Martine Vercelletto

Frontotemporal dementia and its subtypes: a genome-wide association study

Alexander Gerhard, Adrian Danek, Luigi Ferrucci, 2014, The Lancet Neurology.

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

Eric Guedj, Valérie Hahn-Barma, Marie-Odile Habert, 2008, Brain : a journal of neurology.

Lateral Temporal Lobe: An Early Imaging Marker of the Presymptomatic GRN Disease?

Stanley Durrleman, Habib Benali, Olivier Colliot, 2015, Journal of Alzheimer's disease : JAD.

Identification and validation of a blood-based transcriptomic signature (AclarusDx) in the diagnosis of Alzheimer's disease

Bruno Vellas, Jacques Touchon, Martine Vercelletto, 2011, Alzheimer's & Dementia.

Phenotype associated with APP duplication in five families.

Florence Pasquier, Didier Hannequin, Thierry Frebourg, 2006, Brain : a journal of neurology.

Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia.

Nick C. Fox, Pietro Pietrini, Alexander Gerhard, 2018, Nature Medicine.

Demographic, neurological and behavioural characteristics and brain perfusion SPECT in frontal variant of frontotemporal dementia.

Eric Guedj, Mira Didic, Marie-Odile Habert, 2006, Brain : a journal of neurology.

Validation of AclarusDx™, a blood-based transcriptomic signature for the diagnosis of Alzheimer's disease.

Bruno Vellas, Harald Hampel, H. Hampel, 2012, Journal of Alzheimer's disease : JAD.

A genome-wide study reveals rare CNVs exclusive to extreme phenotypes of Alzheimer disease

Claire Paquet, Jérémie Pariente, Bernard Croisile, 2011, European Journal of Human Genetics.