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2009 Journal Article Genome-wide association study identifies eight loci associated with blood pressure.Newton-Chen, C., Johnson, T., Gateva, V., Tobin, M. D., Bochud, M., Coin, L., Najjar, S. S., Zhao, J. H., et al, Wellcome Trust Case Control Consortium, Brown, Matthew A., Bradbury, Linda and Evans, David (2009). Genome-wide association study identifies eight loci associated with blood pressure.. Nature Genetics, 41 (6), 666-676. doi: 10.1038/ng.361 |
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2009 Journal Article Combined effects of <i>MC4R</i> and <i>FTO</i> common genetic variants on obesity in European general populationsCauchi, Stephane, Stutzmann, Fanny, Cavalcanti-Proenca, Christine, Durand, Emmanuelle, Pouta, Anneli, Hartikainen, Anna-Liisa, Marre, Michel, Vol, Sylviane, Tammelin, Tuija, Laitinen, Jaana, Gonzalez-Izquierdo, Arturo, Blakemore, Alexandra I. F., Elliott, Paul, Meyre, David, Balkau, Beverley, Jaervelin, Marjo-Riitta and Froguel, Philippe (2009). Combined effects of MC4R and FTO common genetic variants on obesity in European general populations. Journal of Molecular Medicine-Jmm, 87 (5), 537-546. doi: 10.1007/s00109-009-0451-6 |
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2009 Journal Article Common variants in the region around Osterix are associated with bone mineral density and growth in childhoodTimpson, Nicholas J., Tobias, Jon H., Richards, J. Brent, Soranzo, Nicole, Duncan, Emma L., Sims, Anne-Maree, Whittaker, Pamela, Kumanduri, Vasudev, Zhai, Guangju, Glaser, Beate, Eisman, John, Jones, Graeme, Nicholson, Geoff, Prince, Richard, Seeman, Ego, Spector, Tim D., Brown, Matthew A., Peltonen, Leena, Smith, George Davey, Deloukas, Panos and Evans, David M. (2009). Common variants in the region around Osterix are associated with bone mineral density and growth in childhood. Human Molecular Genetics, 18 (8), 1510-1517. doi: 10.1093/hmg/ddp052 |
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2009 Journal Article Harnessing the information contained within genome-wide association studies to improve individual prediction of complex disease riskEvans, David M., Visscher, Peter M. and Wray, Naomi R. (2009). Harnessing the information contained within genome-wide association studies to improve individual prediction of complex disease risk. Human Molecular Genetics, 18 (18), 3525-3531. doi: 10.1093/hmg/ddp295 |
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2009 Journal Article Six new loci associated with body mass index highlight a neuronal influence on body weight regulationWiller, Cristen J., Speliotes, Elizabeth K., Loos, Ruth J. F., Li, Shengxu, Lindgren, Cecilia M., Heid, Iris M., Berndt, Sonja I., Elliot, Amanda L., Jackson, Anne U., Lamina, Claudia, Lettre, Guillaume, Lim, Noha, Lyon, Helen N., McCarroll, Steven N., Papadakis, Konstantinos, Qi, Lu, Randall, Joshua C., Roccasecca, Rosa Maria, Sanna, Serena, Scheet, Paul, Weedon, Michael N., Wheeler, Eleanor, Zhao, Jing Hua, Jacobs, Leonie C., Prokopenko,, Soranzo, Nicole, Tanaka, Toshiko, Timpson, Nicholas J., Almgran, Peter ... GIANT consortium (2009). Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. Nature Genetics, 41 (1), 25-34. doi: 10.1038/ng.287 |
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2009 Journal Article A genome-wide association study reveals variants in ARL15 that influence adiponectin levelsBrent Richards, J., Waterworth, Dawn, O'Rahilly, Stephen, Hivert, Marie-France, Loos, Ruth J. F., Perry, John R. B., Tanaka, Toshiko, Timpson, Nicholas John, Semple, Robert K., Soranzo, Nicole, Song, Kijoung, Rocha, Nuno, Grundberg, Elin, Dupuis, Josee, Florez, Jose C., Langenberg, Claudia, Prokopenko, Inga, Saxena, Richa, Sladek, Robert, Aulchenko, Yurii, Evans, David, Waeber, Gerard, Erdmann, Jeanette, Burnett, Mary-Susan, Sattar, Naveed, Devaney, Joseph, Willenborg, Christina, Hingorani, Aroon, Witteman, Jaquelin C. M ... Spector, Tim D. (2009). A genome-wide association study reveals variants in ARL15 that influence adiponectin levels. PLoS Genetics, 5 (12) e1000768, e1000768.1-e1000768.10. doi: 10.1371/journal.pgen.1000768 |
