中文

Journal Publications

[41]Li B#, Zhao G, Li K, Wang Z, Fang Z, Wang X, Luo T, Zhang Y, Wang Y, Chen Q, Huang Y, Dong L, Guo J, Tang B, Li J*.Characterizing the Expression Patterns of Parkinson's Disease Associated Genes.Frontiers in Neuroscience, 2021
[42]Li B#, Wang Z, Chen Q, Li K, Wang X, Han Y, LU B, Zhao Y, Zhang R, Jiang L, Pan H, Luo T, Zhang Y, Fang Z, Xiao X, Zhou X, Wang R, Zhou L, Wang Y, Yuan Z, Xia L, Guo J, Tang B, Xia K, Zhao G*, Li J*.GPCards: an integrated database of genotype-phenotype correlations in human genetic diseases.Computational and Structural Biotechnology Journal, 2021
[43]Luo T#, Li K#, Zhao G, Li B, Chen C, Fang Z, Xia L, Wang L, Wang X, Wang Z, Zhang Y, Jiang l, Hu Z, Guo H, Tang B, Liu C, Sun Z, Xia K, Zhou X, Wang Y, Pan H, Zhou Q, Pan Q*, Xia K*, Li J*.De novo mutations in folate related genes associated with common developmental disorders.Computational and Structural Biotechnology Journal, 2021
[44]Li B#, Li K, Tian D, Zhou Q, Xie Y, Fang Z, Wang X, Luo T, Wang Z, Zhang Y, Wang Y, Chen Q, Meng Q, Zhao G*, Li J*.De novo mutation of cancer-related genes associates with particular neurodevelopmental disorders.Journal of Molecular Medicine, 2020
[45]Wang L#, Zhang Y#, Li K#, Wang Z, Wang X, Li B, Zhao G, Fang Z, Ling Z, Luo T, Xia L, Li Y, Guo H, Hu Z, Li J*, Sun Z*, Xia K*.Functional relationships between recessive inherited genes and genes with de novo variants in autism spectrum disorder.Molecular Autism, 2020
[46]Zhao Y#, Qin L#, Pan H, Liu Z, Jiang L, He Y, Zeng Q, Zhou X, Zhou X, Zhou Y, Fang Z, Wang Z, Xiang Y, Yang H, Wang Y, Zhan K, Zhang R, He R, Zhou X, Zhou Z, Yang N, Liang D, Chen J, Zhang X, Zhou Y, Liu H, Deng P, Xu K, Xu K, Zhou C, Zhong J, Xu Q, Sun Q, Li B, Zhao G, Wang T, Chen L, Shang H, Liu.The role of genetics in Parkinson's disease: a large cohort study in Chinese mainland population.Brain, 2020
[47]Zhang Y#, Li N, Li C, Zhang Z, Teng H, Wang Y, Zhao T, Shi L, Zhang K, Xia K, Li J*, Sun Z*.Genetic evidence of gender difference in autism spectrum disorder supports the female-protective effect.Translational Psychiatry, 2020
[48]Zhao G#, Li K#, Li B, Wang Z, Fang Z, Wang X, Zhang Y, Luo T, Zhou Q, Wang L, Xie Y, Wang Y, Chen Q, Xia L, Tang Y, Tang B, Xia K, Li J*.Gene4Denovo: an integrated database and analytic platform for de novo mutations in humans.Nucleic Acids Research, 2020
[49]Li J#, Hu S#, Zhang K, Shi L, Zhang Y, Zhao T, Wang L, He X, Xia K, Liu C, Sun Z*.A comparative study of the genetic components of three subcategories of autism spectrum disorder.Molecular Psychiatry, 2019
[50]Li J#, Zhao T#, Zhang Y, Zhang K, Shi L, Chen Y, Wang X, Sun Z*.Performance evaluation of pathogenicity-computation methods for missense variants.Nucleic Acids Research, 2018
[51]Wang Y#, Zeng C#, Li J#, Zhou Z, Ju X, Xia S, Li Y, Liu A, Teng H, Zhang K, Shi L, Bi C, Xie W, He X, Jia Z, Jiang Y, Cai T, Wu J, Xia K*, Sun ZS*.PAK2 Haploinsufficiency Results in Synaptic Cytoskeleton Impairment and Autism-Related Behavior.Cell Reports, 2018
[52]Li J#, Shi L#, Zhang K, Zhang Y, Hu S, Zhao T, Teng H, Li X, Jiang Y, Ji L, Sun ZS*.Varcards: an integrated genetic and clinical database for coding variations in human genome.Nucleic Acids Research, 2018
[53]Li J#, Wang L#, Guo H, Shi L, Zhang K, Tang M, Hu S, Dong S, Liu Y, Wang T, Yu P, He X, Hu Z, Zhao J, Liu C*, Sun Z*, Xia K*.Targeted sequencing and functional analysis reveal brain-size-related genes and their networks in autism spectrum disorders.Molecular Psychiatry, 2017
[54]Li J#, Wang L#, Yu P, Shi L, Zhang K, Sun ZS*, Xia K*.Vitamin D-related genes are subjected to significant de novo mutation burdens in autism spectrum disorder.American Journal of Medical Genetics part B-Neuropsychiatric Genetics, 2017
[55]Li J#, Cai T#, Jiang Y, Chen H, He X, Chen Y, Li X, Shao Q, Ran X, Li Z, Xia K, Liu C*, Sun Z*, Wu J*.Genes with de novo mutations are shared by four neuropsychiatric disorders discovered from NPdenovo database.Molecular Psychiatry, 2016
[56]Li J#, Jiang Y#, Wang T, Chen H, Xie Q, Shao Q, Ran X, Xia K, Sun ZS*, Wu J*.mirTrios: an integrated pipeline for detection of de novo and rare inherited mutations from trios-based next-generation sequencing.Journal of Medical Genetics, 2015
[57]Ran X#, Li J#, Shao Q, Chen H, Lin Z, Sun ZS*, Wu J*.EpilepsyGene: a genetic resource for genes and mutations related to epilepsy.Nucleic Acids Research, 2015

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Jinchen Li

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