The University of Queensland

COXPD9 an evolving multisystem disease; congenital lactic acidosis, sensorineural hearing loss, hypertrophic cardiomyopathy, cirrhosis and interstitial nephritis

Bursle, Carolyn, Narendra, Anna, Chuk, Raymond, Cardinal, John, Justo, Rob, Lewis, Bruce and Coman, David (2017). COXPD9 an evolving multisystem disease; congenital lactic acidosis, sensorineural hearing loss, hypertrophic cardiomyopathy, cirrhosis and interstitial nephritis. JIMD Reports. (pp. 105-109) edited by Eva Morava, Matthias Baumgartner, Marc Patterson, Shamima Rahman, Johannes Zschocke and Verena Peters. Berlin, Heidelberg: Springer. doi: 10.1007/8904_2016_13

DMP1-CDG (CDG1e) with significant gastrointestinal manifestations; phenotype and genotype expansion

Bursle, Carolyn, Brown, Dominique, Cardinal, John, Connor, Frances, Calvert, Sophie and Coman, David (2017). DMP1-CDG (CDG1e) with significant gastrointestinal manifestations; phenotype and genotype expansion. JIMD Reports. (pp. 27-32) Berlin, Germany: Springer. doi: 10.1007/8904_2016_7

Normal neurodevelopmental outcomes in PNPO deficiency: a case series and literature review

Hatch, J., Coman, D., Clayton, P., Mills, P., Calvert, S., Webster, R. I. and Riney, K. (2016). Normal neurodevelopmental outcomes in PNPO deficiency: a case series and literature review. JIMD Reports. (pp. 91-97) edited by Eva Morava, Matthias Baumgartner, Marc Patterson, Shamima Rahman, Johannes Zschocke and Verena Peters. Berlin, Germany: Springer. doi: 10.1007/8904_2015_482

Hepatic copper accumulation: a novel feature in transient infantile liver failure due to TRMU mutations?

Grover, Z., Lewindon, P., Clousten, A., Shaag, A., Elpeleg, O. and Coman, D. (2015). Hepatic copper accumulation: a novel feature in transient infantile liver failure due to TRMU mutations?. JIMD Reports, Volume 21. (pp. 109-113) edited by Johannes Zschocke, Matthias Baumgartner, Eva Morava, Marc Patterson, Shamima Rahman and Verena Peters. Berlin, Germany: Springer Berlin Heidelberg. doi: 10.1007/8904_2014_402

Impact of Impaired Maternal Vitamin A Status on Infant Eyes

Coman, David and Gole, Glen (2014). Impact of Impaired Maternal Vitamin A Status on Infant Eyes. Handbook of nutrition, diet and the eye. (pp. 377-382) edited by Victor R. Preedy. Burlington, MA United States: Elsevier Science. doi: 10.1016/B978-0-12-401717-7.00038-1

Differential phonological awareness skills in children with classic galactosemia: a descriptive study of four cases

Lewis, Fiona M., Coman, David J., Syrmis, Maryanne, Kilcoyne, Sarah and Murdoch, Bruce E. (2013). Differential phonological awareness skills in children with classic galactosemia: a descriptive study of four cases. JIMD reports: case and research reports. (pp. 45-52) edited by Johannes Zschocke, K. Michael Gibson, Garry Brown, Eva Morava and Verena Peters. Dordrecht, Netherlands: Springer. doi: 10.1007/8904_2012_200

Haploinsufficiency of ZFHX3, encoding a key player in neuronal development, causes syndromic intellectual disability

Pérez Baca, María del Rocío, Jacobs, Eva Z., Vantomme, Lies, Leblanc, Pontus, Bogaert, Elke, Dheedene, Annelies, De Cock, Laurenz, Haghshenas, Sadegheh, Foroutan, Aidin, Levy, Michael A., Kerkhof, Jennifer, McConkey, Haley, Chen, Chun-An, Batzir, Nurit Assia, Wang, Xia, Palomares, María, Carels, Marieke, Agrawal, Pankaj, Armstrong Scott, Daryl, Barkoudah, Elizabeth, Bellini, Melissa, Beneteau, Claire, Bjørgo, Kathrine, Brooks, Alice, Brown, Natasha, Castle, Alison, Castro, Diana, Chorin, Odelia, Cleghorn, Mark ... Callewaert, Bert (2024). Haploinsufficiency of ZFHX3, encoding a key player in neuronal development, causes syndromic intellectual disability. American Journal of Human Genetics, 111 (3), 509-528. doi: 10.1016/j.ajhg.2024.01.013

Brain function in classic galactosemia, a galactosemia network (GalNet) members review

Panis, Bianca, Vos, E. Naomi, Barić, Ivo, Bosch, Annet M., Brouwers, Martijn C. G. J., Burlina, Alberto, Cassiman, David, Coman, David J., Couce, María L., Das, Anibh M., Demirbas, Didem, Empain, Aurélie, Gautschi, Matthias, Grafakou, Olga, Grunewald, Stephanie, Kingma, Sandra D. K., Knerr, Ina, Leão-Teles, Elisa, Möslinger, Dorothea, Murphy, Elaine, Õunap, Katrin, Pané, Adriana, Paci, Sabrina, Parini, Rossella, Rivera, Isabel A., Scholl-Bürgi, Sabine, Schwartz, Ida V. D., Sdogou, Triantafyllia, Shakerdi, Loai A. ... Rubio-Gozalbo, M. Estela (2024). Brain function in classic galactosemia, a galactosemia network (GalNet) members review. Frontiers in Genetics, 15 1355962. doi: 10.3389/fgene.2024.1355962

Development of cancer surveillance guidelines in ataxia telangiectasia: A Delphi‐based consensus survey of international experts

Neves, Renata, De Dios Perez, Blanca, Panek, Rafal, Jagani, Sumit, Wilne, Sophie, Bhatt, Jayesh M., Caputi, Caterina, Cirillo, Emilia, Coman, David J., Dückers, Gregor, Gilbert, Donald L., Kay Koenig, Mary, Mansour, Lobna, McDermott, Elizabeth, Pauni, Micaela, Pignata, Claudio, Perlman, Susan L., Porras, Oscar, Betina Porto, Mariela, Schon, Katherine, Soler‐Palacin, Pere, Nick Russo, Sam, Takagi, Masatoshi, Tischkowitz, Marc, Wainwright, Claire, Dandapani, Madhumita, Glazebrook, Cristine, Suri, Mohnish, Whitehouse, William P. and Dineen, Robert A. (2023). Development of cancer surveillance guidelines in ataxia telangiectasia: A Delphi‐based consensus survey of international experts. Cancer Medicine, 12 (13), 14663-14673. doi: 10.1002/cam4.6075

Erratum: Genotypic and phenotypic spectrum of infantile liver failure due to pathogenic TRMU variants (Genetics in Medicine (2023) 25(6), (S1098360022009534), (10.1016/j.gim.2022.09.015))

Vogel, Georg F., Mozer-Glassberg, Yael, Landau, Yuval E., Schlieben, Lea D., Prokisch, Holger, Feichtinger, René G., Mayr, Johannes A., Brennenstuhl, Heiko, Schröter, Julian, Pechlaner, Agnes, Alkuraya, Fowzan S., Baker, Joshua J., Barcia, Giulia, Baric, Ivo, Braverman, Nancy, Burnyte, Birute, Christodoulou, John, Ciara, Elzbieta, Coman, David, Das, Anibh M., Darin, Niklas, Della Marina, Adela, Distelmaier, Felix, Eklund, Erik A., Ersoy, Melike, Fang, Weiyan, Gaignard, Pauline, Ganetzky, Rebecca D., Gonzales, Emmanuel ... Wortmannd, Saskia (2023). Erratum: Genotypic and phenotypic spectrum of infantile liver failure due to pathogenic TRMU variants (Genetics in Medicine (2023) 25(6), (S1098360022009534), (10.1016/j.gim.2022.09.015)). Genetics in Medicine, 25 (6) 100828, 100828. doi: 10.1016/j.gim.2023.100828

Genotypic and phenotypic spectrum of infantile liver failure due to pathogenic TRMU variants

