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Issue Date
Title
Author(s)
2014
The sheep genome illuminates biology of the rumen and lipid metabolism
Jiang, Y.
;
Xie, M.
;
Chen, W.
;
Talbot, R.
;
Maddox, J.
;
Faraut, T.
;
Wu, C.
;
Muzny, D.
;
Li, Y.
;
Zhang, W.
;
Stanton, J.
;
Brauning, R.
;
Barris, W.
;
Hourlier, T.
;
Aken, B.
;
Searle, S.
;
Adelson, D.
;
Bian, C.
;
Cam, G.
;
Chen, Y.
;
et al.
2014
Fifty thousand years of Arctic vegetation and megafaunal diet
Willerslev, E.
;
Davison, J.
;
Moora, M.
;
Zobel, M.
;
Coissac, E.
;
Edwards, M.
;
Lorenzen, E.
;
Vestergård, M.
;
Gussarova, G.
;
Haile, J.
;
Craine, J.
;
Gielly, L.
;
Boessenkool, S.
;
Epp, L.
;
Pearman, P.
;
Cheddadi, R.
;
Murray, D.
;
Bråthen, K.
;
Yoccoz, N.
;
Binney, H.
;
et al.
2016
A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape
Ried, J.
;
Jeff, J.
;
Chu, A.
;
Bragg-Gresham, J.
;
Van Dongen, J.
;
Huffman, J.
;
Ahluwalia, T.
;
Cadby, G.
;
Eklund, N.
;
Eriksson, J.
;
Esko, T.
;
Feitosa, M.
;
Goel, A.
;
Gorski, M.
;
Hayward, C.
;
Heard-Costa, N.
;
Jackson, A.
;
Jokinen, E.
;
Kanoni, S.
;
Kristiansson, K.
;
et al.
2011
Identification of SOX3 as an XX male sex reversal gene in mice and humans
Sutton, E.
;
Hughes, J.
;
White, S.
;
Sekido, R.
;
Tan, J.
;
Arboleda, V.
;
Rogers, N.
;
Knower, K.
;
Rowley, L.
;
Eyre, H.
;
Rizzoti, K.
;
McAninch, D.
;
Golcalves, J.
;
Slee, J.
;
Turbitt, E.
;
Bruno, D.
;
Bengtsson, H.
;
Harley, V.
;
Vilain, E.
;
Sinclair, A.
;
et al.
2017
Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases
Stessman, H.
;
Xiong, B.
;
Coe, B.
;
Wang, T.
;
Hoekzema, K.
;
Fenckova, M.
;
Kvarnung, M.
;
Gerdts, J.
;
Trinh, S.
;
Cosemans, N.
;
Vives, L.
;
Lin, J.
;
Turner, T.
;
Santen, G.
;
Ruivenkamp, C.
;
Kriek, M.
;
Van Haeringen, A.
;
Aten, E.
;
Friend, K.
;
Liebelt, J.
;
et al.
2018
A genotype-first approach identifies an intellectual disability-overweight syndrome caused by PHIP haploinsufficiency
Jansen, S.
;
Hoischen, A.
;
Coe, B.
;
Carvill, G.
;
van Esch, H.
;
Bosch, D.
;
Andersen, U.
;
Baker, C.
;
Bauters, M.
;
Bernier, R.
;
van Bon, B.
;
Claahsen-van der Grinten, H.
;
Gecz, J.
;
Gilissen, C.
;
Grillo, L.
;
Hackett, A.
;
Kleefstra, T.
;
Koolen, D.
;
Kvarnung, M.
;
Larsen, M.
;
et al.
2017
A recurrent de novo nonsense variant in ZSWIM6 results in severe intellectual disability without frontonasal or limb malformations
Palmer, E.E.
;
Kumar, R.
;
Gordon, C.T.
;
Shaw, M.
;
Hubert, L.
;
Carroll, R.
;
Rio, M.
;
Murray, L.
;
Leffler, M.
;
Dudding-Byth, T.
;
Oufadem, M.
;
Lalani, S.R.
;
Lewis, A.M.
;
Xia, F.
;
Tam, A.
;
Webster, R.
;
Brammah, S.
;
Filippini, F.
;
Pollard, J.
;
Spies, J.
;
et al.
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.
2015
A meta-analysis of gene expression signatures of blood pressure and hypertension
Huan, T.
;
Esko, T.
;
Peters, M.
;
Pilling, L.
;
Schramm, K.
;
Schurmann, C.
;
Chen, B.
;
Liu, C.
;
Joehanes, R.
;
Johnson, A.
;
Yao, C.
;
Ying, S.
;
Courchesne, P.
;
Milani, L.
;
Raghavachari, N.
;
Wang, R.
;
Liu, P.
;
Reinmaa, E.
;
Dehghan, A.
;
Hofman, A.
;
et al.
;
McCarthy, M.
2016
Clinical and molecular analyses of Beckwith–Wiedemann syndrome: comparison between spontaneous conception and assisted reproduction techniques
Tenorio, J.
;
Romanelli, V.
;
Martin-Trujillo, A.
;
Fernández, G.M.
;
Segovia, M.
;
Perandones, C.
;
Pérez Jurado, L.A.
;
Esteller, M.
;
Fraga, M.
;
Arias, P.
;
Gordo, G.
;
Dapía, I.
;
Mena, R.
;
Palomares, M.
;
Pérez de Nanclares, G.
;
Nevado, J.
;
García-Miñaur, S.
;
Santos-Simarro, F.
;
Martinez-Glez, V.
;
Vallespín, E.
;
et al.
;
Hennekam, R.C.M.
;
Biesecker, L.G.
Discover
Author
4
Haak, W.
4
Mallick, S.
4
Rohland, N.
3
Coe, B.
3
Fernandes, D.
3
Kvarnung, M.
3
Mittnik, A.
3
Szécsényi-Nagy, A.
2
Anderlid, B.
2
Broomandkhoshbacht, N.
.
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Subject
7
Humans
4
Female
4
Male
3
Adult
3
Genetic Predisposition to Disease
2
Adolescent
2
Amino Acid Sequence
2
Animals
2
Autistic Disorder
2
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