Displaying 1 - 77 of 77
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Gasparini, L., Shepherd, D., Lange, K., Wang, J., Verhoef, E., Bavin, E., Reilly, S., St Pourcain, B., Wake, M., & Morgan, A. (2024). Combining genetic and early life parent-reported predictors of 11-year language: A two-cohort study. Poster presented at the 16th International Congress for the Study of Child Language (IASCL 2024), Prague, Czech Republic.
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Hollowell, A. C., Gui, A., Hannigan, L., Corfield, E. C., Morgan, M. J., Middeldorp, C., St Pourcain, B., Arichi, T., Dudbrige, F., Johnson, M. H., Havdahl, A. K. S., & Ronald, A. (2024). Genome-wide association meta-analysis of infant fussiness in the first year. Poster presented at the 54th Annual Meeting of the Behavior Genetics Association, London.
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Schlag, F., De Hoyos, L., Verhoef, E., Van den Bedem, S., Verhulst, B., Fisher, S. E., & St Pourcain, B. (2024). Genomic and non-genomic contributions to children’s cognition, language, and social skills: Evidence for independent phenotypic domains with strong gene-environment correlations. Talk presented at the third conference of the European Social Science Genetics Network (ESSGN III). Rotterdam, The Netherlands. 2024-05-29 - 2024-05-30.
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Hollowell, A., Gui, A., Hannigan, L., Corfield, E., Morgan, M. J., Middeldorp, C., St Pourcain, B., Arichi, T., Dudbridge, F., Johnson, M., Havdahl, A., & Ronald, A. (2023). First look results from a genome wide association study of activity levels in infancy. Poster presented at the 53rd Annual Meeting of the Behavior Genetics Association, Murcia, Spain.
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De Hoyos, L., Verhoef, E., Fisher, S. E., Okbay, A., Gordon, R. L., & St Pourcain, B. (2023). Preschool musicality is associated with school-age communication abilities through genes related to rhythmicity. Talk presented at the 53rd Annual Meeting of the Behavior Genetics Association. Murcia, Spain. 2023-06-21 - 2023-06-24.
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St Pourcain, B. (2023). Language and social behaviour are genetically encoded dimensions of mental health. Talk presented at the Center of Neurodevelopmental Disorders at Karolinska Institutet (KIND). Stockholm, Sweden. 2023.
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St Pourcain, B. (2023). Social behaviour as a dimension of neurodevelopmental condition. Talk presented at the research network seminar on “The future of the Autism Birth Cohort Study (ABC Study)” and the NIPH Centre for Genetic Epidemiology and Mental Health Kick-Off Meeting. Oslo, Norway. 2023-10-25.
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Ronald, A., Gui, A., Hollowell, A., Morgan, M., Hannigan, L., Corfield, E., Eilertsen, E., Ystrøm, E., Odintsova, V. V., Hottenga, J.-J., Bartels, M., Boomsma, D. I., Wong, A., Hartman, C. A., Robinson, E. B., Middeldorp, C., St Pourcain, B., Arichi, T., Dudbridge, F., Johnson, M. H. and 1 moreRonald, A., Gui, A., Hollowell, A., Morgan, M., Hannigan, L., Corfield, E., Eilertsen, E., Ystrøm, E., Odintsova, V. V., Hottenga, J.-J., Bartels, M., Boomsma, D. I., Wong, A., Hartman, C. A., Robinson, E. B., Middeldorp, C., St Pourcain, B., Arichi, T., Dudbridge, F., Johnson, M. H., & Havdahl, A. (2023). Heritability of infant fine and gross motor skills. Poster presented at the 53rd Annual Meeting of the Behavior Genetics Association, Murcia, Spain.
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Schlag, F., De Hoyos, L., Admiraal, D., St Pourcain, B., & on behalf of the cognitive working group of the social behaviour project (2023). Genome-wide association meta-analysis of social behaviour during childhood and adolescence. Talk presented at the World Congress of Psychiatric Genetics (WCPG 2023). Montreal, Canada. 2023-10-10 - 2023-10-14.
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Schlag, F., De Hoyos, L., Verhoef, E., Van Bedem, S., Verhulst, B., Fisher, S. E., & St Pourcain, B. (2023). Disentangling the multivariate genomic and residual structure between cognition, language, communication and social traits. Talk presented at the 53rd Annual Meeting of the Behavior Genetics Association. Murcia, Spain. 2023-06-21 - 2023-06-24.
