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Issue Date
Title
Author(s)
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.
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.
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.
2016
Novel germ line DDX41 mutations define families with a lower age of MDS/AML onset and lymphoid malignancies
Lewinsohn, M.
;
Brown, A.L.
;
Weinel, L.M.
;
Phung, C.
;
Rafidi, G.
;
Lee, M.K.
;
Schreiber, A.W.
;
Feng, J.
;
Babic, M.
;
Chong, C.E.
;
Lee, Y.
;
Yong, A.
;
Suthers, G.K.
;
Poplawski, N.
;
Altree, M.
;
Phillips, K.
;
Jaensch, L.
;
Fine, M.
;
D'Andrea, R.J.
;
Lewis, I.D.
;
et al.
2012
Common variants at 6q22 and 17q21 are associated with intracranial volume
Ikram, M.
;
Fornage, M.
;
Smith, A.
;
Seshadri, S.
;
Schmidt, R.
;
Debette, S.
;
Vrooman, H.
;
Sigurdsson, S.
;
Ropele, S.
;
Taal, H.
;
Mook-Kanamori, D.
;
Coker, L.
;
Longstreth Jr, W.
;
Niessen, W.
;
DeStefano, A.
;
Beiser, A.
;
Zijdenbos, A.
;
Struchalin, M.
;
Jack Jr, C.
;
Rivadeneira, F.
;
et al.
2013
PIK3CA and PTEN gene and exon mutation-specific clinicopathologic and molecular associations in colorectal cancer
Day, F.
;
Jorissen, R.
;
Lipton, L.
;
Mouradov, D.
;
Sakthianandeswaren, A.
;
Christie, M.
;
Li, S.
;
Tsui, C.
;
Tie, J.
;
Desai, J.
;
Xu, Z.
;
Molloy, P.
;
Whitehall, V.
;
Leggett, B.
;
Jones, I.
;
McLaughlin, S.
;
Ward, R.
;
Hawkins, N.
;
Ruszkiewicz, A.
;
Moore, J.
;
et al.
2021
Transcriptional signature in microglia associated with Aβ plaque phagocytosis
Grubman, A.
;
Choo, X.Y.
;
Chew, G.
;
Ouyang, J.F.
;
Sun, G.
;
Croft, N.P.
;
Rossello, F.J.
;
Simmons, R.
;
Buckberry, S.
;
Landin, D.V.
;
Pflueger, J.
;
Vandekolk, T.H.
;
Abay, Z.
;
Zhou, Y.
;
Liu, X.
;
Chen, J.
;
Larcombe, M.
;
Haynes, J.M.
;
McLean, C.
;
Williams, S.
;
et al.
Discover
Author
4
Vos, T.
3
Afshin, A.
3
Anderson, H.
3
Andrews, K.
3
Branford, S.
3
Feng, J.
3
Flaxman, A.
3
Phillips, K.
3
Shibuya, K.
2
Abbasi-Kangevari, M.
.
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Subject
47
Middle Aged
45
Female
43
Male
32
Adult
14
Young Adult
13
Adolescent
9
Genetic Predisposition to Disease
9
Risk Factors
9
Treatment Outcome
8
Cohort Studies
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Date issued
15
2020 - 2022
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2010 - 2019
5
2002 - 2009