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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

  • Shishegar, R, Harding, IH, Selvadurai, LP, Corben, LA, Delatycki, MB, Egan, GF, Georgiou-Karistianis, N. Longitudinal investigation of brain activation during motor tasks in Friedreich ataxia: 24-month data from IMAGE-FRDA. Brain Structure and Function 227(3) : 809 -819 2022
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  • King, E, Halliday, J, Archibald, AD, Delatycki, M, Barlow-Stewart, K, Newson, AJ, McClaren, BJ. Development and use of the Australian reproductive genetic carrier screening decision aid. European Journal of Human Genetics 30(2) : 194 -202 2022
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  • Bartlett, E, Archibald, AD, Francis, D, Ling, L, Thomas, R, Chandler, G, Ward, L, O'Farrell, G, Pandelache, A, Delatycki, MB, et al. Paternal retraction of a fragile X allele to normal size, showing normal function over two generations. American Journal of Medical Genetics Part A 188(1) : 304 -309 2022
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  • Fanjul‐Fernández, M, Brown, NJ, Hickey, P, Diakumis, P, Rafehi, H, Bozaoglu, K, Green, CC, Rattray, A, Young, S, Alhuzaimi, D, et al. A family study implicates GBE1 in the etiology of autism spectrum disorder. Human Mutation 43(1) : 16 -29 2022
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  • Khan, W, Corben, LA, Bilal, H, Vivash, L, Delatycki, MB, Egan, GF, Harding, IH. Neuroinflammation in the Cerebellum and Brainstem in Friedreich Ataxia: An [18F]‐FEMPA PET Study. Movement Disorders 37(1) : 218 -224 2022
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