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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. 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.
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. 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.
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. 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. Hum Mol Genet. 2022 Jun 4;31(11):1747-1761. doi: 10.1093/hmg/ddab358. Hum Mol Genet. 2022. PMID: 34897451
1,318 results