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Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's diseaseAssociation of Long Runs of Homozygosity With Alzheimer Disease Among African American IndividualsRarity of the Alzheimer disease-protective APP A673T variant in the United StatesAssociation and heterogeneity at the GAPDH locus in Alzheimer's diseaseCommon variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease.Effects of multiple genetic loci on age at onset in late-onset Alzheimer disease: a genome-wide association studyVariants in the ATP-binding cassette transporter (ABCA7), apolipoprotein E ϵ4,and the risk of late-onset Alzheimer disease in African Americans.Association of MAPT haplotypes with Alzheimer's disease risk and MAPT brain gene expression levels.ALS-FTD complex disorder due to C9ORF72 gene mutation: description of first Polish family.Systems biology approach to late-onset Alzheimer's disease genome-wide association study identifies novel candidate genes validated using brain expression data and Caenorhabditis elegans experiments.Concordant association of insulin degrading enzyme gene (IDE) variants with IDE mRNA, Abeta, and Alzheimer's diseaseAfrican American exome sequencing identifies potential risk variants at Alzheimer disease lociFine mapping of the alpha-T catenin gene to a quantitative trait locus on chromosome 10 in late-onset Alzheimer's disease pedigrees.Genetics of Alzheimer disease in the pre- and post-GWAS eraBrain expression genome-wide association study (eGWAS) identifies human disease-associated variants.Genetic variants in a haplotype block spanning IDE are significantly associated with plasma Abeta42 levels and risk for Alzheimer disease.Alzheimer's disease: early alterations in brain DNA methylation at ANK1, BIN1, RHBDF2 and other loci.Two rare AKAP9 variants are associated with Alzheimer's disease in African Americans.Meta-analysis confirms CR1, CLU, and PICALM as alzheimer disease risk loci and reveals interactions with APOE genotypes.Genetics of Alzheimer's disease: a centennial reviewRare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease.Late-onset Alzheimer's risk variants in memory decline, incident mild cognitive impairment, and Alzheimer's diseaseAssociation of common KIBRA variants with episodic memory and AD risk.LRRTM3 interacts with APP and BACE1 and has variants associating with late-onset Alzheimer's disease (LOAD).Genome-wide association interaction analysis for Alzheimer's disease.TREM2 is associated with increased risk for Alzheimer's disease in African Americans.Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsyGlutathione S-transferase omega genes in Alzheimer and Parkinson disease risk, age-at-diagnosis and brain gene expression: an association study with mechanistic implications.Novel late-onset Alzheimer disease loci variants associate with brain gene expression.Expression and processing analyses of wild type and p.R47H TREM2 variant in Alzheimer's disease brains.Role for the microtubule-associated protein tau variant p.A152T in risk of α-synucleinopathies.Global and local ancestry in African-Americans: Implications for Alzheimer's disease riskIdentifying therapeutic targets for Alzheimer's disease with big data.Evaluating pathogenic dementia variants in posterior cortical atrophy.The presenilin 1 p.Gly206Ala mutation is a frequent cause of early-onset Alzheimer's disease in Hispanics in FloridaGenetic architecture of resilience of executive functioning.Late-onset Alzheimer disease risk variants mark brain regulatory lociTREM2 in neurodegeneration: evidence for association of the p.R47H variant with frontotemporal dementia and Parkinson's diseaseTREM2 p.R47H substitution is not associated with dementia with Lewy bodies.TMEM106B p.T185S regulates TMEM106B protein levels: implications for frontotemporal dementia.
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