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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

  • Nisselle, AE, Delatycki, MB, Collins, V, Metcalfe, S, Aitken, MA, du Sart, D, Halliday, J, Macciocca, I, Wakefield, A, Hill, V, et al. Implementation of HaemScreen, a workplace-based genetic screening program for hemochromatosis.. Clin Genet 65(5) : 358 -367 2004
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  • Turner, G, Lower, KM, White, SM, Delatycki, M, Lampe, AK, Wright, M, Smith, JC, Kerr, B, Schelley, S, Hoyme, HE, et al. The clinical picture of the Börjeson-Forssman-Lehmann syndrome in males and heterozygous females with PHF6 mutations.. Clin Genet 65(3) : 226 -232 2004
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  • Voncken, M, Ioannou, P, Delatycki, MB. Friedreich ataxia-update on pathogenesis and possible therapies.. Neurogenetics 5(1) : 1 -8 2004
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  • Delatycki, MB, Powell, LW, Allen, KJ. Hereditary hemochromatosis genetic testing of at-risk children: what is the appropriate age?. Genet Test 8(2) : 98 -103 2004
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  • Pollard, LM, Sharma, R, Gómez, M, Shah, S, Delatycki, MB, Pianese, L, Monticelli, A, Keats, BJB, Bidichandani, SI. Replication-mediated instability of the GAA triplet repeat mutation in Friedreich ataxia.. Nucleic Acids Res 32(19) : 5962 -5971 2004
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