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2019 Journal Article Publisher correction: Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathwaysDuffy, David L., Zhu, Gu, Li, Xin, Sanna, Marianna, Iles, Mark M., Jacobs, Leonie C., Evans, David M., Yazar, Seyhan, Beesley, Jonathan, Law, Matthew H., Kraft, Peter, Visconti, Alessia, Taylor, John C., Liu, Fan, Wright, Margaret J., Henders, Anjali K., Bowdler, Lisa, Glass, Dan, Ikram, M. Arfan, Uitterlinden, André G., Madden, Pamela A., Heath, Andrew C., Nelson, Elliot C., Green, Adele C., Chanock, Stephen, Barrett, Jennifer H., Brown, Matthew A., Hayward, Nicholas K., MacGregor, Stuart ... Martin, Nicholas G. (2019). Publisher correction: Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways. Nature Communications, 10 (1) 299, 299. doi: 10.1038/s41467-018-08078-w |
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2019 Conference Publication Genes within the context of development: changes in genetic trait architectures during childhood and adolescenceSt Pourcain, Beate, Eaves, Lindon, Verhoef, Ellen, Shapland, Chin Yang, Ring, Susan M., Fisher, Simon E., Medland, Sarah E., Evans, David and Smith, George Davey (2019). Genes within the context of development: changes in genetic trait architectures during childhood and adolescence. 25th World Congress of Psychiatric Genetics (WCPG), Orlando, FL, United States, 13-17 October 2017. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2017.06.071 |
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2019 Journal Article Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorderDemontis, Ditte, Walters, Raymond K., Martin, Joanna, Mattheisen, Manuel, Als, Thomas D., Agerbo, Esben, Baldursson, Gísli, Belliveau, Rich, Bybjerg-Grauholm, Jonas, Bækvad-Hansen, Marie, Cerrato, Felecia, Chambert, Kimberly, Churchhouse, Claire, Dumont, Ashley, Eriksson, Nicholas, Gandal, Michael, Goldstein, Jacqueline I., Grasby, Katrina L., Grove, Jakob, Gudmundsson, Olafur O., Hansen, Christine S., Hauberg, Mads Engel, Hollegaard, Mads V., Howrigan, Daniel P., Huang, Hailiang, Maller, Julian B., Martin, Alicia R., Martin, Nicholas G., Moran, Jennifer ... Kemp, John P. (2019). Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder. Nature Genetics, 51 (1), 63-75. doi: 10.1038/s41588-018-0269-7 |
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2019 Journal Article Calculating Power to Detect Maternal and Offspring Genetic Effects in Genetic Association StudiesMoen, Gunn-Helen, Hemani, Gibran, Warrington, Nicole M. and Evans, David M. (2019). Calculating Power to Detect Maternal and Offspring Genetic Effects in Genetic Association Studies. Behavior Genetics, 49 (3), 327-339. doi: 10.1007/s10519-018-9944-9 |
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2019 Conference Publication Effects of assortative mating on estimates of SNP heritabilityKeller, Matthew, de Candia, Teresa, Jones, Matt, Tahmasbi, Rasool, Evans, Luke, Evans, David, Eaves, Lindon, Yang, Jian, Visscher, Peter and Goddard, Mike (2019). Effects of assortative mating on estimates of SNP heritability. 25th World Congress of Psychiatric Genetics (WCPG), Orlando, FL, United States, 13-17 October 2017. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2017.08.016 |
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2019 Conference Publication Maternal and paternal effects on offspring internalising problems: findings from family data and extended GCTA analysesShahid, Eshim, Eilertsen, Espen, Hammerschlag, Anke, Sallis, Hannah, Qiao, Zhen, Evans, David, Ystrom, Eivind, Bartels, Meike and Middeldorp, Christel M. (2019). Maternal and paternal effects on offspring internalising problems: findings from family data and extended GCTA analyses. 27th World Congress of Psychiatric Genetics (WCPG), Los Angeles, CA, United States, 26-31 October, 2019. Amsterdam, Netherlands: Elsevier BV. doi: 10.1016/j.euroneuro.2019.07.034 |
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2019 Conference Publication A large-scale deep-coverage whole genome sequencing to identify less common and rare variants associated with BMD and fractures: the NHLBI Trans-Omics for Precision Medicine (TOPMED) studyHsu, Yi-Hsiang, Xu, Hanfei, Zhang, Xiaoyu, Liu, Ching-Ti, Montasser, May, Fu, Mao, O'Connell, Jeff, Perry, James, Salimi, Shabnam, Streeten, Elizabeth, Mitchell, Braxton D., Crandall, Carolyn, Delaney, Chris, Justice, Anne, Karasik, David, Wallace, Robert, Evans, David M., Tobias, Jonathan H., Richards, Brent, Blangero, John, Wiggins, Kerri, Jackson, Rebecca and Kiel, Douglas (2019). A large-scale deep-coverage whole genome sequencing to identify less common and rare variants associated with BMD and fractures: the NHLBI Trans-Omics for Precision Medicine (TOPMED) study. Annual Meeting of the American Society for Bone and Mineral Research, Orlando, FL, United States, 20-23 September 2019. Hoboken, NJ, United States: Wiley-Blackwell Publishing. doi: 10.1002/jbmr.3936 |
