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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 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 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 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 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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2018 Conference Publication Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic diseaseBeaumont, Robin N., Warrington, Nicole M., Horikoshi, Momoko, Day, Felix R., Ong, Ken K., McCarthy, Mark I., Perry, John R. B., Freathy, Rachel M. and Evans, David M. (2018). Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic disease. 27th Annual Meeting of the International-Genetic-Epidemiology-Society (IGES), San Diego, Ca, United States, 14-16 October 2018. Hoboken, NJ, United States: John Wiley & Sons. |
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2018 Conference Publication The genetic architecture of hip statistical shape models suggests that endochondral bone formation makes an important contribution to hip shapeBaird, D., Evans, D. S., Gregory, J. S., Saunders, F. R., Giuraniuc, C. V., Barr, R. J., Aspden, R. M., Kamanu, F. K., Kiel, D. P., Orwoll, E. S., Cummings, S. R., Lane, N. E., Mullins, B. H., Williams, F. M., Richards, B., Wilson, S. G., Spector, T. D., Faber, B. G., Lawlor, D. A., Beck, T. J., Evans, D. M., Paternoster, L., Karasikl, D. and Tobias, J. H. (2018). The genetic architecture of hip statistical shape models suggests that endochondral bone formation makes an important contribution to hip shape. OARSI World Congress on Osteoarthritis - Promoting Clinical and Basic Research in Osteoarthritis, Liverpool, England, 26-29 April 2018. London, United Kingdom: Elsevier. |
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2017 Conference Publication Comparison of the response of the NCI60 NSCLC panel with the response of patient-derived NSCLC lines to approved and investigational agentsTeicher, Beverly A., Evans, David, Silvers, Thomas, Selby, Michael, Delosh, Rene, Laudeman, Julie, Ogle, Chad, Reinhart, Russell, Morris, Joel, Kaur, Gurmeet and Doroshow, James (2017). Comparison of the response of the NCI60 NSCLC panel with the response of patient-derived NSCLC lines to approved and investigational agents. Annual Meeting of the American-Association-for-Cancer-Research (AACR), Washington Dc, Apr 01-05, 2017. PHILADELPHIA: AMER ASSOC CANCER RESEARCH. doi: 10.1158/1538-7445.AM2017-348 |
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2017 Conference Publication Small cell lung carcinoma (SCLC) cell line screen of standard of care (etoposide/carboplatin) plus a third agentTeicher, Beverly A., Selby, Michael, Silvers, Thomas, Laudeman, Julie, Reinhart, Russell, Delosh, Rene, Ogle, Chad, Parchment, Ralph, Krushkal, Julia, Sonkin, Dmitriy, Morris, Joel, Kunkel, Mark and Evans, David (2017). Small cell lung carcinoma (SCLC) cell line screen of standard of care (etoposide/carboplatin) plus a third agent. Annual Meeting of the American-Association-for-Cancer-Research (AACR), Washington Dc, Apr 01-05, 2017. PHILADELPHIA: AMER ASSOC CANCER RESEARCH. doi: 10.1158/1538-7445.AM2017-4831 |
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2017 Conference Publication A clinical pharmacodynamic biomarker assay that distinguishes potentially repairable, cytotoxic drug-induced DNA double strand breaks (DSBs) from DSBs associated with apoptotic cell deathDull, Angie B., Wilsker, Deborah, Kinders, Robert J., Parchment, Ralph E., Evans, David, Teicher, Beverly A. and Doroshow, James H. (2017). A clinical pharmacodynamic biomarker assay that distinguishes potentially repairable, cytotoxic drug-induced DNA double strand breaks (DSBs) from DSBs associated with apoptotic cell death. Annual Meeting of the American-Association-for-Cancer-Research (AACR), Washington Dc, Apr 01-05, 2017. PHILADELPHIA: AMER ASSOC CANCER RESEARCH. doi: 10.1158/1538-7445.AM2017-3072 |
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2017 Conference Publication Performing Mendelian randomization using structural equation modelsEvans, David and Warrington, Nicole (2017). Performing Mendelian randomization using structural equation models. 47th Annual Meeting of the Behavior-Genetics-Association (BGA), Oslo Norway, 28 June - 1 July 2017. New York NY United States: Springer. |
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2017 Conference Publication Trait-specific patterns of common genetic factors influence social-communication difficulties and ADHD symptoms during child and adolescent developmentSt Pourcain, Beate, Eaves, Lindon, Evans, David M., Stergiakouli, Evie, Fisher, Simon E., Ring, Susan M., Carey, Gregory and George, Davey Smith (2017). Trait-specific patterns of common genetic factors influence social-communication difficulties and ADHD symptoms during child and adolescent development. 24th World Congress of Psychiatric Genetics (WCPG), Jerusalem Israel, October 30 - November 4 2016. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2016.09.411 |
