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The role of genetics in Parkinson's disease: a large cohort study in Chinese mainland population.
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, Zhang 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 W, Chan P, Xue Z, Wang Q, Guo L, Wang X, Xu C, Zhang Z, Chen T, Lei L, Zhang H, Wang C, Tan J, Yan X, Shen L, Jiang H, Zhang Z, Hu Z, Xia K, Yue Z, Li J, Guo J, Tang B. Zhao Y, et al. Among authors: wang x, wang z, wang y, wang t, wang c, wang q. Brain. 2020 Jul 1;143(7):2220-2234. doi: 10.1093/brain/awaa167. Brain. 2020. PMID: 32613234
GCH1 variants contribute to the risk and earlier age-at-onset of Parkinson's disease: a two-cohort case-control study.
Pan HX, Zhao YW, Mei JP, Fang ZH, Wang Y, Zhou X, Zhou YJ, Zhang R, Zhang KL, Jiang L, Zeng Q, He Y, Wang Z, Liu ZH, Xu Q, Sun QY, Yang Y, Hu YC, Chen YS, Du J, Lei LF, Zhang HN, Wang CY, Yan XX, Shen L, Jiang H, Tan JQ, Li JC, Tang BS, Guo JF. Pan HX, et al. Among authors: wang z, wang y, wang cy. Transl Neurodegener. 2020 Aug 4;9(1):31. doi: 10.1186/s40035-020-00212-3. Transl Neurodegener. 2020. PMID: 32746945 Free PMC article.
ATP10B variants in Parkinson's disease: a large cohort study in Chinese mainland population.
Zhao Y, Pan H, Wang Y, Zeng Q, Fang Z, He R, Xu K, Zhou X, Zhou X, Zhou Z, Li Y, Deng P, Xu Y, Xu Q, Sun Q, Li B, Zhao G, Lei L, Zhang H, Wang C, Tan J, Yan X, Shen L, Jiang H, Li J, Guo J, Tang B, Liu Z. Zhao Y, et al. Among authors: wang y, wang c. Acta Neuropathol. 2021 May;141(5):805-806. doi: 10.1007/s00401-021-02280-9. Epub 2021 Feb 18. Acta Neuropathol. 2021. PMID: 33599816 No abstract available.
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: wang x, wang z, wang y. 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.
UQCRC1 variants in Parkinson's disease: a large cohort study in Chinese mainland population.
Zhao YW, Pan HX, Wang CY, Zeng Q, Wang Y, Fang ZH, Huang J, Li X, Wang X, Zhang X, Liu ZH, Sun QY, Xu Q, Lei LF, Yan XX, Shen L, Jiang H, Tan JQ, Li JC, Tang BS, Zhang HN, Guo JF. Zhao YW, et al. Among authors: wang x, wang y, wang cy. Brain. 2021 Jul 28;144(6):e54. doi: 10.1093/brain/awab137. Brain. 2021. PMID: 33779694 No abstract available.
PSAP variants in Parkinson's disease: a large cohort study in Chinese mainland population.
Zhao YW, Pan HX, Zeng Q, Fang ZH, Liu ZH, Wang Y, Jiang L, He R, Zhou X, Zhou YJ, Xu Q, Sun QY, Li B, Zhao G, Yang Y, Hu YC, Chen YS, Du J, Lei LF, Zhang HN, Wang CY, Yan XX, Shen L, Jiang H, Li JC, Tang BS, Tan JQ, Guo JF. Zhao YW, et al. Among authors: wang y, wang cy. Brain. 2021 Apr 12;144(3):e25. doi: 10.1093/brain/awaa391. Brain. 2021. PMID: 33793763 No abstract available.
GPCards: An integrated database of genotype-phenotype correlations in human genetic diseases.
Li B, Wang Z, Chen Q, Li K, Wang X, Wang Y, Zeng Q, 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. Li B, et al. Among authors: wang x, wang z, wang y, wang r. Comput Struct Biotechnol J. 2021 Mar 22;19:1603-1611. doi: 10.1016/j.csbj.2021.03.011. eCollection 2021. Comput Struct Biotechnol J. 2021. PMID: 33868597 Free PMC article.
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