Presentations

Alagöz, G., Wong, M. M. K., Gräßle, T., Jaeger, C., Morawski, M., Francks, C., Wittig, R. M., Crockford, C., Gunz, P., & Fisher, S. E. (2023). Spatial and single-nucleus transcriptomic profile of the chimpanzee frontal pole. Poster presented at the Society of Molecular Biology and Evolution Meeting (SMBE 2023), Ferrara, Italy.

Francks, C. (2023). Large‐scale genetic studies reveal clues to the developmental origins of human brain asymmetry. Talk presented at Yamada Conference LXXV: Origin of left-right asymmetry in animals. Kobe, Japan. 2023-01-24 - 2023-01-27.

Soheili-Nezhad, S., Schijven, D., Mars, R. B., Fisher, S. E., & Francks, C. (2023). Distinct impact modes of polygenic disposition to dyslexia in the adult brain. Talk presented at the Donders theme II and III meeting. Nijmegen, The Netherlands. 2023-09-02.

Soheili-Nezhad, S., Schijven, D., Mars, R. B., Fisher, S. E., & Francks, C. (2023). Genomic modifiers of dyslexia influence brain microstructure in the general population. Poster presented at the Annual Meeting of the Organization for Human Brain Mapping (OHBM 2023), Montreal, Canada.

Francks, C. (2012). Genes and brain asymmetry. Talk presented at Current Issues in Clinical Neuroscience - The human brain and its development throughout the lifespan. Utrecht, The Netherlands. 2012-05.

Gialluisi, A., Newbury, D. F., Wilcutt, E. G., Olson, R. K., Brandler, W. M., Paracchini, S., Monaco, A. P., Francks, C., & Fisher, S. E. (2012). Genome-wide screening for DNA variants associated with dyslexia and language impairment. Poster presented at the New Frontiers Symposium 2012: Genomics in health and disease - Towards personal genomics, Nijmegen, The Netherlands.

Guadalupe, T., Zwiers, M. P., Arias Vasquez, A., Hoogman, M., Franke, B., Fisher, S. E., & Francks, C. (2012). Genetics of brain asymmetries. Poster presented at the New Frontiers Symposium 2012: Genomics in health and disease - Towards personal genomics, Nijmegen, The Netherlands.

Simpson, N., Ceroni, F., Francks, C., Knight, S. J. L., Monaco, A. P., Fisher, S. E., Newbury, D., & SLI Consortium (2012). Investigating copy number variants within a cohort of individuals with specific language impairment. Poster presented at the European Society of Human Genetics Conference 2012 (ESHG 2012), Nürnberg, Germany.