Xuli Qian

Phenotype Prediction of Pathogenic Nonsynonymous Single Nucleotide Polymorphisms in WFS1

G. Xing, Xin Cao, Luyang Qin, 2015, Scientific Reports.

Probing the Effect of Two Heterozygous Mutations in Codon 723 of SLC26A4 on Deafness Phenotype Based on Molecular Dynamics Simulations

G. Xing, Jun Yao, Qinjun Wei, 2015, Scientific Reports.

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

G. Xing, Jun Yao, Qinjun Wei, 2014, Journal of Translational Medicine.

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

G. Xing, Jun Yao, Qinjun Wei, 2014, Journal of Translational Medicine.

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

G. Xing, Jun Yao, Qinjun Wei, 2017, Journal of Medical Genetics.