On the public citation graph
Identification of heart rate–associated loci and their effects on cardiac conduction and rhythm disorders
0 signed · 416 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1001/jama.2011.1826openalex-snapshot
Temporal Changes in Resting Heart Rate and Deaths From Ischemic Heart Disease
inferredcites →https://doi.org/10.1006/jmcc.1997.0460openalex-snapshot
Dexamethasone-induced Up-regulation of Adrenomedullin and Atrial Natriuretic Peptide Genes in Cultured Rat Ventricular Myocytes
inferredcites →https://doi.org/10.1007/s10147-006-0616-zopenalex-snapshot
The TIMP-1 gene transferred through adenovirus mediation shows a suppressive effect on peritoneal metastases from gastric cancer
inferredcites →https://doi.org/10.1007/s12265-010-9243-1openalex-snapshot
Electrophysiological Mechanisms of the Anti-arrhythmic Effects of Omega-3 Fatty Acids
inferredcites →https://doi.org/10.1016/0002-8703(91)90970-sopenalex-snapshot
Pulse rate, coronary heart disease, and death: The NHANES I Epidemiologic Follow-up Study
inferredcites →https://doi.org/10.1016/0006-2952(93)90283-3openalex-snapshot
Arachidonic acid-induced Ca2+ release from isolated sarcoplasmic reticulum
inferredcites →https://doi.org/10.1016/0091-7435(87)90087-9openalex-snapshot
Incidence and precursors of hypertension in young adults: The Framingham offspring study
inferredcites →https://doi.org/10.1016/0092-8674(90)90273-hopenalex-snapshot
A molecular basis for familial hypertrophic cardiomyopathy: An αβ cardiac myosin heavy chain hybrid gene
inferredcites →https://doi.org/10.1016/j.ahj.2010.08.001openalex-snapshot
PLN-encoded phospholamban mutation in a large cohort of hypertrophic cardiomyopathy cases: Summary of the literature and implications for genetic testing
inferredcites →https://doi.org/10.1016/j.ajhg.2011.10.013openalex-snapshot
Blood Pressure Loci Identified with a Gene-Centric Array
inferredcites →https://doi.org/10.1016/j.atherosclerosis.2008.10.009openalex-snapshot
Tissue Factor Pathway Inhibitor-2 gene methylation is associated with low expression in carotid atherosclerotic plaques
inferredcites →https://doi.org/10.1016/j.atherosclerosis.2009.04.024openalex-snapshot
Tissue factor pathway inhibitor, vascular risk factors and subclinical atherosclerosis: The Multi-Ethnic Study of Atherosclerosis
inferredcites →https://doi.org/10.1016/j.cbi.2010.01.042openalex-snapshot
Acetylcholinesterase: From 3D structure to function
inferredcites →https://doi.org/10.1016/j.febslet.2007.01.095openalex-snapshot
New insights into mitochondrial fusion
inferredcites →https://doi.org/10.1016/j.jacc.2003.05.004openalex-snapshot
NKX2.5mutations in patients with congenital heart disease
inferredcites →https://doi.org/10.1016/j.jvs.2005.02.020openalex-snapshot
Genetic analysis of polymorphisms in biologically relevant candidate genes in patients with abdominal aortic aneurysms
inferredcites →https://doi.org/10.1016/j.tcm.2003.09.006openalex-snapshot
Pacemaker Channels and Sinus Node Arrhythmia
inferredcites →https://doi.org/10.1016/j.yjmcc.2009.01.004openalex-snapshot
Titin-based mechanical signalling in normal and failing myocardium
inferredcites →https://doi.org/10.1016/j.yjmcc.2011.06.008openalex-snapshot
Effects of different small HSPB members on contractile dysfunction and structural changes in a Drosophila melanogaster model for Atrial Fibrillation
inferredcites →https://doi.org/10.1016/s0006-291x(03)00526-6openalex-snapshot
Mutation of the phospholamban promoter associated with hypertrophic cardiomyopathy
inferredcites →https://doi.org/10.1016/s0022-0736(98)80034-4openalex-snapshot
Heritability of ECG measurements in adult male twins
inferredcites →https://doi.org/10.1016/s0026-895x(24)12560-6openalex-snapshot
Expression of Multiple Subtypes of Muscarinic Receptors and Cellular Distribution in the Human Heart
inferredcites →https://doi.org/10.1016/s0092-8674(00)81436-1openalex-snapshot
Molecular Distinction and Angiogenic Interaction between Embryonic Arteries and Veins Revealed by ephrin-B2 and Its Receptor Eph-B4
inferredcites →https://doi.org/10.1016/s0140-6736(10)61259-7openalex-snapshot
Heart rate as a risk factor in chronic heart failure (SHIFT): the association between heart rate and outcomes in a randomised placebo-controlled trial
inferredcites →https://doi.org/10.1016/s1053-2498(02)00557-0openalex-snapshot
Increased expression of extracellular matrix regulators TIMP1 and MMP1 in deteriorating heart failure
inferredcites →https://doi.org/10.1016/s1097-2765(02)00488-4openalex-snapshot
EphrinB Phosphorylation and Reverse Signaling
inferredcites →https://doi.org/10.1038/nature05954openalex-snapshot
A genome-wide transgenic RNAi library for conditional gene inactivation in Drosophila
inferredcites →https://doi.org/10.1038/nature06007openalex-snapshot
Variants conferring risk of atrial fibrillation on chromosome 4q25
inferredcites →https://doi.org/10.1038/nature09629openalex-snapshot
A population-specific HTR2B stop codon predisposes to severe impulsivity
inferredcites →https://doi.org/10.1038/nature10405openalex-snapshot
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
inferredcites →https://doi.org/10.1038/nchembio732openalex-snapshot
High-throughput assay for small molecules that modulate zebrafish embryonic heart rate
inferredcites →https://doi.org/10.1038/ncomms1871openalex-snapshot
Quantitative maps of protein phosphorylation sites across 14 different rat organs and tissues
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.2261openalex-snapshot
Meta-analysis identifies six new susceptibility loci for atrial fibrillation
inferredcites →https://doi.org/10.1038/ng.269openalex-snapshot
Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts
inferredcites →https://doi.org/10.1038/ng.327openalex-snapshot
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants
inferredcites →https://doi.org/10.1038/ng.357openalex-snapshot
A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits
inferredcites →https://doi.org/10.1038/ng.361openalex-snapshot
Genome-wide association study identifies eight loci associated with blood pressure
inferredcites →https://doi.org/10.1038/ng.362openalex-snapshot
Common variants at ten loci modulate the QT interval duration in the QTSCD Study
inferredcites →https://doi.org/10.1038/ng.364openalex-snapshot
Common variants at ten loci influence QT interval duration in the QTGEN Study
inferredcites →https://doi.org/10.1038/ng.384openalex-snapshot
Genome-wide association study of blood pressure and hypertension
inferredcites →https://doi.org/10.1038/ng.416openalex-snapshot
Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry
inferredcites →https://doi.org/10.1038/ng.417openalex-snapshot
A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke
inferredcites →https://doi.org/10.1038/ng.511openalex-snapshot
Several common variants modulate heart rate, PR interval and QRS duration
inferredcites →https://doi.org/10.1038/ng.516openalex-snapshot
Genetic variation in SCN10A influences cardiac conduction
inferredcites →https://doi.org/10.1038/ng.517openalex-snapshot
Genome-wide association study of PR interval
inferredcites →https://doi.org/10.1038/ng.537openalex-snapshot
