Clyde Francks

Presentations

Displaying 1 - 50 of 50
  • 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.
  • 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. Talk presented at the 9th North Sea Laterality Conference on Brain Asymmetry. St Andrews, Scotland. 2024-08-21 - 2024-08-23.
  • 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.
  • Francks, C. (2023). Large‐scale genetic studies reveal clues to the developmental origins of human brain asymmetry. Talk presented at Yamada Conference LXXV: Origin of left-right asymmetry in animals. Kobe, Japan. 2023-01-24 - 2023-01-27.
  • Soheili-Nezhad, S., Schijven, D., Mars, R. B., Fisher, S. E., & Francks, C. (2023). Distinct impact modes of polygenic disposition to dyslexia in the adult brain. Talk presented at the Donders theme II and III meeting. Nijmegen, The Netherlands. 2023-09-02.
  • 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. Talk presented at the Neuromatch Conference (NMC 2022). online. 2022-09-27 - 2022-09-28.
  • Francks, C. (2022). Genetics of human brain asymmetry [invited talk]. Talk presented at the FENS Forum 2022 miniconference: Understanding Behaviour: Molecular, Cellular & Systems Approaches. Paris, France. 2022-07-09.
  • Francks, C. (2022). Imaging genomics group at the Max Planck Institute Nijmegen [invited talk]. Talk presented at the Neurodevelopmental Disorders Principal Investigator meeting, Radboud University Medical Center. Nijmegen, The Netherlands. 2022-04-19.
  • Francks, C. (2022). Imaging genomics of left-right asymmetry in the human brain [invited talk]. Talk presented at the Donders Institute research theme 3 meeting. Nijmegen, The Netherlands. 2022-05-19.
  • Francks, C. (2022). Mapping the brain: Neuroimaging and connectome approaches to study genetic variation in brain function, structure, and behavior [symposium chair]. Talk presented at the Annual Meeting of International Behavioural and Neural Genetics Society. Memphis, TN, USA. 2022-05-24 - 2022-05-27.
  • Francks, C. (2022). Multi-level integrative analysis of brain lateralization for language. Talk presented at the Human Brain Project EBRAINS workshop. Berg en Dal, The Netherlands. 2022-09-05 - 2022-09-07.
  • Francks, C. (2022). Human brain and behavioural asymmetries: Genetic influences and associations with psychiatric disorders [keynote]. Talk presented at the Aphasia Junior days. Nijmegen, The Netherlands. 2022-12-13 - 2022-12-14.
  • Gunz, P., Molz, B., Eising, E., Alagöz, G., Schijven, D., Francks, C., & Fisher, S. E. (2022). Scratching the surface: The genetic bases of brain globularity. Talk presented at the European Society for the study of Human Evolution meeting (ESHE 2022). Tübingen, Germany. 2022-09-21 - 2022-09-25.
  • Molz, B., Gunz, P., Eising, E., Alagöz, G., Schijven, D., Francks, C., & Fisher, S. E. (2022). Deciphering the underlying biological mechanisms of modern human brain shape. Talk presented at the IMPRS Conference 2022. Nijmegen, the Netherlands. 2022-06-01 - 2022-06-03.
  • Sha, Z., Schijven, D., Fisher, S. E., & Francks, C. (2022). Genetic architecture of the white matter connectome of the human brain. Talk presented at the Annual Meeting of International Behavioural and Neural Genetics Society. Memphis, TN, USA. 2022-05-24 - 2022-05-27.

