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Results 1-10 of 36 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
2017
A latent genetic subtype of major depression identified by whole-exome genotyping data in a Mexican-American cohort
Yu, C.
;
Arcos-Burgos, M.
;
Licinio, J.
;
Wong, M.
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.
2018
CYP3A5*3 and ABCB1 61A>G significantly influence dose-adjusted trough blood tacrolimus concentrations in the first three months post-kidney transplantation
Hu, R.
;
Barratt, D.
;
Coller, J.
;
Sallustio, B.
;
Somogyi, A.
2012
Colorectal cancer linkage on chromosomes 4q21, 8q13, 12q24, and 15q22
Cicek, M.
;
Cunningham, J.
;
Fridley, B.
;
Serie, D.
;
Bamlet, W.
;
Diergaarde, B.
;
Haile, R.
;
Le Marchand, L.
;
Krontiris, T.
;
Younghusband, H.
;
Gallinger, S.
;
Newcomb, P.
;
Hopper, J.
;
Jenkins, M.
;
Casey, G.
;
Schumacher, F.
;
Chen, Z.
;
DeRycke, M.
;
Templeton, A.
;
Winship, I.
;
et al.
;
Lo, A.
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.
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.
2018
ADCY9 genetic variants and cardiovascular outcomes with evacetrapib in patients with high-risk vascular disease: a nested case-control study
Nissen, S.
;
Pillai, S.
;
Nicholls, S.
;
Wolski, K.
;
Riesmeyer, J.
;
Weerakkody, G.
;
Foster, W.
;
McErlean, E.
;
Li, L.
;
Bhatnagar, P.
;
Ruotolo, G.
;
Lincoff, A.
2018
Association between the EPHX2 p.Lys55Arg polymorphism and prognosis following an acute coronary syndrome
Oni-Orisan, A.
;
Cresci, S.
;
Jones, P.G.
;
Theken, K.N.
;
Spertus, J.A.
;
Lee, C.R.
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.
Discover
Author
16
et al.
6
Palmer, L.
3
Casson, R.
3
Hewitt, A.
2
Barratt, D.
2
Baune, B.
2
Brown, M.
2
Burdon, K.
2
Cohen-Woods, S.
2
Cremin, K.
.
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31
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25
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Genetic Predisposition to Disease
14
Genome-Wide Association Study
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10
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