Alecia Willis

Clinical Whole-Exome Sequencing for the Diagnosis of Mendelian Disorders

Yaping Yang, Donna M. Muzny, Jeffrey G. Reid et al. · New England Journal of Medicine · 2013 · 1.9K citations · Full text

Molecular Findings Among Patients Referred for Clinical Whole-Exome Sequencing

Yaping Yang, Donna M. Muzny, Fan Xia et al. · JAMA · 2014 · 1.4K citations · Full text

Functional Consequences of PRODH Missense Mutations

Hans‐Ulrich Bender, Shlomo Almashanu, Gary Steel et al. · The American Journal of Human Genetics · 2005 · 149 citations · Full text

Somatic Variant, Genetic Disorder, Genetics +5

Multilocus Analysis of Hypertension: A Hierarchical Approach

Scott M. Williams, Marylyn D. Ritchie, John A. Phillips et al. · Human Heredity · 2004 · 131 citations

Hypertension, Genetics, Genetic Epidemiology +27

Consensus interpretation of the p.Met34Thr and p.Val37Ile variants in GJB2 by the ClinGen Hearing Loss Expert Panel

Jun Shen, Andrea M. Oza, Ignacio del Castillo et al. · Genetics in Medicine · 2019 · 98 citations · Full text

Genetics, P.val37ile Variants, Genetic Epidemiology +5