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Neurology|April 3, 2016
ABCA7 rare variants and Alzheimer disease riskKilan Le Guennec, Gaël Nicolas, Olivier Quenez, et al.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|February 5, 2022
Challenges at the APOE locus: a robust quality control approach for accurate APOE genotypingMichael E Belloy, Sarah J Eger, Yann Le Guen, et al.JAMA|August 10, 2006
Collaborative analysis of alpha-synuclein gene promoter variability and Parkinson diseaseDemetrius M Maraganore, Mariza de Andrade, Alexis Elbaz, et al.International Journal of Molecular Sciences|January 11, 2025
Head-to-Head Comparison of Aptamer- and Antibody-Based Proteomic Platforms in Human Cerebrospinal Fluid Samples from a Real-World Memory Clinic CohortRaquel Puerta, Amanda Cano, Pablo García-González, et al.Journal of Neurology, Neurosurgery, and Psychiatry|February 15, 2013
The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphismStephan Klebe, Jean-Louis Golmard, Michael A Nalls, et al.Fluids and Barriers of the CNS|February 13, 2025
Low prevalence of CWH43 variants among Finnish and Norwegian idiopathic normal pressure hydrocephalus patients: a cohort-based observational studyJoel Räsänen, Seppo Helisalmi, Sami Heikkinen, et al.Neurology|August 14, 2024
Risk Variants Associated With Normal Pressure Hydrocephalus: Genome-Wide Association Study in the FinnGen CohortJoel Räsänen, Sami Heikkinen, Kiira Mäklin, et al.Journal of Alzheimer'S Disease : JAD|June 25, 2016
Evaluation of a Genetic Risk Score to Improve Risk Prediction for Alzheimer's DiseaseVincent Chouraki, Christiane Reitz, Fleur Maury, et al.Nature Genetics|March 19, 2013
Genome-wide association analysis identifies a susceptibility locus for pulmonary arterial hypertensionMarine Germain, Mélanie Eyries, David Montani, et al.Pageof 19