Displaying 1 - 9 of 9
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Carrion Castillo, A., Pepe, A., Fisher, S. E., Tzourio-Mazoyer, N., Mazoyer, B., Joliot, M., Crivello, F., & Francks, C. (2017). Heritability analysis of brain laterality indices using the UK biobank dataset. Poster presented at the Cognomics Conference 2017, Nijmegen, The Netherlands.
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Kong, X., & Francks, C. (2017). Differential gene expression associated with frontal and occipital asymmetries of the human brain. Poster presented at the Annual Meeting of the Organization for Human Brain Mapping, Vancouver, Canada.
Abstract
Rightward frontal and leftward occipital asymmetries in human brain (i.e., brain torque) have been consistently reported in postmortem and in vivo neuroimaging studies. Alterations of these asymmetries may be involved in human disorders including stuttering and depression. However, little is known about the genetic determinants of these asymmetries. In the present study, we aimed to explore the genetic basis of frontal and occipital asymmetries by combining a large sample of MRI images (N = 2326) and a high-resolution gene expression database (Allen Human Brain Atlas, AHBA). -
Postema, M., Carrion Castillo, A., Fisher, S. E., Vingerhoeds, G., & Francks, C. (2017). The genetics of situs inversus totalis without primary ciliary dyskinesia. Poster presented at the Donders Discussions 2017, Nijmegen, The Netherlands.
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Postema, M., Carrion Castillo, A., Fisher, S. E., Vingerhoeds, G., & Francks, C. (2017). The genetics of situs inversus totalis without primary ciliary dyskinesia. Poster presented at the Donders Poster Sessions 2017, Nijmegen, The Netherlands.
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Postema, M., Carrion Castillo, A., Fisher, S. E., Vingerhoeds, G., & Francks, C. (2017). The genetics of situs inversus totalis without primary ciliary dyskinesia. Poster presented at the Cognomics Conference 2017, Nijmegen, The Netherlands.
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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.
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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.
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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.
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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.
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