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2009 Journal Article Genetic variants in the vitamin D receptor are associated with advanced prostate cancer at diagnosis: Findings from the prostate testing for cancer and treatment study and a systematic reviewChen, Lina, Smith, George Davey, Evans, David M., Cox, Angela, Lawlor, Debbie A., Donovan, Jenny, Yuan, Wei, Day, Ian N. M., Martin, Richard M., Lane, Athene, Rodriguez, Santi, Davis, Michael, Zuccolo, Luisa, Collin, Simon M., Hamdy, Freddie, Neal, David and Lewis, Sarah J. (2009). Genetic variants in the vitamin D receptor are associated with advanced prostate cancer at diagnosis: Findings from the prostate testing for cancer and treatment study and a systematic review. Cancer Epidemiology Biomarkers and Prevention, 18 (11), 2874-2881. doi: 10.1158/1055-9965.EPI-09-0544 |
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2008 Journal Article Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's diseaseBarrett, Jeffrey C., Wellcome Trust Case Control Consortium, Brown, Matthew A., Bradbury, Linda A., et al. and Evans, David (2008). Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. Nature Genetics, 40 (8), 955-962. doi: 10.1038/ng.175 |
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2008 Journal Article Common variants near MC4R are associated with fat mass, weight and risk of obesityLoos, Ruth J. F., Evans, David M., Wellcome Trust Case Control Consortium, Brown, Matthew A. and Bradbury, Linda A. (2008). Common variants near MC4R are associated with fat mass, weight and risk of obesity. Nature Genetics, 40 (6), 768-775. doi: 10.1038/ng.140 |
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2008 Journal Article Genome-wide association analysis identifies 20 loci that influence adult heightWeedon, Michael N., Evans, David M., Wellcome Trust Case Control Consortium, Brown, Matthew A. and Bradbury, Linda A. (2008). Genome-wide association analysis identifies 20 loci that influence adult height. Nature Genetics, 40 (5), 575-583. doi: 10.1038/ng.121 |
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2008 Journal Article To what extent do scans of non-synonymous SNPs complement denser genome-wide association studies?Evans, David M., Barrett, Jeffrey C. and Cardon, Lon R. (2008). To what extent do scans of non-synonymous SNPs complement denser genome-wide association studies?. European Journal of Human Genetics, 16 (6), 718-723. doi: 10.1038/sj.ejhg.5202011 |
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2008 Conference Publication Diagnostic capacity of genetic tests in Ankylosing spondylitis can exceed MRI scanningEvans, David, Reveille, John D., Weisman, Michael H., Stone, Millicent A., Ward, Michael M., Savage, Laurie, Zhou, Xiaodong, Wordsworth, B. Paul and Brown, Matthew A. (2008). Diagnostic capacity of genetic tests in Ankylosing spondylitis can exceed MRI scanning. 72nd Annual Scientific Meeting of the American-College-of-Rheumatology/43rd Annual Scientific Meeting of the Association-of-Rheumatology-Health-Professionals, San Francisco Ca, Oct 24-29, 2008. HOBOKEN: WILEY-LISS. |
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2008 Conference Publication Phased genome-wide association study identifies new gene affecting bone mineral densityDuncan, E. L., Addison, K., Brugmans, M., Irwin, D., Evans, D., Eisman, J., Jones, G., Nicholson, G., Prince, R., Seeman, E., Uitterlinden, A., Wark, J., Ralston, S. and Brown, M. A. (2008). Phased genome-wide association study identifies new gene affecting bone mineral density. American Society for Bone and Mineral Research (ASBMR) 30th Annual Meeting, Montreal,Canada, 12 - 16 September 2008. Malden, MA, United States: Wiley-Blackwell. doi: 10.1002/jbmr.5650231306 |