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2017 Conference Publication Genome-wide association study of extreme high bone mass identifies NPR3 as a novel BMD-associated gene and highlights the contribution of common genetic variation to extreme BMD phenotypesGregson, Celia, Newell, Felicity, Leo, Paul, Paternoster, Lavinia, Marshall, Mhairi, Clark, Graeme, Morris, John, Ge, Bing, Bao, Xiao, Bassett, Duncan, Williams, Graham, Youlten, Scott, Croucher, Peter, Smith, George Davey, Evans, David, Kemp, John, Brown, Matthew, Tobias, Jon and Duncan, Emma (2017). Genome-wide association study of extreme high bone mass identifies NPR3 as a novel BMD-associated gene and highlights the contribution of common genetic variation to extreme BMD phenotypes. Annual Meeting of the American-Society-for-Bone-and-Mineral-Research (ASBMR), Denver CO, United States, 8-11 September 2017. Hoboken, NJ United States: Wiley. |
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2017 Conference Publication Genetic links between social-communication traits, ADHD traits and clinical ADHD during developmentSt Pourcain, Beate, Martin, Joanna, Stergiakouli, Evie, Robinson, Elise, Skuse, David, Susan, Ring, Ronald, Angelica, Evans, David, Timpson, Nicholas, Thapar, Anita and Smith, George Davey (2017). Genetic links between social-communication traits, ADHD traits and clinical ADHD during development. 23rd Annual World Congress of Psychiatric Genetics (WCPG), Toronto Canada, Oct 16-20 2015. Amsterdam, Netherlands: Elsevier. |
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2017 Conference Publication Common polygenic risk for ASD and ADHD is associated with childhood linguistic traits within the general population, but with opposite effectsSt Pourcain, Beate, Verhoef, Ellen, Fisher, Simon E., Stergiakouli, Evie, Evans, David E., Ring, Susan M. and Smith, George Davey (2017). Common polygenic risk for ASD and ADHD is associated with childhood linguistic traits within the general population, but with opposite effects. 24th World Congress of Psychiatric Genetics (WCPG), Jerusalem Israel, October 30-November 4 2016. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2016.09.470 |
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2017 Conference Publication Cathepsins B and S Are Novel Biomarkers for Bone Mineral Density: A Mendelian Randomization StudyMorris, John, Kemp, John, Evans, David and Richards, Brent (2017). Cathepsins B and S Are Novel Biomarkers for Bone Mineral Density: A Mendelian Randomization Study. Annual Meeting of the American-Society-for-Bone-and-Mineral-Research (ASBMR), Denver CO, United States, 8-11 September 2017. Hoboken, NJ United States: Wiley. |
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2017 Conference Publication Developmental changes in genetic relationships between traits and disease: Analyses of genetic overlaps between social-communication difficulties, autism spectrum disorders and schizophreniaSt Pourcain, Beate, Robinson, Elise, Bulik-Sullivan, Brendan, Anttila, Verneri, Maller, Julian, Skuse, David, Rings, Susan, Evans, David, Timpson, Nicholas, Ronald, Angelica, Grove, Jakob, Borglum, Anders, Mortensen, Preben Bo, Daly, Mark and Smiths, George Davey (2017). Developmental changes in genetic relationships between traits and disease: Analyses of genetic overlaps between social-communication difficulties, autism spectrum disorders and schizophrenia. 23rd Annual World Congress of Psychiatric Genetics (WCPG), Toronto Canada, Oct 16-20 2015. Amsterdam, Netherlands: Elsevier. |
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2017 Conference Publication Genome-wide association study identifies three novel genetic determinants of dental maturationGrgic, Olja, Medina-Gomez, Carolina, Dhamo, Brunilda, Trajanoska, Katerina, Vucic, Strahinja, Ongkosuwito, Edwin M., Jaddoe, Vincent W. V., Uitterlinden, Andre G., Jarvelin, Marjo-Riitta, Timpson, Nicholas, Evans, David M., Wolvius, Eppo B. and Rivadeneira, Fernando (2017). Genome-wide association study identifies three novel genetic determinants of dental maturation. Annual Meeting of the American-Society-for-Bone-and-Mineral-Research (ASBMR), Denver, CO USA, 8-11 September 2017. Hoboken, NJ United States: Wiley-Blackwell Publishing. |
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2017 Conference Publication Estimating developmental changes within the genetic architecture of social communication traits: a multivariate study of genetic variance in unrelated individualsSt Pourcain, Beate, Eaves, Lindon, Verhoef, Ellen, Shapland, Chin Yang, Ring, Susan M., Fisher, Simon E., Medland, Sarah, Evans, David and Smith, George Davey (2017). Estimating developmental changes within the genetic architecture of social communication traits: a multivariate study of genetic variance in unrelated individuals. 47th Annual Meeting of the Behavior-Genetics-Association (BGA), Oslo Norway, Jun 28-Jul 01, 2017. New York, NY, United States: Springer. |
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2016 Conference Publication Genome-wide association study of 6,939 individuals identifies five novel loci and suggests that prenatal exposure to testosterone is not a major determinant of individual differences in 2D:4D finger ratioWarrington, Nicole, Hemani, Gibran, Hysi, Pirro, Mangino, Massimo, McMahon, George, Hickey, Martha, Wolke, Dieter, Montgomery, Grant, Pennell, Craig, Spector, Tim, Martin, Nicholas, Medland, Sarah and Evans, David (2016). Genome-wide association study of 6,939 individuals identifies five novel loci and suggests that prenatal exposure to testosterone is not a major determinant of individual differences in 2D:4D finger ratio. 46th Annual Meeting of the Behavior-Genetics-Association, Brisbane Australia, Jun 20-23, 2016. NEW YORK: SPRINGER. |
