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For: Cai B, Li B, Kiga N, Thusberg J, Bergquist T, Chen YC, Niknafs N, Carter H, Tokheim C, Beleva-Guthrie V, Douville C, Bhattacharya R, Yeo HTG, Fan J, Sengupta S, Kim D, Cline M, Turner T, Diekhans M, Zaucha J, Pal LR, Cao C, Yu CH, Yin Y, Carraro M, Giollo M, Ferrari C, Leonardi E, Tosatto SCE, Bobe J, Ball M, Hoskins RA, Repo S, Church G, Brenner SE, Moult J, Gough J, Stanke M, Karchin R, Mooney SD. Matching phenotypes to whole genomes: Lessons learned from four iterations of the personal genome project community challenges. Hum Mutat 2017;38:1266-76. [PMID: 28544481 DOI: 10.1002/humu.23265] [Cited by in Crossref: 9] [Cited by in F6Publishing: 5] [Article Influence: 1.8] [Reference Citation Analysis]
Number Citing Articles
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4 Bergquist T, Yan Y, Schaffter T, Yu T, Pejaver V, Hammarlund N, Prosser J, Guinney J, Mooney S. Piloting a model-to-data approach to enable predictive analytics in health care through patient mortality prediction. J Am Med Inform Assoc 2020;27:1393-400. [PMID: 32638010 DOI: 10.1093/jamia/ocaa083] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.5] [Reference Citation Analysis]
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6 Warmerdam R, Lanting P, Deelen P, Franke L; Lifelines Cohort Study. Idéfix: identifying accidental sample mix-ups in biobanks using polygenic scores. Bioinformatics 2021:btab783. [PMID: 34792549 DOI: 10.1093/bioinformatics/btab783] [Reference Citation Analysis]
7 Douville NJ, Kheterpal S, Engoren M, Mathis M, Mashour GA, Hornsby WE, Willer CJ, Douville CB. Genetic mutations associated with susceptibility to perioperative complications in a longitudinal biorepository with integrated genomic and electronic health records. Br J Anaesth 2020;125:986-94. [PMID: 32891412 DOI: 10.1016/j.bja.2020.08.009] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]