Circulation: Genomic and Precision Medicine considers all types of original research articles, including studies conducted in human subjects, laboratory animals, in vitro, and in silico. Articles may include investigations of: clinical genetics as applied to the diagnosis and management of monogenic or oligogenic cardiovascular disorders; the molecular basis of complex cardiovascular disorders, including genome-wide association studies, exome and genome sequencing-based association studies, coding variant association studies, genetic linkage studies, epigenomics, transcriptomics, proteomics, metabolomics, and metagenomics; integration of electronic health record data or patient-generated data with any of the aforementioned approaches, including phenome-wide association studies, or with environmental or lifestyle factors; pharmacogenomics; regulation of gene expression; gene therapy and therapeutic genomic editing; systems biology approaches to the diagnosis and management of cardiovascular disorders; novel methods to perform any of the aforementioned studies; and novel applications of precision medicine. Above all, we seek studies with relevance to human cardiovascular biology and disease.
发行量:Genomic and Precision Medicine考虑所有类型的原始研究文章,包括在人类受试者、实验室动物、体外和计算机模拟中进行的研究。文章可能包括以下方面的研究:应用于单基因或寡基因心血管疾病的诊断和治疗的临床遗传学;复杂心血管疾病的分子基础,包括全基因组关联研究、外显子组和基于基因组测序的关联研究、编码变体关联研究、遗传连锁研究、表观基因组学、转录组学、蛋白质组学、代谢组学和宏基因组学;将电子健康记录数据或患者生成的数据与任何上述方法(包括全表型关联研究)或与环境或生活方式因素整合;药物基因组学;基因表达调节;基因治疗和治疗性基因组编辑;心血管疾病诊断和治疗的系统生物学方法;进行任何上述研究的新方法;和精准医疗的新应用。最重要的是,我们寻求与人类心血管生物学和疾病相关的研究。
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