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Jon-Ruben van Rhijn
Jon-Ruben van Rhijn
Applied sciences teacher/researcher innovative testing
Verified email at hu.nl
Title
Cited by
Cited by
Year
Rapid neuronal differentiation of induced pluripotent stem cells for measuring network activity on micro-electrode arrays
M Frega, SHC Van Gestel, K Linda, J Van Der Raadt, J Keller, ...
JoVE (Journal of Visualized Experiments), e54900, 2017
1522017
Neuronal network dysfunction in a model for Kleefstra syndrome mediated by enhanced NMDAR signaling
M Frega, K Linda, JM Keller, G Gümüş-Akay, B Mossink, JR van Rhijn, ...
Nature communications 10 (1), 4928, 2019
1242019
Ptchd1 deficiency induces excitatory synaptic and cognitive dysfunctions in mouse
DC Ung, G Iacono, H Méziane, E Blanchard, MA Papon, M Selten, ...
Molecular psychiatry 23 (5), 1356-1367, 2018
812018
Cadherin-13 is a critical regulator of GABAergic modulation in human stem-cell-derived neuronal networks
B Mossink, JR Van Rhijn, S Wang, K Linda, MR Vitale, JEM Zöller, ...
Molecular Psychiatry 27 (1), 1-18, 2022
612022
Loss-of-function variants in the schizophrenia risk gene SETD1A alter neuronal network activity in human neurons through the cAMP/PKA pathway
S Wang, JR van Rhijn, I Akkouh, N Kogo, N Maas, A Bleeck, IS Ortiz, ...
Cell reports 39 (5), 2022
312022
Foxp2 loss of function increases striatal direct pathway inhibition via increased GABA release
JR van Rhijn, SE Fisher, SC Vernes, N Nadif Kasri
Brain Structure and Function 223, 4211-4226, 2018
262018
SETD1A mediated H3K4 methylation and its role in neurodevelopmental and neuropsychiatric disorders
S Wang, A Bleeck, N Nadif Kasri, T Kleefstra, JR van Rhijn, D Schubert
Frontiers in Molecular Neuroscience 14, 772000, 2021
182021
Brunner syndrome associated MAOA mutations result in NMDAR hyperfunction and increased network activity in human dopaminergic neurons
JR Van Rhijn, Y Shi, M Bormann, B Mossink, M Frega, H Recaioglu, ...
Neurobiology of disease 163, 105587, 2022
92022
Retinoic acid signaling: A new piece in the spoken language puzzle
JR Van Rhijn, SC Vernes
Frontiers in Psychology 6, 167151, 2015
82015
Neuronal network dysfunction in a human model for Kleefstra syndrome mediated by enhanced NMDAR signaling
M Frega, K Linda, JM Keller, G Gümüş-Akay, B Mossink, JR van Rhijn, ...
bioRxiv, 585596, 2019
72019
Neuronal network dysfunction in a model for Kleefstra syndrome mediated by enhanced NMDAR signaling. Nat. Commun. 10, 1–15
M Frega, K Linda, JM Keller, G Gümüsç-Akay, B Mossink, JR van Rhijn, ...
62019
Brunner Syndrome associated MAOA dysfunction in human induced dopaminergic neurons results in dysregulated NMDAR expression and increased network activity
Y Shi, JR Van Rhijn, M Bormann, B Mossink, M Frega, M Hakobjan, ...
bioRxiv, 741108, 2019
42019
A human in vitro neuronal model for studying homeostatic plasticity at the network level
X Yuan, S Puvogel, JR van Rhijn, U Ciptasari, A Esteve-Codina, M Meijer, ...
Stem cell reports 18 (11), 2222-2239, 2023
32023
Brunner syndrome associated MAOA dysfunction in human dopaminergic neurons results in NMDAR hyperfunction and increased network activity
Y Shi, JR van Rhijn, M Bormann, B Mossink, M Frega, H Recaioglu, ...
bioRxiv, 2020.10. 28.359224, 2020
2020
The cell-type specific contribution of EHMT1 to E/I balance in human in vitro neuronal networks
B Mossink, JR van Rhijn, AHA Verboven, G Parodi, S Wang, M Negwer, ...
The cell-type specific contribution of EHMT1 to neuronal network dysfunction …, 2020
2020
Cadherin 13 interacts with Integrin Beta-1 and Integrin Beta-3 to regulate inhibitory synaptic function in a human neuronal model
B Mossink, J van Rhijn, M Selten, K Linda, E van Hughte, J Bak, M Frega, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 27, 1435-1435, 2019
2019
van Rhijn, JR, Fisher, SE, Vernes, SC, and Nadif-Kasri, N.(2018). Foxp2 loss of function increases striatal direct pathway inhibition via increased GABA release. Submitted.
JR van Rhijn
FOXP2 IN, 201, 2019
2019
Heterozygous DNA-binding domain mutation of Foxp2 impairs striatal inhibition
JR van Rhijn, SE Fisher, SC Vernes, NN Kasri
FOXP2 IN, 93, 2019
2019
Reduced excitatory activity in a human dopaminergic model for FOXP2 homozygous deletion
JR van Rhijn, Y Shi, M Frega, D Schubert, T Maricic, S Pääbo, NN Kasri
FOXP2 IN, 133, 2019
2019
The role of FoxP2 in striatal circuitry
JR Van Rhijn
Radboud University Nijmegen Nijmegen, 2019
2019
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Articles 1–20