Xuli Qian

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

Phenotype Prediction of Pathogenic Nonsynonymous Single Nucleotide Polymorphisms in WFS1

Xuli Qian, Luyang Qin, Guangqian Xing et al. · Scientific Reports · 2015 · 30 citations · Full text

<i>GPRASP2</i>, a novel causative gene mutated in an X-linked recessive syndromic hearing loss

Guangqian Xing, Jun Yao, Chunyu Liu et al. · Journal of Medical Genetics · 2017 · 11 citations · Full text