Common variants in KCNN3 are associated with lone atrial fibrillation
inferredcites →https://doi.org/10.1038/ng.543openalex-snapshot
Multiple common variants for celiac disease influencing immune gene expression
inferredcites →https://doi.org/10.1038/ng.716openalex-snapshot
Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction
inferredcites →https://doi.org/10.1038/ng.768openalex-snapshot
Discovery and genotyping of genome structural polymorphism by sequencing on a population scale
inferredcites →https://doi.org/10.1038/ng.781openalex-snapshot
A rare variant in MYH6 is associated with high risk of sick sinus syndrome
inferredcites →https://doi.org/10.1038/ng.784openalex-snapshot
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
inferredcites →https://doi.org/10.1038/ng.922openalex-snapshot
Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure
inferredcites →https://doi.org/10.1038/ng1526openalex-snapshot
Mutation in myosin heavy chain 6 causes atrial septal defect
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/ng815openalex-snapshot
Mutations of TTN, encoding the giant muscle filament titin, cause familial dilated cardiomyopathy
inferredcites →https://doi.org/10.1054/jcaf.2002.129278openalex-snapshot
Titin: An endosarcomeric protein that modulates myocardial stiffness in DCM
inferredcites →https://doi.org/10.1073/pnas.0510519103openalex-snapshot
A mutation in the human phospholamban gene, deleting arginine 14, results in lethal, hereditary cardiomyopathy
inferredcites →https://doi.org/10.1073/pnas.0904744106openalex-snapshot
GATA6 mutations cause human cardiac outflow tract defects by disrupting semaphorin-plexin signaling
inferredcites →https://doi.org/10.1073/pnas.1010122108openalex-snapshot
Deep bradycardia and heart block caused by inducible cardiac-specific knockout of the pacemaker channel gene Hcn4
inferredcites →https://doi.org/10.1073/pnas.110149597openalex-snapshot
Use of double-stranded RNA interference in Drosophila cell lines to dissect signal transduction pathways
inferredcites →https://doi.org/10.1073/pnas.2434235100openalex-snapshot
The hyperpolarization-activated channel HCN4 is required for the generation of pacemaker action potentials in the embryonic heart
inferredcites →https://doi.org/10.1074/jbc.m107669200openalex-snapshot
Csx/Nkx2-5 Is Required for Homeostasis and Survival of Cardiac Myocytes in the Adult Heart
inferredcites →https://doi.org/10.1080/07420520902924939openalex-snapshot
Clock Genes Display Rhythmic Expression in Human Hearts
inferredcites →https://doi.org/10.1086/497345openalex-snapshot
Handling Marker-Marker Linkage Disequilibrium: Pedigree Analysis with Clustered Markers
inferredcites →https://doi.org/10.1086/519795openalex-snapshot
PLINK: A Tool Set for Whole-Genome Association and Population-Based Linkage Analyses
inferredcites →https://doi.org/10.1093/bioinformatics/btm108openalex-snapshot
GenABEL: an R library for genome-wide association analysis
inferredcites →https://doi.org/10.1093/bioinformatics/btn564openalex-snapshot
SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap
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/cvr/cvp181openalex-snapshot
Mitochondrial OPA1, apoptosis, and heart failure
inferredcites →https://doi.org/10.1093/hmg/ddi202openalex-snapshot
Functional dissection of sequence-specific NKX2-5 DNA binding domain mutations associated with human heart septation defects using a yeast-based system
inferredcites →https://doi.org/10.1093/hmg/ddl117openalex-snapshot
Common genetic variants of the FADS1 FADS2 gene cluster and their reconstructed haplotypes are associated with the fatty acid composition in phospholipids
inferredcites →https://doi.org/10.1093/hmg/ddq303openalex-snapshot
Genome-wide association analysis identifies multiple loci related to resting heart rate
inferredcites →https://doi.org/10.1093/molehr/6.9.811openalex-snapshot
Adrenomedullin is an autocrine regulator of endothelial growth in human endometrium
inferredcites →https://doi.org/10.1093/oxfordjournals.aje.a113046openalex-snapshot
HEART RATE AS A PROGNOSTIC FACTOR FOR CORONARY HEART DISEASE AND MORTALITY: FINDINGS IN THREE CHICAGO EPIDEMIOLOGIC STUDIES
inferredcites →https://doi.org/10.1097/01.psy.0000278973.14218.6bopenalex-snapshot
Correction to De Geus et al. Bivariate Genetic Modeling of Cardiovascular Stress Reactivity: Does Stress Uncover Genetic Variance? (May 2007)
inferredcites →https://doi.org/10.1097/psy.0b013e318049cc2dopenalex-snapshot
Bivariate Genetic Modeling of Cardiovascular Stress Reactivity: Does Stress Uncover Genetic Variance?
inferredcites →https://doi.org/10.1101/gad.13.3.295openalex-snapshot
Roles of ephrinB ligands and EphB receptors in cardiovascular development: demarcation of arterial/venous domains, vascular morphogenesis, and sprouting angiogenesis
inferredcites →https://doi.org/10.1101/gr.772403openalex-snapshot
PANTHER: A Library of Protein Families and Subfamilies Indexed by Function
inferredcites →https://doi.org/10.1111/j.1540-8167.2007.01030.xopenalex-snapshot
Heritability of QT Interval: How Much Is Explained by Genes for Resting Heart Rate?
inferredcites →https://doi.org/10.1111/j.1582-4934.2004.tb00477.xopenalex-snapshot
Expression of phospholipase D isozymes in scar and viable tissue in congestive heart failure due to myocardial infarction
inferredcites →https://doi.org/10.1111/j.1582-4934.2008.00219.xopenalex-snapshot
Atrial extracellular matrix remodelling in patients with atrial fibrillation
inferredcites →https://doi.org/10.1113/jphysiol.2005.100776openalex-snapshot
Properties of ivabradine‐induced block of HCN1 and HCN4 pacemaker channels
inferredcites →https://doi.org/10.1126/science.1081578openalex-snapshot
Dilated Cardiomyopathy and Heart Failure Caused by a Mutation in Phospholamban
inferredcites →https://doi.org/10.1126/science.6484569openalex-snapshot
Retarding Effect of Lowered Heart Rate on Coronary Atherosclerosis
inferredcites →https://doi.org/10.1128/mcb.26.7.2511-2518.2006openalex-snapshot
Hydrops Fetalis, Cardiovascular Defects, and Embryonic Lethality in Mice Lacking the Calcitonin Receptor-Like Receptor Gene
inferredcites →https://doi.org/10.1146/annurev.genom.9.081307.164242openalex-snapshot
Genotype Imputation
inferredcites →https://doi.org/10.1152/ajpheart.00140.2011openalex-snapshot
Effect of dietary omega-3 fatty acids on the heart rate and the heart rate variability responses to myocardial ischemia or submaximal exercise
inferredcites →https://doi.org/10.1152/physiolgenomics.00206.2009openalex-snapshot
High-resolution cardiovascular function confirms functional orthology of myocardial contractility pathways in zebrafish
inferredcites →https://doi.org/10.1159/000435947openalex-snapshot
Heart Rate, Life Expectancy and the Cardiovascular System: Therapeutic Considerations
inferredcites →https://doi.org/10.1161/01.atv.0000254147.89321.cfopenalex-snapshot
Adenovirus-Mediated Expression of Tissue Factor Pathway Inhibitor-2 Inhibits Endothelial Cell Migration and Angiogenesis
inferredcites →https://doi.org/10.1161/01.atv.12.11.1245openalex-snapshot
Experimental atherosclerosis at the carotid bifurcation of the cynomolgus monkey. Localization, compensatory enlargement, and the sparing effect of lowered heart rate.