    Abstract

    White matter tracts form the structural basis of large-scale functional networks in the human brain. We applied brain-wide tractography to diffusion images from 30,810 adult participants (UK Biobank), and found significant heritability for 90 regional connectivity measures and 851 fiber tracts. Multivariate genome-wide association analyses identified 355 independently associated lead SNPs across the genome, of which 77% were not previously associated with human brain metrics. Enrichment analyses implicated neurodevelopmental processes including neurogenesis, neural differentiation, neural migration, neural projection guidance, and axon development, as well as prenatal brain expression especially in stem cells, astrocytes, microglia and neurons. We used the multivariate association profiles of lead SNPs to identify 26 genomic loci implicated in structural connectivity between core regions of the left-hemisphere language network, and also identified 6 loci associated with hemispheric left-right asymmetry of structural connectivity. Polygenic scores for schizophrenia, bipolar disorder, autism spectrum disorder, attention-deficit hyperactivity disorder, reading ability, left-handedness, Alzheimer’s disease, amyotrophic lateral sclerosis, and epilepsy showed significant multivariate associations with structural connectivity, each implicating specific sets of brain regions with trait-relevant functional profiles. This large-scale mapping study revealed common genetic contributions to the human brain's structural connectome in the general adult population, and its links with polygenic disposition to brain disorders and behavioral traits.
  • Sha, Z., Van Rooij, D., Anagnostou, E., Arango, C., Auzias, G., Behrmann, M., Bernhardt, B., Bolte, S., Busatto, G. F., Calderoni, S., Calvo, R., Daly, E., Deruelle, C., Duan, M., Duran, F. L. S., Durston, S., Ecker, C., Ehrlich, S., Fair, D., Fedor, J. and 38 moreSha, Z., Van Rooij, D., Anagnostou, E., Arango, C., Auzias, G., Behrmann, M., Bernhardt, B., Bolte, S., Busatto, G. F., Calderoni, S., Calvo, R., Daly, E., Deruelle, C., Duan, M., Duran, F. L. S., Durston, S., Ecker, C., Ehrlich, S., Fair, D., Fedor, J., Fitzgerald, J., Floris, D. L., Franke, B., Freitag, C. M., Gallagher, L., Glahn, D. C., Haar, S., Hoekstra, L., Jahanshad, N., Jalbrzikowski, M., Janssen, J., King, J. A., Lazaro, L., Luna, B., McGrath, J., Medland, S. E., Muratori, F., Murphy, D. G., Neufeld, J., O’Hearn, K., Oranje, B., Parellada, M., Pariente, J. C., Postema, M., Remnelius, K. L., Retico, A., Rosa, P. G. P., Rubia, K., Shook, D., Tammimies, K., Taylor, M. J., Tosetti, M., Wallace, G. L., Zhou, F., Thompson, P. M., Fisher, S. E., Buitelaar, J. K., & Francks, C. (2022). Subtly altered topological asymmetry of brain structural covariance networks in autism spectrum disorder across 43 datasets from the ENIGMA consortium. Talk presented at the 2022 Society of Biological Psychiatry (SOBP) Annual Meeting. New Orleans, USA. 2022-04-28 - 2022-04-30.
  • Sha, Z., Van Rooij, D., Anagnostou, E., Arango, C., Auzias, G., Behrmann, M., Bernhardt, B., Bolte, S., Busatto, G. F., Calderoni, S., Calvo, R., Daly, E., Deruelle, C., Duan, M., Duran, F. L. S., Durston, S., Ecker, C., Ehrlich, S., Fair, D., Fedor, J. and 38 moreSha, Z., Van Rooij, D., Anagnostou, E., Arango, C., Auzias, G., Behrmann, M., Bernhardt, B., Bolte, S., Busatto, G. F., Calderoni, S., Calvo, R., Daly, E., Deruelle, C., Duan, M., Duran, F. L. S., Durston, S., Ecker, C., Ehrlich, S., Fair, D., Fedor, J., Fitzgerald, J., Floris, D. L., Franke, B., Freitag, C. M., Gallagher, L., Glahn, D. C., Haar, S., Hoekstra, L., Jahanshad, N., Jalbrzikowski, M., Janssen, J., King, J. A., Lazaro, L., Luna, B., McGrath, J., Medland, S. E., Muratori, F., Murphy, D. G., Neufeld, J., O’Hearn, K., Oranje, B., Parellada, M., Pariente, J. C., Postema, M., Remnelius, K. L., Retico, A., Rosa, P. G. P., Rubia, K., Shook, D., Tammimies, K., Taylor, M. J., Tosetti, M., Wallace, G. L., Zhou, F., Thompson, P. M., Fisher, S. E., Buitelaar, J. K., & Francks, C. (2022). Subtly altered topological asymmetry of brain structural covariance networks in autism spectrum disorder across 43 datasets from the ENIGMA consortium. Talk presented at the 28th Annual Meeting of the Organization for Human Brain Mapping (OHBM 2022). Glasgow, Scotland. 2022-06-19 - 2022-06-23.
  • Sha, Z., Schijven, D., Fisher, S. E., & Francks, C. (2022). Genetic architecture of the white matter connectome of the human brain. Talk presented at the World Congress of Psychiatric Genetics (WCPG 2022). Florence, Italy. 2022-09-13 - 2022-09-17.
  • Sha, Z., Schijven, D., Fisher, S. E., & Francks, C. (2022). Genetic architecture of the white matter connectome of the human brain. Talk presented at Theme Discussion (RadboudUMC). online. 2022-10-21.
  • Molz, B., Gunz, P., Schijven, D., Francks, C., & Fisher, S. E. (2021). Deciphering the biological bases of endocranial globularity in modern humans. Talk presented at the Wellcome Trust conference Human Evolution - From Fossils to Ancient and Modern Genomes. online. 2021-11-02 - 2021-11-04.
  • 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. Talk presented at 22nd Annual Genes, Brain & Behavior Meeting. Online. 2021-05-10 - 2021-05-15.
  • 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. Talk presented at the World Congress of Psychiatric Genetics (WCPG 2021). Online. 2021-10-11 - 2021-10-15.
  • 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. Talk presented at the North Sea Meeting on Laterality. online. 2020-08-27.
  • 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.
  • 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.
  • 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.
  • 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., 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.
  • Carrion Castillo, A., Heister, A., Naber, M., van der Leij, A., Franke, B., Francks, C., Maassen, B., & Fisher, S. E. (2016). Association analysis of dyslexia candidate genes in a Dutch longitudinal sample. Talk presented at IWORDD - International Workshop on Reading and Developmental Dyslexia. Bilbao, Spain. 2016-05-05 - 2016-05-07.

