Presentations

Den Hoed, J. (2022). Modeling early stages of human brain development using brain organoids [invited talk]. Talk presented at Radboud Summer School - Induced Pluripotent Stem Cells: Maintenance, Differentiation, and Uses for Regenerative Medicine. Nijmegen, The Netherlands. 2022-07-11 - 2022-07-15.

Wong, M. M. K., Den Hoed, J., Kampen, R. A., Claassen, W., Lütje, L., Heide, M., Huttner, W. B., Van Bon, B. W., & Fisher, S. E. (2022). Delineating the neurobiological pathways involved in SETBP1 haploinsufficiency and related disorders using human brain organoids and transcriptomics. Talk presented at the Simons Searchlight and SETBP1 2022 Family & Research conference. online. 2022-08-04 - 2022-08-07.

Wong, M. M. K., Den Hoed, J., Kampen, R. A., Claassen, W., Lütje, L., Heide, M., Huttner, W. B., Van Bon, B. W., & Fisher, S. E. (2022). Understanding the neurobiology underlying SETBP1-related disorders using gene-editing and human cellular models. Talk presented at the Simons Searchlight and SETBP1 2022 Family & Research conference. online. 2022-08-04 - 2022-08-07.

Wong, M. M. K., Den Hoed, J., Lütje, L., Claassen, W., Heide, M., Huttner, W. B., Van Bon, B. W., & Fisher, S. E. (2021). Understanding the neurobiological pathways involved in speech-related disorders using human brain organoids: a SETBP1 study. Talk presented at the University of Nottingham Stem Cell Network. online. 2021-12-08.

Den Hoed, J., De Boer, E., Voisin, N., Guex, N., Snijders Blok, L., Chrast, J., The DDD study, Manwaring, L., Willing, M., Waheeb, A., Osmond, M., McWalter, K., Vitobello, A., Demurger, F., Lavillaureix, A., Odent, S., Mazel, B., Faivre, L., Thiffault, I., Schwager, C., Amudhavalli, S. M. and 27 moreDen Hoed, J., De Boer, E., Voisin, N., Guex, N., Snijders Blok, L., Chrast, J., The DDD study, Manwaring, L., Willing, M., Waheeb, A., Osmond, M., McWalter, K., Vitobello, A., Demurger, F., Lavillaureix, A., Odent, S., Mazel, B., Faivre, L., Thiffault, I., Schwager, C., Amudhavalli, S. M., Rosenfeld, J. A., Radtke, K., Preiksaitiene, E., Ranza, E., Depienne, C., Kuechler, A., Mohammed, S., Hamzavi Abedi, Y., Bonagura, V. R., Zuccarelli, B., Horist, B., Krishnamurthy, V., Kattentidt-Mouravieva, A. A., Granger, L., Petersen, A., Jones, K. L., Sinnema, M., Stegmann, A. P. A., Newbury-Ecob, R., Kini, U., Newbury, D. F., Gilissen, C., Brunner, H., Kleefstra, T., Reymond, A., Vissers, L. E. L. M., & Fisher, S. E. (2020). Mutation-specific pathophysiological mechanisms in a new SATB1 -associated neurodevelopmental disorder. Talk presented at the 53rd European Human Genetics Conference (ESHG 2020). online. 2020-06-06 - 2020-06-09.

Wong, M. M. K., Den Hoed, J., Heide, M., Huttner, W. B., Van Bon, B. W., & Fisher, S. E. (2020). Uncovering molecular mechanisms and neuronal pathways involved in SETBP1 disorder using human stem cell models. Talk presented at the Quarterly expert meetings for SETBP1 researchers organised by Simons Searchlight and SETBP1 Society. online. 2020-08-06.