RRBS-Analyser: A Comprehensive Web Server for Reduced Representation Bisulfite Sequencing Data AnalysisTao Wang, Jinyu Wu, Zhong Sheng Sun et al.|Human Mutation|2013Cited by 55
Nonrandom occurrence of multiple de novo coding variants in a proband indicates the existence of an oligogenic model in autismYaoqiang Du, Jinyu Wu, Xiao Zhi et al.|Genetics in Medicine|2019Cited by 41
Prioritized High-Confidence Risk Genes for Intellectual Disability Reveal Molecular Convergence During Brain DevelopmentZhenwei Liu, Xiaobing Wang, Jinyu Wu et al.|Frontiers in Genetics|2018Cited by 29
mirDNMR: a gene-centered database of background<i>de novo</i>mutation rates in humanYiyi Jiang, Jinyu Wu, Wei Li et al.|Nucleic Acids Research|2016Cited by 20
A de novo pathogenic <i>CSNK1E</i> mutation identified by exome sequencing in family trios with epileptic encephalopathyZhenwei Liu, Huangqi Xue, Jinyu Wu et al.|Human Mutation|2018Cited by 11