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2011 Journal Article Correction: The genetic basis of spondyloarthritis: SPARTAN/IGAS 2009 (Journal of Rheumatology (2010) 37 (2626-2631))Evans, D. M., Reveille, J. D., Brown, M., Chandran, V., Gladman, D. D., Martin, T. M., McGovern, D., Wordsworth, Paul and Inman, R. D. (2011). Correction: The genetic basis of spondyloarthritis: SPARTAN/IGAS 2009 (Journal of Rheumatology (2010) 37 (2626-2631)). Journal of Rheumatology, 38 (4). doi: 10.3899/jrheum.100892C1 |
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2011 Journal Article The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: evidence from a large collaborative study totaling 4,963 subjectsRizzi, Thais S., Arias-Vasquez, Alejandro, Rommelse, Nanda, Kuntsi, Jonna, Anney, Richard, Asherson, Philip, Buitelaar, Jan, Banaschewski, Tobias, Ebstein, Richard, Ruano, Dina, van der Sluis, Sophie, Markunas, Christina A., Garrett, Melanie E., Ashley-Koch, Allison E., Kollins, Scott H., Anastopoulos, Arthur D., Hansell, Narelle K., Wright, Margaret J., Montgomery, Grant W., Martin, Nicholas G., Harris, Sarah E., Davies, Gail, Tenesa, Albert, Porteous, David J., Starr, John M., Deary, Ian J., St. Pourcain, Beate, Smith, George Davey, Timpson, Nicholas J. ... Posthuma, Danielle (2011). The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: evidence from a large collaborative study totaling 4,963 subjects. American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 156 (2), 145-157. doi: 10.1002/ajmg.b.31149 |
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2011 Journal Article Adult height variants affect birth length and growth rate in childrenPaternoster, Lavinia, Howe, Laura D., Tilling, Kate, Weedon, Michael N., Freathy, Rachel M., Frayling, Timothy M., Kemp, John P., Smith, George Davey, Timpson, Nicholas J., Ring, Susan M., Evans, David M. and Lawlor, Debbie A. (2011). Adult height variants affect birth length and growth rate in children. Human Molecular Genetics, 20 (20) ddr309, 4069-4075. doi: 10.1093/hmg/ddr309 |
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2011 Book Chapter Gene-gene interaction and epistasisEvans, David M. (2011). Gene-gene interaction and epistasis. Analysis of complex disease association studies. (pp. 197-213) edited by Eleftheria Zeggini and Andrew Morris. Amsterdam, Netherlands: Elsevier. doi: 10.1016/B978-0-12-375142-3.10012-4 |
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2011 Journal Article Associations of FTO and MC4R variants with obesity traits in Indians and the role of rural/urban environment as a possible effect modifierTaylor, A. E., Sandeep, M. N., Janipalli, C. S., Giambartolomei, C., Evans, D. M., Kranthi Kumar, M. V., Vinay, D. G., Smitha, P., Gupta, V., Aruna, M., Kinra, S., Sullivan, R. M., Bowen, L., Timpson, N. J., Davey Smith, G., Dudbridge, F., Prabhakaran, D., Ben-Shlomo, Y., Reddy, K. S., Ebrahim, S. and Chandak, G. R. (2011). Associations of FTO and MC4R variants with obesity traits in Indians and the role of rural/urban environment as a possible effect modifier. Journal of Obesity, 2011 307542, 1-7. doi: 10.1155/2011/307542 |
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2011 Journal Article Genome-wide association study identifies four loci associated with eruption of permanent teethGeller, Frank, Feenstra, Bjarke, Zhang, Hao, Shaffer, John R., Hansen, Thomas, Esserlind, Ann-Louise, Boyd, Heather A., Nohr, Ellen A., Timpson, Nicholas J., Fatemifar, Ghazaleh, Paternoster, Lavinia, Evans, David M., Weyant, Robert J., Levy, Steven M., Lathrop, Mark, Smith, George Davey, Murray, Jeffrey C., Olesen, Jes, Werge, Thomas, Marazita, Mary L., Sorensen, Thorkild I. A. and Melbye, Mads (2011). Genome-wide association study identifies four loci associated with eruption of permanent teeth. PLoS Genetics, 7 (9) e1002275, e1002275.1-e1002275.9. doi: 10.1371/journal.pgen.1002275 |
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2011 Book Chapter Mapping complex disease genes using linkage disequilibrium and genomewide association scansPalmer, Lyle J., Timpson, Nicholas J., Evans, David M., Smith, George Davey and Cardon, Lon R. (2011). Mapping complex disease genes using linkage disequilibrium and genomewide association scans. An Introduction to Genetic Epidemiology. (pp. 91-130) Bristol, United Kingdom: Policy Press. |
