photo of

Details

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, Maier, A, Zanin, J, Haebich, KM, North, KN, Orsini, F, Dabscheck, G, Delatycki, MB, Payne, JM. A randomized controlled trial of remote microphone listening devices to treat auditory deficits in children with neurofibromatosis type 1.. Neurol Sci 43(9) : 5637 -5641 2022
    view publication
  • Stutterd, CA, Vanderver, A, Lockhart, PJ, Helman, G, Pope, K, Uebergang, E, Love, C, Delatycki, MB, Thorburn, D, Mackay, MT, et al. Unclassified white matter disorders: A diagnostic journey requiring close collaboration between clinical and laboratory services.. Eur J Med Genet 65(9) : 104551 2022
    view publication
  • Tiller, JM, Keogh, LA, McInerney-Leo, AM, Belcher, A, Barlow-Stewart, K, Boughtwood, T, Gleeson, P, Dowling, G, Prince, A, Bombard, Y, et al. A step forward, but still inadequate: Australian health professionals' views on the genetics and life insurance moratorium.. J Med Genet 59(8) : 817 -826 2022
    view publication
  • Cloney, T, Gallacher, L, Pais, LS, Tan, NB, Yeung, A, Stark, Z, Brown, NJ, McGillivray, G, Delatycki, MB, de Silva, MG, et al. Lessons learnt from multifaceted diagnostic approaches to the first 150 families in Victoria's Undiagnosed Diseases Program.. J Med Genet 59(8) : 748 -758 2022
    view publication
  • Huq, AJ, Thompson, B, Bennett, MF, Bournazos, A, Bommireddipalli, S, Gorelik, A, Schultz, J, Sexton, A, Purvis, R, West, K, et al. Clinical impact of whole-genome sequencing in patients with early-onset dementia.. J Neurol Neurosurg Psychiatry 2022
    view publication