Xin Zhang

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

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 · 109 citations · Full text

Medicine, Genetics, Pediatrics +14

Cosegregation of the G7444A mutation in the mitochondrial COI/tRNA^Ser(UCN) genes with the 12S rRNA A1555G mutation in a Chinese family with aminoglycoside‐induced and nonsyndromic hearing loss

Huijun Yuan, Yaping Qian, Yanjun Xu et al. · American Journal of Medical Genetics Part A · 2005 · 85 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA mutation in 16 Chinese families: Implication for early detection and prevention of deafness

Pu Dai, Xin Liu, Dongyi Han et al. · Biochemical and Biophysical Research Communications · 2005 · 59 citations

Life Sciences, Genetics, Molecular Genetics +17

Prevalence of the GJB2 IVS1+1G >A mutation in Chinese hearing loss patients with monoallelic pathogenic mutation in the coding region of GJB2

Yongyi Yuan, Fei Yu, Guojian Wang et al. · Journal of Translational Medicine · 2010 · 38 citations · Full text

Life Sciences, Genetics, Molecular Genetics +9