Uta Francke
Uta Francke | |
|---|---|
| Born | 1942 |
| Education | Doctor of Medicine, University of Munich, 1967 |
Uta Francke is a German-American physician-geneticist known for her accomplishments in mapping genes to specific chromosome locations and discovering the genes and underlying mutations responsible for Prader-Willi and Rett syndromes. Her work on detailed mapping of human chromosome laid the foundation of the Human Genome Project and discovery of many other rare genetic disorders. She is currently a professor of Genetics and Pediatrics Emerita at Stanford University. She has also served as a consultant to 23andMe Inc since 2007,[1] and as a part-time employee from 2010-2013.[2]
Francke is a past-president of the American Society of Human Genetics (ASHG) and a founding member of the American College of Medical Genetics.
Early life[edit]
Francke was born in 1942 in a small town just north of Frankfurt, Germany. Her father, who had a law degree, fought for Germany in World War II, and her mother was an elementary school teacher. Francke's father died from what was assumed as a heart attack at age 46, when she was 12 years old.[3] Francke became interested in medicine after high school and eventually graduated from University of Munich in 1967 with a M.D.[3] In 1978, Uta Francke got a license to fly a small plane and joined a flying club in New Haven.[3]
Research[edit]
Dr. Uta Francke's research spans across five decades ranging from human and mouse chromosome identification and gene mapping to the discovery of genes involved in heritable disorders and their functions. Her laboratory developed mouse models for human micro-deletion syndromes as well as the original nomenclature for band patterns of mouse chromosomes. Francke has been a HHMI investigator from 1989 to 2000.[4]
She has over 500 peer-reviewed publications with groundbreaking insights into Charcot–Marie–Tooth disease, Marfan syndrome, Prader–Willi syndrome, and Williams syndrome.[5] In 1994, her laboratory discovered the gene for the inherited immunodeficiency Wiskott–Aldrich syndrome. In 1999, she co-discovered the gene for Rett syndrome, an autism-like disorder that is one of the most common causes of developmental mental disability among girls.
Awards[edit]
- Original Member, Highly Cited Researchers database, ISI (2002)
- Antoine Marfan Award, National Marfan Foundation (1996)
- President, International Federation of Human Genetics Societies (2000-2002)
- Elected President, American Society of Human Genetics (1999)
- Elected Member, American Academy of Arts and Sciences (1997)
- Elected Fellow, American Association for the Advancement of Science (1995)
- Elected Member, Institute of Medicine (National Academies) (1990)
- Elected Associate Member, European Molecular Biology Organization (2009)
- Colonel Harland Sanders Lifetime Achievement Award in Genetics, March of Dimes Birth Defects Foundation (2001)
- William Allan Award, American Society for Human Genetics (2012)
- Award for Excellence in Molecular Diagnostics, Association for Molecular Pathology (2014)[6]
References[edit]
- ^ "23andMe's Uta Francke Lauded by ASHG". 23andMe Blog. 2012-11-09. Retrieved 2018-05-25.
- ^ "Uta Francke's Profile". profiles.stanford.edu. Retrieved 2018-05-25.
- ^ a b c Azvolinsky, Anna (2018-05-01). "Rare Disease Geneticist: A Profile of Uta Francke". The Scientist Magazine®. Retrieved 2019-12-16.
- ^ "Uta Francke, MD". HHMI.org. Retrieved 2018-05-25.
- ^ "Uta Francke's Publications". profiles.stanford.edu. Retrieved 2018-05-25.
- ^ "Past Recipients". Association for Molecular Pathology. Retrieved 2023-04-12.
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