Grant Robert Sutherland
Grant Robert Sutherland AC (born 2 June 1945) is an Australian human geneticist and celebrated cytogeneticist. Professor Sutherland was the Director, Department of Cytogenetics and Molecular Genetics, Adelaide Women's and Children's Hospital for 27 years (1975-2002). He developed methods to allow the reliable observation of fragile sites on chromosomes. These studies culminated in the recognition of fragile X syndrome as the most common familial form of intellectual impairment.[1] His group contributed significantly to the mapping of human chromosome 16 and positional cloning of genes on this chromosome. In clinical cytogenetics, he has many publications including a book on genetic counseling for chromosome abnormalities that has become the standard work in this area. He is a past President of the Human Genetics Society of Australasia and of the Human Genome Organisation.[2][3]
Grant Robert Sutherland | |
|---|---|
| Born | 2 June 1945 Bairnsdale, Australia |
| Alma mater | University of Melbourne (BSc), (MSc); University of Edinburgh (PhD), (D.Sc.) |
| Known for | Discovery of chromosomal fragile sites, Cloning of chromosome 16 |
| Awards | Australia Prize (1998), Centenary Medal (2001), Australian Achiever (2001), Companion of the Order of Australia (1998) |
| Scientific career | |
| Fields | Human Genetics |
| Institutions | Women's and Children's Hospital, University of Adelaide |
References
- Sutherland, Grant Robert, (FAA, FRS) (1945-). (2008). In Trove. Retrieved October 2, 2021, from https://nla.gov.au/nla.party-509081
- Australian Academy of Science. "Professor Grant Sutherland". Retrieved 2 October 2021.
- University of Adelaide. "Citation for the Degree of Doctor of Medicine (honoris causa)" (PDF). Retrieved 2 October 2021.