inferredcites →https://doi.org/10.1161/01.cir.0000105900.21445.3dopenalex-snapshot
Involvement of Tissue Factor Pathway Inhibitor in the Coronary Circulation of Patients With Acute Coronary Syndromes
inferredcites →https://doi.org/10.1161/01.cir.69.4.790openalex-snapshot
Autonomic mechanisms in ventricular fibrillation induced by myocardial ischemia during exercise in dogs with healed myocardial infarction. An experimental preparation for sudden cardiac death.
inferredcites →https://doi.org/10.1161/01.cir.95.5.1214openalex-snapshot
Potent and Long-Lasting Vasodilatory Effects of Adrenomedullin in Humans
inferredcites →https://doi.org/10.1161/01.res.0000152325.07495.5aopenalex-snapshot
Connexin 43 Downregulation and Dephosphorylation in Nonischemic Heart Failure Is Associated With Enhanced Colocalized Protein Phosphatase Type 2A
inferredcites →https://doi.org/10.1161/01.res.86.12.1193openalex-snapshot
Gap Junctions in Cardiovascular Disease
inferredcites →https://doi.org/10.1161/circresaha.107.167783openalex-snapshot
A Missense Mutation in the CHRM2 Gene Is Associated With Familial Dilated Cardiomyopathy
inferredcites →https://doi.org/10.1161/circresaha.108.171835openalex-snapshot
Perinatal Loss of Nkx2-5 Results in Rapid Conduction and Contraction Defects
inferredcites →https://doi.org/10.1161/circulationaha.104.507699openalex-snapshot
α-Myosin Heavy Chain
inferredcites →https://doi.org/10.1161/circulationaha.107.706887openalex-snapshot
Point Mutation in the HCN4 Cardiac Ion Channel Pore Affecting Synthesis, Trafficking, and Functional Expression Is Associated With Familial Asymptomatic Sinus Bradycardia
inferredcites →https://doi.org/10.1161/circulationaha.107.712984openalex-snapshot
Omega-3 Fatty Acids and Cardiac Arrhythmias: Prior Studies and Recommendations for Future Research
inferredcites →https://doi.org/10.1161/circulationaha.110.961227openalex-snapshot
Paradigm of Genetic Mosaicism and Lone Atrial Fibrillation
inferredcites →https://doi.org/10.1172/jci113627openalex-snapshot
Molecular cloning and characterization of human cardiac alpha- and beta-form myosin heavy chain complementary DNA clones. Regulation of expression during development and pressure overload in human atrium.
inferredcites →https://doi.org/10.1172/jci119776openalex-snapshot
Myosin heavy chain gene expression in human heart failure.
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/10.1186/1471-2199-9-41openalex-snapshot
Interaction of circadian clock proteins PER2 and CRY with BMAL1 and CLOCK
inferredcites →https://doi.org/10.1186/1476-511x-9-22openalex-snapshot
Postnatal ontogenesis of clock genes in mouse suprachiasmatic nucleus and heart
inferredcites →https://doi.org/10.1186/1479-7364-3-4-371openalex-snapshot
Current software for genotype imputation
inferredcites →https://doi.org/10.1242/dev.059386openalex-snapshot
The fibronectin leucine-rich repeat transmembrane protein Flrt2 is required in the epicardium to promote heart morphogenesis
inferredcites →https://doi.org/10.1253/circj.66.561openalex-snapshot
Novel Point Mutation in the Cardiac Transcription Factor CSX/NKX2.5 Associated With Congenital Heart Disease.
inferredcites →https://doi.org/10.1253/circj.71.1755openalex-snapshot
Higher Heart Rate Predicts the Risk of Developing Hypertension in a Normotensive Screened Cohort
inferredcites →https://doi.org/10.1292/jvms.70.411openalex-snapshot
Transient Expression of Phospholipase D1 during Heart Development in Rats
inferredcites →https://doi.org/10.1371/journal.pgen.1000279openalex-snapshot
Practical Issues in Imputation-Based Association Mapping
inferredcites →https://doi.org/10.1371/journal.pgen.1000338openalex-snapshot
Genome-Wide Association Study of Plasma Polyunsaturated Fatty Acids in the InCHIANTI Study
inferredcites →https://doi.org/10.1371/journal.pgen.1001058openalex-snapshot
Common Inherited Variation in Mitochondrial Genes Is Not Enriched for Associations with Type 2 Diabetes or Related Glycemic Traits
inferredcites →https://doi.org/10.1371/journal.pgen.1001177openalex-snapshot
Genome-Wide Association Study of Blood Pressure Extremes Identifies Variant near UMOD Associated with Hypertension
inferredcites →https://doi.org/10.1371/journal.pgen.1001300openalex-snapshot
Genome-Wide Association Study of Coronary Heart Disease and Its Risk Factors in 8,090 African Americans: The NHLBI CARe Project
inferredcites →https://doi.org/10.1371/journal.pgen.1002793openalex-snapshot
The Metabochip, a Custom Genotyping Array for Genetic Studies of Metabolic, Cardiovascular, and Anthropometric Traits
inferredcites →https://doi.org/10.1371/journal.pone.0005698openalex-snapshot
NKX2-5 Regulates the Expression of β-Catenin and GATA4 in Ventricular Myocytes
inferredcites →https://doi.org/10.1371/journal.pone.0010827openalex-snapshot
Analyses and Comparison of Imputation-Based Association Methods
inferredcites →https://doi.org/10.1371/journal.pone.0031193openalex-snapshot
Identification of New Genes Involved in Human Adipogenesis and Fat Storage
inferredcites →https://doi.org/10.1515/cclm.2008.091openalex-snapshot
Serum levels of the osteoprotegerin, receptor activator of nuclear factor κ-B ligand, metalloproteinase-1 (MMP-1) and tissue inhibitors of MMP-1 levels are increased in men 6 months after acute myocardial infarction
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/ajmg.a.37297openalex-snapshot
Exome analysis of a family with Wolff–Parkinson–White syndrome identifies a novel disease locus
inferred← citeshttps://doi.org/10.1002/ar.23911openalex-snapshot
Filamin‐A as a Balance between Erk/Smad Activities During Cardiac Valve Development
inferred← citeshttps://doi.org/10.1002/clc.22578openalex-snapshot
The Risk of Atrial Fibrillation With Ivabradine Treatment: A Meta‐analysis With Trial Sequential Analysis of More Than 40000 Patients
inferred← citeshttps://doi.org/10.1002/da.22966openalex-snapshot
The association of depression and anxiety with cardiac autonomic activity: The role of confounding effects of antidepressants
inferred← citeshttps://doi.org/10.1002/gepi.22372openalex-snapshot
Statistical methods with exhaustive search in the identification of gene–gene interactions for colorectal cancer
inferred← citeshttps://doi.org/10.1002/jcph.1443openalex-snapshot
β2‐Adrenergic Receptor Gene Affects the Heart Rate Response of β‐Blockers: Evidence From 3 Clinical Studies
