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Integrating gene expression with summary association statistics to identify susceptibility genes for 30 complex traits

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1006/geno.1999.5949openalex-snapshot

Human Aiolos, an Ikaros-Related Zinc Finger DNA Binding Protein: cDNA Cloning, Tissue Expression Pattern, and Chromosomal Mapping

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.2016.02.020openalex-snapshot

Imputing Gene Expression in Uncollected Tissues Within and Beyond GTEx

inferredcites →https://doi.org/10.1016/j.ajhg.2016.05.013openalex-snapshot

Contrasting the Genetic Architecture of 30 Complex Traits from Summary Association Data

inferredcites →https://doi.org/10.1038/nature06758openalex-snapshot

Genetics of gene expression and its effect on disease

inferredcites →https://doi.org/10.1038/nature10251openalex-snapshot

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

inferredcites →https://doi.org/10.1038/nature10659openalex-snapshot

New gene functions in megakaryopoiesis and platelet formation

inferredcites →https://doi.org/10.1038/nature11677openalex-snapshot

Seventy-five genetic loci influencing the human red blood cell

inferredcites →https://doi.org/10.1038/nature12531openalex-snapshot

Transcriptome and genome sequencing uncovers functional variation in humans

inferredcites →https://doi.org/10.1038/nature12873openalex-snapshot

Genetics of rheumatoid arthritis contributes to biology and drug discovery

inferredcites →https://doi.org/10.1038/nature13545openalex-snapshot

Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche

inferredcites →https://doi.org/10.1038/nature13595openalex-snapshot

Biological insights from 108 schizophrenia-associated genetic loci

inferredcites →https://doi.org/10.1038/nature13835openalex-snapshot

Genetic and epigenetic fine mapping of causal autoimmune disease variants

inferredcites →https://doi.org/10.1038/nature14177openalex-snapshot

Genetic studies of body mass index yield new insights for obesity biology

inferredcites →https://doi.org/10.1038/nature14878openalex-snapshot

Whole‐genome sequencing identifies EN1 as a determinant of bone density and fracture

inferredcites →https://doi.org/10.1038/nature15393openalex-snapshot

A global reference for human genetic variation

inferredcites →https://doi.org/10.1038/ng.2213openalex-snapshot

Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits

inferredcites →https://doi.org/10.1038/ng.2383openalex-snapshot

Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

inferredcites →https://doi.org/10.1038/ng.2653openalex-snapshot

The Genotype-Tissue Expression (GTEx) project

inferredcites →https://doi.org/10.1038/ng.2795openalex-snapshot

Common variants associated with plasma triglycerides and risk for coronary artery disease

inferredcites →https://doi.org/10.1038/ng.2797openalex-snapshot

Discovery and refinement of loci associated with lipid levels

inferredcites →https://doi.org/10.1038/ng.2951openalex-snapshot

Heritability and genomics of gene expression in peripheral blood

inferredcites →https://doi.org/10.1038/ng.3097openalex-snapshot

Defining the role of common variation in the genomic and biological architecture of adult human height

inferredcites →https://doi.org/10.1038/ng.3211openalex-snapshot

LD Score regression distinguishes confounding from polygenicity in genome-wide association studies

inferredcites →https://doi.org/10.1038/ng.3359openalex-snapshot

Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations

inferredcites →https://doi.org/10.1038/ng.3367openalex-snapshot

A gene-based association method for mapping traits using reference transcriptome data

inferredcites →https://doi.org/10.1038/ng.3404openalex-snapshot

Partitioning heritability by functional annotation using genome-wide association summary statistics

inferredcites →https://doi.org/10.1038/ng.3406openalex-snapshot

An atlas of genetic correlations across human diseases and traits

inferredcites →https://doi.org/10.1038/ng.3506openalex-snapshot

Integrative approaches for large-scale transcriptome-wide association studies

inferredcites →https://doi.org/10.1038/ng.3538openalex-snapshot

Integration of summary data from GWAS and eQTL studies predicts complex trait gene targets

