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
Milne, SC, Corben, LA, Georgiou-Karistianis, N, Delatycki, MB, Yiu, EM.
Rehabilitation for Individuals With Genetic Degenerative Ataxia: A Systematic Review..
Neurorehabil Neural Repair
31(7)
:
609 -622
2017
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Beecroft, SJ, McLean, CA, Delatycki, MB, Koshy, K, Yiu, E, Haliloglu, G, Orhan, D, Lamont, PJ, Davis, MR, Laing, NG, et al.
Expanding the phenotypic spectrum associated with mutations of DYNC1H1..
Neuromuscul Disord
27(7)
:
607 -615
2017
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Tai, G, Corben, LA, Yiu, EM, Delatycki, MB.
A longitudinal study of the SF-36 version 2 in Friedreich ataxia..
Acta Neurol Scand
136(1)
:
41 -46
2017
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Huq, AJ, Pertile, MD, Davis, AM, Landon, H, James, PA, Kline, CF, Vohra, J, Mohler, PJ, Delatycki, MB.
A Novel Mechanism for Human Cardiac Ankyrin-B Syndrome due to Reciprocal Chromosomal Translocation..
Heart Lung Circ
26(6)
:
612 -618
2017
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