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Results 1-10 of 10 (Search time: 0.005 seconds).
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Issue Date
Title
Author(s)
2014
Prediction of potential cancer-risk regions based on transcriptome data: towards a comprehensive view
Alisoltani, A.
;
Fallahi, H.
;
Ebrahimi, M.
;
Ebrahimi, M.
;
Ebrahimie, E.
;
Coleman, W.
2017
Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domains
Geisheker, M.
;
Heymann, G.
;
Wang, T.
;
Coe, B.
;
Turner, T.
;
Stessman, H.
;
Hoekzema, K.
;
Kvarnung, M.
;
Shaw, M.
;
Friend, K.
;
Liebelt, J.
;
Barnett, C.
;
Thompson, E.
;
Haan, E.
;
Guo, H.
;
Anderlid, B.
;
Nordgren, A.
;
Lindstrand, A.
;
Vandeweyer, G.
;
Alberti, A.
;
et al.
2017
Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing
Jansen, I.E.
;
Ye, H.
;
Heetveld, S.
;
Lechler, M.C.
;
Michels, H.
;
Seinstra, R.I.
;
Lubbe, S.J.
;
Drouet, V.
;
Lesage, S.
;
Majounie, E.
;
Gibbs, J.R.
;
Nalls, M.A.
;
Ryten, M.
;
Botia, J.A.
;
Vandrovcova, J.
;
Simon-Sanchez, J.
;
Castillo-Lizardo, M.
;
Rizzu, P.
;
Blauwendraat, C.
;
Chouhan, A.K.
;
et al.
2020
Can we blame fathers who are obese peri-conception, for increasing chronic disease risk in children?
McPherson, N.O.
2023
Heritable defects in telomere and mitotic function selectively predispose to sarcomas
Ballinger, M.L.
;
Pattnaik, S.
;
Mundra, P.A.
;
Zaheed, M.
;
Rath, E.
;
Priestley, P.
;
Baber, J.
;
Ray-Coquard, I.
;
Isambert, N.
;
Causeret, S.
;
van der Graaf, W.T.A.
;
Puri, A.
;
Duffaud, F.
;
Le Cesne, A.
;
Seddon, B.
;
Chandrasekar, C.
;
Schiffman, J.D.
;
Brohl, A.S.
;
James, P.A.
;
Kurtz, J.-E.
;
et al.
2013
Contribution of copy number variants involving nonsense-mediated mRNA decay pathway genes to neuro-developmental disorders
Nguyen, L.
;
Kim, H.
;
Rosenfeld, J.
;
Shen, Y.
;
Gusella, J.
;
Lacassie, Y.
;
Layman, L.
;
Shaffer, L.
;
Gecz, J.
1998
Analysis of Australian Crohn's disease pedigrees refines the localization for susceptibility to inflammatory bowel disease on chromosome 16
Cavanaugh, J.
;
Callen, D.
;
Wilson, S.
;
Stanford, P.
;
Sraml, M.
;
Gorska, M.
;
Crawford, J.
;
Whitmore, S.
;
Shlegel, C.
;
Foote, S.
;
Kohonen-Corish, M.
;
Pavli, P.
2016
A method to exploit the structure of genetic ancestry space to enhance case-control studies
Bodea, C.A.
;
Neale, B.M.
;
Ripke, S.
;
Barclay, M.
;
Peyrin-Biroulet, L.
;
Chamaillard, M.
;
Colombel, J.F.
;
Cottone, M.
;
Croft, A.
;
D'Incà, R.
;
Halfvarson, J.
;
Hanigan, K.
;
Henderson, P.
;
Hugot, J.P.
;
Karban, A.
;
Kennedy, N.A.
;
Khan, M.A.
;
Lémann, M.
;
Levine, A.
;
Massey, D.
;
et al.
2018
Analysis of 182 cerebral palsy transcriptomes points to dysregulation of trophic signalling pathways and overlap with autism
Van Eyk, C.
;
Corbett, M.
;
Gardner, A.
;
Van Bon, B.
;
Broadbent, J.
;
Harper, K.
;
MacLennan, A.
;
Gecz, J.
2017
Single-nucleotide variant proportion in genes: a new concept to explore major depression based on DNA sequencing data
Yu, C.
;
Baune, B.
;
Licinio, J.
;
Wong, M.
Discover
Author
4
et al.
2
Gecz, J.
1
Alberti, A.
1
Alisoltani, A.
1
Anderlid, B.
1
Baber, J.
1
Ballinger, M.L.
1
Barclay, M.
1
Barnett, C.
1
Baune, B.
.
next >
Subject
9
Humans
5
Female
5
Male
3
Child
2
Adolescent
2
Adult
2
Case-Control Studies
2
Exome
2
Gene Expression Profiling
2
Gene Regulatory Networks
.
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Date issued
2
2020 - 2023
7
2010 - 2019
1
1998 - 1999