Elliott H. Sherr

A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders

Flore Zufferey, Elliott H. Sherr, Noam D. Beckmann et al. · Journal of Medical Genetics · 2012 · 347 citations · Full text

Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities

Debra D’Angelo, Sébastien Lebon, Qixuan Chen et al. · JAMA Psychiatry · 2015 · 290 citations · Full text

Agenesis of the corpus callosum in California 1983–2003: A population‐based study

Hannah C. Glass, Gary M. Shaw, Chen Ma et al. · American Journal of Medical Genetics Part A · 2008 · 251 citations · Full text

<i>GFAP</i> mutations, age at onset, and clinical subtypes in Alexander disease

Morgan J. Prust, Jiaxian Wang, Hiroki Morizono et al. · Neurology · 2011 · 249 citations · Full text

Ultra-rare genetic variation in common epilepsies: a case-control sequencing study

Andrew S. Allen, Susannah T. Bellows, Samuel F. Berkovic et al. · The Lancet Neurology · 2017 · 232 citations · Full text

Allelic Variant, Ultra-rare Genetic Variation, Medicine +8