Familial Sinus Node Disease Caused by a Gain of GIRK (G-Protein Activated Inwardly Rectifying K+ Channel) Channel Function
来源期刊:Circulation: Genomic and Precision MedicineDOI:10.1161/CIRCGEN.118.002238
International Triadin Knockout Syndrome Registry: The Clinical Phenotype and Treatment Outcomes of Patients With Triadin Knockout Syndrome
来源期刊:Circulation: Genomic and Precision MedicineDOI:10.1161/CIRCGEN.118.002419
Rare Missense Variants in TLN1 Are Associated With Familial and Sporadic Spontaneous Coronary Artery Dissection
来源期刊:Circulation: Genomic and Precision MedicineDOI:10.1161/CIRCGEN.118.002437
Serum Magnesium and Calcium Levels and Risk of Atrial Fibrillation: A Mendelian Randomization Study
来源期刊:Circulation: Genomic and Precision MedicineDOI:10.1161/CIRCGEN.118.002349
Key Value of RNA Analysis of MYBPC3 Splice-Site Variants in Hypertrophic Cardiomyopathy
来源期刊:Circulation: Genomic and Precision MedicineDOI:10.1161/CIRCGEN.118.002368
Circulating Markers of Inflammation Persist in Children and Adults With Giant Aneurysms After Kawasaki Disease
来源期刊:Circulation: Genomic and Precision MedicineDOI:10.1161/CIRCGEN.118.002433
Genetic Assessment of Potential Long-Term On-Target Side Effects of PCSK9 (Proprotein Convertase Subtilisin/Kexin Type 9) Inhibitors
来源期刊:Circulation: Genomic and Precision MedicineDOI:10.1161/CIRCGEN.118.002196
High-Resolution Regulatory Maps Connect Vascular Risk Variants to Disease-Related Pathways
来源期刊:Circulation: Genomic and Precision MedicineDOI:10.1161/CIRCGEN.118.002353
Thyroid Function and Dysfunction in Relation to 16 Cardiovascular Diseases: A Mendelian Randomization Study
来源期刊:Circulation: Genomic and Precision MedicineDOI:10.1161/CIRCGEN.118.002468
CYP2C19 Genotype-Guided Antiplatelet Therapy and 30-Day Outcomes After Percutaneous Coronary Intervention
来源期刊:Circulation: Genomic and Precision MedicineDOI:10.1161/CIRCGEN.119.002441
HLA-B*54: 01 Is Associated With Susceptibility to Kawasaki Disease
来源期刊:Circulation: Genomic and Precision MedicineDOI:10.1161/CIRCGEN.118.002365
Novel Biomarkers for the Precisive Diagnosis and Activity Classification of Takayasu Arteritis
来源期刊:Circulation: Genomic and Precision MedicineDOI:10.1161/CIRCGEN.117.002080
Integrative Functional Annotation of 52 Genetic Loci Influencing Myocardial Mass Identifies Candidate Regulatory Variants and Target Genes
来源期刊:Circulation: Genomic and Precision MedicineDOI:10.1161/CIRCGEN.118.002328
Variation in Serum PCSK9 (Proprotein Convertase Subtilisin/Kexin Type 9), Cardiovascular Disease Risk, and an Investigation of Potential Unanticipated Effects of PCSK9 Inhibition: A Genome-Wide Association Study and Mendelian Randomization Study in the HUNT, Norway
来源期刊:Circulation: Genomic and Precision MedicineDOI:10.1161/CIRCGEN.118.002335
Common Genetic Variation in Relation to Brachial Vascular Dimensions and Flow-Mediated Vasodilation
来源期刊:Circulation: Genomic and Precision MedicineDOI:10.1161/CIRCGEN.118.002409
Accuracy of Clinical Diagnostic Criteria for Patients With Vascular Ehlers-Danlos Syndrome in a Tertiary Referral Centre
来源期刊:Circulation: Genomic and Precision MedicineDOI:10.1161/CIRCGEN.117.001996
HeartBioPortal: An Internet-of-Omics for Human Cardiovascular Disease Data
来源期刊:Circulation: Genomic and Precision MedicineDOI:10.1161/CIRCGEN.118.002426
Resting Heart Rate and Cardiovascular Disease: Mendelian Randomization Analysis
来源期刊:Circulation: Genomic and Precision MedicineDOI:10.1161/CIRCGEN.119.002459
Phenotypic Characterization of Individuals With Variants in Cardiovascular Genes in the Absence of a Primary Cardiovascular Indication for Testing
来源期刊:Circulation: Genomic and Precision MedicineDOI:10.1161/CIRCGEN.119.002463