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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

  • Vogel, AP, Brown, SE, Folker, JE, Corben, LA, Delatycki, MB. Dysphagia and swallowing-related quality of life in Friedreich ataxia. Journal of Neurology 261(2) : 392 -399 2014
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  • Evans-Galea, MV, Lockhart, PJ, Galea, CA, Hannan, AJ, Delatycki, MB. Beyond loss of frataxin: the complex molecular pathology of Friedreich ataxia.. Discovery Medicine 17(91) : 25 -35 2014
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  • Massie, J, Delatycki, MB. Cystic Fibrosis Carrier Screening. Paediatric Respiratory Reviews 14(4) : 270 -275 2013
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  • Evans-Galea, MV, Hannan, AJ, Carrodus, N, Delatycki, MB, Saffery, R. Epigenetic modifications in trinucleotide repeat diseases. Trends in Molecular Medicine 19(11) : 655 -663 2013
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  • Seyer, LA, Galetta, K, Wilson, J, Sakai, R, Perlman, S, Mathews, K, Wilmot, GR, Gomez, CM, Ravina, B, Zesiewicz, T, et al. Analysis of the visual system in Friedreich ataxia. Journal of Neurology 260(9) : 2362 -2369 2013
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