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2016 Journal Article A genome-wide association meta-analysis of diarrhoeal disease in young children identifies FUT2 locus and provides plausible biological pathwaysBustamante, Mariona, Standl, Marie, Bassat, Quique, Vilor-Tejedor, Natalia, Medina-Gomez, Carolina, Bonilla, Carolina, Ahluwalia, Tarunveer S., Bacelis, Jonas, Bradfield, Jonathan P., Tiesler, Carla M. T., Rivadeneira, Fernando, Ring, Susan, Vissing, Nadja H., Fink, Nadia R., Jugessur, Astanand, Mentch, Frank D., Ballester, Ferran, Kriebel, Jennifer, Kiefte-de Jong, Jessica C., Wolsk, Helene M., Llop, Sabrina, Thiering, Elisabeth, Beth, Systke A., Timpson, Nicholas J., Andersen, Josefine, Schulz, Holger, Jaddoe, Vincent W. V., Evans, David M., Waage, Johannes ... Sunyer, Jordi (2016). A genome-wide association meta-analysis of diarrhoeal disease in young children identifies FUT2 locus and provides plausible biological pathways. Human Molecular Genetics, 25 (18), 4127-4142. doi: 10.1093/hmg/ddw264 |
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2016 Journal Article Genome-wide association study of copy number variation with lung function identifies a novel signal of association near BANP for forced vital capacityShrine, Nick, Tobin, Martin D., Schurmann, Claudia, Artigas, Maria Soler, Hui, Jennie, Lehtimaki, Terho, Raitakari, Olli T., Pennell, Craig E., Ang, Qi Wei, Strachan, David P., Homuth, Georg, Glaeser, Sven, Felix, Stephan B., Evans, David M., Henderson, John, Granell, Raquel, Palmer, Lyle J., Huffman, Jennifer, Hayward, Caroline, Scotland, Generation, Malarstig, Anders, Musk, Bill, James, Alan L. and Wain, Louise V. (2016). Genome-wide association study of copy number variation with lung function identifies a novel signal of association near BANP for forced vital capacity. BMC Genetics, 17 (1) 116, 1-8. doi: 10.1186/s12863-016-0423-0 |
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2016 Journal Article Erratum to: Heritability and genome-wide analyses of problematic peer relationships during childhood and adolescencePourcain, Beate St, 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 (2016). Erratum to: Heritability and genome-wide analyses of problematic peer relationships during childhood and adolescence. Human Genetics, 135 (8), 965-965. doi: 10.1007/s00439-016-1695-1 |
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2016 Journal Article Joint developmental trajectories of internalizing and externalizing disorders between childhood and adolescenceNivard, Michel G., Lubke, Gitta H., Dolan, Conor V., Evans, David M., St. Pourcain, Beate, Munafo, Marcus R. and Middeldorp, Christel M. (2016). Joint developmental trajectories of internalizing and externalizing disorders between childhood and adolescence. Development and Psychopathology, 29 (3), 1-10. doi: 10.1017/S0954579416000572 |
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2016 Journal Article International genome-wide association study consortium identifies novel loci associated with blood pressure in children and adolescentsParmar, Priyakumari Ganesh, Taal, H. Rob, Timpson, Nicholas J., Thiering, Elisabeth, Lehtimaki, Terho, Marinelli, Marcella, Lind, Penelope A., Howe, Laura D., Verwoert, Germaine, Aalto, Ville, Uitterlinden, Andre G., Briollais, Laurent, Evans, Dave M., Wright, Margie J., Newnham, John P., Whitfield, John B., Lyytikainen, Leo-Pekka, Rivadeneira, Fernando, Boomsma, Dorrett I., Viikari, Jorma, Gillman, Matthew W., St Pourcain, Beate, Hottenga, Jouke-Jan, Montgomery, Grant W., Hofman, Albert, Kahonen, Mika, Martin, Nicholas G., Tobin, Martin D., Raitakari, Ollie ... Palmer, Lyle J. (2016). International genome-wide association study consortium identifies novel loci associated with blood pressure in children and adolescents. Circulation: Cardiovascular Genetics, 9 (3), 266-278. doi: 10.1161/CIRCGENETICS.115.001190 |
