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
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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
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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
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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
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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
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