Olivier Martinaud

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

Mutation of the <i>PDGFRB</i> gene as a cause of idiopathic basal ganglia calcification

Gaël Nicolas, Cyril Pottier, David Maltête et al. · Neurology · 2012 · 275 citations

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

Gaël Nicolas, Cyril Pottier, Camille Charbonnier et al. · Brain · 2013 · 231 citations · Full text

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 · 164 citations · Full text

Neurodegenerative Diseases, Alzheimer's Disease, Disease Risk +11

The pathophysiology of letter-by-letter reading

Laurent Cohen, Carole Henry, Stanislas Dehaene et al. · Neuropsychologia · 2004 · 154 citations

Reading Disabilities, Cognitive Science, Handwriting +9