Jeffrey Stedehouder
Affiliations: | Erasmus Medical Center Rotterdam, Rotterdam, Netherlands |
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Parents
Sign in to add mentor| Steven A. Kushner | grad student | Erasmus MC | ||
| Stephanie Cragg | grad student | 2021-2022 | Oxford | |
| (Postdoctoral scientist) | ||||
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Publications
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| Stedehouder J, Roberts BM, Raina S, et al. (2024) Rapid modulation of striatal cholinergic interneurons and dopamine release by satellite astrocytes. Nature Communications. 15: 10017 |
| Stedehouder J, Brizee D, Slotman JA, et al. (2019) Local axonal morphology guides the topography of interneuron myelination in mouse and human neocortex. Elife. 8 |
| Avagliano Trezza R, Sonzogni M, Bossuyt SNV, et al. (2019) Loss of nuclear UBE3A causes electrophysiological and behavioral deficits in mice and is associated with Angelman syndrome. Nature Neuroscience |
| Stedehouder J, Brizee D, Slotman JA, et al. (2019) Author response: Local axonal morphology guides the topography of interneuron myelination in mouse and human neocortex Elife |
| Amin N, de Vrij FMS, Baghdadi M, et al. (2018) Employed family-based genetic discovery combining linkage analysis and exome sequencing to identify RCL1 as a novel candidate gene for depression, with independent replication in a population-based cohort. Molecular Psychiatry. 23: 1093 |
| Stedehouder J, Brizee D, Shpak G, et al. (2018) Activity-Dependent Myelination of Parvalbumin Interneurons Mediated by Axonal Morphological Plasticity. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 38: 3631-3642 |
| Stedehouder J, Couey JJ, Brizee D, et al. (2017) Fast-spiking Parvalbumin Interneurons are Frequently Myelinated in the Cerebral Cortex of Mice and Humans. Cerebral Cortex (New York, N.Y. : 1991). 27: 5001-5013 |
| Schreiber J, Grimbergen LA, Overwater I, et al. (2017) Mechanisms underlying cognitive deficits in a mouse model for Costello Syndrome are distinct from other RASopathy mouse models. Scientific Reports. 7: 1256 |
| Amin N, de Vrij FM, Baghdadi M, et al. (2017) A rare missense variant in RCL1 segregates with depression in extended families. Molecular Psychiatry |
| Peter S, Ten Brinke MM, Stedehouder J, et al. (2016) Dysfunctional cerebellar Purkinje cells contribute to autism-like behaviour in Shank2-deficient mice. Nature Communications. 7: 12627 |