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Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/bf01066731openalex-snapshot
The investigation of linkage between a quantitative trait and a marker locus
inferredcites →https://doi.org/10.1016/j.ajhg.2010.11.011openalex-snapshot
GCTA: A Tool for Genome-wide Complex Trait Analysis
inferredcites →https://doi.org/10.1016/j.ajhg.2014.03.004openalex-snapshot
Joint Analysis of Functional Genomic Data and Genome-wide Association Studies of 18 Human Traits
inferredcites →https://doi.org/10.1016/j.ajhg.2014.10.004openalex-snapshot
Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases
inferredcites →https://doi.org/10.1016/j.ajhg.2015.04.002openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.ajhg.2015.06.005openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.ajhg.2015.06.007openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.ajhg.2015.09.001openalex-snapshot
Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores
inferredcites →https://doi.org/10.1016/j.cell.2015.07.048openalex-snapshot
Genetic Control of Chromatin States in Humans Involves Local and Distal Chromosomal Interactions
inferredcites →https://doi.org/10.1016/j.cell.2015.08.001openalex-snapshot
Population Variation and Genetic Control of Modular Chromatin Architecture in Humans
inferredcites →https://doi.org/10.1038/mp.2014.145openalex-snapshot
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inferredcites →https://doi.org/10.1038/mp.2014.49openalex-snapshot
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inferredcites →https://doi.org/10.1038/mp.2014.63openalex-snapshot
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inferredcites →https://doi.org/10.1038/nature08185openalex-snapshot
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inferredcites →https://doi.org/10.1038/nature08872openalex-snapshot
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inferredcites →https://doi.org/10.1038/nature11091openalex-snapshot
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inferredcites →https://doi.org/10.1038/nature13595openalex-snapshot
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Microduplications of 16p11.2 are associated with schizophrenia
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Systematic Localization of Common Disease-Associated Variation in Regulatory DNA
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Coordinated Effects of Sequence Variation on DNA Binding, Chromatin Structure, and Transcription
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Extensive Variation in Chromatin States Across Humans
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What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/gepi.22110openalex-snapshot
Integrating eQTL data with GWAS summary statistics in pathway‐based analysis with application to schizophrenia
inferred← citeshttps://doi.org/10.1002/gepi.22131openalex-snapshot
Transcriptome‐wide association studies accounting for colocalization using Egger regression
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A Protein-Centric View of in Vitro Biological Model Systems for Schizophrenia
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Recent Genetics and Epigenetics Approaches to PTSD
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Transcriptome-wide association study identifies novel genes associated with bone mineral density and lean body mass in children
inferred← citeshttps://doi.org/10.1016/j.ajhg.2017.01.031openalex-snapshot
Integrating Gene Expression with Summary Association Statistics to Identify Genes Associated with 30 Complex Traits
inferred← citeshttps://doi.org/10.1016/j.biopsych.2017.06.033openalex-snapshot
No Evidence That Schizophrenia Candidate Genes Are More Associated With Schizophrenia Than Noncandidate Genes
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Statistical methods for genome-wide association studies
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inferred← citeshttps://doi.org/10.1038/s41380-022-01449-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1038/s41380-022-01488-9openalex-snapshot
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Quantitative trait loci mapping of circulating metabolites in cerebrospinal fluid to uncover biological mechanisms involved in brain-related phenotypes
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Transcriptome-wide association study of treatment-resistant depression and depression subtypes for drug repurposing
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Decreased CNNM2 expression in prefrontal cortex affects sensorimotor gating function, cognition, dendritic spine morphogenesis and risk of schizophrenia
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Large-scale transcriptome-wide association study identifies new prostate cancer risk regions
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Genetically regulated eRNA expression predicts chromatin contact frequency and reveals genetic mechanisms at GWAS loci
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Cas13d-mediated isoform-specific RNA knockdown with a unified computational and experimental toolbox
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Genome-wide meta-analysis, functional genomics and integrative analyses implicate new risk genes and therapeutic targets for anxiety disorders
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Probabilistic fine-mapping of transcriptome-wide association studies
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