Presentations

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.