Vogel, Georg F., Mozer-Glassberg, Yael, Landau, Yuval E., Schlieben, Lea D., Prokisch, Holger, Feichtinger, René G., Mayr, Johannes A., Brennenstuhl, Heiko, Schröter, Julian, Pechlaner, Agnes, Alkuraya, Fowzan S., Baker, Joshua J., Barcia, Giulia, Baric, Ivo, Braverman, Nancy, Burnyte, Birute, Christodoulou, John, Ciara, Elzbieta, Coman, David, Das, Anibh M., Darin, Niklas, Della Marina, Adela, Distelmaier, Felix, Eklund, Erik A., Ersoy, Melike, Fang, Weiyan, Gaignard, Pauline, Ganetzky, Rebecca D., Gonzales, Emmanuel ... Wortmann, Saskia (2023). Genotypic and phenotypic spectrum of infantile liver failure due to pathogenic TRMU variants. Genetics in Medicine, 25 (6) 100314, 1-16. doi: 10.1016/j.gim.2022.09.015

DNA methylation episignatures are sensitive and specific biomarkers for detection of patients with KAT6A/KAT6B variants

Vos, Niels, Reilly, Jack, Elting, Mariet W., Campeau, Philippe M., Coman, David, Stark, Zornitza, Tan, Tiong Yang, Amor, David J., Kaur, Simran, StJohn, Miya, Morgan, Angela T., Kamien, Benjamin A., Patel, Chirag, Tedder, Matthew L., Merla, Giuseppe, Prontera, Paolo, Castori, Marco, Muru, Kai, Collins, Felicity, Christodoulou, John, Smith, Janine, Zeev, Bruria Ben, Murgia, Alessandra, Leonardi, Emanuela, Esber, Natacha, Martinez-Monseny, Antonio, Casas-Alba, Didac, Wallis, Matthew, Mannens, Marcel ... Sadikovic, Bekim (2023). DNA methylation episignatures are sensitive and specific biomarkers for detection of patients with KAT6A/KAT6B variants. Epigenomics, 15 (6), 351-367. doi: 10.2217/epi-2023-0079

Correction: Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain development

Kaspi, Antony, Hildebrand, Michael S., Jackson, Victoria E., Braden, Ruth, van Reyk, Olivia, Howell, Tegan, Debono, Simone, Lauretta, Mariana, Morison, Lottie, Coleman, Matthew J., Webster, Richard, Coman, David, Goel, Himanshu, Wallis, Mathew, Dabscheck, Gabriel, Downie, Lilian, Baker, Emma K., Parry-Fielder, Bronwyn, Ballard, Kirrie, Harrold, Eva, Ziegenfusz, Shaun, Bennett, Mark F., Robertson, Erandee, Wang, Longfei, Boys, Amber, Fisher, Simon E., Amor, David J., Scheffer, Ingrid E., Bahlo, Melanie and Morgan, Angela T. (2023). Correction: Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain development. Molecular Psychiatry, 28 (4), 1-3. doi: 10.1038/s41380-022-01879-y

3-Methylglutaconyl-CoA hydratase deficiency: When ascertainment bias confounds a biochemical diagnosis

Hertzog, Ashley, Selvanathan, Arthavan, Pandithan, Dinusha, Kim, Won-Tae, Kava, Maina P., Boneh, Avihu, Coman, David, Tolun, Adviye Ayper and Bhattacharya, Kaustuv (2022). 3-Methylglutaconyl-CoA hydratase deficiency: When ascertainment bias confounds a biochemical diagnosis. JIMD Reports, 63 (6), 568-574. doi: 10.1002/jmd2.12332

Generation of iPSC lines from hereditary spastic paraplegia 56 (SPG56) patients and family members carrying CYP2U1 mutations

Leeson, Hannah C., Goh, Denise, Coman, David and Wolvetang, Ernst J. (2022). Generation of iPSC lines from hereditary spastic paraplegia 56 (SPG56) patients and family members carrying CYP2U1 mutations. Stem Cell Research, 64 102917, 1-5. doi: 10.1016/j.scr.2022.102917

Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain development

Kaspi, Antony, Hildebrand, Michael S., Jackson, Victoria E., Braden, Ruth, van Reyk, Olivia, Howell, Tegan, Debono, Simone, Lauretta, Mariana, Morison, Lottie, Coleman, Matthew J., Webster, Richard, Coman, David, Goel, Himanshu, Wallis, Mathew, Dabscheck, Gabriel, Downie, Lilian, Baker, Emma K., Parry-Fielder, Bronwyn, Ballard, Kirrie, Harrold, Eva, Ziegenfusz, Shaun, Bennett, Mark F., Robertson, Erandee, Wang, Longfei, Boys, Amber, Fisher, Simon E., Amor, David J., Scheffer, Ingrid E., Bahlo, Melanie and Morgan, Angela T. (2022). Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain development. Molecular Psychiatry, 28 (4), 1647-1663. doi: 10.1038/s41380-022-01764-8

N-acetylglutamate synthase deficiency with associated 3-methylglutaconic aciduria: A case report

Selvanathan, Arthavan, Demetriou, Kalliope, Lynch, Matthew, Lipke, Michelle, Bursle, Carolyn, Elliott, Aoife, Inwood, Anita, Foyn, Leanne, McWhinney, Brett, Coman, David and McGill, Jim (2022). N-acetylglutamate synthase deficiency with associated 3-methylglutaconic aciduria: A case report. JIMD Reports, 63 (5), 420-424. doi: 10.1002/jmd2.12318

Metabolic stress and mitochondrial dysfunction in ataxia-telangiectasia

Subramanian, Goutham Narayanan, Yeo, Abrey Jie, Gatei, Magtouf Hnaidi, Coman, David John and Lavin, Martin Francis (2022). Metabolic stress and mitochondrial dysfunction in ataxia-telangiectasia. Antioxidants, 11 (4) 653. doi: 10.3390/antiox11040653

WT1 complete gonadal dysgenesis with membranoproliferative glomerulonephritis: case series and literature review

Anderson, Erin, Aldridge, Melanie, Turner, Ross, Harraway, James, McManus, Sam, Stewart, Anna, Borzi, Peter, Trnka, Peter, Burke, John and Coman, David (2022). WT1 complete gonadal dysgenesis with membranoproliferative glomerulonephritis: case series and literature review. Pediatric Nephrology, 37 (10), 2369-2374. doi: 10.1007/s00467-022-05421-8

PURA-related developmental and epileptic encephalopathy phenotypic and genotypic spectrum

Johannesen, Katrine M., Gardella, Elena, Gjerulfsen, Cathrine E., Bayat, Allan, Rouhl, Rob P.W., Reijnders, Margot, Whalen, Sandra, Keren, Boris, Buratti, Julien, Courtin, Thomas, Wierenga, Klaas J., Isidor, Bertrand, Piton, Amélie, Faivre, Laurence, Garde, Aurore, Moutton, Sébastien, Tran-Mau-Them, Frédéric, Denommé-Pichon, Anne-Sophie, Coubes, Christine, Larson, Austin, Esser, Michael J., Appendino, Juan Pablo, Al-Hertani, Walla, Gamboni, Beatriz, Mampel, Alejandra, Mayorga, Lía, Orsini, Alessandro, Bonuccelli, Alice, Suppiej, Agnese ... Rubboli, Guido (2021). PURA-related developmental and epileptic encephalopathy phenotypic and genotypic spectrum. Neurology: Genetics, 7 (6) e613, e613. doi: 10.1212/NXG.0000000000000613

Patient care standards for primary mitochondrial disease in Australia: an Australian adaptation of the Mitochondrial Medicine Society recommendations

Sue, Carolyn M., Balasubramaniam, Shanti, Bratkovic, Drago, Bonifant, Catherine, Christodoulou, John, Coman, David, Crawley, Karen, Edema‐Hildebrand, Fabienne, Ellaway, Carolyn, Ghaoui, Roula, Kava, Maina, Kearns, Lisa S., Lee, Joy, Liang, Christina, Mackey, David A., Murray, Sean, Needham, Merrilee, Rius, Rocio, Russell, Jacqui, Smith, Nicholas J.C., Thyagarajan, Dominic and Wools, Christine (2021). Patient care standards for primary mitochondrial disease in Australia: an Australian adaptation of the Mitochondrial Medicine Society recommendations. Internal Medicine Journal, 52 (1), 110-120. doi: 10.1111/imj.15505

An anaplerotic approach to correct the mitochondrial dysfunction in ataxia-telangiectasia (A-T)

Yeo, A.J., Subramanian, G.N., Chong, K.L., Gatei, M., Parton, R.G., Coman, D. and Lavin, M.F. (2021). An anaplerotic approach to correct the mitochondrial dysfunction in ataxia-telangiectasia (A-T). Molecular Metabolism, 54 101354, 101354. doi: 10.1016/j.molmet.2021.101354