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2011 Conference Publication Association analyses of 47,500 individuals identifies six fracture loci and 82 BMD loci clustering in biological pathways that regulate osteoblast and osteoclast activityEstrada, K, Evangelou, E, Hsu, YH, Styrkarsdottir, U, Liu, CT, Moayyeri, A, Kaptoge, S, Duncan, E, Amin, N, Kiel, D, Karasik, D, Albagha, OM, Brown, M, Spector, TD, Zillikens, MC, Ohlsson, C, Thorleifsson, G, Reeve, J, Vandenput, L, Pettersson, U, O'Neill, T, Riancho, JA, Ijunggren, O, Rousseau, F, Leslie, WD, Obermayer-Pietsch, B, Alonso, N, Langdahl, B, Nogues, X ... GENOMOS Consortia (2011). Association analyses of 47,500 individuals identifies six fracture loci and 82 BMD loci clustering in biological pathways that regulate osteoblast and osteoclast activity. 3rd Joint Meeting of the European-Calcified-Tissue-Society/International-Bone-and-Mineral-Society, Athens Greece, May 07-11, 2011. NEW YORK: ELSEVIER SCIENCE INC. doi: 10.1016/j.bone.2011.03.070 |
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2011 Journal Article A genome-wide association study to identify genetic determinants of atopy in subjects from the United KingdomWan, Yize I., Strachan, David P., Evans, David M., Henderson, John, McKeever, Tricia, Holloway, John W., Hall, Ian P. and Sayers, Ian (2011). A genome-wide association study to identify genetic determinants of atopy in subjects from the United Kingdom. Journal of Allergy and Clinical Immunology, 127 (1), 223-231. doi: 10.1016/j.jaci.2010.10.006 |
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2010 Conference Publication The genetic basis of spondyloarthritis: SPARTAN/IGAS 2009Evans, David M., Reveille, John D., Brown, Matthew A., Chandran, Vinod, Gladman, Dafna D., Martin, Tammy M., McGovern, Dermot, Wordsworth, Paul and Inman, Robert D. (2010). The genetic basis of spondyloarthritis: SPARTAN/IGAS 2009. Toronto, ON, Canada: Journal of Rheumatology Publishing. doi: 10.3899/jrheum.100892 |
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2010 Journal Article A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1Strange, Amy, Capon, Francesca, Spencer, Chris C. A., Knight, Jo, Weale, Michael E., Allen, Michael H., Barton, Anne, Band, Gavin, Bellenguez, Céline, Bergboer, Judith G. M., Blackwell, Jenefer M., Bramon, Elvira, Bumpstead, Suzannah J., Casas, Juan P., Cork, Michael J., Corvin, Aiden, Deloukas, Panos, Dilthey, Alexander, Duncanson, Audrey, Edkins, Sarah, Estivill, Xavier, Fitzgerald, Oliver, Freeman, Colin, Giardina, Emiliano, Gray, Emma, Hofer, Angelika, Hüffmeier, Ulrike, Hunt, Sarah E., Irvine, Alan D. ... Trembath, Richard C. (2010). A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. Nature Genetics, 42 (11), 985-990. doi: 10.1038/ng.694 |
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2010 Journal Article Follow-up of potential novel Graves' disease susceptibility loci, identified in the UK WTCCC genome-wide nonsynonymous SNP studyNewby, Paul R., Pickles, Oliver J., Mazumdar, Samaresh, Brand, Oliver J., Carr-Smith, Jaqueline D., Pearce, Simon H. S., Franklyn, Jayne A., Wellcome Trust Case Control Consortium, Evans, David M., Simmonds, Matthew J., Gough, Stephen C. L., Brown, Matthew A., Bradbury, Linda and Pointon, Jennifer (2010). Follow-up of potential novel Graves' disease susceptibility loci, identified in the UK WTCCC genome-wide nonsynonymous SNP study. European Journal of Human Genetics, 18 (9), 1021-1026. doi: 10.1038/ejhg.2010.55 |
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2010 Journal Article A variant in LIN28B is Associated with 2D:4D finger-length ratio, a putative retrospective biomarker of prenatal testosterone exposureMedland, Sarah E., Zayats,Tetyana, Glaser, Beate, Nyholt, Dale R., Gordon,Scott D., Wright, Margaret J., Montgomery, Grant W., Campbell, Megan J., Henders, Anjali K., Timpson, Nicholas J., Peltonen, Leena, Wolke, Dieter, Ring, Susan M., Deloukas, Panos, Martin, Nicholas G., Smith, George Davey and Evans, David M. (2010). A variant in LIN28B is Associated with 2D:4D finger-length ratio, a putative retrospective biomarker of prenatal testosterone exposure. American Journal of Human Genetics, 86 (4), 519-525. doi: 10.1016/j.ajhg.2010.02.017 |
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2010 Journal Article Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controlsCraddock, Nick, Hurles, Matthew E., Cardin, Niall, Pearson, Richard D., Plagnol, Vincent, Robson, Samuel, Vukcevic, Damjan, Barnes, Chris, Brown, Matthew A., Evans, David M. and The Wellcome Trust Case Control Consortium (2010). Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls. Nature, 464 (7289), 713-720. doi: 10.1038/nature08979 |
