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Genome-wide association study provides new insights into the genetic architecture and pathogenesis of heart failure
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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/archinternmed.2010.427openalex-snapshot
Antihypertensive Treatment and Development of Heart Failure in Hypertension
inferredcites →https://doi.org/10.1001/jama.292.3.344openalex-snapshot
Trends in Heart Failure Incidence and Survival in a Community-Based Population
inferredcites →https://doi.org/10.1001/jamacardio.2018.1918openalex-snapshot
Is Heart Failure Inherited?
inferredcites →https://doi.org/10.1001/jamacardio.2018.1919openalex-snapshot
A Swedish Nationwide Adoption Study of the Heritability of Heart Failure
inferredcites →https://doi.org/10.1002/gepi.20533openalex-snapshot
MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes
inferredcites →https://doi.org/10.1002/gepi.21758openalex-snapshot
Mendelian Randomization Analysis With Multiple Genetic Variants Using Summarized Data
inferredcites →https://doi.org/10.1007/s00439-011-1054-1openalex-snapshot
Artifact due to differential error when cases and controls are imputed from different platforms
inferredcites →https://doi.org/10.1007/s00439-013-1266-7openalex-snapshot
Imputation across genotyping arrays for genome-wide association studies: assessment of bias and a correction strategy
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.bbrc.2013.12.109openalex-snapshot
CDK inhibitors, p21Cip1 and p27Kip1, participate in cell cycle exit of mammalian cardiomyocytes
inferredcites →https://doi.org/10.1016/j.ccl.2007.08.010openalex-snapshot
Heart Failure in the Twenty-First Century: Is it a Coronary Artery Disease or Hypertension Problem?
inferredcites →https://doi.org/10.1016/j.exger.2017.09.019openalex-snapshot
Causal effects of cardiovascular risk factors on onset of major age-related diseases: A time-to-event Mendelian randomization study
inferredcites →https://doi.org/10.1016/j.jacc.2018.08.2181openalex-snapshot
Dilated Cardiomyopathy Due to BLC2-Associated Athanogene 3 (BAG3) Mutations
inferredcites →https://doi.org/10.1016/j.tips.2016.04.007openalex-snapshot
Breaking BAG: The Co-Chaperone BAG3 in Health and Disease
inferredcites →https://doi.org/10.1038/75556openalex-snapshot
Gene Ontology: tool for the unification of biology
inferredcites →https://doi.org/10.1038/ejhg.2017.51openalex-snapshot
Improved imputation accuracy of rare and low-frequency variants using population-specific high-coverage WGS-based imputation reference panel
inferredcites →https://doi.org/10.1038/nature06258openalex-snapshot
A second generation human haplotype map of over 3.1 million SNPs
inferredcites →https://doi.org/10.1038/nature09534openalex-snapshot
A map of human genome variation from population-scale sequencing
inferredcites →https://doi.org/10.1038/nature10814openalex-snapshot
Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities
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/nature15393openalex-snapshot
A global reference for human genetic variation
inferredcites →https://doi.org/10.1038/nature24277openalex-snapshot
Genetic effects on gene expression across human tissues
inferredcites →https://doi.org/10.1038/ncomms15452openalex-snapshot
A complete tool set for molecular QTL discovery and analysis
inferredcites →https://doi.org/10.1038/ng.216openalex-snapshot
Detection of sharing by descent, long-range phasing and haplotype imputation
inferredcites →https://doi.org/10.1038/ng.2653openalex-snapshot
The Genotype-Tissue Expression (GTEx) project
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.2892openalex-snapshot
A general framework for estimating the relative pathogenicity of human genetic variants
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.3396openalex-snapshot
A comprehensive 1000 Genomes–based genome-wide association meta-analysis of coronary artery disease
inferredcites →https://doi.org/10.1038/ng.3571openalex-snapshot
Fast and accurate long-range phasing in a UK Biobank cohort
inferredcites →https://doi.org/10.1038/ng.3643openalex-snapshot
A reference panel of 64,976 haplotypes for genotype imputation
inferredcites →https://doi.org/10.1038/ng.3708openalex-snapshot
Identification of genomic loci associated with resting heart rate and shared genetic predictors with all-cause mortality
inferredcites →https://doi.org/10.1038/ng.3768openalex-snapshot
Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk
inferredcites →https://doi.org/10.1038/ng2088openalex-snapshot
A new multipoint method for genome-wide association studies by imputation of genotypes
