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Results 1-10 of 12 (Search time: 0.006 seconds).
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PreviewIssue DateTitleAuthor(s)
2008Association of Interleukin-1 gene polymorphisms with central obesity and metabolic syndrome in a coronary heart disease populationCarter, K.; Hung, J.; Powell, B.; Wiltshire, S.; Foo, B.; Leow, Y.; McQuillan, B.; Jennens, M.; McCaskie, P.; Thompson, P.; Beilby, J.; Palmer, L.
2009The association of common genetic variants in the APOA5, LPL and GCK genes with longitudinal changes in metabolic and cardiovascular traitsWebster, R.; Warrington, N.; Weedon, M.; Hattersley, A.; McCaskie, P.; Beilby, J.; Palmer, L.; Frayling, T.
2009Analyses of associations with asthma in four asthma population samples from Canada and AustraliaDaly, D.; Lemire, M.; Akhabir, L.; Chan-Yeung, M.; He, J.; McDonald, T.; Stanford, A.; Stefanowicz, D.; Tripp, B.; Zamar, D.; Bosse, Y.; Ferretti, V.; Montpetit, A.; Tessier, M.; Becker, A.; Kozyrskyj, A.; Beilby, J.; McCaskie, P.; Musk, A.; Warrington, N.; et al.
2009Sequence variants in three loci influence monocyte counts and erythrocyte volumeFerreira, M.; Hottenga, J.; Warrington, N.; Medland, S.; Willemsen, G.; Lawrence, R.; Gordon, S.; de Geus, E.; Henders, A.; Smit, J.; Campbell, M.; Wallace, L.; Evans, D.; Wright, M.; Nyholt, D.; James, A.; Beilby, J.; Penninx, B.; Palmer, L.; Frazer, I.; et al.
2009Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarctionGudbjartsson, D.; Bjornsdottir, U.; Halapi, E.; Helgadottir, A.; Sulem, P.; Jonsdottir, G.; Thorleifsson, G.; Helgadottir, H.; Steinthorsdottir, V.; Stefansson, H.; Williams, C.; Hui, J.; Beilby, J.; Warrington, N.; James, A.; Palmer, L.; Koppelman, G.; Heinzmann, A.; Krueger, M.; Boezen, H.; et al.
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.
2008Investigating the association between K198N coding polymorphism in EDN1 and hypertension, lipoprotein levels, the metabolic syndrome and cardiovascular diseaseWiltshire, S.; Powell, B.; Jennens, M.; McCaskie, P.; Carter, K.; Palmer, L.; Thompson, P.; McQuillan, B.; Hung, J.; Beilby, J.
2008Angiotensinogen gene T235 variant: a marker for the development of persistent microalbuminuria in children and adolescents with type 1 diabetes mellitusGallego, P.; Shephard, N.; Bulsara, M.; van Bockxmeer, F.; Powell, B.; Beilby, J.; Arscott, G.; Le Page, M.; Palmer, L.; Davis, E.; Jones, T.; Choong, C.
2008The apolipoprotein AII rs5082 variant is associated with reduced risk of coronary artery disease in an Australian male populationXiao, J.; Zhang, F.; Wiltshire, S.; Hung, J.; Jennens, M.; Beilby, J.; Thompson, P.; McQuillan, B.; McCaskie, P.; Carter, K.; Palmer, L.; Powell, B.
2013A comprehensive investigation of variants in genes encoding adiponectin (ADIPOQ) and its receptors (ADIPOR1/R2), and their association with serum adiponectin, type 2 diabetes, insulin resistance and the metabolic syndromePeters, K.; Beilby, J.; Cadby, G.; Warrington, N.; Bruce, D.; Davis, W.; Davis, T.; Wiltshire, S.; Knuiman, M.; McQuillan, B.; Palmer, L.; Thompson, P.; Hung, J.