Presentations

Amelink, J., Postema, M., Kong, X., Schijven, D., Carrion Castillo, A., Soheili-Nezhad, S., Sha, Z., Molz, B., Joliot, M., Fisher, S. E., & Francks, C. (2024). Imaging genetics of functional connectivity within the language network reveals links with language-related abilities, dyslexia, and handedness. Poster presented at the IMPRS Conference 2024, Nijmegen, the Netherlands.

Amelink, J., Postema, M., Kong, X., Schijven, D., Carrion Castillo, A., Soheili-Nezhad, S., Sha, Z., Molz, B., Joliot, M., Fisher, S. E., & Francks, C. (2024). Imaging genetics of language network functional connectivity reveals links with language-related abilities, dyslexia and handedness. Talk presented at the third conference of the European Social Science Genetics Network (ESSGN III). Rotterdam, The Netherlands. 2024-05-29 - 2024-05-30.

Amelink, J., Postema, M., Kong, X., Schijven, D., Carrion Castillo, A., Soheili-Nezhad, S., Sha, Z., Molz, B., Joliot, M., Fisher, S. E., & Francks, C. (2024). Imaging genetics of language network functional connectivity reveals links with language-related abilities, dyslexia and handedness. Poster presented at the 57th Annual European Human Genetics Conference (ESHG 2024), Berlin, Germany.

Amelink, J., Postema, M., Kong, X., Schijven, D., Carrion Castillo, A., Soheili-Nezhad, S., Sha, Z., Molz, B., Joliot, M., Fisher, S. E., & Francks, C. (2024). Imaging genetics of language network functional connectivity reveals links with language-related abilities, dyslexia and handedness. Poster presented at the Dutch Neuroscience Meeting (DNM 24), Tiel, The Netherlands.

Amelink, J., Postema, M., Kong, X., Schijven, D., Carrion Castillo, A., Soheili-Nezhad, S., Sha, Z., Molz, B., Joliot, M., Fisher, S. E., & Francks, C. (2024). Imaging genetics of language network functional connectivity reveals links with language-related abilities, dyslexia and handedness. Poster presented at the Highlights in the Language Sciences Conference 2024, Nijmegen, The Netherlands.

Amelink, J., Postema, M., Kong, X., Schijven, D., Carrion Castillo, A., Soheili-Nezhad, S., Sha, Z., Molz, B., Joliot, M., Fisher, S. E., & Francks, C. (2024). Imaging genetics of language network functional connectivity reveals links with language-related abilities, dyslexia and handedness. Poster presented at the Donders Poster Session 2024, Nijmegen, The Netherlands.

Francks, C. (2024). Large-scale genetic studies of human brain asymmetry and handedness [invited talk]. Talk presented at the Maastricht Center for Systems Biology Science Day. Maastricht, The Netherlands. 2024-06-21.

Houwing, D. J., Costa Da Glória, C., & Francks, C. (2024). Perfect imperfections: Mapping molecular asymmetries in the mouse brain. Poster presented at the Spatial Omics conference, Ghent, Belgium.

Houwing, D. J., Costa Da Glória, C., & Francks, C. (2024). Perfect imperfections: Mapping molecular asymmetries in the mouse brain. Talk presented at the 9th North Sea Laterality Conference on Brain Asymmetry. St Andrews, Scotland. 2024-08-21 - 2024-08-23.

Houwing, D. J., Costa Da Glória, C., & Francks, C. (2024). Perfect imperfections: Mapping molecular asymmetries in the mouse brain. Poster presented at the Donders Poster Session 2024, Nijmegen, The Netherlands.

Molz, B., Lana Alberro, M., Eising, E., Schijven, D., Francks, C., & Fisher, S. E. (2024). Evolutionary insights from a population database: Limited consequences of archaic protein-altering variants in present-day humans. Poster presented at the 57th Annual European Human Genetics Conference (ESHG 2024), Berlin, Germany.

Soheili-Nezhad, S., Schijven, D., Mars, R. B., Fisher, S. E., & Francks, C. (2024). Distinct impact modes of polygenic disposition to dyslexia in the adult brain. Poster presented at the FENS Forum 2024, Vienna, Austria.

Soheili-Nezhad, S., Schijven, D., Mars, R. B., Fisher, S. E., & Francks, C. (2024). Distinct impact modes of polygenic disposition to dyslexia in the adult brain. Talk presented at the Language in Interaction consortium meeting. Nijmegen, The Netherlands. 2024-03-25.

Soheili-Nezhad, S., Schijven, D., Mars, R. B., Fisher, S. E., & Francks, C. (2024). Genetic variants predisposing to dyslexia are associated with structural properties of multiple brain networks in 35,231 adults. Poster presented at the Highlights in the Language Sciences Conference 2024, Nijmegen, The Netherlands.

