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Results 11-20 of 25 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
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.
2013Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architectureBerndt, S.; Gustafsson, S.; Mägi, R.; Ganna, A.; Wheeler, E.; Feitosa, M.; Justice, A.; Monda, K.; Croteau-Chonka, D.; Day, F.; Esko, T.; Fall, T.; Ferreira, T.; Gentilini, D.; Jackson, A.; Luan, J.; Randall, J.; Vedantam, S.; Willer, C.; Winkler, T.; et al.
2011Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource StudyFox, E.; Young, J.; Li, Y.; Dreisbach, A.; Keating, B.; Musani, S.; Liu, K.; Morrison, A.; Ganesh, S.; Kutlar, A.; Ramachandran, V.; Polak, J.; Fabsitz, R.; Dries, D.; Farlow, D.; Redline, S.; Adeyemo, A.; Hirschorn, J.; Sun, Y.; Wyatt, S.; et al.
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.
2011Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetesStrawbridge, R.; Dupuis, J.; Prokopenko, I.; Barker, A.; Ahlqvist, E.; Rybin, D.; Petrie, J.; Travers, M.; Bouatia-Naji, N.; Dimas, A.; Nica, A.; Wheeler, E.; Chen, H.; Voight, B.; Taneera, J.; Kanoni, S.; Peden, J.; Turrini, F.; Gustafsson, S.; Zabena, C.; et al.
2013SNP genotyping allows an in-depth characterisation of the genome of sugarcane and other complex autopolyploidsGarcia, A.; Mollinari, M.; Marconi, T.; Serang, O.; Silva, R.; Vieira, M.; Vicentini, R.; Costa, E.; Mancini, M.; Garcia, M.; Pastina, M.; Gazaffi, R.; Martins, E.; Dahmer, N.; Sforça, D.; Silva, C.; Bundock, P.; Henry, R.; Souza, G.; van Sluys, M.-A.; et al.
2011A genome-wide significant linkage for severe depression on chromosome 3: the depression network studyBreen, G.; Webb, B.; Butler, A.; van den Oord, E.; Tozzi, F.; Craddock, N.; Gill, M.; Korszun, A.; Maier, W.; Middleton, L.; Mors, O.; Owen, M.; Cohen-Woods, S.; Perry, J.; Galwey, N.; Upmanyu, R.; Craig, I.; Lewis, C.; Ng, M.; Brewster, S.; et al.
2007Genome wide association study identifies novel breat cancer susceptibility lociEaston, D.; Pooley, K.; Pharoah, P.; Thompson, D.; Ballinger, D.; Struewing, J.; Morrison, J.; Field, H.; Luben, R.; Wareham, N.; Ahmed, S.; Healey, C.; Bowman, R.; Luccarini, C.; Conroy, D.; Shah, M.; Munday, H.; Jordan, C.; Perkins, B.; West, J.; et al.
2007Multicentre search for genetic susceptibility loci in sporadic epilepsy syndrome and seizure types: a case-control studyCavalleri, G.; Weale, M.; Shianna, K.; Singh, R.; Lynch, J.; Grinton, B.; Szoeke, C.; Murphy, K.; Kinirons, P.; O'Rourke, D.; Ge, D.; Depondt, C.; Claeys, K.; Pandolfo, M.; Gumbs, C.; Walley, N.; McNamara, J.; Mulley, J.; Linney, K.; Sheffield, L.; et al.
2007A multicenter study of BRD2 as a risk factor for juvenile myoclonic epilepsyCavalleri, G.; Walley, N.; Soranzo, N.; Mulley, J.; Doherty, C.; Kapoor, A.; Depondt, C.; Lynch, J.; Scheffer, I.; Heils, A.; Gehrmann, A.; Kinirons, P.; Gandhi, S.; Satishchandra, P.; Wood, N.; Anand, A.; Sander, T.; Berkovic, S.; Delanty, N.; Goldstein, D.; et al.