Ronald Worton
Ronald G. Worton OC FRSC (born April 2, 1942) is a Canadian doctor.[1]
Born in
The Hospital for Sick Children in Toronto. Worton became geneticist in chief at the hospital and professor of Medical Genetics at the University of Toronto in 1985. In 1996, he became director of research at the Ottawa General Hospital and chief executive officer of the Ottawa Hospital Research Institute, as well as professor of medicine, University of Ottawa.[2]
Worton and his team identified the
Becker muscular dystrophies. Under his leadership, the genetics department at The Hospital for Sick Children also identified genes associated with cystic fibrosis, Fanconi anemia, Wilson's disease, Wilms' tumor[2] and Tay–Sachs disease.[1]
Worton served four years on the board of the
Human Genome Organization, twelve years as associate director for the Canadian Genetic Diseases network, six years as head of the Canadian Genome Analysis and Technology Program and four years as founding scientific director of the Canadian Stem Cell Network.[3]
He was awarded a Gairdner Foundation International Award in 1989,[4] was named an officer of the Order of Canada in 2012[5] and is a fellow of the Royal Society of Canada.[3] He has also received the E. Mead Johnson Award for pediatrics research.[2] In 2014, Worton was inducted into the Canadian Medical Hall of Fame.[1]
Worton has retired from medical research and lives in Oakville, Ontario, spending his winters in Mesa, Arizona.[6]
References
- ^ a b c "Dr. Ronald Worton". Canadian Medical Hall of Fame. 2014. Archived from the original on 2014-07-18.
- ^ a b c "Ronald G. Worton, D.Sc". University of Manitoba. October 19, 2000.
- ^ a b "Ronald Worton". University of Toronto.
- ^ "Ronald G. Worton PhD". Gairdner Foundation.
- ^ "Rick Hillier, Stuart McLean among 44 Order of Canada recipients". CBC News. September 28, 2012.
- ^ "Dr. Ronald Worton". Ottawa Hospital Research Institute.
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