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Results 1-10 of 12 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
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
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.
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.
2014
Novel approach identifies SNPs in SLC2A10 and KCNK9 with evidence for parent-of-origin effect on Body Mass Index
Hoggart, C.
;
Venturini, G.
;
Mangino, M.
;
Gomez, F.
;
Ascari, G.
;
Zhao, J.
;
Teumer, A.
;
Winkler, T.
;
Tšernikova, N.
;
Luan, J.
;
Mihailov, E.
;
Ehret, G.
;
Zhang, W.
;
Lamparter, D.
;
Esko, T.
;
Macé, A.
;
Rüeger, S.
;
Bochud, P.
;
Barcella, M.
;
Dauvilliers, Y.
;
et al.
;
Visscher, P.
2009
Analyses of associations with asthma in four asthma population samples from Canada and Australia
Daly, D.
;
Lemire, M.
;
Akhabir, L.
;
Chan-Yeung, M.
;
He, J.
;
McDonald, T.
;
Stanford, A.
;
Stefanowicz, D.
;
Tripp, B.
;
Zamar, D.
;
Bosse, Y.
;
Ferretti, V.
;
Montpetit, A.
;
Tessier, M.
;
Becker, A.
;
Kozyrskyj, A.
;
Beilby, J.
;
McCaskie, P.
;
Musk, A.
;
Warrington, N.
;
et al.
2009
Sequence variants in three loci influence monocyte counts and erythrocyte volume
Ferreira, M.
;
Hottenga, J.
;
Warrington, N.
;
Medland, S.
;
Willemsen, G.
;
Lawrence, R.
;
Gordon, S.
;
de Geus, E.
;
Henders, A.
;
Smit, J.
;
Campbell, M.
;
Wallace, L.
;
Evans, D.
;
Wright, M.
;
Nyholt, D.
;
James, A.
;
Beilby, J.
;
Penninx, B.
;
Palmer, L.
;
Frazer, I.
;
et al.
2011
Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource Study
Fox, E.
;
Young, J.
;
Li, Y.
;
Dreisbach, A.
;
Keating, B.
;
Musani, S.
;
Liu, K.
;
Morrison, A.
;
Ganesh, S.
;
Kutlar, A.
;
Ramachandran, V.
;
Polak, J.
;
Fabsitz, R.
;
Dries, D.
;
Farlow, D.
;
Redline, S.
;
Adeyemo, A.
;
Hirschorn, J.
;
Sun, Y.
;
Wyatt, S.
;
et al.
2011
Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes
Strawbridge, R.
;
Dupuis, J.
;
Prokopenko, I.
;
Barker, A.
;
Ahlqvist, E.
;
Rybin, D.
;
Petrie, J.
;
Travers, M.
;
Bouatia-Naji, N.
;
Dimas, A.
;
Nica, A.
;
Wheeler, E.
;
Chen, H.
;
Voight, B.
;
Taneera, J.
;
Kanoni, S.
;
Peden, J.
;
Turrini, F.
;
Gustafsson, S.
;
Zabena, C.
;
et al.
2011
A genome-wide significant linkage for severe depression on chromosome 3: the depression network study
Breen, G.
;
Webb, B.
;
Butler, A.
;
van den Oord, E.
;
Tozzi, F.
;
Craddock, N.
;
Gill, M.
;
Korszun, A.
;
Maier, W.
;
Middleton, L.
;
Mors, O.
;
Owen, M.
;
Cohen-Woods, S.
;
Perry, J.
;
Galwey, N.
;
Upmanyu, R.
;
Craig, I.
;
Lewis, C.
;
Ng, M.
;
Brewster, S.
;
et al.
Discover
Author
3
Warrington, N.
2
Beilby, J.
2
Casson, R.
2
Graham, S.
2
Law, M.
2
Lawrence, R.
2
Palmer, L.
2
Sharma, S.
1
Adeyemo, A.
1
Afawi, Z.
.
next >
Subject
12
Female
12
Humans
7
Genome-Wide Association Study
6
Adult
6
Alleles
5
Genetic Predisposition to Disease
4
Aged
4
Cohort Studies
4
Middle Aged
4
Phenotype
.
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2011
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