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Predictive Accuracy of a Clinical and Genetic Risk Model for Atrial Fibrillation.Circulation: Genomic and Precision Medicine28 dayssaveRefWorksSFX Info
Polygenic Risk Score to Identify Subclinical Coronary Heart Disease Risk in Young Adults.Circulation: Genomic and Precision Medicine28 dayssaveRefWorksSFX Info
Contribution of Noncanonical Splice Variants to TTN Truncating Variant Cardiomyopathy.Circulation: Genomic and Precision Medicine28 dayssaveRefWorksSFX Info
Genome-Wide Association Meta-Analysis Supports Genes Involved in Valve and Cardiac Development to Associate With Mitral Valve Prolapse.Circulation: Genomic and Precision Medicine28 dayssaveRefWorksSFX Info
Genotype-Phenotype Correlation of SCN5A Genotype in Patients With Brugada Syndrome and Arrhythmic Events: Insights From the SABRUS in 392 Probands.Circulation: Genomic and Precision Medicine28 dayssaveRefWorksSFX Info
Rare, Damaging DNA Variants in CORIN and Risk of Coronary Artery Disease: Insights From Functional Genomics and Large-Scale Sequencing Analyses.Circulation: Genomic and Precision Medicine28 dayssaveRefWorksSFX Info
Truncating Variants in OBSCN Gene Associated With Disease-Onset and Outcomes of Hypertrophic Cardiomyopathy.Circulation: Genomic and Precision Medicine28 dayssaveRefWorksSFX Info
Genome-Wide Association Study of Peripheral Artery Disease.Circulation: Genomic and Precision Medicine28 dayssaveRefWorksSFX Info
Prevalence and Outcomes of p.Val142Ile TTR Amyloidosis Cardiomyopathy: A Systematic Review.Circulation: Genomic and Precision Medicine28 dayssaveRefWorksSFX Info
Utility of Genetically Predicted Lp(a) (Lipoprotein [a]) and ApoB Levels for Cardiovascular Risk Assessment.Circulation: Genomic and Precision Medicine28 dayssaveRefWorksSFX Info
Presence of the V122I Variant of Hereditary Transthyretin-Mediated Amyloidosis Among Self-Reported White Individuals in a Sponsored Genetic Testing Program.Circulation: Genomic and Precision Medicine28 dayssaveRefWorksSFX Info
Thrombotic Risk Determined by STAB 2 Variants in a Population-Based Cohort Study.Circulation: Genomic and Precision Medicine28 dayssaveRefWorksSFX Info
MYH7 p.Glu903Gln Is a Pathogenic Variant Associated With Hypertrophic Cardiomyopathy.Circulation: Genomic and Precision Medicine28 dayssaveRefWorksSFX Info
Molecular Management of Multifocal Atrial Tachycardia in Noonan's Syndrome With MEK1/2 Inhibitor Trametinib.Circulation: Genomic and Precision Medicine28 dayssaveRefWorksSFX Info
COL3A1 Missense Variant in a Patient Presenting With Hemoptysis.Circulation: Genomic and Precision Medicine28 dayssaveRefWorksSFX Info
The Propagation of Racial Disparities in Cardiovascular Genomics Research.Circulation: Genomic and Precision Medicine28 dayssaveRefWorksSFX Info
Genetic Testing for Heritable Cardiovascular Diseases in Pediatric Patients: A Scientific Statement From the American Heart Association.Circulation: Genomic and Precision Medicine28 dayssaveRefWorksSFX Info
Correction to: High-Resolution Regulatory Maps Connect Vascular Risk Variants to Disease-Related Pathways.Circulation: Genomic and Precision Medicine28 dayssaveRefWorksSFX Info
Predictive Accuracy of a Clinical and Genetic Risk Model for Atrial Fibrillation.Circulation: Genomic and Precision Medicine37 dayssaveRefWorksSFX Info
Polygenic Risk Score to Identify Subclinical Coronary Heart Disease Risk in Young Adults.Circulation: Genomic and Precision Medicine37 dayssaveRefWorksSFX Info
Contribution of Noncanonical Splice Variants to TTN Truncating Variant Cardiomyopathy.Circulation: Genomic and Precision Medicine37 dayssaveRefWorksSFX Info
Genome-Wide Association Meta-Analysis Supports Genes Involved in Valve and Cardiac Development to Associate With Mitral Valve Prolapse.Circulation: Genomic and Precision Medicine37 dayssaveRefWorksSFX Info
Genotype-Phenotype Correlation of SCN5A Genotype in Patients With Brugada Syndrome and Arrhythmic Events: Insights From the SABRUS in 392 Probands.Circulation: Genomic and Precision Medicine37 dayssaveRefWorksSFX Info
Rare, Damaging DNA Variants in CORIN and Risk of Coronary Artery Disease: Insights From Functional Genomics and Large-Scale Sequencing Analyses.Circulation: Genomic and Precision Medicine37 dayssaveRefWorksSFX Info
Truncating Variants in OBSCN Gene Associated With Disease-Onset and Outcomes of Hypertrophic Cardiomyopathy.Circulation: Genomic and Precision Medicine37 dayssaveRefWorksSFX Info
Genome-Wide Association Study of Peripheral Artery Disease.Circulation: Genomic and Precision Medicine37 dayssaveRefWorksSFX Info
