Hongsheng Chen

发表

A novel frameshift mutation of SMPX causes a rare form of X-linked nonsyndromic hearing loss in a Chinese family

X. Liu, Zhengmao Hu, Yong Feng, 2017, PloS one.

Biallelic Intronic AAGGG Expansion of RFC1 is Related to Multiple System Atrophy

T. Ashizawa, K. Xia, B. Tang, 2020, Annals of neurology.

Identification and functional analysis of a novel mutation in the SOX10 gene associated with Waardenburg syndrome type IV.

Yong Feng, L. Mei, Hongsheng Chen, 2014, Gene.

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

K. Xia, Yong Feng, L. Mei, 2011, Human Genetics.

Functional analysis of MITF gene mutations associated with Waardenburg syndrome type 2

Yong Feng, L. Mei, Hongsheng Chen, 2012, FEBS letters.

Extrusion pump ABCC1 was first linked with nonsyndromic hearing loss in humans by stepwise genetic analysis

X. Liu, S. Blanton, Zhengmao Hu, 2019, Genetics in Medicine.

MITF Is Mutated in Type 1 Waardenburg Syndrome With Unusual Phenotype

Yong Feng, L. Mei, Hongsheng Chen, 2020, Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology.

Novel mutations in the SOX10 gene in the first two Chinese cases of type IV Waardenburg syndrome.

K. Xia, Zhengmao Hu, Yong Feng, 2011, Biochemical and biophysical research communications.

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

K. Xia, Zhengmao Hu, Yong Feng, 2010, Biochemical and biophysical research communications.

LEF-1 Regulates Tyrosinase Gene Transcription In Vitro

Yong Feng, Zhijie Niu, L. Mei, 2015, PloS one.

Functional analysis of a nonstop mutation in MITF gene identified in a patient with Waardenburg syndrome type 2

Yong Feng, Zhijie Niu, L. Mei, 2017, Journal of Human Genetics.

Application of a New Genetic Deafness Microarray for Detecting Mutations in the Deaf in China

Q. Pan, Yong Feng, L. Mei, 2016, PloS one.

Novel and recurrent non-truncating mutations of the MITF basic domain: genotypic and phenotypic variations in Waardenburg and Tietz syndromes

V. Drouin‐Garraud, H. Dollfus, C. Baumann, 2012, European Journal of Human Genetics.

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

D. Yan, Yong Feng, L. Mei, 2019, Neural plasticity.

A New Genetic Diagnostic for Enlarged Vestibular Aqueduct Based on Next-Generation Sequencing

Yong Feng, L. Mei, Hongsheng Chen, 2016, PloS one.

Establishment of an iPSC line (CSUXHi003-A) from a patient with Waardenburg syndrome type Ⅱ caused by a MITF mutation.

Yong Feng, L. Mei, Hongsheng Chen, 2021, Stem cell research.

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

Yong Feng, Jing Liu, Shu-shan Sang, 2019, Front. Genet..

Identification of a Novel CNV at 8q13 in a Family With Branchio‐Oto‐Renal Syndrome and Epilepsy

Hui Guo, Yong Feng, Hongsheng Chen, 2020, The Laryngoscope.

Exome Sequencing Identifies a Novel CEACAM16 Mutation Associated with Autosomal Dominant Nonsyndromic Hearing Loss DFNA4B in a Chinese Family

J. Yu, X. Liu, Jianguo Zhang, 2014, Journal of Human Genetics.

Exome sequencing identifies a novel missense mutation of WFS1 as the cause of non-syndromic low-frequency hearing loss in a Chinese family.

X. Liu, Zhengmao Hu, Yong Feng, 2017, International journal of pediatric otorhinolaryngology.

A novel ABHD12 nonsense variant in Usher syndrome type 3 family with genotype-phenotype spectrum review.

X. Liu, Yong Feng, Jing Liu, 2019, Gene.

A novel mutation in the SMPX gene associated with X-linked nonsyndromic sensorineural hearing loss in a Chinese family

Yong Feng, Shu-shan Sang, Zhijie Niu, 2018, Journal of Human Genetics.

Mutations in TMEM43 cause autosomal dominant auditory neuropathy spectrum disorder via interaction with connexin-mediated passive conductance channels

W. Park, Eunyoung Yi, S. Blanton, 2020, bioRxiv.

Reproductive guidance through prenatal diagnosis and genetic counseling for recessive hereditary hearing loss in high-risk families.

M. Li, Yong Feng, Shu-shan Sang, 2018, International journal of pediatric otorhinolaryngology.

A rapid improved multiplex ligation detection reaction method for the identification of gene mutations in hereditary hearing loss

Yong Feng, L. Mei, Hongsheng Chen, 2019, PloS one.

[An investigation of SLC26A4 gene mutation in nonsydromic hearing impairment in Hunan province of China].

Yong Feng, L. Mei, Hongsheng Chen, 2010, Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery.

ELMOD3, a novel causative gene, associated with human autosomal dominant nonsyndromic and progressive hearing loss

X. Liu, M. Li, D. Yan, 2018, Human Genetics.

Gene localization in a Chinese family with autosomal dominant non-syndromic deafness

K. Xia, Zhengmao Hu, Yong Feng, 2011, Acta oto-laryngologica.

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

K. Xia, Yong Feng, L. Mei, 2012, Human Genetics.

[Analysis of nuclear localization and signal function of MITF protein predisposing to Warrdenburg syndrome].

Hongsheng Chen, Juan Feng, Jiada Li, 2015, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

A nonsense TMEM43 variant leads to disruption of connexin-linked function and autosomal dominant auditory neuropathy spectrum disorder

W. Park, Eunyoung Yi, S. Blanton, 2021, Proceedings of the National Academy of Sciences.

Acoustic Assessment of Tone Production of Prelingually-Deafened Mandarin-Speaking Children With Cochlear Implants

S. Xie, Li Xu, Y. Mao, 2020, Frontiers in Neuroscience.

Establishment of an iPSC line (CSUXHi004-A) from a patient with Waardenburg syndrome type I caused by a PAX3 splice mutation.

Yong Feng, Jing Liu, L. Mei, 2021, Stem cell research.

ELMOD3, a novel causative gene, associated with human autosomal dominant nonsyndromic and progressive hearing loss

X. Liu, M. Li, D. Yan, 2018, Human Genetics.