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. 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.

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). 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.

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.

Alagöz, G., Molz, B., Eising, E., Schijven, D., Francks, C., Stein, J. L., & Fisher, S. E. (2022). Using neuroimaging genomics to investigate the evolution of human brain structure. Poster presented at the Reconstructing the human past: Using ancient and modern genomics symposium (EMBL), Heidelberg, Germany.

Amelink, J., Postema, M., Kong, X., Sha, Z., Schijven, D., Molz, B., Joliot, M., Fisher, S. E., & Francks, C. (2022). Genetic correlates of intra- and interhemispheric resting state functional language connectivity. Poster presented at the IMPRS Conference 2022, Nijmegen, the Netherlands.

Molz, B., Gunz, P., Eising, E., Alagöz, G., Schijven, D., Francks, C., & Fisher, S. E. (2022). Insights into the biological bases of modern human brain shape. Poster presented at the 28th Annual Meeting of the Organization for Human Brain Mapping (OHBM 2022), Glasgow, Scotland.

Schijven, D., Postema, M., ENIGMA-Schizophrenia Working Group, Fisher, S. E., Franke, B., Glahn, D. C., Gur, R. C., Hashimoto, R., Jahanshad, N., Luders, E., Medland, S. E., Thompson, P. M., Turner, J. A., Van Erp, T. G. M., & Francks, C. (2022). Large-scale analysis of brain structural asymmetries in schizophrenia via the ENIGMA Consortium. Poster presented at the 28th Annual Meeting of the Organization for Human Brain Mapping (OHBM 2022), Glasgow, Scotland.

Sha, Z., Schijven, D., Fisher, S. E., & Francks, C. (2022). Genetic architecture of the white matter connectome of the human brain. Poster presented at the FENS Forum 2022, Paris, France.

Alagöz, G., Molz, B., Eising, E., Schijven, D., Francks, C., Stein, J., & Fisher, S. E. (2021). Common DNA variants associated with neuroanatomy of language-related cortical regions are enriched in human gained enhancers. Poster presented at the Wellcome Trust conference Human Evolution - From Fossils to Ancient and Modern Genomes, online.

Den Hoed, J., Van der Spek, J., Snijders Blok, L., Dingemans, A. J. M., Schijven, D., Barakat, T. S., Bebin, E. M., Beck-Wödl, S., Beunders, G., Brown, N. J., Brunet, T., Brunner, H. G., Campeau, P. M., Čuturilo, G., Gilissen, C., Haack, T. B., Husain, R. A., Kamien, B., Lim, S. C., Magg, J. and 16 moreDen Hoed, J., Van der Spek, J., Snijders Blok, L., Dingemans, A. J. M., Schijven, D., Barakat, T. S., Bebin, E. M., Beck-Wödl, S., Beunders, G., Brown, N. J., Brunet, T., Brunner, H. G., Campeau, P. M., Čuturilo, G., Gilissen, C., Haack, T. B., Husain, R. A., Kamien, B., Lim, S. C., Magg, J., Maver, A., Monteil, D. C., Ockeloen, C. W., Richmond, C., Riess, A., Schwaibold, E. M. C., Simon, M. E. H., Spranger, S., Tan, T. Y., Thompson, M. L., De Vries, B. B., Wilkins, E. J., Willemsen, M. H., Vissers, L. E. L. M., Fisher, S. E., & Kleefstra, T. (2021). Inherited variants in CHD3 demonstrate variable expressivity in Snijders Blok-Campeau syndrome. Poster presented at the ASHG 2021 Annual Meeting, online.

Molz, B., Alagöz, G., Schijven, D., Francks, C., Stein, J., & Fisher, S. E. (2021). Cortical surface area is influenced by genetic variation in enhancers gained during human evolution. Poster presented at the 27th Annual Meeting of the Organization for Human Brain Mapping (OHBM 2021), online.

Schijven, D., Fisher, S. E., Franke, B., Glahn, D. C., Gur, R. C., Hashimoto, R., Jahanshad, N., Medland, S. E., Thompson, P. M., Van Erp, T. G. M., Turner, J. A., Francks, C., & ENIGMA-Schizophrenia working group (2021). Large-scale ENIGMA Consortium analysis of brain anatomical asymmetries in schizophrenia. Poster presented at the 2021 Society of Biological Psychiatry (SOBP) Annual Meeting, online.

Sha, Z., Schijven, D., & Francks, C. (2021). Patterns of brain asymmetry associated with polygenic risks for autism and schizophrenia implicate language and executive functions but not brain masculinization. Poster presented at the 51st Annual Meeting of the Behavior Genetics Association, Online.

Postema, M., Pepe, A., Carrion Castillo, A., Schijven, D., Kong, X., Tzourio-Mazoyer, N., Crivello, F., Mazoyer, B., Fisher, S. E., Joliot, M., & Francks, C. (2020). Genetic influences on left-right asymmetry of functional connectivity in the human brain. Poster presented at the IMPRS conference 2020, online.

Sha, Z., Schijven, D., Carrion Castillo, A., Joliot, M., Mazoyer, B., Fisher, S. E., Crivello, F., & Francks, C. (2020). The genetic architecture of structural left-right asymmetry of the human brain. Poster presented at the World Congress of Psychiatric Genetics (WCPG 2020), online.

Sha, Z., Schijven, D., Carrion Castillo, A., Joliot, M., Mazoyer, B., Fisher, S. E., Crivello, F., & Francks, C. (2020). The genetic architecture of structural left-right asymmetry of the human brain. Poster presented at the Neurogenetics Conference, online.