Valerie Gartner

The Undiagnosed Diseases Network: Accelerating Discovery about Health and Disease

Rachel Ramoni, John J. Mulvihill, David R. Adams et al. · The American Journal of Human Genetics · 2017 · 188 citations · Full text

Public Health, Biomedical Informatics, Health Informatics +13

A Syndromic Neurodevelopmental Disorder Caused by De Novo Variants in EBF3

Hsiao‐Tuan Chao, Mariska Davids, Elizabeth A. Burke et al. · The American Journal of Human Genetics · 2016 · 121 citations · Full text

Medicine, Genetics, Molecular Genetics +14

Positive selection within the genomes of SARS-CoV-2 and other Coronaviruses independent of impact on protein function

Alejandro Berrío, Valerie Gartner, Gregory A. Wray · PeerJ · 2020 · 57 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Looking beyond the exome: a phenotype-first approach to molecular diagnostic resolution in rare and undiagnosed diseases

Loren D.M. Peña, Yong‐Hui Jiang, Kelly Schoch et al. · Genetics in Medicine · 2017 · 52 citations

Life Sciences, Genetics, Molecular Genetics +16

A Recurrent De Novo Variant in NACC1 Causes a Syndrome Characterized by Infantile Epilepsy, Cataracts, and Profound Developmental Delay

Kelly Schoch, Linyan Meng, Szabolcs Szelinger et al. · The American Journal of Human Genetics · 2017 · 51 citations · Full text

Medicine, Genetics, Molecular Genetics +16