Tao Yang

发表

A novel splice site mutation in EYA4 causes DFNA10 hearing loss

M. Bahlo, R. Gardner, H. Dahl, 2007, American journal of medical genetics. Part A.

Carcinoembryonic antigen-related cell adhesion molecule 16 interacts with α-tectorin and is mutated in autosomal dominant hearing loss (DFNA4)

Todd E. Scheetz, Adam P. DeLuca, A. Eliot Shearer, 2011, Proceedings of the National Academy of Sciences.

A Dominant Mutation in the Stereocilia‐Expressing Gene TBC1D24 is a Probable Cause for Nonsyndromic Hearing Impairment

Tao Yang, Hao Wu, Luping Zhang, 2014, Human mutation.

Molecular basis of hearing loss associated with enlarged vestibular aqueduct

Tao Yang, Hao Wu, Xiaoyu Yu, 2019, Journal of Bio-X Research.

A 7666-bp genomic deletion is frequent in Chinese Han deaf patients with non-syndromic enlarged vestibular aqueduct but without bi-allelic SLC26A4 mutations.

Penghui Chen, Tao Yang, Hao Wu, 2015, International journal of pediatric otorhinolaryngology.

The influence of mutations in the SLC26A4 gene on the temporal bone in a population with enlarged vestibular aqueduct.

J. Meinzen-Derr, M. Halsted, D. Choo, 2007, Archives of otolaryngology--head & neck surgery.

Molecular etiology of hearing impairment associated with nonsyndromic enlarged vestibular aqueduct in East China

Tao Yang, Hao Wu, Y. Chai, 2013, American journal of medical genetics. Part A.

Association of leukocyte telomere length and the risk of age-related hearing impairment in Chinese Hans

Han Liu, Tao Yang, Hao Wu, 2017, Scientific Reports.

Identification and study of a FBN1 gene mutation in a Chinese family with ectopia lentis

Shangzhi Huang, Tao Yang, Shui-Hu Zhang, 2012, Molecular vision.

Disruption of Hars2 in Cochlear Hair Cells Causes Progressive Mitochondrial Dysfunction and Hearing Loss in Mice

Hu Peng, Tao Yang, Hao Wu, 2021, Frontiers in Cellular Neuroscience.

Identification of a novel three-nucleotide duplication in ECM1 in Chinese siblings affected with Lipoid Proteinosis.

D. Ma, Tao Yang, Tieshan Zhu, 2020, Clinica chimica acta; international journal of clinical chemistry.

THOC1 deficiency leads to late-onset nonsyndromic hearing loss through p53-mediated hair cell apoptosis

Fuping Qian, Dong Liu, R. Chai, 2019, bioRxiv.

Identification of a novel mutation of the gene for gap junction protein α3 (GJA3) in a Chinese family with congenital cataract

Shangzhi Huang, Tao Yang, Yali Feng, 2014, Molecular Biology Reports.

Title: THOC1 deficiency leads to late-onset nonsyndromic hearing loss through p53-mediated hair cell apoptosis Running title: A mutation in THOC1 causes hearing loss

Fuping Qian, Dong Liu, R. Chai, 2019 .

Genetic heterogeneity of deafness phenotypes linked to DFNA4

H. Zenner, C. Pusch, N. Blin, 2005, American journal of medical genetics. Part A.

Targeted Next-Generation Sequencing Identified Compound Heterozygous Mutations in MYO15A as the Probable Cause of Nonsyndromic Deafness in a Chinese Han Family

Hu Peng, Tao Yang, Hao Wu, 2020, Neural plasticity.

Mutations of KCNJ10 together with mutations of SLC26A4 cause digenic nonsyndromic hearing loss associated with enlarged vestibular aqueduct syndrome.

P. Wangemann, P. Snyder, Richard J. H. Smith, 2009, American journal of human genetics.

Recurrent PAX 6 mutation in a Chinese family with congenital aniridia, progressive cataracts and mental retardation

Tao Yang, Si-quan Zhu, D. Chen, 2018, European journal of ophthalmology.

Molecular etiology and genotype-phenotype correlation of Chinese Han deaf patients with type I and type II Waardenburg Syndrome

Tao Yang, Xiaohu Li, Hao Wu, 2016, Scientific Reports.

chr19_34670, a newly identified miRNA, represses rapid tumor growth of cystic vestibular schwannomas by targeting transforming growth factor α and inhibiting MAPK pathway

Penghui Chen, Tao Yang, Shuang Yan, 2017 .

MiR-205 inhibits sporadic vestibular schwannoma cells proliferation by targeting cyclin-dependent kinase 14.

Tao Yang, Shuang Yan, Hao Wu, 2020, World neurosurgery.

Machine learning-based genetic diagnosis models for hereditary hearing loss by the GJB2, SLC26A4 and MT-RNR1 variants

Xiaomei Luo, Tao Yang, Hao Wu, 2021, EBioMedicine.

