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A Bayesian framework for efficient and accurate variant prediction.
Qian D, Li S, Tian Y, Clifford JW, Sarver BAJ, Pesaran T, Gau CL, Elliott AM, Lu HM, Black MH. Qian D, et al. Among authors: li s. PLoS One. 2018 Sep 13;13(9):e0203553. doi: 10.1371/journal.pone.0203553. eCollection 2018. PLoS One. 2018. PMID: 30212499 Free PMC article.
Genotype-phenotype associations among panel-based TP53+ subjects.
Rana HQ, Clifford J, Hoang L, LaDuca H, Black MH, Li S, McGoldrick K, Speare V, Dolinsky JS, Gau CL, Garber JE. Rana HQ, et al. Among authors: li s. Genet Med. 2019 Nov;21(11):2478-2484. doi: 10.1038/s41436-019-0541-y. Epub 2019 May 20. Genet Med. 2019. PMID: 31105275 Free article.
Validation of a prostate cancer polygenic risk score.
Black MH, Li S, LaDuca H, Lo MT, Chen J, Hoiness R, Gutierrez S, Tippin-Davis B, Lu HM, Gielzak M, Wiley K, Shi Z, Wei J, Zheng SL, Helfand BT, Isaacs W, Xu J. Black MH, et al. Among authors: li s. Prostate. 2020 Nov;80(15):1314-1321. doi: 10.1002/pros.24058. Epub 2020 Aug 17. Prostate. 2020. PMID: 33258481 Free PMC article.
Multigene Panel Testing Provides a New Perspective on Lynch Syndrome.
Espenschied CR, LaDuca H, Li S, McFarland R, Gau CL, Hampel H. Espenschied CR, et al. Among authors: li s. J Clin Oncol. 2017 Aug 1;35(22):2568-2575. doi: 10.1200/JCO.2016.71.9260. Epub 2017 May 17. J Clin Oncol. 2017. PMID: 28514183 Free PMC article.
Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline CDH1 sequence variants.
Lee K, Krempely K, Roberts ME, Anderson MJ, Carneiro F, Chao E, Dixon K, Figueiredo J, Ghosh R, Huntsman D, Kaurah P, Kesserwan C, Landrith T, Li S, Mensenkamp AR, Oliveira C, Pardo C, Pesaran T, Richardson M, Slavin TP, Spurdle AB, Trapp M, Witkowski L, Yi CS, Zhang L, Plon SE, Schrader KA, Karam R. Lee K, et al. Among authors: li s. Hum Mutat. 2018 Nov;39(11):1553-1568. doi: 10.1002/humu.23650. Hum Mutat. 2018. PMID: 30311375 Free PMC article.
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