Nael Nadif Kasri, Ph.D
Affiliations: | Cns | Radboud university medical centre |
Area:
Synaptic plasticity, epigenetics, intellectual disabilityWebsite:
Http://Naidfkasri-lab.comGoogle:
"Nael Nadif Kasri"Mean distance: 16.86 (cluster 6)
Parents
Sign in to add mentor| Humbert de Smedt | grad student | 2000-2004 | KU Leuven |
| Linda Van Aelst | grad student | 2005-2010 | CSHL |
Children
Sign in to add trainee| Wei Ba | grad student | 2011-2016 | Radboud university medical centre |
| Marco Benevento | grad student | 2011-2016 | Radboud university medical centre |
| Martijn M. Selten | grad student | 2011-2016 | Radboud university medical centre |
| Jon-Ruben van Rhijn | grad student | 2013-2017 | Radboud university medical centre |
| Kartin Linda | grad student | 2014-2018 | Radboud university medical centre |
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Publications
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| Mihailovich M, Germain PL, Shyti R, et al. (2024) Multiscale modeling uncovers 7q11.23 copy number variation-dependent changes in ribosomal biogenesis and neuronal maturation and excitability. The Journal of Clinical Investigation. 134 |
| Yuan X, Puvogel S, van Rhijn JR, et al. (2023) A human in vitro neuronal model for studying homeostatic plasticity at the network level. Stem Cell Reports. 18: 2222-2239 |
| Lewerissa EI, Nadif Kasri N, Linda K. (2023) Epigenetic regulation of genes: Implications for neurodevelopmental disorders. Autophagy. 1-14 |
| Doorn N, van Hugte EJH, Ciptasari U, et al. (2023) An in silico and in vitro human neuronal network model reveals cellular mechanisms beyond Na1.1 underlying Dravet syndrome. Stem Cell Reports |
| Giansante G, Mazzoleni S, Zippo AG, et al. (2023) Neuronal network activity and connectivity are impaired in a conditional knockout mouse model with PCDH19 mosaic expression. Molecular Psychiatry |
| Wang S, Rhijn JV, Akkouh I, et al. (2022) Loss-of-function variants in the schizophrenia risk gene SETD1A alter neuronal network activity in human neurons through the cAMP/PKA pathway. Cell Reports. 39: 110790 |
| van Rhijn JR, Shi Y, Bormann M, et al. (2021) Brunner syndrome associated MAOA mutations result in NMDAR hyperfunction and increased network activity in human dopaminergic neurons. Neurobiology of Disease. 163: 105587 |
| Wang S, Bleeck A, Nadif Kasri N, et al. (2021) SETD1A Mediated H3K4 Methylation and Its Role in Neurodevelopmental and Neuropsychiatric Disorders. Frontiers in Molecular Neuroscience. 14: 772000 |
| Linda K, Lewerissa EI, Verboven AHA, et al. (2021) Imbalanced autophagy causes synaptic deficits in a human model for neurodevelopmental disorders. Autophagy. 1-20 |
| Mossink B, van Rhijn JR, Wang S, et al. (2021) Cadherin-13 is a critical regulator of GABAergic modulation in human stem-cell-derived neuronal networks. Molecular Psychiatry |