Marco Benevento - Publications

Affiliations: 
2011-2016 CNS Radboud university medical centre 

8 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, 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
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  0.584
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  0.681
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  0.597
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  0.588
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  0.603
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, 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  0.658
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  0.591
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  0.5
Show low-probability matches.