    Abstract

    Dyslexia is a common learning disability with a known genetic component. Several candidate genes have been implicated in dyslexia susceptibility, such as ROBO1, KIAA0319, and DCDC2. Associations with variants in these genes have also been reported for a variety of psychometric measures that tackle underlying processes that might be impaired in dyslexic people. In this study, we first conducted a literature review to select single nucleotide polymorphisms (SNPs) in dyslexia candidate genes that had been repeatedly implicated in multiple studies. We then assessed the selected SNPs for association in a well-phenotyped longitudinal dataset: the Dutch Dyslexia Program longitudinal sample. We tested for association with several quantitative traits, including word and nonword reading fluency, rapid naming, phoneme deletion and nonword repetition, and took advantage of the longitudinal nature of the sample to examine if associations were stable across four developmental time-points (from 7 to 12 years). Two SNPs in the KIAA0319 gene were found to be nominally associated with rapid naming, and further analysis revealed that these associations were stable across different ages.
  • Francks, C. (2016). Genetics of atypical language lateralization. Talk presented at the MULTI-LATERAL consortium meeting. Bordeaux, France. 2016-07-05.
  • Francks, C. (2016). Multi-level integrated analysis of brain lateralization for language. Talk presented at the Human Brain Project summit meeting. Florence, Italy. 2016-10-14.
  • Francks, C. (2016). Multi-level integrated analysis of brain lateralization for language. Talk presented at the FLAG-ERA partnering project kick-off meeting. Budapest, Hungary. 2016-04-13.
  • Francks, C. (2016). The genetic bases of brain lateralization. Talk presented at the Language in Interaction Summerschool on Human Language: From Genes and Brains to Behavior. Berg en Dal, The Netherlands. 2016-07-03 - 2016-07-14.

