Anne Lortie

Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy

Patrick Cossette, Lidong Liu, Katéri Brisebois et al. · Nature Genetics · 2002 · 648 citations

Molecular Neuroscience, Genetic Disorder, Genetics +9

Incidence of acquired demyelination of the CNS in Canadian children

Brenda Banwell, J. Kennedy, Douglas L. Arnold et al. · Neurology · 2009 · 366 citations

Clinical, environmental, and genetic determinants of multiple sclerosis in children with acute demyelination: a prospective national cohort study

Brenda Banwell, Amit Bar‐Or, Douglas L. Arnold et al. · The Lancet Neurology · 2011 · 314 citations

Neurological Disorder, Medicine, Genetic Epidemiology +10

CACNA1A haploinsufficiency causes cognitive impairment, autism and epileptic encephalopathy with mild cerebellar symptoms

Léna Damaj, Alexis Lupien‐Meilleur, Anne Lortie et al. · European Journal of Human Genetics · 2015 · 206 citations · Full text

Neurodevelopmental Disorders, Epileptic Encephalopathy, Corticobasal Degeneration +12

The genetic landscape of infantile spasms

Jacques L. Michaud, Mathieu Lachance, Fadi F. Hamdan et al. · Human Molecular Genetics · 2014 · 188 citations · Full text