Anita Rauch
University of Zurich(CH)
Publications by Year
Research Areas
Genomic variations and chromosomal abnormalities, Genetics and Neurodevelopmental Disorders, Genomics and Rare Diseases, Congenital heart defects research, RNA modifications and cancer
Most-Cited Works
- → Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study(2012)1,063 cited
- → Germline KRAS mutations cause Noonan syndrome(2006)738 cited
- → Transcription Factor E2-2 Is an Essential and Specific Regulator of Plasmacytoid Dendritic Cell Development(2008)650 cited
- → Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes(2010)506 cited
- → Diagnostic yield of various genetic approaches in patients with unexplained developmental delay or mental retardation(2006)445 cited
- → Mutations in the Pericentrin ( PCNT ) Gene Cause Primordial Dwarfism(2008)393 cited
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