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Issue Date
Title
Author(s)
2018
A global cline in a colour polymorphism suggests a limited contribution of gene flow towards the recovery of a heavily exploited marine mammal
Hoffman, J.I.
;
Bauer, E.
;
Paijmans, A.J.
;
Humble, E.
;
Beckmann, L.M.
;
Kubetschek, C.
;
Christaller, F.
;
Kröcker, N.
;
Fuchs, B.
;
Moreras, A.
;
Shihlomule, Y.D.
;
Bester, M.N.
;
Cleary, A.C.
;
De Bruyn, P.J.N.
;
Forcada, J.
;
Goebel, M.E.
;
Goldsworthy, S.D.
;
Guinet, C.
;
Hoelzel, A.R.
;
Lydersen, C.
;
et al.
2017
YY1 haploinsufficiency causes an intellectual disability syndrome featuring transcriptional and chromatin dysfunction
Gabriele, M.
;
Vulto-van Silfhout, A.
;
Germain, P.
;
Vitriolo, A.
;
Kumar, R.
;
Douglas, E.
;
Haan, E.
;
Kosaki, K.
;
Takenouchi, T.
;
Rauch, A.
;
Steindl, K.
;
Frengen, E.
;
Misceo, D.
;
Pedurupillay, C.
;
Stromme, P.
;
Rosenfeld, J.
;
Shao, Y.
;
Craigen, W.
;
Schaaf, C.
;
Rodriguez-Buritica, D.
;
et al.
2017
Lost in translation: returning germline genetic results in genome-scale cancer research
Johns, A.
;
McKay, S.
;
Humphris, J.
;
Pinese, M.
;
Chantrill, L.
;
Mead, R.
;
Tucker, K.
;
Andrews, L.
;
Goodwin, A.
;
Leonard, C.
;
High, H.
;
Nones, K.
;
Waddell, N.
;
Patch, A.
;
Merrett, N.
;
Pavlakis, N.
;
Kassahn, K.
;
Samra, J.
;
Miller, D.
;
Chang, D.
;
et al.
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.
2011
Abdominal aortic aneurysm is associated with a variant in low-density lipoprotein receptor-related protein 1
Bown, M.J.
;
Jones, G.T.
;
Harrison, S.C.
;
Wright, B.J.
;
Bumpstead, S.
;
Baas, A.F.
;
Gretarsdottir, S.
;
Badger, S.A.
;
Bradley, D.T.
;
Burnand, K.
;
Child, A.H.
;
Clough, R.E.
;
Cockerill, G.
;
Hafez, H.
;
Scott, D.J.A.
;
Futers, S.
;
Johnson, A.
;
Sohrabi, S.
;
Smith, A.
;
Thompson, M.M.
;
et al.
2019
Quantifying between-cohort and between-sex genetic heterogeneity in major depressive disorder
Trzaskowski, M.
;
Mehta, D.
;
Peyrot, W.J.
;
Hawkes, D.
;
Davies, D.
;
Howard, D.M.
;
Kemper, K.E.
;
Sidorenko, J.
;
Maier, R.
;
Ripke, S.
;
Mattheisen, M.
;
Baune, B.T.
;
Grabe, H.J.
;
Heath, A.C.
;
Jones, L.
;
Jones, I.
;
Madden, P.A.F.
;
McIntosh, A.M.
;
Breen, G.
;
Lewis, C.M.
;
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.
2018
Genome-wide gene-environment interaction in depression: a systematic evaluation of candidate genes: the childhood trauma working-group of PGC-MDD
Van der Auwera, S.
;
Peyrot, W.
;
Milaneschi, Y.
;
Hertel, J.
;
Baune, B.
;
Breen, G.
;
Byrne, E.
;
Dunn, E.
;
Fisher, H.
;
Homuth, G.
;
Levinson, D.
;
Lewis, C.
;
Mills, N.
;
Mullins, N.
;
Nauck, M.
;
Pistis, G.
;
Preisig, M.
;
Rietschel, M.
;
Ripke, S.
;
Sullivan, P.
;
et al.
2018
Developing reproducible bioinformatics analysis workflows for heterogeneous computing environments to support African genomics
Baichoo, S.
;
Souilmi, Y.
;
Panji, S.
;
Botha, G.
;
Meintjes, A.
;
Hazelhurst, S.
;
Bendou, H.
;
de Beste, E.
;
Mpangase, P.
;
Souiai, O.
;
Alghali, M.
;
Yi, L.
;
O'Connor, B.
;
Crusoe, M.
;
Armstrong, D.
;
Aron, S.
;
Joubert, F.
;
Ahmed, A.
;
Mbiyavanga, M.
;
van Heusden, P.
;
et al.
2014
Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies
Bras, J.
;
Guerreiro, R.
;
Darwent, L.
;
Parkkinen, L.
;
Ansorge, O.
;
Escott-Price, V.
;
Hernandez, D.G.
;
Nalls, M.A.
;
Clark, L.N.
;
Honig, L.S.
;
Marder, K.
;
Van Der Flier, W.M.
;
Lemstra, A.
;
Scheltens, P.
;
Rogaeva, E.
;
St George-Hyslop, P.
;
Londos, E.
;
Zetterberg, H.
;
Ortega-Cubero, S.
;
Pastor, P.
;
et al.
Discover
Author
4
Haak, W.
4
Mallick, S.
4
Rohland, N.
3
Coe, B.
3
Fernandes, D.
3
Kvarnung, M.
3
Mittnik, A.
3
Ripke, S.
3
Szécsényi-Nagy, A.
2
Anderlid, B.
.
next >
Subject
8
Humans
5
Female
5
Male
3
Adult
3
Animals
3
Genetic Predisposition to Disease
3
Mice, Inbred C57BL
2
Adolescent
2
Amino Acid Sequence
2
Autistic Disorder
.
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