Qingwen Zhu

SLC26A4 c.919-2A>G varies among Chinese ethnic groups as a cause of hearing loss

Pu Dai, Qi Li, Deliang Huang et al. · Genetics in Medicine · 2008 · 65 citations

The mitochondrial tRNAAla T5628C variant may have a modifying role in the phenotypic manifestation of the 12S rRNA C1494T mutation in a large Chinese family with hearing loss

Dongyi Han, Pu Dai, Qingwen Zhu et al. · Biochemical and Biophysical Research Communications · 2007 · 42 citations

Biology, Mitochondrial Function, Genetic Disorder +7

A novel EYA4 mutation causing hearing loss in a Chinese DFNA family and genotype-phenotype review of EYA4 in deafness

Aiping Huang, Yongyi Yuan, Yan-Ping Liu et al. · Journal of Translational Medicine · 2015 · 21 citations · Full text

Assessment of Hearing Screening Combined With Limited and Expanded Genetic Screening for Newborns in Nantong, China

Qingwen Zhu, Mu-Ting Li, Xun Zhuang et al. · JAMA Network Open · 2021 · 20 citations · Full text

A novel pore-region mutation, c.887G > A (p.G296D) in KCNQ4, causing hearing loss in a Chinese family with autosomal dominant non-syndromic deafness 2

Bangqing Huang, Xue Gao, Jin‐Cao Xu et al. · BMC Medical Genetics · 2017 · 13 citations · Full text