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2015 Journal Article A genome-wide approach to children's aggressive behavior: the EAGLE consortiumPappa, Irene, St Pourcain, Beate, Benke, Kelly, Cavadino, Alana, Hakulinen, Christian, Nivard, Michel G., Nolte, Ilja M., Tiesler, Carla M. T., Bakermans-Kranenburg, Marian J., Davies, Gareth E., Evans, David M., Geoffroy, Marie-Claude, Grallert, Harald, Groen-Blokhuis, Maria M., Hudziak, James J., Kemp, John P., Keltikangas-Järvinen, Liisa, McMahon, George, Mileva-Seitz, Viara R., Motazedi, Ehsan, Power, Christine, Raitakari, Olli T., Ring, Susan M., Rivadeneira, Fernando, Rodriguez, Alina, Scheet, Paul A., Seppälä, Ilkka, Snieder, Harold, Standl, Marie ... Tiemeier, Henning (2015). A genome-wide approach to children's aggressive behavior: the EAGLE consortium. American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 171 (5), 1-11. doi: 10.1002/ajmg.b.32333 |
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2015 Journal Article TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transportSchmidts, Miriam, Hou, Yuqing, Cortes, Claudio R., Mans, Dorus A., Huber, Celine, Boldt, Karsten, Patel, Mitali, van Reeuwijk, Jeroen, Plaza, Jean-Marc, van Beersum, Sylvia E. C., Yap, Zhi Min, Letteboer, Stef J. F., Taylor, S. Paige, Herridge, Warren, Johnson, Colin A., Scambler, Peter J., Ueffing, Marius, Kayserili, Hulya, Krakow, Deborah, King, Stephen M., Beales, Philip L., Al-Gazali, Lihadh, Wicking, Carol, Cormier-Daire, Valerie, Roepman, Ronald, Mitchison, Hannah M., Witman, George B., Al-Turki, Saeed, Anderson, Carl ... Zheng, Hou-Feng (2015). TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport. Nature Communications, 6 (7074) 7074, 1-13. doi: 10.1038/ncomms8074 |
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2015 Journal Article Major histocompatibility complex associations of ankylosing spondylitis are complex and involve further epistasis with ERAP1Cortes, Adrian, Pulit, Sara L., Leo, Paul J., Pointon, Jenny J., Robinson, Philip C., Weisman, Michael H., Ward, Michael, Gensler, Lianne S., Zhou, Xiaodong, Garchon, Henri-J., Chiocchia, Gilles, Nossent, Johannes, Lie, Benedicte A., Forre, Oystein, Tuomilehto, Jaakko, Laiho, Kari, Bradbury, Linda A., Elewaut, Dirk, Burgos-Vargas, Ruben, Stebbings, Simon, Appleton, Louise, Farrah, Claire, Lau, Jonathan, Haroon, Nigil, Mulero, Juan, Blanco, Francisco J., Gonzalez-Gay, Miguel A., Lopez-Larrea, C., Bowness, Paul ... Brown, Matthew A. (2015). Major histocompatibility complex associations of ankylosing spondylitis are complex and involve further epistasis with ERAP1. Nature Communications, 6 (7146) 7146, 1-8. doi: 10.1038/ncomms8146 |
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2015 Journal Article Data Resource Profile: Accessible Resource for Integrated Epigenomic Studies (ARIES)Relton, Caroline L., Gaunt, Tom, MCardle, Wendy, Ho, Haren, Shihab, Hashem, Woodward, Geoff, Lyttleton, Oliver, Evans, David M., Reik, Wolf, Paul, Yu-Lee, Ticz, Gabriella, Ozanne, Susan E., Wipat, Anil, Flanagan, Keith, Lister, Allyson, Heijmans, Bastiaan T., Ring, Susan M. and Smith, George Davey (2015). Data Resource Profile: Accessible Resource for Integrated Epigenomic Studies (ARIES). International Journal of Epidemiology, 44 (4), 1181-1190. doi: 10.1093/ije/dyv072 |
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2015 Journal Article Genetic variants in adult bone mineral density and fracture risk genes are associated with the rate of bone mineral density acquisition in adolescenceWarrington, Nicole M., Kemp, John P., Tilling, Kate, Tobias, Jonathan H. and Evans, David M. (2015). Genetic variants in adult bone mineral density and fracture risk genes are associated with the rate of bone mineral density acquisition in adolescence. Human Molecular Genetics, 24 (14) ddv143, 4158-4166. doi: 10.1093/hmg/ddv143 |
