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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

  • Rance, G, Corben, L, Barker, E, Carew, P, Chisari, D, Rogers, M, Dowell, R, Jamaluddin, S, Bryson, R, Delatycki, MB. Auditory perception in individuals with Friedreich's ataxia.. Audiol Neurootol 15(4) : 229 -240 2010
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  • Fielding, J, Corben, L, Cremer, P, Millist, L, White, O, Delatycki, M. Disruption to higher order processes in Friedreich ataxia.. Neuropsychologia 48(1) : 235 -242 2010
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  • Folker, J, Murdoch, B, Cahill, L, Delatycki, M, Corben, L, Vogel, A. Dysarthria in Friedreich's ataxia: a perceptual analysis.. Folia Phoniatr Logop 62(3) : 97 -103 2010
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  • Hulsebos, TJM, Kenter, SB, Jakobs, ME, Baas, F, Chong, B, Delatycki, MB. SMARCB1/INI1 maternal germ line mosaicism in schwannomatosis.. Clin Genet 77(1) : 86 -91 2010
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  • Ioannou, L, Massie, J, Collins, V, McClaren, B, Delatycki, MB. Population-based genetic screening for cystic fibrosis: attitudes and outcomes.. Public Health Genomics 13(7-8) : 449 -456 2010
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