Chia-hsiang Chen

Taoyuan, TNQ, Taiwan

Last Updated: 09/26/2026

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Found 59 publications

Deletion of Fbxo25 causes excessive repetitive behavior, impaired recognition memory, reduced dendritic complexity, and aberrant protein expression in mice.

Deletion of Fbxo25 causes excessive repetitive behavior, impaired recognition memory, reduced dendritic complexity, and aberrant protein expression in mice.

Journal: Progress in neurobiology

Published: August 19, 2025

Altered odor perception in Dlgap2 mutant mice, a mouse model of autism spectrum disorder.

Altered odor perception in Dlgap2 mutant mice, a mouse model of autism spectrum disorder.

Journal: Behavioural brain research

Published: August 09, 2024

Neuregulin 2 Is a Candidate Gene for Autism Spectrum Disorder.

Neuregulin 2 Is a Candidate Gene for Autism Spectrum Disorder.

Journal: International journal of molecular sciences

Published: March 26, 2024

Whole Genome Sequencing Revealed Inherited Rare Oligogenic Variants Contributing to Schizophrenia and Major Depressive Disorder in Two Families.

Whole Genome Sequencing Revealed Inherited Rare Oligogenic Variants Contributing to Schizophrenia and Major Depressive Disorder in Two Families.

Journal: International journal of molecular sciences

Published: May 04, 2023

Actin-related protein 6 facilitates proneural protein-induced gene activation for rapid neural differentiation.

Actin-related protein 6 facilitates proneural protein-induced gene activation for rapid neural differentiation.

Journal: Development (Cambridge, England)

Published: June 21, 2022

Altered synaptic protein expression, aberrant spine morphology, and impaired spatial memory in Dlgap2 mutant mice, a genetic model of autism spectrum disorder.

Altered synaptic protein expression, aberrant spine morphology, and impaired spatial memory in Dlgap2 mutant mice, a genetic model of autism spectrum disorder.

Journal: Cerebral cortex (New York, N.Y. : 1991)

Published: May 24, 2022

Two Genetic Mechanisms in Two Siblings with Intellectual Disability, Autism Spectrum Disorder, and Psychosis.

Two Genetic Mechanisms in Two Siblings with Intellectual Disability, Autism Spectrum Disorder, and Psychosis.

Journal: Journal of personalized medicine

Published: May 16, 2022

Identification of rare mutations of the vasoactive intestinal peptide receptor 2 gene in schizophrenia.

Identification of rare mutations of the vasoactive intestinal peptide receptor 2 gene in schizophrenia.

Journal: Psychiatric genetics

Published: March 30, 2022

Decreased Cerebral Amyloid-β Depositions in Patients With a Lifetime History of Major Depression With Suspected Non-Alzheimer Pathophysiology.

Decreased Cerebral Amyloid-β Depositions in Patients With a Lifetime History of Major Depression With Suspected Non-Alzheimer Pathophysiology.

Journal: Frontiers in aging neuroscience

Published: January 19, 2022

Middle-Aged Worker Bees Express Higher Innate Immunity than Young Worker Bees in the Abdomen without the Digestive Tract of Worker Bees Reared in an Incubator.

Middle-Aged Worker Bees Express Higher Innate Immunity than Young Worker Bees in the Abdomen without the Digestive Tract of Worker Bees Reared in an Incubator.

Journal: Insects

Published: December 23, 2021

Involvement of Rare Mutations of SCN9A, DPP4, ABCA13, and SYT14 in Schizophrenia and Bipolar Disorder.

Involvement of Rare Mutations of SCN9A, DPP4, ABCA13, and SYT14 in Schizophrenia and Bipolar Disorder.

Journal: International journal of molecular sciences

Published: November 19, 2021

Translational Study of Copy Number Variations in Schizophrenia.

Translational Study of Copy Number Variations in Schizophrenia.

Journal: International journal of molecular sciences

Published: November 17, 2021

Showing 1-12 of 59

Last Updated: 09/26/2026