Tao Yang

Transcriptional Control of SLC26A4 Is Involved in Pendred Syndrome and Nonsyndromic Enlargement of Vestibular Aqueduct (DFNB4)

Tao Yang, Hilmar Viđarsson, Sandra Rodrigo-Blomqvist et al. · The American Journal of Human Genetics · 2007 · 215 citations

Life Sciences, Genetics, Molecular Genetics +10

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

Mei Zhu, Tao Yang, Shu‐Chen Wei et al. · The American Journal of Human Genetics · 2003 · 201 citations · Full text

Medicine, Genetics, Molecular Genetics +12

Mutations of KCNJ10 Together with Mutations of SLC26A4 Cause Digenic Nonsyndromic Hearing Loss Associated with Enlarged Vestibular Aqueduct Syndrome

Tao Yang, José Gurrola, Hao Wu et al. · The American Journal of Human Genetics · 2009 · 180 citations · Full text

Medicine, Genetics, Molecular Genetics +14

Genetic etiology study of the non-syndromic deafness in Chinese Hans by targeted next-generation sequencing

Tao Yang, Xiaoming Wei, Yongchuan Chai et al. · Orphanet Journal of Rare Diseases · 2013 · 178 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

Utilizing Ethnic-Specific Differences in Minor Allele Frequency to Recategorize Reported Pathogenic Deafness Variants

A. Eliot Shearer, Robert W. Eppsteiner, Kevin T. Booth et al. · The American Journal of Human Genetics · 2014 · 154 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12