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Verhoef, E., De Hoyos, L., Schlag, F., Dale, P. S., Kidd, E., Fisher, S. E., & St Pourcain, B. (2023). Developing language in a developing body: A genetic perspective. Talk presented at Many Paths to Language (MPaL 2023). Nijmegen, The Netherlands. 2023-10-25 - 2023-10-27.
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Verhoef, E., De Hoyos González, L., Schlag, F., Dale, P. S., Fisher, S. E., & St Pourcain, B. (2023). Developing language in a developing body: A genetic perspective. Talk presented at the 53rd Annual Meeting of the Behavior Genetics Association. Murcia, Spain. 2023-06-21 - 2023-06-24.
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Bignardi, G., Schaare, H. L., Verhulst, B., St Pourcain, B., Fisher, S. E., Eickhoff, S. B., & Valk, S. L. (2022). A functional gradient association study of aesthetic sensitivity. Poster presented at the workshop Gradients of Brain Organization, Cambridge, UK.
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Bignardi, G., Schaare, H. L., Verhulst, B., St Pourcain, B., Fisher, S. E., Eickhoff, S. B., & Valk, S. L. (2022). A functional gradient association study of aesthetic sensitivity. Poster presented at the 28th Annual Meeting of the Organization for Human Brain Mapping (OHBM 2022), Glasgow, Scotland.
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Bignardi, G., Schaare, H. L., Verhulst, B., St Pourcain, B., Fisher, S. E., Eickhoff, S. B., & Valk, S. L. (2022). Brain-wide alterations of the principal gradient of human brain functional connectivity relate to aesthetic sensitivity. Poster presented at the 2022 Biennial Congress of the International Association of Empirical Aesthetics (IAEA 2022), Philadelphia, PA, USA.
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Bignardi, G., Schaare, H. L., Verhulst, B., St Pourcain, B., Fisher, S. E., Eickhoff, S. B., & Valk, S. L. (2022). Brain-wide functional alterations of the principal gradients of human brain connectivity relate to aesthetic sensitivity. Talk presented at the Visual Science of Art Conference (VSAC 2022). Amsterdam, The Netherlands. 2022-08-24 - 2022-08-27.
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De Hoyos, L., Barendse, M. T., Schlag, F., Van Donkelaar, M. M. J., Verhoef, E., Shapland, C. Y., Buitelaar, J., Verhulst, B., Fisher, S. E., Rai, D., & St Pourcain, B. (2022). Structural models of genome-wide covariance identify multiple genetic influences across ASD symptoms. Talk presented at the 52nd Annual Meeting of the Behavior Genetics Association. Los Angeles, CA, USA. 2022-06-22 - 2022-06-25.
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De Hoyos, L., Barendse, M. T., Schlag, F., Van Donkelaar, M. M. J., Verhoef, E., Shapland, C. Y., Buitelaar, J., Verhulst, B., Fisher, S. E., Rai, D., & St Pourcain, B. (2022). Structural models of genome-wide covariance identify multiple genetic influences across ASD symptoms. Poster presented at the World Congress of Psychiatric Genetics (WCPG 2022), Florence, Italy.
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De Hoyos, L., Barendse, M. T., Schlag, F., Van Donkelaar, M. M. J., Verhoef, E., Shapland, C. Y., Buitelaar, J., Verhulst, B., Fisher, S. E., Rai, D., & St Pourcain, B. (2022). Structural models of genome-wide covariance identify multiple genetic influences across ASD symptoms. Poster presented at the IMPRS Conference 2022, Nijmegen, the Netherlands.
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St Pourcain, B., Verhoef, E., Grove, J., Shapland, C. Y., Demontis, D., Burgess, S., Rai, D., & Børglum, A. D. (2022). Polygenic pleiotropy within ASD and ADHD genetic architectures: shared risk alleles with discordant polygenic effects. Talk presented at the SFARI Spring 2022 Investigator Meeting. New York, NY, USA. 2022-04-09.
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St Pourcain, B., & the EAGLE Consortium (2022). Structural models of genomic covariance: The developmental genetic architecture of language acquisition [invited talk]. Talk presented at the Department of Biological Psychology, Vrije Universiteit Amsterdam. online. 2022-01-20.
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St Pourcain, B. (2022). Studying genetic overlap between ASD risk and related traits: From disorder-specific profiles to polygenic pleiotropy [invited talk]. Talk presented at the Seaver Autism Center Seminar Series. online. 2022-06-15.
