Dongyi Han

Maternally Inherited Aminoglycoside-Induced and Nonsyndromic Deafness Is Associated with the Novel C1494T Mutation in the Mitochondrial 12S rRNA Gene in a Large Chinese Family

Hui Zhao, Ronghua Li, Qiuju Wang et al. · The American Journal of Human Genetics · 2004 · 422 citations · Full text

Mendelian Disorder, Mitochondrial Function, Genetic Disorder +10

GJB2 mutation spectrum in 2063 Chinese patients with nonsyndromic hearing impairment

Pu Dai, Fei Yu, Bing Han et al. · Journal of Translational Medicine · 2009 · 190 citations · Full text

Comprehensive molecular etiology analysis of nonsyndromic hearing impairment from typical areas in China

Yongyi Yuan, Yiwen You, Deliang Huang et al. · Journal of Translational Medicine · 2009 · 152 citations · Full text

Loss-of-Function Mutations in the PRPS1 Gene Cause a Type of Nonsyndromic X-linked Sensorineural Deafness, DFN2

Xue Zhong Liu, Dongyi Han, Jianzhong Li et al. · The American Journal of Human Genetics · 2009 · 123 citations · Full text

Developmental Biology, Genetic Disorder, Prps1 Gene Cause +5

Vibrant Soundbridge implantation via the third window in two Chinese patients with severe bilateral congenital aural atresia

Shiming Yang, Yihui Zou, Jianan Li et al. · Acta Oto-Laryngologica · 2013 · 90 citations