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Ling-Yun Mei · SciRah

Researcher profile · Semantic Scholar

Ling-Yun Mei

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Ling-Yun Mei — researcher profile on SciRah

h-index: 18
Works: 96
Citations: 859

Most-cited papers

Novel mutations of PAX3, MITF, and SOX10 genes in Chinese patients with type I or type II Waardenburg syndrome.
Hong-Sheng Chen, Lu Jiang, Zhi-guo Xie, Ling-Yun Mei +4 more
2010Biochemical and Biophysical Research Communications - BBRC71 citations
Semantic Scholar
Genetic insights, disease mechanisms, and biological therapeutics for Waardenburg syndrome
Sida Huang, Jian Song, Chu-Feng He, Xin-Zhang Cai +3 more
2021Gene Therapy52 citations
Semantic Scholar
Functional analysis of Waardenburg syndrome-associated PAX3 and SOX10 mutations: report of a dominant-negative SOX10 mutation in Waardenburg syndrome type II
Hua Zhang, Hong-Sheng Chen, Hun-Jin Luo, Jing An +8 more
2012Human Genetics47 citations
Semantic Scholar
Multivariate analysis of prognostic factors for idiopathic sudden sensorineural hearing loss treated with adjuvant hyperbaric oxygen therapy
Shao-Bing Xie, Q. Qiang, Ling-Yun Mei, Chu-Feng He +3 more
2017European Archives of Oto-Rhino-Laryngology44 citations
Semantic Scholar
Proband Whole-Exome Sequencing Identified Genes Responsible for Autosomal Recessive Non-Syndromic Hearing Loss in 33 Chinese Nuclear Families
Shu-Shan Sang, Jie Ling, Xue-Zhong Liu, Ling-Yun Mei +11 more
2019Frontiers in Genetics29 citations Open access
Semantic Scholar
A nonsense TMEM43 variant leads to disruption of connexin-linked function and autosomal dominant auditory neuropathy spectrum disorder
M. Jang, D. Oh, Eunyoung Yi, Xue-Zhong Liu +40 more
2021Proceedings of the National Academy of Sciences of the United States of America27 citations Open access
Semantic Scholar
New Genotypes and Phenotypes in Patients with 3 Subtypes of Waardenburg Syndrome Identified by Diagnostic Next-Generation Sequencing
Wu Li, Ling-Yun Mei, Hong-Sheng Chen, Xin-Zhang Cai +6 more
2019Journal of Neural Transplantation and Plasticity27 citations Open access
Semantic Scholar
Exome sequencing identifies POU4F3 as the causative gene for a large Chinese family with non-syndromic hearing loss
Xin-Zhang Cai, Y. Li, L. Xia, Yun Peng +7 more
2016Journal of Human Genetics25 citations
Semantic Scholar
Extrusion pump ABCC1 was first linked with nonsyndromic hearing loss in humans by stepwise genetic analysis
Meng Li, Ling-Yun Mei, Chu-Feng He, Hong-Sheng Chen +19 more
2019Genetics in Medicine24 citations Open access
Semantic Scholar
Functional analysis of MITF gene mutations associated with Waardenburg syndrome type 2
Hua Zhang, Hun-Jin Luo, Hong-Sheng Chen, Ling-Yun Mei +4 more
2012FEBS Letters24 citations Open access
Semantic Scholar
LEF-1 Regulates Tyrosinase Gene Transcription In Vitro
Xue-Ping Wang, Yalan Liu, Hong-Sheng Chen, Ling-Yun Mei +7 more
2015PLoS ONE23 citations Open access
Semantic Scholar
Effect of systemic lupus erythematosus and rheumatoid arthritis on sudden sensorineural hearing loss
Shao-Bing Xie, Hong-Ting Ning, Yong-Chuan She, Qian-Cheng Jing +5 more
2019The Laryngoscope22 citations
Semantic Scholar
A New Genetic Diagnostic for Enlarged Vestibular Aqueduct Based on Next-Generation Sequencing
Yalan Liu, Lili Wang, Yong Feng, Chu-Feng He +7 more
2016PLoS ONE22 citations Open access
Semantic Scholar
Novel mutations in the SOX10 gene in the first two Chinese cases of type IV Waardenburg syndrome.
Lu Jiang, Hong-Sheng Chen, Wen Jiang, Zheng-Mao Hu +6 more
2011Biochemical and Biophysical Research Communications - BBRC22 citations
Semantic Scholar
ABCC1 deficiency potentiated noise-induced hearing loss in mice by impairing cochlear antioxidant capacity
Jing Liu, Yijiang Bai, Yong Feng, Xian-Ling Liu +8 more
2024Redox Biology21 citations Open access
Semantic Scholar
Functional analysis of a nonstop mutation in MITF gene identified in a patient with Waardenburg syndrome type 2
Jie Sun, Zi-Qi Hao, Hun-Jin Luo, Chu-Feng He +7 more
2017Journal of Human Genetics21 citations Open access
Semantic Scholar
Exome Sequencing Identifies a Novel CEACAM16 Mutation Associated with Autosomal Dominant Nonsyndromic Hearing Loss DFNA4B in a Chinese Family
