| Year |
Citation |
Score |
| 2023 |
Yuan X, Puvogel S, van Rhijn JR, Ciptasari U, Esteve-Codina A, Meijer M, Rouschop S, van Hugte EJH, Oudakker A, Schoenmaker C, Frega M, Schubert D, Franke B, Nadif Kasri N. A human in vitro neuronal model for studying homeostatic plasticity at the network level. Stem Cell Reports. 18: 2222-2239. PMID 37863044 DOI: 10.1016/j.stemcr.2023.09.011 |
0.388 |
|
| 2023 |
Lewerissa EI, Nadif Kasri N, Linda K. Epigenetic regulation of genes: Implications for neurodevelopmental disorders. Autophagy. 1-14. PMID 37674294 DOI: 10.1080/15548627.2023.2250217 |
0.334 |
|
| 2023 |
Doorn N, van Hugte EJH, Ciptasari U, Mordelt A, Meijer HGE, Schubert D, Frega M, Nadif Kasri N, van Putten MJAM. An in silico and in vitro human neuronal network model reveals cellular mechanisms beyond Na1.1 underlying Dravet syndrome. Stem Cell Reports. PMID 37419110 DOI: 10.1016/j.stemcr.2023.06.003 |
0.338 |
|
| 2023 |
Giansante G, Mazzoleni S, Zippo AG, Ponzoni L, Ghilardi A, Maiellano G, Lewerissa E, van Hugte E, Nadif Kasri N, Francolini M, Sala M, Murru L, Bassani S, Passafaro M. Neuronal network activity and connectivity are impaired in a conditional knockout mouse model with PCDH19 mosaic expression. Molecular Psychiatry. PMID 36997609 DOI: 10.1038/s41380-023-02022-1 |
0.428 |
|
| 2022 |
Wang S, Rhijn JV, Akkouh I, Kogo N, Maas N, Bleeck A, Ortiz IS, Lewerissa E, Wu KM, Schoenmaker C, Djurovic S, van Bokhoven H, Kleefstra T, Nadif Kasri N, Schubert D. Loss-of-function variants in the schizophrenia risk gene SETD1A alter neuronal network activity in human neurons through the cAMP/PKA pathway. Cell Reports. 39: 110790. PMID 35508131 DOI: 10.1016/j.celrep.2022.110790 |
0.713 |
|
| 2021 |
van Rhijn JR, Shi Y, Bormann M, Mossink B, Frega M, Recaioglu H, Hakobjan M, Klein Gunnewiek T, Schoenmaker C, Palmer E, Faivre L, Kittel-Schneider S, Schubert D, Brunner H, Franke B, ... Nadif Kasri N, et al. Brunner syndrome associated MAOA mutations result in NMDAR hyperfunction and increased network activity in human dopaminergic neurons. Neurobiology of Disease. 163: 105587. PMID 34923109 DOI: 10.1016/j.nbd.2021.105587 |
0.424 |
|
| 2021 |
Wang S, Bleeck A, Nadif Kasri N, Kleefstra T, van Rhijn JR, Schubert D. SETD1A Mediated H3K4 Methylation and Its Role in Neurodevelopmental and Neuropsychiatric Disorders. Frontiers in Molecular Neuroscience. 14: 772000. PMID 34803610 DOI: 10.3389/fnmol.2021.772000 |
0.405 |
|
| 2021 |
Linda K, Lewerissa EI, Verboven AHA, Gabriele M, Frega M, Klein Gunnewiek TM, Devilee L, Ulferts E, Hommersom M, Oudakker A, Schoenmaker C, van Bokhoven H, Schubert D, Testa G, Koolen DA, ... ... Nadif Kasri N, et al. Imbalanced autophagy causes synaptic deficits in a human model for neurodevelopmental disorders. Autophagy. 1-20. PMID 34286667 DOI: 10.1080/15548627.2021.1936777 |
0.442 |
|
| 2021 |
Mossink B, van Rhijn JR, Wang S, Linda K, Vitale MR, Zöller JEM, van Hugte EJH, Bak J, Verboven AHA, Selten M, Negwer M, Latour BL, van der Werf I, Keller JM, Klein Gunnewiek TM, ... ... Nadif Kasri N, et al. Cadherin-13 is a critical regulator of GABAergic modulation in human stem-cell-derived neuronal networks. Molecular Psychiatry. PMID 33972691 DOI: 10.1038/s41380-021-01117-x |
0.803 |
|
| 2021 |
Schörnig M, Ju X, Fast L, Ebert S, Weigert A, Kanton S, Schaffer T, Nadif Kasri N, Treutlein B, Peter BM, Hevers W, Taverna E. Comparison of induced neurons reveals slower structural and functional maturation in humans than in apes. Elife. 10. PMID 33470930 DOI: 10.7554/eLife.59323 |
