol phenotypes in community-ascertained families. 2010 World Congress on International Society for Biomedical Research on Alcoholism, Paris, France, 13-16 September 2010. Hoboken, NJ, U.S.A.: Wiley-Blackwell Publishing. doi: 10.1111/j.1530-0277.2010.01292_3.x

  • Heritability of FMRI response in young adult twins

    Blokland, G, McMahon, K, Thompson, P, Martin, N, de Zubicaray, G and Wright, MJ (2010). Heritability of FMRI response in young adult twins. 40th Annual Meeting of Behavior-Genetics-Association, Pennsylvania PA, MAY, 2009. NEW YORK: SPRINGER.

  • Multivariate group-wise genetic analysis of white matter integrity using orientation distribution functions

    Lepore, Natasha, Brun, Caroline, Descoteaux, Maxime, Lee, Agatha D., Barysheva, Marina, Chou, Yi-Yu, de Zubicaray, Greig, McMahon, Katie, Wright, Margaret J., Martin, Nicholas G., Gee, James C. and Thompson, Paul M. (2010). Multivariate group-wise genetic analysis of white matter integrity using orientation distribution functions. MICCAI Workshop on Computational Diffusion MRI, Beijiing, China, 20-24 September 2010.

  • Multivariate variance-components analysis in DTI

    Lee, Agatha D., Leporé, Natasha, de Leeuw, Jan, Brun, Caroline C., Barysheva, Marina, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2010). Multivariate variance-components analysis in DTI. 2010 7th IEEE International Symposium on Biomedical Imaging: From Nano to Macro, Rotterdam, Netherlands, 14-17 April 2010. Piscataway, NJ, U.S.A.: I E E E. doi: 10.1109/ISBI.2010.5490199

  • Psychiatric vulnerability in nonheterosexuals

    Zietsch, B. P., Verweij, K. J. H., Bailey, J. M., Wright, M. J. and Martin, N. G. (2010). Psychiatric vulnerability in nonheterosexuals. The 40th Annual Behavior Genetics Association meeting, Seoul, Korea, 2-5 June 2010. New York, NY, U.S.A.: Springer New York. doi: 10.1007/s10519-010-9392-7

  • Relating fiber crossing in HARDI to intellectual function

    Aganj, Iman, Jahanshad, Neda, Lenglet, Christophe, Toga, Arthur W., McMahon, Katie L., de Zubicaray, Greig I., Wright, Margaret J., Martin, Nicholas G., Sapiro, Guillermo and Thompson, Paul M. (2010). Relating fiber crossing in HARDI to intellectual function. 16th annual meeting of the Organization for Human Brain Mapping, Barcelona, Spain, 6-10 June 2010.

  • Scalar connectivity measures from fast-marching tractography reveal heritability of white matter architecture

    Patel, V, Chiang, MC, Thompson, PM, McMahon, KL, de Zubicaray, GI, Martin, NG, Wright, MJ and Toga, AW (2010). Scalar connectivity measures from fast-marching tractography reveal heritability of white matter architecture. ISBI 2010 7th IEEE International Symposium on Biomedical Imaging: From Nano to Macro, Rotterdam, Netherlands, 14-17 April 2010. Piscataway, NJ, U.S.A.: Institute of Electrical and Electronic Engineers (IEEE). doi: 10.1109/ISBI.2010.5490187

  • Genetic and Environmental Influences on the Co-morbidity Between Depression, Panic Disorder, Agoraphobia, and Social Phobia: A Twin Study

    Mosing, Miriam A., Gordon, Scott D., Medland, Sarah E., Statham, Dixie J., Nelson, Elliot C., Heath, Andrew C., Martin, Nicholas G. and Wray, Naomi R. (2009). Genetic and Environmental Influences on the Co-morbidity Between Depression, Panic Disorder, Agoraphobia, and Social Phobia: A Twin Study. United States: John Wiley & Sons, Inc.. doi: 10.1002/da.20611

  • The cholinesterases: Analysis by pharmacogenomics in man

    Valle, A. M., Radic, Z., Rana, B. K., Whitfield, J. B., O'Connor, D. T., Martin, N. G. and Taylor, P. (2008). The cholinesterases: Analysis by pharmacogenomics in man. 9th International Meeting on Cholinesterases, Suzhou Peoples R China, May 06-10, 2007. CLARE: ELSEVIER IRELAND LTD. doi: 10.1016/j.cbi.2008.04.042