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2015 Journal Article A genome-wide association study of body mass index across early life and childhoodWarrington, Nicole M., Howe, Laura D., Paternoster, Lavinia, Kaakinen, Marika, Herrala, Sauli, Huikari, Ville, Wu, Yan Yan, Kemp, John P., Timpson, Nicholas J., Pourcain, Beate St, Smith, George Davey, Tilling, Kate, Jarvelin, Marjo-Riitta, Pennell, Craig E., Evans, David M., Lawlor, Debbie A., Briollais, Laurent and Palmer, Lyle J. (2015). A genome-wide association study of body mass index across early life and childhood. International Journal of Epidemiology, 44 (2) dyv077, 700-712. doi: 10.1093/ije/dyv077 |
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2015 Journal Article Shared genetic influences between attention-deficit/hyperactivity disorder (ADHD) traits in children and clinical ADHDStergiakouli, Evie, Martin, Joanna, Hamshere, Marian L., Langley, Kate, Evans, David M., St Pourcain, Beate, Timpson, Nicholas J., Owen, Michael J., O'Donovan, Michael, Thapar, Anita and Davey Smith, George (2015). Shared genetic influences between attention-deficit/hyperactivity disorder (ADHD) traits in children and clinical ADHD. Journal of the American Academy of Child and Adolescent Psychiatry, 54 (4), 322-327. doi: 10.1016/j.jaac.2015.01.010 |
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2015 Journal Article Cardiometabolic effects of genetic upregulation of the interleukin 1 receptor antagonist: A Mendelian randomisation analysisFreitag, Daniel, Butterworth, Adam S, Willeit, Peter, Howson, Joanna M M, Burgess, Stephen, Kaptoge, Stephen, Young, Robin, Ho, Weang Kee, Wood, Angela M, Sweeting, Michael, Spackman, Sarah, Staley, James R, Ramond, Anna, Harshfield, Eric, Nielsen, Sune F, Grande, Peer, Lange, Leslie A, Bown, Matthew J, Jones, Gregory T, Scott, Robert A, Bevan, Steve, Porcu, Eleonora, Thorleifsson, Gudmar, Zeng, Lingyao, Kessler, Thorsten, Nikpay, Majid, Do, Ron, Zhang, Weihua, Hopewell, Jemma C ... Houlston, Richard S (2015). Cardiometabolic effects of genetic upregulation of the interleukin 1 receptor antagonist: A Mendelian randomisation analysis. The Lancet Diabetes and Endocrinology, 3 (4), 243-253. doi: 10.1016/S2213-8587(15)00034-0 |
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2015 Journal Article Genome-wide association study of blood lead shows multiple associations near ALADWarrington, Nicole M., Zhu, Gu, Dy, Veronica, Heath, Andrew C., Madden, Pamela A. F., Hemani, Gibran, Kemp, John P., Mcmahon, George, St Pourcain, Beate, Timpson, Nicholas J., Taylor, Caroline M., Golding, Jean, Lawlor, Debbie A., Steer, Colin, Montgomery, Grant W., Martin, Nicholas G., Smith, George Davey, Evans, David M. and Whitfield, John B. (2015). Genome-wide association study of blood lead shows multiple associations near ALAD. Human Molecular Genetics, 24 (13) ddv112, 3871-3879. doi: 10.1093/hmg/ddv112 |
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2015 Journal Article Whole-genome sequence-based analysis of thyroid functionTaylor, Peter N., Porcu, Eleonora, Chew, Shelby, Campbell, Purdey J., Traglia, Michela, Brown, Suzanne J., Mullin, Benjamin H., Shihab, Hashem A., Min, Josine, Walter, Klaudia, Memari, Yasin, Huang, Jie, Barnes, Michael R., Beilby, John P., Charoen, Pimphen, Danecek, Petr, Dudbridge, Frank, Forgetta, Vincenzo, Greenwood, Celia, Grundberg, Elin, Johnson, Andrew D., Hui, Jennie, Lim, Ee M., McCarthy, Shane, Muddyman, Dawn, Panicker, Vijay, Perry, John R. B., Bell, Jordana T., Yuan, Wei ... Yang, Jian (2015). Whole-genome sequence-based analysis of thyroid function. Nature Communications, 6 (1) 5681, 5681.1-5681.10. doi: 10.1038/ncomms6681 |
