Displaying 1 - 14 of 14
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Carrion Castillo, A., Pepe, A., Kong, X., Fisher, S. E., Mazoyer, B., Tzourio-Mazoyer, N., Crivello, F., & Francks, C. (2019). Genetics of planum temporale asymmetry: Limited relevance to disorders and cognitive variability. Poster presented at the 25th Annual Meeting of the Organization for Human Brain Mapping (OHBM 2019), Rome, Italy.
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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.
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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.
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Francks, C. (2019). Genetics of human brain laterality. Talk presented at the workshop Capturing Developmental Brain Dynamics, Lorentz Center. Leiden, The Netherlands. 2019-04-15 - 2019-04-19.
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Kong, X., Tzourio-Mazoyer, N., Joliot, M., Fedorenko, E., Liu, J., Fisher, S. E., & Francks, C. (2019). Gene expression correlates of the cortical network underlying sentence processing. Poster presented at the 25th Annual Meeting of the Organization for Human Brain Mapping (OHBM 2019), Rome, Italy.
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Kong, X., Tzourio-Mazoyer, N., Joliot, M., Fedorenko, E., Liu, J., Fisher, S. E., & Francks, C. (2019). Gene expression correlates of the human language network. Poster presented at Crossing the Boundaries: Language in Interaction Symposium, Nijmegen, The Netherlands.
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Kong, X., Boedhoe, P., ENIGMA-OCD Working Group, Thompson, P., Stein, D., Van den Heuvel, O. A., & Francks, C. (2019). Mapping cortical and subcortical asymmetry in OCD: Findings from the ENIGMA Consortium. Poster presented at the 25th Annual Meeting of the Organization for Human Brain Mapping (OHBM 2019), Rome, Italy.
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Postema, M., Van Rooij, D., ENIGMA ASD Working Group, Thompson, P. M., Fisher, S. E., Buitelaar, J. K., & Francks, C. (2019). Altered structural brain asymmetry in autism spectrum disorder: Analysis via the ENIGMA Consortium. Poster presented at the 25th Annual Meeting of the Organization for Human Brain Mapping (OHBM 2019), Rome, Italy.
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Postema, M., Carrion Castillo, A., Fisher, S. E., Vingerhoeds, G., & Francks, C. (2019). No clear monogenic links between left-handedness and situs inversu. Poster presented at the Cognomics Conference 2019, Nijmegen, The Netherlands.
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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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