Presentations

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.

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.

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.

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.

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.

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.

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.

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.

Eising, E., Carrion Castillo, A., Vino, A., Shriberg, L. D., & Fisher, S. E. (2017). Childhood apraxia of speech is caused by genes that control gene expression during fetal brain development. Poster presented at the 11th Genomics of Rare Disease conference, Hinxton, UK.