Pu Dai

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

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 · Full text

Developmental Anomaly, Developmental Biology, Mendelian Disorder +9

Concurrent Hearing and Genetic Screening of 180,469 Neonates with Follow-up in Beijing, China

Pu Dai, Li-Hui Huang, Guo-Jian Wang et al. · The American Journal of Human Genetics · 2019 · 106 citations · Full text

Early Diagnosis, Pediatric Otolaryngology, Genetics +14