Xiangbin U. Jia

Center For Medical Genetics And Hunan Key Laboratory Of Medical Genetics
Changsha, China

Last Updated: 09/26/2026

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Found 20 publications

The association between the residential environment and arthritis among the elderly in China: evidence from cohort and cross-sectional studies.

The association between the residential environment and arthritis among the elderly in China: evidence from cohort and cross-sectional studies.

Journal: Journal of global health

Published: August 14, 2026

X-linked SYTL4 missense variant disrupts RAB27A-dependent vesicle trafficking and synaptic transmission in autism.

X-linked SYTL4 missense variant disrupts RAB27A-dependent vesicle trafficking and synaptic transmission in autism.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: July 30, 2026

Genomic landscape of rare variants in a Chinese autism cohort and discovery of novel risk genes.

Genomic landscape of rare variants in a Chinese autism cohort and discovery of novel risk genes.

Journal: Molecular psychiatry

Published: January 05, 2026

Haplotype-resolved long-read sequencing reveals parent-of-origin effects of tandem-repeat variation in autism spectrum disorder.

Haplotype-resolved long-read sequencing reveals parent-of-origin effects of tandem-repeat variation in autism spectrum disorder.

Journal: Science bulletin

Published: December 19, 2025

MSL2 disruption leads to autism-like behaviors, impairs neurogenesis, and alters histone H4K16 acetylation.

MSL2 disruption leads to autism-like behaviors, impairs neurogenesis, and alters histone H4K16 acetylation.

Journal: Cellular and molecular life sciences : CMLS

Published: October 15, 2025

Evidence supporting the role of GIGYF2 in synapse development and autism.

Evidence supporting the role of GIGYF2 in synapse development and autism.

Journal: Molecular psychiatry

Published: July 07, 2025

Disrupting integrator complex subunit INTS6 causes neurodevelopmental disorders and impairs neurogenesis and synapse development.

Disrupting integrator complex subunit INTS6 causes neurodevelopmental disorders and impairs neurogenesis and synapse development.

Journal: The Journal of clinical investigation

Published: January 28, 2025

Csde1 Mediates Neurogenesis via Post-transcriptional Regulation of the Cell Cycle.

Csde1 Mediates Neurogenesis via Post-transcriptional Regulation of the Cell Cycle.

Journal: Neuroscience bulletin

Published: November 01, 2024

Naa15 Haploinsufficiency and De Novo Missense Variants Associate With Neurodevelopmental Disorders and Interfere With Neurogenesis and Neuron Development.

Naa15 Haploinsufficiency and De Novo Missense Variants Associate With Neurodevelopmental Disorders and Interfere With Neurogenesis and Neuron Development.

Journal: Autism research : official journal of the International Society for Autism Research

Published: July 29, 2024

KCTD10 regulates brain development by destabilizing brain disorder-associated protein KCTD13.

KCTD10 regulates brain development by destabilizing brain disorder-associated protein KCTD13.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: March 15, 2024

CELF2 Deficiency Demonstrates Autism-Like Behaviors and Interferes with Late Development of Cortical Neurons in Mice.

CELF2 Deficiency Demonstrates Autism-Like Behaviors and Interferes with Late Development of Cortical Neurons in Mice.

Journal: Molecular neurobiology

Published: October 13, 2023

GIGYF1 disruption associates with autism and impaired IGF-1R signaling.

GIGYF1 disruption associates with autism and impaired IGF-1R signaling.

Journal: The Journal of clinical investigation

Published: March 02, 2022

Showing 1-12 of 20

Last Updated: 09/26/2026