Tao Yang (T Yang)

Publication Activity (10 Years)

Years Active: 2016-2021
Publications (10 Years): 13

Top Topics

Dna Methylation

Muscular Dystrophy

Top Venues

Neural plasticity

Clinical genetics

American journal of medical genetics. Part A

This page only lists publications with an associated author ORCID identifier.

Publications

Xueshuang Mei, Yaqi Zhou, Muhammad Amjad, Weiqiang Yang, Rufei Zhu, Muhammad Asif, Hafiz Muhammad Jafar Hussain, Tao Yang, Furhan Iqbal, Hongyi Hu
Next-Generation Sequencing Identifies Pathogenic Variants in HGF, POU3F4, TECTA, and MYO7A in Consanguineous Pakistani Deaf Families. Neural plasticity 2021 (2021)
Pengcheng Xu, Jun Xu, Hu Peng, Tao Yang
Compound Heterozygous Mutations in TMC1 and MYO15A Are Associated with Autosomal Recessive Nonsyndromic Hearing Loss in Two Chinese Han Families. Neural plasticity 2020 (2020)
Luping Zhang, Yu Gao, Ru Zhang, Feifei Sun, Cheng Cheng, Fuping Qian, Xuchu Duan, Guanyun Wei, Cheng Sun, Xiuhong Pang, Penghui Chen, Renjie Chai, Tao Yang, Hao Wu, Dong Liu
THOC1 deficiency leads to late-onset nonsyndromic hearing loss through p53-mediated hair cell apoptosis. PLoS genetics 16 (8) (2020)
Xiaoyu Yu, Yun Lin, Jun Xu, Tuanjie Che, Lin Li, Tao Yang, Hao Wu
Molecular epidemiology of Chinese Han deaf patients with bi-allelic and mono-allelic GJB2 mutations. Orphanet journal of rare diseases 15 (1) (2020)
Longhao Wang, Lin Zhao, Hu Peng, Jun Xu, Yun Lin, Tao Yang, Hao Wu
Targeted Next-Generation Sequencing Identified Compound Heterozygous Mutations in MYO15A as the Probable Cause of Nonsyndromic Deafness in a Chinese Han Family. Neural plasticity 2020 (2020)
Songfeng Zou, Xueshuang Mei, Weiqiang Yang, Rvfei Zhu, Tao Yang, Hongyi Hu
Whole-exome sequencing identifies rare pathogenic and candidate variants in sporadic Chinese Han deaf patients. Clinical genetics 97 (2) (2019)
Xue-Ling Wang, Chengbin Wang, Hu Peng, Tao Yang, Hao Wu
A Novel p.G141R Mutation in ILDR1 Leads to Recessive Nonsyndromic Deafness DFNB42 in Two Chinese Han Families. Neural plasticity 2018 (2018)
L He, X Pang, H Liu, Y Chai, H Wu, Tao Yang
Targeted next-generation sequencing and parental genotyping in sporadic Chinese Han deaf patients. Clinical genetics 93 (4) (2018)
Xiuhong Pang, Xiaoyong Zheng, Xuhui Kong, Yongchuan Chai, Yu Wang, Hua Qian, Bo Yang, Chao Wu, Jiusheng Chu, Tao Yang
A homozygous MITF mutation leads to familial Waardenburg syndrome type 4. American journal of medical genetics. Part A 179 (2) (2018)
Penghui Chen, Yongchuan Chai, Haijin Liu, Gen Li, Chengbin Wang, Tao Yang, Hao Wu
Postnatal Development of Microglia-Like Cells in Mouse Cochlea. Neural plasticity 2018 (2018)
Xiao-Long Zhou, Long-Xia He, Li-Jia Yu, Yong Wang, Xi-Jin Wang, En-Duo Wang, Tao Yang
Mutations in KARS cause early-onset hearing loss and leukoencephalopathy: Potential pathogenic mechanism. Human mutation 38 (12) (2017)
Penghui Chen, Longxia He, Xiuhong Pang, Xiaowen Wang, Tao Yang, Hao Wu
NLRP3 Is Expressed in the Spiral Ganglion Neurons and Associated with Both Syndromic and Nonsyndromic Sensorineural Deafness. Neural plasticity 2016 (2016)
Longxia He, Xiuhong Pang, Penghui Chen, Hao Wu, Tao Yang
Mutation in the Hair Cell Specific Gene POU4F3 Is a Common Cause for Autosomal Dominant Nonsyndromic Hearing Loss in Chinese Hans. Neural plasticity 2016 (2016)