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2010 Journal Article Functional Gene Group Analysis Reveals a Role of Synaptic Heterotrimeric G Proteins in Cognitive AbilityRuano, Dina, Abecasis, Goncalo R., Glaser, Beate, Lips, Esther S., Cornelisse, L. Niels, de Jong, Arthur P. H., Evans, David M., Smith, George Davey, Timpson, Nicolas J., Smit, August B., Heutink, Peter, Verhage, Mathhijs and Posthuma, Danielle (2010). Functional Gene Group Analysis Reveals a Role of Synaptic Heterotrimeric G Proteins in Cognitive Ability. American Journal of Human Genetics, 86 (2), 113-125. doi: 10.1016/j.ajhg.2009.12.006 |
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2010 Journal Article A new highly penetrant form of obesity due to deletions on chromosome 16p11.2Walters, R. G., Jacquemont, S., Valsesia, A., De Smith, A. J., Martinet, D., Andersson, J., Falchi, M., Chen, F., Andrieux, J., Lobbens, S., Delobel, B., Stutzmann, F., El-Sayed Moustafa, J. S., Chevre, J.-C., Lecoeur, C., Vatin, V., Bouquillon, S., Buxton, J. L., Boute, O., Holder-Espinasse, M., Cuisset, J.-M., Lemaitre, M.-P., Ambresin, A.-E., Brioschi, A., Gaillard, M., Giusti, V., Fellmann, F., Ferrarini, A., Hadjikhani, N. ... Beckmann, J. S. (2010). A new highly penetrant form of obesity due to deletions on chromosome 16p11.2. Nature, 463 (7281), 671-675. doi: 10.1038/nature08727 |
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2010 Journal Article Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility lociReveille, John D., Sims, Anne-Marie, Danoy, Patrick, Evans, David M., Leo, Paul, Pointon, Jennifer J., Jin, Rui, Zhou, Xiaodong, Bradbury, Linda A., Appleton, Louise H., Davis, John C., Diekman, Laura, Doan, Tracey, Dowling, Alison, Duan, Ran, Duncan, Emma L., Farrar, Claire, Hadler, Johanna, Harvey, David, Karaderi, Tugce, Mogg, Rebecca, Pomeroy, Emma, Pryce, Karena, Taylor, Jacqueline, Savage, Laurie, Deloukas, Panos, Kumanduri, Vasudev, Peltonen, Leena, Ring, Sue M. ... Brown, Mathew A. (2010). Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci. Nature Genetics, 42 (2), 123-127. doi: 10.1038/ng.513 |
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2010 Journal Article Quantitative trait loci for CD4:CD8 lymphocyte ratio are associated with risk of type 1 diabetes and HIV-1 immune controlFerreira, Mar, Mangino, M, Brumme, CJ, Zhao, ZZ, Medland, SE, Wright, MJ, Nyholt, DR, Gordon, S, Campbell, M, McEvoy, BP, Henders, A, Evans, DM, Lanchbury, JS, Pereyra, F, Walker, BD, Haas, DW, Soranzo, N, Spector, TD, de Bakker, PIW, Frazer, IH, Montgomery, GW, Martin, NG and Int HIV Controllers Study (2010). Quantitative trait loci for CD4:CD8 lymphocyte ratio are associated with risk of type 1 diabetes and HIV-1 immune control. American Journal of Human Genetics, 86 (1), 88-92. doi: 10.1016/j.ajhg.2009.12.008 |
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2010 Journal Article Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weightFreathy, Rachel M., Mook-Kanamor, Dennis O., Sovio, Ulla, Prokopenko, Inga, Timpson, Nicholas J., Berry, Diane J., Warrington, Nicole M., Widen, Elisabeth, Hottenga, Jouke Jan, Kaakinen, Marika, Lange, Leslie A., Bradfield, Jonathan P., Kerkhof, Marjan, Marsh, Julie A., Magi, Reedik, Chen, Chih-Mei, Lyon, Helen N., Kirin, Mirna, Adair, Linda S., Aulchenko, Yurii S., Bennett, Amanda J., Borja, Judith B., Bouatia-Naji, Nabila, Charoen, Pimphen, Coin, Lachlan ..J. M., Cousminer, Diana L., De Geus, Eco J. C., Deloukas, Panos, Elliott, Paul ... McCarthy, Mark I. (2010). Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight. Nature Genetics, 42 (5), 430-435. doi: 10.1038/ng.567 |
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2010 Journal Article OPG and RANK polymorphisms are both associated with cortical bone mineral density: Findings from a metaanalysis of the avon longitudinal study of parents and children and Gothenburg osteoporosis and obesity determinants cohortsPaternoster, L., Ohlsson, C., Sayers, A., Vandenput, L., Lorentzon, M., Evans, D. M. and Tobias, J. H. (2010). OPG and RANK polymorphisms are both associated with cortical bone mineral density: Findings from a metaanalysis of the avon longitudinal study of parents and children and Gothenburg osteoporosis and obesity determinants cohorts. Journal of Clinical Endocrinology and Metabolism, 95 (8), 3940-3948. doi: 10.1210/jc.2010-0025 |
