Ludivine Chamard

APP, PSEN1, and PSEN2 mutations in early-onset Alzheimer disease: A genetic screening study of familial and sporadic cases

Hélène-Marie Lanoiselée, Gaël Nicolas, David Wallon et al. · PLoS Medicine · 2017 · 583 citations · Full text

Seizures in dominantly inherited Alzheimer disease

Aline Zaréa, Camille Charbonnier, Anne Rovelet‐Lecrux et al. · Neurology · 2016 · 105 citations

Screening of dementia genes by whole-exome sequencing in early-onset Alzheimer disease: input and lessons

Gaël Nicolas, David Wallon, Camille Charbonnier et al. · European Journal of Human Genetics · 2015 · 94 citations · Full text

Sequencing, Alzheimer's Disease, Whole-exome Sequencing +13

Logopenic syndrome in posterior cortical atrophy

Éloi Magnin, Géraldine Sylvestre, Flora Lenoir et al. · Journal of Neurology · 2012 · 57 citations

Corticobasal Degeneration, Neuroanatomy, Neurological Disorder +7

Executive and Attentional Disorders, Epilepsy and Porencephalic Cyst in Autosomal Recessive Cerebellar Ataxia Type 3 Due to <b><i>ANO10</i></b> Mutation

Ludivine Chamard, Géraldine Sylvestre, Éloi Magnin · European Neurology · 2016 · 20 citations