Delineating the Smith-Kingsmore syndrome phenotype: Investigation of 16 patients with the MTOR c.5395G > A p.(Glu1799Lys) missense variant

Poole, Rebecca L., Curry, Philippa D. K., Marcinkute, Ruta, Brewer, Carole, Coman, David, Hobson, Emma, Johnson, Diana, Lynch, Sally Ann, Saggar, Anand, Searle, Claire, Scurr, Ingrid, Turnpenny, Peter D., Vasudevan, Pradeep and Tatton-Brown, Katrina (2021). Delineating the Smith-Kingsmore syndrome phenotype: Investigation of 16 patients with the MTOR c.5395G > A p.(Glu1799Lys) missense variant. American Journal of Medical Genetics, Part A, 185 (8), 2445-2454. doi: 10.1002/ajmg.a.62350

New insights into carnitine-acylcarnitine translocase deficiency from 23 cases: management challenges and potential therapeutic approaches

Ryder, Bryony, Inbar-Feigenberg, Michal, Glamuzina, Emma, Halligan, Rebecca, Vara, Roshni, Elliot, Aoife, Coman, David, Minto, Tahlee, Lewis, Katherine, Schiff, Manuel, Vijay, Suresh, Akroyd, Rhonda, Thompson, Sue, MacDonald, Anita, Woodward, Abigail J. M., Gribben, Joanne. E. L., Grunewald, Stephanie, Belaramani, Kiran, Hall, Madeleine, van der Haak, Natalie, Devanapalli, Beena, Tolun, Adviye Ayper, Wilson, Callum and Bhattacharya, Kaustuv (2021). New insights into carnitine-acylcarnitine translocase deficiency from 23 cases: management challenges and potential therapeutic approaches. Journal of Inherited Metabolic Disease, 44 (4), 903-915. doi: 10.1002/jimd.12371

Application of genome sequencing from blood to diagnose mitochondrial diseases

Rius, Rocio, Compton, Alison G., Baker, Naomi L., Welch, Annemarie E., Coman, David, Kava, Maina P., Minoche, Andre E., Cowley, Mark J., Thorburn, David R. and Christodoulou, John (2021). Application of genome sequencing from blood to diagnose mitochondrial diseases. Genes, 12 (4) 607, 1-13. doi: 10.3390/genes12040607

Triple P for parents of children with phenylketonuria: a nonrandomized trial

Mitchell, Amy E., Morawska, Alina, Kirby, Grace, McGill, James, Coman, David and Inwood, Anita (2021). Triple P for parents of children with phenylketonuria: a nonrandomized trial. Journal of Pediatric Psychology, 46 (2), 208-218. doi: 10.1093/jpepsy/jsaa100

Impaired endoplasmic reticulum-mitochondrial signaling in ataxia-telangiectasia

Yeo, Abrey J., Kok, Chong L., Gatei, Magtouf, Zou, Dongxiu, Stewart, Romal, Withey, Sarah, Wolvetang, Ernst, Parton, Robert G., Brown, Adam D., Kastan, Michael B., Coman, David and Lavin, Martin F. (2021). Impaired endoplasmic reticulum-mitochondrial signaling in ataxia-telangiectasia. iScience, 24 (1) 101972, 101972. doi: 10.1016/j.isci.2020.101972

International consensus guidelines for phosphoglucomutase 1 deficiency (PGM1-CDG): diagnosis, follow-up, and management

Altassan, Ruqaiah, Radenkovic, Silvia, Edmondson, Andrew C., Barone, Rita, Brasil, Sandra, Cechova, Anna, Coman, David, Donoghue, Sarah, Falkenstein, Kristina, Ferreira, Vanessa, Ferreira, Carlos, Fiumara, Agata, Francisco, Rita, Freeze, Hudson, Grunewald, Stephanie, Honzik, Tomas, Jaeken, Jaak, Krasnewich, Donna, Lam, Christina, Lee, Joy, Lefeber, Dirk, Marques-da-Silva, Dorinda, Pascoal, Carlota, Quelhas, Dulce, Raymond, Kimiyo M., Rymen, Daisy, Seroczynska, Malgorzata, Serrano, Mercedes, Sykut-Cegielska, Jolanta ... Morava, Eva (2021). International consensus guidelines for phosphoglucomutase 1 deficiency (PGM1-CDG): diagnosis, follow-up, and management. Journal of Inherited Metabolic Disease, 44 (1), 148-163. doi: 10.1002/jimd.12286

Expanding the genetic landscape of Rett syndrome to include lysine acetyltransferase 6A (KAT6A)

Kaur, Simranpreet, Van Bergen, Nicole J., Ben-Zeev, Bruria, Leonardi, Emanuela, Tan, Tiong Y., Coman, David, Kamien, Benjamin, White, Susan M., St John, Miya, Phelan, Dean, Rigbye, Kristin, Lim, Sze Chern, Torres, Michelle C., Marty, Melanie, Savva, Elena, Zhao, Teresa, Massey, Sean, Murgia, Alessandra, Gold, Wendy A. and Christodoulou, John (2020). Expanding the genetic landscape of Rett syndrome to include lysine acetyltransferase 6A (KAT6A). Journal of Genetics and Genomics, 47 (10), 650-654. doi: 10.1016/j.jgg.2020.09.003

A synonymous UPF3B variant causing a speech disorder implicates NMD as a regulator of neurodevelopmental disorder gene networks

Domingo, Deepti, Nawaz, Urwah, Corbett, Mark, Espinoza, Josh L., Tatton-Brown, Katrina, Coman, David, Wilkinson, Miles F., Gecz, Jozef and Jolly, Lachlan A. (2020). A synonymous UPF3B variant causing a speech disorder implicates NMD as a regulator of neurodevelopmental disorder gene networks. Human Molecular Genetics, 29 (15), 2568-2578. doi: 10.1093/hmg/ddaa151

Severe childhood speech disorder: Gene discovery highlights transcriptional dysregulation

Hildebrand, Michael S., Jackson, Victoria E., Scerri, Thomas S., Van Reyk, Olivia, Coleman, Matthew, Braden, Ruth O., Turner, Samantha, Rigbye, Kristin A., Boys, Amber, Barton, Sarah, Webster, Richard, Fahey, Michael, Saunders, Kerryn, Parry-Fielder, Bronwyn, Paxton, Georgia, Hayman, Michael, Coman, David, Goel, Himanshu, Baxter, Anne, Ma, Alan, Davis, Noni, Reilly, Sheena, Delatycki, Martin, Liégeois, Frederique J., Connelly, Alan, Gecz, Jozef, Fisher, Simon E., Amor, David J., Scheffer, Ingrid E. ... Morgan, Angela T. (2020). Severe childhood speech disorder: Gene discovery highlights transcriptional dysregulation. Neurology, 94 (20), e2148-e2167. doi: 10.1212/WNL.0000000000009441

The diagnostic utility of genome sequencing in a pediatric cohort with suspected mitochondrial disease

Riley, Lisa G., Cowley, Mark J., Gayevskiy, Velimir, Minoche, Andre E., Puttick, Clare, Thorburn, David R., Rius, Rocio, Compton, Alison G., Menezes, Minal J., Bhattacharya, Kaustuv, Coman, David, Ellaway, Carolyn, Alexander, Ian E., Adams, Louisa, Kava, Maina, Robinson, Jacqui, Sue, Carolyn M., Balasubramaniam, Shanti and Christodoulou, John (2020). The diagnostic utility of genome sequencing in a pediatric cohort with suspected mitochondrial disease. Genetics in Medicine, 22 (7), 1254-1261. doi: 10.1038/s41436-020-0793-6

Behçet disease-like symptoms with a novel COPA mutation

Anderson, E., Hatch, J., Cardinal, J., Langguth, D. and Coman, D. (2020). Behçet disease-like symptoms with a novel COPA mutation. Case Reports in Genetics, 2020, 1-4. doi: 10.1155/2020/8414857

Hypoglycemia in CDG patients due to PMM2 mutations: follow up on hyperinsulinemic patients

Moravej, Hossein, Altassan, Ruqaiah, Jaeken, Jaak, Enns, Gregory M., Ellaway, Carolyn, Balasubramaniam, Shanti, De Lonlay, Pascale, Coman, David, Mercimek-Andrews, Saadet, Witters, Peter and Morava, Eva (2020). Hypoglycemia in CDG patients due to PMM2 mutations: follow up on hyperinsulinemic patients. JIMD Reports, 51 (1), 76-81. doi: 10.1002/jmd2.12085

