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Issue Date
Title
Author(s)
2008
X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment
Dibbens, L.
;
Tarpey, P.
;
Hynes, K.
;
Bayly, M.
;
Scheffer, I.
;
Smith, R.
;
Bomar, J.
;
Sutton, E.
;
Vandeleur, L.
;
Shoubridge, C.
;
Edkins, S.
;
Turner, S.
;
Stevens, C.
;
O'Meara, S.
;
Tofts, C.
;
Barthorpe, S.
;
Buck, G.
;
Cole, J.
;
Halliday, K.
;
Jones, D.
;
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.
2018
Cortical abnormalities in bipolar disorder: an MRI analysis of 6503 individuals from the ENIGMA Bipolar Disorder Working Group
Hibar, D.
;
Westlye, L.
;
Doan, N.
;
Jahanshad, N.
;
Cheung, J.
;
Ching, C.
;
Versace, A.
;
Bilderbeck, A.
;
Uhlmann, A.
;
Mwangi, B.
;
Krämer, B.
;
Overs, B.
;
Hartberg, C.
;
Abé, C.
;
Dima, D.
;
Grotegerd, D.
;
Sprooten, E.
;
Bøen, E.
;
Jimenez, E.
;
Howells, F.
;
et al.
2018
Genomic dissection of bipolar disorder and schizophrenia, including 28 subphenotypes
Ruderfer, D.M.
;
Ripke, S.
;
McQuillin, A.
;
Boocock, J.
;
Stahl, E.A.
;
Pavlides, J.M.W.
;
Mullins, N.
;
Charney, A.W.
;
Ori, A.P.S.
;
Loohuis, L.M.O.
;
Domenici, E.
;
Di Florio, A.
;
Papiol, S.
;
Kalman, J.L.
;
Trubetskoy, V.
;
Adolfsson, R.
;
Agartz, I.
;
Agerbo, E.
;
Akil, H.
;
Albani, D.
;
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.
2017
Electrophysiological, cognitive and clinical profiles of at-risk mental state: the longitudinal minds in transition (MinT) study
Atkinson, R.J.
;
Fulham, W.R.
;
Michie, P.T.
;
Ward, P.B.
;
Todd, J.
;
Stain, H.
;
Langdon, R.
;
Thienel, R.
;
Paulik, G.
;
Cooper, G.
;
Anthes, L.
;
Bowen, D.
;
Case, V.
;
Clark, S.
;
Collins-Langworthy, J.
;
Curtis, J.
;
Ehlkes, T.
;
Haddow, T.
;
Lawrence, C.
;
Logan, S.
;
et al.
;
Hashimoto, K.
2014
Inactivating mutations in NPC1L1 and protection from coronary heart disease
Stitziel, N.O.
;
Won, H.H.
;
Morrison, A.C.
;
Peloso, G.M.
;
Do, R.
;
Lange, L.A.
;
Fontanillas, P.
;
Gupta, N.
;
Duga, S.
;
Goel, A.
;
Farrall, M.
;
Saleheen, D.
;
Ferrario, P.
;
König, I.
;
Asselta, R.
;
Merlini, P.A.
;
Marziliano, N.
;
Notarangelo, M.F.
;
Schick, U.
;
Auer, P.
;
et al.
2018
Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection
Pardiñas, 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.
2020
Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression
Craig, J.E.
;
Han, X.
;
Qassim, A.
;
Hassall, M.
;
Cooke Bailey, J.N.
;
Kinzy, T.G.
;
Khawaja, A.P.
;
An, J.
;
Marshall, H.
;
Gharahkhani, P.
;
Igo, R.P.
;
Graham, S.L.
;
Healey, P.R.
;
Ong, J.-S.
;
Zhou, T.
;
Siggs, O.
;
Law, M.H.
;
Souzeau, E.
;
Ridge, B.
;
Hysi, P.G.
;
et al.
2014
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
Nalls, M.A.
;
Pankratz, N.
;
Lill, C.M.
;
Do, C.B.
;
Hernandez, D.G.
;
Saad, M.
;
DeStefano, A.L.
;
Kara, E.
;
Bras, J.
;
Sharma, M.
;
Schulte, C.
;
Keller, M.F.
;
Arepalli, S.
;
Letson, C.
;
Edsall, C.
;
Stefansson, H.
;
Liu, X.
;
Pliner, H.
;
Lee, J.H.
;
Cheng, R.
;
et al.
Discover
Author
3
Ahmed, S.
3
Warrington, N.
2
Alabiad, C.
2
Beilby, J.
2
Bueno-de-Mesquita, H.
2
Cavalleri, G.
2
Choi, D.
2
Czene, K.
2
Czyz, C.
2
Dailey, R.
.
next >
Subject
37
Humans
24
Female
20
Male
20
Polymorphism, Single Nucleotide
17
Genetic Predisposition to Disease
16
Adult
16
Genome-Wide Association Study
15
Middle Aged
13
Genotype
8
Aged
.
next >
Date issued
31
2010 - 2020
7
2007 - 2009