Lynette S. Penney

Phenotypic Heterogeneity of Genomic Disorders and Rare Copy-Number Variants

Santhosh Girirajan, Jill A. Rosenfeld, Bradley P. Coe et al. · New England Journal of Medicine · 2012 · 620 citations · Full text

Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance

Frank J. Kaiser, Morad Ansari, Diana Braunholz et al. · Human Molecular Genetics · 2014 · 146 citations · Full text

Genetics, Immunodeficiencies, Genetic Epidemiology +27

A Fifth Locus for Bardet-Biedl Syndrome Maps to Chromosome 2q31

Terry‐Lynn Young, Lynette S. Penney, Michael O. Woods et al. · The American Journal of Human Genetics · 1999 · 125 citations · Full text

Cytogenetics, Genetic Disorder, Genetics +7

The complex behavioral phenotype of 15q13.3 microdeletion syndrome

Mark N. Ziats, Robin P. Goin‐Kochel, Leandra N. Berry et al. · Genetics in Medicine · 2016 · 99 citations · Full text

Genetic Disorder, Genetics, Medicine +2

Germline Mutations in MAP3K6 Are Associated with Familial Gastric Cancer

Daniel Gaston, Samantha Hansford, Carla Oliveíra et al. · PLoS Genetics · 2014 · 66 citations · Full text

Oncology, Gastrointestinal Oncology, Medicine +12