Mutation in the Hair Cell Specific Gene POU4F3 Is a Common Cause for Autosomal Dominant Nonsyndromic Hearing Loss in Chinese Hans

T. Yang, Penghui Chen, Tao Yang, 2016, Neural plasticity.

A novel splicing mutation of the FRMD7 gene in a Chinese family with X-linked congenital nystagmus

Jing Shen, Shangzhi Huang, Tao Yang, 2012, Molecular vision.

Mutations in KARS cause early‐onset hearing loss and leukoencephalopathy: Potential pathogenic mechanism

E. Wang, Tao Yang, Xiao-Long Zhou, 2017, Human mutation.

Detection and Functional Verification of Noncanonical Splice Site Mutations in Hereditary Deafness

Penghui Chen, Tao Yang, Hao Wu, 2021, Frontiers in Genetics.

Screening for delayed-onset hearing loss in preschool children who previously passed the newborn hearing screening.

Yu Wang, Zhiwu Huang, Hao Wu, 2011, International journal of pediatric otorhinolaryngology.

The effect of GJB2 and SLC26A4 gene mutations on rehabilitative outcomes in pediatric cochlear implant patients

Tao Yang, Hao Wu, Qi Huang, 2013, European Archives of Oto-Rhino-Laryngology.

Association of leukocyte telomere length and the risk of age-related hearing impairment in Chinese Hans

Han Liu, Tao Yang, Hao Wu, 2017, Scientific Reports.

Association of GRM7 Variants with Different Phenotype Patterns of Age-Related Hearing Impairment in an Elderly Male Han Chinese Population

Xiaojie Jin, Jing Sun, Tao Yang, 2013, PloS one.

Mutations in the γ-Actin Gene (ACTG1) Are Associated with Dominant Progressive Deafness (DFNA20/26)

S. Leal, A. Dewan, Richard J. H. Smith, 2003 .

Gene expression profiles between cystic and solid vestibular schwannoma indicate susceptible molecules and pathways in the cystic formation of vestibular schwannoma

Tao Yang, Shuang Yan, Hao Wu, 2019, Functional & Integrative Genomics.

Characterization of Spectrum, de novo Rate and Genotype-Phenotype Correlation of Dominant GJB2 Mutations in Chinese Hans

Tao Yang, Y. Chai, X. Pang, 2014, PloS one.

Compound Heterozygous Mutations in TMC1 and MYO15A Are Associated with Autosomal Recessive Nonsyndromic Hearing Loss in Two Chinese Han Families

Hu Peng, Tao Yang, Pengcheng Xu, 2020, Neural plasticity.

Identification of novel mutations of PKD1 gene in Chinese patients with autosomal dominant polycystic kidney disease by targeted next-generation sequencing.

Y. Meng, Shangzhi Huang, Mingrong Zhang, 2014, Clinica chimica acta; international journal of clinical chemistry.

Genotypic and phenotypic characterization of Chinese patients with osteogenesis imperfecta

Yiyang Wu, Chendan Jiang, Jinsong Gao, 2019, Human mutation.

Characterization of a knock-in mouse model of the homozygous p.V37I variant in Gjb2

Zhiwu Huang, Hao Wu, Ling Mei, 2016, Scientific Reports.

Mutation analysis of seven consanguineous Uyghur families with non-syndromic deafness.

Tao Yang, Y. Chai, X. Pang, 2014, International journal of pediatric otorhinolaryngology.

Next-Generation Sequencing Identifies Pathogenic Variants in HGF, POU3F4, TECTA, and MYO7A in Consanguineous Pakistani Deaf Families

M. Asif, F. Iqbal, Weiqiang Yang, 2021, Neural plasticity.

Carrier re-sequencing reveals rare but benign variants in recessive deafness genes

Penghui Chen, Tao Yang, X. Pang, 2017, Scientific Reports.

Identification of a novel mutation of the gene for gap junction protein α3 (GJA3) in a Chinese family with congenital cataract

Shangzhi Huang, Tao Yang, Yali Feng, 2014, Molecular Biology Reports.

The European GWAS-identified risk SNP rs457717 within IQGAP2 is not associated with age-related hearing impairment in Han male Chinese population

Xiaojie Jin, Tao Yang, Z. Fan, 2016, European Archives of Oto-Rhino-Laryngology.

Autosomal dominant nonsyndromic hearing impairment.

G. Camp, W. McGuirt, Tao Yang, 1999, American journal of medical genetics.

Gene expression profiles between cystic and solid vestibular schwannoma indicate susceptible molecules and pathways in the cystic formation of vestibular schwannoma

Tao Yang, Shuang Yan, Hao Wu, 2019, Functional & Integrative Genomics.

Carrier re-sequencing reveals rare but benign variants in recessive deafness genes

T. Yang, Penghui Chen, Tao Yang, 2017, Scientific Reports.

THOC1 deficiency leads to late-onset nonsyndromic hearing loss through p53-mediated hair cell apoptosis

T. Yang, Fuping Qian, Dong Liu, 2019, bioRxiv.

Identification of a novel FBN1 gene mutation in a Chinese family with Marfan syndrome

Shangzhi Huang, Tao Yang, Bo Meng, 2011, Molecular vision.