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Brain Connectivity|January 12, 2021
Resting-State Functional Connectivity Disruption as a Pathological Biomarker in Autosomal Dominant Alzheimer DiseaseRobert X Smith, Jeremy F Strain, Aaron Tanenbaum, et al.
Brain : a Journal of Neurology|March 22, 2019
Clinical, pathophysiological and genetic features of motor symptoms in autosomal dominant Alzheimer's diseaseJonathan Vöglein, Katrina Paumier, Mathias Jucker, et al.
Nature Communications|November 18, 2024
Comparative neurofilament light chain trajectories in CSF and plasma in autosomal dominant Alzheimer's diseaseAnna Hofmann, Lisa M Häsler, Marius Lambert, et al.
Brain Communications|May 24, 2024
Molecular neuroimaging in dominantly inherited versus sporadic early-onset Alzheimer's diseaseLeonardo Iaccarino, Jorge J Llibre-Guerra, Eric McDade, et al.
Annals of Neurology|January 7, 2015
Protective variant for hippocampal atrophy identified by whole exome sequencingKwangsik Nho, Sungeun Kim, Shannon L Risacher, et al.
NPJ Dementia|February 19, 2026
15 years of longitudinal genetic, clinical, cognitive, imaging, and biochemical measures in DIANAlisha J Daniels, Eric McDade, Jorge J Llibre-Guerra, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|July 25, 2017
Presymptomatic atrophy in autosomal dominant Alzheimer's disease: A serial magnetic resonance imaging studyKirsi M Kinnunen, David M Cash, Teresa Poole, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|April 1, 2022
Biomarker clustering in autosomal dominant Alzheimer's diseasePatrick H Luckett, Charlie Chen, Brian A Gordon, et al.
Medrxiv : the Preprint Server for Health Sciences|August 16, 2024
15 Years of Longitudinal Genetic, Clinical, Cognitive, Imaging, and Biochemical Measures in DIANAlisha J Daniels, Eric McDade, Jorge J Llibre-Guerra, et al.
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