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
Li, A, Geyer, FC, Blecua, P, Lee, JY, Selenica, P, Brown, DN, Pareja, F, Lee, SSK, Kumar, R, Rivera, B, et al.
Homologous recombination DNA repair defects in PALB2-associated breast cancers..
NPJ Breast Cancer
5:
23
2019
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Tankard, RM, Bennett, MF, Degorski, P, Delatycki, MB, Lockhart, PJ, Bahlo, M.
Detecting Expansions of Tandem Repeats in Cohorts Sequenced with Short-Read Sequencing Data..
Am J Hum Genet
103(6)
:
858 -873
2018
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Lin, KY, Delatycki, M, Corben, L, Cheung, M, Ferrari, V, Fogel, M, Moir, S, Peverill, R.
Abstract 16863: Cardiac Magnetic Resonance T1 Mapping as a Window Into the Myocardium in Friedreich Ataxia.
Circulation
138(Suppl_1)
:
2018
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Archibald, AD, Smith, MJ, Burgess, T, Scarff, KL, Elliott, J, Hunt, CE, Barns-Jenkins, C, Holt, C, Sandoval, K, Kumar, VS, et al.
Correction: Reproductive genetic carrier screening for cystic fibrosis, fragile X syndrome, and spinal muscular atrophy in Australia: outcomes of 12,000 tests..
Genet Med
20(11)
:
1485
2018
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Forbes Shepherd, R, Lewis, A, Keogh, LA, Werner-Lin, A, Delatycki, MB, Forrest, LE.
A Systematic Review of How Young People Live with Inherited Disease: What Can We Learn for Li-Fraumeni Syndrome?.
J Adolesc Young Adult Oncol
7(5)
:
525 -545
2018
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