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PreviewIssue DateTitleAuthor(s)
2019Association of chromosome 9p21 with subsequent coronary heart disease events A GENIUS-CHD study of individual participant dataPatel, R.S.; Schmidt, A.F.; Tragante, V.; McCubrey, R.O.; Holmes, M.; Howe, L.J.; Direk, K.; Akerblom, A.; Leander, K.; Virani, S.S.; Kaminski, K.A.; Muehlschlegel, J.D.; Dube, M.-P.; Allayee, H.; Almgren, P.; Alver, M.; Baranova, E.; Behlouli, H.; Boeckx, B.; Braund, P.S.; et al.
2020A phenome-wide association and Mendelian Randomisation study of polygenic risk for depression in UK BiobankShen, X.; Howard, D.M.; Adams, M.J.; Hill, W.D.; Clarke, T.K.; Adams, M.J.; Clarke, T.K.; McIntosh, A.M.; Deary, I.J.; Wray, N.R.; Ripke, S.; Mattheisen, M.; Trzaskowski, M.; Byrne, E.M.; Abdellaoui, A.; Agerbo, E.; Air, T.M.; Andlauer, T.F.M.; Bacanu, S.A.; Bækvad-Hansen, M.; et al.
2014Common variants near ABCA1, AFAP1 and GMDS confer risk of primary open-angle glaucomaGharahkhani, P.; Burdon, K.; Fogarty, R.; Sharma, S.; Hewitt, A.; Martin, S.; Law, M.; Cremin, K.; Bailey, J.; Loomis, S.; Pasquale, L.; Haines, J.; Hauser, M.; Viswanathan, A.; McGuffin, P.; Topouzis, F.; Foster, P.; Graham, S.; Casson, R.; Chehade, M.; et al.
2013Genetic variants associated with increased risk of malignant pleural mesothelioma: a genome-wide association studyMatullo, G.; Guarrera, S.; Betti, M.; Fiorito, G.; Ferrante, D.; Voglino, F.; Cadby, G.; Di Gaetano, C.; Rosa, F.; Russo, A.; Hirvonen, A.; Casalone, E.; Tunesi, S.; Padoan, M.; Giordano, M.; Aspesi, A.; Casadio, C.; Ardissone, F.; Ruffini, E.; Betta, P.; et al.; Miao, X.-P.
2021Variation in the risk of colorectal cancer in families with Lynch syndrome: a retrospective cohort studyWin, A.K.; Dowty, J.G.; Reece, J.C.; Lee, G.; Templeton, A.S.; Plazzer, J.P.; Buchanan, D.D.; Akagi, K.; Aksoy, S.; Alonso, A.; Alvarez, K.; Amor, D.J.; Ankathil, R.; Aretz, S.; Arnold, J.L.; Aronson, M.; Austin, R.; Backman, A.S.; Bajwa-ten Broeke, S.W.; Barca-Tierno, V.; et al.
2015Association of the colorectal CpG island methylator phenotype with molecular features, risk factors, and family historyWeisenberger, D.; Levine, A.; Long, T.; Buchanan, D.; Walters, R.; Clendenning, M.; Rosty, C.; Joshi, A.; Stern, M.; Le Marchand, L.; Lindor, N.; Daftary, D.; Gallinger, S.; Selander, T.; Bapat, B.; Newcomb, P.; Campbell, P.; Casey, G.; Ahnen, D.; Baron, J.; et al.
2011Progesterone receptor gene variants and risk of endometrial cancerO'Mara, T.; Fahey, P.; Ferguson, K.; Marquart, L.; Lambrechts, D.; Despierre, E.; Vergote, I.; Amant, F.; Hall, P.; Liu, J.; Czene, K.; SASBAC,; Rebbeck, T.; WISE Study Group,; AOCS Management Group,; SEARCH,; Ahmed, S.; Dunning, A.; Gregory, C.; Shah, M.; et al.

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