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Results 1-10 of 28 (Search time: 0.003 seconds).
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Issue Date
Title
Author(s)
2010
FunctSNP: an R package to link SNPs to functional knowledge and dbAutoMaker: a suite of Perl scripts to build SNP databases
Goodswen, S.
;
Gondro, C.
;
Watson-Haigh, N.
;
Kadarmideen, H.
2010
Genetic variants regulating insulin receptor signalling are associated with the severity of liver damage in patients with non-alcoholic fatty liver disease
Dongiovanni, P.
;
Valenti, L.
;
Rametta, R.
;
Daly, A.
;
Nobili, V.
;
Mozzi, E.
;
Leathart, J.
;
Pietrobattista, A.
;
Burt, A.
;
Maggioni, M.
;
Fracanzani, A.
;
Lattuada, E.
;
Zappa, M.
;
Roviaro, G.
;
Marchesini, G.
;
Day, C.
;
Fargion, S.
2010
The longitudinal association of common susceptibility variants for type 2 diabetes and obesity with fasting glucose level and BMI
Webster, R.
;
Warrington, N.
;
Beilby, J.
;
Frayling, T.
;
Palmer, L.
2010
Genome-wide association study identifies five loci associated with lung function
Repapi, E.
;
Sayers, I.
;
Wain, L.
;
Burton, P.
;
Johnson, T.
;
Obeidat, M.
;
Zhao J-, H.
;
Ramasamy, A.
;
Zhai, G.
;
Vitart, V.
;
Huffman, J.
;
Igl, W.
;
Albrecht, E.
;
Deloukas, P.
;
Henderson, J.
;
Granell, R.
;
McArdle, W.
;
Rudnicka, A.
;
Wellcome Trust Case Control Consortium,
;
Barroso, I.
;
et al.
2010
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
Speliotes, E.
;
Palmer, L.
2010
Association between erythropoietin gene polymorphisms and diabetic retinopathy
Abhary, S.
;
Burdon, K.
;
Casson, R.
;
Goggin, M.
;
Petrovsky, N.
;
Craig, J.
2010
The Bipolar Association case-control study (BACCS)and meta-analysis: no association with the 5,10-methylenetetrahydrofolate reductase gene and bipolar disorder
Cohen-Woods, S.
;
Craig, I.
;
Gaysina, D.
;
Gray, J.
;
Gunasinghe, C.
;
Craddock, N.
;
Elkin, A.
;
Jones, L.
;
Kennedy, J.
;
King, N.
;
Korszun, A.
;
Knight, J.
;
Owen, M.
;
Parikh, S.
;
Strauss, J.
;
Sterne, A.
;
Tozzi, F.
;
Perry, J.
;
Muglia, P.
;
Vincent, J.
;
et al.
2010
Familial concordance of breast cancer pathology as an indicator of genotype in multiple-case families
Balleine, R.
;
Provan, P.
;
Pupo, G.
;
Pathmanathan, N.
;
Cummings, M.
;
Farshid, G.
;
Salisbury, E.
;
Bilous, A.
;
Byth, K.
;
Mann, G.
2010
Association of PPARĪ³ allelic variation, osteoprotegerin and abdominal aortic aneurysm
Moran, C.
;
Clancy, P.
;
Biros, E.
;
Blanco-Martin, B.
;
McCaskie, P.
;
Palmer, L.
;
Coomans, D.
;
Norman, P.
;
Golledge, J.
2010
Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies
Elks, C.
;
Perry, J.
;
Sulem, P.
;
Chasman, D.
;
Franceschini, N.
;
He, C.
;
Lunetta, K.
;
Visser, J.
;
Byrne, E.
;
Cousminer, D.
;
Gudbjartsson, D.
;
Esko, T.
;
Feenstra, B.
;
Hottenga, J.
;
Koller, D.
;
Kutalik, Z.
;
Lin, P.
;
Mangino, M.
;
Marongiu, M.
;
McArdle, P.
;
et al.
Discover
Author
6
et al.
4
Cohen-Woods, S.
4
Palmer, L.
3
Craig, J.
3
Muglia, P.
3
Perry, J.
3
Speliotes, E.
2
Berndt, S.
2
Burdon, K.
2
Craig, I.
.
next >
Subject
26
Humans
13
Female
13
Genotype
11
Genetic Predisposition to Disease
11
Male
10
Genome-Wide Association Study
8
Adult
7
Alleles
7
Phenotype
5
Case-Control Studies
.
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