inferred← citeshttps://doi.org/10.1007/978-1-4614-0965-6_10openalex-snapshot
The Genetic Determinants of Common Obesity-Susceptibility
inferred← citeshttps://doi.org/10.1007/978-3-030-45457-9_17openalex-snapshot
Hereditary Cardiac Conduction Diseases
inferred← citeshttps://doi.org/10.1007/978-3-319-44203-7_16openalex-snapshot
Hereditary Cardiac Conduction Diseases
inferred← citeshttps://doi.org/10.1007/978-3-319-52031-5_11openalex-snapshot
The Genetic Determinants of Common Obesity-Susceptibility
inferred← citeshttps://doi.org/10.1007/978-3-319-66114-8_15openalex-snapshot
Inherited Conduction Disease and Atrial Fibrillation
inferred← citeshttps://doi.org/10.1007/978-3-7091-1883-2_62openalex-snapshot
Human Genetics of Arrhythmias
inferred← citeshttps://doi.org/10.1007/978-981-13-1429-2_1openalex-snapshot
Genome-Wide Association Studies of Hypertension and Several Other Cardiovascular Diseases
inferred← citeshttps://doi.org/10.1007/s00018-016-2400-1openalex-snapshot
Development of the cardiac pacemaker
inferred← citeshttps://doi.org/10.1007/s00059-020-04913-3openalex-snapshot
Association of T66A polymorphism in CASQ2 with PR interval in a Chinese population
inferred← citeshttps://doi.org/10.1007/s00103-016-2323-xopenalex-snapshot
12 Jahre AFNET. Vom Forschungsnetzwerk zur Academic Research Organisation
inferred← citeshttps://doi.org/10.1007/s00125-022-05653-1openalex-snapshot
Separating the direct effects of traits on atherosclerotic cardiovascular disease from those mediated by type 2 diabetes
inferred← citeshttps://doi.org/10.1007/s00246-019-02166-4openalex-snapshot
Tbx3-Mediated Regulation of Cardiac Conduction System Development and Function: Potential Contributions of Alternative RNA Processing
inferred← citeshttps://doi.org/10.1007/s00395-015-0468-7openalex-snapshot
Loss of dihydrolipoyl succinyltransferase (DLST) leads to reduced resting heart rate in the zebrafish
inferred← citeshttps://doi.org/10.1007/s00395-016-0557-2openalex-snapshot
Coding and non-coding variants in the SHOX2 gene in patients with early-onset atrial fibrillation
inferred← citeshttps://doi.org/10.1007/s00439-022-02502-4openalex-snapshot
Identifying shared genetic factors underlying epilepsy and congenital heart disease in Europeans
inferred← citeshttps://doi.org/10.1007/s00439-024-02661-6openalex-snapshot
Genetic evidence for T-wave area from 12-lead electrocardiograms to monitor cardiovascular diseases in patients taking diabetes medications
inferred← citeshttps://doi.org/10.1007/s00439-024-02684-zopenalex-snapshot
Fine mapping of candidate effector genes for heart rate
inferred← citeshttps://doi.org/10.1007/s00592-019-01344-3openalex-snapshot
Association between resting heart rate and incident diabetes risk: a Mendelian randomization study
inferred← citeshttps://doi.org/10.1007/s10522-016-9665-5openalex-snapshot
Lifetime regular exercise affects the incident of different arrhythmias and improves organismal health in aging female Drosophila melanogaster
inferred← citeshttps://doi.org/10.1007/s10539-023-09904-2openalex-snapshot
Gradualism, natural selection, and the randomness of mutation–fisher, Kimura, and Orr, connecting the dots
inferred← citeshttps://doi.org/10.1007/s10654-013-9866-zopenalex-snapshot
The Rotterdam Study: 2014 objectives and design update
inferred← citeshttps://doi.org/10.1007/s10654-015-0082-xopenalex-snapshot
The Rotterdam Study: 2016 objectives and design update
inferred← citeshttps://doi.org/10.1007/s10654-017-0321-4openalex-snapshot
The Rotterdam Study: 2018 update on objectives, design and main results
inferred← citeshttps://doi.org/10.1007/s11033-021-06517-4openalex-snapshot
Genetic predictors of sick sinus syndrome
inferred← citeshttps://doi.org/10.1007/s11356-022-24542-zopenalex-snapshot
Toxicity assessment of hexafluoropropylene oxide-dimer acid on morphology, heart physiology, and gene expression during zebrafish (Danio rerio) development
inferred← citeshttps://doi.org/10.1007/s12020-017-1331-4openalex-snapshot
Circulating microRNA-1a is a biomarker of Graves’ disease patients with atrial fibrillation
inferred← citeshttps://doi.org/10.1007/s12192-017-0787-8openalex-snapshot
The growing world of small heat shock proteins: from structure to functions
inferred← citeshttps://doi.org/10.1007/s12551-018-0435-2openalex-snapshot
Genomic approaches for the elucidation of genes and gene networks underlying cardiovascular traits
inferred← citeshttps://doi.org/10.1016/b978-0-12-802002-9.00014-5openalex-snapshot
Complexity of Molecular Genetics in the Inherited Cardiac Arrhythmias
inferred← citeshttps://doi.org/10.1016/b978-0-12-822951-4.00004-7openalex-snapshot
Genomic basis of heart rate and rhythm generation
inferred← citeshttps://doi.org/10.1016/b978-0-443-13868-3.00040-5openalex-snapshot
Genetic methods to evaluate evidence for causal effect of coffee on health
inferred← citeshttps://doi.org/10.1016/j.ajhg.2013.10.012openalex-snapshot
Beyond GWASs: Illuminating the Dark Road from Association to Function
inferred← citeshttps://doi.org/10.1016/j.ajhg.2016.06.025openalex-snapshot
GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability
inferred← citeshttps://doi.org/10.1016/j.ajhg.2022.08.004openalex-snapshot
Identification and single-base gene-editing functional validation of a cis-EPO variant as a genetic predictor for EPO-increasing therapies
inferred← citeshttps://doi.org/10.1016/j.amjcard.2014.05.040openalex-snapshot
A Genome-Wide Association Study to Identify Genomic Modulators of Rate Control Therapy in Patients With Atrial Fibrillation
inferred← citeshttps://doi.org/10.1016/j.amjcard.2016.06.013openalex-snapshot
Association Between Heart Rate at Rest and Incident Atrial Fibrillation (from the Copenhagen Electrocardiographic Study)
inferred← citeshttps://doi.org/10.1016/j.amjcard.2018.01.048openalex-snapshot
Observational and Genetic Associations of Resting Heart Rate With Aortic Valve Calcium
inferred← citeshttps://doi.org/10.1016/j.bbadis.2014.04.025openalex-snapshot
Systems genetics: From GWAS to disease pathways
inferred← citeshttps://doi.org/10.1016/j.bone.2019.02.009openalex-snapshot
Using zebrafish to study skeletal genomics
inferred← citeshttps://doi.org/10.1016/j.cellsig.2021.109947openalex-snapshot
Subtype-dependent regulation of Gβγ signalling
