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PreviewIssue DateTitleAuthor(s)
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.
2016Identity by descent fine mapping of familial adult myoclonus epilepsy (FAME) to 2p11.2–2q11.2Henden, L.; Freytag, S.; Afawi, Z.; Baldassari, S.; Berkovic, S.; Bisulli, F.; Canafoglia, L.; Casari, G.; Crompton, D.; Depienne, C.; Gecz, J.; Guerrini, R.; Helbig, I.; Hirsch, E.; Keren, B.; Klein, K.; Labauge, P.; LeGuern, E.; Licchetta, L.; Mei, D.; et al.
2008Estimating the ancestral recombinations graph (ARG) as compatible networks of SNP patternsParida, L.; Mele, M.; Calafell, F.; Bertranpetit, J.; Schurr, T.; Santos, F.; Quintana-Murci, L.; Comas, D.; Tyler-Smith, C.; Zalloua, P.; Balanovska, E.; Balanovsky, O.; Behar, D.; Mitchell, R.; Jin, L.; Soodyall, H.; Pitchappan, R.; Cooper, A.; Royyuru, A.; Rosset, S.; et al.; Cooper, Alan
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.
2012A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistancePalmer, L.; Manning, A.K.; Hivert M-, F.; Scott, R.A.; Grimsby, J.L.; Bouatia-Naji, N.; Chen, H.; Rybin, D.; Liu C-, T.; Bielak, L.F.; Prokopenko, I.; Amin, N.; Barnes, D.; Cadby, G.; Hottenga J-, J.; Ingelsson, E.; Jackson, A.U.; Johnson, T.; Kanoni, S.; Ladenvall, C.; et al.
2012Refinement of the associations between risk of colorectal cancer and polymorphisms on chromosomes 1q41 and 12q13.13Spain, S.; Carvajal-Carmona, L.; Howarth, K.; Jones, A.; Su, Z.; Cazier, J.; Williams, J.; Aaltonen, L.; Pharoah, P.; Kerr, D.; Cheadle, J.; Li, L.; Casey, G.; Vodicka, P.; Sieber, O.; Lipton, L.; Gibbs, P.; Martin, N.; Montgomery, G.; Young, J.; et al.
2014Common variants near ABCA1, AFAP1 and GMDS confer risk of primary open-angle glaucomaGharahkhani, P.; Burdon, K.; Fogarty, R.; Sharma, S.; Hewitt, A.; Martin, S.; Law, M.; Cremin, K.; Bailey, J.; Loomis, S.; Pasquale, L.; Haines, J.; Hauser, M.; Viswanathan, A.; McGuffin, P.; Topouzis, F.; Foster, P.; Graham, S.; Casson, R.; Chehade, M.; et al.
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.
2012Impact of common variation in bone-related genes on type 2 diabetes and related traitsBillings, L.; Hsu, Y.; Ackerman, R.; Dupuis, J.; Voight, B.; Rasmussen-Torvik, L.; Hercberg, S.; Lathrop, M.; Barnes, D.; Langenberg, C.; Hui, J.; Fu, M.; Bouatia-Naji, N.; Lecoeur, C.; An, P.; Magnusson, P.; Surakka, I.; Ripatti, S.; Christiansen, L.; Dalgard, C.; 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.

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