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Results 1-10 of 26 (Search time: 0.003 seconds).
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Issue Date
Title
Author(s)
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
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
Nalls, M.A.
;
Pankratz, N.
;
Lill, C.M.
;
Do, C.B.
;
Hernandez, D.G.
;
Saad, M.
;
DeStefano, A.L.
;
Kara, E.
;
Bras, J.
;
Sharma, M.
;
Schulte, C.
;
Keller, M.F.
;
Arepalli, S.
;
Letson, C.
;
Edsall, C.
;
Stefansson, H.
;
Liu, X.
;
Pliner, H.
;
Lee, J.H.
;
Cheng, R.
;
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.
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.
2015
Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk
Painter, J.
;
O'Mara, T.
;
Batra, J.
;
Cheng, T.
;
Lose, F.
;
Dennis, J.
;
Michailidou, K.
;
Tyrer, J.
;
Ahmed, S.
;
Ferguson, K.
;
Healey, C.
;
Kaufmann, S.
;
Hillman, K.
;
Walpole, C.
;
Moya, L.
;
Pollock, P.
;
Jones, A.
;
Howarth, K.
;
Martin, L.
;
Gorman, M.
;
et al.
2016
A splicing-regulatory polymorphism in DRD2 disrupts ZRANB2 binding, impairs cognitive functioning and increases risk for schizophrenia in six Han Chinese samples
Cohen, O.
;
Weickert, T.
;
Hess, J.
;
Paish, L.
;
McCoy, S.
;
Rothmond, D.
;
Galletly, C.
;
Liu, D.
;
Weinberg, D.
;
Huang, X.
;
Xu, Q.
;
Shen, Y.
;
Zhang, D.
;
Yue, W.
;
Yan, J.
;
Wang, L.
;
Lu, T.
;
He, L.
;
Shi, Y.
;
Xu, M.
;
et al.
2015
Efficacy of thiopurines and adalimumab in preventing Crohn's disease recurrence in high-risk patients - a POCER study analysis
De Cruz, P.
;
Kamm, M.A.
;
Hamilton, A.L.
;
Ritchie, K.J.
;
Krejany, E.O.
;
Gorelik, A.
;
Liew, D.
;
Prideaux, L.
;
Lawrance, I.C.
;
Andrews, J.M.
;
Bampton, P.A.
;
Jakobovits, S.
;
Florin, T.H.
;
Gibson, P.R.
;
Debinski, H.
;
Gearry, R.B.
;
Macrae, F.A.
;
Leong, R.W.
;
Kronborg, I.
;
Radford-Smith, G.
;
et al.
2015
Association of cardiometabolic multimorbidity with mortality
Emerging Risk Factors Collaboration,
;
Di Angelantonio, E.
;
Kaptoge, S.
;
Wormser, D.
;
Willeit, P.
;
Butterworth, A.
;
Bansal, N.
;
O'Keeffe, L.
;
Gao, P.
;
Wood, A.
;
Burgess, S.
;
Freitag, D.
;
Pennells, L.
;
Peters, S.
;
Hart, C.
;
Haheim, L.
;
Gillum, R.
;
Nordestgaard, B.
;
Psaty, B.
;
Yeap, B.
;
et al.
2015
BOB CAT: a large-scale review and delphi consensus for management of Barrett's esophagus with no dysplasia, indefinite for, or low-grade dysplasia
Bennett, C.
;
Moayyedi, P.
;
Corley, D.
;
Decaestecker, J.
;
Falck-Ytter, Y.
;
Falk, G.
;
Vakil, N.
;
Sanders, S.
;
Vieth, M.
;
Inadomi, J.
;
Aldulaimi, D.
;
Ho, K.
;
Odze, R.
;
Meltzer, S.
;
Quigley, E.
;
Gittens, S.
;
Watson, P.
;
Zaninotto, G.
;
Iyer, P.
;
Alexandre, L.
;
et al.
2015
Association of the colorectal CpG island methylator phenotype with molecular features, risk factors, and family history
Weisenberger, D.
;
Levine, A.
;
Long, T.
;
Buchanan, D.
;
Walters, R.
;
Clendenning, M.
;
Rosty, C.
;
Joshi, A.
;
Stern, M.
;
Le Marchand, L.
;
Lindor, N.
;
Daftary, D.
;
Gallinger, S.
;
Selander, T.
;
Bapat, B.
;
Newcomb, P.
;
Campbell, P.
;
Casey, G.
;
Ahnen, D.
;
Baron, J.
;
et al.
Discover
Author
2
Ahmed, S.
2
Barber, R.
2
Bueno-de-Mesquita, H.
2
Casson, R.
2
Ferguson, K.
2
Forouzanfar, M.
2
Gallinger, S.
2
Graham, S.
2
Law, M.
2
Lim, S.
.
next >
Subject
25
Humans
18
Female
14
Male
11
Middle Aged
10
Adult
10
Aged
8
Genetic Predisposition to Disease
8
Polymorphism, Single Nucleotide
6
Case-Control Studies
6
Genotype
.
next >
Date issued
3
2018
7
2016
6
2015
5
2014
2
2013
2
2012
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2011