Elsa Rossignol, Ph.D/MD
Affiliations: | Neurosciences | Université de Montréal, Montréal, Canada |
Area:
EpilepsyWebsite:
https://recherche.chusj.org/fr/Axes-de-recherche/Bio?id=5b83741d-1d9c-447f-8498-c8f3f5cc3126Google:
"https://scholar.google.ca/citations?user=wQD13gEAAAAJ&hl=en"Mean distance: (not calculated yet)
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Publications
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| Toudji I, Toumi A, Chamberland É, et al. (2023) Interneuron odyssey: molecular mechanisms of tangential migration. Frontiers in Neural Circuits. 17: 1256455 |
| Lupien-Meilleur A, Jiang X, Lachance M, et al. (2021) Reversing frontal disinhibition rescues behavioural deficits in models of CACNA1A-associated neurodevelopment disorders. Molecular Psychiatry |
| Jiang X, Raju PK, D'Avanzo N, et al. (2019) Both gain-of-function and loss-of-function de novo CACNA1A mutations cause severe developmental epileptic encephalopathies in the spectrum of Lennox-Gastaut syndrome. Epilepsia |
| Murakami Y, Nguyen TTM, Baratang N, et al. (2019) Mutations in PIGB Cause an Inherited GPI Biosynthesis Defect with an Axonal Neuropathy and Metabolic Abnormality in Severe Cases. American Journal of Human Genetics |
| Bell S, Rousseau J, Peng H, et al. (2019) Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons. American Journal of Human Genetics |
| Finelli MJ, Aprile D, Castroflorio E, et al. (2018) The epilepsy-associated protein TBC1D24 is required for normal development, survival and vesicle trafficking in mammalian neurons. Human Molecular Genetics |
| Jiang X, Lupien-Meilleur A, Tazerart S, et al. (2018) Remodeled cortical inhibition prevents motor seizures in generalized epilepsy. Annals of Neurology |
| Eid L, Lachance M, Hickson G, et al. (2018) Ex Utero Electroporation and Organotypic Slice Cultures of Embryonic Mouse Brains for Live-Imaging of Migrating GABAergic Interneurons. Journal of Visualized Experiments : Jove |
| Piard J, Hu JH, Campeau PM, et al. (2017) FRMPD4 Mutations Cause X-linked Intellectual Disability and Disrupt Dendritic Spine Morphogenesis. Human Molecular Genetics |
| Hamdan FF, Myers CT, Cossette P, et al. (2017) High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies. American Journal of Human Genetics. 101: 664-685 |