inferred← citeshttps://doi.org/10.1016/j.cjca.2023.07.011openalex-snapshot
Association Analyses of Predicted Loss-of-Function Variants Prioritized 15 Genes as Blood Pressure Regulators
inferred← citeshttps://doi.org/10.1016/j.cvdhj.2022.06.001openalex-snapshot
Deep learning on resting electrocardiogram to identify impaired heart rate recovery
inferred← citeshttps://doi.org/10.1016/j.devcel.2020.11.020openalex-snapshot
Modeling Human TBX5 Haploinsufficiency Predicts Regulatory Networks for Congenital Heart Disease
inferred← citeshttps://doi.org/10.1016/j.ebiom.2022.104288openalex-snapshot
Genetic determinants of cardiometabolic and pulmonary phenotypes and obstructive sleep apnoea in HCHS/SOL
inferred← citeshttps://doi.org/10.1016/j.expneurol.2015.03.016openalex-snapshot
Drosophila and experimental neurology in the post-genomic era
inferred← citeshttps://doi.org/10.1016/j.forsciint.2019.109944openalex-snapshot
Identifying blood-specific age-related DNA methylation markers on the Illumina MethylationEPIC® BeadChip
inferred← citeshttps://doi.org/10.1016/j.gene.2014.03.045openalex-snapshot
Insight into genetic determinants of resting heart rate
inferred← citeshttps://doi.org/10.1016/j.gene.2025.149269openalex-snapshot
The role of genetic polymorphisms in KCNN2 in cardiovascular complications in patients with renal failure
inferred← citeshttps://doi.org/10.1016/j.hlc.2019.06.726openalex-snapshot
Impact of Oxidative Stress on Long-Term Heart Rate Variability: Linear Versus Non-Linear Heart Rate Dynamics
inferred← citeshttps://doi.org/10.1016/j.hrcr.2020.03.003openalex-snapshot
The missense variant p.(Gly482Arg) in HCN4 is responsible for fetal tachy-bradycardia syndrome
inferred← citeshttps://doi.org/10.1016/j.hrthm.2017.06.018openalex-snapshot
Genome-wide association study of heart rate and its variability in Hispanic/Latino cohorts
inferred← citeshttps://doi.org/10.1016/j.hrthm.2018.10.036openalex-snapshot
2018 ACC/AHA/HRS guideline on the evaluation and management of patients with bradycardia and cardiac conduction delay: Executive summary
inferred← citeshttps://doi.org/10.1016/j.hrthm.2018.10.037openalex-snapshot
2018 ACC/AHA/HRS guideline on the evaluation and management of patients with bradycardia and cardiac conduction delay
inferred← citeshttps://doi.org/10.1016/j.hrthm.2022.08.024openalex-snapshot
GJA1 gene polymorphism is a genetic predictor of recurrence after pulmonary vein isolation in patients with paroxysmal atrial fibrillation
inferred← citeshttps://doi.org/10.1016/j.hrthm.2022.09.005openalex-snapshot
“Can we ablate your atrial fibrillation? Let’s check your bloodwork.” Genetic profiling and its role in ablation for atrial fibrillation
inferred← citeshttps://doi.org/10.1016/j.hrthm.2024.02.050openalex-snapshot
Symptomatic bradyarrhythmias in the athlete—Underlying mechanisms and treatments
inferred← citeshttps://doi.org/10.1016/j.ijcard.2015.01.048openalex-snapshot
CASP3 genetic variants and susceptibility to atrial fibrillation in Chinese Han population
inferred← citeshttps://doi.org/10.1016/j.ijcard.2015.11.127openalex-snapshot
Genome-wide rare copy number variations contribute to genetic risk for transposition of the great arteries
inferred← citeshttps://doi.org/10.1016/j.ijcha.2015.03.001openalex-snapshot
Cumulative effects of common genetic variants on risk of sudden cardiac death
inferred← citeshttps://doi.org/10.1016/j.intimp.2024.113520openalex-snapshot
Use of mendelian randomization to assess the causal associations of circulating plasma proteins with 12-lead ECG parameters
inferred← citeshttps://doi.org/10.1016/j.jacadv.2025.102282openalex-snapshot
Ivabradine and Atrial Fibrillation Incidence
inferred← citeshttps://doi.org/10.1016/j.jacc.2014.05.045openalex-snapshot
HCN4 Mutations in Multiple Families With Bradycardia and Left Ventricular Noncompaction Cardiomyopathy
inferred← citeshttps://doi.org/10.1016/j.jacc.2017.09.005openalex-snapshot
A Missense Variant in PLEC Increases Risk of Atrial Fibrillation
inferred← citeshttps://doi.org/10.1016/j.jacc.2018.10.044openalex-snapshot
2018 ACC/AHA/HRS Guideline on the Evaluation and Management of Patients With Bradycardia and Cardiac Conduction Delay
inferred← citeshttps://doi.org/10.1016/j.jacc.2019.03.519openalex-snapshot
Effects of Calcium, Magnesium, and Potassium Concentrations on Ventricular Repolarization in Unselected Individuals
inferred← citeshttps://doi.org/10.1016/j.jacc.2019.08.1055openalex-snapshot
Genome-Wide Assessment for Resting Heart Rate and Shared Genetics With Cardiometabolic Traits and Type 2 Diabetes
inferred← citeshttps://doi.org/10.1016/j.jacc.2022.07.014openalex-snapshot
The Athlete’s Heart—Challenges and Controversies
inferred← citeshttps://doi.org/10.1016/j.jacep.2020.10.009openalex-snapshot
Sex-Specific Ventricular Arrhythmias and Mortality in Cardiac Resynchronization Therapy Recipients
inferred← citeshttps://doi.org/10.1016/j.jelectrocard.2016.07.022openalex-snapshot
Genome-wide association studies and resting heart rate
inferred← citeshttps://doi.org/10.1016/j.pbiomolbio.2021.05.006openalex-snapshot
HCN4 current during human sinoatrial node-like action potentials
inferred← citeshttps://doi.org/10.1016/j.psychres.2024.115982openalex-snapshot
Genetic and polygenic investigation of heart rate variability to identify biomarkers associated with Anxiety disorders
inferred← citeshttps://doi.org/10.1016/j.tcm.2013.09.001openalex-snapshot
From GWAS to function: Genetic variation in sodium channel gene enhancer influences electrical patterning
inferred← citeshttps://doi.org/10.1016/j.tcm.2015.02.013openalex-snapshot
New approaches to establish genetic causality
inferred← citeshttps://doi.org/10.1016/j.tem.2015.10.004openalex-snapshot
GWAS as a Driver of Gene Discovery in Cardiometabolic Diseases
inferred← citeshttps://doi.org/10.1016/j.xgen.2026.101164openalex-snapshot
Discovery and characterization of gene-by-environment and epistatic genetic effects in a vertebrate model
inferred← citeshttps://doi.org/10.1016/j.xops.2023.100288openalex-snapshot
Genome-wide Association Studies of Retinal Vessel Tortuosity Identify Numerous Novel Loci Revealing Genes and Pathways Associated With Ocular and Cardiometabolic Diseases
inferred← citeshttps://doi.org/10.1016/j.yjmcc.2015.10.028openalex-snapshot
Genetics meets epigenetics: Genetic variants that modulate noncoding RNA in cardiovascular diseases
