Hsin-yao Tsai

Yuli Branch
Hualien City, TNQ 98142, Taiwan

Last Updated: 09/26/2026

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Found 16 publications

Genetic Analysis of the HSPA1A, HSPA1B, and HSPA1L Genes in Patients with Schizophrenia from Taiwan.

Genetic Analysis of the HSPA1A, HSPA1B, and HSPA1L Genes in Patients with Schizophrenia from Taiwan.

Journal: Genes

Published: May 21, 2026

Transcriptomic and proteomic analyses of SH-SY5Y neuroblastoma cells treated with amisulpride.

Transcriptomic and proteomic analyses of SH-SY5Y neuroblastoma cells treated with amisulpride.

Journal: Acta neuropsychiatrica

Published: September 16, 2025

Identification of rare missense variants of ionotropic glutamate receptor N-methyl- D -aspartate 2 genes in patients with schizophrenia.

Identification of rare missense variants of ionotropic glutamate receptor N-methyl- D -aspartate 2 genes in patients with schizophrenia.

Journal: Psychiatric genetics

Published: April 24, 2025

Indicators of HSV1 Infection, ECM-Receptor Interaction, and Chromatin Modulation in a Nuclear Family with Schizophrenia.

Indicators of HSV1 Infection, ECM-Receptor Interaction, and Chromatin Modulation in a Nuclear Family with Schizophrenia.

Journal: Journal of personalized medicine

Published: August 10, 2023

Identification of rare missense mutations in the glutamate ionotropic receptor AMPA type subunit genes in schizophrenia.

Identification of rare missense mutations in the glutamate ionotropic receptor AMPA type subunit genes in schizophrenia.

Journal: Psychiatric genetics

Published: January 09, 2023

Ultrarare Loss-of-Function Mutations in the Genes Encoding the Ionotropic Glutamate Receptors of Kainate Subtypes Associated with Schizophrenia Disrupt the Interaction with PSD95.

Ultrarare Loss-of-Function Mutations in the Genes Encoding the Ionotropic Glutamate Receptors of Kainate Subtypes Associated with Schizophrenia Disrupt the Interaction with PSD95.

Journal: Journal of personalized medicine

Published: April 07, 2022

Transcriptomic and Proteomic Analysis of CRISPR/Cas9-Mediated ARC-Knockout HEK293 Cells.

Transcriptomic and Proteomic Analysis of CRISPR/Cas9-Mediated ARC-Knockout HEK293 Cells.

Journal: International journal of molecular sciences

Published: April 01, 2022

Identification of ultra-rare missense mutations associated with familial schizophrenia by whole-exome sequencing.

Identification of ultra-rare missense mutations associated with familial schizophrenia by whole-exome sequencing.

Journal: Schizophrenia research

Published: May 24, 2021

Sequencing of the coding regions of GNBIL on chromosome 22q11.2 as a risk gene of schizophrenia.

Sequencing of the coding regions of GNBIL on chromosome 22q11.2 as a risk gene of schizophrenia.

Journal: Psychiatry research

Published: February 04, 2021

Differential Expression of Multiple Disease-Related Protein Groups Induced by Valproic Acid in Human SH-SY5Y Neuroblastoma Cells.

Differential Expression of Multiple Disease-Related Protein Groups Induced by Valproic Acid in Human SH-SY5Y Neuroblastoma Cells.

Journal: Brain sciences

Published: July 10, 2020

Genetic analysis of the NR2E1 gene as a candidate gene of schizophrenia.

Genetic analysis of the NR2E1 gene as a candidate gene of schizophrenia.

Journal: Psychiatry research

Published: May 18, 2020

Multiple Rare Risk Coding Variants in Postsynaptic Density-Related Genes Associated With Schizophrenia Susceptibility.

Multiple Rare Risk Coding Variants in Postsynaptic Density-Related Genes Associated With Schizophrenia Susceptibility.

Journal: Frontiers in genetics

Published: January 03, 2020

Showing 1-12 of 16

Last Updated: 09/26/2026