Elsa Rossignol, Ph.D/MD

Neurosciences Université de Montréal, Montréal, Canada 
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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
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