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Systems genetics identifies modifiers of Alzheimer’s disease risk and resilience
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1001/jamaneurol.2015.1424openalex-snapshot
Genetic Modifiers of Age at Onset in Carriers of the G206A Mutation inPSEN1With Familial Alzheimer Disease Among Caribbean Hispanics
inferredcites →https://doi.org/10.1002/ana.10507openalex-snapshot
PRNP Val129 homozygosity increases risk for early‐onset Alzheimer's disease
inferredcites →https://doi.org/10.1007/s00210-005-1052-8openalex-snapshot
Functional characterization and physiological relevance of the TRPC3/6/7 subfamily of cation channels
inferredcites →https://doi.org/10.1007/s00401-016-1533-5openalex-snapshot
Cerebrospinal fluid soluble TREM2 is higher in Alzheimer disease and associated with mutation status
inferredcites →https://doi.org/10.1016/j.bbr.2014.12.018openalex-snapshot
TRPC3 channels critically regulate hippocampal excitability and contextual fear memory
inferredcites →https://doi.org/10.1016/j.bbr.2016.05.007openalex-snapshot
Transcriptional signatures of brain aging and Alzheimer’s disease: What are our rodent models telling us?
inferredcites →https://doi.org/10.1016/j.biopsych.2014.05.006openalex-snapshot
Alzheimer’s Disease Risk Genes and Mechanisms of Disease Pathogenesis
inferredcites →https://doi.org/10.1016/j.brainresbull.2015.12.003openalex-snapshot
Toward more predictive genetic mouse models of Alzheimer's disease
inferredcites →https://doi.org/10.1016/j.cell.2013.03.030openalex-snapshot
Integrated Systems Approach Identifies Genetic Nodes and Networks in Late-Onset Alzheimer’s Disease
inferredcites →https://doi.org/10.1016/j.jalz.2015.10.010openalex-snapshot
Unraveling the mechanistic complexity of Alzheimer's disease through systems biology
inferredcites →https://doi.org/10.1016/j.neurobiolaging.2007.02.017openalex-snapshot
Genetic loci modulating amyloid-beta levels in a mouse model of Alzheimer's disease
inferredcites →https://doi.org/10.1016/j.neurobiolaging.2014.10.004openalex-snapshot
Systemic administration of fibroblast growth factor-2 (FGF2) reduces BACE1 expression and amyloid pathology in APP23 mice
inferredcites →https://doi.org/10.1016/s0959-4388(99)80027-0openalex-snapshot
Hippocampus and context in classical conditioning
inferredcites →https://doi.org/10.1037//0735-7044.98.2.269openalex-snapshot
Opiate modulation of the active and inactive components of the postshock reaction: Parallels between naloxone pretreatment and shock intensity.
inferredcites →https://doi.org/10.1038/nature10413openalex-snapshot
Mouse genomic variation and its effect on phenotypes and gene regulation
inferredcites →https://doi.org/10.1038/ncomms9382openalex-snapshot
Genome-wide association meta-analysis identifies five modifier loci of lung disease severity in cystic fibrosis
inferredcites →https://doi.org/10.1038/ncomms9876openalex-snapshot
TRPC6 specifically interacts with APP to inhibit its cleavage by γ-secretase and reduce Aβ production
inferredcites →https://doi.org/10.1038/ng.2802openalex-snapshot
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
inferredcites →https://doi.org/10.1038/nn.3786openalex-snapshot
Alzheimer's disease: early alterations in brain DNA methylation at ANK1, BIN1, RHBDF2 and other loci
inferredcites →https://doi.org/10.1038/nrg2664openalex-snapshot
The genetics of inbreeding depression
inferredcites →https://doi.org/10.1038/nrn960openalex-snapshot
Calcium dyshomeostasis and intracellular signalling in alzheimer's disease
inferredcites →https://doi.org/10.1038/nrneurol.2012.263openalex-snapshot
Apolipoprotein E and Alzheimer disease: risk, mechanisms and therapy
inferredcites →https://doi.org/10.1038/sj.cdd.4401803openalex-snapshot
FGF-2 overexpression opposes the beta amyloid toxic injuries to the vascular endothelium
