Mathilde Sauvée

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 · 609 citations · Full text

Life Sciences, Genetics, Neurology +17

Phenotypic spectrum of probable and genetically-confirmed idiopathic basal ganglia calcification

Gaël Nicolas, Cyril Pottier, Camille Charbonnier et al. · Brain · 2013 · 233 citations · Full text

Medicine, Neurology, Neuroscience +12

Contribution to Alzheimer's disease risk of rare variants in TREM2, SORL1, and ABCA7 in 1779 cases and 1273 controls

Céline Bellenguez, Camille Charbonnier, Benjamin Grenier‐Boley et al. · Neurobiology of Aging · 2017 · 170 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Focal electrical intracerebral stimulation of a face-sensitive area causes transient prosopagnosia

Jacques Jonas, Médéric Descoins, Laurent Koessler et al. · Neuroscience · 2012 · 121 citations

Medicine, Neurology, Neuroscience +12

The French Series of Autosomal Dominant Early Onset Alzheimer's Disease Cases: Mutation Spectrum and Cerebrospinal Fluid Biomarkers

David Wallon, Stéphane Rousseau, Anne Rovelet‐Lecrux et al. · Journal of Alzheimer s Disease · 2012 · 120 citations

Life Sciences, Genetics, Neurology +17