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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

  • Ong, SY, Khoo, T, Nicoll, AJ, Gurrin, L, Worland, T, Pateria, P, Ramm, LE, Testro, A, Anderson, GJ, Skoien, R, et al. Utility and limitations of Hepascore and transient elastography to detect advanced hepatic fibrosis in HFE hemochromatosis.. Sci Rep 11(1) : 14654 2021
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  • Tai, G, Corben, LA, Woodcock, IR, Yiu, EM, Delatycki, MB. Determining the Validity of Conducting Rating Scales in Friedreich Ataxia through Video.. Mov Disord Clin Pract 8(5) : 688 -693 2021
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  • Cousens, NE, Tiller, J, Meiser, B, Barlow-Stewart, K, Rowley, S, Ko, Y-A, Mahale, S, Campbell, IG, Kaur, R, Bankier, A, et al. Evaluation of two population screening programmes for BRCA1/2 founder mutations in the Australian Jewish community: a protocol paper.. BMJ Open 11(6) : e041186 2021
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  • Tiller, J, Delatycki, MB. Genetic discrimination in life insurance: a human rights issue.. J Med Ethics 2021
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  • Chopra, M, McEntagart, M, Clayton-Smith, J, Platzer, K, Shukla, A, Girisha, KM, Kaur, A, Kaur, P, Pfundt, R, Veenstra-Knol, H, et al. Heterozygous ANKRD17 loss-of-function variants cause a syndrome with intellectual disability, speech delay, and dysmorphism.. Am J Hum Genet 108(6) : 1138 -1150 2021
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