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Transcriptomic profiling of unmethylated full mutation carriers implicates TET3 in FMR1 CGG repeat expansion methylation dynamics in fragile X syndrome
Farmiloe, G., Bejczy, V., Tabolacci, E., Willemsen, R. & Jacobs, F., 26 Apr 2025, In: JOURNAL OF NEURODEVELOPMENTAL DISORDERS. 17, 15 p., 22.Research output: Contribution to journal › Article* › Academic › peer-review
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ZNF91 is an endogenous repressor of the molecular phenotype associated with X-linked dystonia-parkinsonism (XDP)
Rosenkrantz, J. L., Brandorff, J. E., Raghib, S., Kapadia, A., Vaine, C. A., Bragg, D. C., Farmiloe, G. & Jacobs, F. M. J., 13 Aug 2024, In: Proceedings of the National Academy of Sciences. 121, 33, 12 p., e2401217121.Research output: Contribution to journal › Article* › Academic › peer-review
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Emergence of the ZNF675 Gene During Primate Evolution–Influenced Human Neurodevelopment Through Changing HES1 Autoregulation
Lodewijk, G. A., de Geus, M., Guimarães, R. L. F. P. & Jacobs, F. M. J., Jul 2024, In: The journal of comparative neurology. 532, 7, 13 p., e25648.Research output: Contribution to journal › Article* › Academic › peer-review
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