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University of Illinois at Chicago


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1.        Li JC, Cai T, Jiang Y, Chen HQ, He X, Chen C, Li XF, Shao QZ, Ran X, Li ZS, Xia K, Liu CY*, Sun ZS*, Wu JY*. Genes with de novo mutations are shared by four neuropsychiatric disorders discovered from NPdenovo database. Molecular Psychiatry, 2015. (IF=15.147, accepted)
2.        Ran X, Li JC, Shao QZ, Chen HQ, Lin ZD, Sun ZS*£¬Wu JY*.  EpilepsyGene: a genetic resource for genes and mutations related to epilepsy. Nucleic Acids Research, 43(Database issue): D893-9£¬2014. (IF=8.808)
3.        Xie Q, Liu Q, Mao FB, Cai WS, Wu HH, You MC, Wang Z, Chen BY, Sun ZS, Wu JY(*), A Bayesian Framework to Identify Methylcytosines from High-Throughput Bisulfite Sequencing Data, PLoS Computational Biology, 2014, 10(9): e1003853. (IF=4.829)

4.        Ran X, Cai  WJ, Huang  XF, Liu Q, Lu F, Qu J, Wu, JY*£¬Jin ZB*. RetinoGenetics: a comprehensive mutation database for genes related to inherited retinal degeneration. Database (Oxford£©, 2014, doi: 10.1093/database/bau047£¬2014. (IF=4.457)
5.        Li JC, Jiang Y, Wang T, Chen HQ, Xie Q, Shao  QZ,  Ran X£¬Xia K£¬Sun ZS*£¬Wu JY*. mirTrios: an integrated pipeline for detection of de novo and rare inherited mutations from trios-based next-generation sequencing. Journal of Medical Genetics, doi: 10.1136/jmedgenet-2014-102656£¬2014. (IF=5.636)
6.        Wang T, Liu Q, Li XF, Wang XB, Li JC, Zhu XC, Sun ZS(*), Wu JY(*), RRBS-analyser: a comprehensive web server for reduced representation bisulfite sequencing data analysis, Human Mutation, 2013, 34(12): 1606-10. (IF=5.05)
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