0.312 |
|
| 2020 |
Mossink B, Negwer M, Schubert D, Nadif Kasri N. The emerging role of chromatin remodelers in neurodevelopmental disorders: a developmental perspective. Cellular and Molecular Life Sciences : Cmls. PMID 33263776 DOI: 10.1007/s00018-020-03714-5 |
0.311 |
|
| 2020 |
Negwer M, Piera K, Hesen R, Lütje L, Aarts L, Schubert D, Nadif Kasri N. EHMT1 regulates Parvalbumin-positive interneuron development and GABAergic input in sensory cortical areas. Brain Structure & Function. PMID 32975655 DOI: 10.1007/s00429-020-02149-9 |
0.344 |
|
| 2020 |
Klein Gunnewiek TM, Van Hugte EJH, Frega M, Guardia GS, Foreman K, Panneman D, Mossink B, Linda K, Keller JM, Schubert D, Cassiman D, Rodenburg R, Vidal Folch N, Oglesbee D, Perales-Clemente E, ... ... Nadif Kasri N, et al. m.3243A > G-Induced Mitochondrial Dysfunction Impairs Human Neuronal Development and Reduces Neuronal Network Activity and Synchronicity. Cell Reports. 31: 107538. PMID 32320658 DOI: 10.1016/j.celrep.2020.107538 |
0.3 |
|
| 2020 |
Frega M, Selten M, Mossink B, Keller JM, Linda K, Moerschen R, Qu J, Koerner P, Jansen S, Oudakker A, Kleefstra T, van Bokhoven H, Zhou H, Schubert D, Nadif Kasri N. Distinct Pathogenic Genes Causing Intellectual Disability and Autism Exhibit a Common Neuronal Network Hyperactivity Phenotype. Cell Reports. 30: 173-186.e6. PMID 31914384 DOI: 10.1016/J.Celrep.2019.12.002 |
0.807 |
|
| 2019 |
Frega M, Linda K, Keller JM, Gümüş-Akay G, Mossink B, van Rhijn JR, Negwer M, Klein Gunnewiek T, Foreman K, Kompier N, Schoenmaker C, van den Akker W, van der Werf I, Oudakker A, Zhou H, ... ... Nadif Kasri N, et al. Neuronal network dysfunction in a model for Kleefstra syndrome mediated by enhanced NMDAR signaling. Nature Communications. 10: 4928. PMID 31666522 DOI: 10.1038/S41467-019-12947-3 |
0.403 |
|
| 2018 |
van Rhijn JR, Fisher SE, Vernes SC, Nadif Kasri N. Foxp2 loss of function increases striatal direct pathway inhibition via increased GABA release. Brain Structure & Function. PMID 30187194 DOI: 10.1007/S00429-018-1746-6 |
0.301 |
|
| 2018 |
Selten M, van Bokhoven H, Nadif Kasri N. Inhibitory control of the excitatory/inhibitory balance in psychiatric disorders. F1000research. 7: 23. PMID 29375819 DOI: 10.12688/F1000Research.12155.1 |
0.8 |
|
| 2017 |
Iacono G, Benevento M, Dubos A, Herault Y, van Bokhoven H, Nadif Kasri N, Stunnenberg HG. Integrated transcriptional analysis unveils the dynamics of cellular differentiation in the developing mouse hippocampus. Scientific Reports. 7: 18073. PMID 29273784 DOI: 10.1038/s41598-017-18287-w |
0.677 |
|
| 2017 |
Linda K, Fiuza C, Nadif Kasri N. The promise of induced pluripotent stem cells for neurodevelopmental disorders. Progress in Neuro-Psychopharmacology & Biological Psychiatry. PMID 29128445 DOI: 10.1016/j.pnpbp.2017.11.009 |
0.329 |
|
| 2017 |
Arbogast T, Iacono G, Chevalier C, Afinowi NO, Houbaert X, van Eede MC, Laliberte C, Birling MC, Linda K, Meziane H, Selloum M, Sorg T, Nadif Kasri N, Koolen DA, Stunnenberg HG, et al. Mouse models of 17q21.31 microdeletion and microduplication syndromes highlight the importance of Kansl1 for cognition. Plos Genetics. 13: e1006886. PMID 28704368 DOI: 10.1371/Journal.Pgen.1006886 |
0.309 |
|
| 2017 |
