Search


Current filters:


Start a new search
Add filters:

Use filters to refine the search results.


Results 1-10 of 28 (Search time: 0.003 seconds).
Item hits:
PreviewIssue DateTitleAuthor(s)
2010FunctSNP: an R package to link SNPs to functional knowledge and dbAutoMaker: a suite of Perl scripts to build SNP databasesGoodswen, S.; Gondro, C.; Watson-Haigh, N.; Kadarmideen, H.
2010Genetic variants regulating insulin receptor signalling are associated with the severity of liver damage in patients with non-alcoholic fatty liver diseaseDongiovanni, 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.
2010The longitudinal association of common susceptibility variants for type 2 diabetes and obesity with fasting glucose level and BMIWebster, R.; Warrington, N.; Beilby, J.; Frayling, T.; Palmer, L.
2010Genome-wide association study identifies five loci associated with lung functionRepapi, 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.
2010Association analyses of 249,796 individuals reveal 18 new loci associated with body mass indexSpeliotes, E.; Palmer, L.
2010Association between erythropoietin gene polymorphisms and diabetic retinopathyAbhary, S.; Burdon, K.; Casson, R.; Goggin, M.; Petrovsky, N.; Craig, J.
2010The Bipolar Association case-control study (BACCS)and meta-analysis: no association with the 5,10-methylenetetrahydrofolate reductase gene and bipolar disorderCohen-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.
2010Familial concordance of breast cancer pathology as an indicator of genotype in multiple-case familiesBalleine, R.; Provan, P.; Pupo, G.; Pathmanathan, N.; Cummings, M.; Farshid, G.; Salisbury, E.; Bilous, A.; Byth, K.; Mann, G.
2010Association of PPARĪ³ allelic variation, osteoprotegerin and abdominal aortic aneurysmMoran, C.; Clancy, P.; Biros, E.; Blanco-Martin, B.; McCaskie, P.; Palmer, L.; Coomans, D.; Norman, P.; Golledge, J.
2010Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studiesElks, 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.