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Results 11-20 of 82 (Search time: 0.004 seconds).
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PreviewIssue DateTitleAuthor(s)
2020Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progressionCraig, J.E.; Han, X.; Qassim, A.; Hassall, M.; Cooke Bailey, J.N.; Kinzy, T.G.; Khawaja, A.P.; An, J.; Marshall, H.; Gharahkhani, P.; Igo, R.P.; Graham, S.L.; Healey, P.R.; Ong, J.-S.; Zhou, T.; Siggs, O.; Law, M.H.; Souzeau, E.; Ridge, B.; Hysi, P.G.; 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.
2014Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's diseaseNalls, M.A.; Pankratz, N.; Lill, C.M.; Do, C.B.; Hernandez, D.G.; Saad, M.; DeStefano, A.L.; Kara, E.; Bras, J.; Sharma, M.; Schulte, C.; Keller, M.F.; Arepalli, S.; Letson, C.; Edsall, C.; Stefansson, H.; Liu, X.; Pliner, H.; Lee, J.H.; Cheng, R.; et al.
2016A genome-wide association study in multiple system atrophySailer, A.; Scholz, S.W.; Nalls, M.A.; Schulte, C.; Federoff, M.; Price, T.R.; Lees, A.; Ross, O.A.; Dickson, D.W.; Mok, K.; Mencacci, N.E.; Schottlaender, L.; Chelban, V.; Ling, H.; O'Sullivan, S.S.; Wood, N.W.; Traynor, B.J.; Ferrucci, L.; Federoff, H.J.; Mhyre, T.R.; et al.
2018Genetics of the thrombomodulin-endothelial cell protein C receptor system and the risk of early-onset ischemic strokeCole, J.W.; Xu, H.; Ryan, K.; Jaworek, T.; Dueker, N.; McArdle, P.; Gaynor, B.; Cheng, Y.C.; O'Connell, J.; Bevan, S.; Malik, R.; Ahmed, N.U.; Amouyel, P.; Anjum, S.; Bis, J.C.; Crosslin, D.; Danesh, J.; Engelter, S.T.; Fornage, M.; Frossard, P.; et al.; Ko, S.-B.
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.
2012Refinement of the associations between risk of colorectal cancer and polymorphisms on chromosomes 1q41 and 12q13.13Spain, S.; Carvajal-Carmona, L.; Howarth, K.; Jones, A.; Su, Z.; Cazier, J.; Williams, J.; Aaltonen, L.; Pharoah, P.; Kerr, D.; Cheadle, J.; Li, L.; Casey, G.; Vodicka, P.; Sieber, O.; Lipton, L.; Gibbs, P.; Martin, N.; Montgomery, G.; Young, J.; et al.
2011Genome-wide association analysis identifies variants associated with nonalcoholic fatty liver disease that have distinct effects on metabolic traitsSpeliotes, E.; Yerges-Armstrong, L.; Wu, J.; Hernaez, R.; Kim, L.; Palmer, C.; Gudnason, V.; Eiriksdottir, G.; Garcia, M.; Launer, L.; Nalls, M.; Clark, J.; Mitchell, B.; Shuldiner, A.; Butler, J.; Tomas, M.; Hoffmann, U.; Hwang, S.; Massaro, J.; O’Donnell, C.; et al.; McCarthy, M.I.
2015Novel IL1RAPL1 mutations associated with intellectual disability impair synaptogenesisRamos-Brossier, M.; Montani, C.; Lebrun, N.; Gritti, L.; Martin, C.; Seminatore-Nole, C.; Toussaint, A.; Moreno, S.; Poirier, K.; Dorseuil, O.; Chelly, J.; Hackett, A.; Gecz, J.; Bieth, E.; Faudet, A.; Heron, D.; Kooy, R.; Loeys, B.; Humeau, Y.; Sala, C.; et al.
2012Identification of common variants associated with human hippocampal and intracranial volumesStein, J.L.; Medland, S.E.; Vasquez, A.A.; Hibar, D.P.; Senstad, R.E.; Winkler, A.M.; Toro, R.; Appel, K.; Bartecek, R.; Bergmann, Ø.; Bernard, M.; Brown, A.A.; Cannon, D.M.; Chakravarty, M.M.; Christoforou, A.; Domin, M.; Grimm, O.; Hollinshead, M.; Holmes, A.J.; Homuth, G.; et al.

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