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Issue Date
Title
Author(s)
2017
Interaction between the FTO gene, body mass index and depression: meta-analysis of 13701 individuals
Rivera, M.
;
Locke, A.E.
;
Corre, T.
;
Czamara, D.
;
Wolf, C.
;
Ching-Lopez, A.
;
Milaneschi, Y.
;
Kloiber, S.
;
Cohen-Woods, S.
;
Rucker, J.
;
Aitchison, K.J.
;
Bergmann, S.
;
Boomsma, D.I.
;
Craddock, N.
;
Gill, M.
;
Holsboer, F.
;
Hottenga, J.J.
;
Korszun, A.
;
Kutalik, Z.
;
Lucae, S.
;
et al.
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
ClinGen Myeloid Malignancy Variant Curation Expert Panel recommendations for germline RUNX1 variants
Luo, X.
;
Feurstein, S.
;
Mohan, S.
;
Porter, C.C.
;
Jackson, S.A.
;
Keel, S.
;
Chicka, M.
;
Brown, A.L.
;
Kesserwan, C.
;
Agarwal, A.
;
Luo, M.
;
Li, Z.
;
Ross, J.E.
;
Baliakas, P.
;
Pineda-Alvarez, D.
;
DiNardo, C.D.
;
Bertuch, A.A.
;
Mehta, N.
;
Vulliamy, T.
;
Wang, Y.
;
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.
2018
Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection
PardiƱas, A.
;
Holmans, P.
;
Pocklington, A.
;
Escott-Price, V.
;
Ripke, S.
;
Carrera, N.
;
Legge, S.
;
Bishop, S.
;
Cameron, D.
;
Hamshere, M.
;
Han, J.
;
Hubbard, L.
;
Lynham, A.
;
Mantripragada, K.
;
Rees, E.
;
MacCabe, J.
;
McCarroll, S.
;
Baune, B.
;
Breen, G.
;
Byrne, E.
;
et al.
2013
A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinsons disease
Holmans, P.
;
Moskvina, V.
;
Jones, L.
;
Sharma, M.
;
Vedernikov, A.
;
Buchel, F.
;
Sadd, M.
;
Bras, J.M.
;
Bettella, F.
;
Nicolaou, N.
;
Simon-Sanchez, J.
;
Mittag, F.
;
Gibbs, J.R.
;
Schulte, C.
;
Durr, A.
;
Guerreiro, R.
;
Hernandez, D.
;
Brice, A.
;
Stefansson, H.
;
Majamaa, K.
;
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.
Discover
Author
4
Casey, G.
3
Babic, M.
3
Brown, A.L.
3
Burdon, K.
3
Cohen-Woods, S.
3
Craddock, N.
3
Gallinger, S.
3
Gill, M.
3
Korszun, A.
2
Ahmed, S.
.
next >
Subject
38
Humans
29
Female
24
Male
21
Polymorphism, Single Nucleotide
17
Middle Aged
15
Adult
13
Aged
13
Genome-Wide Association Study
10
Risk Factors
9
Case-Control Studies
.
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Date issued
8
2020 - 2023
32
2010 - 2019
1
2007 - 2009