  • An imaging study of Australian twins: Quantifying genetic and environmental influences on fMRI and Hardi phenotypes

    Wright, Margaret, Blokland, Gabriella, Chiang, Ming- Chang, McMahon, Katy, Martin, Nicholas, Toga, Arthur, de Zubicaray, Greig and Thompson, Paul (2008). An imaging study of Australian twins: Quantifying genetic and environmental influences on fMRI and Hardi phenotypes. Forty-Eighth Annual Meeting of the Society for Psychophysiological Research, Austin, TX, U.S.A., 1 – 5 October 2008. Malden, MA, U.S.A.: Blackwell Publishing.

  • Genome-wide scan for loci influencing the P3: An endophenotype for psychopathology

    Wright, Margaret J., Luciano, Michelle, Hansell, Narelle K., Geffen, Gina M., Montgomery, Grant W. and Martin, Nicholas G. (2006). Genome-wide scan for loci influencing the P3: An endophenotype for psychopathology. World Congress on Alcohol Research (ISBRA 2006), Sydney, Australia, 10 - 13 September 2006. Oxford: Blackwell Publishing. doi: 10.1111/j.1530-0277.2006.00197.x

  • Risk of premature ovarian failure in twins

    Gosden, RG, Treloar, SA, Martin, NG, Cherkas, LF, Spector, TD and Silber, SJ (2005). Risk of premature ovarian failure in twins. Conjoint Annual Meeting of the American-Society-for-Reproductive-Medicine/Canadian-Fertility-and-Andrology-Society, Montreal Canada, Oct 15-19, 2005. NEW YORK: ELSEVIER SCIENCE INC. doi: 10.1016/j.fertnstert.2005.07.287

  • A genomic wide screen of the P3(00) ERP component: Preliminary findings

    Wright, M. J., Luciano, M., Hansell, N. K., Geffen, G. M. and Martin, N. G. (2004). A genomic wide screen of the P3(00) ERP component: Preliminary findings. Behavior Genetics Association 34th Annual Meeting , Aix en Provence, France, June 2004. New York, NY United States: Springer.

  • Linkage analyses of ERP slow wave measures of working memory

    Hansell, Narelle K., Wright, M. J., Geffen, G. M., Geffen, L. B. and Martin, N. G. (2004). Linkage analyses of ERP slow wave measures of working memory. 34th Annual Meeting of the Behavior Genetics Association, Provence, France, 27 - 30 June 2004. New York, NY, United States: Springer New York. doi: 10.1007/s10519-004-5590-5

  • Bladder neck mobility is a heritable trait

    Dietz, H. P., Hansell, N., Grace, M., Eldridge, A., Martin, N. and Clarke, B. (2003). Bladder neck mobility is a heritable trait. 28th Annual IUGA Meeting, Buenos Aires, Argentina, 28-31 October, 2003. Surrey, U.K.: Springer-Verlag London Ltd. doi: 10.1007/s00192-003-1108-6

  • ERP endophenotypes of cognitive ability: A genetic study

    Hansell, N. K., Wright, M. J., Geffen, G. M., Geffen, L. B. and Martin, N. G. (2003). ERP endophenotypes of cognitive ability: A genetic study. 3rd Victorian Postgraduates in Psychology Conference, RMIT University, Victoria, 23 Nov 2002. Melbourne, VIC, Australia: John Wiley & Sons.

  • Genetic association and cellular function of MC1R variant alleles in human pigmentation

    Sturm, R. A., Duffy, D. L., Box, N. F., Newton, R. A., Shepherd, A. G., Chen, W., Marks, L. H., Leonard, J. H. and Martin, N. G. (2003). Genetic association and cellular function of MC1R variant alleles in human pigmentation. Fifth International Melanocortin Meeting, Sunriver, Oregon, August 25-28, 2002. New York, U.S.: The Academy. doi: 10.1111/j.1749-6632.2003.tb03199.x

  • Genetic covariation among ERP and performance measures of a working memory delayed-response task, information processing, and psychometric IQ

    Hartsell, N., Wright, M. J., Geffen, G. M., Geffen, L. and Martin, N. (2002). Genetic covariation among ERP and performance measures of a working memory delayed-response task, information processing, and psychometric IQ. 42nd Annual Meeting of the Society of Psychophysiological Research, Washington, DC, U.S.A., October 2-6, 2002. Malden, MA: Blackwell Publishing.