Prevalence and Outcomes of p.Val142Ile TTR Amyloidosis Cardiomyopathy: A Systematic Review.Circulation: Genomic and Precision Medicine37 dayssaveRefWorksSFX Info
Utility of Genetically Predicted Lp(a) (Lipoprotein [a]) and ApoB Levels for Cardiovascular Risk Assessment.Circulation: Genomic and Precision Medicine37 dayssaveRefWorksSFX Info
Presence of the V122I Variant of Hereditary Transthyretin-Mediated Amyloidosis Among Self-Reported White Individuals in a Sponsored Genetic Testing Program.Circulation: Genomic and Precision Medicine37 dayssaveRefWorksSFX Info
Thrombotic Risk Determined by STAB 2 Variants in a Population-Based Cohort Study.Circulation: Genomic and Precision Medicine37 dayssaveRefWorksSFX Info
MYH7 p.Glu903Gln Is a Pathogenic Variant Associated With Hypertrophic Cardiomyopathy.Circulation: Genomic and Precision Medicine37 dayssaveRefWorksSFX Info
Molecular Management of Multifocal Atrial Tachycardia in Noonan's Syndrome With MEK1/2 Inhibitor Trametinib.Circulation: Genomic and Precision Medicine37 dayssaveRefWorksSFX Info
COL3A1 Missense Variant in a Patient Presenting With Hemoptysis.Circulation: Genomic and Precision Medicine37 dayssaveRefWorksSFX Info
The Propagation of Racial Disparities in Cardiovascular Genomics Research.Circulation: Genomic and Precision Medicine37 dayssaveRefWorksSFX Info
Genetic Testing for Heritable Cardiovascular Diseases in Pediatric Patients: A Scientific Statement From the American Heart Association.Circulation: Genomic and Precision Medicine37 dayssaveRefWorksSFX Info
Correction to: High-Resolution Regulatory Maps Connect Vascular Risk Variants to Disease-Related Pathways.Circulation: Genomic and Precision Medicine37 dayssaveRefWorksSFX Info
Clinical Conditions and Their Impact on Utility of Genetic Scores for Prediction of Acute Coronary Syndrome.Circulation: Genomic and Precision Medicine90 dayssaveRefWorksSFX Info
Pathogenic Variants Associated With Dilated Cardiomyopathy Predict Outcome in Pediatric Myocarditis.Circulation: Genomic and Precision Medicine90 dayssaveRefWorksSFX Info
Impact of Genetic Testing for Cardiomyopathy on Emotional Well-Being and Family Dynamics: A Study of Parents and Adolescents.Circulation: Genomic and Precision Medicine90 dayssaveRefWorksSFX Info
Associations of Genetically Predicted Lp(a) (Lipoprotein [a]) Levels With Cardiovascular Traits in Individuals of European and African Ancestry.Circulation: Genomic and Precision Medicine90 dayssaveRefWorksSFX Info
Multiethnic Genome-Wide Association Study of Subclinical Atherosclerosis in Individuals With Type 2 Diabetes.Circulation: Genomic and Precision Medicine90 dayssaveRefWorksSFX Info
Burden of Cardiomyopathic Genetic Variation in Lethal Pediatric Myocarditis.Circulation: Genomic and Precision Medicine90 dayssaveRefWorksSFX Info
Rare Coding Variants Associated With Electrocardiographic Intervals Identify Monogenic Arrhythmia Susceptibility Genes: A Multi-Ancestry Analysis.Circulation: Genomic and Precision Medicine90 dayssaveRefWorksSFX Info
Clinical Genetic Risk Variants Inform a Functional Protein Interaction Network for Tetralogy of Fallot.Circulation: Genomic and Precision Medicine90 dayssaveRefWorksSFX Info
Sex-Specific Associations of Genetically Predicted Circulating Lp(a) (Lipoprotein(a)) and Hepatic LPA Gene Expression Levels With Cardiovascular Outcomes: Mendelian Randomization and Observational Analyses.Circulation: Genomic and Precision Medicine90 dayssaveRefWorksSFX Info
Estimating the Posttest Probability of Long QT Syndrome Diagnosis for Rare KCNH2 Variants.Circulation: Genomic and Precision Medicine90 dayssaveRefWorksSFX Info
Sugar-Sweetened Beverage Consumption May Modify Associations Between Genetic Variants in the CHREBP (Carbohydrate Responsive Element Binding Protein) Locus and HDL-C (High-Density Lipoprotein Cholesterol) and Triglyceride Concentrations.Circulation: Genomic and Precision Medicine90 dayssaveRefWorksSFX Info
Association of Plasma Branched-Chain Amino Acid With Biomarkers of Inflammation and Lipid Metabolism in Women.Circulation: Genomic and Precision Medicine90 dayssaveRefWorksSFX Info
Susceptibility Locus for Pregnancy-Associated Spontaneous Coronary Artery Dissection.Circulation: Genomic and Precision Medicine90 dayssaveRefWorksSFX Info
Clinical Impact of Copy Number Variation on the Genetic Diagnosis of Syndromic Aortopathies.Circulation: Genomic and Precision Medicine90 dayssaveRefWorksSFX Info
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