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Issue Date
Title
Author(s)
2018
Cortical abnormalities in bipolar disorder: an MRI analysis of 6503 individuals from the ENIGMA Bipolar Disorder Working Group
Hibar, D.
;
Westlye, L.
;
Doan, N.
;
Jahanshad, N.
;
Cheung, J.
;
Ching, C.
;
Versace, A.
;
Bilderbeck, A.
;
Uhlmann, A.
;
Mwangi, B.
;
Krämer, B.
;
Overs, B.
;
Hartberg, C.
;
Abé, C.
;
Dima, D.
;
Grotegerd, D.
;
Sprooten, E.
;
Bøen, E.
;
Jimenez, E.
;
Howells, F.
;
et al.
2017
Developing consensus-based priority outcome domains for trials in kidney transplantation: a multinational Delphi Survey with patients, caregivers, and health professionals
Sautenet, B.
;
Tong, A.
;
Manera, K.
;
Chapman, J.
;
Warrens, A.
;
Rosenbloom, D.
;
Wong, G.
;
Gill, J.
;
Budde, K.
;
Rostaing, L.
;
Marson, L.
;
Josephson, M.
;
Reese, P.
;
Pruett, T.
;
Hanson, C.
;
O'Donoghue, D.
;
Tam-Tham, H.
;
Halimi, J.
;
Shen, J.
;
Kanellis, J.
;
et al.
2017
Electrophysiological, cognitive and clinical profiles of at-risk mental state: the longitudinal minds in transition (MinT) study
Atkinson, R.J.
;
Fulham, W.R.
;
Michie, P.T.
;
Ward, P.B.
;
Todd, J.
;
Stain, H.
;
Langdon, R.
;
Thienel, R.
;
Paulik, G.
;
Cooper, G.
;
Anthes, L.
;
Bowen, D.
;
Case, V.
;
Clark, S.
;
Collins-Langworthy, J.
;
Curtis, J.
;
Ehlkes, T.
;
Haddow, T.
;
Lawrence, C.
;
Logan, S.
;
et al.
;
Hashimoto, K.
2018
A four-gene lincRNA expression signature predicts risk in multiple cohorts of acute myeloid leukemia patients
Beck, D.
;
Thoms, J.
;
Palu, C.
;
Herold, T.
;
Shah, A.
;
Olivier, J.
;
Boelen, L.
;
Huang, Y.
;
Chacon, D.
;
Brown, A.
;
Babic, M.
;
Hahn, C.
;
Perugini, M.
;
Zhou, X.
;
Huntly, B.
;
Schwarzer, A.
;
Klusmann, J.-H.
;
Berdel, W.
;
Wörmann, B.
;
Büchner, T.
;
et al.
2014
Inactivating mutations in NPC1L1 and protection from coronary heart disease
Stitziel, N.O.
;
Won, H.H.
;
Morrison, A.C.
;
Peloso, G.M.
;
Do, R.
;
Lange, L.A.
;
Fontanillas, P.
;
Gupta, N.
;
Duga, S.
;
Goel, A.
;
Farrall, M.
;
Saleheen, D.
;
Ferrario, P.
;
König, I.
;
Asselta, R.
;
Merlini, P.A.
;
Marziliano, N.
;
Notarangelo, M.F.
;
Schick, U.
;
Auer, P.
;
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.
2014
Tumor mismatch repair immunohistochemistry and DNA MLH1 methylation testing of patients with endometrial cancer diagnosed at age younger than 60 years optimizes triage for population-level germline mismatch repair gene mutation testing
Buchanan, D.
;
Tan, Y.
;
Walsh, M.
;
Clendenning, M.
;
Metcalf, A.
;
Ferguson, K.
;
Arnold, S.
;
Thompson, B.
;
Lose, F.
;
Parsons, M.
;
Walters, R.
;
Pearson, S.
;
Cummings, M.
;
Oehler, M.
;
Blomfield, P.
;
Quinn, M.
;
Kirk, J.
;
Stewart, C.
;
Obermair, A.
;
Young, J.
;
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.
2013
A phase 2 trial of ponatinib in Philadelphia chromosome-positive leukemias
Cortes, J.E.
;
Kim, D.W.
;
Pinilla-Ibarz, J.
;
Le Coutre, P.
;
Paquette, R.
;
Chuah, C.
;
Nicolini, F.E.
;
Apperley, J.F.
;
Khoury, H.J.
;
Talpaz, M.
;
DiPersio, J.
;
DeAngelo, D.J.
;
Abruzzese, E.
;
Rea, D.
;
Baccarani, M.
;
Müller, M.C.
;
Gambacorti-Passerini, C.
;
Wong, S.
;
Lustgarten, S.
;
Rivera, V.M.
;
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.
Discover
Author
7
Bloemenkamp, K.
6
Porath, M.
5
Gecz, J.
5
Vos, T.
4
Choi, D.
4
Czyz, C.
4
Dailey, R.
4
Dolman, P.
4
Foster, J.
4
Grossniklaus, H.
.
next >
Subject
19
Child
16
Genetic Predisposition to Disease
15
Mutation
14
Case-Control Studies
14
Child, Preschool
14
Genome-Wide Association Study
14
Treatment Outcome
13
Pregnancy
12
Genotype
12
Infant, Newborn
.
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