Jeffrey Stedehouder

Affiliations: 
Erasmus Medical Center Rotterdam, Rotterdam, Netherlands 
Google:
"Jeffrey Stedehouder"
Mean distance: 16.21
 

Parents

Sign in to add mentor
Steven A. Kushner grad student Erasmus MC
Stephanie Cragg grad student 2021-2022 Oxford
 (Postdoctoral scientist)
BETA: Related publications

Publications

You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

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
Stedehouder J, Kushner SA. (2016) Myelination of parvalbumin interneurons: a parsimonious locus of pathophysiological convergence in schizophrenia Molecular Psychiatry
See more...