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Results 1-10 of 13 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
2015
Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers
Onengut-Gumuscu, S.
;
Chen, W.-M.
;
Burren, O.
;
Cooper, N.J.
;
Quinlan, A.R.
;
Mychaleckyj, J.C.
;
Farber, E.
;
Bonnie, J.K.
;
Szpak, M.
;
Schofield, E.
;
Achuthan, P.
;
Guo, H.
;
Fortune, M.D.
;
Stevens, H.
;
Walker, N.M.
;
Ward, L.D.
;
Kundaje, A.
;
Kellis, M.
;
Daly, M.J.
;
Barrett, J.C.
;
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
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.
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.
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.
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.
2015
Causal mechanisms and balancing selection inferred from genetic associations with polycystic ovary syndrome
Day, F.
;
Hinds, D.
;
Tung, J.
;
Stolk, L.
;
Styrkarsdottir, U.
;
Saxena, R.
;
Bjonnes, A.
;
Broer, L.
;
Dunger, D.
;
Halldorsson, B.
;
Lawlor, D.
;
Laval, G.
;
Mathieson, I.
;
McCardle, W.
;
Louwers, Y.
;
Meun, C.
;
Ring, S.
;
Scott, R.
;
Sulem, P.
;
Uitterlinden, A.
;
et al.
2015
Copy number variants in patients with intellectual disability affect the regulation of ARX transcription factor gene
Ishibashi, M.
;
Manning, E.
;
Shoubridge, C.
;
Krecsmarik, M.
;
Hawkins, T.
;
Giacomotto, J.
;
Zhao, T.
;
Mueller, T.
;
Bader, P.
;
Cheung, S.
;
Stankiewicz, P.
;
Bain, N.
;
Hackett, A.
;
Reddy, C.
;
Mechaly, A.
;
Peers, B.
;
Wilson, S.
;
Lenhard, B.
;
Bally-Cuif, L.
;
Gecz, J.
;
et al.
2016
X chromosome dose and sex bias in autoimmune diseases: increased prevalence of 47,XXX in systemic lupus erythematosus and Sjögren's syndrome
Liu, K.
;
Kurien, B.
;
Zimmerman, S.
;
Kaufman, K.
;
Taft, D.
;
Kottyan, L.
;
Lazaro, S.
;
Weaver, C.
;
Ice, J.
;
Adler, A.
;
Chodosh, J.
;
Radfar, L.
;
Rasmussen, A.
;
Stone, D.
;
Lewis, D.
;
Li, S.
;
Koelsch, K.
;
Igoe, A.
;
Talsania, M.
;
Kumar, J.
;
et al.
2016
Replication of association of the apolipoprotein A1-C3-A4 gene cluster with the risk of gout
Rasheed, H.
;
Phipps-Green, A.J.
;
Topless, R.
;
Smith, M.D.
;
Hill, C.
;
Lester, S.
;
Rischmueller, M.
;
Janssen, M.
;
Jansen, T.L.
;
Joosten, L.A.
;
Radstake, T.R.
;
Riches, P.L.
;
Tausche, A.K.
;
Lioté, F.
;
So, A.
;
Van Rij, A.
;
Jones, G.T.
;
McCormick, S.P.
;
Harrison, A.A.
;
Stamp, L.K.
;
et al.
Discover
Author
2
Ahmed, S.
2
Alabiad, C.
2
Choi, D.
2
Czyz, C.
2
Dailey, R.
2
Dolman, P.
2
Dubovy, S.
2
Ferguson, K.
2
Foster, J.
2
Grossniklaus, H.
.
next >
Subject
13
Humans
9
Male
8
Adult
7
Middle Aged
4
Genetic Predisposition to Disease
4
Genotype
4
Polymorphism, Single Nucleotide
4
Risk Factors
3
Aged
3
Genome-Wide Association Study
.
next >
Date issued
1
2019
1
2018
1
2017
2
2016
6
2015
1
2014
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2011