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2016 Journal Article The case for genome-wide association studies of bone acquisition in paediatric and adolescent populationsKemp, John P, Medina-Gomez, Carolina, Tobias, Jonathan H, Rivadeneira, Fernando and Evans, David M (2016). The case for genome-wide association studies of bone acquisition in paediatric and adolescent populations. BoneKEy reports, 5, 796. doi: 10.1038/bonekey.2016.23 |
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2016 Journal Article Childhood gene-environment interactions and age-dependent effects of genetic variants associated with refractive error and myopia: the CREAM ConsortiumFan, Qiao, Guo, Xiaobo, Tideman, J. Willem L., Williams, Katie M., Yazar, Seyhan, Hosseini, S. Mohsen, Howe, Laura D., St Pourcain, Beate, Evans, David M., Timpson, Nicholas J., McMahon, George, Hysi, Pirro G., Krapohl, Eva, Wang, Ya Xing, Jonas, Jost B., Baird, Paul Nigel, Wang, Jie Jin, Cheng, Ching-Yu, Teo, Yik-Ying, Wong, Tien-Yin, Ding, Xiaohu, Wojciechowski, Robert, Young, Terri L., Parssinen, Olavi, Oexle, Konrad, Pfeiffer, Norbert, Bailey-Wilson, Joan E., Paterson, Andrew D., Klaver, Caroline C. W. ... Guggenheim, Jeremy A. (2016). Childhood gene-environment interactions and age-dependent effects of genetic variants associated with refractive error and myopia: the CREAM Consortium. Scientific Reports, 6 (1) 25853, 25853. doi: 10.1038/srep25853 |
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2016 Journal Article Genome-wide association study identifies 74 loci associated with educational attainmentOkbay, Aysu, Beauchamp, Jonathan P., Fontana, Mark Alan, Lee, James J., Pers, Tune H., Rietveld, Cornelius A., Turley, Patrick, Chen, Guo-Bo, Emilsson, Valur, Meddens, S. Fleur W., Oskarsson, Sven, Pickrell, Joseph K., Thom, Kevin, Timshel, Pascal, de Vlaming, Ronald, Abdellaoui, Abdel, Ahluwalia, Tarunveer S., Bacelis, Jonas, Baumbach, Clemens, Bjornsdottir, Gyda, Brandsma, Johannes H., Concas, Maria Pina, Derringer, Jaime, Furlotte, Nicholas A., Galesloot, Tessel E., Girotto, Giorgia, Gupta, Richa, Hall, Leanne M., Harris, Sarah E. ... Benjamin, Daniel J. (2016). Genome-wide association study identifies 74 loci associated with educational attainment. Nature, 533 (7604), 539-542. doi: 10.1038/nature17671 |
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2016 Journal Article Exome-wide study of ankylosing spondylitis demonstrates additional shared genetic background with inflammatory bowel diseaseRobinson, Philip C., Leo, Paul J, Pointon, Jennifer J., Harris, Jessica, Cremin, Katie, Bradbury, Linda A., Stebbings, Simon, Harrison, Andrew A., Australian Osteoporosis Genetics Consortium, Wellcome Trust Case Control Consortium, Management Committee, Data and Analysis Group, DNA, Genotyping, Data QC and Informatics Group, Publications Committee, Duncan, Emma L., Evans, David M., Wordsworth, Paul B. and Brown, Matthew A. (2016). Exome-wide study of ankylosing spondylitis demonstrates additional shared genetic background with inflammatory bowel disease. NPJ Genomic Medicine, 1 (1) 16008, 16008-6. doi: 10.1038/npjgenmed.2016.8 |
