Presentations

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.