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Issue Date
Title
Author(s)
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.
2020
Global age-sex-specific fertility, mortality, healthy life expectancy (HALE), and population estimates in 204 countries and territories, 1950–2019: a comprehensive demographic analysis for the Global Burden of Disease Study 2019
Wang, H.
;
Abbas, K.M.
;
Abbasifard, M.
;
Abbasi-Kangevari, M.
;
Abbastabar, H.
;
Abd-Allah, F.
;
Abdelalim, A.
;
Abolhassani, H.
;
Abreu, L.G.
;
Abrigo, M.R.M.
;
Abushouk, A.I.
;
Adabi, M.
;
Adair, T.
;
Adebayo, O.M.
;
Adedeji, I.A.
;
Adekanmbi, V.
;
Adeoye, A.M.
;
Adetokunboh, O.O.
;
Advani, S.M.
;
Afshin, A.
;
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.
2021
Clonal evolution and clinical implications of genetic abnormalities in blastic transformation of chronic myeloid leukaemia
Ochi, Y.
;
Yoshida, K.
;
Huang, Y.-J.
;
Kuo, M.-C.
;
Nannya, Y.
;
Sasaki, K.
;
Mitani, K.
;
Hosoya, N.
;
Hiramoto, N.
;
Ishikawa, T.
;
Branford, S.
;
Shanmuganathan, N.
;
Ohyashiki, K.
;
Takahashi, N.
;
Takaku, T.
;
Tsuchiya, S.
;
Kanemura, N.
;
Nakamura, N.
;
Ueda, Y.
;
Yoshihara, S.
;
et al.
2018
Long-term outcome of catheter ablation for treatment of bundle branch re-entrant tachycardia
Pathak, R.
;
Fahed, J.
;
Santangeli, P.
;
Hyman, M.
;
Liang, J.
;
Kubala, M.
;
Hayashi, T.
;
Muser, D.
;
Pathak, M.
;
Kochar, A.
;
Castro, S.
;
Garcia, F.
;
Frankel, D.
;
Supple, G.
;
Schaller, R.
;
Lin, D.
;
Riley, M.
;
Deo, R.
;
Epstein, A.
;
Zado, E.
;
et al.
2018
Aspirin in patients with previous percutaneous coronary intervention undergoing noncardiac surgery
Graham, M.
;
Sessler, D.
;
Parlow, J.
;
Biccard, B.
;
Guyatt, G.
;
Leslie, K.
;
Chan, M.
;
Meyhoff, C.
;
Xavier, D.
;
Sigamani, A.
;
Kumar, P.
;
Mrkobrada, M.
;
Cook, D.
;
Tandon, V.
;
Alvarez-Garcia, J.
;
Villar, J.
;
Painter, T.
;
Landoni, G.
;
Fleischmann, E.
;
Lamy, A.
;
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.
2020
Causes of blindness and vision impairment in 2020 and trends over 30 years, and prevalence of avoidable blindness in relation to VISION 2020: the Right to Sight: an analysis for the Global Burden of Disease Study
Bourne, R.R.A.
;
Briant, P.S.
;
Flaxman, S.R.
;
Taylor, H.R.B.
;
Jonas, J.B.
;
Abdoli, A.A.
;
Abrha, W.A.
;
Abualhasan, A.
;
Abu-Gharbieh, E.G.
;
Adal, T.G.
;
Afshin, A.
;
Ahmadieh, H.
;
Alemayehu, W.
;
Alemzadeh, S.A.S.
;
Alfaar, A.S.
;
Alipour, V.
;
Androudi, S.
;
Arabloo, J.
;
Arditi, A.B.
;
Aregawi, B.B.
;
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.
Discover
Author
5
Vos, T.
4
Branford, S.
4
Levi, C.
3
Aboyans, V.
3
Anderson, C.S.
3
Anderson, H.
3
Andrews, K.
3
Baccarani, M.
3
Brown, A.L.
3
Casson, R.
.
next >
Subject
99
Humans
94
Middle Aged
90
Female
62
Adult
43
Aged, 80 and over
21
Young Adult
20
Adolescent
20
Treatment Outcome
15
Genetic Predisposition to Disease
15
Polymorphism, Single Nucleotide
.
next >
Date issued
26
2020 - 2023
65
2010 - 2019
8
2002 - 2009