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Results 21-30 of 68 (Search time: 0.014 seconds).
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PreviewIssue DateTitleAuthor(s)
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.
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.
2013Genetic variants associated with increased risk of malignant pleural mesothelioma: a genome-wide association studyMatullo, G.; Guarrera, S.; Betti, M.; Fiorito, G.; Ferrante, D.; Voglino, F.; Cadby, G.; Di Gaetano, C.; Rosa, F.; Russo, A.; Hirvonen, A.; Casalone, E.; Tunesi, S.; Padoan, M.; Giordano, M.; Aspesi, A.; Casadio, C.; Ardissone, F.; Ruffini, E.; Betta, P.; et al.; Miao, X.-P.
2012A genome-wide association search for type 2 diabetes genes in African AmericansPalmer, N.; McDonough, C.; Hicks, P.; Roh, B.; Wing, M.; Sandy An, S.; Hester, J.; Cooke, J.; Bostrom, M.; Rudock, M.; Talbert, M.; Lewis, J.; DIAGRAM Consortium,; MAGIC Consortium,; Ferrara, A.; Lu, L.; Ziegler, J.; Sale, M.; Divers, J.; Shriner, D.; et al.; Kronenberg, F.
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.
2012Colorectal and other cancer risks for carriers and noncarriers from families with a DNA mismatch repair gene mutation: a prospective cohort studyWin, A.; Young, J.; Lindor, N.; Tucker, K.; Ahnen, D.; Young, G.; Buchanan, D.; Clendenning, M.; Giles, G.; Winship, I.; Macrae, F.; Goldblatt, J.; Southey, M.; Arnold, J.; Thibodeau, S.; Gunawardena, S.; Bapat, B.; Baron, J.; Casey, G.; Gallinger, S.; et al.
2018A genome-wide association study of diabetic kidney disease in subjects with type 2 diabetesVan Zuydam, N.R.; Ahlqvist, E.; Sandholm, N.; Deshmukh, H.; William Rayner, N.; Abdalla, M.; Ladenvall, C.; Ziemek, D.; Fauman, E.; Robertson, N.R.; McKeigue, P.M.; Valo, E.; Forsblom, C.; Harjutsalo, V.; Perna, A.; Rurali, E.; Loredana Marcovecchio, M.; Igo, R.P.; Salem, R.M.; Perico, N.; et al.
2011A comprehensive evaluation of potential lung function associated genes in the SpiroMeta general population sampleObeidat, M.; Wain, L.; Shrine, N.; Kalsheker, N.; Soler Artigas, M.; Repapi, E.; Burton, P.; Johnson, T.; Ramasamy, A.; Zhao, J.-H.; Zhai, G.; Huffman, J.; Vitart, V.; Albrecht, E.; Igl, W.; Hartikainen, A.-L.; Pouta, A.; Cadby, G.; Hui, J.; Palmer, L.; et al.; Semple, M.G.
2016Novel germ line DDX41 mutations define families with a lower age of MDS/AML onset and lymphoid malignanciesLewinsohn, M.; Brown, A.L.; Weinel, L.M.; Phung, C.; Rafidi, G.; Lee, M.K.; Schreiber, A.W.; Feng, J.; Babic, M.; Chong, C.E.; Lee, Y.; Yong, A.; Suthers, G.K.; Poplawski, N.; Altree, M.; Phillips, K.; Jaensch, L.; Fine, M.; D'Andrea, R.J.; Lewis, I.D.; 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.

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