Geeske van Woerden
Affiliations: | Erasmus Medical Center Rotterdam, Rotterdam, Netherlands |
Area:
learning and memoryGoogle:
"Geeske van Woerden"Mean distance: 16.3 (cluster 6) | S | N | B | C | P |
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Publications
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Küry S, Stanton JE, van Woerden G, et al. (2024) Unveiling the crucial neuronal role of the proteasomal ATPase subunit gene in neurodevelopmental proteasomopathies. Medrxiv : the Preprint Server For Health Sciences |
Rigter PMF, de Konink C, Dunn MJ, et al. (2024) Role of CAMK2D in neurodevelopment and associated conditions. American Journal of Human Genetics |
Ebstein F, Küry S, Most V, et al. (2023) PSMC3 proteasome subunit variants are associated with neurodevelopmental delay and type I interferon production. Science Translational Medicine. 15: eabo3189 |
Rigter PMF, Wallaard I, Aghadavoud Jolfaei M, et al. (2022) Adult gene reinstatement restores the learning and plasticity deficits of knockout mice. Iscience. 25: 105303 |
van Woerden GM, Senden R, de Konink C, et al. (2022) The MAP3K7 gene: further delineation of clinical characteristics and genotype/phenotype correlations. Human Mutation |
Proietti Onori M, Koene LMC, Schäfer CB, et al. (2021) RHEB/mTOR hyperactivity causes cortical malformations and epileptic seizures through increased axonal connectivity. Plos Biology. 19: e3001279 |
Proietti Onori M, van Woerden GM. (2021) Role of calcium/calmodulin-dependent kinase 2 in neurodevelopmental disorders. Brain Research Bulletin. 171: 209-220 |
van Woerden GM, Bos M, de Konink C, et al. (2021) TAOK1 is associated with neurodevelopmental disorder and essential for neuronal maturation and cortical development. Human Mutation |
Sonzogni M, Zhai P, Mientjes EJ, et al. (2020) Assessing the requirements of prenatal UBE3A expression for rescue of behavioral phenotypes in a mouse model for Angelman syndrome. Molecular Autism. 11: 70 |
Tonazzini I, Van Woerden GM, Masciullo C, et al. (2019) The role of ubiquitin ligase E3A in polarized contact guidance and rescue strategies in UBE3A-deficient hippocampal neurons. Molecular Autism. 10: 41 |