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2009

Journal Article

A genome-wide association study reveals variants in ARL15 that influence adiponectin levels

Brent 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

A genome-wide association study reveals variants in ARL15 that influence adiponectin levels

2008

Journal Article

Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease

Barrett, 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

Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease

2008

Journal Article

Common variants near MC4R are associated with fat mass, weight and risk of obesity

Loos, 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

Common variants near MC4R are associated with fat mass, weight and risk of obesity

2008

Journal Article

Genome-wide association analysis identifies 20 loci that influence adult height

Weedon, 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

Genome-wide association analysis identifies 20 loci that influence adult height

2008

Journal Article

A genome-wide scan for Eysenckian personality dimensions in adolescent twin sibships: Psychoticism, Extraversion, Neuroticism, and Lie

Gillespie, 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

A genome-wide scan for Eysenckian personality dimensions in adolescent twin sibships: Psychoticism, Extraversion, Neuroticism, and Lie

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

To what extent do scans of non-synonymous SNPs complement denser genome-wide association studies?

2007

Journal Article

Localization of type 1 diabetes susceptibility to the MHC class I genes HLA-B and HLA-A

Nejentsev, 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

Localization of type 1 diabetes susceptibility to the MHC class I genes HLA-B and HLA-A

2007

Journal Article

Rheumatoid arthritis association at 6q23

Thompson, 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

Rheumatoid arthritis association at 6q23

2007

Journal Article

Association scan of 14,000 nonsynonymous SNP's in four diseases identifies autoimmunity variants

Wellcome 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

Association scan of 14,000 nonsynonymous SNP's in four diseases identifies autoimmunity variants

2007

Journal Article

A second generation human haplotype map of over 3.1 million SNPs

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., 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

A second generation human haplotype map of over 3.1 million SNPs

2007

Journal Article

Genome-wide detection and characterization of positive selection in human populations

Sabeti 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

Genome-wide detection and characterization of positive selection in human populations

2007

Journal Article

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

The Wellcome Trust Case Control Consortium, Bradbury, L. A., Brown, M. A. and Evans, D. (2007). Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature, 447 (7145), 661-678. doi: 10.1038/nature05911

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

2007

Journal Article

Genomewide scans of red cell indices suggest linkage on chromosome 6q23

Iliadou, A., Evans, D. M., Zhu, G., Duffy, D. L., Frazer, I. H., Montgomery, G. W. and Martin, N. G. (2007). Genomewide scans of red cell indices suggest linkage on chromosome 6q23. Journal of Medical Genetics, 44 (1), 24-30. doi: 10.1136/jmg.2006.043521

Genomewide scans of red cell indices suggest linkage on chromosome 6q23

2006

Journal Article

Genome-wide association: a promising start to a long race

Evans, David M. and Cardon, Lon R. (2006). Genome-wide association: a promising start to a long race. Trends in Genetics, 22 (7), 350-354. doi: 10.1016/j.tig.2006.05.001

Genome-wide association: a promising start to a long race

2006

Journal Article

Two-stage two-locus models in genome-wide association

Evans D.M., Marchini J., Morris A.P. and Cardon L.R. (2006). Two-stage two-locus models in genome-wide association. PLoS Genetics, 2 (9), 1424-1432. doi: 10.1371/journal.pgen.0020157

Two-stage two-locus models in genome-wide association

2006

Journal Article

A note on the power to detect transmission distortion in parent-child trios via the transmission disequilibrium test.

Evans D.M., Morris A.P., Cardon L.R. and Sham P.C. (2006). A note on the power to detect transmission distortion in parent-child trios via the transmission disequilibrium test.. Behavior genetics, 36 (6), 947-950. doi: 10.1007/s10519-006-9087-2

A note on the power to detect transmission distortion in parent-child trios via the transmission disequilibrium test.

2006

Journal Article

Genome-wide scan of IQ finds significant linkage to a quantitative trait locus on 2q

Luciano, M., Wright, M. J., Duffy, D. L., Wainwright, M. A., Zhu, G., Evans, D. M., Geffen, G. M., Montgomery, G. W. and Martin, N. G. (2006). Genome-wide scan of IQ finds significant linkage to a quantitative trait locus on 2q. Behavior Genetics, 36 (1), 45-55. doi: 10.1007/s10519-005-9003-1

Genome-wide scan of IQ finds significant linkage to a quantitative trait locus on 2q

2005

Journal Article

A haplotype map of the human genome

Belmont J.W., Boudreau A., Leal S.M., Hardenbol P., Pasternak S., Wheeler D.A., Willis T.D., Yu F., Yang H., 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., Zhao H., Zhou J., Barry R., Blumenstiel B., Camargo A., Defelice M., Faggart M. ... Stewart J. (2005). A haplotype map of the human genome. Nature, 437 (7063), 1299-1320. doi: 10.1038/nature04226

A haplotype map of the human genome

2005

Journal Article

Teenage acne is influenced by genetic factors

Evans, D. M., Kirk, K. M., Nyholt, D. R., Novac, C. and Martin, N. G. (2005). Teenage acne is influenced by genetic factors. British Journal of Dermatology, 152 (3), 579-581. doi: 10.1111/j.1365-2133.2005.06387.x

Teenage acne is influenced by genetic factors

2005

Journal Article

Genetically indistinguishable SNPs and their influence on inferring the location of disease-associated variants

Lawrence, Robert, Evans, David M., Morris, Andrew P., Ke, Xiayi, Hunt, Sarah, Paolucci, Marta, Ragoussis, Jiannis, Deloukas, Panos, Bentley, David and Cardon, Lon R. (2005). Genetically indistinguishable SNPs and their influence on inferring the location of disease-associated variants. Genome Research, 15 (11), 1503-1510. doi: 10.1101/gr.4217605

Genetically indistinguishable SNPs and their influence on inferring the location of disease-associated variants