Genetic abnormalities in a large cohort of Coffin–Siris syndrome patients

Sekiguchi, Futoshi, Tsurusaki, Yoshinori, Okamoto, Nobuhiko, Teik, Keng Wee, Mizuno, Seiji, Suzumura, Hiroshi, Isidor, Bertrand, Ong, Winnie Peitee, Haniffa, Muzhirah, White, Susan M., Matsuo, Mari, Saito, Kayoko, Phadke, Shubha, Kosho, Tomoki, Yap, Patrick, Goyal, Manisha, Clarke, Lorne A., Sachdev, Rani, McGillivray, George, Leventer, Richard J., Patel, Chirag, Yamagata, Takanori, Osaka, Hitoshi, Hisaeda, Yoshiya, Ohashi, Hirofumi, Shimizu, Kenji, Nagasaki, Keisuke, Hamada, Junpei, Dateki, Sumito ... Matsumoto, Naomichi (2019). Genetic abnormalities in a large cohort of Coffin–Siris syndrome patients. Journal of Human Genetics, 64 (12), 1173-1186. doi: 10.1038/s10038-019-0667-4

Psychosocial functioning in children with phenylketonuria: relationships between quality of life and parenting indicators

Morawska, Alina, Mitchell, Amy E., Etel, Evren, Kirby, Grace, McGill, James, Coman, David and Inwood, Anita (2019). Psychosocial functioning in children with phenylketonuria: relationships between quality of life and parenting indicators. Child: Care, Health and Development, 46 (1) cch.12727, 56-65. doi: 10.1111/cch.12727

Defective protein prenylation in a spectrum of patients with mevalonate kinase deficiency

Munoz, Marcia A., Jurczyluk, Julie, Simon, Anna, Hissaria, Pravin, Arts, Rob J. W., Coman, David, Boros, Christina, Mehra, Sam and Rogers, Michael J. (2019). Defective protein prenylation in a spectrum of patients with mevalonate kinase deficiency. Frontiers in Immunology, 10 (AUG) 1900, 1900. doi: 10.3389/fimmu.2019.01900

SLC35A2-CDG: functional characterization, expanded molecular, clinical, and biochemical phenotypes of 30 unreported individuals

Ng, Bobby G., Sosicka, Paulina, Agadi, Satish, Almannai, Mohammed, Bacino, Carlos A., Barone, Rita, Botto, Lorenzo D., Burton, Jennifer E., Carlston, Colleen, Chung, Brian Hon-Yin, Cohen, Julie S., Coman, David, Dipple, Katrina M., Dorrani, Naghmeh, Dobyns, William B., Elias, Abdallah F., Epstein, Leon, Gahl, William A., Garozzo, Domenico, Hammer, Trine Bjørg, Haven, Jaclyn, Héron, Delphine, Herzog, Matthew, Hoganson, George E., Hunter, Jesse M., Jain, Mahim, Juusola, Jane, Lakhani, Shenela, Lee, Hane ... Freeze, Hudson H. (2019). SLC35A2-CDG: functional characterization, expanded molecular, clinical, and biochemical phenotypes of 30 unreported individuals. Human Mutation, 40 (7) humu.23731, 908-925. doi: 10.1002/humu.23731

A novel familial 9q31.2q32 microdeletion: muscle cramping, somnolence, fatigue, sensorineural hearing loss, pubertal delay, and short stature

Ramineni, Anand K., Burgess, Trent, Cruickshanks, Penny and Coman, David (2019). A novel familial 9q31.2q32 microdeletion: muscle cramping, somnolence, fatigue, sensorineural hearing loss, pubertal delay, and short stature. Clinical Case Reports, 7 (2), 304-310. doi: 10.1002/ccr3.1970

International clinical guidelines for the management of phosphomannomutase 2-congenital disorders of glycosylation: diagnosis, treatment and follow up

Altassan, Ruqaiah, Péanne, Romain, Jaeken, Jaak, Barone, Rita, Bidet, Muad, Borgel, Delphine, Brasil, Sandra, Cassiman, David, Cechova, Anna, Coman, David, Corral, Javier, Correia, Joana, de la Morena-Barrio, María Eugenia, de Lonlay, Pascale, Dos Reis, Vanessa, Ferreira, Carlos R., Fiumara, Agata, Francisco, Rita, Freeze, Hudson, Funke, Simone, Gardeitchik, Thatjana, Gert, Matthijs, Girad, Muriel, Giros, Marisa, Grünewald, Stephanie, Hernández-Caselles, Trinidad, Honzik, Tomas, Hutter, Marlen, Krasnewich, Donna ... Morava, Eva (2019). International clinical guidelines for the management of phosphomannomutase 2-congenital disorders of glycosylation: diagnosis, treatment and follow up. Journal of Inherited Metabolic Disease, 42 (1), 5-28. doi: 10.1002/jimd.12024

Keeping an eye on congenital disorders of O-glycosylation: a systematic literature review

Francisco, Rita, Pascoal, Carlota, Marques-da-Silva, Dorinda, Morava, Eva, Gole, Glen A., Coman, David, Jaeken, Jaak and Dos Reis Ferreira, Vanessa (2019). Keeping an eye on congenital disorders of O-glycosylation: a systematic literature review. Journal of Inherited Metabolic Disease, 42 (1), 29-48. doi: 10.1002/jimd.12025

Congenital Glaucoma: a Novel Ocular Manifestation of Hajdu-Cheney Syndrome

Swan, L., Gole, G., Sabesan, V., Cardinal, J. and Coman, D. (2018). Congenital Glaucoma: a Novel Ocular Manifestation of Hajdu-Cheney Syndrome. Case Reports in Genetics, 2018, 1-4. doi: 10.1155/2018/2508345

Xq26.3 Duplication in a Boy With Motor Delay and Low Muscle Tone Refines the X-Linked Acrogigantism Genetic Locus

Trivellin, Giampaolo, Sharwood, Erin, Hijazi, Hadia, Carvalho, Claudia M. B., Yuan, Bo, Tatton-Brown, Katrina, Coman, David, Lupski, James R., Cotterill, Andrew M., Lodish, Maya B. and Stratakis, Constantine A. (2018). Xq26.3 Duplication in a Boy With Motor Delay and Low Muscle Tone Refines the X-Linked Acrogigantism Genetic Locus. Journal of the Endocrine Society, 2 (10), 1100-1108. doi: 10.1210/js.2018-00156

SYNE1-related autosomal recessive cerebellar ataxia, congenital cerebellar hypoplasia, and cognitive impairment

Swan, Lauren, Cardinal, John and Coman, David (2018). SYNE1-related autosomal recessive cerebellar ataxia, congenital cerebellar hypoplasia, and cognitive impairment. Clinics and Practice, 8 (3), 91-93. doi: 10.4081/cp.2018.1071

Squalene synthase deficiency: clinical, biochemical, and molecular characterization of a defect in cholesterol biosynthesis

Coman, David, Vissers, Lisenka E. L. M., Riley, Lisa G., Kwint, Michael P., Hauck, Roxanna, Koster, Janet, Geuer, Sinje, Hopkins, Sarah, Hallinan, Barbra, Sweetman, Larry, Engelke, Udo F. H., Burrow, T Andrew, Cardinal, John, McGill, James, Inwood, Anita, Gurnsey, Christine, Waterham, Hans R., Christodoulou, John, Wevers, Ron A. and Pitt, James (2018). Squalene synthase deficiency: clinical, biochemical, and molecular characterization of a defect in cholesterol biosynthesis. American Journal of Human Genetics, 103 (1), 125-130. doi: 10.1016/j.ajhg.2018.05.004

Ocular manifestations of a novel proximal 19p13.3 microdeletion

Swan, L. and Coman, D. (2018). Ocular manifestations of a novel proximal 19p13.3 microdeletion. Case Reports in Genetics, 2018, 2492437-5. doi: 10.1155/2018/2492437

Transient neonatal zinc deficiency in exclusively breastfed preterm infants

Watson, Lauren, Cartwright, David, Jardine, Luke A, Pincus, David, Koorts, Pieter, Kury, Sebastien, Bezieau, Stephanie, George, Shane, Moloney, Susan, Holt, Johanna and Coman, David (2018). Transient neonatal zinc deficiency in exclusively breastfed preterm infants. Journal of Paediatrics and Child Health, 54 (3), 319-322. doi: 10.1111/jpc.13780

Tread carefully: a functional variant in the human NADPH oxidase 4 (NOX4) is not disease causing