Ung DC, Iacono G, Méziane H, Blanchard E, Papon MA, Selten M, van Rhijn JR, Montjean R, Rucci J, Martin S, Fleet A, Birling MC, Marouillat S, Roepman R, Selloum M, ... ... Nadif Kasri N, et al. Ptchd1 deficiency induces excitatory synaptic and cognitive dysfunctions in mouse. Molecular Psychiatry. PMID 28416808 DOI: 10.1038/Mp.2017.39 |
0.82 |
|
| 2017 |
Miceli S, Nadif Kasri N, Joosten J, Huang C, Kepser L, Proville R, Selten MM, van Eijs F, Azarfar A, Homberg JR, Celikel T, Schubert D. Reduced Inhibition within Layer IV of Sert Knockout Rat Barrel Cortex is Associated with Faster Sensory Integration. Cerebral Cortex (New York, N.Y. : 1991). 1-17. PMID 28158484 DOI: 10.1093/Cercor/Bhx016 |
0.755 |
|
| 2017 |
Frega M, van Gestel SH, Linda K, van der Raadt J, Keller J, Van Rhijn JR, Schubert D, Albers CA, Nadif Kasri N. Rapid Neuronal Differentiation of Induced Pluripotent Stem Cells for Measuring Network Activity on Micro-electrode Arrays. Journal of Visualized Experiments : Jove. PMID 28117798 DOI: 10.3791/54900 |
0.308 |
|
| 2016 |
Bart Martens M, Frega M, Classen J, Epping L, Bijvank E, Benevento M, van Bokhoven H, Tiesinga P, Schubert D, Nadif Kasri N. Euchromatin histone methyltransferase 1 regulates cortical neuronal network development. Scientific Reports. 6: 35756. PMID 27767173 DOI: 10.1038/srep35756 |
0.779 |
|
| 2016 |
Ba W, Nadif Kasri N. RhoGTPases at the synapse: An embarrassment of choice. Small Gtpases. 1-8. PMID 27492682 DOI: 10.1080/21541248.2016.1206352 |
0.774 |
|
| 2016 |
Benevento M, Iacono G, Selten M, Ba W, Oudakker A, Frega M, Keller J, Mancini R, Lewerissa E, Kleefstra T, Stunnenberg HG, Zhou H, van Bokhoven H, Nadif Kasri N. Histone Methylation by the Kleefstra Syndrome Protein EHMT1 Mediates Homeostatic Synaptic Scaling. Neuron. PMID 27373831 DOI: 10.1016/J.Neuron.2016.06.003 |
0.779 |
|
| 2016 |
Ba W, Selten MM, van der Raadt J, van Veen H, Li LL, Benevento M, Oudakker AR, Lasabuda RS, Letteboer SJ, Roepman R, van Wezel RJ, Courtney MJ, van Bokhoven H, Nadif Kasri N. ARHGAP12 Functions as a Developmental Brake on Excitatory Synapse Function. Cell Reports. PMID 26854232 DOI: 10.1016/J.Celrep.2016.01.037 |
0.764 |
|
| 2015 |
Ba W, Yan Y, Reijnders MR, Schuurs-Hoeijmakers JH, Feenstra I, Bongers EM, Bosch DG, de Leeuw N, Pfundt R, Gilissen C, de Vries PF, Veltman JA, Hoischen A, Mefford HC, Eichler EE, ... ... Nadif Kasri N, et al. TRIO loss of function is associated with mild intellectual disability and affects dendritic branching and synapse function. Human Molecular Genetics. PMID 26721934 DOI: 10.1093/Hmg/Ddv618 |
0.774 |
|
| 2015 |
Rivero O, Selten MM, Sich S, Popp S, Bacmeister L, Amendola E, Negwer M, Schubert D, Proft F, Kiser D, Schmitt AG, Gross C, Kolk SM, Strekalova T, van den Hove D, ... ... Nadif Kasri N, et al. Cadherin-13, a risk gene for ADHD and comorbid disorders, impacts GABAergic function in hippocampus and cognition. Translational Psychiatry. 5: e655. PMID 26460479 DOI: 10.1038/Tp.2015.152 |
0.804 |
|
| 2015 |
Koolen DA, Pfundt R, Linda K, Beunders G, Veenstra-Knol HE, Conta JH, Fortuna AM, Gillessen-Kaesbach G, Dugan S, Halbach S, Abdul-Rahman OA, Winesett HM, Chung WK, Dalton M, Dimova PS, ... ... Nadif Kasri N, et al. The Koolen-de Vries syndrome: a phenotypic comparison of patients with a 17q21.31 microdeletion versus a KANSL1 sequence variant. European Journal of Human Genetics : Ejhg. PMID 26306646 DOI: 10.1038/ejhg.2015.178 |
0.72 |
|
| 2015 |
