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.

Alagöz, G., Eising, E., Bignardi, G., Mekki, Y. N., Doust, C., Luciano, M., Fisher, S. E., & Gordon, R. L. (2023). Novel genomic evidence for shared biology between musical rhythm and language skills. Talk presented at the 53rd Annual Meeting of the Behavior Genetics Association. Murcia, Spain. 2023-06-21 - 2023-06-24.

Alagöz, G., Eising, E., Doust, C., Mekki, Y., 23andMe Research Team, Fisher, S. E., & Gordon, R. L. (2022). Investigating the evolution of common DNA variants associated with reading and rhythm traits. Poster presented at the World Congress of Psychiatric Genetics (WCPG 2022), Florence, Italy.

Alagöz, G., Molz, B., Eising, E., Schijven, D., Francks, C., Stein, J. L., & Fisher, S. E. (2022). Using neuroimaging genomics to investigate the evolution of human brain structure. Poster presented at the Reconstructing the human past: Using ancient and modern genomics symposium (EMBL), Heidelberg, Germany.

Gunz, P., Molz, B., Eising, E., Alagöz, G., Schijven, D., Francks, C., & Fisher, S. E. (2022). Scratching the surface: The genetic bases of brain globularity. Talk presented at the European Society for the study of Human Evolution meeting (ESHE 2022). Tübingen, Germany. 2022-09-21 - 2022-09-25.

Molz, B., Gunz, P., Eising, E., Alagöz, G., Schijven, D., Francks, C., & Fisher, S. E. (2022). Deciphering the underlying biological mechanisms of modern human brain shape. Talk presented at the IMPRS Conference 2022. Nijmegen, the Netherlands. 2022-06-01 - 2022-06-03.

Molz, B., Gunz, P., Eising, E., Alagöz, G., Schijven, D., Francks, C., & Fisher, S. E. (2022). Insights into the biological bases of modern human brain shape. Poster presented at the 28th Annual Meeting of the Organization for Human Brain Mapping (OHBM 2022), Glasgow, Scotland.

Alagöz, G., Molz, B., Eising, E., Schijven, D., Francks, C., Stein, J., & Fisher, S. E. (2021). Common DNA variants associated with neuroanatomy of language-related cortical regions are enriched in human gained enhancers. Poster presented at the Wellcome Trust conference Human Evolution - From Fossils to Ancient and Modern Genomes, online.

Doust, C., Fontanillas, P., Eising, E., Gordon, S. D., GenLang Consortium, Martin, N. G., Bates, T. C., Fisher, S. E., & Luciano, M. (2020). Discovery of genome-wide significant risk loci for dyslexia. Poster presented at the World Congress of Psychiatric Genetics (WCPG 2020), 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.

Eising, E., Niarchou, M., 23andMe Research Team, GenLang QTL-GWAS Working Group, Davis, L., Fisher, S. E., & Gordon, R. (2020). Novel investigation of pleiotropy of rhythm and language traits. Poster presented at the World Congress of Psychiatric Genetics (WCPG 2020), online.

Lyu, B., Tsvetanov, K., Tyler, L., Clarke, A., Eising, E., Fisher, S. E., & Amos, W. (2020). Pattern-based genome-wide relatedness analysis of human brain structure. Poster presented at the 27th Annual Meeting of the Cognitive Neuroscience Society (CNS 2020), 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.

Henson, R., Suri, S., Kievit, R., Rowe, J., Chan, D., Tyler, L., Eising, E., CamCAN, & Fisher, S. E. (2019). Testing the antagonistic pleiotropy hypothesis of ApoE with cognitive and brain data from a healthy cohort. Poster presented at the BNA (British Neuroscience Association) 2019: Festival of Neuroscience, Dublin, Ireland.

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.

Eising, E. (2018). Exploring genes and pathways involved in migraine. Talk presented at the Amsterdamse Neurologen Vereeniging. Amsterdam, The Netherlands. 2018.

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.

Eising, E., Huisman, S. M. H., Mahfouz, A., Vijfhuizen, L. S., Ferrari, M. D., Terwindt, G. M., Nyholt, D. R., Lelieveldt, B. F. P., Reinders, M. J. T., Van den Maagdenberg, A. M. J. M., & the International Headache Genetics Consortium (2015). Integrating brain gene expression data with genome-wide association data links several brain regions and gene functions to migraine pathophysiology. Poster presented at the first Target Validation using Genomics and Informatics Conference, 2015, Hinxton, UK.

Eising, E., Huisman, S. M. H., De Leeuw, C., Vijfhuizen, L. S., Anttila, V., Terwindt, G. M., Ferrari, M. D., Palotie, A., Nyholt, D. R., De Vries, B., Posthuma, H., Lelieveldt, B. F. P., Reinders, M. J., Van Den Maagdenberg, A. M. J. M., & the IHGC consortium (2015). Integrating migraine GWAS data with brain expression information for functional interpretation of migraine-associated SNPsin. Talk presented at the 17th International headache conference (IHC). Valencia, Spain. 2015-05-14 - 2015-05-17.

Eising, E., De Vries, B., Shyti, R., Vijfhuizen, L. S., Broos, L. A. M., Datson, N. A., Tolner, E. A., ’t Hoen, P. A. C., Ferrari, M. D., & Van den Maagdenberg, A. M. J. M. (2013). Dysregulation of inflammatory pathways in a Familial Hemiplegic Migraine 1 mouse model after the induction of cortical spreading depression. Poster presented at he American Society of Human Genetics (ASHG) Conference, 2013, Boston, USA.

Eising, E., De Vries, B., Broos, L. A., Ferrari, M. D., ’t Hoen, P. A. C., & Van den Maagdenberg, A. M. J. M. (2012). Gene expression profiling in Familial Hemiplegic Migraine mice. Talk presented at the Genetica Retraite (Dutch human genetics conference). Rolduc, The Netherlands.