Nafisinia, Michael, Menezes, Minal Juliet, Gold, Wendy Anne, Riley, Lisa, Hatch, Joshua, Cardinal, John, Coman, David and Christodoulou, John (2018). Tread carefully: a functional variant in the human NADPH oxidase 4 (NOX4) is not disease causing. Molecular Genetics and Metabolism, 123 (3), 382-387. doi: 10.1016/j.ymgme.2018.01.007

Keeping an eye on congenital disorders of O-glycosylation: a systematic literature review

Francisco, R., Pascoal, C., Marques-da-Silva, D., Morava, E., Gole, G. A., Coman, D., Jaeken, J. and Dos Reis Ferreira, Vanessa (2018). Keeping an eye on congenital disorders of O-glycosylation: a systematic literature review. Journal of Inherited Metabolic Disease, 1-16. doi: 10.1007/s10545-017-0119-2

Leber Hereditary Optic Neuropathy and Longitudinally Extensive Transverse Myelitis

Bursle, C., Riney, K., Stringer, J., Moore, D., Gole, G., Kearns, L. S., Mackey, D. A. and Coman, D. (2017). Leber Hereditary Optic Neuropathy and Longitudinally Extensive Transverse Myelitis. JIMD Reports, 42, 53-60. doi: 10.1007/8904_2017_79

An overview of combined D-2- and L-2-hydroxyglutaric aciduria: functional analysis of CIC variants

Pop, Ana, Williams, Monique, Struys, Eduard A., Monné, Magnus, Jansen, Erwin E. W., De Grassi, Anna, Kanhai, Warsha A., Scarcia, Pasquale, Ojeda, Matilde R. Fernandez, Porcelli, Vito, van Dooren, Silvy J. M., Lennertz, Pascal, Nota, Benjamin, Abdenur, Jose E., Coman, David, Das, Anibh Martin, El-Gharbawy, Areeg, Nuoffer, Jean-Marc, Polic, Branka, Santer, René, Weinhold, Natalie, Zuccarelli, Britton, Palmieri, Ferdinando, Palmieri, Luigi and Salomons, Gajja S. (2017). An overview of combined D-2- and L-2-hydroxyglutaric aciduria: functional analysis of CIC variants. Journal of Inherited Metabolic Disease, 41 (2), 169-180. doi: 10.1007/s10545-017-0106-7

Mitochondrial Trifunctional Protein Deficiency: Severe Cardiomyopathy and Cardiac Transplantation

Bursle, C, Weintraub, R, Ward, C, Justo, R, Cardinal, J and Coman, D (2017). Mitochondrial Trifunctional Protein Deficiency: Severe Cardiomyopathy and Cardiac Transplantation. JIMD reports, 40, 91-95. doi: 10.1007/8904_2017_68

X-Linked Lissencephaly With Absent Corpus Callosum and Abnormal Genitalia: An Evolving Multisystem Syndrome With Severe Congenital Intestinal Diarrhea Disease

Coman, David, Fullston, Tom, Shoubridge, Cheryl, Leventer, Richard, Wong, Flora, Nazaretian, Simon, Simpson, Ian, Gecz, Josef and McGillivray, George (2017). X-Linked Lissencephaly With Absent Corpus Callosum and Abnormal Genitalia: An Evolving Multisystem Syndrome With Severe Congenital Intestinal Diarrhea Disease. Child Neurology Open, 4, 1-6. doi: 10.1177/2329048X17738625

GNAO1-related movement disorder with life-threatening exacerbations: movement phenomenology and response to DBS

Waak, Michaela, Mohammad, Shekeeb S., Coman, David, Sinclair, Kate, Copeland, Lisa, Silburn, Peter, Coyne, Terry, McGill, Jim, O'Regan, Mary, Selway, Richard, Symonds, Joseph, Grattan-Smith, Padraic, Lin, Jean-Pierre, Dale, Russell C. and Malone, Stephen (2017). GNAO1-related movement disorder with life-threatening exacerbations: movement phenomenology and response to DBS. Journal of Neurology, Neurosurgery and Psychiatry, 89 (2), 220-+. doi: 10.1136/jnnp-2017-315653

Fumarate hydratase is a critical metabolic regulator of hematopoietic stem cell functions

Guitart, Amelie V., Panagopoulou, Theano I., Villacreces, Arnaud, Vukovic, Milica, Sepulveda, Catarina, Allen, Lewis, Carter, Roderick N., van de Lagemaat, Louie N., Morgan, Marcos, Giles, Peter, Sas, Zuzanna, Gonzalez, Marta Vila, Lawson, Hannah, Paris, Jasmin, Edwards-Hicks, Joy, Schaak, Katrin, Subramani, Chithra, Gezer, Deniz, Armesilla-Diaz, Alejandro, Wills, Jimi, Easterbrook, Aaron, Coman, David, So, Chi Wai Eric, O'Carroll, Donal, Vernimmen, Douglas, Rodrigues, Neil P., Pollard, Patrick J., Morton, Nicholas M., Finch, Andrew and Kranc, Kamil R. (2017). Fumarate hydratase is a critical metabolic regulator of hematopoietic stem cell functions. The Journal of Experimental Medicine, 214 (3), 719-735. doi: 10.1084/jem.20161087

Persistent Hyperinsulinism in Kabuki Syndrome 2: Case Report and Literature Review

Gole, Hobia, Chuk, Raymond and Coman, David (2016). Persistent Hyperinsulinism in Kabuki Syndrome 2: Case Report and Literature Review. Clinics and Practice, 6 (3) 848, 1-3. doi: 10.4081/cp.2016.848

De Novo Mutations in SLC1A2 and CACNA1A Are Important Causes of Epileptic Encephalopathies

Myers, Candace T., McMahon, Jacinta M., Schneider, Amy L., Petrovski, Slavé, Allen, Andrew S., Carvill, Gemma L., Zemel, Matthew, Saykally, Julia E., LaCroix, Amy J., Heinzen, Erin L., Hollingsworth, Georgina, Nikanorova, Marina, Corbett, Mark, Gecz, Jozef, Coman, David, Freeman, Jeremy, Calvert, Sophie, Gill, Deepak, Carney, Patrick, Lerman-Sagie, Tally, Sampaio, Hugo, Cossette, Patrick, Delanty, Norman, Dlugos, Dennis, Eichler, Evan E., Epstein, Michael P., Glauser, Tracy, Johnson, Michael R., Kuzniecky, Ruben ... Epi4K Consortium (2016). De Novo Mutations in SLC1A2 and CACNA1A Are Important Causes of Epileptic Encephalopathies. American Journal of Human Genetics, 99 (2), 287-298. doi: 10.1016/j.ajhg.2016.06.003

Erratum to: Spondyloenchondrodysplasia Due to Mutations in ACP5: A Comprehensive Survey

Briggs, Tracy A., Rice, Gillian I., Adib, Navid, Ades, Lesley, Barete, Stephane, Baskar, Kannan, Baudouin, Veronique, Cebeci, Ayse N., Clapuyt, Philippe, Coman, David, De Somer, Lien, Finezilber, Yael, Frydman, Moshe, Guven, Ayla, Heritier, Sébastien, Karall, Daniela, Kulkarni, Muralidhar L., Lebon, Pierre, Levitt, David, Le Merrer, Martine, Linglart, Agnes, Livingston, John H., Navarro, Vincent, Okenfuss, Ericka, Puel, Anne, Revencu, Nicole, Scholl-Bürgi, Sabine, Vivarelli, Marina, Wouters, Carine ... Crow, Yanick J. (2016). Erratum to: Spondyloenchondrodysplasia Due to Mutations in ACP5: A Comprehensive Survey. Journal of Clinical Immunology, 36 (5), 529-530. doi: 10.1007/s10875-016-0287-0

Spondyloenchondrodysplasia due to mutations in ACP5: a comprehensive survey

Briggs, Tracy A., Rice, Gillian I., Adib, Navid, Ades, Lesley, Barete, Stephane, Baskar, Kannan, Baudouin, Veronique, Cebeci, Ayse N., Clapuyt, Philippe, Coman, David, De Somer, Lien, Finezilber, Yael, Frydman, Moshe, Guven, Ayla, Heritier, Sébastien, Karall, Daniela, Kulkarni, Muralidhar L., Lebon, Pierre, Levitt, David, Le Merrer, Martine, Linglart, Agnes, Livingston, John H., Navarro, Vincent, Okenfuss, Ericka, Puel, Anne, Revencu, Nicole, Scholl-Bürgi, Sabine, Vivarelli, Marina, Wouters, Carine ... Crow, Yanick J. (2016). Spondyloenchondrodysplasia due to mutations in ACP5: a comprehensive survey. Journal of Clinical Immunology, 36 (3), 220-234. doi: 10.1007/s10875-016-0252-y

