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Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's diseaseThe gene encoding nicastrin, a major gamma-secretase component, modifies risk for familial early-onset Alzheimer disease in a Dutch population-based sampleMolecular genetics of early-onset Alzheimer's disease revisitedThe genetic landscape of Alzheimer disease: clinical implications and perspectivesLarge meta-analysis establishes the ACE insertion-deletion polymorphism as a marker of Alzheimer's diseaseAPP duplication is sufficient to cause early onset Alzheimer's dementia with cerebral amyloid angiopathyITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: a genome-wide association studyThe CALHM1 P86L polymorphism is a genetic modifier of age at onset in Alzheimer's disease: a meta-analysis study.Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease.Identification and description of three families with familial Alzheimer disease that segregate variants in the SORL1 gene.CMT-associated mutations in glycyl- and tyrosyl-tRNA synthetases exhibit similar pattern of toxicity and share common genetic modifiers in Drosophila.Current status on Alzheimer disease molecular genetics: from past, to present, to future.A novel locus for dementia with Lewy bodies: a clinically and genetically heterogeneous disorder.Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degenerationLinkage and association studies identify a novel locus for Alzheimer disease at 7q36 in a Dutch population-based samplePolymorphisms in the GluR2 gene are not associated with amyotrophic lateral sclerosisLonger leukocyte telomere length is associated with smaller hippocampal volume among non-demented APOE ε3/ε3 subjectsGlobal investigation and meta-analysis of the C9orf72 (G4C2)n repeat in Parkinson diseaseTMEM106B is associated with frontotemporal lobar degeneration in a clinically diagnosed patient cohortPromoter mutations that increase amyloid precursor-protein expression are associated with Alzheimer disease.Meta-analysis of the association between variants in SORL1 and Alzheimer disease.Genome-wide association interaction analysis for Alzheimer's disease.Both common variations and rare non-synonymous substitutions and small insertion/deletions in CLU are associated with increased Alzheimer risk.Reduced secreted clusterin as a mechanism for Alzheimer-associated CLU mutations.Reduced secretion and altered proteolytic processing caused by missense mutations in progranulin.sTREM2 cerebrospinal fluid levels are a potential biomarker for microglia activity in early-stage Alzheimer's disease and associate with neuronal injury markers.A genomewide screen for late-onset Alzheimer disease in a genetically isolated Dutch populationAmyloid precursor protein mutation E682K at the alternative β-secretase cleavage β'-site increases Aβ generation.A pan-European study of the C9orf72 repeat associated with FTLD: geographic prevalence, genomic instability, and intermediate repeats.Phenotypic characteristics of Alzheimer patients carrying an ABCA7 mutation.Diffusion Kurtosis Imaging: A Possible MRI Biomarker for AD Diagnosis?A comprehensive study of the genetic impact of rare variants in SORL1 in European early-onset Alzheimer's diseasePolymorphism of brain derived neurotrophic factor influences β amyloid load in cognitively intact apolipoprotein E ε4 carriers.Molecular pathogenesis of frontotemporal lobar degeneration: basic science seminar in neurology.Molecular genetics of Alzheimer's disease: an update.Invited article: the Alzheimer disease-frontotemporal lobar degeneration spectrum.Rare Variants in PLD3 Do Not Affect Risk for Early-Onset Alzheimer Disease in a European Consortium Cohort.TBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis.The pursuit of susceptibility genes for Alzheimer's disease: progress and prospects.Role of progranulin as a biomarker for Alzheimer's disease.
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