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2015 Journal Article Genomic influences on alcohol problems in a population-based sample of young adultsEdwards, Alexis C., Aliev, Fazil, Wolen, Aaron R., Salvatore, Jessica E., Gardner, Charles O., McMahon, George, Evans, David M., Macleod, John, Hickman, Matthew, Dick, Danielle M. and Kendler, Kenneth S. (2015). Genomic influences on alcohol problems in a population-based sample of young adults. Addiction, 110 (3), 461-470. doi: 10.1111/add.12822 |
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2015 Journal Article A novel common variant in DCST2 is associated with length in early life and height in adulthoodvan der Valk, Ralf J. P., Kreiner-Moller, Eskil, Kooijman, Marjolein N., Guxens, Monica, Stergiakouli, Evangelia, Saaf, Annika, Bradfield, Jonathan P., Geller, Frank, Hayes, M. Geoffrey, Cousminer, Diana L., Koerner, Antje, Thiering, Elisabeth, Curtin, John A., Myhre, Ronny, Huikari, Ville, Joro, Raimo, Kerkhof, Marjan, Warrington, Nicole M., Pitkanen, Niina, Ntalla, Ioanna, Horikoshi, Momoko, Veijola, Riitta, Freathy, Rachel M., Teo, Yik-Ying, Barton, Sheila J., Evans, David M., Kemp, John P., St Pourcain, Beate, Ring, Susan M. ... for the Early Growth Genetics (EGG) Consortium (2015). A novel common variant in DCST2 is associated with length in early life and height in adulthood. Human Molecular Genetics, 24 (4) ddu510, 1155-1168. doi: 10.1093/hmg/ddu510 |
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2015 Journal Article Associations of vitamin D pathway genes with circulating 25-hydroxyvitamin-D, 1,25-dihydroxyvitamin-D, and prostate cancer: a nested case–control studyGilbert, Rebecca, Bonilla, Carolina, Metcalfe, Chris, Lewis, Sarah, Evans, David M., Fraser, William D., Kemp, John P., Donovan, Jenny L., Hamdy, Freddie C., Neal, David E., Lane, J. Athene, Smith, George Davey, Lathrop, Mark and Martin, Richard M. (2015). Associations of vitamin D pathway genes with circulating 25-hydroxyvitamin-D, 1,25-dihydroxyvitamin-D, and prostate cancer: a nested case–control study. Cancer Causes and Control, 26 (2), 205-218. doi: 10.1007/s10552-014-0500-5 |
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2015 Journal Article Genetic dissection of acute anterior uveitis reveals similarities and differences in associations observed with ankylosing spondylitisRobinson, Philip C., Claushuis, Theodora A. M., Cortes, Adrian, Martin, Tammy M., Evans, David M., Leo, Paul, Mukhopadhyay, Pamela, Bradbury, Linda A., Cremin, Katie, Harris, Jessica, Maksymowych, Walter P., Inman, Robert D., Rahman, Proton, Haroon, Nigil, Gensler, Lianne, Powell, Joseph E., Van Der Horst-Bruinsma, Irene E., Hewitt, Alex W., Craig, Jamie E., Lim, Lyndell L., Wakefield, Denis, McCluskey, Peter, Voigt, Valentina, Fleming, Peter, Spondyloarthritis Research Consortium of Canada, Australio-Anglo-American Spondylitis Consortium, International Genetics of Ankylosing Spondylitis Consortium, Wellcome Trust Case Control Study 2, Degli-Esposti, Mariapia ... Brown, Matthew A. (2015). Genetic dissection of acute anterior uveitis reveals similarities and differences in associations observed with ankylosing spondylitis. Arthritis and Rheumatology, 67 (1), 140-151. doi: 10.1002/art.38873 |
