Presentations

Carrion Castillo, A., Francks, C., Franke, B., & Fisher, S. E. (2014). Identification of rare variants from exome sequencing in a large family with dyslexia. Poster presented at the 64th Annual Meeting of the American Society of Human Genetics, San Diego, USA.

Francks, C. (2014). Genome-wide screening for DNA variants associated with reading and language traits. Talk presented at the International Workshop Dyslexia. Erfurt, Germany. 2014-05-10.

Francks, C. (2014). The genetics of human brain asymmetries. Talk presented at the Neurofunctional Imaging Group of Bordeaux University. Bordeaux, France. 2014-07-05.

Guadalupe, T., Zwiers, M., Wittfeld, K., Teumer, A., Vasquez, A. A., Hoogman, M., Hagoort, P., Fernandez, G., Grabe, H., Fisher, S. E., & Francks, C. (2014). Asymmetry within and around the planum temporale is sexually dimorphic and influenced by genes involved in steroid biology. Poster presented at the Sixth Annual Meeting of the Society for the Neurobiology of Language (SNL 2014), Amsterdam.

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.