Qinjun Wei

Identification of OSBPL2 as a novel candidate gene for progressive nonsyndromic hearing loss by whole-exome sequencing

Guangqian Xing, Jun Yao, Bin Wu et al. · Genetics in Medicine · 2014 · 64 citations · Full text

Developmental Biology, Genetic Disorder, Whole-exome Sequencing +11

Targeted genomic capture and massively parallel sequencing to identify novel variants causing Chinese hereditary hearing loss

Qinjun Wei, Hongmei Zhu, Xuli Qian et al. · Journal of Translational Medicine · 2014 · 50 citations · Full text

Maternally inherited non-syndromic hearing loss associated with mitochondrial 12S rRNA A827G mutation in a Chinese family

Guangqian Xing, Zhibin Chen, Qinjun Wei et al. · Biochemical and Biophysical Research Communications · 2006 · 46 citations

Biology, Chinese Family, Mendelian Disorder +13

Deletion of OSBPL2 in auditory cells increases cholesterol biosynthesis and drives reactive oxygen species production by inhibiting AMPK activity

Hongshun Wang, Changsong Lin, Jun Yao et al. · Cell Death and Disease · 2019 · 41 citations · Full text

Mitochondrial 12S rRNA A827G mutation is involved in the genetic susceptibility to aminoglycoside ototoxicity

Guangqian Xing, Zhibin Chen, Qinjun Wei et al. · Biochemical and Biophysical Research Communications · 2006 · 39 citations

Mitochondrial Function, Biochemistry, Medicine +9