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Results 1-10 of 15 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
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.
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.
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.
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.
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.
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.
2018
A genome-wide association study of diabetic kidney disease in subjects with type 2 diabetes
Van Zuydam, N.R.
;
Ahlqvist, E.
;
Sandholm, N.
;
Deshmukh, H.
;
William Rayner, N.
;
Abdalla, M.
;
Ladenvall, C.
;
Ziemek, D.
;
Fauman, E.
;
Robertson, N.R.
;
McKeigue, P.M.
;
Valo, E.
;
Forsblom, C.
;
Harjutsalo, V.
;
Perna, A.
;
Rurali, E.
;
Loredana Marcovecchio, M.
;
Igo, R.P.
;
Salem, R.M.
;
Perico, N.
;
et al.
2015
The International SSRI Pharmacogenomics Consortium (ISPC): a genome-wide association study of antidepressant treatment response
Biernacka, J.
;
Sangkuhl, K.
;
Jenkins, G.
;
Whaley, R.
;
Barman, P.
;
Batzler, A.
;
Altman, R.
;
Arolt, V.
;
Brockmöller, J.
;
Chen, C.
;
Domschke, K.
;
Hall-Flavin, D.
;
Hong, C.
;
Illi, A.
;
Ji, Y.
;
Kampman, O.
;
Kinoshita, T.
;
Leinonen, E.
;
Liou, Y.
;
Mushiroda, T.
;
et al.
Discover
Author
2
Butler, A.
2
Casson, R.
2
Cohen-Woods, S.
2
Craddock, N.
2
Domschke, K.
2
Gharahkhani, P.
2
Gill, M.
2
Korszun, A.
2
MAGIC Consortium,
2
Maier, W.
.
next >
Subject
13
Female
12
Aged
10
Adult
9
Genome-Wide Association Study
6
Cohort Studies
6
Genetic Predisposition to Disease
6
Genotype
4
Case-Control Studies
4
Phenotype
3
Age of Onset
.
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