X. Pang

发表

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.

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.

Mono-allelic mutations of SLC26A4 is over-presented in deaf patients with non-syndromic enlarged vestibular aqueduct.

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

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

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

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.

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

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

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 .

A homozygous MITF mutation leads to familial Waardenburg syndrome type 4

T. Yang, Y. Chai, X. Pang, 2018, American journal of medical genetics. Part A.

A 1.6-Mb Microdeletion in Chromosome 17q22 Leads to NOG-Related Symphalangism Spectrum Disorder without Intellectual Disability

T. Yang, Penghui Chen, Y. Chai, 2015, PloS one.

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.

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

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

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, Hao Wu, 2016, Neural plasticity.

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.

p53 performs an essential role in mediating the oncogenic stimulus triggered by loss of expression of neurofibromatosis type 2 during in vitro tumor progression

Hao Wu, X. Pang, L. Xue, 2017, Oncology letters.

Identification and Characterization of a Cryptic Genomic Deletion-Insertion in EYA1 Associated with Branchio-Otic Syndrome

Y. Chai, X. Pang, Changling Sun, 2021, Neural plasticity.

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.

Targeted next‐generation sequencing and parental genotyping in sporadic Chinese Han deaf patients

T. Yang, H. Liu, Y. Chai, 2018, Clinical genetics.

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.

The homozygous p.V37I variant of GJB2 is associated with diverse hearing phenotypes

Y. Chen, D. Chen, Y. Chai, 2015, Clinical genetics.

Identification of both MT-RNR1 m.1555A>G and bi-allelic GJB2 mutations in probands with non-syndromic hearing loss.

T. Yang, Hao Wu, Y. Chai, 2014, International journal of pediatric otorhinolaryngology.

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

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

Targeted Next-Generation Sequencing in Uyghur Families with Non-Syndromic Sensorineural Hearing Loss

T. Yang, Hao Wu, Y. Chai, 2015, PloS one.

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

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

A Novel Missense Mutation of NOG Interferes With the Dimerization of NOG and Causes Proximal Symphalangism Syndrome in a Chinese Family

T. Yang, Hao Wu, Y. Chai, 2015, The Annals of otology, rhinology, and laryngology.

Molecular etiology of non‐dominant, non‐syndromic, mild‐to‐moderate childhood hearing impairment in Chinese Hans

T. Yang, Hao Wu, Y. Chai, 2014, American journal of medical genetics. Part A.