    Abstract

    A degree of functional lateralization is characteristic of various aspects of human cognition, including aspects of language processing, which show left hemisphere dominance in most people. Left-right asymmetries of the human brain and behaviour are likely to arise from lateralized genetic-developmental programs that originate in the early embryo. In adults, a recent study of gene expression data from superior temporal and auditory cortex found subtle, quantitative lateralization of genes involved in synaptic transmission and neuronal electrophysiology. These observations are consistent with functional lateralization of this cortical region for language. Genetic polymorphisms that may have small, modifying effects on brain and behavioral asymmetries are starting to be identified through association studies, although core genetic mechanisms of asymmetrical brain development are not known. A major challenge will be to understand how neuronal circuits of the left and right hemisphere become differently fine-tuned, at the molecular level, to preferentially support particular cognitive functions. Through analyzing the inter-hemispheric genetic contrast, powerful insights may be gained into the exact properties of the left hemisphere's architecture which are particularly supportive of language-related functions
  • Guadalupe, T., & Francks, C. (2016). ENIGMA laterality group. Talk presented at the Enhancing Neuroimaging Genetics through Meta-Analysis consortium meeting. Geneva, Switzerland. 2016-06-24.
  • De Kovel, C. G. F., & Francks, C. (2016). Testing for lateralisation of gene expression in the human embryonic spinal cord. Talk presented at the North Sea Laterality 2016. Groningen, The Netherlands. 2016-09-01 - 2016-09-03.
  • Francks, C. (2015). The genetics of human brain asymmetries. Talk presented at the Hanse-Wissenschaftkolleg Workshop on Hemispheric Asymmetries: Language, Handedness and Beyond. Delmenhorst, Germany. 2015-11-21.
  • Guadalupe, T., & Francks, C. (2015). ENIGMA laterality group. Talk presented at the Enhancing Neuroimaging Genetics through Meta-Analysis consortium meeting. North Shore Oahu, Hawaii, USA. 2015-06-12.
  • 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.
  • Francks, C. (2013). Defending the discipline of genetics. Talk presented at the Donders Institute Theme 1 Meeting. Nijmegen, The Netherlands. 2013-06-20.
  • Francks, C. (2013). Genetics of brain asymmetries and left handedness. Talk presented at MPI Proudly Presents, Max Planck Institute for Psycholinguistics. Nijmegen, The Netherlands. 2013-06-18.
  • Francks, C. (2013). Genetics of brain asymmetries and left handedness. Talk presented at the Ruhr-University Bochum Institute of Cognitive Neuroscience. Bochum, Germany. 2013-08-05.
  • Francks, C., & Guadalupe, T. (2013). Genetics of left-handedness and brain asymmetries. Talk presented at the Workshop on Cerebral Lateralization. Nijmegen, The Netherlands. 2013-05.
  • Francks, C. (2013). Genetics of left-handedness and brain asymmetry. Talk presented at the workshop Handedness and Language, at the Netherlands Institute for Advanced Study in the Humanities and Social Sciences. Wassenaar, The Netherlands. 2013-11-28 - 2013-11-29.
  • Francks, C. (2013). Individual differences in brain asymmetry. Talk presented at the Donders Institute Theme 1 Meeting. Nijmegen, The Netherlands. 2013-01-17.
  • Guadalupe, T., Zwiers, M. P., Wittfeld, K., Teumer, A., Arias Vasquez, A., Hoogman, M., Hagoort, P., Van Bokhoven, H., Fernandez, G., Buitelaar, J., Franke, B., Fisher, S. E., Grabe, H. J., & Francks, C. (2013). Genome-wide association scanning for asymmetry of the human planum temporale. Talk presented at the Cognomics Symposium 2013. Nijmegen, The Netherlands. 2013-09-10 - 2013-09-11.
  • 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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