Presentations

Claassen, W., Den Hoed, J., Wong, M. M. K., Lütje, L., Heide, M., Huttner, W. B., & Fisher, S. E. (2022). Investigating the role of CHD3 in early brain development using brain organoids. Poster presented at the IMPRS conference 2022, Nijmegen, The Netherlands.

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., Lütje, L., Claassen, W., Van Bon, B., & Fisher, S. E. (2022). Uncovering neurobiological pathways involved in SETBP1 haploinsufficiency disorder during early development using human brain organoids. Poster presented at the FENS Forum 2022, Paris, France.

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., Van Bon, B., & Fisher, S. E. (2022). Uncovering neurobiological pathways involved in SETBP1 haploinsufficiency disorder during early development using human brain organoids. Poster presented at the Fachbeirat 2022 at the Max Planck Institute for Psycholinguistics, Nijmegen, The Netherlands.

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. Poster presented at the 53rd European Human Genetics Conference (ESHG 2020), online.

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.