inferredcites →https://doi.org/10.1038/nmeth.2307openalex-snapshot
Improved whole-chromosome phasing for disease and population genetic studies
inferredcites →https://doi.org/10.1038/nprot.2014.071openalex-snapshot
Quality control and conduct of genome-wide association meta-analyses
inferredcites →https://doi.org/10.1038/nrcardio.2016.25openalex-snapshot
Epidemiology and aetiology of heart failure
inferredcites →https://doi.org/10.1038/s41467-017-01261-5openalex-snapshot
Functional mapping and annotation of genetic associations with FUMA
inferredcites →https://doi.org/10.1038/s41467-017-02317-2openalex-snapshot
Causal associations between risk factors and common diseases inferred from GWAS summary data
inferredcites →https://doi.org/10.1038/s41586-018-0175-2openalex-snapshot
Genomic atlas of the human plasma proteome
inferredcites →https://doi.org/10.1038/s41586-018-0579-zopenalex-snapshot
The UK Biobank resource with deep phenotyping and genomic data
inferredcites →https://doi.org/10.1038/s41588-018-0133-9openalex-snapshot
Multi-ethnic genome-wide association study for atrial fibrillation
inferredcites →https://doi.org/10.1038/s41588-021-00913-zopenalex-snapshot
Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression
inferredcites →https://doi.org/10.1038/srep45040openalex-snapshot
1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function
inferredcites →https://doi.org/10.1056/nejmoa020245openalex-snapshot
Obesity and the Risk of Heart Failure
inferredcites →https://doi.org/10.1093/aje/kwx246openalex-snapshot
Comparison of Sociodemographic and Health-Related Characteristics of UK Biobank Participants With Those of the General Population
inferredcites →https://doi.org/10.1093/bioinformatics/btq340openalex-snapshot
METAL: fast and efficient meta-analysis of genomewide association scans
inferredcites →https://doi.org/10.1093/bioinformatics/btu704openalex-snapshot
minimac2: faster genotype imputation
inferredcites →https://doi.org/10.1093/biostatistics/kxq039openalex-snapshot
Methods for testing association between uncertain genotypes and quantitative traits
inferredcites →https://doi.org/10.1093/eurheartj/ehab670openalex-snapshot
Corrigendum to: 2021 ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure: Developed by the Task Force for the diagnosis and treatment of acute and chronic heart failure of the European Society of Cardiology (ESC) With the special contribution of the Heart Failure…
inferredcites →https://doi.org/10.1093/eurheartj/ehr105openalex-snapshot
A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy
inferredcites →https://doi.org/10.1093/eurheartj/ehs370openalex-snapshot
Corrigendum to: ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure 2012’[Eur Heart J 2012;33:1787–1847, doi:10.1093/eurheartj/ehs104
inferredcites →https://doi.org/10.1093/eurheartj/eht251openalex-snapshot
A genome-wide association study identifies 6p21 as novel risk locus for dilated cardiomyopathy
inferredcites →https://doi.org/10.1093/eurheartj/ehw128openalex-snapshot
2016 ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure
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/dyv080openalex-snapshot
Mendelian randomization with invalid instruments: effect estimation and bias detection through Egger regression
inferredcites →https://doi.org/10.1093/ije/dyx034openalex-snapshot
MendelianRandomization: an R package for performing Mendelian randomization analyses using summarized data
inferredcites →https://doi.org/10.1093/nar/gkt1229openalex-snapshot
The NHGRI GWAS Catalog, a curated resource of SNP-trait associations
inferredcites →https://doi.org/10.1093/nar/gku864openalex-snapshot
svaseq: removing batch effects and other unwanted noise from sequencing data
inferredcites →https://doi.org/10.1093/nar/gkw1133openalex-snapshot
The new NHGRI-EBI Catalog of published genome-wide association studies (GWAS Catalog)
inferredcites →https://doi.org/10.1111/acel.12824openalex-snapshot
Altered modulation of lamin A/C‐HDAC2 interaction and p21 expression during oxidative stress response in HGPS
inferredcites →https://doi.org/10.1111/j.0006-341x.1999.00997.xopenalex-snapshot
Genomic Control for Association Studies
inferredcites →https://doi.org/10.1136/bmj.327.7414.557openalex-snapshot
Measuring inconsistency in meta-analyses
inferredcites →https://doi.org/10.1161/cir.0000000000000558openalex-snapshot
Heart Disease and Stroke Statistics—2018 Update: A Report From the American Heart Association
inferredcites →https://doi.org/10.1161/circgenetics.109.895763openalex-snapshot
