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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.
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.
2021
Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries
Gharahkhani, P.
;
Jorgenson, E.
;
Hysi, P.
;
Khawaja, A.P.
;
Pendergrass, S.
;
Han, X.
;
Ong, J.S.
;
Hewitt, A.W.
;
Segrè, A.V.
;
Rouhana, J.M.
;
Hamel, A.R.
;
Igo, R.P.
;
Choquet, H.
;
Qassim, A.
;
Josyula, N.S.
;
Cooke Bailey, J.N.
;
Bonnemaijer, P.W.M.
;
Iglesias, A.
;
Siggs, O.M.
;
Young, T.L.
;
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.
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.
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.
2018
Association of serotonin transporter gene AluJb methylation with major depression, amygdala responsiveness, 5-HTTLPR/rs25531 polymorphism, and stress
Schneider, I.
;
Kugel, H.
;
Redlich, R.
;
Grotegerd, D.
;
Bürger, C.
;
Bürkner, P.-C.
;
Opel, N.
;
Dohm, K.
;
Zaremba, D.
;
Meinert, S.
;
Schröder, N.
;
Straßburg, A.
;
Schwarte, K.
;
Schettler, C.
;
Ambrée, O.
;
Rust, S.
;
Domschke, K.
;
Arolt, V.
;
Heindel, W.
;
Baune, B.
;
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
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.
2019
GWAS on longitudinal growth traits reveals different genetic factors influencing infant, child, and adult BMI
Alves, A.C.
;
De Silva, N.M.G.
;
Karhunen, V.
;
Sovio, U.
;
Das, S.
;
Rob Taal, H.
;
Warrington, N.M.
;
Lewin, A.M.
;
Kaakinen, M.
;
Cousminer, D.L.
;
Thiering, E.
;
Timpson, N.J.
;
Bond, T.A.
;
Lowry, E.
;
Brown, C.D.
;
Estivill, X.
;
Lindi, V.
;
Bradfield, J.P.
;
Geller, F.
;
Speed, D.
;
et al.
Discover
Author
8
Warrington, N.
7
Esko, T.
7
Palmer, L.
5
Bouatia-Naji, N.
5
Feitosa, M.
5
Winkler, T.
4
Berndt, S.
4
Casson, R.
4
Cohen-Woods, S.
4
Gharahkhani, P.
.
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Subject
16
Aged
16
Middle Aged
15
Alleles
14
Phenotype
13
Chromosome Mapping
12
Body Mass Index
10
Cohort Studies
10
Genetic Variation
10
Genome, Human
10
Risk Factors
.
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Date issued
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2020 - 2021
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2010 - 2019
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2007 - 2009