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2017

Conference Publication

Performing Mendelian randomization using structural equation models

Evans, 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.

Performing Mendelian randomization using structural equation models

2017

Conference Publication

Trait-specific patterns of common genetic factors influence social-communication difficulties and ADHD symptoms during child and adolescent development

St 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

Trait-specific patterns of common genetic factors influence social-communication difficulties and ADHD symptoms during child and adolescent development

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 phenotypes

Gregson, 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.

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

2017

Conference Publication

Genetic links between social-communication traits, ADHD traits and clinical ADHD during development

St 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.

Genetic links between social-communication traits, ADHD traits and clinical ADHD during development

2017

Conference Publication

Common polygenic risk for ASD and ADHD is associated with childhood linguistic traits within the general population, but with opposite effects

St 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

Common polygenic risk for ASD and ADHD is associated with childhood linguistic traits within the general population, but with opposite effects

2017

Conference Publication

Cathepsins B and S Are Novel Biomarkers for Bone Mineral Density: A Mendelian Randomization Study

Morris, 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.

Cathepsins B and S Are Novel Biomarkers for Bone Mineral Density: A Mendelian Randomization Study

2017

Conference Publication

Developmental changes in genetic relationships between traits and disease: Analyses of genetic overlaps between social-communication difficulties, autism spectrum disorders and schizophrenia

St 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.

Developmental changes in genetic relationships between traits and disease: Analyses of genetic overlaps between social-communication difficulties, autism spectrum disorders and schizophrenia

2017

Conference Publication

Genome-wide association study identifies three novel genetic determinants of dental maturation

Grgic, 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.

Genome-wide association study identifies three novel genetic determinants of dental maturation

2017

Conference Publication

Estimating developmental changes within the genetic architecture of social communication traits: a multivariate study of genetic variance in unrelated individuals

St 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.

Estimating developmental changes within the genetic architecture of social communication traits: a multivariate study of genetic variance in unrelated individuals

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 ratio

Warrington, 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.

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

2016

Conference Publication

Trait-specific patterns of common genetic factors influence social communication difficulties and ADHD symptoms during development

St Pourcain, Beate, Eaves, Lindon, Evans, David, Fisher, Simon, Carey, Greg and Smith, George Davey (2016). Trait-specific patterns of common genetic factors influence social communication difficulties and ADHD symptoms during development. 46th Annual Meeting of the Behavior-Genetics-Association, Brisbane Australia, Jun 20-23, 2016. NEW YORK: SPRINGER.

Trait-specific patterns of common genetic factors influence social communication difficulties and ADHD symptoms during development

2016

Conference Publication

LD hub and MR-base: online platforms for preforming LD score regression and Mendelian randomization analysis using GWAS summary data

Zheng, Jie, Haycock, Philip, Hemani, Gibran, Elsworth, Benjamin, Shihab, Hashem, Laurin, Charles, Erzurumluoglu, Mesut, Howe, Laurence, Wade, Kaitlin, Warrington, Nicole, Finucane, Hilary, Price, Alkes, Anttila, Verneri, Paternoster, Lavinia, Martin, Richard, Relton, Caroline, Gaunt, Tom, Smith, George Davey, Neale, Benjamin and Evans, David (2016). LD hub and MR-base: online platforms for preforming LD score regression and Mendelian randomization analysis using GWAS summary data. 46th Annual Meeting of the Behavior-Genetics-Association, Brisbane Australia, Jun 20-23, 2016. NEW YORK: SPRINGER.

LD hub and MR-base: online platforms for preforming LD score regression and Mendelian randomization analysis using GWAS summary data

2016

Conference Publication

New opportunities for structural equation modelling in the post GWAS era

Evans, David (2016). New opportunities for structural equation modelling in the post GWAS era. 46th Annual Meeting of the Behavior-Genetics-Association, Brisbane Australia, Jun 20-23, 2016. NEW YORK: SPRINGER.

New opportunities for structural equation modelling in the post GWAS era

2016

Conference Publication

Locus Discovery in Genome-wide Association Studies using Bivariate Analysis

Warrington, Nicole M. and Evans, David M. (2016). Locus Discovery in Genome-wide Association Studies using Bivariate Analysis. Annual Meeting of the International-Genetic-Epidemiology-Society, Toronto Canada, Oct 24-26, 2016. HOBOKEN: WILEY-BLACKWELL.

Locus Discovery in Genome-wide Association Studies using Bivariate Analysis

2016

Conference Publication

Detecting parent of origin effects using GREML of transmitted genotypes

Laurin, Charles, Hemani, Gibran and Evans, David (2016). Detecting parent of origin effects using GREML of transmitted genotypes. 46th Annual Meeting of the Behavior-Genetics-Association, Brisbane Australia, Jun 20-23, 2016. NEW YORK: SPRINGER.

Detecting parent of origin effects using GREML of transmitted genotypes

2016

Conference Publication

Can Mendelian randomization inform drug development research for neurobehavioural conditions? A study of Alzheimer's disease

Brion, Marie-Jo, Benyamin, Beben, Smith, George Davey, McGrath, John and Evans, David (2016). Can Mendelian randomization inform drug development research for neurobehavioural conditions? A study of Alzheimer's disease. 46th Annual Meeting of the Behavior-Genetics-Association, Brisbane Australia, Jun 20-23, 2016. NEW YORK: SPRINGER.

Can Mendelian randomization inform drug development research for neurobehavioural conditions? A study of Alzheimer's disease

2016

Conference Publication

Investigation into the genetic architecture of Giant Cell Arteritis through a genome-wide association study

De 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.

Investigation into the genetic architecture of Giant Cell Arteritis through a genome-wide association study

2016

Conference Publication

Longitudinal Expression Profiling of T Lymphocytes in Patients with Active to Quiescent Giant Cell Arteritis

De 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.

Longitudinal Expression Profiling of T Lymphocytes in Patients with Active to Quiescent Giant Cell Arteritis

2016

Conference Publication

Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population

Robinson, Elise B., St Pourcain, Beate, Anttilal, Verneri, Kosmicki, Jack, Bulik-Sullivan, Brendan, Grove, Jakob, Maller, Julian, Samocha, Kaitlin E., Sanders, Stephan, Ripke, Stephan, Martin, Joanna, Hollegaard, Mads V., Werge, Thomas, Hougaard, David M., Neale, Benjamin M., Evans, David M., Skuse, David, Mortensen, Preben Bo, Borglum, 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. 71st Annual Scientific Convention and Meeting, Unknown, Unknown. Philadelphia, PA United States: Elsevier.

Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population

2016

Conference Publication

Using Mendelian randomization to investigate a possible causal relationship between adiposity and increased bone mineral density at different skeletal sites in children

Kemp, 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.

Using Mendelian randomization to investigate a possible causal relationship between adiposity and increased bone mineral density at different skeletal sites in children