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Verhoef, E., Allegrini, A. G., Jansen, P. R., Lange, K., Wang, C. A., Morgan, A. T., Ahluwalia, T. S., Christos, S., EAGLE working group, Fisher, S. E., & St Pourcain, B. (2022). Genome-wide analyses of infant and toddler vocabulary size: links with ADHD and cognitive traits. Talk presented at the World Congress of Psychiatric Genetics (WCPG 2022). Florence, Italy. 2022-09-13 - 2022-09-17.
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Verhoef, E., Ahluwalia, T. S., Jansen, P., Lange, K., Allegrini, A., Wang, C., Symeonides, C., Morgan, A., EAGLE working group, Fisher, S. E., & St Pourcain, B. (2022). Genome-wide association meta-analysis of expressive and receptive vocabulary from infancy to early childhood. Poster presented at TOK day - Taalontwikkeling Kinderen (in Nederland en Vlaanderen), Nijmegen, the Netherlands.
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Barendse, M. T., Klassmann, A., De Hoyos, L., Rai, D., Fisher, S. E., & St Pourcain, B. (2021). Structural equation modelling in the genomics era: State-of-the-art and future developments. Talk presented at the World Congress of Psychiatric Genetics (WCPG 2021). online. 2021-10-11 - 2021-10-15.
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De Hoyos, L., Barendse, M. T., Van Donkelaar, M. M. J., Verhoef, E., Fisher, S. E., Rai, D., & St Pourcain, B. (2021). Structural models of genome-wide covariance explain variation in autism spectrum disorder symptoms. Poster presented at the World Congress of Psychiatric Genetics (WCPG 2021), online.
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De Hoyos, L., Barendse, M. T., Van Donkelaar, M. M. J., Verhoef, E., Fisher, S. E., Rai, D., & St Pourcain, B. (2021). Genetic clustering of co-occurring symptoms in people with autism: A multivariate genetic variance analysis of genetic relationship matrices in the SPARK sample. Poster presented at the International Society for Autism Research (INSAR) 2021 Annual Meeting, online.
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De Hoyos, L., Barendse, M. T., Van Donkelaar, M. M. J., Verhoef, E., Fisher, S. E., Rai, D., & St Pourcain, B. (2021). Genetic clustering of co-occurring symptoms in people with autism: A multivariate genetic variance analysis of genetic relationship matrices in the SPARK sample. Talk presented at the European Human Genetics Conference (ESHG 2021). online. 2021-08-28 - 2021-08-31.
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St Pourcain, B., & the EAGLE Consortium (2021). Structural models of multivariate genetic architectures in the genomics era: Insights into the developmental origins of reading and verbal intelligence [invited talk]. Talk presented at the Multifactorial meeting at the Department of Human Genetics, Radboud University Medical Center. online. 2021-05-18.
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Schlag, F., Allegrini, A. G., Buitelaar, J., Verhoef, E., Van Donkelaar, M. M. J., Plomin, R., Rimfeld, K., Fisher, S. E., & St Pourcain, B. (2021). Polygenic risk for psychiatric disorder reveals distinct association profiles across social behaviour in the general population. Poster presented at the World Congress of Psychiatric Genetics (WCPG 2021), online.
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Verhoef, E., Ahluwalia, T., Jansen, P., Lange, K., Allegrini, A., Wang, C., Symeonides, C., Morgan, A., EAGLE working group, Fisher, S. E., & St Pourcain, B. (2021). Genome-wide association meta-analysis of expressive and receptive vocabulary from infancy to early childhood. Poster presented at the World Congress of Psychiatric Genetics (WCPG 2021), online.
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Verhoef, E., Grove, J., Shapland, C. Y., Demontis, D., Burgess, S., Rai, D., Børglum, A. D., & St Pourcain, B. (2021). Polygenic pleiotropy within ASD and ADHD genetic architectures: shared risk alleles with discordant polygenic effects. Talk presented at the Cognomics workshop. Nijmegen, The Netherlands. 2021-06-28 - 2021-06-29.
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Verhoef, E., Grove, J., Shapland, C. Y., Demontis, D., Burgess, S., Rai, D., Børglum, A. D., & St Pourcain, B. (2021). Polygenic pleiotropy within ASD and ADHD genetic architectures: shared risk alleles with discordant polygenic effects. Talk presented at the World Congress of Psychiatric Genetics (WCPG 2021). online. 2021-10-12 - 2021-10-14.