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2016 Journal Article Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general populationRobinson, Elise B., St Pourcain, Beate, Anttila, Verneri, Kosmicki, Jack A., Bulik-Sullivan, Brendan, Grove, Jakob, Maller, Julian, Samocha, Kaitlin E., Sanders, Stephan J., Ripke, Stephan, Martin, Joanna, Hollegaard, Mads V., Werge, Thomas, Hougaard, David M., Neale, Benjamin M., Evans, David M., Skuse, David, Mortensen, Preben Bo, Børglum, Anders D., Ronald, Angelica, Smith, George Davey and Daly, Mark J. (2016). Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population. Nature Genetics, 48 (5), 552-555. doi: 10.1038/ng.3529 |
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2016 Journal Article Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive errorFan, Qiao, Verhoeven, Virginie J. M., Wojciechowski, Robert, Barathi, Veluchamy A., Hysi, Pirro G., Guggenheim, Jeremy A., Hoehn, Rene, Vitart, Veronique, Khawaja, Anthony P., Yamashiro, Kenji, Hosseini, S. Mohsen, Lehtimaki, Terho, Lu, Yi, Haller, Toomas, Xie, Jing, Delcourt, Cecile, Pirastu, Mario, Wedenoja, Juho, Gharahkhani, Puya, Venturini, Cristina, Miyake, Masahiro, Hewitt, Alex W., Guo, Xiaobo, Mazur, Johanna, Huffman, Jenifer E., Williams, Katie M., Polasek, Ozren, Campbell, Harry, Rudan, Igor ... Makela, Kari Matti (2016). Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error. Nature Communications, 7 (1) 11008, 11008-11008. doi: 10.1038/ncomms11008 |
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2016 Journal Article Common genetic variants influence whorls in fingerprint patternsHo, Yvonne Y. W., Evans, David M., Montgomery, Grant W., Henders, Anjali K., Kemp, John P., Timpson, Nicholas J., Pourcain, Beate St., Heath, Andrew C., Madden, Pamela A. F., Loesch, Danuta Z., McNevin, Dennis, Daniel, Runa, Davey-Smith, George, Martin, Nicholas G. and Medland, Sarah E. (2016). Common genetic variants influence whorls in fingerprint patterns. Journal of Investigative Dermatology, 136 (4), 859-862. doi: 10.1016/j.jid.2015.10.062 |
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2016 Journal Article Systematic identification of genetic influences on methylation across the human life courseGaunt, Tom R., Shihab, Hashem A., Hemani, Gibran, Min, Josine L., Woodward, Geoff, Lyttleton, Oliver, Zheng, Jie, Duggirala, Aparna, McArdle, Wendy L., Ho, Karen, Ring, Susan M., Evans, David M., Smith, George Davey and Relton, Caroline L. (2016). Systematic identification of genetic influences on methylation across the human life course. Genome Biology, 17 (1) 61, 61. doi: 10.1186/s13059-016-0926-z |
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2016 Journal Article Genetic evidence for causal relationships between maternal obesity-related traits and birth weightTyrrell, Jessica, Richmond, Rebecca C., Palmer, Tom M., Feenstra, Bjarke, Rangarajan, Janani, Metrustry, Sarah, Cavadino, Alana, Paternoster, Lavinia, Armstrong, Loren L., De Silva, N. Maneka G., Wood, Andrew R., Horikoshi, Momoko, Geller, Frank, Myhre, Ronny, Bradfield, Jonathan P., Kreiner-Moller, Eskil, Huikari, Ville, Painter, Jodie N., Hottenga, Jouke-Jan, Allard, Catherine, Berry, Diane J., Bouchard, Luigi, Das, Shikta, Evans, David M., Hakonarson, Hakon, Hayes, M. Geoffrey, Heikkinen, Jani, Hofman, Albert, Knight, Bridget ... Freathy, Rachel M. (2016). Genetic evidence for causal relationships between maternal obesity-related traits and birth weight. Journal of the American Medical Association, 315 (11), 1129-1140. doi: 10.1001/jama.2016.1975 |
