Ethan M. Lange

REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants

Nilah M. Ioannidis, Joseph H. Rothstein, Vikas Pejaver et al. · The American Journal of Human Genetics · 2016 · 2.8K citations · Full text

Genome-wide Association Study, Allelic Variant, Genotype-phenotype Association +14

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

Daniel Taliun, Daniel Harris, Michael D. Kessler et al. · Nature · 2021 · 2.2K citations · Full text

Inherited causes of clonal haematopoiesis in 97,691 whole genomes

Alexander G. Bick, Joshua S. Weinstock, Satish K. Nandakumar et al. · Nature · 2020 · 698 citations · Full text

Genetic Disorder, Genetics, Hematology +3

Germline Mutations in <i>HOXB13</i> and Prostate-Cancer Risk

Charles M. Ewing, Anna M. Ray, Ethan M. Lange et al. · New England Journal of Medicine · 2012 · 656 citations · Full text

Rare and low-frequency coding variants alter human adult height

Eirini Marouli, Mariaelisa Graff, Carolina Medina‐Gómez et al. · Nature · 2017 · 647 citations · Full text

Allelic Variant, Genetics, Statistical Genetics +2