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 (1945-06-02) 2 June 1945
Bairnsdale, Australia
Alma materUniversity of Melbourne
(BSc), (MSc);
University of Edinburgh (PhD), (D.Sc.)
Known forDiscovery of chromosomal fragile sites,
Cloning of chromosome 16
AwardsAustralia Prize (1998),
Centenary Medal (2001),
Australian Achiever (2001),
Companion of the Order of Australia (1998)
Scientific career
FieldsHuman Genetics
InstitutionsWomen's and Children's Hospital, University of Adelaide

References

  1. Sutherland, Grant Robert, (FAA, FRS) (1945-). (2008). In Trove. Retrieved October 2, 2021, from https://nla.gov.au/nla.party-509081
  2. Australian Academy of Science. "Professor Grant Sutherland". Retrieved 2 October 2021.
  3. University of Adelaide. "Citation for the Degree of Doctor of Medicine (honoris causa)" (PDF). Retrieved 2 October 2021.


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