Yongyi Yuan

GJB2 mutation spectrum in 2063 Chinese patients with nonsyndromic hearing impairment

Pu Dai, Fei Yu, Bing Han et al. · Journal of Translational Medicine · 2009 · 193 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

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 · 153 citations · Full text

Medicine, Molecular Biology, Molecular Genetics +11

Digenic inheritance of non-syndromic deafness caused by mutations at the gap junction proteins Cx26 and Cx31

Xue-Zhong Liu, Yongyi Yuan, Denise Yan et al. · Human Genetics · 2008 · 116 citations

Life Sciences, Genetics, Molecular Genetics +16

The prevalence of the 235delC GJB2 mutation in a Chinese deaf population

Pu Dai, Fei Yu, Bing Han et al. · Genetics in Medicine · 2007 · 87 citations · Full text

Life Sciences, Genetics, Molecular Genetics +10

Molecular Epidemiology and Functional Assessment of Novel Allelic Variants of SLC26A4 in Non-Syndromic Hearing Loss Patients with Enlarged Vestibular Aqueduct in China

Yongyi Yuan, Weiwei Guo, Jie Tang et al. · PLoS ONE · 2012 · 86 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17