Honghan Wang, Xin-Wei Wang, Chu-Feng He, Hai-bo Li +19 more
2015Journal of Human Genetics20 citations Open access
Semantic Scholar
ELMOD3, a novel causative gene, associated with human autosomal dominant nonsyndromic and progressive hearing loss
Wu Li, Jie Sun, Jie Ling, Jia-Da Li +18 more
2018Human Genetics19 citations
Semantic Scholar
Wnt signaling pathway involvement in genotypic and phenotypic variations in Waardenburg syndrome type 2 with MITF mutations
Xue-Ping Wang, Yalan Liu, Ling-Yun Mei, Chu-Feng He +5 more
2018Journal of Human Genetics18 citations Open access
Semantic Scholar
A novel frameshift mutation of SMPX causes a rare form of X-linked nonsyndromic hearing loss in a Chinese family
Zhi-Jie Niu, Yong Feng, Ling-Yun Mei, Jie Sun +10 more
2017PLoS ONE18 citations Open access
Semantic Scholar
Identification and functional analysis of a novel mutation in the SOX10 gene associated with Waardenburg syndrome type IV.
Honghan Wang, Hong-Sheng Chen, Hai-bo Li, Hua Zhang +8 more
2014Gene18 citations Open access
Semantic Scholar
A rapid improved multiplex ligation detection reaction method for the identification of gene mutations in hereditary hearing loss
Yalan Liu, Chang-Min Hu, Chang Liu, Deyuan Liu +6 more
2019PLoS ONE16 citations Open access
Semantic Scholar
Downregulation of p66Shc can reduce oxidative stress and apoptosis in oxidative stress model of marginal cells of stria vascularis in Sprague Dawley rats
Cong Hao, Xuewen Wu, R. Zhou, Hao Zhang +7 more
2019Drug Design, Development and Therapy16 citations Open access
Semantic Scholar
Elmod3 knockout leads to progressive hearing loss and abnormalities in cochlear hair cell stereocilia.
Wu Li, Yong Feng, Anhai Chen, Taoxi Li +10 more
2019Human Molecular Genetics16 citations Open access
Semantic Scholar
Application of a New Genetic Deafness Microarray for Detecting Mutations in the Deaf in China
Hong-Tao Wu, Yong Feng, Lu Jiang, Q. Pan +8 more
2016PLoS ONE15 citations Open access
Semantic Scholar
Otological manifestations in branchiootorenal spectrum disorder: A systematic review and meta‐analysis
Anhai Chen, Jian Song, F. Acke, Ling-Yun Mei +3 more
2021Clinical Genetics13 citations
Semantic Scholar
Short-term effects of intravenous batroxobin in treatment of sudden sensorineural hearing loss: a propensity score-matched study
Mengzhu Jiang, Hu-Ping Huang, Ling-Yun Mei, Chu-Feng He +5 more
2023Frontiers in Neurology11 citations Open access
Semantic Scholar
A novel mutation in the SMPX gene associated with X-linked nonsyndromic sensorineural hearing loss in a Chinese family
Yuyuan Deng, Zhi-Jie Niu, Liang-Liang Fan, Jie Ling +12 more
2018Journal of Human Genetics11 citations
Semantic Scholar
Exome sequencing identifies a novel missense mutation of WFS1 as the cause of non-syndromic low-frequency hearing loss in a Chinese family.
Zhi-Jie Niu, Yong Feng, Zheng-Mao Hu, Jia-Da Li +11 more
2017International Journal of Pediatric Otorhinolaryngology11 citations
Semantic Scholar
A Model of Waardenburg Syndrome Using Patient-Derived iPSCs With a SOX10 Mutation Displays Compromised Maturation and Function of the Neural Crest That Involves Inner Ear Development
Jie Wen, Jian Song, Yijiang Bai, Yalan Liu +5 more
2021Frontiers in Cell and Developmental Biology10 citations Open access
Semantic Scholar
[An investigation of SLC26A4 gene mutation in nonsydromic hearing impairment in Hunan province of China].
Lu Jiang, Yong Feng, Hong-Sheng Chen, Chu-Feng He +1 more
2010Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery10 citations
Semantic Scholar
A novel splicing mutation in SMPX is linked to nonsyndromic progressive hearing loss.
Zhi-Jie Niu, D. Yan, Sara E. Bressler, Ling-Yun Mei +2 more
2018International Journal of Pediatric Otorhinolaryngology9 citations
Semantic Scholar
A comprehensive genotype–phenotype evaluation of eight Chinese probands with Waardenburg syndrome
Sijun Li, Mengyao Qin, Shuang Mao, Ling-Yun Mei +4 more
2022BMC Medical Genomics8 citations Open access
Semantic Scholar
Identification and functional analysis of a novel mutation in the PAX3 gene associated with Waardenburg syndrome type I.
Zhi-Jie Niu, Jia-Da Li, Fen Tang, Jie Sun +8 more
2018Gene8 citations
Semantic Scholar