inferredcites →https://doi.org/10.1038/ng.3570openalex-snapshot

Detection and interpretation of shared genetic influences on 42 human traits

inferredcites →https://doi.org/10.1038/ng.520openalex-snapshot

New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

inferredcites →https://doi.org/10.1038/ni.2363openalex-snapshot

Aiolos promotes TH17 differentiation by directly silencing Il2 expression

inferredcites →https://doi.org/10.1038/nn.4399openalex-snapshot

Gene expression elucidates functional impact of polygenic risk for schizophrenia

inferredcites →https://doi.org/10.1038/nprot.2013.092openalex-snapshot

Large-scale gene function analysis with the PANTHER classification system

inferredcites →https://doi.org/10.1038/nrg3891openalex-snapshot

The role of regulatory variation in complex traits and disease

inferredcites →https://doi.org/10.1056/nejmoa1502214openalex-snapshot

FTO Obesity Variant Circuitry and Adipocyte Browning in Humans

inferredcites →https://doi.org/10.1084/jem.20140455openalex-snapshot

CCDC88B is a novel regulator of maturation and effector functions of T cells during pathological inflammation

inferredcites →https://doi.org/10.1093/biomet/34.1-2.28openalex-snapshot

THE GENERALIZATION OF ‘STUDENT'S’ PROBLEM WHEN SEVERAL DIFFERENT POPULATION VARLANCES ARE INVOLVED

inferredcites →https://doi.org/10.1093/hmg/ddu328openalex-snapshot

Mendelian randomization: genetic anchors for causal inference in epidemiological studies

inferredcites →https://doi.org/10.1093/ije/dyg070openalex-snapshot

‘Mendelian randomization’: can genetic epidemiology contribute to understanding environmental determinants of disease?*

inferredcites →https://doi.org/10.1093/ije/dym225openalex-snapshot

Cohort Profile: The Cardiovascular Risk in Young Finns Study

inferredcites →https://doi.org/10.1093/nar/gkt1229openalex-snapshot

The NHGRI GWAS Catalog, a curated resource of SNP-trait associations

inferredcites →https://doi.org/10.1101/018150openalex-snapshot

Fulfilling the promise of Mendelian randomization

inferredcites →https://doi.org/10.1101/019885openalex-snapshot

Detection and interpretation of shared genetic influences on 40 human traits

inferredcites →https://doi.org/10.1126/science.1235488openalex-snapshot

GWAS of 126,559 Individuals Identifies Genetic Variants Associated with Educational Attainment

inferredcites →https://doi.org/10.1177/1403494814541597openalex-snapshot

Cardiovascular risk factors in 2011 and secular trends since 2007: The Cardiovascular Risk in Young Finns Study

inferredcites →https://doi.org/10.1186/s13073-015-0257-9openalex-snapshot

Erratum to: Clinical metagenomic identification of Balamuthia mandrillaris encephalitis and assembly of the draft genome: the continuing case for reference genome sequencing

inferredcites →https://doi.org/10.1186/s13073-016-0338-4openalex-snapshot

Predicting gene targets from integrative analyses of summary data from GWAS and eQTL studies for 28 human complex traits

inferredcites →https://doi.org/10.1371/journal.pgen.1000888openalex-snapshot

Trait-Associated SNPs Are More Likely to Be eQTLs: Annotation to Enhance Discovery from GWAS

inferredcites →https://doi.org/10.1371/journal.pgen.1000895openalex-snapshot

Candidate Causal Regulatory Effects by Integration of Expression QTLs with Complex Trait Genetic Associations

inferredcites →https://doi.org/10.1371/journal.pgen.1003608openalex-snapshot

Prediction of Complex Human Traits Using the Genomic Best Linear Unbiased Predictor

inferredcites →https://doi.org/10.1371/journal.pgen.1004958openalex-snapshot

Tissue-Specific Effects of Genetic and Epigenetic Variation on Gene Regulation and Splicing

inferredcites →https://doi.org/10.1371/journal.pmed.1001474openalex-snapshot

The Role of Adiposity in Cardiometabolic Traits: A Mendelian Randomization Analysis

inferredcites →https://doi.org/10.2337/db08-1607openalex-snapshot

Changes in Insulin Sensitivity and Insulin Release in Relation to Glycemia and Glucose Tolerance in 6,414 Finnish Men

inferredcites →https://doi.org/10.2337/db10-0502openalex-snapshot

Common Variants at 10 Genomic Loci Influence Hemoglobin A1C Levels via Glycemic and Nonglycemic Pathways

inferredcites →https://doi.org/10.2337/db11-1378openalex-snapshot

Hyperglycemia and a Common Variant of GCKR Are Associated With the Levels of Eight Amino Acids in 9,369 Finnish Men

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1007/s11920-018-0898-7openalex-snapshot

Recent Genetics and Epigenetics Approaches to PTSD

inferred← citeshttps://doi.org/10.1016/j.ajhg.2017.09.022openalex-snapshot

Local Genetic Correlation Gives Insights into the Shared Genetic Architecture of Complex Traits

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