Qi‐Jie Zhang

Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia

Wan‐Jin Chen, Yu Lin, Zhi‐Qi Xiong et al. · Nature Genetics · 2011 · 477 citations

Transcriptional Regulation, Mendelian Disorder, Genetic Disorder +6

Genetic Spectrum and Variability in Chinese Patients with Amyotrophic Lateral Sclerosis

Zhijun Liu, Hui-Xia Lin, Qiao Wei et al. · Aging and Disease · 2019 · 63 citations · Full text

Molecular analysis of SMN1, SMN2, NAIP, GTF2H2, and H4F5 genes in 157 Chinese patients with spinal muscular atrophy

Jin He, Qi‐Jie Zhang, Qifang Lin et al. · Gene · 2013 · 56 citations

Genetic Disorder, Medicine, Genetics +9

Novel SLC20A2 mutations identified in southern Chinese patients with idiopathic basal ganglia calcification

Wan‐Jin Chen, Xiang‐Ping Yao, Qi‐Jie Zhang et al. · Gene · 2013 · 46 citations

Medicine, Experimental Neuropathology, Pathology +7

Disruption of splicing-regulatory elements using CRISPR/Cas9 to rescue spinal muscular atrophy in human iPSCs and mice

Jin-Jing Li, Xiang Lin, Cheng Tang et al. · National Science Review · 2019 · 28 citations · Full text