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PreviewIssue DateTitleAuthor(s)
2017Relations between lipoprotein(a) concentrations, LPA genetic variants, and the risk of mortality in patients with established coronary heart disease: a molecular and genetic association studyZewinger, S.; Kleber, M.E.; Tragante, V.; McCubrey, R.O.; Schmidt, A.F.; Direk, K.; Laufs, U.; Werner, C.; Koenig, W.; Rothenbacher, D.; Mons, U.; Breitling, L.P.; Brenner, H.; Jennings, R.T.; Petrakis, I.; Triem, S.; Klug, M.; Filips, A.; Blankenberg, S.; Waldeyer, C.; et al.
2012Colorectal cancer linkage on chromosomes 4q21, 8q13, 12q24, and 15q22Cicek, M.; Cunningham, J.; Fridley, B.; Serie, D.; Bamlet, W.; Diergaarde, B.; Haile, R.; Le Marchand, L.; Krontiris, T.; Younghusband, H.; Gallinger, S.; Newcomb, P.; Hopper, J.; Jenkins, M.; Casey, G.; Schumacher, F.; Chen, Z.; DeRycke, M.; Templeton, A.; Winship, I.; et al.; Lo, A.
2019Myocilin gene Gln368Ter variant penetrance and association with glaucoma in population-based and registry-based studiesHan, X.; Souzeau, E.; Ong, J.S.; An, J.; Siggs, O.M.; Burdon, K.P.; Best, S.; Goldberg, I.; Healey, P.R.; Graham, S.L.; Ruddle, J.B.; Mills, R.A.; Landers, J.; Galanopoulos, A.; White, A.J.R.; Casson, R.; Mackey, D.A.; Hewitt, A.W.; Gharahkhani, P.; Craig, J.E.; et al.
2013The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphismKlebe, S.; Golmard, J.-L.; Nalls, M.A.; Saad, M.; Singleton, A.B.; Bras, J.M.; Hardy, J.; Simon-Sanchez, J.; Heutink, P.; Kuhlenbaeumer, G.; Charfi, R.; Klein, C.; Hagenah, J.; Gasser, T.; Wurster, I.; Lesage, S.; Lorenz, D.; Deuschl, G.; Durif, F.; Pollak, P.; 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.
2018A genome-wide association study of diabetic kidney disease in subjects with type 2 diabetesVan Zuydam, N.R.; Ahlqvist, E.; Sandholm, N.; Deshmukh, H.; William Rayner, N.; Abdalla, M.; Ladenvall, C.; Ziemek, D.; Fauman, E.; Robertson, N.R.; McKeigue, P.M.; Valo, E.; Forsblom, C.; Harjutsalo, V.; Perna, A.; Rurali, E.; Loredana Marcovecchio, M.; Igo, R.P.; Salem, R.M.; Perico, N.; et al.
2015The International SSRI Pharmacogenomics Consortium (ISPC): a genome-wide association study of antidepressant treatment responseBiernacka, J.; Sangkuhl, K.; Jenkins, G.; Whaley, R.; Barman, P.; Batzler, A.; Altman, R.; Arolt, V.; Brockmöller, J.; Chen, C.; Domschke, K.; Hall-Flavin, D.; Hong, C.; Illi, A.; Ji, Y.; Kampman, O.; Kinoshita, T.; Leinonen, E.; Liou, Y.; Mushiroda, T.; 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.