Recurrent muscle weakness with rhabdomyolysis, metabolic crises, and cardiac arrhythmia due to bi-allelic TANGO2 mutations

Lalani, Seema R., Liu, Pengfei, Rosenfeld, Jill A., Watkin, Levi B., Chiang, Theodore, Leduc, Magalie S., Zhu, Wenmiao, Ding, Yan, Pan, Shujuan, Vetrini, Francesco, Miyake, Christina Y., Shinawi, Marwan, Gambin, Tomasz, Eldomery, Mohammad K., Akdemir, Zeynep Hande Coban, Emrick, Lisa, Wilnai, Yael, Schelley, Susan, Koenig, Mary Kay, Memon, Nada, Farach, Laura S., Coe, Bradley P., Azamian, Mahshid, Hernandez, Patricia, Zapata, Gladys, Jhangiani, Shalini N., Muzny, Donna M., Lotze, Timothy, Clark, Gary ... Yang, Yaping (2016). Recurrent muscle weakness with rhabdomyolysis, metabolic crises, and cardiac arrhythmia due to bi-allelic TANGO2 mutations. American Journal of Human Genetics, 98 (2), 347-357. doi: 10.1016/j.ajhg.2015.12.008

De Novo 3q22.3q24 Microdeletion in a Patient With Blepharophimosis–Ptosis–Epicanthus Inversus Syndrome, Dandy-Walker Malformation, and Wisconsin Syndrome

Ramineni, Anand and Coman, David (2016). De Novo 3q22.3q24 Microdeletion in a Patient With Blepharophimosis–Ptosis–Epicanthus Inversus Syndrome, Dandy-Walker Malformation, and Wisconsin Syndrome. Child Neurology Open, 3, 1-6. doi: 10.1177/2329048x16666362

PNPO Deficiency and Cirrhosis: Expanding the Clinical Phenotype?

Coman, D., Lewindon, P., Clayton, P. and Riney, K. (2016). PNPO Deficiency and Cirrhosis: Expanding the Clinical Phenotype?. JIMD Reports, 25, 71-75. doi: 10.1007/8904_2015_456

Pediatric Hereditary Neuralgic Amyotrophy : Successful Treatment With Intravenous Immunoglobulin and Insights Into SEPT9 Pathogenesis

Chuk, Raymond, Sheppard, Megan, Wallace, Geoff and Coman, David (2016). Pediatric Hereditary Neuralgic Amyotrophy : Successful Treatment With Intravenous Immunoglobulin and Insights Into SEPT9 Pathogenesis. Child Neurology Open, 3 2329048X1666897, 1-3. doi: 10.1177/2329048x16668970

Allan-Herndon-Dudley syndrome with unusual profound sensorineural hearing loss

Gagliardi, Lucia, Nataren, Nathalie, Feng, Jinghua, Schreiber, Andreas W., Hahn, Christopher N., Conwell, Louise S., Coman, David and Scott, Hamish S. (2015). Allan-Herndon-Dudley syndrome with unusual profound sensorineural hearing loss. American Journal of Medical Genetics, Part A, 167 (8), 1872-1876. doi: 10.1002/ajmg.a.37075

Septic arthritis of the temporomandibular joint in an infant

Chuk, Raymond, Arvier, John, Laing, Barbara and Coman, David (2015). Septic arthritis of the temporomandibular joint in an infant. Clinics and Practice, 5 (2) 736, 53-55. doi: 10.4081/cp.2015.736

Glucose transporter 1 deficiency syndrome and hemiplegic migraines as a dominant presenting clinical feature

Mohammad, Shekeeb S., Coman, David and Calvert, Sophie (2014). Glucose transporter 1 deficiency syndrome and hemiplegic migraines as a dominant presenting clinical feature. Journal of Paediatrics and Child Health, 50 (12), 1025-1026. doi: 10.1111/jpc.12613

Pre-linguistic communication skill development in an infant with a diagnosis of galactosemia

Lewis, Fiona M., Coman, David J., Kilcoyne, Sarah, Murdoch, Bruce E. and Syrmis, Maryanne (2014). Pre-linguistic communication skill development in an infant with a diagnosis of galactosemia. Developmental Neurorehabilitation, 17 (5), 291-297. doi: 10.3109/17518423.2012.753479

Early markers of vulnerable language skill development in galactosaemia

Lewis, Fiona M., Coman, David J. and Syrnis, Maryanne (2014). Early markers of vulnerable language skill development in galactosaemia. Early Child Development and Care, 184 (12), 1787-1799. doi: 10.1080/03004430.2013.878712

Age at assessment a critical factor when monitoring early communicative skills in children with galactosaemia

Lewis, Fiona M., DeJonge, Shannon M. and Coman, David J. (2014). Age at assessment a critical factor when monitoring early communicative skills in children with galactosaemia. Early Child Development and Care, 184 (11), 1636-1647. doi: 10.1080/03004430.2013.871275

Mutations in SH3PXD2B cause Borrone dermato-cardio-skeletal syndrome

Wilson, Gabrielle R., Sunley, Jasmine, Smith, Katherine R., Pope, Kate, Bromhead, Catherine J., Fitzpatrick, Elizabeth, Di Rocco, Maja, Van Steensel, Maurice, Coman, David J., Leventer, Richard J., Delatycki, Martin B., Amor, David J., Bahlo, Melanie and Lockhart, Paul J. (2014). Mutations in SH3PXD2B cause Borrone dermato-cardio-skeletal syndrome. European Journal of Human Genetics, 22 (6), 741-747. doi: 10.1038/ejhg.2013.229

Charting a seven-year trajectory of language outcomes for a child with galactosemia

Lewis, Fiona M., Coman, David J., Syrmis, Maryann, Kilcoyne, Sarah and Murdoch, Bruce E. (2013). Charting a seven-year trajectory of language outcomes for a child with galactosemia. Journal of Developmental and Behavioral Pediatrics, 34 (6), 414-418. doi: 10.1097/DBP.0b013e31829a7be1

Pediatric acute liver failure: etiology, outcomes, and the role of serial pediatric end-stage liver disease scores

Rajanayagam, Jeremy, Coman, David, Cartwright, David and Lewindon, Peter J. (2013). Pediatric acute liver failure: etiology, outcomes, and the role of serial pediatric end-stage liver disease scores. Pediatric Transplantation, 17 (4), 362-368. doi: 10.1111/petr.12083

Fumarase deficiency in dichorionic diamniotic twins

Tregoning, S., Salter, W., Thorburn, D.R., Durkie, M., Panayi, M., Wu, J.Y., Easterbrook, A. and Coman, D.J. (2013). Fumarase deficiency in dichorionic diamniotic twins. Twin Research and Human Genetics, 16 (6), 1117-1120. doi: 10.1017/thg.2013.72

Impaired language abilities and pre-linguistic communication skills in a child with a diagnosis of galactosaemia

Lewis, Fiona M., Coman, David J., Syrmis, Maryanne, Kilcoyne, Sarah and Murdoch, Bruce E. (2012). Impaired language abilities and pre-linguistic communication skills in a child with a diagnosis of galactosaemia. Early Child Development and Care, 183 (12), 1747-1757. doi: 10.1080/03004430.2012.751101

Extended newborn screening: An update for the general paediatrician

Coman, David and Bhattacharya, Kaustuv (2012). Extended newborn screening: An update for the general paediatrician. Journal of Paediatrics and Child Health, 48 (2), E68-E72. doi: 10.1111/j.1440-1754.2011.02199.x

IgG N-glycans as potential biomarkers for determining galactose tolerance in Classical Galactosaemia

Coss, K.P., Byrne, J.C., Coman, D.J., Adamczyk, B., Abrahams, J.L., Saldova, R., Brown, A.Y., Walsh, O., Hendroff, U., Carolan, C., Rudd, P.M. and Treacy, E.P. (2012). IgG N-glycans as potential biomarkers for determining galactose tolerance in Classical Galactosaemia. Molecular Genetics and Metabolism, 105 (2), 1-9. doi: 10.1016/j.ymgme.2011.10.018

Enzyme replacement therapy and extended newborn screening for mucopolysaccharidoses: opinions of treating physicians

