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Results 1-10 of 13 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
2013
Common variants in mendelian kidney disease genes and their association with renal function
Parsa, A.
;
Fuchsberger, C.
;
Köttgen, A.
;
O'Seaghdha, C.
;
Pattaro, C.
;
De Andrade, M.
;
Chasman, D.
;
Teumer, A.
;
Endlich, K.
;
Olden, M.
;
Chen, M.
;
Tin, A.
;
Kim, Y.
;
Taliun, D.
;
Li, M.
;
Feitosa, M.
;
Gorski, M.
;
Yang, Q.
;
Hundertmark, C.
;
Foster, M.
;
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.
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.
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.
2016
A genome-wide association study in multiple system atrophy
Sailer, A.
;
Scholz, S.W.
;
Nalls, M.A.
;
Schulte, C.
;
Federoff, M.
;
Price, T.R.
;
Lees, A.
;
Ross, O.A.
;
Dickson, D.W.
;
Mok, K.
;
Mencacci, N.E.
;
Schottlaender, L.
;
Chelban, V.
;
Ling, H.
;
O'Sullivan, S.S.
;
Wood, N.W.
;
Traynor, B.J.
;
Ferrucci, L.
;
Federoff, H.J.
;
Mhyre, T.R.
;
et al.
2012
Refinement of the associations between risk of colorectal cancer and polymorphisms on chromosomes 1q41 and 12q13.13
Spain, S.
;
Carvajal-Carmona, L.
;
Howarth, K.
;
Jones, A.
;
Su, Z.
;
Cazier, J.
;
Williams, J.
;
Aaltonen, L.
;
Pharoah, P.
;
Kerr, D.
;
Cheadle, J.
;
Li, L.
;
Casey, G.
;
Vodicka, P.
;
Sieber, O.
;
Lipton, L.
;
Gibbs, P.
;
Martin, N.
;
Montgomery, G.
;
Young, J.
;
et al.
2012
Identification of common variants associated with human hippocampal and intracranial volumes
Stein, J.L.
;
Medland, S.E.
;
Vasquez, A.A.
;
Hibar, D.P.
;
Senstad, R.E.
;
Winkler, A.M.
;
Toro, R.
;
Appel, K.
;
Bartecek, R.
;
Bergmann, Ø.
;
Bernard, M.
;
Brown, A.A.
;
Cannon, D.M.
;
Chakravarty, M.M.
;
Christoforou, A.
;
Domin, M.
;
Grimm, O.
;
Hollinshead, M.
;
Holmes, A.J.
;
Homuth, G.
;
et al.
2015
Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk
Painter, J.
;
O'Mara, T.
;
Batra, J.
;
Cheng, T.
;
Lose, F.
;
Dennis, J.
;
Michailidou, K.
;
Tyrer, J.
;
Ahmed, S.
;
Ferguson, K.
;
Healey, C.
;
Kaufmann, S.
;
Hillman, K.
;
Walpole, C.
;
Moya, L.
;
Pollock, P.
;
Jones, A.
;
Howarth, K.
;
Martin, L.
;
Gorman, M.
;
et al.
2018
A genome-wide association study of diabetic kidney disease in subjects with type 2 diabetes
Van Zuydam, N.R.
;
Ahlqvist, E.
;
Sandholm, N.
;
Deshmukh, H.
;
William Rayner, N.
;
Abdalla, M.
;
Ladenvall, C.
;
Ziemek, D.
;
Fauman, E.
;
Robertson, N.R.
;
McKeigue, P.M.
;
Valo, E.
;
Forsblom, C.
;
Harjutsalo, V.
;
Perna, A.
;
Rurali, E.
;
Loredana Marcovecchio, M.
;
Igo, R.P.
;
Salem, R.M.
;
Perico, N.
;
et al.
Discover
Author
3
Schulte, C.
2
Holmans, P.
2
Howarth, K.
2
Jones, A.
2
Nalls, M.A.
2
Sharma, M.
2
Stefansson, H.
1
Aaltonen, L.
1
Abdalla, M.
1
Ahlqvist, E.
.
next >
Subject
11
Humans
7
Genetic Predisposition to Disease
6
Genetic Loci
5
Female
4
Adult
4
Alleles
4
Case-Control Studies
4
Male
3
Gene Frequency
3
Risk Factors
.
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Date issued
1
2019
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2018
1
2016
3
2015
1
2014
3
2013
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2012