| 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 | 286 | 2012 |
| 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 | 280 | 2012 |
| Inhibitory control of the excitatory/inhibitory balance in psychiatric disorders M Selten, H van Bokhoven, NN Kasri F1000Research 7, 2018 | 211 | 2018 |
| 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 | 186 | 2004 |
| 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 | 177 | 2004 |
| 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 | 163 | 2009 |
| 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 | 158 | 2017 |
| 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 | 145 | 2016 |
| 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 | 144 | 2017 |
| 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 | 127 | 2019 |
| 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 | 125 | 2015 |
| 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 | 124 | 2004 |
| Rho-linked genes and neurological disorders N Nadif Kasri, L Van Aelst Pflügers Archiv-European Journal of Physiology 455, 787-797, 2008 | 123 | 2008 |
| 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 | 122 | 2013 |
| 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 | 111 | 2016 |
| 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 | 108 | 2015 |
| 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 | 102 | 2014 |
| 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 | 100 | 2009 |
| 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 | 98 | 2016 |
| 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 | 95 | 2002 |
