Chia-Hsiang Chen

Deep exon resequencing of DLGAP2 as a candidate gene of autism spectrum disorders.

Runs of homozygosity associated with speech delay in autism in a taiwanese han population: evidence for the recessive model.

Genetic analysis of GABRB3 as a candidate gene of autism spectrum disorders.

Association analysis of GABRB3 promoter variants with heroin dependence.

Autism-associated gene Dlgap2 mutant mice demonstrate exacerbated aggressive behaviors and orbitofrontal cortex deficits.

Genome-wide Association Study of Autism Spectrum Disorder in the East Asian Populations.

Genome-Wide Association Study for Autism Spectrum Disorder in Taiwanese Han Population.

Complex genomic variants contribute toward the genetic architecture of autism spectrum disorder.

Dosage of copy number variation at 22q11.2 mediates changes in cognition, social function and brain structure in autism spectrum disorder.

Development of a Melting Curve-Based Allele-Specific PCR of Apolipoprotein E (APOE) Genotyping Method for Genomic DNA, Guthrie Blood Spot, and Whole Blood.

FamPipe: An Automatic Analysis Pipeline for Analyzing Sequencing Data in Families for Disease Studies.

Clinical and molecular characterization of three genomic rearrangements at chromosome 22q13.3 associated with autism spectrum disorder.

Seroprevalence survey of selective anti-neuronal autoantibodies in patients with first-episode schizophrenia and chronic schizophrenia.

High resolution analysis of rare copy number variants in patients with autism spectrum disorder from Taiwan.

Neuroligin 2 R215H Mutant Mice Manifest Anxiety, Increased Prepulse Inhibition, and Impaired Spatial Learning and Memory.