Call for Paper

CVG&G_CoverInternational Journal for applied and translational genetic and genomic approaches to cardiovascular medicine and surgery

Editor in Chief: Professor Dhavendra Kumar, MD FRCP FRCPCH FACMG
Consultant in Clinical Genetics/ Cardiovascular Genetics Institute of Cancer and Genetics Cardiff University School of Medicine University Hospital of Wales, Cardiff, UK and The Genomic Policy Unit Faculty of Life Sciences and Education The University of South Wales, UK

‘Cardiovascular Genetics and Genomics’ is an open-access online journal publishing original research, meta analyses, reviews, case commentaries and updates on recent development focusing on genetic and genomic aspects of wide range of cardiovascular conditions. The journal particularly focuses on delineation of the clinical phenotypes, new genes and variants, genotype-phenotype correlations, basic and clinically applied molecular genetics, next generation sequencing and new therapeutic developments (drugs & devices). The original cardiovascular research will highlight the omics: proteomics, metabolomics, functional genomics and systems biology – as well as clinical trials in the burgeoning field of pharmacogenomics related to cardiovascular medicine. The journal also features current and comprehensive reviews in the areas of recent advances in cardiovascular development, Mendelian cardiovascular conditions, new diagnostic and therapeutic progress, and controversies in cardiovascular genetics. The journal shall also include clinical case reports and studies, book reviews, and letters to the editor.

The following categories (not limited) of papers and articles are published in Cardiovascular Genetics & Genomics:

  • Cardiovascular development; congenital heart disease
  • Inherited cardiomyopathy-Hypertrophic cardiomyopathy (HCM), Dilated cardiomyopathy, Arryhthmogenic right ventricular cardiomyopathy (ARVC)
  • Cardiovascular genes- Sarcomere, cytoskeletal, junctional, ion channel; ciliopathies, RAS/MAPK, mitochondrial and others
  • Inherited arrhythmia- Long QT Syndrome (LQTS); Short QT Syndrome
  • Brugada syndrome, Catecholaminergic polymorphic ventricular tachycardia (CPVT)
  • Inherited vascular/ connective diseases: Marfan syndrome, Loeys-Dietz syndrome, Ehlers-Danlos syndrome and other connective tissue genetic diseases
  • Hypertension- systemic and pulmonary arterial
  • Inherited metabolic disease with cardiovascular phenotypes
  • Sudden unexplained/cardiac death (infant and adult)
  • Inherited neuromuscular disorders with cardiovascular phenotypes
  • Complex cardiovascular disease (coronary artery disease; atrial fibrillation etc.)
  • Molecular cardiology- diagnostic, experimental, applied and translational
  • Cardiovascular pharmacogenetics & pharmacogenomics
  • Bio-banking and cardiovascular genomics databases
  • Gene, Stem cell and somatic cell therapy in cardiovascular diseases
  • Surgical and non-invasive therapy for inherited cardiovascular conditions
  • Education and training in cardiovascular genetics and genomics
  • Ethical, legal, social issues related to cardiovascular genetics and genomics

Manuscripts of original research papers, review articles, commentaries and opinions and conference reports are invited for publication in Cardiovascular Genetics and Genomics. All manuscripts should be submitted online as an email attachment to cardiovasculargeneticsgenomics@gmail.com. Submitted manuscripts are independently peer-reviewed and all accepted manuscripts published online/print subject to copyright agreement. The journal is open-access as per terms and conditions available from the publishers the Genomic Medicine Foundation (UK) Ltd, a not-for-profit company registered in England and Wales (Registered Number 8749919). For all enquiries and information please visit www.genomicmedicine.org or write to cardiovasculargeneticsgenomics@gmail.com.