Benevento M, van de Molengraft M, van Westen R, van Bokhoven H, Nadif Kasri N. The role of chromatin repressive marks in cognition and disease: A focus on the repressive complex GLP/G9a. Neurobiology of Learning and Memory. 124: 88-96. PMID 26143996 DOI: 10.1016/j.nlm.2015.06.013 |
0.687 |
|
| 2015 |
Olde Loohuis NF, Ba W, Stoerchel PH, Kos A, Jager A, Schratt G, Martens GJ, van Bokhoven H, Nadif Kasri N, Aschrafi A. MicroRNA-137 Controls AMPA-Receptor-Mediated Transmission and mGluR-Dependent LTD. Cell Reports. 11: 1876-84. PMID 26095359 DOI: 10.1016/J.Celrep.2015.05.040 |
0.677 |
|
| 2015 |
Iqbal Z, Willemsen MH, Papon MA, Musante L, Benevento M, Hu H, Venselaar H, Wissink-Lindhout WM, Vulto-van Silfhout AT, Vissers LE, de Brouwer AP, Marouillat S, Wienker TF, Ropers HH, Kahrizi K, ... Nadif Kasri N, et al. Homozygous SLC6A17 mutations cause autosomal-recessive intellectual disability with progressive tremor, speech impairment, and behavioral problems. American Journal of Human Genetics. 96: 386-96. PMID 25704603 DOI: 10.1016/J.Ajhg.2015.01.010 |
0.753 |
|
| 2014 |
Nakano-Kobayashi A, Tai Y, Nadif Kasri N, Van Aelst L. The X-linked mental retardation protein OPHN1 interacts with Homer1b/c to control spine endocytic zone positioning and expression of synaptic potentiation. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 34: 8665-71. PMID 24966368 DOI: 10.1523/JNEUROSCI.0894-14.2014 |
0.666 |
|
| 2014 |
Willemsen MH, Ba W, Wissink-Lindhout WM, de Brouwer AP, Haas SA, Bienek M, Hu H, Vissers LE, van Bokhoven H, Kalscheuer V, Nadif Kasri N, Kleefstra T. Involvement of the kinesin family members KIF4A and KIF5C in intellectual disability and synaptic function. Journal of Medical Genetics. 51: 487-94. PMID 24812067 DOI: 10.1136/Jmedgenet-2013-102182 |
0.736 |
|
| 2014 |
Balemans MC, Ansar M, Oudakker AR, van Caam AP, Bakker B, Vitters EL, van der Kraan PM, de Bruijn DR, Janssen SM, Kuipers AJ, Huibers MM, Maliepaard EM, Walboomers XF, Benevento M, Nadif Kasri N, et al. Reduced Euchromatin histone methyltransferase 1 causes developmental delay, hypotonia, and cranial abnormalities associated with increased bone gene expression in Kleefstra syndrome mice. Developmental Biology. 386: 395-407. PMID 24362066 DOI: 10.1016/J.Ydbio.2013.12.016 |
0.69 |
|
| 2013 |
Ba W, van der Raadt J, Nadif Kasri N. Rho GTPase signaling at the synapse: implications for intellectual disability. Experimental Cell Research. 319: 2368-74. PMID 23769912 DOI: 10.1016/j.yexcr.2013.05.033 |
0.735 |
|
| 2011 |
Nadif Kasri N, Nakano-Kobayashi A, Van Aelst L. Rapid synthesis of the X-linked mental retardation protein OPHN1 mediates mGluR-dependent LTD through interaction with the endocytic machinery. Neuron. 72: 300-15. PMID 22017989 DOI: 10.1016/j.neuron.2011.09.001 |
0.618 |
|
| 2010 |
Nadif Kasri N, Van Aelst L. Spines and Mental Disorders Encyclopedia of Neuroscience. 329-335. DOI: 10.1016/B978-008045046-9.01797-6 |
0.54 |
|
| 2009 |
Nadif Kasri N, Nakano-Kobayashi A, Malinow R, Li B, Van Aelst L. The Rho-linked mental retardation protein oligophrenin-1 controls synapse maturation and plasticity by stabilizing AMPA receptors. Genes & Development. 23: 1289-302. PMID 19487570 DOI: 10.1101/Gad.1783809 |
0.682 |
|
| 2008 |
Nadif Kasri N, Van Aelst L. Rho-linked genes and neurological disorders. Pflã¼Gers Archiv : European Journal of Physiology. 455: 787-97. PMID 18004590 DOI: 10.1007/s00424-007-0385-1 |
0.647 |
|
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