KatherineARauenMD, PhD

Clinical Genetics

Professor, Pediatrics, UC Davis School of Medicine

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Office
2825 50th St Rm 2284
Uc Davis Mind Institute
Sacramento, CA 95817
Phone+1 916-703-0235

Fax+1 916-703-0243

University of California (San Francisco)Residency, Medical Genetics and Genomics, 1997 - 2000
University of California (San Francisco)Residency, Pediatrics, 1995 - 1997
University of California, Irvine, School of MedicineClass of 1995
University of California, DavisPh.D., Genetics, 1985 - 1992
University of California, DavisMS, Physiology, 1981 - 1985

Presidential Early Career Awards for Scientists and Engineers United States Goverment, 2013

PubMed

33 citations
MEK inhibitors for neurofibromatosis type 1 manifestations: Clinical evidence and consensus.
Peter M K de Blank, Andrea M Gross, Srivandana Akshintala, Jaishri O Blakeley, Gideon Bollag
Neuro-Oncology. 2022-11-02
180 citations
The RASopathies.
Katherine A Rauen
Annual Review of Genomics and Human Genetics. 2013-01-01
307 citations
Revised diagnostic criteria for neurofibromatosis type 1 and Legius syndrome: an international consensus recommendation.
Eric Legius, Ludwine Messiaen, Pierre Wolkenstein, P Pancza, Robert A. Avery
Genetics in Medicine. 2021-05-19

Journal Articles

Proceedings of the Fifth International RASopathies Symposium: When Development and Cancer Intersect
David A Stevenson, Katherine A Rauen, Bruce D Gelb, Corinne M Linardic, Suma Shankar, Brigitte C Widemann, Karen Gripp, Maxim Itkin, American Journal of Medical Genetics Part A
Expanding the Clinical Phenotype of Individuals with a 3-Bp in-Frame Deletion of the NF1 Gene (c.2970_2972del): An Update of Genotype–Phenotype Correlation
Rachel K Hachen, Elizabeth K Schorry, Arthur S Aylsworth, Katherine A Rauen, Ashraf Syed, Daryl A Scott, Lois J Starr, Donald G Basel, Lynne M Bird, Leah W Burke, Mari..., Nature

New Genetic Models of Autism Point to Cellular Roots of DiseaseDecember 6th, 2017
UC Davis Health’s Partnership in Telegenomics Improves Accessibility to Genetic Medicine with Telemedicine RobotsSeptember 2nd, 2021

Genetic Syndromes Of The RAS/MAPK Pathway: From Bedside To Bench And BackEunice Kennedy Shriver National Institute Of Child Health &Human Development2009
Elucidation Of The Genetic Etiology Of Costello SyndromeEunice Kennedy Shriver National Institute Of Child Health &Human Development2005–2009
1st Costello Syndrome SymposiumEunice Kennedy Shriver National Institute Of Child Health &Human Development2007
Clinical Investigation Of The Patient With Chromosome AberrationsNational Center For Research Resources2004–2005