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Role Clinical Geneticist
Group Clinical Services
Professor Martin Delatycki is a co-director of the Bruce Lefroy Centre at the Murdoch Children's Research Institute (MCRI) and a clinical geneticist at the Victorian Clinical Genetics Services (VCGS). Martin studied medicine at the University of Melbourne and trained in paediatrics at The Royal Children’s Hospital (RCH).

Martin subsequently trained in Clinical Genetics at VCGS and then obtained his PhD for work on Friedreich ataxia through the MCRI. His research and clinical interests are neurogenetics and community genetics. Martin has over 250 publications and has obtained over $5 million in research funding.
Professor Martin Delatycki is a co-director of the Bruce Lefroy Centre at the Murdoch Children's Research Institute (MCRI) and a clinical geneticist at the Victorian Clinical Genetics Services (VCGS). Martin studied medicine at the University of...
Professor Martin Delatycki is a co-director of the Bruce Lefroy Centre at the Murdoch Children's Research Institute (MCRI) and a clinical geneticist at the Victorian Clinical Genetics Services (VCGS). Martin studied medicine at the University of Melbourne and trained in paediatrics at The Royal Children’s Hospital (RCH).

Martin subsequently trained in Clinical Genetics at VCGS and then obtained his PhD for work on Friedreich ataxia through the MCRI. His research and clinical interests are neurogenetics and community genetics. Martin has over 250 publications and has obtained over $5 million in research funding.

Top Publications

  • Massie, J, Delatycki, M. Letters to the Editor. Journal of Paediatrics and Child Health 44(4) : 233 -233 2008
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  • Brody, KM, Taylor, JM, Wilson, GR, Delatycki, MB, Lockhart, PJ. Regional and cellular localisation of Parkin co-regulated gene in developing and adult mouse brain.. Brain Res 1201: 177 -186 2008
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  • Fahey, MC, White, O, Cremer, PD, Millist, L, Aw, S, Corben, LA, Churchyard, A, Delatycki, MB. 458: Vestibular, saccadic and fixation abnormalities in genetically confirmed Friedreich Ataxia. Journal of Clinical Neuroscience 15(3) : 362 -363 2008
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  • Allen, KJ, Nisselle, AE, Collins, VR, Williamson, R, Delatycki, MB. Asymptomatic individuals at genetic risk of haemochromatosis take appropriate steps to prevent disease related to iron overload.. Liver Int 28(3) : 363 -369 2008
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  • Duncan, RE, Gillam, L, Savulescu, J, Williamson, R, Rogers, JG, Delatycki, MB. "You're one of us now": young people describe their experiences of predictive genetic testing for Huntington disease (HD) and familial adenomatous polyposis (FAP).. Am J Med Genet C Semin Med Genet 148C(1) : 47 -55 2008
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