Presentations

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., 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.