Nael Nadif Kasri, Ph.D - Publications

Affiliations: 
Cns Radboud university medical centre 
Area:
Synaptic plasticity, epigenetics, intellectual disability
Website:
Http://Naidfkasri-lab.com

24 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any innacuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2019 van der Raadt J, van Gestel SHC, Nadif Kasri N, Albers CA. ONECUT transcription factors induce neuronal characteristics and remodel chromatin accessibility. Nucleic Acids Research. PMID 31049588 DOI: 10.1093/nar/gkz273  0.96
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  0.76
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  0.76
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  0.4
2016 Olde Loohuis NF, Nadif Kasri N, Glennon JC, van Bokhoven H, Hébert SS, Kaplan BB, Martens GJ, Aschrafi A. The schizophrenia risk gene MIR137 acts as a hippocampal gene network node orchestrating the expression of genes relevant to nervous system development and function. Progress in Neuro-Psychopharmacology & Biological Psychiatry. PMID 26925706 DOI: 10.1016/j.pnpbp.2016.02.009  1
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  1
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  0.96
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  0.36
2015 Brouwer M, Zhou H, Nadif Kasri N. Choices for Induction of Pluripotency: Recent Developments in Human Induced Pluripotent Stem Cell Reprogramming Strategies. Stem Cell Reviews. PMID 26424535 DOI: 10.1007/s12015-015-9622-8  1
2015 Kos A, Aschrafi A, Nadif Kasri N. The Multifarious Hippocampal Functions of MicroRNA-137. The Neuroscientist : a Review Journal Bringing Neurobiology, Neurology and Psychiatry. PMID 26396150 DOI: 10.1177/1073858415608356  0.32
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  0.76
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  1
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  1
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  0.6
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  1
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  1
2013 Balemans MC, Kasri NN, Kopanitsa MV, Afinowi NO, Ramakers G, Peters TA, Beynon AJ, Janssen SM, van Summeren RC, Eeftens JM, Eikelenboom N, Benevento M, Tachibana M, Shinkai Y, Kleefstra T, et al. Hippocampal dysfunction in the Euchromatin histone methyltransferase 1 heterozygous knockout mouse model for Kleefstra syndrome. Human Molecular Genetics. 22: 852-66. PMID 23175442 DOI: 10.1093/hmg/dds490  1
2012 Olde Loohuis NF, Kos A, Martens GJ, Van Bokhoven H, Nadif Kasri N, Aschrafi A. MicroRNA networks direct neuronal development and plasticity. Cellular and Molecular Life Sciences : Cmls. 69: 89-102. PMID 21833581 DOI: 10.1007/s00018-011-0788-1  1
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  1
2010 Nadif Kasri N, Van Aelst L. Spines and Mental Disorders Encyclopedia of Neuroscience. 329-335. DOI: 10.1016/B978-008045046-9.01797-6  1
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  0.48
2009 Nakano-Kobayashi A, Kasri NN, Newey SE, Van Aelst L. The Rho-linked mental retardation protein OPHN1 controls synaptic vesicle endocytosis via endophilin A1. Current Biology : Cb. 19: 1133-9. PMID 19481455 DOI: 10.1016/j.cub.2009.05.022  0.64
2008 Kasri NN, Govek EE, Van Aelst L. Characterization of oligophrenin-1, a RhoGAP lost in patients affected with mental retardation: lentiviral injection in organotypic brain slice cultures. Methods in Enzymology. 439: 255-66. PMID 18374170 DOI: 10.1016/S0076-6879(07)00419-3  0.72
2008 Nadif Kasri N, Van Aelst L. Rho-linked genes and neurological disorders. PflüGers Archiv : European Journal of Physiology. 455: 787-97. PMID 18004590 DOI: 10.1007/s00424-007-0385-1  1
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