Wenqi Zeng

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

Xiang Li, Aaron Elliott, Xiang Li, 2014, Genetics in Medicine.

A human de novo mutation in MYH10 phenocopies the loss of function mutation in mice

W. Chung, Lan Yu, K. Gonzalez, 2013, Rare diseases.

ELP2 is a novel gene implicated in neurodevelopmental disabilities

A. Fatemi, E. Chao, S. Srivastava, 2015, American journal of medical genetics. Part A.

Neurexin 1α structural variants associated with autism

C. Skinner, C. Schwartz, S. Sommer, 2008, Neuroscience Letters.

Genetic analysis of the GRIK2 modifier effect in Huntington's disease

T. Gillis, M. MacDonald, J. Gusella, 2006, BMC Neuroscience.