Coman, David J., Hayes, Ian M, Collins, Veronica, Sahhar, Margaret, Wraith, J. Ed and Delatycki, Martin B (2011). Enzyme replacement therapy and extended newborn screening for mucopolysaccharidoses: opinions of treating physicians. Journal of Inherited Metabolic Disease, 1, 9-15. doi: 10.1007/8904_2011_9

Language skills in a child with Leber hereditary optic neuropathy following intrathecal chemotherapy for acute lymphoblastic leukemia

Lewis, Fiona M., Coman, David J. and Murdoch, Bruce E. (2010). Language skills in a child with Leber hereditary optic neuropathy following intrathecal chemotherapy for acute lymphoblastic leukemia. Pediatric Hematology and Oncology, 27 (8), 626-635. doi: 10.3109/08880018.2010.503340

Enzyme replacement therapy for mucopolysaccharidosis VI from 8 weeks of age – a sibling control study

McGill, J. J., Inwood, A. C., Coman, D. J., Lipke, M. L., de Lore, D, Swiedler, S. J. and Hopwood, J. J. (2010). Enzyme replacement therapy for mucopolysaccharidosis VI from 8 weeks of age – a sibling control study. Clinical Genetics, 77 (5), 492-498. doi: 10.1111/j.1399-0004.2009.01324.x

Galactosemia, a single gene disorder with epigenetic consequences

Coman, David J., Murray, David W., Byrne, Jennifer C., Rudd, Pauline M., Bagadlia, Paola M., Doran, Peter D. and Treacy, Eileen P. (2010). Galactosemia, a single gene disorder with epigenetic consequences. Pediatric Research, 67 (3), 286-292. doi: 10.1203/PDR.0b013e3181cbd542

Three Mendelian disorders (chronic granulomatous disease, retinitis pigmentosa, ornithine transcarbamylase deficiency) in a young woman with an X chromosome deletion, del(X)(p11.4p21.1)

Coman, David, Yaplito-Lee, Joy, La, Phung, Nasioulas, Steven, Bruno, Damien, Slater, Howard R., Stock-Myer, Sharyn E., Lynch, Elly L. and Gardner, R.J. McKinlay (2010). Three Mendelian disorders (chronic granulomatous disease, retinitis pigmentosa, ornithine transcarbamylase deficiency) in a young woman with an X chromosome deletion, del(X)(p11.4p21.1). Molecular Genetics and Metabolism, 99 (3), 329. doi: 10.1016/j.ymgme.2009.11.006

Mutations in the nuclear localization sequence of the Aristaless related homeobox; Sequestration of mutant ARX with IPO13 disrupts normal subcellular distribution of the transcription factor and retards cell division

Shoubridge, Cheryl, Tan, May, Fullston, Tod, Cloosterman, Desiree, Coman, David, McGillivray, George, Mancini, Grazia, Kleefstra, Tjitske and Gécz, Jozef (2010). Mutations in the nuclear localization sequence of the Aristaless related homeobox; Sequestration of mutant ARX with IPO13 disrupts normal subcellular distribution of the transcription factor and retards cell division. PathoGenetics, 3 (1) 1. doi: 10.1186/1755-8417-3-1

Trisomy 16 mosaicism at chorionic villus sampling and amniocentesis with a normal physical and intellectual outcome

Coman, D., Gardner, R. J., Pertile, M. D. and Kannu, P. (2010). Trisomy 16 mosaicism at chorionic villus sampling and amniocentesis with a normal physical and intellectual outcome. Fetal diagnosis and therapy, 28 (2), 117-118. doi: 10.1159/000316404

Molecular basis of EEC (ectrodactyly, ectodermal dysplasia, clefting) syndrome: Five new mutations in the DNA-binding domain of the TP63 gene and genotype–phenotype correlation

Clements, S. E., Techanukul, T., Coman, D., Mellerio, J. E. and McGrath, J.A. (2009). Molecular basis of EEC (ectrodactyly, ectodermal dysplasia, clefting) syndrome: Five new mutations in the DNA-binding domain of the TP63 gene and genotype–phenotype correlation. British Journal of Dermatology, 162 (1), 201-207. doi: 10.1111/j.1365-2133.2009.09496.x

Detection of cryptic pathogenic copy number variations and constitutional loss of heterozygosity using high resolution SNP microarray analysis in 117 patients referred for cytogenetic analysis and impact on clinical practice

Bruno, D. L., Ganesamoorthy, D., Schoumans, J., Bankier, A., Coman, D., Delatycki, M., Gardner, R. J. M., Hunter, M., James, P. A., Kannu, P., McGillivray, G., Pachter, N., Peters, H., Rieubland, C., Savarirayan, R., Scheffer, I. E., Sheffield, L., Tan, T., White, S. M., Yeung, A., Bowman, Z., Ngo, C., Choy, K. W., Cacheux, V., Wong, L., Amor, D. J. and Slater, H. R. (2009). Detection of cryptic pathogenic copy number variations and constitutional loss of heterozygosity using high resolution SNP microarray analysis in 117 patients referred for cytogenetic analysis and impact on clinical practice. Journal of Medical Genetics, 46 (2), 123-131. doi: 10.1136/jmg.2008.062604

Prenatal cardiac ultrasound finding in congenital disorder of glycosylation type 1a

Malhotra, A., Pateman, A., Chalmers, R., Coman, D. and Menahem, S. (2009). Prenatal cardiac ultrasound finding in congenital disorder of glycosylation type 1a. Fetal Diagnosis and Therapy: clinical advances and basic research, 25 (1), 54-57. doi: 10.1159/000196816

Unrelated cord blood transplantation in a girl with Hoyeraal–Hreidarsson syndrome

Coman, D., Herbert, A. R., McGill, J., Lockwood, L. and Hallahan, A. R. (2008). Unrelated cord blood transplantation in a girl with Hoyeraal–Hreidarsson syndrome. Bone Marrow Transplantation, 42 (4), 293-294. doi: 10.1038/bmt.2008.163

New indications and controversies in arginine therapy

Coman, David, Yaplito-Lee, Joy and Boneh, Avihu (2008). New indications and controversies in arginine therapy. Clinical Nutrition, 27 (4), 489-496. doi: 10.1016/j.clnu.2008.05.007

Spondylocostal dysostosis in a pregnancy complicated by confined placental mosaicism for tetrasomy 9p

Coman, David, Bacic, Sonya, Boys, Amber, Sparrow, Duncan B., Dunwoodie, Sally L., Savarirayan, Ravi and Amor, David J. (2008). Spondylocostal dysostosis in a pregnancy complicated by confined placental mosaicism for tetrasomy 9p. American Journal of Medical Genetics, Part A, 146 (15), 1972-1976. doi: 10.1002/ajmg.a.32299

The skeletal manifestations of the congenital disorders of glycosylation

Coman, D., Irving, M., Kannu, P., Jaeken, J. and Savarirayan, Ravi (2008). The skeletal manifestations of the congenital disorders of glycosylation. Clinical Genetics, 73 (6), 507-515. doi: 10.1111/j.1399-0004.2008.01015.x

Enzyme Replacement Therapy for Mucopolysaccharidoses: Opinions of Patients and Families

Coman, David J., Hayes, Ian M., Collins, Veronica, Sahhar, Margaret, Wraith, J. Ed and Delatycki, Martin B. (2008). Enzyme Replacement Therapy for Mucopolysaccharidoses: Opinions of Patients and Families. Journal of Pediatrics, 152 (5), 723-727. doi: 10.1016/j.jpeds.2007.10.015

A novel splice site mutation in EYA4 causes DFNA10 hearing loss (American Journal of Medical Genetics 143,14, (1599-1604))

Hildebrand, Michael S., Coman, D., Yang, T., Gardner, R. J., Rose, E., Smith, R. J., Bahlo, M. and Dahl, H. H. (2008). A novel splice site mutation in EYA4 causes DFNA10 hearing loss (American Journal of Medical Genetics 143,14, (1599-1604)). American Journal of Medical Genetics, Part A, 146 (8), 1099-1099. doi: 10.1002/ajmg.a.32134

Primary skeletal dysplasia as a major manifesting feature in an infant with congenital disorder of glycosylation type Ia [4]

Coman, D., Bostock, D., Hunter, M., Kannu, P., Irving, M., Mayne, V., Fietz, M., Jaeken, J. and Savarirayan, R. (2008). Primary skeletal dysplasia as a major manifesting feature in an infant with congenital disorder of glycosylation type Ia [4]. American Journal of Medical Genetics, Part A, 146 (3), 389-392. doi: 10.1002/ajmg.a.32119

Diagnostic dilemma's: The congenital disorders of glycosylation are clinical chameleons

Coman, David J. (2008). Diagnostic dilemma's: The congenital disorders of glycosylation are clinical chameleons. European Journal of Human Genetics, 16 (1), 2-4. doi: 10.1038/sj.ejhg.5201962

Dysmorphism and the inborn errors of metabolism: The importance of the paediatrician

Coman, D., McGill, J. and Savarirayan, Ravi (2008). Dysmorphism and the inborn errors of metabolism: The importance of the paediatrician. Perinatology, 10 (1-2), 1-22.

