Circulation. Genomic and Precision Medicine
Overview
Circulation. Genomic and precision medicine is a reputable scientific journal that focuses on cutting-edge research in the field of genomics and precision medicine. It publishes high-quality articles exploring the genetic basis of diseases, personalized therapies, and advancements in genomic technologies. This journal serves as a valuable resource for researchers, clinicians, and policymakers interested in the intersection of genomics and precision medicine.
Details
Details
Abbr.
Circ Genom Precis Med
Start
2018
End
Continuing
Frequency
Bimonthly
e-ISSN
2574-8300
Country
United States
Language
English
Specialties
Genetics
Cardiology & Vascular Diseases
Cardiology & Vascular Diseases
Metrics
Metrics
h-index / Ranks: 3337
96
SJR / Ranks: 743
2670
CiteScore / Ranks: 1928
8.70
JIF / Ranks: 780
7.4
Recent Articles
1.
Gagnon E, Gill D, Chabot D, Cronje H, Yuan S, Brennan S, et al.
Circ Genom Precis Med
. 2025 Mar;
:e004933.
PMID: 40052268
Background: Therapies targeting the LPL (lipoprotein lipase) pathway are under development for cardiometabolic disease. Insights into their efficacy-both alone and in combination with existing lipid-lowering therapies-modes of action, and safety...
2.
Khera R, Asnani A, Krive J, Addison D, Zhu H, Vasbinder A, et al.
Circ Genom Precis Med
. 2025 Feb;
:e000097.
PMID: 39989357
Artificial intelligence is poised to transform cardio-oncology by enabling personalized care for patients with cancer, who are at a heightened risk of cardiovascular disease due to both the disease and...
3.
Asatryan B, Rieder M, Murray B, Muller S, Tichnell C, Gasperetti A, et al.
Circ Genom Precis Med
. 2025 Feb;
:e004878.
PMID: 39968648
Background: Pathogenic/likely pathogenic (LP) desmin () variants cause heterogeneous cardiomyopathy and skeletal myopathy phenotypes. Limited data suggest a high incidence of major adverse cardiac events (MACEs), including cardiac conduction disease,...
4.
Vatta M, Regalado E, Parfenov M, Swartzlander D, Nagl A, Mannello M, et al.
Circ Genom Precis Med
. 2025 Feb;
:e004982.
PMID: 39968638
Background: Truncating variants (TTNtvs) in the titin () gene have been associated with cardiomyopathies or arrhythmias (C/A) and autosomal recessive neuromuscular diseases (NM). However, the clinical significance of TTNtvs across...
5.
Kang S, Moon J, Lee S, Kim S, Kang J, Kim H, et al.
Circ Genom Precis Med
. 2025 Feb;
:e004998.
PMID: 39945096
No abstract available.
6.
Lo A, Mew T, Mew C, Guppy-Coles K, Dahiya A, Ng A, et al.
Circ Genom Precis Med
. 2025 Feb;
:e004806.
PMID: 39936296
Background: It remains challenging to determine which hypertrophic cardiomyopathy (HCM) family members will subsequently develop HCM. Standard 2-dimensional and conventional Doppler echocardiography have been unable to reliably distinguish HCM genotype-positive...
7.
Ruhrman Shahar N, Yagel D, Marek-Yagel D, Greenberg R, Isakov O, Naftali M, et al.
Circ Genom Precis Med
. 2025 Jan;
18(1):e004864.
PMID: 39866098
No abstract available.
8.
Fan W, Wu C, Wong N
Circ Genom Precis Med
. 2025 Jan;
18(1):e004631.
PMID: 39851061
Background: Lipoprotein(a) [Lp(a)] is a predictor of atherosclerotic cardiovascular disease (ASCVD); however, there are few algorithms incorporating Lp(a), especially from real-world settings. We developed an electronic health record (EHR)-based risk...
9.
Urbut S, Cho S, Paruchuri K, Truong B, Haidermota S, Peloso G, et al.
Circ Genom Precis Med
. 2025 Jan;
18(1):e004681.
PMID: 39851049
Background: Earlier identification of high coronary artery disease (CAD) risk individuals may enable more effective prevention strategies. However, existing 10-year risk frameworks are ineffective at earlier identification. We sought to...
10.
Huang K, Ashraf M, Rohani L, Luo Y, Sacayanan A, Huang H, et al.
Circ Genom Precis Med
. 2025 Jan;
18(1):e004412.
PMID: 39851047
Background: Protein-truncating mutations in the titin gene are associated with increased risk of atrial fibrillation. However, little is known about the underlying pathophysiology. Methods: We identified a heterozygous titin truncating...