
Uta Francke
Medical Genetics / Clinical Genetics (M.D.)
Credentials: · ·
History
- 1970–1971
UCLA Medical Genetics and Genomics Fellowship (1971) CA

- 1963–1967
Research
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
Nature Genetics · 1999 · 3,827 citations
Science · 1985 · 1,727 citations
Human proto-oncogene c-kit: a new cell surface receptor tyrosine kinase for an unidentified ligand
The EMBO Journal · 1987 · 1,537 citations
- BD
18 papers · 17 as a resident

13 papers · 2 as a fellow
- MB
10 papers

8 papers
- BL
7 papers

6 papers

6 papers
- NS
6 papers
Grants
- 2002–2007
Imprinted SnoRNA Genes in the PWS Deletion Region
National Institute of Child Health and Human Development · R01
Contact PI · $1.1M · Stanford University
- 2001–2007
Function of Genes in Williams Syndrome Deletion Region
National Institute of Child Health and Human Development · R01
Contact PI · $2.2M · Stanford University
- 2004–2006
General Clinical Research Center
National Center for Research Resources · M01
Project lead · $11.2K · Stanford University
- 2000–2005
Postdoctoral Training in Medical Genetics
National Institute of General Medical Sciences · T32
Contact PI · $772.4K · Stanford University


