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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.
2020Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK BiobankColeman, J.R.I.; Peyrot, W.J.; Purves, K.L.; Davis, K.A.S.; Rayner, C.; Choi, S.W.; Hübel, C.; Gaspar, H.A.; Kan, C.; Van der Auwera, S.; Adams, M.J.; Lyall, D.M.; Choi, K.W.; Wray, N.R.; Ripke, S.; Mattheisen, M.; Trzaskowski, M.; Byrne, E.M.; Abdellaoui, A.; Adams, M.J.; et al.
2020The Genetics of the Mood Disorder Spectrum: Genome-wide Association Analyses of More Than 185,000 Cases and 439,000 ControlsColeman, J.R.I.; Gaspar, H.A.; Bryois, J.; Byrne, E.M.; Forstner, A.J.; Holmans, P.A.; de Leeuw, C.A.; Mattheisen, M.; McQuillin, A.; Whitehead Pavlides, J.M.; Pers, T.H.; Ripke, S.; Stahl, E.A.; Steinberg, S.; Trubetskoy, V.; Trzaskowski, M.; Wang, Y.; Abbott, L.; Abdellaoui, A.; Adams, M.J.; et al.
2020The genetic architecture of the human cerebral cortexGrasby, K.L.; Jahanshad, N.; Painter, J.N.; Colodro-Conde, L.; Bralten, J.; Hibar, D.P.; Lind, P.A.; Pizzagalli, F.; Ching, C.R.K.; McMahon, M.A.B.; Shatokhina, N.; Zsembik, L.C.P.; Thomopoulos, S.I.; Zhu, A.H.; Strike, L.T.; Agartz, I.; Alhusaini, S.; Almeida, M.A.A.; Alnæs, D.; Amlien, I.K.; et al.
2020An intraocular pressure polygenic risk score stratifies multiple primary open-angle glaucoma parameters including treatment intensityQassim, A.; Souzeau, E.; Siggs, O.M.; Hassall, M.M.; Han, X.; Griffiths, H.L.; Frost, N.A.; Vallabh, N.A.; Kirwan, J.F.; Menon, G.; Cree, A.J.; Galanopoulos, A.; Agar, A.; Healey, P.R.; Graham, S.L.; Landers, J.; Casson, R.J.; Gharahkhani, P.; Willoughby, C.E.; Hewitt, A.W.; 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.
2020Common genetic variation indicates separate causes for periventricular and deep white matter hyperintensitiesArmstrong, N.J.; Mather, K.A.; Sargurupremraj, M.; Knol, M.J.; Malik, R.; Satizabal, C.L.; Yanek, L.R.; Wen, W.; Gudnason, V.G.; Dueker, N.D.; Elliott, L.T.; Hofer, E.; Hofer, E.; Bis, J.; Jahanshad, N.; Li, S.; Logue, M.A.; Logue, M.A.; Luciano, M.; Scholz, M.; et al.
2020Genomic analysis of male puberty timing highlights shared genetic basis with hair colour and lifespanHollis, B.; Day, F.R.; Busch, A.S.; Thompson, D.J.; Soares, A.L.G.; Timmers, P.R.H.J.; Kwong, A.; Easton, D.F.; Joshi, P.K.; Timpson, N.J.; The PRACTICAL Consortium,; 23andMe Research Team,; Ong, K.K.; Perry, J.R.B.; Eeles, R.A.; Henderson, B.E.; Haiman, C.A.; Kote-Jarai, Z.; Schumacher, F.R.; Olama, A.A.A.; et al.