inferredcites →https://doi.org/10.1042/bj20051246openalex-snapshot
Cellular cholesterol controls TRPC3 function: evidence from a novel dominant-negative knockdown strategy
inferredcites →https://doi.org/10.1073/pnas.051632698openalex-snapshot
Activation of Trp3 by inositol 1,4,5-trisphosphate receptors through displacement of inhibitory calmodulin from a common binding domain
inferredcites →https://doi.org/10.1073/pnas.0808793106openalex-snapshot
Selective and direct inhibition of TRPC3 channels underlies biological activities of a pyrazole compound
inferredcites →https://doi.org/10.1093/bioinformatics/btg112openalex-snapshot
R/qtl: QTL mapping in experimental crosses
inferredcites →https://doi.org/10.1093/brain/aws234openalex-snapshot
Cognitive impairment, decline and fluctuations in older community-dwelling subjects with Lewy bodies
inferredcites →https://doi.org/10.1093/brain/aww330openalex-snapshot
Interleukin-2 improves amyloid pathology, synaptic failure and memory in Alzheimer’s disease mice
inferredcites →https://doi.org/10.1093/gerona/52a.2.m117openalex-snapshot
Heritability for Alzheimer's Disease: The Study of Dementia in Swedish Twins
inferredcites →https://doi.org/10.1093/hmg/ddl157openalex-snapshot
Mapping genetic modulators of amyloid plaque deposition in TgCRND8 transgenic mice
inferredcites →https://doi.org/10.1101/024588openalex-snapshot
Genomic analysis of allele-specific expression in the mouse liver
inferredcites →https://doi.org/10.1111/bpa.12365openalex-snapshot
The Relationship of Cerebral Vessel Pathology to Brain Microinfarcts
inferredcites →https://doi.org/10.1126/science.1566067openalex-snapshot
Alzheimer's Disease: The Amyloid Cascade Hypothesis
inferredcites →https://doi.org/10.1126/science.aad8373openalex-snapshot
Complement and microglia mediate early synapse loss in Alzheimer mouse models
inferredcites →https://doi.org/10.1126/scitranslmed.aaf2362openalex-snapshot
Tau and Aβ imaging, CSF measures, and cognition in Alzheimer’s disease
inferredcites →https://doi.org/10.1161/strokeaha.110.595082openalex-snapshot
Microinfarct Pathology, Dementia, and Cognitive Systems
inferredcites →https://doi.org/10.1161/strokeaha.111.623462openalex-snapshot
Cerebrovascular Disease Pathology and Parkinsonian Signs in Old Age
inferredcites →https://doi.org/10.1186/1471-2105-9-559openalex-snapshot
WGCNA: an R package for weighted correlation network analysis
inferredcites →https://doi.org/10.1186/1471-2156-5-7openalex-snapshot
A new set of BXD recombinant inbred lines from advanced intercross populations in mice
inferredcites →https://doi.org/10.1186/1750-1326-10-1openalex-snapshot
Aβ reduction in BACE1 heterozygous null 5XFAD mice is associated with transgenic APP level
inferredcites →https://doi.org/10.1186/s13059-014-0550-8openalex-snapshot
Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2
inferredcites →https://doi.org/10.1186/s13059-016-0974-4openalex-snapshot
The Ensembl Variant Effect Predictor
inferredcites →https://doi.org/10.1212/01.wnl.0000219668.47116.e6openalex-snapshot
Neuropathology of older persons without cognitive impairment from two community-based studies
inferredcites →https://doi.org/10.1212/01.wnl.0000271090.28148.24openalex-snapshot
Mixed brain pathologies account for most dementia cases in community-dwelling older persons
inferredcites →https://doi.org/10.1212/wnl.0000000000000596openalex-snapshot
Symptom onset in autosomal dominant Alzheimer disease
inferredcites →https://doi.org/10.1212/wnl.0000000000002175openalex-snapshot
Cerebral amyloid angiopathy and cognitive outcomes in community-based older persons
inferredcites →https://doi.org/10.1212/wnl.41.4.479openalex-snapshot
The Consortium to Establish a Registry for Alzheimer's Disease (CERAD)
inferredcites →https://doi.org/10.1371/journal.pone.0050976openalex-snapshot
Expression of Novel Alzheimer’s Disease Risk Genes in Control and Alzheimer’s Disease Brains