Association of Genome-Wide Variation With the Risk of Incident Heart Failure in Adults of European and African Ancestry
inferredcites →https://doi.org/10.1161/circheartfailure.109.899070openalex-snapshot
Chronic Kidney Disease and the Risk of Heart Failure in Men
inferredcites →https://doi.org/10.1161/circheartfailure.112.000171openalex-snapshot
Resting Heart Rate and the Risk of Heart Failure in Healthy Adults
inferredcites →https://doi.org/10.1161/circresaha.113.300268openalex-snapshot
Epidemiology of Heart Failure
inferredcites →https://doi.org/10.1161/circresaha.113.300282openalex-snapshot
Genetic Cardiomyopathies Causing Heart Failure
inferredcites →https://doi.org/10.1161/circresaha.113.301667openalex-snapshot
Parsing Good Versus Bad Signaling Pathways in the Heart
inferredcites →https://doi.org/10.1161/circulationaha.115.018614openalex-snapshot
Atrial Fibrillation Begets Heart Failure and Vice Versa
inferredcites →https://doi.org/10.1161/circulationaha.118.035774openalex-snapshot
Phenotypic Refinement of Heart Failure in a National Biobank Facilitates Genetic Discovery
inferredcites →https://doi.org/10.1172/jci36277openalex-snapshot
Calsarcin-2 deficiency increases exercise capacity in mice through calcineurin/NFAT activation
inferredcites →https://doi.org/10.1172/jci84840openalex-snapshot
Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function
inferredcites →https://doi.org/10.1186/1471-2105-11-134openalex-snapshot
ProbABEL package for genome-wide association analysis of imputed data
inferredcites →https://doi.org/10.1186/s13073-017-0410-8openalex-snapshot
Genetics and genomics of dilated cardiomyopathy and systolic heart failure
inferredcites →https://doi.org/10.1186/s13742-015-0047-8openalex-snapshot
Second-generation PLINK: rising to the challenge of larger and richer datasets
inferredcites →https://doi.org/10.1242/jcs.063859openalex-snapshot
CHAP is a newly identified Z-disc protein essential for heart and skeletal muscle function
inferredcites →https://doi.org/10.1371/journal.pcbi.1004219openalex-snapshot
MAGMA: Generalized Gene-Set Analysis of GWAS Data
inferredcites →https://doi.org/10.1371/journal.pgen.1000529openalex-snapshot
A Flexible and Accurate Genotype Imputation Method for the Next Generation of Genome-Wide Association Studies
inferredcites →https://doi.org/10.1371/journal.pgen.1004383openalex-snapshot
Bayesian Test for Colocalisation between Pairs of Genetic Association Studies Using Summary Statistics
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/10.1371/journal.pone.0172995openalex-snapshot
Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy
inferredcites →https://doi.org/10.2337/db16-1253openalex-snapshot
An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans
inferredcites →https://doi.org/10.34944/dspace/4648openalex-snapshot
Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics
inferredcites →https://doi.org/10.7554/elife.34408openalex-snapshot
The MR-Base platform supports systematic causal inference across the human phenome
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.ijbiomac.2024.135125openalex-snapshot
Potentially causal association between immunoglobulin G N-glycans and cardiometabolic diseases: Bidirectional two-sample Mendelian randomization study
inferred← citeshttps://doi.org/10.1038/s41598-024-82698-9openalex-snapshot
CpG methylation changes associated with hyperglycemia in type 1 diabetes occur at angiogenic glomerular and retinal gene loci
inferred← citeshttps://doi.org/10.1134/s0026893325700281openalex-snapshot
Genetic Aspects of the Application of Tissue-Engineered Constructs in Regenerative Therapy in Cardiology: An Analytical Review
inferred← citeshttps://doi.org/10.21203/rs.3.rs-776922/v1openalex-snapshot
Coffee Types and Cardiac Metabolic Risks: Large-scale Cross-phenotype Association Study and Mendelian Randomization Analysis
inferred← citeshttps://doi.org/10.21203/rs.3.rs-86424/v1openalex-snapshot
Genetic and Causal Relationship Between Coffee Intake and Cardiometabolic Risks: Cross-Phenotype Association And Mendelian Randomization Analysis
inferred← citeshttps://doi.org/10.3389/fgene.2021.746677openalex-snapshot
Evaluating Causal Relationship Between Metabolites and Six Cardiovascular Diseases Based on GWAS Summary Statistics
inferred← citeshttps://doi.org/10.7554/elife.57345openalex-snapshot
Dynamic effects of genetic variation on gene expression revealed following hypoxic stress in cardiomyocytes
inferred← citeshttps://doi.org/10.7554/elife.72452openalex-snapshot
Disease consequences of higher adiposity uncoupled from its adverse metabolic effects using Mendelian randomisation
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