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Issue Date
Title
Author(s)
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.
2019
Disruptive variants of CSDE1 associate with autism and interfere with neuronal development and synaptic transmission
Guo, H.
;
Li, Y.
;
Shen, L.
;
Wang, T.
;
Jia, X.
;
Liu, L.
;
Xu, T.
;
Ou, M.
;
Hoekzema, K.
;
Wu, H.
;
Gillentine, M.A.
;
Liu, C.
;
Ni, H.
;
Peng, P.
;
Zhao, R.
;
Zhang, Y.
;
Phornphutkul, C.
;
Stegmann, A.P.A.
;
Prada, C.E.
;
Hopkin, R.J.
;
et al.
2019
Association of chromosome 9p21 with subsequent coronary heart disease events A GENIUS-CHD study of individual participant data
Patel, R.S.
;
Schmidt, A.F.
;
Tragante, V.
;
McCubrey, R.O.
;
Holmes, M.
;
Howe, L.J.
;
Direk, K.
;
Akerblom, A.
;
Leander, K.
;
Virani, S.S.
;
Kaminski, K.A.
;
Muehlschlegel, J.D.
;
Dube, M.-P.
;
Allayee, H.
;
Almgren, P.
;
Alver, M.
;
Baranova, E.
;
Behlouli, H.
;
Boeckx, B.
;
Braund, P.S.
;
et al.
2021
Targeted gene panels identify a high frequency of pathogenic germline variants in patients diagnosed with a hematological malignancy and at least one other independent cancer
Singhal, D.
;
Hahn, C.N.
;
Feurstein, S.
;
Wee, L.Y.A.
;
Moma, L.
;
Kutyna, M.M.
;
Chhetri, R.
;
Eshraghi, L.
;
Schreiber, A.W.
;
Feng, J.
;
Wang, P.P.-S.
;
Babic, M.
;
Parker, W.T.
;
Gao, S.
;
Moore, S.
;
Das, S.
;
Thomas, D.
;
Pattnaik, S.
;
Brown, A.L.
;
D'Andrea, R.J.
;
et al.
2017
Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domains
Geisheker, M.
;
Heymann, G.
;
Wang, T.
;
Coe, B.
;
Turner, T.
;
Stessman, H.
;
Hoekzema, K.
;
Kvarnung, M.
;
Shaw, M.
;
Friend, K.
;
Liebelt, J.
;
Barnett, C.
;
Thompson, E.
;
Haan, E.
;
Guo, H.
;
Anderlid, B.
;
Nordgren, A.
;
Lindstrand, A.
;
Vandeweyer, G.
;
Alberti, A.
;
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.
2020
Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank
Coleman, J.R.I.
;
Peyrot, W.J.
;
Purves, K.L.
;
Davis, K.A.S.
;
Rayner, C.
;
Choi, S.W.
;
Hübel, C.
;
Gaspar, H.A.
;
Kan, C.
;
Van der Auwera, S.
;
Adams, M.J.
;
Lyall, D.M.
;
Choi, K.W.
;
Wray, N.R.
;
Ripke, S.
;
Mattheisen, M.
;
Trzaskowski, M.
;
Byrne, E.M.
;
Abdellaoui, A.
;
Adams, M.J.
;
et al.
2020
A phenome-wide association and Mendelian Randomisation study of polygenic risk for depression in UK Biobank
Shen, X.
;
Howard, D.M.
;
Adams, M.J.
;
Hill, W.D.
;
Clarke, T.K.
;
Adams, M.J.
;
Clarke, T.K.
;
McIntosh, A.M.
;
Deary, I.J.
;
Wray, N.R.
;
Ripke, S.
;
Mattheisen, M.
;
Trzaskowski, M.
;
Byrne, E.M.
;
Abdellaoui, A.
;
Agerbo, E.
;
Air, T.M.
;
Andlauer, T.F.M.
;
Bacanu, S.A.
;
Bækvad-Hansen, M.
;
et al.
2021
Implementing gene curation for hereditary cancer susceptibility in Australia: achieving consensus on genes with clinical utility
Tudini, E.
;
Davidson, A.L.
;
Dressel, U.
;
Andrews, L.
;
Antill, Y.
;
Crook, A.
;
Field, M.
;
Gattas, M.
;
Harris, R.
;
Kirk, J.
;
Pachter, N.
;
Salmon, L.
;
Susman, R.
;
Townshend, S.
;
Trainer, A.H.
;
Tucker, K.M.
;
Mitchell, G.
;
James, P.A.
;
Ward, R.L.
;
Mar Fan, H.
;
et al.
2020
Common genetic variation indicates separate causes for periventricular and deep white matter hyperintensities
Armstrong, N.J.
;
Mather, K.A.
;
Sargurupremraj, M.
;
Knol, M.J.
;
Malik, R.
;
Satizabal, C.L.
;
Yanek, L.R.
;
Wen, W.
;
Gudnason, V.G.
;
Dueker, N.D.
;
Elliott, L.T.
;
Hofer, E.
;
Hofer, E.
;
Bis, J.
;
Jahanshad, N.
;
Li, S.
;
Logue, M.A.
;
Logue, M.A.
;
Luciano, M.
;
Scholz, M.
;
et al.
Discover
Author
3
Babic, M.
3
Friend, K.
3
Guo, H.
2
Abdellaoui, A.
2
Adams, M.J.
2
Ahmed, S.
2
Aoude, L.
2
Bonazzi, V.
2
Brown, A.L.
2
Burdon, K.
.
next >
Subject
41
Humans
35
Male
21
Polymorphism, Single Nucleotide
20
Middle Aged
18
Adult
16
Aged
13
Genome-Wide Association Study
11
Genotype
10
Case-Control Studies
10
Pedigree
.
next >
Date issued
8
2020 - 2023
31
2010 - 2019
2
2002 - 2009