Circulation. Genomic and precision medicine
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publication venue for
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High-Risk Nonclassical Long-QT Syndrome Genotypes: Spectrum of Genetic and Phenotypic Features.
17:e004554.
2024
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Current State and Future of Polygenic Risk Scores in Cardiometabolic Disease: A Scoping Review.
16:286-313.
2023
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Rationale, Design, and the Baseline Characteristics of the RHDGen (The Genetics of Rheumatic Heart Disease) Network Study†.
16:e003641.
2023
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Cost-Effectiveness of Polygenic Risk Scores to Guide Statin Therapy for Cardiovascular Disease Prevention.
15:e003423.
2022
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Variant Reinterpretation in Survivors of Cardiac Arrest With Preserved Ejection Fraction (the Cardiac Arrest Survivors With Preserved Ejection Fraction Registry) by Clinicians and Clinical Commercial Laboratories.
14:e003235.
2021
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Polygenic Risk Score for Low-Density Lipoprotein Cholesterol Is Associated With Risk of Ischemic Heart Disease and Enriches for Individuals With Familial Hypercholesterolemia.
14:e003106.
2021
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Identification of Circulating Proteins Associated With Blood Pressure Using Mendelian Randomization.
13:e002605.
2020
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Association of Chromosome 9p21 With Subsequent Coronary Heart Disease Events.
12:e002471.
2019
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Subsequent Event Risk in Individuals With Established Coronary Heart Disease.
12:e002470.
2019
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Novel Association of a De Novo
CALM2
Mutation With Long QT Syndrome and Hypertrophic Cardiomyopathy.
11:e002255.
2018
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Polygenic Contribution in Individuals With Early-Onset Coronary Artery Disease.
11:e001849.
2018
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Transcript of Interview with Authors: Sebastien Theriault and Guillaume Pare.
11.
2018
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Impact of Selection Bias on Estimation of Subsequent Event Risk.
10:e001616.
2017
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Genetic Testing in the Evaluation of Unexplained Cardiac Arrest.
10:e001686.
2017
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Identification of Cadherin 2 (
CDH2
) Mutations in Arrhythmogenic Right Ventricular Cardiomyopathy.
10:e001605.
2017
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Mendelian Randomization Studies Do Not Support a Role for Vitamin D in Coronary Artery Disease.
9:349-356.
2016
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Effect of Bile Acid Sequestrants on the Risk of Cardiovascular Events.
8:618-627.
2015
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Association Between Shortened Leukocyte Telomere Length and Cardiometabolic Outcomes.
8:82-90.
2015
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Common Low-Density Lipoprotein Receptor p.G116S Variant Has a Large Effect on Plasma Low-Density Lipoprotein Cholesterol in Circumpolar Inuit Populations.
8:100-105.
2015
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Evaluation of Genes Encoding for the Transient Outward Current (Ito) Identifies the
KCND2
Gene as a Cause of J-Wave Syndrome Associated With Sudden Cardiac Death.
7:782-789.
2014
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Genotype-Positive Status in Patients With Hypertrophic Cardiomyopathy Is Associated With Higher Rates of Heart Failure Events.
7:416-422.
2014
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A Genome-Wide Association Study for Coronary Artery Disease Identifies a Novel Susceptibility Locus in the Major Histocompatibility Complex.
5:217-225.
2012
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Effect of
PON1
Q192R Genetic Polymorphism on Clopidogrel Efficacy and Cardiovascular Events in the Clopidogrel in the Unstable Angina to Prevent Recurrent Events Trial and the Atrial Fibrillation Clopidogrel Trial With Irbesartan for Prevention of Vascular Events.
5:250-256.
2012
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Excess of Rare Variants in Non–Genome-Wide Association Study Candidate Genes in Patients With Hypertriglyceridemia.
5:66-72.
2012
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Association of Variation at the
ABO
Locus With Circulating Levels of Soluble Intercellular Adhesion Molecule-1, Soluble P-selectin, and Soluble E-selectin.
4:681-686.
2011
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Multiple Genetic Loci Influence Serum Urate Levels and Their Relationship With Gout and Cardiovascular Disease Risk Factors.
3:523-530.
2010
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Multiple Genetic Loci Influence Serum Urate Levels and Their Relationship With Gout and Cardiovascular Disease Risk Factors.
3:523-530.
2010
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Fine Mapping of the Insulin-Induced Gene 2 Identifies a Variant Associated With LDL Cholesterol and Total Apolipoprotein B Levels.
3:454-461.
2010
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Extremes of Unexplained Variation as a Phenotype.
3:215-221.
2010
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Comprehensive Analysis of Genomic Variation in the
LPA
Locus and Its Relationship to Plasma Lipoprotein(a) in South Asians, Chinese, and European Caucasians.
3:39-46.
2010
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Novel Associations of CPS1, MUT, NOX4, and DPEP1 With Plasma Homocysteine in a Healthy Population.
2:142-150.
2009
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Novel Loci, Including Those Related to Crohn Disease, Psoriasis, and Inflammation, Identified in a Genome-Wide Association Study of Fibrinogen in 17 686 Women.
2:134-141.
2009
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Genetic Variants Associated With Myocardial Infarction Risk Factors in Over 8000 Individuals From Five Ethnic Groups.
2:16-25.
2009
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Polymorphism in the
CETP
Gene Region, HDL Cholesterol, and Risk of Future Myocardial Infarction.
2:26-33.
2009
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Genetic Loci Associated With Plasma Concentration of Low-Density Lipoprotein Cholesterol, High-Density Lipoprotein Cholesterol, Triglycerides, Apolipoprotein A1, and Apolipoprotein B Among 6382 White Women in Genome-Wide Analysis With Replication.
1:21-30.
2008
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