Lingyun Mei

Novel mutations of PAX3, MITF, and SOX10 genes in Chinese patients with type I or type II Waardenburg syndrome

Hongsheng Chen, Lu Jiang, Zhiguo Xie et al. · Biochemical and Biophysical Research Communications · 2010 · 68 citations

Sox10 Genes, Disease Mechanism, Genetic Disorder +9

Multivariate analysis of prognostic factors for idiopathic sudden sensorineural hearing loss treated with adjuvant hyperbaric oxygen therapy

Shaobing Xie, Qingfen Qiang, Lingyun Mei et al. · European Archives of Oto-Rhino-Laryngology · 2017 · 47 citations

Prognostic Factors, Aural Rehabilitation, Pediatric Otolaryngology +7

Functional analysis of Waardenburg syndrome-associated PAX3 and SOX10 mutations: report of a dominant-negative SOX10 mutation in Waardenburg syndrome type II

Hua Zhang, Hongsheng Chen, Hunjin Luo et al. · Human Genetics · 2011 · 43 citations

Disease Mechanism, Genetic Disorder, Medicine +9

Proband Whole-Exome Sequencing Identified Genes Responsible for Autosomal Recessive Non-Syndromic Hearing Loss in 33 Chinese Nuclear Families

Shushan Sang, Jie Ling, Xuezhong Liu et al. · Frontiers in Genetics · 2019 · 37 citations · Full text

New Genotypes and Phenotypes in Patients with 3 Subtypes of Waardenburg Syndrome Identified by Diagnostic Next-Generation Sequencing

Wu Li, Lingyun Mei, Hongsheng Chen et al. · Neural Plasticity · 2019 · 32 citations · Full text