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Genome-wide association study using whole-genome sequencing identifies risk loci for Parkinson's disease in Chinese population.
Pan H, Liu Z, Ma J, Li Y, Zhao Y, Zhou X, Xiang Y, Wang Y, Zhou X, He R, Xie Y, Zhou Q, Yuan K, Xu Q, Sun Q, Wang J, Yan X, Zhang H, Wang C, Lei L, Liu W, Wang X, Ding X, Wang T, Xue Z, Zhang Z, Chen L, Wang Q, Liu Y, Tang J, Zhang X, Peng S, Wang C, Ding J, Liu C, Wang L, Chen H, Shen L, Jiang H, Wu X, Tan H, Luo D, Xiao S, Chen X, Tan J, Hu Z, Chen C, Xia K, Zhang Z, Foo JN, Blauwendraat C, Nalls MA, Singleton AB, Liu J, Chan P, Zheng H, Li J, Guo J, Yang J, Tang B; Parkinson’s Disease & Movement Disorders Multicenter Database and Collaborative Network in China (PD-MDCNC). Pan H, et al. Among authors: zhou x, zhou q. NPJ Parkinsons Dis. 2023 Feb 9;9(1):22. doi: 10.1038/s41531-023-00456-6. NPJ Parkinsons Dis. 2023. PMID: 36759515 Free PMC article.
De novo mutations in folate-related genes associated with common developmental disorders.
Luo T, Li K, Ling Z, Zhao G, Li B, Wang Z, Wang X, Han Y, Xia L, Zhang Y, Zhou Q, Fang Z, Wang Y, Chen Q, Zhou X, Pan H, Zhao Y, Wang Y, Dong L, Huang Y, Hu Z, Pan Q, Xia K, Li J. Luo T, et al. Among authors: zhou x, zhou q. Comput Struct Biotechnol J. 2021 Mar 1;19:1414-1422. doi: 10.1016/j.csbj.2021.02.011. eCollection 2021. Comput Struct Biotechnol J. 2021. PMID: 33777337 Free PMC article.
Gene4PD: A Comprehensive Genetic Database of Parkinson's Disease.
Li B, Zhao G, Zhou Q, Xie Y, Wang Z, Fang Z, Lu B, Qin L, Zhao Y, Zhang R, Jiang L, Pan H, He Y, Wang X, Luo T, Zhang Y, Wang Y, Chen Q, Liu Z, Guo J, Tang B, Li J. Li B, et al. Among authors: zhou q. Front Neurosci. 2021 Apr 26;15:679568. doi: 10.3389/fnins.2021.679568. eCollection 2021. Front Neurosci. 2021. PMID: 33981200 Free PMC article.
Genetic landscape of human mitochondrial genome using whole-genome sequencing.
Wang Y, Zhao G, Fang Z, Pan H, Zhao Y, Wang Y, Zhou X, Wang X, Luo T, Zhang Y, Wang Z, Chen Q, Dong L, Huang Y, Zhou Q, Xia L, Li B, Guo J, Xia K, Tang B, Li J. Wang Y, et al. Among authors: zhou x, zhou q. Hum Mol Genet. 2022 Jun 4;31(11):1747-1761. doi: 10.1093/hmg/ddab358. Hum Mol Genet. 2022. PMID: 34897451
Performance Comparison of Computational Methods for the Prediction of the Function and Pathogenicity of Non-coding Variants.
Wang Z, Zhao G, Li B, Fang Z, Chen Q, Wang X, Luo T, Wang Y, Zhou Q, Li K, Xia L, Zhang Y, Zhou X, Pan H, Zhao Y, Wang Y, Wang L, Guo J, Tang B, Xia K, Li J. Wang Z, et al. Among authors: zhou x, zhou q. Genomics Proteomics Bioinformatics. 2023 Jun;21(3):649-661. doi: 10.1016/j.gpb.2022.02.002. Epub 2022 Mar 8. Genomics Proteomics Bioinformatics. 2023. PMID: 35272052 Free PMC article.
Interactions of genetic risks for autism and the broad autism phenotypes.
Dong L, Wang Y, Wang X, Luo T, Zhou Q, Zhao G, Li B, Xia L, Xia K, Li J. Dong L, et al. Among authors: zhou q. Front Psychiatry. 2023 Mar 21;14:1110080. doi: 10.3389/fpsyt.2023.1110080. eCollection 2023. Front Psychiatry. 2023. PMID: 37102084 Free PMC article.
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