Wenqi Zeng

Enhanced utility of family-centered diagnostic exome sequencing with inheritance model–based analysis: results from 500 unselected families with undiagnosed genetic conditions

Kelly D. Farwell, Layla Shahmirzadi, Dima El‐Khechen et al. · Genetics in Medicine · 2014 · 462 citations · Full text

Biotin-Responsive Basal Ganglia Disease Maps to 2q36.3 and Is Due to Mutations in SLC19A3

Wenqi Zeng, Eiman A. Al-Yamani, James S. Acierno et al. · The American Journal of Human Genetics · 2005 · 215 citations · Full text

Neurodegenerative Diseases, Molecular Neuroscience, Medicine +8

Neurexin 1α structural variants associated with autism

Yan Jin, Katie Noltner, Jinong Feng et al. · Neuroscience Letters · 2008 · 152 citations

Structural Variants, Molecular Neuroscience, Neurogenomics +6

<i>ELP2</i> is a novel gene implicated in neurodevelopmental disabilities

Julie S. Cohen, Siddharth Srivastava, Kelly D. Farwell et al. · American Journal of Medical Genetics Part A · 2015 · 73 citations

Congenital lethal motor neuron disease with a novel defect in ribosome biogenesis

Russell J. Butterfield, Tamara J. Stevenson, Lingyan Xing et al. · Neurology · 2014 · 61 citations · Full text