David Sillence

David Sillence, AM is the foundation chair (Professor) of Medical Genetics in the University of Sydney. An honours graduate of the University of Sydney, he obtained his MD in Medical Genetics from the University of Melbourne 1978 in Bone Dysplasias.

David Sillence was a founding member of the Human Genetics Society of Australasia (1978), the Australian Teratology Society (1981), the Australian Faculty of Public Health Medicine (1990), and the American College of Medical Genetics (1993) and has held office in the Human Genetics Society of Australasia from 1981 to 2000, often with more than one concurrent position. He has also held office in the Royal Australasian College of Physicians from 1994 to 2000. He has been a member of many committees within the School of Public Health and Tropical Medicine, and the University of Sydney. He currently serves on the education committee of the Human Genetics Society of Australasia, the International Nomenclature Committee for Constitutional Disorders of the Skeletal, the International Mucopolysaccharidosis type I expert committee, the National Fabry Disease and MPS expert committees for the LSDP.

David Sillence was instrumental in establishing the first working party to write guidelines for training in Clinical Genetics in Australia and was granted Clinical Geneticist status (1987) through the grandfather clause. This certification model has been used by other Special Interest Groups within the Human Genetics Society of Australasia. He has been involved in a considerable amount of collaborative research as well as those within his department. He has published over 130 original articles, has contributed over 30 book chapters, 8 books/monographs, and has contributed to conference proceedings more than a dozen times. He has been a peer reviewer/editor to 8 different groups/journals.[1][2]

David Sillence created the first classification system for Osteogenesis Imperfecta that he later developed further to be the world standard. It enabled progress into the molecular causes of the disorder and collagen mutations. (Sillence DO, Senn A, Danks DM (1979). "Genetic heterogeneity in osteogenesis imperfecta". J. Med. Genet. 16 (2): 101–16. doi:10.1136/jmg.16.2.101. PMID 458828.)

In 2012, David delivered the Human Genetics Society of Australasia Oration, a prestigious lecture given by a senior member of the HGSA who has contributed significantly to the discipline over many years.[3] David was made a Member of the Order of Australia (AM) in the 2013 Australia Day Honours.

References
  1. "Informationen zum Thema scientificcommons". En.scientificcommons.org. Retrieved 26 February 2019.
  2. "Archived copy". Archived from the original on 2011-07-16. Retrieved 2009-08-25.CS1 maint: archived copy as title (link)
  3. "Archived copy" (PDF). Archived from the original (PDF) on 2012-03-18. Retrieved 2012-08-26.CS1 maint: archived copy as title (link)
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