photo of

Details

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

  • Kennerson, ML, Yiu, EM, Chuang, DT, Kidambi, A, Tso, S-C, Ly, C, Chaudhry, R, Drew, AP, Rance, G, Delatycki, MB, et al. A new locus for X-linked dominant Charcot-Marie-Tooth disease (CMTX6) is caused by mutations in the pyruvate dehydrogenase kinase isoenzyme 3 (PDK3) gene.. Hum Mol Genet 22(7) : 1404 -1416 2013
    view publication
  • Stark, Z, Massie, J, McClaren, B, Ioannou, L, Cousens, N, Lewis, S, Metcalfe, S, Delatycki, MB. Current practice and attitudes of Australian obstetricians toward population-based carrier screening for inherited conditions.. Twin Res Hum Genet 16(2) : 601 -607 2013
    view publication
  • Yiu, E, Tai, G, Peverill, R, Lee, K, Croft, K, Mori, T, Stephenson, S, Lockhart, P, Sarsero, J, Churchyard, A, et al. An Open Label Clinical Pilot Study of Resveratrol as a Treatment for Friedreich Ataxia (S43.006). Neurology 80(7_supplement) : 2013
    view publication
  • Kennerson, M, Yiu, E, Chuang, D, Kidambi, A, Tso, S-C, Ly, C, Chaudhry, R, Drew, A, Rance, G, Delatycki, M, et al. A Combination of Linkage Analysis and Exome Sequencing Identifies a New Gene for X-linked Charcot-Marie-Tooth Neuropathy (S26.007). Neurology 80(7_supplement) : 2013
    view publication
  • Lynch, DR, Pandolfo, M, Schulz, JB, Perlman, S, Delatycki, MB, Payne, RM, Shaddy, R, Fischbeck, KH, Farmer, J, Kantor, P, et al. Common data elements for clinical research in Friedreich's ataxia.. Mov Disord 28(2) : 190 -195 2013
    view publication