Recent insights into the molecular genetics of dementiaRADEMAKERS, Rosa; ROVELET-LECRUX, Anne.Trends in neurosciences (Regular edition). 2009, Vol 32, Num 8, pp 451-461, issn 0166-2236, 11 p.Article

Regional distribution of synaptic markers and APP correlate with distinct clinicopathological features in sporadic and familial Alzheimer's diseaseSHINOHARA, Mitsuru; FUJIOKA, Shinsuke; PETERSEN, Ronald C et al.Brain. 2014, Vol 137, pp 1533-1549, issn 0006-8950, 17 p., 5Article

APP locus duplication causes autosomal dominant early-onset alzheimer disease with cerebral amyloid angiopathyROVELET-LECRUX, Anne; HANNEQUIN, Didier; DUBAS, Frédéric et al.Nature genetics. 2006, Vol 38, Num 1, pp 24-26, issn 1061-4036, 3 p.Article

Mutation of the PDGFRB gene as a cause of idiopathic basal ganglia calcificationNICOLAS, Gaël; POTTIER, Cyril; MARTINAUD, Olivier et al.Neurology. 2013, Vol 80, Num 2, pp 181-187, issn 0028-3878, 7 p.Article

Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family membersFINCH, Nicole; BAKER, Matt; DICKSON, Dennis W et al.Brain. 2009, Vol 132, pp 583-591, issn 0006-8950, 9 p., 3Article

Phenotypic spectrum of probable and genetically-confirmed idiopathic basal ganglia calcificationNICOLAS, Gaël; POTTIER, Cyril; MARTINAUD, Olivier et al.Brain. 2013, Vol 136, pp 3395-3407, issn 0006-8950, 13 p., 11Article

A genome-wide study reveals rare CNVs exclusive to extreme phenotypes of Alzheimer diseaseROVELET-LECRUX, Anne; LEGALLIC, Solenn; PUEL, Michele et al.European journal of human genetics. 2012, Vol 20, Num 6, pp 613-617, issn 1018-4813, 5 p.Article

Phenotype variability in progranulin mutation carriers : a clinical, neuropsychological, imaging and genetic studyLE BER, Isabelle; CAMUZAT, Agnès; PUEL, Michèle et al.Brain. 2008, Vol 131, pp 732-746, issn 0006-8950, 15 p., 3Article