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Verhoef, E., Grove, J., Shapland, C. Y., Demontis, D., Burgess, S., Rai, D., Børglum, A. D., & St Pourcain, B. (2021). Shared risk alleles with discordant polygenic effects: Disentangling the genetic overlap between ASD and ADHD. Talk presented at the European Mathematical Genetics Meeting 2021. online. 2021-04-22 - 2021-04-23.
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Eising, E., St Pourcain, B., Francks, C., Fisher, S. E., & the Quantitative Trait Working Group of the GenLang consortium (2019). A genome-wide association screen of quantitative www.genlang.org speech, language and reading traits in >18,000 people in the GenLang consortium. Poster presented at Cognomics conference, Nijmegen.
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Eising, E., St Pourcain, B., Francks, C., & Fisher, S. E. (2020). A GWAS meta-analysis of quantitative reading and language traits in >33,000 people in the GenLang consortium. Poster presented at the World Congress of Psychiatric Genetics (WCPG 2020), online.
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St Pourcain, B., Verhoef, E., Smith, G. D., Fisher, S. E., Verhulst, B., Dale, P. S., & Shapland, C. Y. (2020). The multivariate genetic architecture of language and literacy-related abilities. Poster presented at the 50th Annual Meeting of the Behavior Genetics Association, online.
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Schlag, F., Van Donkelaar, M. M. J., Buitelaar, J., Verhoef, E., Shapland, C. Y., Fisher, S. E., & St Pourcain, B. (2020). Distinct association profiles between polygenic risk for psychiatric disorder and social skill sets in the general population. Poster presented at the 50th Annual Meeting of the Behavior Genetics Association, online.
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Schlag, F., Van Donkelaar, M. M. J., Verhoef, E., Buitelaar, J., Shapland, C. Y., Fisher, S. E., & St Pourcain, B. (2020). Distinct association profiles between polygenic risk for psychiatric disorder and social skill sets in the general population. Talk presented at the World Congress of Psychiatric Genetics (WCPG 2020). online. 2020-10-16 - 2020-10-22.
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Shapland, C. Y., Verhoef, E., Smith, G. D., Fisher, S. E., Verhulst, B., Dale, P., & St Pourcain, B. (2020). The multivariate genetic architecture of language- and literacy-related abilities: Genetic evidence for different cognitive skill sets. Talk presented at Many Paths to Language (MPaL 2020). online. 2020-10-22 - 2020-10-23.
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Van der Ven, J., Verhoef, E., Olislagers, M., Vermeulen, J., Dale, P., Fisher, S. E., & St Pourcain, B. (2020). Exploring genetic relationships between early motor, personal-social and language development. Poster presented at the 50th Annual Meeting of the Behavior Genetics Association, online.
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Van Donkelaar, M. M. J., Verhoef, E., Fisher, S. E., Rai, D., & St Pourcain, B. (2020). Disentangling autism heterogeneity through multivariate genetic analyses. Poster presented at the World Congress of Psychiatric Genetics (WCPG 2020), online.
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Vermeulen, J. R., Schlag, F., Verhoef, E., Figaroa, C., Van der Ven, J., Fisher, S. E., & St Pourcain, B. (2020). Exploring genetic relationships between musicality and social behavior. Poster presented at the 50th Annual Meeting of the Behavior Genetics Association, online.
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Eising, E., Allegrini, A., Barr, C., Van Bergen, E., Boomsma, D. I., Van Donkelaar, M. M. J., Franken, M. C. J. P., Gruen, J., Jansen, P. R., De Jong, P.., Luciano, M., Newbury, D., Nöthen, M. M., Paracchini, S., Price, K., Rimfeld, K., Schulte-Körne, G., Shapland, C. Y., Simpson, N., Smith, S. and 10 moreEising, E., Allegrini, A., Barr, C., Van Bergen, E., Boomsma, D. I., Van Donkelaar, M. M. J., Franken, M. C. J. P., Gruen, J., Jansen, P. R., De Jong, P.., Luciano, M., Newbury, D., Nöthen, M. M., Paracchini, S., Price, K., Rimfeld, K., Schulte-Körne, G., Shapland, C. Y., Simpson, N., Smith, S., Timpson, N., Tomblin, J. B., Truong, D. T., Wang, C., Whitehouse, A., De Zeeuw, E. L., Zhu, G., St Pourcain, B., Francks, C., & Fisher, S. E. (2019). A genome-wide association screen of quantitative reading and language traits in >22,000 people in the GenLang consortium. Poster presented at the American Society of Human Genetics 69th Annual Meeting (ASHG 2019), Houston, TX, USA.
