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Issue Date
Title
Author(s)
2017
Epiregulin and EGFR interactions are involved in pain processing
Martin, L.J.
;
Smith, S.B.
;
Khoutorsky, A.
;
Magnussen, C.A.
;
Samoshkin, A.
;
Sorge, R.E.
;
Cho, C.
;
Yosefpour, N.
;
Sivaselvachandran, S.
;
Tohyama, S.
;
Cole, T.
;
Khuong, T.M.
;
Mir, E.
;
Gibson, D.G.
;
Wieskopf, J.S.
;
Sotocinal, S.G.
;
Austin, J.S.
;
Meloto, C.B.
;
Gitt, J.H.
;
Gkogkas, C.
;
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.
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.
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.
2015
Novel IL1RAPL1 mutations associated with intellectual disability impair synaptogenesis
Ramos-Brossier, M.
;
Montani, C.
;
Lebrun, N.
;
Gritti, L.
;
Martin, C.
;
Seminatore-Nole, C.
;
Toussaint, A.
;
Moreno, S.
;
Poirier, K.
;
Dorseuil, O.
;
Chelly, J.
;
Hackett, A.
;
Gecz, J.
;
Bieth, E.
;
Faudet, A.
;
Heron, D.
;
Kooy, R.
;
Loeys, B.
;
Humeau, Y.
;
Sala, C.
;
et al.
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.
2016
A splicing-regulatory polymorphism in DRD2 disrupts ZRANB2 binding, impairs cognitive functioning and increases risk for schizophrenia in six Han Chinese samples
Cohen, O.
;
Weickert, T.
;
Hess, J.
;
Paish, L.
;
McCoy, S.
;
Rothmond, D.
;
Galletly, C.
;
Liu, D.
;
Weinberg, D.
;
Huang, X.
;
Xu, Q.
;
Shen, Y.
;
Zhang, D.
;
Yue, W.
;
Yan, J.
;
Wang, L.
;
Lu, T.
;
He, L.
;
Shi, Y.
;
Xu, M.
;
et al.
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.
2014
Novel approach identifies SNPs in SLC2A10 and KCNK9 with evidence for parent-of-origin effect on Body Mass Index
Hoggart, C.
;
Venturini, G.
;
Mangino, M.
;
Gomez, F.
;
Ascari, G.
;
Zhao, J.
;
Teumer, A.
;
Winkler, T.
;
Tšernikova, N.
;
Luan, J.
;
Mihailov, E.
;
Ehret, G.
;
Zhang, W.
;
Lamparter, D.
;
Esko, T.
;
Macé, A.
;
Rüeger, S.
;
Bochud, P.
;
Barcella, M.
;
Dauvilliers, Y.
;
et al.
;
Visscher, P.
Discover
Author
2
Maier, W.
2
Mors, O.
2
Ng, M.
2
Owen, M.
2
Timpson, N.J.
1
23andMe Research Team,
1
Abdalla, M.
1
Adeyemo, A.
1
Altman, R.
1
Alves, A.C.
.
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Genome-Wide Association Study
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Middle Aged
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Genetic Predisposition to Disease
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Cohort Studies
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Genotype
5
Young Adult
4
Alleles
4
Case-Control Studies
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