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Neurobiology of Aging|August 10, 2017
Contribution to Alzheimer's disease risk of rare variants in TREM2, SORL1, and ABCA7 in 1779 cases and 1273 controlsCéline Bellenguez, Camille Charbonnier, Benjamin Grenier-Boley, et al.
Alzheimer'S Research & Therapy|July 19, 2022
Prodromal characteristics of dementia with Lewy bodies: baseline results of the MEMENTO memory clinics nationwide cohortFrederic Blanc, Vincent Bouteloup, Claire Paquet, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|June 15, 2026
Provider and patient perspectives on the diagnosis and treatment of Alzheimer's disease: A global perspective from the Global Alzheimer's Leadership Series (GoALS)Philippe Amouyel, Sandrine Andrieu, Angela Bradshaw, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|February 20, 2018
Plasma amyloid levels within the Alzheimer's process and correlations with central biomarkersOlivier Hanon, Jean-Sébastien Vidal, Sylvain Lehmann, et al.
Plos Medicine|August 21, 2020
Age and the association between apolipoprotein E genotype and Alzheimer disease: A cerebrospinal fluid biomarker-based case-control studyHana Saddiki, Aurore Fayosse, Emmanuel Cognat, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|February 21, 2022
Plasma amyloid beta predicts conversion to dementia in subjects with mild cognitive impairment: The BALTAZAR studyOlivier Hanon, Jean-Sébastien Vidal, Sylvain Lehmann, et al.
Acta Neuropathologica Communications|February 13, 2022
A postzygotic de novo NCDN mutation identified in a sporadic FTLD patient results in neurochondrin haploinsufficiency and altered FUS granule dynamicsGaël Nicolas, Myriam Sévigny, François Lecoquierre, et al.
European Journal of Human Genetics : EJHG|June 30, 2018
Primary brain calcification: an international study reporting novel variants and associated phenotypesEliana Marisa Ramos, Miryam Carecchio, Roberta Lemos, et al.
Plos Medicine|March 29, 2017
APP, PSEN1, and PSEN2 mutations in early-onset Alzheimer disease: A genetic screening study of familial and sporadic casesHélène-Marie Lanoiselée, Gaël Nicolas, David Wallon, et al.
Neurology|May 13, 2021
Primary Progressive Aphasia Associated With <i>GRN</i> Mutations: New Insights Into the Nonamyloid Logopenic VariantDario Saracino, Sophie Ferrieux, Marie Noguès-Lassiaille, et al.
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