Qian Xin

An intronic variant associated with systemic lupus erythematosus changes the binding affinity of Yinyang1 to downregulate WDFY4

Hailing Zhao, Wanling Yang, Ruojun Qiu et al. · Genes and Immunity · 2012 · 50 citations · Full text

Immunogenetics, Autoimmune Disease, Systemic Lupus Erythematosus +12

Whole-Exome Sequencing Identifies a Variant in<i>TMEM132E</i>Causing Autosomal-Recessive Nonsyndromic Hearing Loss DFNB99

Jiangxia Li, Xiaohan Zhao, Qian Xin et al. · Human Mutation · 2014 · 45 citations

Genetics, Pathology, Molecular Genetics +22

Exome sequencing reveals a heterozygous DLX5 mutation in a Chinese family with autosomal-dominant split-hand/foot malformation

Xue Wang, Qian Xin, Lin Li et al. · European Journal of Human Genetics · 2014 · 37 citations · Full text

Developmental Anomaly, Chinese Family, Developmental Biology +9

Gene–gene interactions of <scp>IRF5</scp>, <scp>STAT4</scp>, <scp>IKZF1</scp> and <scp>ETS1</scp> in systemic lupus erythematosus

Jie Dang, Shiying Shan, Jingjing Li et al. · Tissue Antigens · 2014 · 34 citations

A novel label-free dual-mode aptasensor based on the mutual regulation of silver nanoclusters and MoSe2 nanosheets for reliable detection of ampicillin

Pengfei Fan, Qian Xin, Qianji Li et al. · Analytica Chimica Acta · 2023 · 34 citations

Nanomedicine, Engineering, Bioanalysis +7