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2019 Conference Publication Identification and Validation of Targets for Osteoporosis: Evidence from Whole exome Sequencing in 42,263 individuals, CRISPR-Cas9 and murine modelsLaurent, Laetitia, Zhou, Sirui, Forgetta, Vincenzo, Richards, J. Brent, Kemp, John P., Evans, David M., Pramatarova, Albena, Croucher, Peter I., Williams, Graham R., Bassett, J. H. Duncan and Goltzman, David (2019). Identification and Validation of Targets for Osteoporosis: Evidence from Whole exome Sequencing in 42,263 individuals, CRISPR-Cas9 and murine models. Annual Meeting of the American Society for Bone and Mineral Research, Orlando, FL, United States, 20-23 September, 2019. Hoboken, NJ United States: Wiley-Blackwell Publishing. doi: 10.1002/jbmr.3936 |
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2019 Conference Publication Using Mendelian randomization to estimate the causal effect of maternal (intrauterine) exposures on late onset offspring outcomesEvans, David, Warrington, Nicole, Partida, Gabriel Cuellar and Hwang, Daniel (2019). Using Mendelian randomization to estimate the causal effect of maternal (intrauterine) exposures on late onset offspring outcomes. 49th Annual Meeting of the Behavior Genetics Association (BGA), Stockholm, Sweden, 26-29 June, 2019. New York, NY, United States: Springer New York LLC. doi: 10.1007/s10519-019-09973-8 |
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2018 Journal Article Antibody response to common human viruses is shaped by genetic factorsHayward, Tanisha A., Zhu, Gu, Warrington, Nicole M., Wong, Yide, Ryan, Rachael Y.M., Murray, Abella M., Haigh, Oscar, Martin, Nicholas G., Miles, John J. and Evans, David M. (2018). Antibody response to common human viruses is shaped by genetic factors. Journal of Allergy and Clinical Immunology, 143 (4), 1640-1643. doi: 10.1016/j.jaci.2018.11.039 |
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2018 Journal Article Genetic determinants of glucose levels in pregnancy: genetic risk scores analysis and GWAS in the Norwegian STORK cohortMoen, Gunn-Helen, LeBlanc, Marissa, Sommer, Christine, Prasad, Rashmi B., Lekva, Tove, Normann, Kjersti R., Qvigstad, Elisabeth, Groop, Leif, Birkeland, Kåre I., Evans, David M. and Frøslie, Kathrine F. (2018). Genetic determinants of glucose levels in pregnancy: genetic risk scores analysis and GWAS in the Norwegian STORK cohort. European Journal of Endocrinology, 179 (6), 363-372. doi: 10.1530/EJE-18-0478 |
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2018 Journal Article Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathwaysDuffy, David L., Zhu, Gu, Li, Xin, Sanna, Marianna, Iles, Mark M., Jacobs, Leonie C., Evans, David M., Yazar, Seyhan, Beesley, Jonathan, Law, Matthew H., Kraft, Peter, Visconti, Alessia, Taylor, John C., Lui, Fan, Wright, Margaret J., Henders, Anjali K., Bowdler, Lisa, Glass, Dan, Ikram, Arfan M., Uitterlinden, André G., Madden, Pamela A., Heath, Andrew C., Nelson, Elliot C., Green, Adele C., Chanock, Stephen, Barrett, Jennifer H., Brown, Matthew A., Hayward, Nicholas K., MacGregor, Stuart ... Martin, Nicholas G. (2018). Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways. Nature Communications, 9 (1) 4774, 4774. doi: 10.1038/s41467-018-06649-5 |
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2018 Journal Article Imputation-based analysis of MICA alleles in the susceptibility to ankylosing spondylitisCortes, Adrian, Gladman, Dafna, Raychaudhuri, Soumya, Cui, Jing, Wheeler, Lawrie, Brown, Matthew A., International Genetics of Ankylosing Spondylitis Consortium (IGAS) and Evans, David (2018). Imputation-based analysis of MICA alleles in the susceptibility to ankylosing spondylitis. Annals of the Rheumatic Diseases, 77 (11), 1691-1692. doi: 10.1136/annrheumdis-2018-213413 |
