John D. Overton

De novo mutations revealed by whole-exome sequencing are strongly associated with autism

Stephan Sanders, Michael T. Murtha, Abha R. Gupta et al. · Nature · 2012 · 2.1K citations

Neurodevelopmental Disorders, Syndromic Autism, Whole-exome Sequencing +9

De novo mutations in histone-modifying genes in congenital heart disease

Samir Zaidi, Murim Choi, Hiroko Wakimoto et al. · Nature · 2013 · 949 citations · Full text

Genomic Analysis of Non- <i>NF2</i> Meningiomas Reveals Mutations in <i>TRAF7</i> , <i>KLF4</i> , <i>AKT1</i> , and <i>SMO</i>

Victoria Clark, E. Zeynep Erson‐Omay, Akdes Serin et al. · Science · 2013 · 850 citations · Full text

Genetic and Pharmacologic Inactivation of ANGPTL3 and Cardiovascular Disease

Frederick E. Dewey, Viktoria Gusarova, Richard L. Dunbar et al. · New England Journal of Medicine · 2017 · 836 citations · Full text

A Protein-Truncating <i>HSD17B13</i> Variant and Protection from Chronic Liver Disease

Noura S. Abul‐Husn, Xiping Cheng, Alexander Li et al. · New England Journal of Medicine · 2018 · 768 citations · Full text