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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: li j, li k, li b. 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.
Cross-Disorder Analysis of De Novo Mutations in Neuropsychiatric Disorders.
Li K, Fang Z, Zhao G, Li B, Chen C, Xia L, Wang L, Luo T, Wang X, Wang Z, Zhang Y, Jiang Y, Pan Q, Hu Z, Guo H, Tang B, Liu C, Sun Z, Xia K, Li J. Li K, et al. Among authors: li j, li b. J Autism Dev Disord. 2022 Mar;52(3):1299-1313. doi: 10.1007/s10803-021-05031-7. Epub 2021 May 10. J Autism Dev Disord. 2022. PMID: 33970367 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: li j, li b. 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: li j, li k, li b. 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.
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: li j, li b. Brain. 2020 Jul 1;143(7):2220-2234. doi: 10.1093/brain/awaa167. Brain. 2020. PMID: 32613234
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: li j, li k. 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.
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: li y, li j, li b. 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.
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: li b, li jc. Brain. 2021 Apr 12;144(3):e25. doi: 10.1093/brain/awaa391. Brain. 2021. PMID: 33793763 No abstract available.
42,389 results
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