Yanli Wang
Department Of Otolaryngology Head And Neck Surgery, Ldey.cn
Lanzhou, China
Lanzhou, China
Last Updated: 09/26/2026
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Found 11 publications
Study on the Mechanism of Hearing Loss Induced by USH2A Gene Knockout.
Journal: Human mutation
Published: May 19, 2025
A Novel Mutation Located in the N-Terminal Domain of MYO15A Caused Sensorineural Hearing Loss.
Journal: Molecular genetics & genomic medicine
Published: July 30, 2024
Research on congenital severe-to-profound sensorineural hearing loss associated with central lucency of the bony island of the lateral semicircular canal.
Journal: Acta oto-laryngologica
Published: February 25, 2023
The effect of SLC26A4 gene mutations on long-term rehabilitative outcomes in cochlear implant patients.
Journal: Acta oto-laryngologica
Published: February 13, 2023
Screening of SLC26A4 Gene Hotspots in 2673 Patients Associated with Sensorineural Hearing Loss in Northwestern China.
Journal: The journal of international advanced otology
Published: April 14, 2022
Analysis of GJB2 Gene Mutations in 1330 Deafness Cases of Major Ethnic Groups in Northwest China.
Journal: Inquiry : a journal of medical care organization, provision and financing
Published: February 25, 2022
Verification of an iPSC line (LZUi002-A) from a patient with a novel mutation in the TBL1X gene.
Journal: Stem cell research
Published: January 25, 2022
Surgical management of mucosal contact headache.
Journal: American journal of otolaryngology
Published: October 25, 2021
Associations between GJB2, mitochondrial 12S rRNA, SLC26A4 mutations, and hearing loss among three ethnicities.
Journal: BioMed research international
Published: February 27, 2014
A systematic review and meta-analysis of common mutations of SLC26A4 gene in Asian populations.
Journal: International journal of pediatric otorhinolaryngology
Published: June 15, 2013
Showing 1-11 of 11
Last Updated: 09/26/2026