  • Genetic influences on the relationship between EEG and intelligence

    Smit, C. M., Wright, M. J., Geffen, G. M., Geffen, L. B. and Martin, N. G. (2002). Genetic influences on the relationship between EEG and intelligence. 8th National Conference of the APS College of Clinical Neuropsychologists , Maroochydore, QLD Australia, 3–6 October 2002 . Oxford, United Kingdom: Wiley-Blackwell.

  • Stringent genetic programming of DNA methylation in humans

    Aung, H. T., Harrison, D. K., Findlay, I., Mattick, J. S., Martin, N. and Carroll, B. J. (2002). Stringent genetic programming of DNA methylation in humans. Australian Human Gene Mapping Meeting, Hobart, 4-6 December, 2002.

  • Approaching the genetics of intelligence through processing speed and working memory constructs

    Luciano, M., Smith, G., Wright, M. J., Geffen, G. M., Geffen, L. B. and Martin, N. G. (2001). Approaching the genetics of intelligence through processing speed and working memory constructs. The Third International Spearman Seminar, Sydney, Australia, 28-30 November 2001.

  • Heritability of measures from elementary cognitivce tasks and their relationship with IQ: A twin study

    Luciano, M., Smith, G., Wright, M. J., Geffen, G. M., Geffen, L. B. and Martin, N. G. (2001). Heritability of measures from elementary cognitivce tasks and their relationship with IQ: A twin study. It Runs in the Family: Twins and Families in Biomedical and Behavioural Research, Melbourne, Australia, 6-7 April 2001.

  • Inspection time, choice reaction time and IQ: Are they influenced by the same genes

    Luciano, M., Smith, G., Wright, M. J., Geffen, G. M., Geffen, L. B. and Martin, N. G. (2001). Inspection time, choice reaction time and IQ: Are they influenced by the same genes. 1st Australian Personality and Individual Differences Conferee, Wollongong, NSW, 15 February 2001.

  • Quantitative trait loci underlying variation in blood cell concentrations

    Evans, D. M., Zhu, G., Frazer, I. H. and Martin, N. G. (2001). Quantitative trait loci underlying variation in blood cell concentrations. It Runs in the Family: Twins and Families in Biome, Melbourne, Australia, 6-7 April, 2001. Cambridge, MA: Cell Press.

  • A twin study of psychometric intelligence and efficiency of information processing

    Smith, G. A., Luciano, M., Geffen, G. M., Geffen, L., Wright, M. J. and Martin, N. G. (2000). A twin study of psychometric intelligence and efficiency of information processing. 30th Annual Meeting of the Behavior Genetics Association, Burlington, Vermont, USA, June 29 - July 1, 2000. Westport, Conn.: Kluwer. doi: 10.1023/A:1017371222025

  • Psychophysiological phenotypes of cognition: The P3 and SW components

    Wright, M. J., Hansell, N., Geffen, G. M., Geffen, L., Smith, G. and Martin, N. (2000). Psychophysiological phenotypes of cognition: The P3 and SW components. 30th Annual Meeting of the Behavior Genetics Association, Burlington, Vermont, USA, June 29 - July 1, 2000. Westport, United States: Kluwer. doi: 10.1023/A:1017371222025

  • Genetic and social determinants of initiation and age at onset of smoking in Australian twins

    Heath, A., Kirk, K. M., Meyer, J. M. and Martin, N. G. (1999). Genetic and social determinants of initiation and age at onset of smoking in Australian twins. Westport, Conneticut: Greenwood Periodicals. doi: 10.1023/A:1021670703806

  • Is there an association between normal cognitive functioning and trinucleotide repeat expansion at loci involved in neurodegenerative disorders?

