Else Eising

Presentations

Displaying 1 - 14 of 14
  • 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 2020 Virtual World Congress of Psychiatric Genetics, Virtual.
  • 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 2020 Virtual World Congress of Psychiatric Genetics.
  • 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 2020 Virtual World Congress of Psychiatric Genetics.
  • 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., & 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.
  • 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.
  • 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.

Share this page