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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.
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.
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.
2012
A genome-wide association search for type 2 diabetes genes in African Americans
Palmer, N.
;
McDonough, C.
;
Hicks, P.
;
Roh, B.
;
Wing, M.
;
Sandy An, S.
;
Hester, J.
;
Cooke, J.
;
Bostrom, M.
;
Rudock, M.
;
Talbert, M.
;
Lewis, J.
;
DIAGRAM Consortium,
;
MAGIC Consortium,
;
Ferrara, A.
;
Lu, L.
;
Ziegler, J.
;
Sale, M.
;
Divers, J.
;
Shriner, D.
;
et al.
;
Kronenberg, F.
2016
A splicing-regulatory polymorphism in DRD2 disrupts ZRANB2 binding, impairs cognitive functioning and increases risk for schizophrenia in six Han Chinese samples
Cohen, O.
;
Weickert, T.
;
Hess, J.
;
Paish, L.
;
McCoy, S.
;
Rothmond, D.
;
Galletly, C.
;
Liu, D.
;
Weinberg, D.
;
Huang, X.
;
Xu, Q.
;
Shen, Y.
;
Zhang, D.
;
Yue, W.
;
Yan, J.
;
Wang, L.
;
Lu, T.
;
He, L.
;
Shi, Y.
;
Xu, M.
;
et al.
Discover
Author
3
Beilin, L.
3
Bouatia-Naji, N.
3
Casson, R.
3
Domschke, K.
3
Esko, T.
3
Mook-Kanamori, D.
3
Sharma, S.
3
Speliotes, E.
3
Warrington, N.
3
Winkler, T.
.
next >
Subject
33
Humans
32
Female
21
Genome-Wide Association Study
15
Adult
14
Genetic Predisposition to Disease
11
Aged
11
Middle Aged
10
Genetic Loci
10
Genotype
6
Alleles
.
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Date issued
3
2018
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2016
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2014
3
2013
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2012
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2011
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2010