inferred← citeshttps://doi.org/10.1016/j.yjmcc.2017.05.009openalex-snapshot
Altered long non-coding RNA expression profile in rabbit atria with atrial fibrillation: TCONS_00075467 modulates atrial electrical remodeling by sponging miR-328 to regulate CACNA1C
inferred← citeshttps://doi.org/10.1016/j.yjmcc.2018.05.005openalex-snapshot
Mutation of the Na+/K+-ATPase Atp1a1a.1 causes QT interval prolongation and bradycardia in zebrafish
inferred← citeshttps://doi.org/10.1016/j.yjmcc.2023.04.004openalex-snapshot
The role of P21-activated kinase (Pak1) in sinus node function
inferred← citeshttps://doi.org/10.1017/cbo9781139519502.033openalex-snapshot
Research: Mediators and Moderators
inferred← citeshttps://doi.org/10.1017/s0007114524001971openalex-snapshot
Associations of the serum n-6 PUFA concentrations with exercise-induced myocardial ischaemia in middle-aged and older men
inferred← citeshttps://doi.org/10.1017/thg.2015.8openalex-snapshot
Genetic Contribution to the Variance of Blood Pressure and Heart Rate: A Systematic Review and Meta-Regression of Twin Studies
inferred← citeshttps://doi.org/10.1038/aps.2018.30openalex-snapshot
miRNAS in cardiovascular diseases: potential biomarkers, therapeutic targets and challenges
inferred← citeshttps://doi.org/10.1038/cr.2014.113openalex-snapshot
Baf250a orchestrates an epigenetic pathway to repress the Nkx2.5-directed contractile cardiomyocyte program in the sinoatrial node
inferred← citeshttps://doi.org/10.1038/ejhg.2017.50openalex-snapshot
Missing heritability: is the gap closing? An analysis of 32 complex traits in the Lifelines Cohort Study
inferred← citeshttps://doi.org/10.1038/ncomms15805openalex-snapshot
Genetic loci associated with heart rate variability and their effects on cardiac disease risk
inferred← citeshttps://doi.org/10.1038/ncomms8200openalex-snapshot
Translational regulation shapes the molecular landscape of complex disease phenotypes
inferred← citeshttps://doi.org/10.1038/ng.3014openalex-snapshot
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization
inferred← citeshttps://doi.org/10.1038/ng.3654openalex-snapshot
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
inferred← citeshttps://doi.org/10.1038/ng.3708openalex-snapshot
Identification of genomic loci associated with resting heart rate and shared genetic predictors with all-cause mortality
inferred← citeshttps://doi.org/10.1038/ng.3768openalex-snapshot
Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk
inferred← citeshttps://doi.org/10.1038/nmeth.2997openalex-snapshot
Annotation of loci from genome-wide association studies using tissue-specific quantitative interaction proteomics
inferred← citeshttps://doi.org/10.1038/nprot.2013.092openalex-snapshot
Large-scale gene function analysis with the PANTHER classification system
inferred← citeshttps://doi.org/10.1038/nrcardio.2013.186openalex-snapshot
Genetics of sudden cardiac death caused by ventricular arrhythmias
inferred← citeshttps://doi.org/10.1038/s10038-020-0742-xopenalex-snapshot
IDDCA syndrome in a Chinese infant due to GNB5 biallelic mutations
inferred← citeshttps://doi.org/10.1038/s41398-020-0765-2openalex-snapshot
Genetic overlap between psychotic experiences in the community across age and with psychiatric disorders
inferred← citeshttps://doi.org/10.1038/s41431-018-0295-zopenalex-snapshot
Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits
inferred← citeshttps://doi.org/10.1038/s41467-018-03395-6openalex-snapshot
Genetic study links components of the autonomous nervous system to heart-rate profile during exercise
inferred← citeshttps://doi.org/10.1038/s41467-018-04148-1openalex-snapshot
Thirty loci identified for heart rate response to exercise and recovery implicate autonomic nervous system
inferred← citeshttps://doi.org/10.1038/s41467-018-04766-9openalex-snapshot
PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity
inferred← citeshttps://doi.org/10.1038/s41467-018-04931-0openalex-snapshot
Promoter interactome of human embryonic stem cell-derived cardiomyocytes connects GWAS regions to cardiac gene networks
inferred← citeshttps://doi.org/10.1038/s41467-018-06805-xopenalex-snapshot
Large-scale genome-wide enrichment analyses identify new trait-associated genes and pathways across 31 human phenotypes
inferred← citeshttps://doi.org/10.1038/s41467-018-07348-xopenalex-snapshot
Examining the current standards for genetic discovery and replication in the era of mega-biobanks
inferred← citeshttps://doi.org/10.1038/s41467-019-09014-2openalex-snapshot
DNA damage-induced PARP1 activation confers cardiomyocyte dysfunction through NAD+ depletion in experimental atrial fibrillation
inferred← citeshttps://doi.org/10.1038/s41467-019-09407-3openalex-snapshot
Phenotypes associated with genes encoding drug targets are predictive of clinical trial side effects
inferred← citeshttps://doi.org/10.1038/s41467-020-17329-8openalex-snapshot
Preservation of microvascular barrier function requires CD31 receptor-induced metabolic reprogramming
inferred← citeshttps://doi.org/10.1038/s41467-020-20578-2openalex-snapshot
Identification and analysis of splicing quantitative trait loci across multiple tissues in the human genome
inferred← citeshttps://doi.org/10.1038/s41467-022-28244-5openalex-snapshot
CRISPR-Cas9 induces large structural variants at on-target and off-target sites in vivo that segregate across generations
inferred← citeshttps://doi.org/10.1038/s41467-023-39521-2openalex-snapshot
Genetic insights into resting heart rate and its role in cardiovascular disease
inferred← citeshttps://doi.org/10.1038/s41467-024-54337-4openalex-snapshot
Single-cell transcriptome analysis reveals CD34 as a marker of human sinoatrial node pacemaker cardiomyocytes
inferred← citeshttps://doi.org/10.1038/s41467-024-55496-0openalex-snapshot
Rapid and accurate multi-phenotype imputation for millions of individuals
inferred← citeshttps://doi.org/10.1038/s41467-025-59425-7openalex-snapshot
Natural genetic variation quantitatively regulates heart rate and dimension
inferred← citeshttps://doi.org/10.1038/s41559-017-0167openalex-snapshot
Dietary adaptation of FADS genes in Europe varied across time and geography
inferred← citeshttps://doi.org/10.1038/s41569-018-0031-yopenalex-snapshot
Transcriptional regulation of the cardiac conduction system