[Study of the anatomy related to cochlear implantation guided by HRCT].
Xuebin He, Yong Feng, Deng-Ming Chen, Ling-Yun Mei +2 more
2011Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery8 citations
Semantic Scholar
PAX3 mutation suppress otic progenitors proliferation and induce apoptosis by inhibiting WNT1/β-catenin signaling pathway in WS1 patient iPSC-derived inner ear organoids.
Sijun Li, Chu-Feng He, Ling-Yun Mei, Xuewen Wu +2 more
2024Biochemical and Biophysical Research Communications - BBRC7 citations
Semantic Scholar
Digenic mutations involving both the BSND and GJB2 genes detected in Bartter syndrome type IV.
Honghan Wang, Yong Feng, Hai-bo Li, Hong Wu +4 more
2017International Journal of Pediatric Otorhinolaryngology7 citations
Semantic Scholar
A Novel EYA1 Mutation Causing Alternative RNA Splicing in a Chinese Family With Branchio-Oto Syndrome: Implications for Molecular Diagnosis and Clinical Application
Anhai Chen, Jie Ling, Xin Peng, Xian-Ling Liu +12 more
2023Clinical and Experimental Otorhinolaryngology6 citations Open access
Semantic Scholar
Susceptibility of immature spiral ganglion neurons to aminoglycoside-induced ototoxicity is mediated by the TRPV1 channel in mice.
Yijiang Bai, Jing Liu, Xue-Wen Wu, Bo Pang +8 more
2023Hearing Research6 citations
Semantic Scholar
Next-generation sequencing-based mutation analysis of genes associated with enlarged vestibular aqueduct in Chinese families
Yalan Liu, Jie Wen, Shu-Shan Sang, Ling-Yun Mei +4 more
2020European Archives of Oto-Rhino-Laryngology6 citations
Semantic Scholar
Modeling of pigmentation disorders associated with MITF mutation in Waardenburg syndrome revealed an impaired melanogenesis pathway in iPS‐derived melanocytes
Jie Wen, Jian Song, Jiale Chen, Zhili Feng +7 more
2023Pigment Cell & Melanoma Research5 citations
Semantic Scholar
Gene regulation analysis of patient-derived iPSCs and its CRISPR-corrected control provides a new tool for studying perturbations of ELMOD3 c.512A>G mutation during the development of inherited hearing loss
Xian-Ling Liu, Jie Wen, Xue-Zhong Liu, Anhai Chen +10 more
2023PLoS ONE5 citations Open access
Semantic Scholar
Establishment of an iPSC line (CSUXHi004-A) from a patient with Waardenburg syndrome type I caused by a PAX3 splice mutation.
Jie Wen, Chu-Feng He, Yong Feng, Jian Song +6 more
2021Stem Cell Research5 citations Open access
Semantic Scholar
Reproductive guidance through prenatal diagnosis and genetic counseling for recessive hereditary hearing loss in high-risk families.
Yuyuan Deng, Shu-Shan Sang, Jie Wen, Yalan Liu +10 more
2018International Journal of Pediatric Otorhinolaryngology5 citations
Semantic Scholar
Functional analysis of a SOX10 gene mutation associated with Waardenburg syndrome II.
Xue-Ping Wang, Zi-Qi Hao, Yalan Liu, Ling-Yun Mei +5 more
2017Biochemical and Biophysical Research Communications - BBRC5 citations
Semantic Scholar
Identification of a family with van der Hoeve’s syndrome harboring a novel COL1A1 mutation and generation of patient-derived iPSC lines and CRISPR/Cas9-corrected isogenic iPSCs
Sijun Li, Ling-Yun Mei, Chu-Feng He, Xin-Zhang Cai +5 more
2024Human Cell4 citations Open access
Semantic Scholar
Establishment of two iPSC lines from healthy donor with heterozygous mutation in the SLC26A4 gene.
Sijun Li, Chu-Feng He, Qi Feng, Yijiang Bai +6 more
2022Stem Cell Research4 citations Open access
Semantic Scholar
[The analysis of nystagmus in patients with posterior canal benign paroxysmal positional vertigoin positioning test].
X. Cui, Yong Feng, Ling-Yun Mei, Chu-Feng He +3 more
2015Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery4 citations
Semantic Scholar
[An analysis of a large hereditary postlingually deaf families and detecting mutation of the deafness genes].
Yong Feng, Chu-Feng He, Jian-Yun Xiao, Jiansheng Fang +5 more
2002Lin chuang er bi yan hou ke za zhi = Journal of clinical otorhinolaryngology4 citations
Semantic Scholar
A novel frameshift mutation in the DIAPH1 gene causes a Chinese family autosomal dominant nonsyndromic hearing loss: Mutation in DIAPH1 causes hearing loss.
Qi Feng, Lu Jiang, Shuai Zhang, Chu-Feng He +2 more
2024Gene3 citations
Semantic Scholar

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