inferredcites →https://doi.org/10.1371/journal.pone.0079771openalex-snapshot
Alzheimer’s Disease: Analyzing the Missing Heritability
inferredcites →https://doi.org/10.1371/journal.pone.0125897openalex-snapshot
DBA/2J Genetic Background Exacerbates Spontaneous Lethal Seizures but Lessens Amyloid Deposition in a Mouse Model of Alzheimer’s Disease
inferredcites →https://doi.org/10.1371/journal.pone.0144052openalex-snapshot
Network Topology Analysis of Post-Mortem Brain Microarrays Identifies More Alzheimer’s Related Genes and MicroRNAs and Points to Novel Routes for Fighting with the Disease
inferredcites →https://doi.org/10.1523/jneurosci.0033-12.2012openalex-snapshot
Reducing Human Apolipoprotein E Levels Attenuates Age-Dependent Aβ Accumulation in Mutant Human Amyloid Precursor Protein Transgenic Mice
inferredcites →https://doi.org/10.1523/jneurosci.1202-06.2006openalex-snapshot
Intraneuronal β-Amyloid Aggregates, Neurodegeneration, and Neuron Loss in Transgenic Mice with Five Familial Alzheimer's Disease Mutations: Potential Factors in Amyloid Plaque Formation
inferredcites →https://doi.org/10.2174/156720512801322573openalex-snapshot
Overview and Findings from the Religious Orders Study
inferredcites →https://doi.org/10.2174/156720512801322663openalex-snapshot
Overview and Findings from the Rush Memory and Aging Project
inferredcites →https://doi.org/10.2353/ajpath.2010.100346openalex-snapshot
Aβ Accelerates the Spatiotemporal Progression of Tau Pathology and Augments Tau Amyloidosis in an Alzheimer Mouse Model
inferredcites →https://doi.org/10.3389/fgene.2014.00088openalex-snapshot
Using mice to model Alzheimer's dementia: an overview of the clinical disease and the preclinical behavioral changes in 10 mouse models
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.bcp.2020.113945openalex-snapshot
Alzheimer’s disease beyond amyloid: Can the repetitive failures of amyloid-targeted therapeutics inform future approaches to dementia drug discovery?
inferred← citeshttps://doi.org/10.1016/j.nbd.2021.105558openalex-snapshot
Pursuit of precision medicine: Systems biology approaches in Alzheimer's disease mouse models
inferred← citeshttps://doi.org/10.1016/j.nlm.2019.107069openalex-snapshot
Regulation of intrinsic excitability: Roles for learning and memory, aging and Alzheimer’s disease, and genetic diversity
inferred← citeshttps://doi.org/10.1038/s41598-021-93085-zopenalex-snapshot
Machine learning compensates fold-change method and highlights oxidative phosphorylation in the brain transcriptome of Alzheimer’s disease
inferred← citeshttps://doi.org/10.1101/2024.01.09.574219openalex-snapshot
Hippocampus Glutathione S Reductase Potentially Confers Genetic Resilience to Cognitive Decline in the AD-BXD Mouse Population
inferred← citeshttps://doi.org/10.1101/746222openalex-snapshot
PLD3 is a neuronal lysosomal phospholipase D associated with β-amyloid plaques and cognitive function in Alzheimer’s disease
inferred← citeshttps://doi.org/10.1101/lm.051839.120openalex-snapshot
Identifying the molecular systems that influence cognitive resilience to Alzheimer's disease in genetically diverse mice
inferred← citeshttps://doi.org/10.1111/gbb.12538openalex-snapshot
Age‐related deterioration of motor function in male and female 5xFAD mice from 3 to 16 months of age
inferred← citeshttps://doi.org/10.1186/s13024-020-00412-5openalex-snapshot
A novel systems biology approach to evaluate mouse models of late-onset Alzheimer’s disease
inferred← citeshttps://doi.org/10.1186/s13064-026-00236-xopenalex-snapshot
Modifier gene identification reveals therapeutic pathways for adult and childhood dementias
inferred← citeshttps://doi.org/10.1371/journal.pgen.1009406openalex-snapshot
PLD3 is a neuronal lysosomal phospholipase D associated with β-amyloid plaques and cognitive function in Alzheimer’s disease
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