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A Statistical Framework for Mapping Risk Genes from De Novo Mutations in Whole-Genome-Sequencing Studies.
Liu Y, Liang Y, Cicek AE, Li Z, Li J, Muhle RA, Krenzer M, Mei Y, Wang Y, Knoblauch N, Morrison J, Zhao S, Jiang Y, Geller E, Ionita-Laza I, Wu J, Xia K, Noonan JP, Sun ZS, He X. Liu Y, et al. Among authors: jiang y. Am J Hum Genet. 2018 Jun 7;102(6):1031-1047. doi: 10.1016/j.ajhg.2018.03.023. Epub 2018 May 10. Am J Hum Genet. 2018. PMID: 29754769 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: jiang y. 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.
Integrative analyses prioritize GNL3 as a risk gene for bipolar disorder.
Meng Q, Wang L, Dai R, Wang J, Ren Z, Liu S, Xia Y, Jiang Y, Duan F, Wang K, Liu C, Chen C. Meng Q, et al. Among authors: jiang y. Mol Psychiatry. 2020 Nov;25(11):2672-2684. doi: 10.1038/s41380-020-00866-5. Epub 2020 Aug 21. Mol Psychiatry. 2020. PMID: 32826963
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