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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

  • Wang, Y, Gurrin, LC, Wluka, AE, Bertalli, NA, Osborne, NJ, Delatycki, MB, Giles, GG, English, DR, Hopper, JL, Simpson, JA, et al. HFE C282Y homozygosity is associated with an increased risk of total hip replacement for osteoarthritis.. Semin Arthritis Rheum 41(6) : 872 -878 2012
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  • Delatycki, MB, Wolthuizen, M, Collins, V, Varley, E, Craven, J, Allen, KJ, Gurrin, LC, Aitken, M, Trembath, MK, Bond, L, et al. ironXS: high-school screening for hereditary haemochromatosis is acceptable and feasible.. Eur J Hum Genet 20(5) : 505 -509 2012
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  • Szmulewicz, D, MacDougall, H, Curthoys, I, O'Leary, S, Paine, M, Cremer, P, Delatycki, M, Corben, L, Halmagyi, M. Impairment of the Vestibulo-Cerebellar Interaction in Friedreich's Ataxia (P02.252). Neurology 78(Meeting Abstracts 1) : p02.252 -p02.252 2012
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  • Evans-Galea, MV, Carrodus, N, Rowley, SM, Corben, LA, Tai, G, Saffery, R, Galati, JC, Wong, NC, Craig, JM, Lynch, DR, et al. FXN methylation predicts expression and clinical outcome in Friedreich ataxia.. Ann Neurol 71(4) : 487 -497 2012
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  • Delatycki, MB. The ethics of screening for disease.. Pathology 44(2) : 63 -68 2012
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