List of works by Zhuozhi Wang

A Comprehensive Workflow for Read Depth-Based Identification of Copy-Number Variation from Whole-Genome Sequence Data

scientific article published in January 2018

A high-resolution copy-number variation resource for clinical and population genetics

scientific article published on 11 December 2014

Brain-expressed exons under purifying selection are enriched for de novo mutations in autism spectrum disorder

scientific article

Clinically relevant copy number variations detected in cerebral palsy

scientific article

Complete Disruption of Autism-Susceptibility Genes by Gene Editing Predominantly Reduces Functional Connectivity of Isogenic Human Neurons

article

Complete Disruption of Autism-Susceptibility Genes by Gene Editing Predominantly Reduces Functional Connectivity of Isogenic Human Neurons

Compound heterozygous mutations in the noncoding RNU4ATAC cause Roifman Syndrome by disrupting minor intron splicing.

scientific article

Convergence of genes and cellular pathways dysregulated in autism spectrum disorders

scientific article

Copy number variation in Han Chinese individuals with autism spectrum disorder

scientific article

Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes

scientific article published on 30 December 2013

Genome-wide characteristics of de novo mutations in autism

scientific article published on August 2016

Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test.

scientific article

Molecular Diagnostic Yield of Chromosomal Microarray Analysis and Whole-Exome Sequencing in Children With Autism Spectrum Disorder

scientific article published on September 2015

Rare copy number variation discovery and cross-disorder comparisons identify risk genes for ADHD.

scientific article

Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder

scientific article published on 6 March 2017