Anne Rovelet‐Lecrux

APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy

Anne Rovelet‐Lecrux, Didier Hannequin, Grégory Raux et al. · Nature Genetics · 2005 · 1.2K citations

Alzheimer's Disease, Cerebral Amyloid Angiopathy, Dementia +9

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

Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family members

NiCole A. Finch, Matthew B. Baker, Richard Crook et al. · Brain · 2009 · 377 citations · Full text

Phenotype variability in progranulin mutation carriers: a clinical, neuropsychological, imaging and genetic study

Isabelle Le Ber, Agnès Camuzat, Didier Hannequin et al. · Brain · 2008 · 344 citations

Corticobasal Degeneration, Genetics, Brain Perfusion Profiles +22

A Polymorphism in CALHM1 Influences Ca2+ Homeostasis, Aβ Levels, and Alzheimer's Disease Risk

Ute Dreses‐Werringloer, Jean‐Charles Lambert, Valérie Vingtdeux et al. · Cell · 2008 · 320 citations · Full text

Alzheimer's Disease, Disease Risk, Aβ Levels +6