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
Nisselle, AE, Delatycki, MB, Collins, V, Metcalfe, S, Aitken, MA, du Sart, D, Halliday, J, Macciocca, I, Wakefield, A, Hill, V, et al.
Implementation of HaemScreen, a workplace-based genetic screening program for hemochromatosis..
Clin Genet
65(5)
:
358 -367
2004
view publication
Turner, G, Lower, KM, White, SM, Delatycki, M, Lampe, AK, Wright, M, Smith, JC, Kerr, B, Schelley, S, Hoyme, HE, et al.
The clinical picture of the Börjeson-Forssman-Lehmann syndrome in males and heterozygous females with PHF6 mutations..
Clin Genet
65(3)
:
226 -232
2004
view publication
Voncken, M, Ioannou, P, Delatycki, MB.
Friedreich ataxia-update on pathogenesis and possible therapies..
Neurogenetics
5(1)
:
1 -8
2004
view publication
Delatycki, MB, Powell, LW, Allen, KJ.
Hereditary hemochromatosis genetic testing of at-risk children: what is the appropriate age?.
Genet Test
8(2)
:
98 -103
2004
view publication
Pollard, LM, Sharma, R, Gómez, M, Shah, S, Delatycki, MB, Pianese, L, Monticelli, A, Keats, BJB, Bidichandani, SI.
Replication-mediated instability of the GAA triplet repeat mutation in Friedreich ataxia..
Nucleic Acids Res
32(19)
:
5962 -5971
2004
view publication