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2018 Journal Article Genome analyses of >200,000 individuals identify 58 loci for chronic inflammation and highlight pathways that link inflammation and complex disordersLigthart, Symen, Vaez, Ahmad, Võsa, Urmo, Stathopoulou, Maria G., de Vries, Paul S., Prins, Bram P., Van der Most, Peter J., Tanaka, Toshiko, Naderi, Elnaz, Rose, Lynda M., Wu, Ying, Karlsson, Robert, Barbalic, Maja, Lin, Honghuang, Pool, René, Zhu, Gu, Macé, Aurélien, Sidore, Carlo, Trompet, Stella, Mangino, Massimo, Sabater-Lleal, Maria, Kemp, John P., Abbasi, Ali, Kacprowski, Tim, Verweij, Niek, Smith, Albert V., Huang, Tao, Marzi, Carola, Feitosa, Mary F. ... Alizadeh, Behrooz Z. (2018). Genome analyses of >200,000 individuals identify 58 loci for chronic inflammation and highlight pathways that link inflammation and complex disorders. American Journal of Human Genetics, 103 (5), 691-706. doi: 10.1016/j.ajhg.2018.09.009 |
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2018 Journal Article Identification of novel loci associated with hip shape: a meta-analysis of genomewide association studiesBaird, Denis A., Evans, Daniel S., Kamanu, Frederick K., Gregory, Jennifer S., Saunders, Fiona R., Giuraniuc, Claudiu V., Barr, Rebecca J., Aspden, Richard M., Jenkins, Deborah, Kiel, Douglas P., Orwoll, Eric S., Cummings, Steven R., Lane, Nancy E., Mullin, Benjamin H., Williams, Frances M. K., Richards, J Brent, Wilson, Scott G., Spector, Tim D., Faber, Benjamin G., Lawlor, Deborah A., Grundberg, Elin, Ohlsson, Claes, Pettersson-Kymmer, Ulrika, Capellini, Terence D., Richard, Daniel, Beck, Thomas J., Evans, David M., Paternoster, Lavinia, Karasik, David and Tobias, Jonathan H. (2018). Identification of novel loci associated with hip shape: a meta-analysis of genomewide association studies. Journal of Bone and Mineral Research, 34 (2), 241-251. doi: 10.1002/jbmr.3605 |
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2018 Journal Article Genome-wide association study of extreme high bone mass: contribution of common genetic variation to extreme BMD phenotypes and potential novel BMD-associated genesGregson, Celia L., Newell, Felicity, Leo, Paul J., Clark, Graeme R., Paternoster, Lavinia, Marshall, Mhairi, Forgetta, Vincenzo, Morris, John A., Ge, Bing, Bao, Xiao, Duncan Bassett, J. H., Williams, Graham R., Youlten, Scott E., Croucher, Peter I., Davey Smith, George, Evans, David M., Kemp, John P., Brown, Matthew A., Tobias, Jon H. and Duncan, Emma L. (2018). Genome-wide association study of extreme high bone mass: contribution of common genetic variation to extreme BMD phenotypes and potential novel BMD-associated genes. Bone, 114, 62-71. doi: 10.1016/j.bone.2018.06.001 |
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2018 Journal Article Assessing the role of DNA methylation-derived neutrophil-to-lymphocyte ratio in rheumatoid arthritisAmbatipudi, Srikant, Sharp, Gemma C., Clarke, Sarah L. N., Plant, Darren, Tobias, Jonathan H., Evans, David M., Barton, Anne and Belton, Caroline L. (2018). Assessing the role of DNA methylation-derived neutrophil-to-lymphocyte ratio in rheumatoid arthritis. Journal of Immunology Research, 2018 2624981, 1-10. doi: 10.1155/2018/2624981 |
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2018 Journal Article Are serum concentrations of vitamin B-12 causally related to cardiometabolic risk factors and disease? A Mendelian randomization studyMoen, Gunn-Helen, Qvigstad, Elisabeth, Birkeland, Kåre I., Evans, David M. and Sommer, Christine (2018). Are serum concentrations of vitamin B-12 causally related to cardiometabolic risk factors and disease? A Mendelian randomization study. The American Journal of Clinical Nutrition, 108 (2), 398-404. doi: 10.1093/ajcn/nqy101 |
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2018 Conference Publication Fluocinolone acetonide ( FAc) 0.2 mg intravitreal implant in the treatment of diabetic macular edema (DME)Liu, John, Coney, Joseph, Schartman, Jerome, Miller, David G., Zegarra, Hernando and Rao, Llewelyn (2018). Fluocinolone acetonide ( FAc) 0.2 mg intravitreal implant in the treatment of diabetic macular edema (DME). Annual Meeting of the Association-for-Research-in-Vision-and-Ophthalmology (ARVO), Honolulu Hi, Apr 21-May 03, 2018. ROCKVILLE: ASSOC RESEARCH VISION OPHTHALMOLOGY INC. |
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2018 Conference Publication Intravitreal Aflibercept Injection (IAI) for Moderately Severe to Severe Nonproliferative Diabetic Retinopathy (NPDR): The Phase 3 PANORAMA StudyBrown, David M. (2018). Intravitreal Aflibercept Injection (IAI) for Moderately Severe to Severe Nonproliferative Diabetic Retinopathy (NPDR): The Phase 3 PANORAMA Study. Annual Meeting of the Association-for-Research-in-Vision-and-Ophthalmology (ARVO), Honolulu Hi, Apr 21-May 03, 2018. ROCKVILLE: ASSOC RESEARCH VISION OPHTHALMOLOGY INC. |
