Yun Lin
Department Of Otolaryngology Head And Neck Surgery
Shanghai, 200011, China
Shanghai, 200011, China
Last Updated: 09/26/2026
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Found 19 publications
ATP6V1C1 deficiency impairs auditory and vestibular hair cell function and leads to sensorineural hearing loss in humans and mice.
Journal: Journal of genetics and genomics = Yi chuan xue bao
Published: August 04, 2025
Etrasimod as induction and maintenance treatment for patients with moderately to severely active ulcerative colitis in East Asia (ENLIGHT UC): a randomised, double-blind, placebo-controlled, multicentre, phase 3 study.
Journal: The lancet. Gastroenterology & hepatology
Published: April 22, 2025
Safety, tolerability, pharmacokinetics, and pharmacodynamics of etrasimod in healthy Chinese adults: a randomized, double-blind, placebo-controlled dose-escalation phase 1 study.
Journal: Frontiers in pharmacology
Published: November 05, 2024
Genetic and phenotypic analysis of MYO15A rare variants associated with autosomal recessive hearing loss
Journal: Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery
Published: October 13, 2023
Disruption of Hars2 in Cochlear Hair Cells Causes Progressive Mitochondrial Dysfunction and Hearing Loss in Mice.
Journal: Frontiers in cellular neuroscience
Published: October 29, 2021
Biallelic p.V37I variant in GJB2 is associated with increasing incidence of hearing loss with age.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: August 11, 2021
Identification and Characterization of a Cryptic Genomic Deletion-Insertion in EYA1 Associated with Branchio-Otic Syndrome.
Journal: Neural plasticity
Published: February 23, 2021
Targeted Next-Generation Sequencing Identifies Separate Causes of Hearing Loss in One Deaf Family and Variable Clinical Manifestations for the p.R161C Mutation in SOX10.
Journal: Neural plasticity
Published: April 22, 2020
Targeted Next-Generation Sequencing Identified Compound Heterozygous Mutations in MYO15A as the Probable Cause of Nonsyndromic Deafness in a Chinese Han Family.
Journal: Neural plasticity
Published: February 20, 2020
Molecular epidemiology of Chinese Han deaf patients with bi-allelic and mono-allelic GJB2 mutations.
Molecular epidemiology of Chinese Han deaf patients with bi-allelic and mono-allelic GJB2 mutations.
Journal: Orphanet journal of rare diseases
Published: October 24, 2019
EYA1 mutations leads to Branchio-Oto syndrome in two Chinese Han deaf families.
Journal: International journal of pediatric otorhinolaryngology
Published: December 27, 2018
Comparison of patients' tolerance between computed tomography enterography and double-balloon enteroscopy.
Journal: Patient preference and adherence
Published: October 31, 2017
Last Updated: 09/26/2026