Deletions revealing recessive genes: Deletions that reveal recessive genes

Coman, David J. and Gardner, R.J. McKinlay (2007). Deletions revealing recessive genes: Deletions that reveal recessive genes. European Journal of Human Genetics, 15 (11), 1103-1104. doi: 10.1038/sj.ejhg.5201919

Two siblings with 46,XY DSD, congenital adrenal hypoplasia, aniridia, craniofacial, and skeletal abnormalities and intrauterine growth retardation: A new syndrome?

Coman, David J., White, Susan M. and Amor, David J. (2007). Two siblings with 46,XY DSD, congenital adrenal hypoplasia, aniridia, craniofacial, and skeletal abnormalities and intrauterine growth retardation: A new syndrome?. American Journal of Medical Genetics, Part A, 143 (18), 2085-2088. doi: 10.1002/ajmg.a.31894

A novel splice site mutation in EYA4 causes DFNA10 hearing loss

Hildebrand, Michael S., Coman, David, Yang, Tao, Gardner, R.J. McKinlay, Rose, Elizabeth, Smith, Richard J.H., Bahlo, Melanie and Dahl, Hans-Henrik M. (2007). A novel splice site mutation in EYA4 causes DFNA10 hearing loss. American Journal of Medical Genetics, Part A, 143 (14), 1599-1604. doi: 10.1002/ajmg.a.31860

Congenital disorder of glycosylation type 1a: Three siblings with a mild neurological phenotype

Coman, D., McGill, J., MacDonald, R., Morris, D., Klingberg, S., Jaeken, J. and Appleton, D. (2007). Congenital disorder of glycosylation type 1a: Three siblings with a mild neurological phenotype. Journal of Clinical Neuroscience, 14 (7), 668-672. doi: 10.1016/j.jocn.2006.04.008

Carbamyl phosphate synthase deficiency: Diagnosed during pregnancy in a 41-year-old

Eather, G., Coman, D., Lander, C. and McGill, J. (2006). Carbamyl phosphate synthase deficiency: Diagnosed during pregnancy in a 41-year-old. Journal of Clinical Neuroscience, 13 (6), 702-706. doi: 10.1016/j.jocn.2005.07.014

Long-term follow-up of patients with idiopathic infantile hypercalcaemia

Huang J., Coman D., McTaggart S.J. and Burke J.R. (2006). Long-term follow-up of patients with idiopathic infantile hypercalcaemia. Pediatric Nephrology, 21 (11), 1676-1680. doi: 10.1007/s00467-006-0217-0

Renal transplantation in a 14-year-old girl with vitamin B12-responsive cblA-type methylmalonic acidaemia

Coman D., Huang J., McTaggart S., Sakamoto O., Ohura T., McGill J. and Burke J. (2006). Renal transplantation in a 14-year-old girl with vitamin B12-responsive cblA-type methylmalonic acidaemia. Pediatric Nephrology, 21 (2), 270-273. doi: 10.1007/s00467-005-2071-x

Seizures, ataxia, developmental delay and the general paediatrician: Glucose transporter 1 deficiency syndrome

Coman, David J., Sinclair, K. G., Burke, C. J., Appleton, D. B., Pelekanos, J. T., ONeil, C. M., Wallace, G. B., Bowling, F. G., Wang, D., De Vivo, D. C. and McGill, J. J. (2006). Seizures, ataxia, developmental delay and the general paediatrician: Glucose transporter 1 deficiency syndrome. Journal of Paediatrics and Child Health, 42 (5), 263-267. doi: 10.1111/j.1440-1754.2006.00852.x

Congenital disorder of glycosylation type Ia in a 6-year-old girl with a mild intellectual phenotype: Two novel PMM2 mutations

Coman, David, Klingberg, S., Morris, D., McGill, J. and Mercer, H. (2005). Congenital disorder of glycosylation type Ia in a 6-year-old girl with a mild intellectual phenotype: Two novel PMM2 mutations. Journal of Inherited Metabolic Disease, 28 (6), 1189-1190. doi: 10.1007/s10545-005-0166-y

Severe hypernatraemic dehydration in a breast-fed neonate

Coman, David and Mercer, Hilary (2005). Severe hypernatraemic dehydration in a breast-fed neonate. Journal of Paediatrics and Child Health, 41 (8), 458-459. doi: 10.1111/j.1440-1754.2005.00670.x

The Australian Genomic Health Alliance Mitochondrial Flagship - A national approach to genomic diagnostics

Thorburn, D., Baker, N., Balasubramaniam, S., Bratkovic, D., Coman, D., Compton, A., Delatycki, M., Ellaway, C., Fahey, M., Fletcher, J., Frazier, A., Ghaoui, R., Goel, H., Hock, D., Kava, M., Lake, N., Lamont, P., Lee, J., Panetta, J., Phillips, L., Rius, R., Ryan, M., Smith, N., Stroud, D., Tchan, M., Walsh, M., Wallis, M., Welch, A., Wools, C. and Christodoulou, J. (2020). The Australian Genomic Health Alliance Mitochondrial Flagship - A national approach to genomic diagnostics. LONDON: SPRINGERNATURE.

Dizygotic twins with skeletal dysplasia and resistance to hormones signalling through G protein-coupled receptors and the Gsa/cAMP/PKA pathway - severe craniosynostosis and hypertrophic cardiomyopathy

Sharwood, Erin F., McGill, Michael, Koorts, P. J., Coman, David and Conwell, Louise S. (2015). Dizygotic twins with skeletal dysplasia and resistance to hormones signalling through G protein-coupled receptors and the Gsa/cAMP/PKA pathway - severe craniosynostosis and hypertrophic cardiomyopathy. International Society of Paediatric and Adolescent Diabetes / Australasian Paediatric Endocrine Group Annual Scientific Meeting, Brisbane, Queensland, Australia, October 2015.

Dizygotic twins with skeletal dysplasia and resistance to hormones signalling through G protein-coupled receptors and the Gsa/cAMP/PKA pathway - severe craniosynostosis and hypertrophic cardiomyopathy

Sharwood, E. F., McGill, M., Koorts, P. J., Coman, D. and Conwell, L. S. (2015). Dizygotic twins with skeletal dysplasia and resistance to hormones signalling through G protein-coupled receptors and the Gsa/cAMP/PKA pathway - severe craniosynostosis and hypertrophic cardiomyopathy. Children's Health Queensland Research Conference, Brisbane, Queensland, Australia, December 2015.

Information processing in a child with Galactosaemia: an examination using behavioural and neuropysiological measures

Lewis, Fiona M., Knueppfer, Christina and Coman, David J. (2015). Information processing in a child with Galactosaemia: an examination using behavioural and neuropysiological measures. Federation of European Societies of Neuropsychology, Tampere, Finland, 9-11 September 2015. doi: 10.13140/RG.2.1.3218.9923

Early communicative skills in galactosaemia

Lewis, F. M., Coman, D. J., Kilcoyne, S., Syrmis, M. and Murdoch, B. E. (2012). Early communicative skills in galactosaemia. Developmental Neurorehabilitation Conference, Jasper, Canada, 15-16 December 2012.

Stability of language skills despite marked leukoencephalopathic changes in a child with Leber Hereditary Optic Neuropathy following CNS-directed leukaemia treatment

Lewis, Fiona M, Coman, David J and Murdoch, Bruce E (2011). Stability of language skills despite marked leukoencephalopathic changes in a child with Leber Hereditary Optic Neuropathy following CNS-directed leukaemia treatment. XX World Congress of Neurology, Marrakech, Morocco, 12-17 November 2011.

The emergence and development of language in infants and children with a diagnosis of galactosaemia

Coman, David J., Lewis, Fiona M., Murdoch, Bruce E. and Syrmis, Maryann (2011). The emergence and development of language in infants and children with a diagnosis of galactosaemia. 3rd Annual Australasian Clinical Metabolic Meeting, Brisbane, QLD, Australia Australia, 18-19 March 2011.