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Results 1-10 of 29 (Search time: 0.004 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
Disruptive variants of CSDE1 associate with autism and interfere with neuronal development and synaptic transmission
Guo, H.
;
Li, Y.
;
Shen, L.
;
Wang, T.
;
Jia, X.
;
Liu, L.
;
Xu, T.
;
Ou, M.
;
Hoekzema, K.
;
Wu, H.
;
Gillentine, M.A.
;
Liu, C.
;
Ni, H.
;
Peng, P.
;
Zhao, R.
;
Zhang, Y.
;
Phornphutkul, C.
;
Stegmann, A.P.A.
;
Prada, C.E.
;
Hopkin, R.J.
;
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.
2021
Targeted gene panels identify a high frequency of pathogenic germline variants in patients diagnosed with a hematological malignancy and at least one other independent cancer
Singhal, D.
;
Hahn, C.N.
;
Feurstein, S.
;
Wee, L.Y.A.
;
Moma, L.
;
Kutyna, M.M.
;
Chhetri, R.
;
Eshraghi, L.
;
Schreiber, A.W.
;
Feng, J.
;
Wang, P.P.-S.
;
Babic, M.
;
Parker, W.T.
;
Gao, S.
;
Moore, S.
;
Das, S.
;
Thomas, D.
;
Pattnaik, S.
;
Brown, A.L.
;
D'Andrea, R.J.
;
et al.
2019
GWAS on longitudinal growth traits reveals different genetic factors influencing infant, child, and adult BMI
Alves, A.C.
;
De Silva, N.M.G.
;
Karhunen, V.
;
Sovio, U.
;
Das, S.
;
Rob Taal, H.
;
Warrington, N.M.
;
Lewin, A.M.
;
Kaakinen, M.
;
Cousminer, D.L.
;
Thiering, E.
;
Timpson, N.J.
;
Bond, T.A.
;
Lowry, E.
;
Brown, C.D.
;
Estivill, X.
;
Lindi, V.
;
Bradfield, J.P.
;
Geller, F.
;
Speed, D.
;
et al.
2020
Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank
Coleman, J.R.I.
;
Peyrot, W.J.
;
Purves, K.L.
;
Davis, K.A.S.
;
Rayner, C.
;
Choi, S.W.
;
Hübel, C.
;
Gaspar, H.A.
;
Kan, C.
;
Van der Auwera, S.
;
Adams, M.J.
;
Lyall, D.M.
;
Choi, K.W.
;
Wray, N.R.
;
Ripke, S.
;
Mattheisen, M.
;
Trzaskowski, M.
;
Byrne, E.M.
;
Abdellaoui, A.
;
Adams, M.J.
;
et al.
2020
Common genetic variation indicates separate causes for periventricular and deep white matter hyperintensities
Armstrong, N.J.
;
Mather, K.A.
;
Sargurupremraj, M.
;
Knol, M.J.
;
Malik, R.
;
Satizabal, C.L.
;
Yanek, L.R.
;
Wen, W.
;
Gudnason, V.G.
;
Dueker, N.D.
;
Elliott, L.T.
;
Hofer, E.
;
Hofer, E.
;
Bis, J.
;
Jahanshad, N.
;
Li, S.
;
Logue, M.A.
;
Logue, M.A.
;
Luciano, M.
;
Scholz, M.
;
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.
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.
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.
Discover
Author
3
Babic, M.
2
Ahmed, S.
2
Aoude, L.
2
Bonazzi, V.
2
Brown, A.L.
2
Burdon, K.
2
Butler, A.
2
Casson, R.
2
Cohen-Woods, S.
2
Craddock, N.
.
next >
Subject
7
Genotype
7
Pedigree
7
Risk Factors
6
Alleles
6
Case-Control Studies
6
Young Adult
5
Adolescent
5
Gene Frequency
5
Genetic Association Studies
4
Child
.
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