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Dena Matalon

Dena Matalon

Clinical Associate Professor, University of Texas at Austin
BIOGRAPHICAL SKETCH
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NAME: Matalon, Dena
eRA COMMONS USER NAME (credential, e.g., agency login): matalond
POSITION TITLE: Clinical Associate Professor
EDUCATION/TRAINING
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FIELD OF STUDY


University of Texas at Austin; Austin, TX

Jefferson Medical College; Philadelphia, PA

Children's Hospital of Philadelphia; Philadelphia, PA B.S.

M.D.

Residency 05/2007

05/2013

06/2017 Honors Biology

Medical Degree

Pediatrics and Genetics

A. Personal Statement
I am a pediatrician and geneticist with clinical expertise in a wide range of genetically based syndromes. In several publications, my work has better characterized or expanded the phenotypes for genetic syndromes including 17q12/HNF1B deletions (Prenat Diag, 2023), congenital heart disease in the RASopathies (Am J Med Genet A, 2021), and episignature in a neurodevelopmental disorder (Genet Med, 2023). This work contributes to the recognition and appropriate diagnosis leading to improved management and genetic counseling. Currently, I am involved in the Genomics Research to Elucidate the Genetics of Rare disease (GREGoR) Consortium which is a national consortium focused on applying new technologies to discover genetic causes in undiagnosed patients. Finally, my recent work has focused on limiting bias and unfair discrimination in genetic testing (Genet Med, 2023).

B. Positions and Honors
Positions and Employment:
2/2023- present Clinical Associate Professor, Department of Pediatrics, Division of Medical Genetics, Stanford University, Stanford, CA
01/2022- present Director, Perinatal Genetics, Stanford University, Stanford CA
Other Experience and Professional Memberships
2024- Vice-Chair, ACMG Social, Ethical and Legal Issues Committee
Honors

2024 Won, The Berger-Reynolds Distinguished Packard Fellow
2023 Nominated, Department of Pediatrics Annual Advocacy Award
2022 Nominated, Early Career Clinical Excellence Award

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