inferred← citeshttps://doi.org/10.1038/s41569-025-01227-xopenalex-snapshot
The cardiac conduction system: development, function and therapeutic targets
inferred← citeshttps://doi.org/10.1038/s41586-021-03604-1openalex-snapshot
An atlas of gene regulatory elements in adult mouse cerebrum
inferred← citeshttps://doi.org/10.1038/s41588-018-0058-3openalex-snapshot
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes
inferred← citeshttps://doi.org/10.1038/s41588-018-0133-9openalex-snapshot
Multi-ethnic genome-wide association study for atrial fibrillation
inferred← citeshttps://doi.org/10.1038/s41588-019-0499-3openalex-snapshot
Allele-specific NKX2-5 binding underlies multiple genetic associations with human electrocardiographic traits
inferred← citeshttps://doi.org/10.1038/s41588-022-01284-9openalex-snapshot
Cross-ancestry genome-wide analysis of atrial fibrillation unveils disease biology and enables cardioembolic risk prediction
inferred← citeshttps://doi.org/10.1038/s41588-024-01978-2openalex-snapshot
The impact of common and rare genetic variants on bradyarrhythmia development
inferred← citeshttps://doi.org/10.1038/s41598-020-58563-wopenalex-snapshot
Automated high-throughput heartbeat quantification in medaka and zebrafish embryos under physiological conditions
inferred← citeshttps://doi.org/10.1038/s41598-020-68567-1openalex-snapshot
Translating GWAS-identified loci for cardiac rhythm and rate using an in vivo image- and CRISPR/Cas9-based approach
inferred← citeshttps://doi.org/10.1038/s41598-021-82117-3openalex-snapshot
Minor allele of GJA1 gene polymorphism is associated with higher heart rate during atrial fibrillation
inferred← citeshttps://doi.org/10.1038/s41598-021-84135-7openalex-snapshot
A genome-wide association and polygenic risk score study on abnormal electrocardiogram in a Chinese population
inferred← citeshttps://doi.org/10.1038/s41598-021-93979-yopenalex-snapshot
A Mendelian randomization analysis of the relationship between cardioembolic risk factors and ischemic stroke
inferred← citeshttps://doi.org/10.1038/s42003-023-05376-yopenalex-snapshot
Phenotypic but not genetically predicted heart rate variability associated with all-cause mortality
inferred← citeshttps://doi.org/10.1038/s42003-024-06703-7openalex-snapshot
Dual color optogenetic tool enables heart arrest, bradycardic, and tachycardic pacing in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1038/s44161-025-00692-4openalex-snapshot
Region-specific gene expression and sex inform about disease susceptibility in the aorta
inferred← citeshttps://doi.org/10.1038/s44325-024-00032-8openalex-snapshot
Atrial cardiomyopathy in endurance athletes
inferred← citeshttps://doi.org/10.1080/00365513.2019.1566567openalex-snapshot
Resting heart rate and relation to disease and longevity: past, present and future
inferred← citeshttps://doi.org/10.1080/15622975.2022.2043561openalex-snapshot
Associations of common genetic risk variants of the muscarinic acetylcholine receptor M2 with cardiac autonomic dysfunction in patients with schizophrenia
inferred← citeshttps://doi.org/10.1093/ajcn/nqab014openalex-snapshot
Cardiovascular symptoms affect the patterns of habitual coffee consumption
inferred← citeshttps://doi.org/10.1093/ajh/hpv082openalex-snapshot
Clock Genes Explain a Large Proportion of Phenotypic Variance in Systolic Blood Pressure and This Control Is Not Modified by Environmental Temperature
inferred← citeshttps://doi.org/10.1093/bfgp/elt029openalex-snapshot
Genomics of cardiac electrical function
inferred← citeshttps://doi.org/10.1093/bfgp/elt031openalex-snapshot
Gene regulatory elements of the cardiac conduction system
inferred← citeshttps://doi.org/10.1093/cvr/cvaa144openalex-snapshot
Genome-wide association studies of cardiac electrical phenotypes
inferred← citeshttps://doi.org/10.1093/cvr/cvab370openalex-snapshot
Animal models and animal-free innovations for cardiovascular research: current status and routes to be explored. Consensus document of the ESC Working Group on Myocardial Function and the ESC Working Group on Cellular Biology of the Heart
inferred← citeshttps://doi.org/10.1093/cvr/cvv006openalex-snapshot
Animal and in silico models for the study of sarcomeric cardiomyopathies
inferred← citeshttps://doi.org/10.1093/eurheartj/ehac049openalex-snapshot
Genome-wide association study reveals novel genetic loci: a new polygenic risk score for mitral valve prolapse
inferred← citeshttps://doi.org/10.1093/eurheartj/ehv173openalex-snapshot
Cardiovascular disease and sudden cardiac death: between genetics and genomics
inferred← citeshttps://doi.org/10.1093/eurheartj/ehx487openalex-snapshot
Big data from electronic health records for early and late translational cardiovascular research: challenges and potential
inferred← citeshttps://doi.org/10.1093/europace/eut348openalex-snapshot
Pacemaker activity of the human sinoatrial node: effects of HCN4 mutations on the hyperpolarization-activated current
inferred← citeshttps://doi.org/10.1093/europace/euw038openalex-snapshot
Quantitative analysis ofPKP2and neighbouring genes in a patient with arrhythmogenic right ventricular cardiomyopathy caused by heterozygousPKP2deletion
inferred← citeshttps://doi.org/10.1093/europace/eux061openalex-snapshot
Left bundle branch block: from cardiac mechanics to clinical and diagnostic challenges
inferred← citeshttps://doi.org/10.1093/function/zqac055openalex-snapshot
Slowing Heart Rate Protects Against Pathological Cardiac Hypertrophy
inferred← citeshttps://doi.org/10.1093/hmg/ddv106openalex-snapshot
Cardiac deficiency of single cytochrome oxidase assembly factor scox induces p53-dependent apoptosis in a Drosophila cardiomyopathy model
inferred← citeshttps://doi.org/10.1093/hmg/ddw058openalex-snapshot
Twenty-eight genetic loci associated with ST-T-wave amplitudes of the electrocardiogram
inferred← citeshttps://doi.org/10.1093/hmg/ddx043openalex-snapshot
Conditional eQTL analysis reveals allelic heterogeneity of gene expression
inferred← citeshttps://doi.org/10.1093/hmg/ddx113openalex-snapshot
Discovery of novel heart rate-associated loci using the Exome Chip
inferred← citeshttps://doi.org/10.1093/hmg/ddz269openalex-snapshot
Impact of sex hormone-binding globulin on the human phenome
inferred← citeshttps://doi.org/10.1093/ije/dyt268openalex-snapshot
