Xue Gao

Beijing, China

Last Updated: 09/26/2026

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Found 38 publications

A novel GRHL2 nonsense variant impairs auditory function via a gain-of-function mechanism in autosomal dominant hearing loss.

A novel GRHL2 nonsense variant impairs auditory function via a gain-of-function mechanism in autosomal dominant hearing loss.

Journal: Acta oto-laryngologica

Published: December 10, 2025

Reevaluation of Enlarged Vestibular Aqueduct.

Reevaluation of Enlarged Vestibular Aqueduct.

Journal: JAMA otolaryngology-- head & neck surgery

Published: October 09, 2025

A cohort study of neonatal hearing testing and genetic screening for variants associated with susceptibility to aminoglycoside antibiotic-induced hearing loss in Beijing, China.

A cohort study of neonatal hearing testing and genetic screening for variants associated with susceptibility to aminoglycoside antibiotic-induced hearing loss in Beijing, China.

Journal: Medicine

Published: June 30, 2025

A Novel Frameshift Variant c.1023_1029del (p.Asp342ArgfsTer54) Leading to Extended Incorrect Protein C Termini in HOMER2 Causing Autosomal Dominant Nonsyndromic Hearing Loss.

A Novel Frameshift Variant c.1023_1029del (p.Asp342ArgfsTer54) Leading to Extended Incorrect Protein C Termini in HOMER2 Causing Autosomal Dominant Nonsyndromic Hearing Loss.

Journal: Journal of clinical laboratory analysis

Published: January 31, 2025

Recessive variants in TWNK cause syndromic and non-syndromic post-synaptic auditory neuropathy through MtDNA replication defects.

Recessive variants in TWNK cause syndromic and non-syndromic post-synaptic auditory neuropathy through MtDNA replication defects.

Journal: Human genetics

Published: January 23, 2025

Reliability and validity of the Clinical pHysical rEsilience assEssment Scale (CHEES) in community-dwelling older adults.

Reliability and validity of the Clinical pHysical rEsilience assEssment Scale (CHEES) in community-dwelling older adults.

Journal: Experimental gerontology

Published: January 02, 2025

Hearing impairment detected by the whisper test is associated with physio-cognitive decline syndrome in community-dwelling older adults.

Hearing impairment detected by the whisper test is associated with physio-cognitive decline syndrome in community-dwelling older adults.

Journal: The journal of nutrition, health & aging

Published: November 25, 2024

Research progress on GSDME-mediated cell pyroptosis resulting in GSDME type hearing loss

Research progress on GSDME-mediated cell pyroptosis resulting in GSDME type hearing loss

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: September 30, 2024

Targeted Linked-Read Sequencing for Direct Haplotype Phasing of Parental GJB2/SLC26A4 Alleles: A Universal and Dependable Noninvasive Prenatal Diagnosis Method Applied to Autosomal Recessive Nonsyndromic Hearing Loss in At-Risk Families.

Targeted Linked-Read Sequencing for Direct Haplotype Phasing of Parental GJB2/SLC26A4 Alleles: A Universal and Dependable Noninvasive Prenatal Diagnosis Method Applied to Autosomal Recessive Nonsyndromic Hearing Loss in At-Risk Families.

Journal: The Journal of molecular diagnostics : JMD

Published: November 07, 2023

MPZL2-a common autosomal recessive deafness gene related to moderate sensorineural hearing loss in the Chinese population.

MPZL2-a common autosomal recessive deafness gene related to moderate sensorineural hearing loss in the Chinese population.

Journal: BMC medical genomics

Published: July 17, 2023

Cochlear implantation in a patient with congenital microtia, cochlear hypoplasia, venous anomalies of the temporal bone and laryngomalacia: Challenges and surgical considerations.

Cochlear implantation in a patient with congenital microtia, cochlear hypoplasia, venous anomalies of the temporal bone and laryngomalacia: Challenges and surgical considerations.

Journal: Medicine

Published: February 17, 2023

Addition of an affected family member to a previously ascertained autosomal recessive nonsyndromic hearing loss pedigree and systematic phenotype-genotype analysis of splice-site variants in MYO15A.

Addition of an affected family member to a previously ascertained autosomal recessive nonsyndromic hearing loss pedigree and systematic phenotype-genotype analysis of splice-site variants in MYO15A.

Journal: BMC medical genomics

Published: June 17, 2022

Showing 1-12 of 38

Last Updated: 09/26/2026