Displaying 1 - 10 of 10
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Eising, E. (2024). Exploring the genetics of stuttering. Talk presented at the NCCR Symposium "From Genes to Communication". Geneva. 2024-06-10 - 2024-06-11.
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Eising, E., Rebattu, V., Boomsma, D. I., Pool, R., Franken, M.-C.-J., & Fisher, S. E. (2024). Exploring the genetics of stuttering persistence. Poster presented at the 54th Annual Meeting of the Behavior Genetics Association, London.
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Eising, E. (2024). Monogenic contributions to speech delay. Talk presented at the CRE Symposium ‘What’s new since FOXP2: new developments in speech and language neurobiology’. London. 2024-06-07.
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Eising, E. (2024). Exploring the genetics of stuttering persistence. Talk presented at the Symposium “Speech and Language Disorders: Lessons from Genetics”. Nijmegen, The Netherlands. 2024-09-13.
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De Heus, E. V., Eising, E., Fisher, S. E., de Jong, P. F., & Van Bergen, E. (2024). Disentangling dyslexia: Towards early identification through biological and non-biological factors. Poster presented at the 54th Annual Meeting of the Behavior Genetics Association, London.
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De Heus, E., Eising, E., Fisher, S. E., De Jong, P. F., & Van Bergen, E. (2024). Disentangling dyslexia: towards early identification through biological and non-biological factors. Poster presented at the Highlights in the Language Sciences Conference 2024, Nijmegen, The Netherlands.
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Molz, B., Lana Alberro, M., Eising, E., Schijven, D., Francks, C., & Fisher, S. E. (2024). Evolutionary insights from a population database: Limited consequences of archaic protein-altering variants in present-day humans. Poster presented at the 57th Annual European Human Genetics Conference (ESHG 2024), Berlin, Germany.
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Szilagyi, I. A., Vino, A., De boer, J., Eising, E., Hintz, F., Meyer, A. S., & Fisher, S. E. (2024). Polygenic profile of individual differences in language skills in a Dutch cohort. Poster presented at the Highlights in the Language Sciences Conference 2024, Nijmegen, The Netherlands.
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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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Eising, E. (2018). Exploring genes and pathways involved in migraine. Talk presented at the Amsterdamse Neurologen Vereeniging. Amsterdam, The Netherlands. 2018.
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