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Authors whose works are in public domain in at least one jurisdiction

List of works by Chia-Hsiang Chen

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Genome-wide association study of treatment refractory schizophrenia in Han Chinese

scientific journal article
High-resolution copy number variation analysis of schizophrenia in Japan.

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

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

scientific article published on 28 August 2015
Increased gene expression of FOXP1 in patients with autism spectrum disorders

scientific article published on July 2013
Genetic analysis of GABRB3 as a candidate gene of autism spectrum disorders

scientific article
Role of the DLGAP2 gene encoding the SAP90/PSD-95-associated protein 2 in schizophrenia

scientific article published on 08 January 2014
Narcolepsy–cataplexy and schizophrenia in adolescents

scientific article published on October 26, 2013
Genetic analysis of the DLGAP1 gene as a candidate gene for schizophrenia.

scientific article published on 31 August 2012
Exonic resequencing of the DLGAP3 gene as a candidate gene for schizophrenia

scientific article published on 13 February 2013
Runs of homozygosity associated with speech delay in autism in a taiwanese han population: evidence for the recessive model

scientific article
Genetic analysis of GABRB3 at 15q12 as a candidate gene of schizophrenia.

scientific article published in August 2014
Seroprevalence survey of selective anti-neuronal autoantibodies in patients with first-episode schizophrenia and chronic schizophrenia.

scientific article published on 21 March 2017
Rare mutations and hypermethylation of the ARC gene associated with schizophrenia

scientific article published on 24 July 2016
Chronic methamphetamine treatment reduces the expression of synaptic plasticity genes and changes their DNA methylation status in the mouse brain

scientific article
Association Analysis of GABRB3 Promoter Variants with Heroin Dependence

scientific article published on July 15, 2014
Neuroligin 2 R215H Mutant Mice Manifest Anxiety, Increased Prepulse Inhibition, and Impaired Spatial Learning and Memory

scientific article published on 27 November 2017
High resolution analysis of rare copy number variants in patients with autism spectrum disorder from Taiwan

scientific article published on 20 September 2017
Resequencing of early growth response 2 (EGR2) gene revealed a recurrent patient-specific mutation in schizophrenia.

scientific article published on 6 June 2015
Development of a Melting Curve-Based Allele-Specific PCR of Apolipoprotein E (APOE) Genotyping Method for Genomic DNA, Guthrie Blood Spot, and Whole Blood

scientific article published on April 14, 2016
Clinical and molecular characterization of three genomic rearrangements at chromosome 22q13.3 associated with autism spectrum disorder

scientific article published on 11 November 2016
Impairment of social behaviors in Arhgef10 knockout mice

scientific article published on 13 February 2018
ARHGEF10 knockout inhibits platelet aggregation and protects mice from thrombus formation

scientific article published on 11 August 2017
FamPipe: An Automatic Analysis Pipeline for Analyzing Sequencing Data in Families for Disease Studies

scientific article
Construction and Analysis of Protein-Protein Interaction Network of Heroin Use Disorder

scientific article published on 21 March 2019
Whole Genome Sequencing Revealed Inherited Rare Oligogenic Variants Contributing to Schizophrenia and Major Depressive Disorder in Two Families

scientific article published in 2023
A Simple Cell-based Immunofluorescence Assay to Detect Autoantibody Against the N-Methyl-D-Aspartate (NMDA) Receptor in Blood

scientific article published on 9 January 2018
Neuropsychiatric complications in a patient with Marfan syndrome.

scientific article published in August 2013
Neuregulin 2 Is a Candidate Gene for Autism Spectrum Disorder

scientific article published in 2024

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