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==See also==
==See also==
* [[Zhen-yi Wang]]
* [[List of graduates of University of Hong Kong]]
* [[List of graduates of University of Hong Kong]]



Revision as of 22:16, 18 May 2010

Yuet Wai Kan
簡悅威
Born1936 (age 87–88)
CitizenshipUnited States
Canada
Alma materUniversity of Hong Kong
Known forhuman blood diseases
prenatal diagnosis
DNA diagnosis
DNA polymorphism
AwardsAllan Award (1984)
Gairner Int'l Award (1984)
Lasker Award (1991)
Shaw Prize (2004)
Scientific career
Fieldshuman genetics
Medicine
InstitutionsUniversity of Hong Kong
Queen Mary Hospital
Brigham and Women's Hospital
University of Pittsburgh
MIT
McGill University
Penn
Children's Hospital Boston
Harvard Medical School
San Francisco General Hospital
HHMI
UCSF

Yuet Wai Kan FRS (Chinese: 簡悅威, also written as Yuet-Wai Kan) (born 1936 in Hong Kong), is a Canadian and American medical scientist and physician. He is the current Louis K. Diamond Professor of Hematology and the head of the Division of Molecular Medicine and Diagnostics at the University of California, San Francisco. He is the former President of the American Society of Hematology (ASH)

Biography

Kan was born in Hong Kong in 1936. His brother, Sir Yuet Keung Kan, was the Senior Unofficial Member of the Legislative Council and Executive Council of Hong Kong.

Kan graduated with an M.B.B.S. (in 1958) and M.D. (in 1980) both from the University of Hong Kong School of Medicine. He did his medical training at Queen Mary Hospital, then went to USA for further study.[1]

Since 1976, Kan has been a research investigator of the Howard Hughes Medical Institute.

Kan served as the president of the American Society of Hematology (ASH) in 1990.

Kan is currently a professor in the Department of Laboratory Medicine at the University of California, San Francisco.

Research

Kan is regarded as a pioneer of applying molecular biology and genetics into clinical medicine. Kan was the first to establish that a single DNA mutation could lead to a human disease, and the first to diagnose a human disease by using DNA [2].

Kan has made many fundamental contributions to our understanding of human blood diseases. Kan was the first to discover the gene deletion in human alpha-thalassemia; he was the first to discover a point-mutation causing human beta-thalassemia; with Golbus' help, he was the first to carry out prenatal diagnosis (for a haemoglobinopathy).[3]

Kan is best known for his groundbreaking works in sickle cell and thalassemia. He is the first person who used fetal DNA diagnosis techniques to study these diseases. Kan's work led to the innovation of DNA diagnosis.[4]

Kan discovered DNA polymorphism, which nowadays is widely used in genetic analysis for human diseases.[5]

Honors and awards

See also

References