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Eising, E., St Pourcain, B., Francks, C., Fisher, S. E., & the Quantitative Trait Working Group of the GenLang consortium (2019). A genome-wide association screen of quantitative speech, language and reading traits in >18,000 people in the GenLang consortium. Poster presented at the Lorentz Center workshop Capturing Developmental Brain Dynamics, Leiden, The Netherlands.
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St Pourcain, B. (2019). Advantages of large international consortia on child development: The EArly Genetics and Lifecourse Epidemiology (EAGLE) Consortium. Talk presented at the 18th International Congress of the European Society for Child and Adolescent Psychiatry. Vienna, Austria. 2019-06-30 - 2019-07-02.
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St Pourcain, B. (2019). New approaches to understand genetic and residual relatedness among complex phenotypes. Talk presented at the Academy Colloquium "Deciphering the biology of human musicality through state-of-the-art genomics". Amsterdam, The Netherlands. 2019-06-20 - 2019-06-22.
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St Pourcain, B., Grove, J., Shapland, C. Y., Demontis, D., Burgess, S., Rai, D., Børglum, A. D., & Verhoef, E. (2019). Shared polygenetic variation between ASD and ADHD exerts opposite association patterns with educational attainment. Talk presented at the 49th Annual Meeting of the Behavior Genetics Association. Stockholm, Sweden. 2019-06-26 - 2019-06-29.
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Van Donkelaar, M. M. J., Figaroa, C., Verhoef, E., Fisher, S. E., Rai, D., & St Pourcain, B. (2019). Exploring the genetic architecture of co-occurring symptoms in autism. Poster presented at the 27th World Congress of Psychiatric Genetics, Los Angeles, CA, USA.
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Verhoef, E., Dale, P. S., Fisher, S. E., Shapland, C. Y., & St Pourcain, B. (2019). Modelling stability and change in the genetic architecture of language and literacy development. Talk presented at the 49th Annual Meeting of the Behavior Genetics Association. Stockholm, Sweden. 2019-06-26 - 2019-06-29.
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Eising, E., St Pourcain, B., Francks, C., Fisher, S. E., & the Quantitative Trait Working Group of the GenLang consortium (2018). A genome-wide association screen of quantitative speech, language and reading traits in >14,000 people in the GenLang consortium. Poster presented at the 26th World Congress of Psychiatric Genetics 2018, Glasgow, UK.
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Gunz, P., Tilot, A. K., Wittfeld, K., Teumer, A., Shapland, C. Y., Van Erp, T. G. M., Dannemann, M., Vernot, B., Neubauer, S., Guadalupe, T., Fernandez, G., Brunner, H., Enard, W., Fallon, J., Hosten, N., Völker, U., Profico, A., Di Vincenzo, F., Manzi, G., Kelso, J. and 7 moreGunz, P., Tilot, A. K., Wittfeld, K., Teumer, A., Shapland, C. Y., Van Erp, T. G. M., Dannemann, M., Vernot, B., Neubauer, S., Guadalupe, T., Fernandez, G., Brunner, H., Enard, W., Fallon, J., Hosten, N., Völker, U., Profico, A., Di Vincenzo, F., Manzi, G., Kelso, J., St Pourcain, B., Hublin, J.-J., Franke, B., Pääbo, S., Macciardi, F., Grabe, H. J., & Fisher, S. E. (2018). Neanderthal introgression sheds light on modern human brain globularity. Talk presented at the 8th Annual Meeting of the European Society for the Study of Human Evolution. Faro, Portugal. 2018-09-13 - 2019-09-15.
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St Pourcain, B. (2018). Distinct developmental profiles in genetic overlap between psychiatric disorder and population-based social communication difficulties. Talk presented at the Special Lecture Series of the University of Edinburgh. Edinburgh, UK. 2018-09-19.
