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Results 1-10 of 33 (Search time: 0.002 seconds).
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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.
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.
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.
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.
2011
Genome-wide association analysis identifies variants associated with nonalcoholic fatty liver disease that have distinct effects on metabolic traits
Speliotes, 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.
2015
Novel IL1RAPL1 mutations associated with intellectual disability impair synaptogenesis
Ramos-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.
2013
Genetic variants associated with increased risk of malignant pleural mesothelioma: a genome-wide association study
Matullo, 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.
2011
Association between common variation at the FTO locus and changes in body mass index from infancy to late childhood: the complex nature of genetic association through growth and development
Sovio, U.
;
Mook-Kanamori, D.
;
Warrington, N.
;
Lawrence, R.
;
Briollais, L.
;
Palmer, C.
;
Cecil, J.
;
Sandling, J.
;
Syvanen, A.
;
Kaakinen, M.
;
Beilin, L.
;
Millwood, I.
;
Bennett, A.
;
Laitneen, J.
;
Pouta, A.
;
Molitor, J.
;
Smith, G.
;
Ben-Shlomo, Y.
;
Jaddoe, V.
;
Palmer, L.
;
et al.
;
Gibson, G.
2013
Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits
Randall, J.
;
Winkler, T.
;
Kutalik, Z.
;
Berndt, S.
;
Jackson, A.
;
Monda, K.
;
Kilpelainen, T.
;
Esko, T.
;
Magi, R.
;
Li, S.
;
Workalemahu, T.
;
Feitosa, M.
;
Croteau-Chonka, D.
;
Day, F.
;
Fall, T.
;
Ferreira, T.
;
Gustafsson, S.
;
Locke, A.
;
Mathieson, I.
;
Scherag, A.
;
et al.
;
Gibson, G.
Discover
Author
3
Beilin, L.
3
Bouatia-Naji, N.
3
Esko, T.
3
Mook-Kanamori, D.
3
Speliotes, E.
3
Warrington, N.
3
Winkler, T.
2
Albrecht, E.
2
Barker, A.
2
Berndt, S.
.
next >
Subject
5
Phenotype
5
Risk Factors
4
Aged, 80 and over
4
Genome, Human
4
GIANT Consortium
4
Infant
4
Pedigree
4
Young Adult
3
Animals
3
Body Height
.
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