Adeline Rollin‐Sillaire

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

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

Seizures in dominantly inherited Alzheimer disease

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

17q21.31 duplication causes prominent tau-related dementia with increased MAPT expression

Kilan Le Guennec, Olivier Quenez, Gaël Nicolas et al. · Molecular Psychiatry · 2016 · 97 citations

Neurodegenerative Diseases, Alzheimer's Disease, Increased Mapt Expression +7

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