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- W2980751820 abstract "An increasing amount of evidence demonstrates that immune dysfunction and neuroinflammation contribute to the pathogenesis and progression of late-onset Alzheimer's disease (LOAD). To identify and characterize the transcriptomic and genetic contributors to immune dysfunction in LOAD, we have designed a comprehensive analysis framework for performing clinical segregation analysis, co-expression modeling, functional enrichment, and gene perturbation testing by integrating clinical neuropathological, gene expression, and genotype data. We applied our analysis framework to 503 human subjects from the Religious Orders Study and Memory and Aging Project (ROSMAP) to map and compare functional gene networks, transcription factors, and genomic loci studies to decipher their contributions to disease progression. We identified deregulation in gene networks involving immune response, synaptic function, and Hippo signaling. One module contains 191 genes, including ABI3, CD33, HLA-DRA, HLA-DMB, IL10RA, MS4A4A, TREM2, and TYROBP and is strongly associated with microglial function. Segregation analysis revealed an association between network organization and cognitive decline in these functionally enriched modules. A reduction in co-regulated genes indicates changes in several key signaling nodes associated with microglia activation and inflammatory response. Finally, we identified HLA and MAPT alleles in association with LOAD." @default.
- W2980751820 created "2019-10-25" @default.
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- W2980751820 date "2019-07-01" @default.
- W2980751820 modified "2023-09-28" @default.
- W2980751820 title "P4-477: COMBINED GENOME-WIDE NETWORK ANALYSIS REVEALS PERTURBATIONS TO IMMUNE SYSTEM, SYNAPTIC AND HIPPO SIGNALING IN ASSOCIATION WITH COGNITIVE DECLINE IN LATE-ONSET ALZHEIMER'S DISEASE" @default.
- W2980751820 doi "https://doi.org/10.1016/j.jalz.2019.08.023" @default.
- W2980751820 hasPublicationYear "2019" @default.
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