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St Pourcain, B., Vitart, V., Zeggini, E., Dedoussis, G., Jaddoe, V., Pennell, C. E., Bønnelykke, K., Martinez, D., Walter, K., Shapland, C. Y., Jackson, A., Timmers, P., Wilson, J. F., Hayward, C., Davey Smith, G., Min, J. L., Iotchkova, V., Cole, T. J., UK10K Consortium, Bisgaard, H., ENIGMA Consortium, CHARGE Consortium, Fisher, S. E. and 8 moreSt Pourcain, B., Vitart, V., Zeggini, E., Dedoussis, G., Jaddoe, V., Pennell, C. E., Bønnelykke, K., Martinez, D., Walter, K., Shapland, C. Y., Jackson, A., Timmers, P., Wilson, J. F., Hayward, C., Davey Smith, G., Min, J. L., Iotchkova, V., Cole, T. J., UK10K Consortium, Bisgaard, H., ENIGMA Consortium, CHARGE Consortium, Fisher, S. E., Timpson, N., Fernandez, D., Sunyer, J., Ahluwalia, T. S., Wang, C., Felix, J., Tachmazidou, I., & Haworth, S. (2018). Low frequency genetic variation in TP53 is associated with final head circumference. Talk presented at the Behaviour Genetics Association meeting 2018. Cambridge, MA, USA. 2018-06-20 - 2018-06-23.
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Schlag, F., Buitelaar, J., Grove, J., Verhoef, E., Shapland, C. Y., Demontis, D., iPSYCH-Broad-PGC ASD Consortium, Davey Smith, D., Rai, D., Fisher, S. E., Børglum, A. D., & St Pourcain, B. (2018). Exploring the developmental genetic architecture of social behaviour: Evidence for genetic overlap with ASD and ADHD. Talk presented at the 26th World Congress of Psychiatric Genetics 2018. Glasgow, UK. 2018-10-11 - 2018-10-15.
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Shapland, C. Y., Haworth, C., Hayward, C., Tachmazidou, I., Felix, J., Wang, C., Ahluwalia, T. S., Sunyer, J., Fernandez, D., Timpson, N., Fisher, S. E., CHARGE Consortium, ENIGMA Consortium, Bisgaard, H., UK10K Consortium, Cole, T. J., Iotchkova, V., Min, J. L., Davey Smith, G., Wilson, J. F., Timmers, P., Jackson, A., Walter, K. and 8 moreShapland, C. Y., Haworth, C., Hayward, C., Tachmazidou, I., Felix, J., Wang, C., Ahluwalia, T. S., Sunyer, J., Fernandez, D., Timpson, N., Fisher, S. E., CHARGE Consortium, ENIGMA Consortium, Bisgaard, H., UK10K Consortium, Cole, T. J., Iotchkova, V., Min, J. L., Davey Smith, G., Wilson, J. F., Timmers, P., Jackson, A., Walter, K., Martinez, D., Bønnelykke, K., Pennell, C. E., Jaddoe, V., Dedoussis, G., Zeggini, E., Vitart, V., & St Pourcain, B. (2018). Low frequency genetic variation in TP53 is associated with final head circumference. Talk presented at the MPI Proudly Presents series. Nijmegen, The Netherlands. 2018-06-20.
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Verhoef, E., Grove, J., Shapland, C. Y., Demontis, D., Burgess, S., iPSYCH-Broad-PGC ASD Consortium, Davey Smith, G., Rai, D., Fisher, S. E., Børglum, A. D., & St Pourcain, B. (2018). Opposite genetic effects for polygenic ASD risk shared with and independent of ADHD: Evidence for a cancelling-out hypothesis studying genetic overlap with language and literacy. Talk presented at the 26th World Congress of Psychiatric Genetics 2018. Glasgow, UK. 2018-10-11 - 2018-11-15.
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Verhoef, E., Shapland, C. Y., Dale, P. S., Fisher, S. E., & St Pourcain, B. (2018). Understanding the genetic architecture of language- and literacy-related abilities during mid-childhood and adolescence: Evidence for genetically shared factors with early vocabulary. Poster presented at the 48th Behavior Genetics Annual Meeting, Boston, MA, USA.
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Haworth, S., Shapland, C. Y., Hayward, C., Tachmazidou, I., Felix, J., Wang, C., Ahluwalia, T. S., Sunyer, J., Fernandez, D., Timpson, N., Fisher, S. E., CHARGE Consortium, ENIGMA Consortium, Bisgaard, H., UK10K Consortium, Cole, T. J., Iotchkova, V., Min, J. L., Davey Smith, G., Wilson, J. F., Timmers, P., Jackson, A., Walter, K. and 8 moreHaworth, S., Shapland, C. Y., Hayward, C., Tachmazidou, I., Felix, J., Wang, C., Ahluwalia, T. S., Sunyer, J., Fernandez, D., Timpson, N., Fisher, S. E., CHARGE Consortium, ENIGMA Consortium, Bisgaard, H., UK10K Consortium, Cole, T. J., Iotchkova, V., Min, J. L., Davey Smith, G., Wilson, J. F., Timmers, P., Jackson, A., Walter, K., Martinez, D., Bønnelykke, K., Pennell, C. E., Jaddoe, V., Dedoussis, G., Zeggini, E., Vitart, V., & St Pourcain, B. (2017). Low frequency genetic variation in TP53 is associated with final head circumference. Talk presented at the Cognomics Conference 2017. Nijmegen, The Netherlands. 2017-09-07 - 2017-09-08.
