Xiaomeng Wang

87 #, Xiangya Road
Changsha, 410008, China

Last Updated: 09/26/2026

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Found 16 publications

Prioritizing de novo potential non-canonical splicing variants in neurodevelopmental disorders.

Prioritizing de novo potential non-canonical splicing variants in neurodevelopmental disorders.

Journal: EBioMedicine

Published: March 11, 2023

Interactions of genetic risks for autism and the broad autism phenotypes.

Interactions of genetic risks for autism and the broad autism phenotypes.

Journal: Frontiers in psychiatry

Published: November 30, 2022

Severity of Autism Spectrum Disorder Symptoms Associated with de novo Variants and Pregnancy-Induced Hypertension.

Severity of Autism Spectrum Disorder Symptoms Associated with de novo Variants and Pregnancy-Induced Hypertension.

Journal: Journal of autism and developmental disorders

Published: November 10, 2022

Study on the expression and function of chordin-like 1 in oral squamous cell carcinoma.

Study on the expression and function of chordin-like 1 in oral squamous cell carcinoma.

Journal: Oral diseases

Published: January 22, 2022

Genetic landscape of human mitochondrial genome using whole-genome sequencing.

Genetic landscape of human mitochondrial genome using whole-genome sequencing.

Journal: Human molecular genetics

Published: October 11, 2021

A novel defined hypoxia-related gene signature to predict the prognosis of oral squamous cell carcinoma.

A novel defined hypoxia-related gene signature to predict the prognosis of oral squamous cell carcinoma.

Journal: Annals of translational medicine

Published: August 26, 2021

Cross-Disorder Analysis of De Novo Mutations in Neuropsychiatric Disorders.

Cross-Disorder Analysis of De Novo Mutations in Neuropsychiatric Disorders.

Journal: Journal of autism and developmental disorders

Published: April 14, 2021

Performance Comparison of Computational Methods for the Prediction of the Function and Pathogenicity of Non-coding Variants.

Performance Comparison of Computational Methods for the Prediction of the Function and Pathogenicity of Non-coding Variants.

Journal: Genomics, proteomics & bioinformatics

Published: March 26, 2021

Gene4PD: A Comprehensive Genetic Database of Parkinson's Disease.

Gene4PD: A Comprehensive Genetic Database of Parkinson's Disease.

Journal: Frontiers in neuroscience

Published: March 19, 2021

Cross-Disorder Analysis of De Novo Variants Increases the Power of Prioritising Candidate Genes.

Cross-Disorder Analysis of De Novo Variants Increases the Power of Prioritising Candidate Genes.

Journal: Life (Basel, Switzerland)

Published: January 29, 2021

Characterizing the Expression Patterns of Parkinson's Disease Associated Genes.

Characterizing the Expression Patterns of Parkinson's Disease Associated Genes.

Journal: Frontiers in neuroscience

Published: November 22, 2020

GPCards: An integrated database of genotype-phenotype correlations in human genetic diseases.

GPCards: An integrated database of genotype-phenotype correlations in human genetic diseases.

Journal: Computational and structural biotechnology journal

Published: November 19, 2020

Showing 1-12 of 16

Last Updated: 09/26/2026