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Issue Date
Title
Author(s)
2015
Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers
Onengut-Gumuscu, S.
;
Chen, W.-M.
;
Burren, O.
;
Cooper, N.J.
;
Quinlan, A.R.
;
Mychaleckyj, J.C.
;
Farber, E.
;
Bonnie, J.K.
;
Szpak, M.
;
Schofield, E.
;
Achuthan, P.
;
Guo, H.
;
Fortune, M.D.
;
Stevens, H.
;
Walker, N.M.
;
Ward, L.D.
;
Kundaje, A.
;
Kellis, M.
;
Daly, M.J.
;
Barrett, J.C.
;
et al.
2018
A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers
Zhang, M.
;
Ferrari, R.
;
Tartaglia, M.C.
;
Keith, J.
;
Surace, E.I.
;
Wolf, U.
;
Sato, C.
;
Grinberg, M.
;
Liang, Y.
;
Xi, Z.
;
Dupont, K.
;
McGoldrick, P.
;
Weichert, A.
;
McKeever, P.M.
;
Schneider, R.
;
McCorkindale, M.D.
;
Manzoni, C.
;
Rademakers, R.
;
Graff-Radford, N.R.
;
Dickson, D.W.
;
et al.
2017
Epiregulin and EGFR interactions are involved in pain processing
Martin, L.J.
;
Smith, S.B.
;
Khoutorsky, A.
;
Magnussen, C.A.
;
Samoshkin, A.
;
Sorge, R.E.
;
Cho, C.
;
Yosefpour, N.
;
Sivaselvachandran, S.
;
Tohyama, S.
;
Cole, T.
;
Khuong, T.M.
;
Mir, E.
;
Gibson, D.G.
;
Wieskopf, J.S.
;
Sotocinal, S.G.
;
Austin, J.S.
;
Meloto, C.B.
;
Gitt, J.H.
;
Gkogkas, C.
;
et al.
2017
Relations between lipoprotein(a) concentrations, LPA genetic variants, and the risk of mortality in patients with established coronary heart disease: a molecular and genetic association study
Zewinger, 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.
2018
Association of serotonin transporter gene AluJb methylation with major depression, amygdala responsiveness, 5-HTTLPR/rs25531 polymorphism, and stress
Schneider, I.
;
Kugel, H.
;
Redlich, R.
;
Grotegerd, D.
;
Bürger, C.
;
Bürkner, P.-C.
;
Opel, N.
;
Dohm, K.
;
Zaremba, D.
;
Meinert, S.
;
Schröder, N.
;
Straßburg, A.
;
Schwarte, K.
;
Schettler, C.
;
Ambrée, O.
;
Rust, S.
;
Domschke, K.
;
Arolt, V.
;
Heindel, W.
;
Baune, B.
;
et al.
2019
Myocilin gene Gln368Ter variant penetrance and association with glaucoma in population-based and registry-based studies
Han, 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.
2019
GWAS on longitudinal growth traits reveals different genetic factors influencing infant, child, and adult BMI
Alves, A.C.
;
De Silva, N.M.G.
;
Karhunen, V.
;
Sovio, U.
;
Das, S.
;
Rob Taal, H.
;
Warrington, N.M.
;
Lewin, A.M.
;
Kaakinen, M.
;
Cousminer, D.L.
;
Thiering, E.
;
Timpson, N.J.
;
Bond, T.A.
;
Lowry, E.
;
Brown, C.D.
;
Estivill, X.
;
Lindi, V.
;
Bradfield, J.P.
;
Geller, F.
;
Speed, D.
;
et al.
2013
The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism
Klebe, 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.
2020
A phenome-wide association and Mendelian Randomisation study of polygenic risk for depression in UK Biobank
Shen, 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.
2014
Common variants near ABCA1, AFAP1 and GMDS confer risk of primary open-angle glaucoma
Gharahkhani, 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.
Discover
Author
3
Mook-Kanamori, D.
3
Palmer, L.
3
Sharma, S.
3
Souzeau, E.
3
Speliotes, E.
3
Winkler, T.
2
Abdellaoui, A.
2
Ahlqvist, E.
2
Albrecht, E.
2
An, J.
.
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Subject
45
Humans
41
Female
26
Genome-Wide Association Study
19
Adult
16
Genetic Predisposition to Disease
16
Middle Aged
15
Aged
14
Genotype
10
Genetic Loci
9
Alleles
.
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Date issued
41
2010 - 2020
4
2008 - 2009