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St Pourcain, B., Eaves, L. J., Verhoef, E., Shapland, C. Y., Ring, S. M., Fisher, S. E., Medland, S., Evans, D. M., & Davey Smith, G. (2017). Genes within the context of development: Changes in genetic trait architectures during childhood and adolescence. Talk presented at the 25th World Congress of Psychiatric Genetics 2017. Orlando, FL, USA. 2017-10-13 - 2017-10-17.
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St Pourcain, B., Eaves, J. L., Ring, S. M., Fisher, S. E., Medland, S., Evans, D. M., & Davey Smith, G. (2017). Modelling changes in genetic variances during development - The re-birth of twin modelling strategies in the GWAS era. Talk presented at the Mendelian Randomization Conference. Bristol, UK. 2017-07-11 - 2017-07-13.
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St Pourcain, B., Vitart, V., Zeggini, E., Dedoussis, G., Jaddoe, V., Pennell, C. E., Bønnelykke, K., Martinez, D., Tachmazidou, I., Walter, K., Shapland, C. Y., Jackson, A., Cleal, H., Huffmann, J., Davey Smith, G., Min, J. L., Iotchkova, V., UK10K Consortium, Bisgaard, H., ENIGMA Consortium, CHARGE Consortium, Fisher, S. E., Timpson, N. and 9 moreSt Pourcain, B., Vitart, V., Zeggini, E., Dedoussis, G., Jaddoe, V., Pennell, C. E., Bønnelykke, K., Martinez, D., Tachmazidou, I., Walter, K., Shapland, C. Y., Jackson, A., Cleal, H., Huffmann, J., Davey Smith, G., Min, J. L., Iotchkova, V., UK10K Consortium, Bisgaard, H., ENIGMA Consortium, CHARGE Consortium, Fisher, S. E., Timpson, N., Fernandez, D., Sunyer, J., Ahluwalia, T. S., Wang, C., Felix, J., Prins, B., Hayward, C., Shapland, C. Y., & Haworth, S. (2017). Low frequency genetic variation in TP53 is associated with final head circumference. Poster presented at the American Society for Human Genetics meeting 2017, Orlando, FL, USA.
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Verhoef, E., Shapland, C. Y., Fisher, S. E., & St Pourcain, B. (2017). The genetic architecture of early vocabulary (15-38 months). Talk presented at Many Paths to Language (MPaL). Nijmegen, The Netherlands. 2017-10-06 - 2017-10-08.
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Verhoef, E., Demontis, D., Burgess, S., Shapland, C. Y., Neale, B. M., Faraone, S. V., Viechtbauer, W., PGC-iPSYCH consortium, Stergiakouli, E., Davey Smith, G., Fisher, S. E., Børglum, A. D., & St Pourcain, B. (2017). Polygenic risk for ADHD is associated with reading- and spelling related traits beyond pleiotropic effects due to educational attainment. Talk presented at the 25th World Congress of Psychiatric Genetics 2017. Orlando, FL, USA. 2017-10-13 - 2017-10-17.
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Verhoef, E., Demontis, D., Shapland, C. Y., Neale, B. M., Faraone, S. V., Viechtbauer, W., Stergiakouli, E., Davey Smith, G., Fisher, S. E., PGC-iPSYCH consortium, Børglum, A. D., & St Pourcain, B. (2017). Polygenic risk for ADHD is associated with reading- and spelling-related traits. Talk presented at the Cognomics Conference 2017. Nijmegen, The Netherlands. 2017-09-07 - 2017-09-08.
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St Pourcain, B., Eaves, L. J., Ring, S. M., Fisher, S. E., Medland, S., Evans, D. M., Carey, G., & Smith, G. D. (2016). Developmental changes within the genetic architecture of social communication behaviour: A multivariate study of genetic variance in unrelated individuals. Poster presented at the 24th World Congress of Psychiatric Genetics 2016, Jerusalem, Israel.