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2015 Conference Publication Multi-ethnic genome-wide association study of 21,000 cases and 95,000 controls identifies 11 novel risk loci for atopic dermatitisPaternoster, L., Standl, M., Baurecht, H., Evans, D. M. and Weidinger, S. (2015). Multi-ethnic genome-wide association study of 21,000 cases and 95,000 controls identifies 11 novel risk loci for atopic dermatitis. 45th Annual Meeting of the European Society for Dermatological Research, Rotterdam, the Netherlands, 09-12 September 2015. London, United Kingdom: Nature Publishing Group. doi: 10.1038/jid.2015.271 |
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2015 Conference Publication The relationship between lower back pain, inflammatory markers and genetic variants robustly associated with risk of Ankylosing Spondylitis in a population-based cohortKatikireddi, V, Baker, P. and Evans, D. (2015). The relationship between lower back pain, inflammatory markers and genetic variants robustly associated with risk of Ankylosing Spondylitis in a population-based cohort. Australian Rheumatology Associationin conjunction with Rheumatology Health Professionals Association, 56th Annual Scientific Meeting, Adelaide, Australia, 23–26 May, 2015. Richmond, Australia: Wiley-Blackwell Publishing Asia. doi: 10.1111/imj.12752 |
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2015 Journal Article Mendelian randomization: new applications in the coming age of hypothesis free causalityEvans, David M. and Smith, George Davey (2015). Mendelian randomization: new applications in the coming age of hypothesis free causality. Annual Review of Genomics and Human Genetics, 16 (1), 327-350. doi: 10.1146/annurev-genom-090314-050016 |
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2015 Journal Article Assumption-free estimation of the genetic contribution to refractive error across childhoodGuggenheim, Jeremy A., St Pourcain, Beate, McMahon, George, Timpson, Nicholas J., Evans, David M. and Williams, Cathy (2015). Assumption-free estimation of the genetic contribution to refractive error across childhood. Molecular Vision, 21, 621-632. |
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2014 Journal Article Heritability and genome-wide analyses of problematic peer relationships during childhood and adolescenceSt Pourcain, Beate, Haworth, C. M. A., Davis, O. S. P., Wang, Kai, Timpson, Nicholas J., Evans, David M., Kemp, John P., Ronald, Angelica, Price, Tom, Meaburn, Emma, Ring, Susan M., Golding, Jean, Hakonarson, Hakon, Plomin, R. and Smith, George Davey (2014). Heritability and genome-wide analyses of problematic peer relationships during childhood and adolescence. Human Genetics, 134 (6), 539-551. doi: 10.1007/s00439-014-1514-5 |
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2014 Journal Article Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortiumLi, Qing, Wojciechowski, Robert, Simpson, Claire L., Hysi, Pirro G., Verhoeven, Virginie J. M., Ikram, Mohammad Kamran, Hohn, Rene, Vitart, Veronique, Hewitt, Alex W., Oexle, Konrad, Makela, Kari-Matti, MacGregor, Stuart, Pirastu, Mario, Fan, Qiao, Cheng, Ching-Yu, St Pourcain, Beate, McMahon, George, Kemp, John P., Northstone, Kate, Rahi, Jugnoo S., Cumberland, Phillippa M., Martin, Nicholas G., Sanfilippo, Paul G., Lu, Yi, Wang, Ya Xing, Hayward, Caroline, Polasek, Ozren, Campbell, Harry, Bencic, Goran ... Guggenheim, Jeremy A. (2014). Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium. Human Genetics, 134 (2), 131-146. doi: 10.1007/s00439-014-1500-y |
