Durand, C M
Centre National de la Recherche Scientifique · Institut Pasteur · Sorbonne Paris Cité · Gènes, synapses et cognition · Université Paris Diderot
7 papers on CoChatORCID 0000-0002-3890-0632
Most cited papers
- Verified
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders
Durand, C. M., Betancur, C., Boeckers, T. M., Bockmann, J., Chaste, P., Fauchereau, F., Nygren, G., Rastam, M., Gillberg, I. C., Anckarsäter, H., et al. (2007) · Nature Genetics
Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research
Cited by 1,602
- Verified
Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: A Gradient of Severity in Cognitive Impairments
Leblond, C. S., Nava, C., Polge, A., Gauthier, J., Huguet, G., Lumbroso, S., Giuliano, F., Stordeur, C., Depienne, C., Mouzat, K., et al. (2014) · PLoS Genetics
Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research
Cited by 630
- Verified
Abnormal melatonin synthesis in autism spectrum disorders
Melke, J., Goubran Botros, H., Chaste, P., Betancur, C., Nygren, G., Anckarsäter, H., Rastam, M., Ståhlberg, O., Gillberg, I. C., Delorme, R., et al. (2008) · Molecular Psychiatry
Circadian rhythm and melatoninAutism Spectrum Disorder Research
Cited by 511
- Verified
SHANK3 mutations identified in autism lead to modification of dendritic spine morphology via an actin-dependent mechanism
Durand, C. M., Perroy, J., Loll, F., Perrais, D., Fagni, L., Bourgeron, T., Montcouquiol, M., & Sans, N. (2012) · Molecular Psychiatry
Genetics and Neurodevelopmental DisordersNeuroscience and Neuropharmacology Research
Cited by 316
- Verified
The planar polarity protein Scribble1 is essential for neuronal plasticity and brain function
Moreau, M. M., Piguel, N., Papouin, T., Koehl, M., Durand, C. M., Rubio, M. E., Loll, F., Richard, E. M., Mazzocco, C., Racca, C., et al. (2010) · Journal of Neuroscience
Neuroscience and Neuropharmacology ResearchGenetics and Neurodevelopmental Disorders
Cited by 69
- Verified
Genetic variations of the melatonin pathway in patients with attention-deficit and hyperactivity disorders: The melatonin pathway in ADHD
Chaste, P., Clement, N., Botros, H. G., Guillaume, J.-L., Konyukh, M., Pagan, C., Scheid, I., Nygren, G., Anckarsäter, H., Rastam, M., et al. (2011) · Journal of Pineal Research
Circadian rhythm and melatoninAttention Deficit Hyperactivity Disorder
Cited by 67
- Verified
Scribble1/AP2 complex coordinates NMDA receptor endocytic recycling
Piguel, N. H., Fievre, S., Blanc, J.-M., Carta, M., Moreau, M. M., Moutin, E., Pinheiro, V. L., Medina, C., Ezan, J., Lasvaux, L., et al. (2014) · Cell Reports
Neuroscience and Neuropharmacology ResearchCellular transport and secretion
Cited by 52
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