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Results 1-10 of 19 (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
Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection
Pardiñas, A.
;
Holmans, P.
;
Pocklington, A.
;
Escott-Price, V.
;
Ripke, S.
;
Carrera, N.
;
Legge, S.
;
Bishop, S.
;
Cameron, D.
;
Hamshere, M.
;
Han, J.
;
Hubbard, L.
;
Lynham, A.
;
Mantripragada, K.
;
Rees, E.
;
MacCabe, J.
;
McCarroll, S.
;
Baune, B.
;
Breen, G.
;
Byrne, E.
;
et al.
2014
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
Nalls, M.A.
;
Pankratz, N.
;
Lill, C.M.
;
Do, C.B.
;
Hernandez, D.G.
;
Saad, M.
;
DeStefano, A.L.
;
Kara, E.
;
Bras, J.
;
Sharma, M.
;
Schulte, C.
;
Keller, M.F.
;
Arepalli, S.
;
Letson, C.
;
Edsall, C.
;
Stefansson, H.
;
Liu, X.
;
Pliner, H.
;
Lee, J.H.
;
Cheng, R.
;
et al.
2016
A genome-wide association study in multiple system atrophy
Sailer, A.
;
Scholz, S.W.
;
Nalls, M.A.
;
Schulte, C.
;
Federoff, M.
;
Price, T.R.
;
Lees, A.
;
Ross, O.A.
;
Dickson, D.W.
;
Mok, K.
;
Mencacci, N.E.
;
Schottlaender, L.
;
Chelban, V.
;
Ling, H.
;
O'Sullivan, S.S.
;
Wood, N.W.
;
Traynor, B.J.
;
Ferrucci, L.
;
Federoff, H.J.
;
Mhyre, T.R.
;
et al.
2012
Identification of common variants associated with human hippocampal and intracranial volumes
Stein, J.L.
;
Medland, S.E.
;
Vasquez, A.A.
;
Hibar, D.P.
;
Senstad, R.E.
;
Winkler, A.M.
;
Toro, R.
;
Appel, K.
;
Bartecek, R.
;
Bergmann, Ø.
;
Bernard, M.
;
Brown, A.A.
;
Cannon, D.M.
;
Chakravarty, M.M.
;
Christoforou, A.
;
Domin, M.
;
Grimm, O.
;
Hollinshead, M.
;
Holmes, A.J.
;
Homuth, G.
;
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.
2015
Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk
Painter, J.
;
O'Mara, T.
;
Batra, J.
;
Cheng, T.
;
Lose, F.
;
Dennis, J.
;
Michailidou, K.
;
Tyrer, J.
;
Ahmed, S.
;
Ferguson, K.
;
Healey, C.
;
Kaufmann, S.
;
Hillman, K.
;
Walpole, C.
;
Moya, L.
;
Pollock, P.
;
Jones, A.
;
Howarth, K.
;
Martin, L.
;
Gorman, M.
;
et al.
2012
Common variants at 12q15 and 12q24 are associated with infant head circumference
Taal, H.
;
St Pourcain, B.
;
Thiering, E.
;
Das, S.
;
Mook-Kanamori, D.
;
Warrington, N.
;
Kaakinen, M.
;
Kreiner-Møller, E.
;
Bradfield, J.
;
Freathy, R.
;
Geller, F.
;
Guxens, M.
;
Cousminer, D.
;
Kerkhof, M.
;
Timpson, N.
;
Arfan Ikram, M.
;
Beilin, L.
;
Bønnelykke, K.
;
Buxton, J.
;
Charoen, P.
;
et al.
Discover
Author
4
Esko, T.
4
Warrington, N.
3
Beilin, L.
3
Cousminer, D.
3
Mook-Kanamori, D.
3
Taal, H.
3
Timpson, N.
2
Amin, N.
2
Berndt, S.
2
Bradfield, J.
.
next >
Subject
19
Humans
17
Genome-Wide Association Study
12
Female
10
Male
8
Genetic Predisposition to Disease
7
Case-Control Studies
5
Adolescent
5
Genetic Markers
4
Alleles
4
Body Height
.
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