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Results 11-20 of 38 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2015Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer riskPainter, 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.
2016A splicing-regulatory polymorphism in DRD2 disrupts ZRANB2 binding, impairs cognitive functioning and increases risk for schizophrenia in six Han Chinese samplesCohen, O.; Weickert, T.; Hess, J.; Paish, L.; McCoy, S.; Rothmond, D.; Galletly, C.; Liu, D.; Weinberg, D.; Huang, X.; Xu, Q.; Shen, Y.; Zhang, D.; Yue, W.; Yan, J.; Wang, L.; Lu, T.; He, L.; Shi, Y.; Xu, M.; et al.
2014Novel approach identifies SNPs in SLC2A10 and KCNK9 with evidence for parent-of-origin effect on Body Mass IndexHoggart, C.; Venturini, G.; Mangino, M.; Gomez, F.; Ascari, G.; Zhao, J.; Teumer, A.; Winkler, T.; Tšernikova, N.; Luan, J.; Mihailov, E.; Ehret, G.; Zhang, W.; Lamparter, D.; Esko, T.; Macé, A.; Rüeger, S.; Bochud, P.; Barcella, M.; Dauvilliers, Y.; et al.; Visscher, P.
2015Single nucleotide variations in CLCN6 identified in patients with benign partial epilepsies in infancy and/or febrile seizuresYamamoto, T.; Shimojima, K.; Sangu, N.; Komoike, Y.; Ishii, A.; Abe, S.; Yamashita, S.; Imai, K.; Kubota, T.; Fukasawa, T.; Okanishi, T.; Enoki, H.; Tanabe, T.; Saito, A.; Furukawa, T.; Shimizu, T.; Milligan, C.; Petrou, S.; Heron, S.; Dibbens, L.; et al.; Ishii, R.
2015The International SSRI Pharmacogenomics Consortium (ISPC): a genome-wide association study of antidepressant treatment responseBiernacka, J.; Sangkuhl, K.; Jenkins, G.; Whaley, R.; Barman, P.; Batzler, A.; Altman, R.; Arolt, V.; Brockmöller, J.; Chen, C.; Domschke, K.; Hall-Flavin, D.; Hong, C.; Illi, A.; Ji, Y.; Kampman, O.; Kinoshita, T.; Leinonen, E.; Liou, Y.; Mushiroda, T.; et al.
2012Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in womenPalmer, L.; Fox, C.S.; Liu, Y.; White, C.C.; Feitosa, M.; Smith, A.V.; Heard-Costa, N.; Lohman, K.; GIANT Consortium,; MAGIC Consortium,; GLGC Consortium,; Johnson, A.D.; Foster, M.C.; Greenawalt, D.M.; Griffin, P.; Ding, J.; Newman, A.B.; Tylavsky, F.; Miljkovic, I.; Kritchevsky, S.B.; et al.; Bray, M.
2012FTO genotype is associated with phenotypic variability of body mass indexYang, J.; Loos, R.; Powell, J.; Medland, S.; Speliotes, E.; Chasman, D.; Rose, L.; Thorleifsson, G.; Steinthorsdottir, V.; Mägi, R.; Waite, L.; Smith, A.; Yerges-Armstrong, L.; Monda, K.; Hadley, D.; Mahajan, A.; Li, G.; Kapur, K.; Vitart, V.; Huffman, J.; et al.
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.
2012Common variants at 12q15 and 12q24 are associated with infant head circumferenceTaal, H.; St Pourcain, B.; Thiering, E.; Das, S.; Mook-Kanamori, D.; Warrington, N.; Kaakinen, M.; Kreiner-Møller, E.; Bradfield, J.; Freathy, R.; Geller, F.; Guxens, M.; Cousminer, D.; Kerkhof, M.; Timpson, N.; Arfan Ikram, M.; Beilin, L.; Bønnelykke, K.; Buxton, J.; Charoen, P.; et al.
2013GWAS of 126,559 individuals identifies genetic variants associated with educational attainmentRietveld, C.; Medland, S.; Derringer, J.; Yang, J.; Esko, T.; Martin, N.; Westra, H.-J.; Shakhbazov, K.; Abdellaoui, A.; Agrawal, A.; Albrecht, E.; Alizadeh, B.; Amin, N.; Barnard, J.; Baumeister, S.; Benke, K.; Bielak, L.; Boatman, J.; Boyle, P.; Davies, G.; et al.

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