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
Pandolfo, M, Arpa, J, Delatycki, MB, Le Quan Sang, KH, Mariotti, C, Munnich, A, Sanz-Gallego, I, Tai, G, Tarnopolsky, MA, Taroni, F, et al.
Deferiprone in Friedreich ataxia: a 6-month randomized controlled trial..
Ann Neurol
76(4)
:
509 -521
2014
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Delatycki, M, Trembath, K.
I20 The Impact Of Lifestyle On The Onset Of Huntington Disease.
Journal of Neurology Neurosurgery & Psychiatry
85(Suppl 1)
:
a64 -a64
2014
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Corben, LA, Kashuk, SR, Akhlaghi, H, Jamadar, S, Delatycki, MB, Fielding, J, Johnson, B, Georgiou-Karistianis, N, Egan, GF.
Myelin paucity of the superior cerebellar peduncle in individuals with Friedreich ataxia: an MRI magnetization transfer imaging study..
J Neurol Sci
343(1-2)
:
138 -143
2014
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Smith, KR, Leventer, RJ, Mackay, MT, Pope, K, Gillies, G, Delatycki, MB, Amor, DJ, Bahlo, M, Lockhart, PJ.
Identification of a novel RNF213 variant in a family with heterogeneous intracerebral vasculopathy..
Int J Stroke
9(6)
:
E26 -E27
2014
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Evans-Galea, MV, Pébay, A, Dottori, M, Corben, LA, Ong, SH, Lockhart, PJ, Delatycki, MB.
Cell and gene therapy for Friedreich ataxia: progress to date..
Hum Gene Ther
25(8)
:
684 -693
2014
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