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2016 Journal Article Association of forced vital capacity with the developmental gene NCOR2Minelli, Cosetta, Dean, Charlotte H., Hind, Matthew, Alves, Alexessander Couto, Amaral, Andre F. S., Siroux, Valerie, Huikari, Ville, Artigas, Maria Soler, Evans, David M., Loth, Daan W., Bosse, Yohan, Postma, Dirkje S., Sin, Don, Thompson, John, Demenais, Florence, Henderson, John, Bouzigon, Emmanuelle, Jarvis, Deborah, Jarvelin, Marjo-Riitta and Burney, Peter (2016). Association of forced vital capacity with the developmental gene NCOR2. Plos One, 11 (2) e0147388, e0147388-e0147388. doi: 10.1371/journal.pone.0147388 |
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2016 Journal Article New loci for body fat percentage reveal link between adiposity and cardiometabolic disease riskLu, Yingchang, Day, Felix R., Gustafsson, Stefan, Buchkovich, Martin L., Na, Jianbo, Bataille, Veronique, Cousminer, Diana L., Dastani, Zari, Drong, Alexander W., Esko, Tonu, Evans, David M., Falchi, Mario, Feitosa, Mary F., Ferreira, Teresa, Hedman, Asa K., Haring, Robin, Hysi, Pirro G., Iles, Mark M., Justice, Anne E., Kanoni, Stavroula, Lagou, Vasiliki, Li, Rui, Li, Xin, Locke, Adam, Lu, Chen, Magi, Reedik, Perry, John R. B., Pers, Tune H., Qi, Qibin ... Loos, Ruth J. F. (2016). New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk. Nature Communications, 7 (1) 10495, 10495-10495. doi: 10.1038/ncomms10495 |
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2016 Conference Publication Using Mendelian randomization to investigate a possible causal relationship between adiposity and increased bone mineral density at different skeletal sites in childrenKemp, John, Sayers, Adrian, Smith, George Davey, Tobias, Jonathan and Evans, David (2016). Using Mendelian randomization to investigate a possible causal relationship between adiposity and increased bone mineral density at different skeletal sites in children. 46th Annual Meeting of the Behavior Genetics Association, Brisbane, Australia, 20-23 June 2016. New York, NY, United States: Springer. |
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2016 Conference Publication Investigation into the genetic architecture of Giant Cell Arteritis through a genome-wide association studyDe Smit, Elisabeth, Hill, Catherine, Merriman, Tony, Cremin, Katie, Leo, Paul, McKelvie, Penny, Evans, David, Brown, Matta and Hewitt, Alex W. (2016). Investigation into the genetic architecture of Giant Cell Arteritis through a genome-wide association study. Annual Meeting of the Association for Research in Vision and Ophthalmology (ARVO), Seattle, WA, United States, May 01-05, 2016. Rockville, MD, United States: Association for Research in Vision and Ophthalmology. |
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2016 Journal Article Effect of Regulatory Requirement for Patient-Specific Prescriptions for Off-label Medications on the Use of Intravitreal BevacizumabHolfinger, Steven, Miller, Alexander G., Rao, Llewelyn J., Rowland, Douglas Y., Hornik, Joan H. and Miller, David G. (2016). Effect of Regulatory Requirement for Patient-Specific Prescriptions for Off-label Medications on the Use of Intravitreal Bevacizumab. Jama Ophthalmology, 134 (1), 45-48. doi: 10.1001/jamaophthalmol.2015.4331 |
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2016 Conference Publication Longitudinal Expression Profiling of T Lymphocytes in Patients with Active to Quiescent Giant Cell ArteritisDe Smit, Elisabeth, Clarke, Linda, Ngygen, Khoa, Shuey, Neil, Hill, Catherine, Anderson, Lisa, Evans, David, Brown, Matt A., Powell, Joseph and Hewitt, Alex W. (2016). Longitudinal Expression Profiling of T Lymphocytes in Patients with Active to Quiescent Giant Cell Arteritis. The Royal Australian and New Zealand College of Ophthalmologists, 48th Annual Scientific Congress, Melbourne, VIC Australia, 19–23 November 2016. Richmond, VIC Australia: Wiley-Blackwell. |