Cohort Profile: Estonian Biobank of the Estonian Genome Center, University of Tartu
inferred← citeshttps://doi.org/10.1093/jb/mvy096openalex-snapshot
Genome analyses for the Tohoku Medical Megabank Project towards establishment of personalized healthcare
inferred← citeshttps://doi.org/10.1093/molbev/msy202openalex-snapshot
Detection of Shared Balancing Selection in the Absence of Trans-Species Polymorphism
inferred← citeshttps://doi.org/10.1093/nar/gkv1262openalex-snapshot
The anatomical distribution of genetic associations
inferred← citeshttps://doi.org/10.1093/nar/gkw1186openalex-snapshot
PATZ1 down-regulates FADS1 by binding to rs174557 and is opposed by SP1/SREBP1c
inferred← citeshttps://doi.org/10.1097/fjc.0000000000000559openalex-snapshot
Genomics of Cardiovascular Measures of Autonomic Tone
inferred← citeshttps://doi.org/10.1097/md.0000000000004312openalex-snapshot
KCNN2 polymorphisms and cardiac tachyarrhythmias
inferred← citeshttps://doi.org/10.1101/121012openalex-snapshot
Novel locus influencing retinal venular tortuosity is also associated with risk of coronary artery disease
inferred← citeshttps://doi.org/10.1101/170142openalex-snapshot
Flipping the odds of drug development success through human genomics
inferred← citeshttps://doi.org/10.1101/2021.04.19.21255650openalex-snapshot
Genetic determinants of interventricular septal anatomy and the risk of ventricular septal defects and hypertrophic cardiomyopathy
inferred← citeshttps://doi.org/10.1101/2021.09.06.21263189openalex-snapshot
Trans-ancestry genome-wide analysis of atrial fibrillation provides new insights into disease biology and enables polygenic prediction of cardioembolic risk
inferred← citeshttps://doi.org/10.1101/2022.02.27.22268990openalex-snapshot
Multitrait Genome-Wide Analysis in the UK Biobank Reveals Novel and Distinct Variants Influencing Cardiovascular Traits in Africans and Europeans
inferred← citeshttps://doi.org/10.1101/2025.01.10.25320367openalex-snapshot
Ivabradine and Atrial Fibrillation Incidence: A Nested Matching Study
inferred← citeshttps://doi.org/10.1101/2025.04.24.650462openalex-snapshot
Discovery and characterisation of gene by environment and epistatic genetic effects in a vertebrate model
inferred← citeshttps://doi.org/10.1101/2025.07.08.663711openalex-snapshot
Exploring cardiac phenotypes of Drosophila orthologues of human genes associated to Brugada Syndrome (BrS)
inferred← citeshttps://doi.org/10.1101/319509openalex-snapshot
Clustering of Type 2 Diabetes Genetic Loci by Multi-Trait Associations Identifies Disease Mechanisms and Subtypes
inferred← citeshttps://doi.org/10.1101/363457openalex-snapshot
GWAS of QRS Duration Identifies New Loci Specific to Hispanic/Latino Populations Swenson Hispanic/Latino QRS GWAS
inferred← citeshttps://doi.org/10.1101/621334openalex-snapshot
Genome-wide association study of plasma triglycerides, phospholipids and relation to cardio-metabolic risk factors
inferred← citeshttps://doi.org/10.1101/835603openalex-snapshot
Modeling human TBX5 haploinsufficiency predicts regulatory networks for congenital heart disease
inferred← citeshttps://doi.org/10.1101/cshperspect.a037408openalex-snapshot
Development of the Cardiac Conduction System
inferred← citeshttps://doi.org/10.1101/cshperspect.a039230openalex-snapshot
Human Genomics and Drug Development
inferred← citeshttps://doi.org/10.1111/eci.12892openalex-snapshot
Heart rate as a predictor of cardiovascular risk
inferred← citeshttps://doi.org/10.1111/jce.13788openalex-snapshot
Potential use of ivabradine for treatment of atrial fibrillation
inferred← citeshttps://doi.org/10.1111/joim.12373openalex-snapshot
Low resting heart rates are associated with new‐onset atrial fibrillation in patients with vascular disease: results of the ONTARGET / TRANSCEND studies
inferred← citeshttps://doi.org/10.1113/jp284241openalex-snapshot
Genome‐wide association studies: utility and limitations for research in physiology
inferred← citeshttps://doi.org/10.1126/sciadv.abf1444openalex-snapshot
Cardiac cell type–specific gene regulatory programs and disease risk association
inferred← citeshttps://doi.org/10.1126/scitranslmed.aad3744openalex-snapshot
A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart disease
inferred← citeshttps://doi.org/10.1128/mcb.01156-14openalex-snapshot
Estrogen-Related Receptor α (ERRα) and ERRγ Are Essential Coordinators of Cardiac Metabolism and Function
inferred← citeshttps://doi.org/10.1136/bjsports-2015-095294openalex-snapshot
Exercise genomics—a paradigm shift is needed: a commentary
inferred← citeshttps://doi.org/10.1136/heartjnl-2014-305482openalex-snapshot
Atrial fibrillation associated with ivabradine treatment: meta-analysis of randomised controlled trials
inferred← citeshttps://doi.org/10.1136/jmedgenet-2016-104112openalex-snapshot
A genome-wide interaction analysis of tricyclic/tetracyclic antidepressants and RR and QT intervals: a pharmacogenomics study from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium
inferred← citeshttps://doi.org/10.1136/openhrt-2014-000187openalex-snapshot
Genetic variation at the human connexin 43 locus but not at the connexin 40 locus is associated with left bundle branch block
inferred← citeshttps://doi.org/10.1146/annurev-pharmtox-031120-115815openalex-snapshot
Pharmacologic Approach to Sinoatrial Node Dysfunction
inferred← citeshttps://doi.org/10.1152/ajpcell.00271.2016openalex-snapshot
Differential effects of inhibitory G protein isoforms on G protein-gated inwardly rectifying K+ currents in adult murine atria
inferred← citeshttps://doi.org/10.1152/physiolgenomics.00004.2015openalex-snapshot
Genome-wide association studies and contribution to cardiovascular physiology
inferred← citeshttps://doi.org/10.1152/physiolgenomics.00157.2020openalex-snapshot
The role of resistance to inhibitors of cholinesterase 8b in the control of heart rate
inferred← citeshttps://doi.org/10.1155/2020/3854630openalex-snapshot
Association of Maternal Diabetes Mellitus and Polymorphisms of theNKX2.5Gene in Children with Congenital Heart Disease: A Single Centre-Based Case-Control Study
inferred← citeshttps://doi.org/10.1159/000496150openalex-snapshot
Genome-Wide Association Studies of Hypertension and Several Other Cardiovascular Diseases
showing the first 200 of 292 · page through all 292
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.