Wong, M. M. K., Sha, Z., Luetje, L., Kong, X., Velthuijs, N., Van Heukelum, S., Schijven, D., Mhlanga, M., Van de Berg, W., Jonkman, L., Fisher, S. E., & Francks, C. (2024). The neocortical infrastructure for language involves region-specific patterns of laminar gene expression. Poster presented at the Highlights in the Language Sciences Conference 2024, Nijmegen, The Netherlands.

Carrion Castillo, A., Tzourio-Mazoyer, N., Kavaklioglu, T., Badillo, S., Chavent, M., Saracco, J., Fisher, S. E., Mazoyer, B., & Francks, C. (2018). Atypical lateralization for sentence production, reading, and listening: detection with multivariate clustering and search for associated rare genetic variants using whole genome sequencing. Talk presented at the International Workshop on Imaging Genetics of Human Brain Laterality. Nijmegen, The Netherlands. 2018-01-30.

Carrion Castillo, A., Tzourio-Mazoyer, N., Kavaklioglu, T., Badillo, S., Chavent, M., Saracco, J., Fisher, S. E., Mazoyer, B., & Francks, C. (2018). Genome sequencing for rightward hemispheric language dominance. Poster presented at the 11th FENS Forum of Neuroscience (FENS 2018), Berlin, Germany.

Carrion Castillo, A., Fisher, S. E., & Francks, C. (2018). Planum temporale asymmetry is heritable in the UK biobank (N=12,236). Poster presented at the 26th World Congress of Psychiatric Genetics 2018, Glasgow, UK.

Eising, E., St Pourcain, B., Francks, C., Fisher, S. E., & the Quantitative Trait Working Group of the GenLang consortium (2018). A genome-wide association screen of quantitative speech, language and reading traits in >14,000 people in the GenLang consortium. Poster presented at the 26th World Congress of Psychiatric Genetics 2018, Glasgow, UK.

Kong, X., Boedhoe, P., ENIGMA OCD Working Group, Thompson, P., Van den Heuvel, O. A., & Francks, C. (2018). A survey of altered brain anatomical asymmetry in Obsessive-Compulsive Disorder. Poster presented at the 73rdAnnual Meeting of the Society of Biological Psychiatry (SOBP 2018), New York, NY, USA.

Kong, X., & Francks, C. (2018). Mapping brain asymmetry: Updates from the ENIGMA Lateralization Group. Talk presented at the ENIGMA Consortium Chairs Annual Retreat 2018. New York, NY, USA. 2018-05-08.

Kong, X., Mathias, S. R., Guadalupe, T., ENIGMA Laterality Working Group, Glahn, D. C., Franke, B., Crivello, F., Tzourio-Mazoyer, N., Fisher, S. E., Thompson, P. M., & Francks, C. (2018). Mapping cortical brain asymmetry in 17,141 healthy individuals worldwide via the ENIGMA Consortium. Poster presented at the 24th Annual Meeting of the Organization for Human Brain Mapping (OHBM 2018), Singapore.

Postema, M., Fisher, S. E., & Francks, C. (2018). Alterations of brain laterality in psychiatric, behavioural and developmental disorders. Talk presented at the MPI Research Progress Presentations. Nijmegen, The Netherlands. 2018-11-22.

Postema, M., Hoogman, M., van Rooij, D., Fisher, S. E., Franke, B., Buitelaar, J. E., & Francks, C. (2018). Exploring structural brain asymmetries in various disorders through the ENIGMA consortium. Talk presented at the MPI Proudly Presents series. Nijmegen, The Netherlands. 2018-06-20.

Postema, M., Carrion Castillo, A., Fisher, S. E., Vingerhoeds, G., & Francks, C. (2018). The genetics of situs inversus totalis without primary ciliary dyskinesia. Talk presented at the 6th North Sea Laterality International Meeting 2018. Dundee, UK. 2018-08-22 - 2018-08-24.

Postema, M., Carrion Castillo, A., Fisher, S. E., Vingerhoeds, G., & Francks, C. (2018). The genetics of situs inversus totalis without primary ciliary dyskinesia. Poster presented at the Donders Poster Sessions 2018, Nijmegen, The Netherlands.

Postema, M., Carrion Castillo, A., Fisher, S. E., Vingerhoeds, G., & Francks, C. (2018). The genetics of situs inversus totalis without primary ciliary dyskinesia. Poster presented at the American Society of Human Genetics 68th Annual Meeting (ASHG 2018), San Diego, CA, USA.

Postema, M., Carrion Castillo, A., Fisher, S. E., Vingerhoets, G., & Francks, C. (2018). The genetics of situs inversus totalis without primary ciliary dyskinesia. Talk presented at the MPI workshop "Imaging Genetics of Human Brain Laterality". Nijmegen, The Netherlands. 2018-01-30.