    Wright, M. J., Smith, G., Geffen, G. M., Geffen, L. and Martin, N. (1999). Is there an association between normal cognitive functioning and trinucleotide repeat expansion at loci involved in neurodegenerative disorders?. 29th Annual Meeting of the Behaviour Genetics Association, Vancouver, British Columbia, Canada, July 4-7, 1999. Westport, United States: Kluwer. doi: 10.1023/A:1021614018034

  • Common genetic risk factors for conduct disorder and alcohol dependence

    Slutske, WS, Heath, AC, Dinwiddie, SH, Madden, PAF, Bucholz, KK, Dunne, MP, Statham, DJ and Martin, NG (1998). Common genetic risk factors for conduct disorder and alcohol dependence. Meeting of the Society-for-Research-in-Psychopathology, Atlanta Georgia, Sep, 1996. WASHINGTON: AMER PSYCHOLOGICAL ASSOC. doi: 10.1037/0021-843X.107.3.363

  • Molecular biology of alcohol dependence, a complex polygenic disorder

    Whitfield, JB, Nightingale, BN, O'Brien, ME, Heath, AC, Birley, AJ and Martin, NG (1998). Molecular biology of alcohol dependence, a complex polygenic disorder. 1st IFCC Roche Conference on Recent Progress in Molecular biology Technology, Singapore Singapore, Mar 15-18, 1998. BERLIN: WALTER DE GRUYTER & CO. doi: 10.1515/CCLM.1998.111

  • Modeling genetic and environmental influences in the etiology of conduct disorder: A study of 2,682 adult twin pairs

    Slutske, WS, Heath, AC, Dinwiddie, SH, Madden, PAF, Bucholz, KK, Dunne, MP, Statham, DJ and Martin, NG (1997). Modeling genetic and environmental influences in the etiology of conduct disorder: A study of 2,682 adult twin pairs. World Congress on Psychiatric Genetics, Cardiff Wales, Aug-Sep -, 1995. WASHINGTON: AMER PSYCHOLOGICAL ASSOC. doi: 10.1037/0021-843X.106.2.266

  • GENETIC INFLUENCES ON ALCOHOL-CONSUMPTION PATTERNS AND PROBLEM DRINKING - RESULTS FROM THE AUSTRALIAN NH-AND-MRC TWIN PANEL FOLLOW-UP SURVEY

    HEATH, AC and MARTIN, NG (1994). GENETIC INFLUENCES ON ALCOHOL-CONSUMPTION PATTERNS AND PROBLEM DRINKING - RESULTS FROM THE AUSTRALIAN NH-AND-MRC TWIN PANEL FOLLOW-UP SURVEY. Conference on Genetic Susceptibility, Biological Markers of Vulnerability and Alcoholic Subtypes, Farmington Ct, Oct 22-23, 1992. NEW YORK: NEW YORK ACAD SCIENCES. doi: 10.1111/j.1749-6632.1994.tb24699.x

  • RISK-FACTORS FOR ATHEROSCLEROSIS IN TWINS

    DUFFY, DL, OCONNELL, DL, HELLER, RF and MARTIN, NG (1993). RISK-FACTORS FOR ATHEROSCLEROSIS IN TWINS. Genetic Analysis Workshop 8: Issues in the Analysis of Complex Diseases and Their Risk Factors ( GAW8 ), Watsonville Ca, Nov 08-10, 1992. NEW YORK: WILEY-LISS. doi: 10.1002/gepi.1370100638

  • IS THE GENETICS OF MOLINESS SIMPLY THE GENETICS OF SUN EXPOSURE - A PATH-ANALYSIS OF NEVUS COUNTS AND RISK-FACTORS IN BRITISH TWINS

    DUFFY, DL, MACDONALD, AM, EASTON, DF, PONDER, BAJ and MARTIN, NG (1992). IS THE GENETICS OF MOLINESS SIMPLY THE GENETICS OF SUN EXPOSURE - A PATH-ANALYSIS OF NEVUS COUNTS AND RISK-FACTORS IN BRITISH TWINS. 7Th Genetic Analysis Workshop : Issues in Gene Mapping and Detection of Major Genes ( Gaw 7 ), Dayton Oh, Oct 14-16, 1990. BASEL: KARGER. doi: 10.1159/000133243

Other Outputs

PhD and MPhil Supervision

Current Supervision

  • Genetic architecture of differences in symptomatology and treatment response in major depressive disorder

    Doctor Philosophy — Associate Advisor

    Other advisors:

  • Genetic architecture of complex respiratory and sleep-related human traits

    Doctor Philosophy — Associate Advisor

  • Statistical genetic approaches in eye disease

    Doctor Philosophy — Associate Advisor

Completed Supervision

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ORCID: 0000-0003-4069-8020

Scopus ID: 57216717619

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