Astrocytes are endogenous regulators of basal transmission at central synapses A Panatier, J Vallée, M Haber, KK Murai, JC Lacaille, R Robitaille Cell 146 (5), 785-798, 2011 | 718 | 2011 |
Autism-related deficits via dysregulated eIF4E-dependent translational control CG Gkogkas, A Khoutorsky, I Ran, E Rampakakis, T Nevarko, ... Nature 493 (7432), 371-377, 2013 | 591 | 2013 |
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 | 591 | 2007 |
Translational control of hippocampal synaptic plasticity and memory by the eIF2α kinase GCN2 M Costa-Mattioli, D Gobert, H Harding, B Herdy, M Azzi, M Bruno, ... Nature 436 (7054), 1166-1170, 2005 | 490 | 2005 |
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 | 478 | 2006 |
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 |
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 | 422 | 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 | 395 | 2009 |
Characterization of an RNA granule from developing brain G Elvira, S Wasiak, V Blandford, XK Tong, A Serrano, X Fan, ... Molecular & cellular proteomics 5 (4), 635-651, 2006 | 342 | 2006 |
Stratum lacunosum-moleculare interneurons of hippocampal CA1 region. I. Intracellular response characteristics, synaptic responses, and morphology JC Lacaille, PA Schwartzkroin Journal of Neuroscience 8 (4), 1400-1410, 1988 | 309 | 1988 |
Stratum lacunosum-moleculare interneurons of hippocampal CA1 region. II. Intrasomatic and intradendritic recordings of local circuit synaptic interactions JC Lacaille, PA Schwartzkroin Journal of Neuroscience 8 (4), 1411-1424, 1988 | 298 | 1988 |
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 | 281 | 2013 |
De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment FF Hamdan, H Daoud, D Rochefort, A Piton, J Gauthier, M Langlois, ... The American Journal of Human Genetics 87 (5), 671-678, 2010 | 270 | 2010 |
Interneuron diversity series: hippocampal interneuron classifications–making things as simple as possible, not simpler G Maccaferri, JC Lacaille Trends in neurosciences 26 (10), 564-571, 2003 | 269 | 2003 |
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 | 237 | 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 | 236 | 2011 |
Metformin ameliorates core deficits in a mouse model of fragile X syndrome I Gantois, A Khoutorsky, J Popic, A Aguilar-Valles, E Freemantle, R Cao, ... Nature medicine 23 (6), 674-677, 2017 | 219 | 2017 |
Pharmacogenetic inhibition of eIF4E-dependent Mmp9 mRNA translation reverses fragile X syndrome-like phenotypes CG Gkogkas, A Khoutorsky, R Cao, SM Jafarnejad, M Prager-Khoutorsky, ... Cell reports 9 (5), 1742-1755, 2014 | 211 | 2014 |
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 | 204 | 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 | 195 | 2009 |