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eIF2α phosphorylation bidirectionally regulates the switch from short-to long-term synaptic plasticity and memory M Costa-Mattioli, D Gobert, E Stern, K Gamache, R Colina, C Cuello, ... Cell 129 (1), 195-206, 2007 | 584 | 2007 |
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Local circuit interactions between oriens/alveus interneurons and CA1 pyramidal cells in hippocampal slices: electrophysiology and morphology JC Lacaille, AL Mueller, DD Kunkel, PA Schwartzkroin Journal of Neuroscience 7 (7), 1979-1993, 1987 | 476 | 1987 |
GABAergic network activation of glial cells underlies hippocampal heterosynaptic depression A Serrano, N Haddjeri, JC Lacaille, R Robitaille Journal of Neuroscience 26 (20), 5370-5382, 2006 | 474 | 2006 |
Excess of de novo deleterious mutations in genes associated with glutamatergic systems in nonsyndromic intellectual disability FF Hamdan, J Gauthier, Y Araki, DT Lin, Y Yoshizawa, K Higashi, AR Park, ... The American Journal of Human Genetics 88 (3), 306-316, 2011 | 421 | 2011 |
Mutations in SYNGAP1 in Autosomal Nonsyndromic Mental Retardation FF Hamdan, J Gauthier, D Spiegelman, A Noreau, Y Yang, S Pellerin, ... New England Journal of Medicine 360 (6), 599-605, 2009 | 389 | 2009 |
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Mutations in SYNGAP1 Cause Intellectual Disability, Autism, and a Specific Form of Epilepsy by Inducing Haploinsufficiency MH Berryer, FF Hamdan, LL Klitten, RS Møller, L Carmant, ... Human mutation 34 (2), 385-394, 2013 | 274 | 2013 |
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A hebbian form of long-term potentiation dependent on mGluR1a in hippocampal inhibitory interneurons Y Perez, F Morin, JC Lacaille Proceedings of the National Academy of Sciences 98 (16), 9401-9406, 2001 | 238 | 2001 |
De novo SYNGAP1 mutations in nonsyndromic intellectual disability and autism FF Hamdan, H Daoud, A Piton, J Gauthier, S Dobrzeniecka, MO Krebs, ... Biological psychiatry 69 (9), 898-901, 2011 | 233 | 2011 |
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Axonal sprouting of CA1 pyramidal cells in hyperexcitable hippocampal slices of kainate‐treated rats Y Perez, F Morin, C Beaulieu, JC Lacaille European Journal of Neuroscience 8 (4), 736-748, 1996 | 203 | 1996 |
De novo STXBP1 mutations in mental retardation and nonsyndromic epilepsy FF Hamdan, A Piton, J Gauthier, A Lortie, F Dubeau, S Dobrzeniecka, ... Annals of Neurology: Official Journal of the American Neurological …, 2009 | 192 | 2009 |