David D. Weaver

A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay

Santhosh Girirajan, Jill A. Rosenfeld, Gregory M. Cooper et al. · Nature Genetics · 2010 · 674 citations · Full text

Medicine, Genetics, Molecular Genetics +10

Mutations in EZH2 Cause Weaver Syndrome

William T. Gibson, Rebecca L. Hood, Shing H. Zhan et al. · The American Journal of Human Genetics · 2011 · 328 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Wiedemann-Beckwith syndrome: presentation of clinical and cytogenetic data on 22 new cases and review of the literature

Mark J. Pettenati, Jonathan L. Haines, Rodney R. Higgins et al. · Human Genetics · 1986 · 301 citations

Life Sciences, Genetics, Pathology +12

Mutations in PIEZO2 Cause Gordon Syndrome, Marden-Walker Syndrome, and Distal Arthrogryposis Type 5

Margaret J. McMillin, Anita E. Beck, Jessica X. Chong et al. · The American Journal of Human Genetics · 2014 · 218 citations · Full text

Life Sciences, Genetics, Molecular Genetics +4

A new overgrowth syndrome with accelerated skeletal maturation, unusual facies, and camptodactyly

David D. Weaver, C. Benjamin Graham, I. T. Thomas et al. · The Journal of Pediatrics · 1974 · 179 citations

Medicine, Developmental Biology, Genetics +16