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Results 1-10 of 93 (Search time: 0.002 seconds).
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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.
2019
GooD4Mum: a general practice-based quality improvement collaborative for diabetes prevention in women with previous gestational diabetes
O'Reilly, S.L.
;
Dunbar, J.A.
;
Best, J.D.
;
Versace, V.
;
Ford, D.
;
Young, A.
;
Shih, S.
;
Bills, R.
;
Shepherdley, W.
;
Janus, E.D.
;
Carter, R.
;
Oats, J.
;
Skinner, T.
;
Ackland, M.
;
Phillips, P.
;
Nankervis, A.
;
Johnson, G.
;
Catford, J.
;
Jeffries, B.
;
Rasa, J.
;
et al.
2019
Preferred learning modalities and practice for critical skills: a global survey of paediatric emergency medicine clinicians
Craig, S.S.
;
Auerbach, M.
;
Cheek, J.A.
;
Babl, F.E.
;
Oakley, E.
;
Nguyen, L.
;
Rao, A.
;
Dalton, S.
;
Lyttle, M.D.
;
Mintegi, S.
;
Nagler, J.
;
Mistry, R.D.
;
Dixon, A.
;
Rino, P.
;
Kohn-Loncarica, G.
;
Dalziel, S.R.
;
Tzimenatos, L.
;
Mistry, R.
;
Brown, K.
;
Powell, E.
;
et al.
2019
Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2
Corbett, M.A.
;
Kroes, T.
;
Veneziano, L.
;
Bennett, M.F.
;
Florian, R.
;
Schneider, A.L.
;
Coppola, A.
;
Licchetta, L.
;
Franceschetti, S.
;
Suppa, A.
;
Wenger, A.
;
Mei, D.
;
Pendziwiat, M.
;
Kaya, S.
;
Delledonne, M.
;
Straussberg, R.
;
Xumerle, L.
;
Regan, B.
;
Crompton, D.
;
van Rootselaar, A.-F.
;
et al.
2019
Association of HIV preexposure prophylaxis with incidence of sexually transmitted infections among individuals at high risk of HIV infection
Traeger, M.W.
;
Cornelisse, V.J.
;
Asselin, J.
;
Price, B.
;
Roth, N.J.
;
Willcox, J.
;
Tee, B.K.
;
Fairley, C.K.
;
Chang, C.C.
;
Armishaw, J.
;
Vujovic, O.
;
Penn, M.
;
Cundill, P.
;
Forgan-Smith, G.
;
Gall, J.
;
Pickett, C.
;
Lal, L.
;
Mak, A.
;
Spelman, T.D.
;
Long, N.
;
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.
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.
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.
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.
Discover
Author
5
Vos, T.
4
Buchanan, D.
4
Choi, D.
4
Clendenning, M.
4
Czyz, C.
4
Dailey, R.
4
Dolman, P.
4
Foster, J.
4
Grossniklaus, H.
4
Harrington, C.
.
next >
Subject
81
Male
80
Female
74
Adult
62
Aged
30
Young Adult
27
Adolescent
25
Aged, 80 and over
16
Genetic Predisposition to Disease
16
Treatment Outcome
15
Mutation
.
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Date issued
15
2019
7
2018
3
2017
9
2016
20
2015
7
2014
10
2013
11
2012
9
2011
2
2010
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