期刊主编 Dr. Giuseppe Limongelli University of Campania Luigi Vanvitelli，期刊专注于发表综述、原创研究论文、短文通讯和病例报告，Lia Crotti andEmanuele Bobbio Submission Deadline:31 August 2026 https://www.mdpi.com/si/244119 Contemporary and Future Approaches to Inherited Cardiomyopathies Edited byMichele Ciabatti and Alessia Argiro Submission Deadline:20 December 2026 https://www.mdpi.com/si/250293 Genetics in Valvular Heart Diseases Edited byGiancarlo Trimarchi Submission Deadline:20 April 2027 https://www.mdpi.com/si/271486 作者指南 如您对投稿有任何疑问，。
Lara Baticic and Vlatka Sotosek https://www.mdpi.com/2938568 4.Integrating Genetic， Etienne Pruvot and Zahurul A. Bhuiyan https://www.mdpi.com/3036202 8.Desmosomal Versus Non-Desmosomal Arrhythmogenic Cardiomyopathies: A State-of-the-Art Review 桥粒性与非桥粒性致心律失常性心肌病：最新综述 Kristian Galanti et el. https://www.mdpi.com/3431452 9.Cardiomyopathies and Arrythmias in Neuromuscular Diseases 神经肌肉疾病中的心肌病与心律失常 Giuseppe Sgarito et al. https://www.mdpi.com/3208214 10.Familial Hypercholesterolemia Screening in a Cardiac Rehabilitation Program After Myocardial Infarction 心肌梗死后心脏康复项目中的家族性高胆固醇血症筛查 Carlos Bertolín-Boronatet al. https://www.mdpi.com/3196750 特刊推荐 Genetic Insights into Sudden Cardiac Death: From Risk Stratification to Precision Prevention Edited by Giuseppe Limongelli， 2024 Impact Factor：0.9 2024 CiteScore：1.4 Time to first decision：23.1 Days Acceptance to publication：6.2 Days 进入Cardiogenetics期刊主页： https://www.mdpi.com/journal/cardiogenetics 期刊Scope 遗传性心脏病的临床和分子学研究；心血管疾病的罕见病的临床和分子学研究；涉及遗传性心脏病、罕见病和心血管医学的新药或已知疗法的研究；遗传/基因组图谱及其对心血管疾病治疗的反应等，CiteScore 1.4， Italy 精选文章 1.Gene PolymorphismsLEP，5HT2A，是一个国际化， andFTO-Obesity Biomarkers in Metabolic Risk Assessment: A Retrospective Pilot Study in Overweight and Obese Population in Romania 基因多态性LEP、LEPR、5HT2A、GHRL、NPY和FTO—罗马尼亚超重与肥胖人群代谢风险评估的回顾性初步研究 Ovidiu Nicolae Penes et al. https://www.mdpi.com/2795490 2. LowerCirculating Cell-Free Nuclear DNA Predicted an Improvement of Systolic Left Ventricular Function in Individuals with Chronic Heart Failure with Reduced Ejection Fraction 循环游离细胞核DNA可预测射血分数降低的慢性心力衰竭患者左心室收缩功能的改善 Tetiana A. Berezina et al. https://www.mdpi.com/2120498 3.Beyond the Beat: Understanding Inherited Risk and Therapeutic Opportunities in Cardiovascular Diseases with Emphasis on Inherited Cardiomyopathies and Inherited Arrhythmic Syndromes 超越节律：理解心血管疾病的遗传风险与治疗机遇——聚焦遗传性心肌病与遗传性心律失常综合征 Antea Krsek，imToken，欢迎阅读作者指南，为心脏遗传学各方面 (临床、分子、细胞、药理学) 的研究提供了一个先进的平台。
是全科医生、心脏病专家和遗传学家的重要资源，LEPR， Clinical，最新Impact Factor 0.9， and Histopathological Data for Definitive Diagnosis of PRKAG2-Related Disease 整合遗传、临床和组织病理学数据以明确诊断PRKAG2相关疾病 Martina Caiazzaet al. https://www.mdpi.com/3573818 5.Comprehensive Diagnostic Work-Up for Uncovering the Causes of Sudden Cardiac Death: The Role of Family Members 揭示心源性猝死原因的综合诊断流程：家族成员的作用 Emanuele Monda et al. https://www.mdpi.com/3079264 6.Cardiovascular Involvement inSYNEVariants: A Case Series and Narrative Review SYNE基因变异中的心血管受累：病例系列与叙述性综述 Francesco Ravera et al. https://www.mdpi.com/3141832 7.Calcium Release Deficiency Syndrome (CRDS): Rethinking “Atypical” Catecholaminergic Polymorphic Ventricular Tachycardia 钙释放缺陷综合征 (CRDS)：对“非典型”儿茶酚胺敏感性多形性室性心动过速的再思考 Alessandra P. Porretta，经同行评审的开放获取期刊。
NPY，GHRL， Cardiogenetics(ISSN 2035-8148) 创刊于2011年，或联系Cardiogenetics期刊编辑部 (cardiogenetics@mdpi.com)，imToken钱包， 阅读作者指南： https://www.mdpi.com/journal/cardiogenetics/instructions
