Guang W. He

800 Dongchuan Road
Shanghai, 200240, China

Last Updated: 09/26/2026

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Found 128 publications

Identification of somatostatin+ inhibitory engrams for extinction in the basolateral amygdala.

Identification of somatostatin+ inhibitory engrams for extinction in the basolateral amygdala.

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

Published: March 20, 2026

De novo variants in MAGED1 suggest a role in intellectual disability pathogenesis.

De novo variants in MAGED1 suggest a role in intellectual disability pathogenesis.

Journal: Neurobiology of disease

Published: February 12, 2026

DeepGene-BC: Deep Learning-Based Breast Cancer Subtype Prediction via Somatic Point Mutation Profiles.

DeepGene-BC: Deep Learning-Based Breast Cancer Subtype Prediction via Somatic Point Mutation Profiles.

Journal: Cancers

Published: January 07, 2026

Dysregulation of RUNX1 isoforms drives mitochondrial defects during neural differentiation in down syndrome.

Dysregulation of RUNX1 isoforms drives mitochondrial defects during neural differentiation in down syndrome.

Journal: Mitochondrion

Published: September 24, 2025

Machine learning prediction for AML based on 3D genome selected circRNA.

Machine learning prediction for AML based on 3D genome selected circRNA.

Journal: NPJ systems biology and applications

Published: September 07, 2025

Pathogenic mutations disrupt stress granules assembly in patients with DDX3X neurodevelopmental disorder.

Pathogenic mutations disrupt stress granules assembly in patients with DDX3X neurodevelopmental disorder.

Journal: Human molecular genetics

Published: April 13, 2025

PSTP: accurate residue-level phase separation prediction using protein conformational and language model embeddings.

PSTP: accurate residue-level phase separation prediction using protein conformational and language model embeddings.

Journal: Briefings in bioinformatics

Published: January 18, 2025

The role of CSNK1A1 and its de novo mutations in infantile spasms syndrome.

The role of CSNK1A1 and its de novo mutations in infantile spasms syndrome.

Journal: Human molecular genetics

Published: December 24, 2024

Gene Doping Detection From the Perspective of 3D Genome.

Gene Doping Detection From the Perspective of 3D Genome.

Journal: Drug testing and analysis

Published: September 26, 2024

Intermittent Vibration Induces Sleep via an Allatostatin A-GABA Signaling Pathway and Provides Broad Benefits in Alzheimer's Disease Models.

Intermittent Vibration Induces Sleep via an Allatostatin A-GABA Signaling Pathway and Provides Broad Benefits in Alzheimer's Disease Models.

Journal: Advanced science (Weinheim, Baden-Wurttemberg, Germany)

Published: September 23, 2024

Identification of Schizophrenia-Risk Regulatory Variant rs1399178 in the Non-coding Region With Its Impact on NRF1 Binding.

Identification of Schizophrenia-Risk Regulatory Variant rs1399178 in the Non-coding Region With Its Impact on NRF1 Binding.

Journal: CNS neuroscience & therapeutics

Published: September 19, 2024

Mutations in the spliceosomal gene SNW1 cause neurodevelopment disorders with microcephaly.

Mutations in the spliceosomal gene SNW1 cause neurodevelopment disorders with microcephaly.

Journal: The Journal of clinical investigation

Published: August 20, 2024

Showing 1-12 of 128

Last Updated: 09/26/2026