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Nadif Kasri Nael
Nadif Kasri Nael
RadboudUMC, Donders institute for Brain cognition and behaviour
Verified email at donders.ru.nl - Homepage
Title
Cited by
Cited by
Year
Disruption of an EHMT1-associated chromatin-modification module causes intellectual disability
T Kleefstra, JM Kramer, K Neveling, MH Willemsen, TS Koemans, ...
The American Journal of Human Genetics 91 (1), 73-82, 2012
2852012
MicroRNA networks direct neuronal development and plasticity
NFM Olde Loohuis, A Kos, GJM Martens, H Van Bokhoven, N Nadif Kasri, ...
Cellular and Molecular Life Sciences 69, 89-102, 2012
2802012
Inhibitory control of the excitatory/inhibitory balance in psychiatric disorders
M Selten, H van Bokhoven, NN Kasri
F1000Research 7, 2018
2102018
Regulation of InsP3 receptor activity by neuronal Ca2+‐binding proteins
NN Kasri, AM Holmes, G Bultynck, JB Parys, MD Bootman, K Rietdorf, ...
The EMBO journal 23 (2), 312-321, 2004
1862004
Caspase-3-induced truncation of type 1 inositol trisphosphate receptor accelerates apoptotic cell death and induces inositol trisphosphate-independent calcium release during …
Z Assefa, G Bultynck, K Szlufcik, NN Kasri, E Vermassen, J Goris, ...
Journal of Biological Chemistry 279 (41), 43227-43236, 2004
1772004
The Rho-linked mental retardation protein oligophrenin-1 controls synapse maturation and plasticity by stabilizing AMPA receptors
NN Kasri, A Nakano-Kobayashi, R Malinow, B Li, L Van Aelst
Genes & development 23 (11), 1289-1302, 2009
1632009
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
1582017
The Koolen-de Vries syndrome: a phenotypic comparison of patients with a 17q21. 31 microdeletion versus a KANSL1 sequence variant
DA Koolen, R Pfundt, K Linda, G Beunders, HE Veenstra-Knol, JH Conta, ...
European Journal of Human Genetics 24 (5), 652-659, 2016
1452016
Epigenetic etiology of intellectual disability
S Iwase, NG Bérubé, Z Zhou, NN Kasri, E Battaglioli, M Scandaglia, ...
Journal of Neuroscience 37 (45), 10773-10782, 2017
1432017
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
1272019
Cadherin-13, a risk gene for ADHD and comorbid disorders, impacts GABAergic function in hippocampus and cognition
O Rivero, MM Selten, S Sich, S Popp, L Bacmeister, E Amendola, ...
Translational psychiatry 5 (10), e655-e655, 2015
1252015
Thimerosal stimulates Ca2+ flux through inositol 1,4,5-trisphosphate receptor type 1, but not type 3, via modulation of an isoform-specific Ca2+-dependent …
G Bultynck, K Szlufcik, NN Kasri, Z Assefa, G Callewaert, L Missiaen, ...
Biochemical Journal 381 (1), 87-96, 2004
1242004
Rho-linked genes and neurological disorders
N Nadif Kasri, L Van Aelst
Pflügers Archiv-European Journal of Physiology 455, 787-797, 2008
1232008
Rho GTPase signaling at the synapse: implications for intellectual disability
W Ba, J van der Raadt, NN Kasri
Experimental cell research 319 (15), 2368-2374, 2013
1222013
Choices for induction of pluripotency: recent developments in human induced pluripotent stem cell reprogramming strategies
M Brouwer, H Zhou, N Nadif Kasri
Stem Cell Reviews and Reports 12, 54-72, 2016
1112016
MicroRNA-137 controls AMPA-receptor-mediated transmission and mGluR-dependent LTD
NFMO Loohuis, W Ba, PH Stoerchel, A Kos, A Jager, G Schratt, ...
Cell reports 11 (12), 1876-1884, 2015
1082015
Involvement of the kinesin family members KIF4A and KIF5C in intellectual disability and synaptic function
MH Willemsen, W Ba, WM Wissink-Lindhout, APM de Brouwer, SA Haas, ...
Journal of medical genetics 51 (7), 487-494, 2014
1022014
The Rho-linked mental retardation protein OPHN1 controls synaptic vesicle endocytosis via endophilin A1
A Nakano-Kobayashi, NN Kasri, SE Newey, L Van Aelst
Current Biology 19 (13), 1133-1139, 2009
1002009
TRIO loss of function is associated with mild intellectual disability and affects dendritic branching and synapse function
W Ba, Y Yan, MRF Reijnders, JHM Schuurs-Hoeijmakers, I Feenstra, ...
Human molecular genetics 25 (5), 892-902, 2016
982016
Localization and function of a calmodulin–apocalmodulin-binding domain in the N-terminal part of the type 1 inositol 1, 4, 5-trisphosphate receptor
I Sienaert, NN Kasri, S Vanlingen, JB Parys, G Callewaert, L Missiaen, ...
Biochemical Journal 365 (1), 269-277, 2002
952002
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