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2008 Conference Publication Genome-wide association study identifies klotho and other novel loci as contributors to BMD variation in postmenopausal womenDuncan, E. L., Rivadeneira, F., Sims, A., Dowling, A., Doan, T., Arp, P. P., Jhamai, M., Moorhouse, M., Evans, D., Eisman, J., Jones, G., Nicholson, G., Prince, R., Seeman, E., Wass, J. A. H., Hofman, A., Pols, H. A., Brown, M. A. and Uitterlinden, A. G. (2008). Genome-wide association study identifies klotho and other novel loci as contributors to BMD variation in postmenopausal women. 35th European Symposium on Calcified Tissues, Barcelona, Spain, 24-28 May 2008. New York, United States: Springer. |
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2008 Journal Article A genome-wide scan for Eysenckian personality dimensions in adolescent twin sibships: Psychoticism, Extraversion, Neuroticism, and LieGillespie, Nathan A., Zhu, Gu, Evans, David M., Medland, Sarah E., Wright, Margie J. and Martin, Nick G. (2008). A genome-wide scan for Eysenckian personality dimensions in adolescent twin sibships: Psychoticism, Extraversion, Neuroticism, and Lie. Journal of Personality, 76 (6), 1415-1445. doi: 10.1111/j.1467-6494.2008.00527.x |
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2007 Journal Article Localization of type 1 diabetes susceptibility to the MHC class I genes HLA-B and HLA-ANejentsev, S., Howson, J. M. M., Walker, N. M., Szeszko, J., Field, S. F., Stevens, H. E., Reynolds, P., Hardy, M., King, E., Masters, J., Hulme, J., Maier, L. M., Smyth, D., Bailey, R., Cooper, J. D., Ribas, G., Campbell, R. D., The Wellcome Trust Case Control Consortium, Bradbury, Linda A., Brown, Matthew A. and Evans, David (2007). Localization of type 1 diabetes susceptibility to the MHC class I genes HLA-B and HLA-A. Nature, 450 (7171), 887-892. doi: 10.1038/nature06406 |
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2007 Journal Article Rheumatoid arthritis association at 6q23Thompson, Wendy, Wellcome Trust Case Control Consortium, Brown, Matthew A., Bradbury, Linda A., et al. and Evans, David (2007). Rheumatoid arthritis association at 6q23. Nature Genetics, 39 (12), 1431-1433. doi: 10.1038/ng.2007.32 |
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2007 Journal Article Association scan of 14,000 nonsynonymous SNP's in four diseases identifies autoimmunity variantsWellcome Trust Case control Consortium, The Australo-Anglo-American Spondylitis Consortium, Sims, A-M., Bradbury, L. A., Brown, M. A., Doan, T., Dowling, A. and Evans, D. (2007). Association scan of 14,000 nonsynonymous SNP's in four diseases identifies autoimmunity variants. Nature Genetics, 39 (11), 1329-1337. doi: 10.1038/ng.2007.17 |
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2007 Journal Article A second generation human haplotype map of over 3.1 million SNPsFrazer, K.A., Ballinger, D.G., Cox, D.R., Hinds, D.A., Stuve, L.L., Gibbs, R.A., Belmont, J.W., Boudreau, A., Hardenbol, P., Leal, S.M., Pasternak, S., Wheeler, D.A., Willis, T.D., Yu, F., Yang, H., Zeng, C., Gao, Y., Hu, H., Hu, W., Li, C., Lin, W., Liu, S., Pan, H., Tang, X., Wang, J., Wang, W., Yu, J., Zhang, B., Zhang, Q. ... Stewart, J. (2007). A second generation human haplotype map of over 3.1 million SNPs. Nature, 449 (7164), 851-861. doi: 10.1038/nature06258 |
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2007 Journal Article Genome-wide detection and characterization of positive selection in human populationsSabeti P.C., Varilly P., Fry B., Lohmueller J., Hostetter E., Cotsapas C., Xie X., Byrne E.H., McCarroll S.A., Gaudet R., Schaffner S.F., Lander E.S., Frazer K.A., Ballinger D.G., Cox D.R., Hinds D.A., Stuve L.L., Gibbs R.A., Belmont J.W., Boudreau A., Hardenbol P., Leal S.M., Pasternak S., Wheeler D.A., Willis T.D., Yu F., Yang H., Zeng C., Gao Y. ... Stewart J. (2007). Genome-wide detection and characterization of positive selection in human populations. Nature, 449 (7164), 913-918. doi: 10.1038/nature06250 |
