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Results 1-10 of 49 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
2013
Common variants in mendelian kidney disease genes and their association with renal function
Parsa, A.
;
Fuchsberger, C.
;
Köttgen, A.
;
O'Seaghdha, C.
;
Pattaro, C.
;
De Andrade, M.
;
Chasman, D.
;
Teumer, A.
;
Endlich, K.
;
Olden, M.
;
Chen, M.
;
Tin, A.
;
Kim, Y.
;
Taliun, D.
;
Li, M.
;
Feitosa, M.
;
Gorski, M.
;
Yang, Q.
;
Hundertmark, C.
;
Foster, M.
;
et al.
2018
Genomic dissection of bipolar disorder and schizophrenia, including 28 subphenotypes
Ruderfer, D.M.
;
Ripke, S.
;
McQuillin, A.
;
Boocock, J.
;
Stahl, E.A.
;
Pavlides, J.M.W.
;
Mullins, N.
;
Charney, A.W.
;
Ori, A.P.S.
;
Loohuis, L.M.O.
;
Domenici, E.
;
Di Florio, A.
;
Papiol, S.
;
Kalman, J.L.
;
Trubetskoy, V.
;
Adolfsson, R.
;
Agartz, I.
;
Agerbo, E.
;
Akil, H.
;
Albani, D.
;
et al.
2017
Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits
Justice, A.
;
Winkler, T.
;
Feitosa, M.
;
Graff, M.
;
Fisher, V.
;
Young, K.
;
Barata, L.
;
Deng, X.
;
Czajkowski, J.
;
Hadley, D.
;
Ngwa, J.
;
Ahluwalia, T.
;
Chu, A.
;
Heard-Costa, N.
;
Lim, E.
;
Perez, J.
;
Eicher, J.
;
Kutalik, Z.
;
Xue, L.
;
Mahajan, A.
;
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.
2013
A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinsons disease
Holmans, P.
;
Moskvina, V.
;
Jones, L.
;
Sharma, M.
;
Vedernikov, A.
;
Buchel, F.
;
Sadd, M.
;
Bras, J.M.
;
Bettella, F.
;
Nicolaou, N.
;
Simon-Sanchez, J.
;
Mittag, F.
;
Gibbs, J.R.
;
Schulte, C.
;
Durr, A.
;
Guerreiro, R.
;
Hernandez, D.
;
Brice, A.
;
Stefansson, H.
;
Majamaa, K.
;
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
Refinement of the associations between risk of colorectal cancer and polymorphisms on chromosomes 1q41 and 12q13.13
Spain, S.
;
Carvajal-Carmona, L.
;
Howarth, K.
;
Jones, A.
;
Su, Z.
;
Cazier, J.
;
Williams, J.
;
Aaltonen, L.
;
Pharoah, P.
;
Kerr, D.
;
Cheadle, J.
;
Li, L.
;
Casey, G.
;
Vodicka, P.
;
Sieber, O.
;
Lipton, L.
;
Gibbs, P.
;
Martin, N.
;
Montgomery, G.
;
Young, J.
;
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.
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.
Discover
Author
7
Esko, T.
6
Feitosa, M.
5
Albrecht, E.
5
Cadby, G.
5
Huffman, J.
5
Jackson, A.
5
Johnson, T.
5
Smith, A.
5
Winkler, T.
4
Berndt, S.
.
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Subject
46
Humans
41
Polymorphism, Single Nucleotide
27
Female
23
Male
19
Genetic Loci
19
Genetic Predisposition to Disease
14
Adult
13
Case-Control Studies
11
Genotype
11
Phenotype
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Date issued
4
2018
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2016
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2015
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2014
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2013
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2012
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2011
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2010