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Results 161-166 of 166 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2014A common 16p11.2 inversion underlies the joint susceptibility to asthma and obesityGonzález, J.R.; Cáceres, A.; Esko, T.; Cuscó, I.; Puig, M.; Esnaola, M.; Reina, J.; Siroux, V.; Bouzigon, E.; Nadif, R.; Reinmaa, E.; Milani, L.; Bustamante, M.; Jarvis, D.; Antó, J.M.; Sunyer, J.; Demenais, F.; Kogevinas, M.; Metspalu, A.; Cáceres, M.; et al.
2010Bayesian methods for meta-analysis of causal relationships estimated using genetic instrumental variablesThompson, S.; Burgess, S.; CRP CHD Genetics Collaboration,
2011Progesterone receptor gene variants and risk of endometrial cancerO'Mara, T.; Fahey, P.; Ferguson, K.; Marquart, L.; Lambrechts, D.; Despierre, E.; Vergote, I.; Amant, F.; Hall, P.; Liu, J.; Czene, K.; SASBAC,; Rebbeck, T.; WISE Study Group,; AOCS Management Group,; SEARCH,; Ahmed, S.; Dunning, A.; Gregory, C.; Shah, M.; et al.
2010A novel syndrome of paediatric cataract, dysmorphism, ectodermal features, and developmental delay in Australian Aboriginal family maps to 1p35.3-p36.32Hattersley, K.; Laurie, K.; Liebelt, J.; Gecz, J.; Durkin, S.; Craig, J.; Burden, K.
2012Association of genetic variants in the TMCO1 gene with clinical parameters related to glaucoma and characterization of the protein in the eyeSharma, S.; Burdon, K.; Chidlow, G.; Klebe, S.; Crawford, A.; Dimasi, D.; Dave, A.; Martin, S.; Javadiyan, S.; Wood, J.; Casson, R.; Danoy, P.; Griggs, K.; Hewitt, A.; Landers, J.; Mitchell, P.; Mackey, D.; Craig, J.
2013Epistasis with HLA DR3 implicates the P2X7 receptor in the pathogenesis of primary Sjögren's syndromeLester, S.; Stokes, L.; Skarratt, K.; Gu, B.; Sivils, K.; Lessard, C.; Wiley, J.; Rischmueller, M.

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