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St Pourcain, B. (2016). The genetic continuity of Autism Spectrum Disorders and other psychiatric illness with related traits in the general population. Talk presented at the Radboud Research Round. Nijmegen, The Netherlands. 2016-02-18.
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St Pourcain, B. (2016). The genetic continuity of psychiatric symptoms in the general population: dimensional views of ASD, ADHD and schizophrenia. Talk presented at the Department of Biological Psychology, Vrije Universiteit. Amsterdam, The Netherlands. 2016-04-05.
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St Pourcain, B., Eaves, L. J., Evans, D. M., Fisher, S. E., Carey, G., & Smith, G. D. (2016). Trait-specific patterns of common genetic factors influence social communication difficulties and ADHD symptoms during development. Talk presented at the Behaviour Genetics Association Meeting 2016. Brisbane, Australia. 2016-06-20 - 2016-06-23.
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Verhoef, E., Fisher, S. E., Stergiakouli, E., Evans, D., Ring, S., Smith, G. D., & St Pourcain, B. (2016). Common polygenic risk for ASD and ADHD is associated with childhood linguistic traits within the general population, but with opposite effects. Talk presented at the 24th World Congress of Psychiatric Genetics 2016. Jerusalem, Israel. 2016-10-30 - 2016-11-03.
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Haworth, S., Felix, J., Prims, B., Blewitt, I., Tachmazidou, I., Medina-Gomez, C., Rivadeneira, F., Ring, S., Davey Smith, G., Evans, D., Timpson, N., Iotchkova, V., Ritchie, G., UK10, C., Dedoussis, G., Vincent Jaddoe, V. W. V., Zeggini, E., & St Pourcain, B. (2015). Analysis of common and less frequent genetic variation for head circumference: Next-generation genetic association studies within the UK10K COHORTS project. Poster presented at the 9th annual Genomics of Common Diseases, Cambridge, UK.
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Middeldorp, C. M., Nivard, M., Gage, S., Hottenga, J.-J., van Beijsterveldt, T., Baselmans, B., Ligthart, L., St Pourcain, B., Munafo, M., & Boomsma, D. (2015). The genetic overlap between schizophrenia and childhood sychopathology. Poster presented at the 23rd World Congress of Psychiatric Genetics 2015, Toronto, Canada.
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St Pourcain, B., Robinson, E., Bulik-Sullivan, B., Anttila, V., Maller, J., Skuse, D., Ring, S., Evans, D., Timpson, N., Ronald, A., Grove, J., Borglum, A., Mortensen, P. B., Daly, M., & Smith, G. D. (2015). Developmental changes in genetic relationships between traits and disease: Analyses of genetic overlaps between social-communication difficulties, autism spectrum disorders and schizophrenia. Poster presented at the 23rd World Congress of Psychiatric Genetics 2015, Toronto, Canada.
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St Pourcain, B., Martin, J., Stergiakouli, E., Robinson, E., Skuse, D., Susan, R., Ronald, A., Evans, D., Timpson, N., Thapar, A., & Smith, G. D. (2015). Genetic links between social-communication traits, ADHD traits and clinical ADHD during development. Talk presented at the 23rd World Congress of Psychiatric Genetics 2015. Toronto, Canada. 2015-10-16 - 2015-10-20.
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Robinson, E., St Pourcain, B., Anttila, V., Bulik-Sullivan, B., Kosmicki, J., Samocha, K., Maller, J., Skuse, D., Grove, J., Mortensen, P. B., Borglum, A., Neale, B., Ronald, A., Smith, G. D., & Daly, M. (2015). Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population. Talk presented at the 23rd World Congress of Psychiatric Genetics 2015. Toronto, Canada. 2015-10-16 - 2015-10-20.
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Stergiakouli, E., Martin, J., Hamshere, M., St Pourcain, B., Timpson, N., Thapar, A., & Smith, G. D. (2015). Shared genetic effects between clinical ADHD and smoking, alcohol and breastfeeding in mothers from the general population. Talk presented at the 23rd World Congress of Psychiatric Genetics 2015. Toronto, Canada. 2015-10-16 - 2015-10-20.
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Stergiakouli, E., Martin, J., Hamshere, M., Heron, J., St Pourcain, B., Timpson, N., Thapar, A., & Smith, G. D. (2015). Polygenic risk scores for clinical ADHD are associated with impaired educational achievement and lower IQ in children and adults from the general population. Poster presented at the 23rd World Congress of Psychiatric Genetics 2015, Toronto, Canada.
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