Circulation-Genomic and Precision Medicine
ISSN:2574-8300

Circulation-Genomic and Precision Medicine

CIRC-GENOM PRECIS ME
学科领域:医学
是否预警:不在预警名单内
是否OA:
录用周期:-
新锐分区:医学1区
年发文量:40
影响因子:5.5
JCR分区:Q1

基本信息

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。
2574-8300SCIE/Scopus收录
5.5
5.9
2026年3月发布
点击查看历史分区趋势    >
大类学科小类学科Top期刊综述期刊
医学1区
CARDIAC & CARDIOVASCULAR SYSTEMS 心脏和心血管系统
2区
GENETICS & HEREDITY 遗传学
1区
N/A
WOS期刊SCI分区  2024-2025最新升级版
按JIF指标学科分区收集子录JIF分区JIF排名百分位
学科:CARDIAC & CARDIOVASCULAR SYSTEMS
SCIE
Q1
40/231
学科:GENETICS & HEREDITY
SCIE
Q1
20/192
按JCR指标学科分区收集子录JCR分区JCR排名百分位
学科:CARDIAC & CARDIOVASCULAR SYSTEMS
SCIE
Q1
37/231
学科:GENETICS & HEREDITY
SCIE
Q1
19/192
暂无h-index数据
40
3%---Biochemistry, Genetics and Molecular Biology-Genetics
3.6%
时间预警情况
2026年03月发布的新锐学术版不在预警名单中
2025年03月发布的2025版不在预警名单中
2024年02月发布的2024版不在预警名单中
2023年01月发布的2023版不在预警名单中
2021年12月发布的2021版不在预警名单中
2020年12月发布的2020版不在预警名单中
85.00%22.3%3.13%
CiteScore:8.60
SJR:1.924
SNIP:1.125
学科类别分区排名百分位
大类:Medicine
小类:Cardiology and Cardiovascular Medicine
Q1
48 / 397
大类:Medicine
小类:Genetics (clinical)
Q1
14 / 100
大类:Medicine
小类:Genetics
Q1
58 / 348

期刊高被引文献

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

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