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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

  • Paznekas, WA, Karczeski, B, Vermeer, S, Lowry, RB, Delatycki, M, Laurence, F, Koivisto, PA, Van Maldergem, L, Boyadjiev, SA, Bodurtha, JN, et al. GJA1 mutations, variants, and connexin 43 dysfunction as it relates to the oculodentodigital dysplasia phenotype.. Hum Mutat 30(5) : 724 -733 2009
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  • Delatycki, MB. Evaluating the progression of Friedreich ataxia and its treatment.. J Neurol 256 Suppl 1: 36 -41 2009
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  • Taylor, JM, Wu, R-M, Lin, C-H, Delatycki, MB, Lockhart, PJ. Lack of evidence for association of a parkin promoter polymorphism with early-onset Parkinson's disease in a Chinese population.. Parkinsonism Relat Disord 15(2) : 149 -152 2009
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  • Bruno, DL, Ganesamoorthy, D, Schoumans, J, Bankier, A, Coman, D, Delatycki, M, Gardner, RJM, Hunter, M, James, PA, Kannu, P, et al. Detection of cryptic pathogenic copy number variations and constitutional loss of heterozygosity using high resolution SNP microarray analysis in 117 patients referred for cytogenetic analysis and impact on clinical practice.. J Med Genet 46(2) : 123 -131 2009
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  • Taylor, JM, Delatycki, MB, Lockhart, PJ. Identification and validation of control cell lines for accurate parkin dosage analysis.. J Neurosci Methods 176(2) : 68 -71 2009
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