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Journal of Arrhythmia, ISSN 1880-4276, 10/2016, Volume 32, Issue 5, pp. 389 - 397
Abstract Inherited arrhythmias, such as cardiomyopathies and cardiac ion channelopathies, along with coronary heart disease (CHD) are three most common... 
Cardiovascular | Cardiac ion channelopathies | Inherited arrhythmias | Cardiomyopathies | Genetic counseling | Genetic testing | ventricular arrhythmia | GWAS | WES | ARVD/C | sudden cardiac death | genome wide association study | dilated cardiomyopathy | heart failure | ventricular fibrillation | BrS | Brugada syndrome | long QT syndrome | arrhythmogenic right ventricular dysplasia/cardiomyopathy | next generation sequencing | LQTS | ICD | whole exome sequencing | DCM | implantable cardioverter defibrillator | catecholaminergic polymorphic ventricular tachycardia | HCM | CPVT | SCD | coronary heart disease | hypertrophic cardiomyopathy | NGS | CHD | Diagnosis | Arrhythmia | Analysis | Genetic screening | Cardiac arrhythmia | Genotype & phenotype | Cardiomyopathy | Long QT syndrome | Cardiovascular disease | Genomes | Gene loci | Clinical medicine | Mutation | Patients | ARVD | NGS, next generation sequencing | VA, ventricular arrhythmia | C, arrhythmogenic right ventricular dysplasia | SCD, sudden cardiac death | DCM, dilated cardiomyopathy | Review | VF, ventricular fibrillation | LQTS, long QT syndrome | BrS, Brugada syndrome | WES, whole exome sequencing | HF, heart failure | CHD, coronary heart disease | CPVT, catecholaminergic polymorphic ventricular tachycardia | GWAS, genome wide association study | cardiomyopathy | ICD, implantable cardioverter defibrillator | HCM, hypertrophic cardiomyopathy
Journal Article
American Heart Journal, ISSN 0002-8703, 2012, Volume 163, Issue 5, pp. 753 - 760.e2
Journal Article
Nature genetics, ISSN 1061-4036, 2013, Volume 45, Issue 9, pp. 1044 - 1049
Journal Article
Mayo Clinic Proceedings, ISSN 0025-6196, 04/2013, Volume 88, Issue 4, p. 309
Journal Article
Scientific Reports, 12/2018, Volume 8, Issue 1, pp. 1 - 12
Congenital long QT syndrome (LQTS) caused by compound mutations is usually associated with more severe clinical phenotypes. We identified a LQTS family... 
Immunocytochemistry | Long QT syndrome | KCNQ1 protein | Potassium channels (voltage-gated) | Mutation | Isoproterenol | Mammalian cells
Journal Article
Journal Article
Journal of the American College of Cardiology, ISSN 0735-1097, 04/2019, Volume 73, Issue 14, pp. 1756 - 1765
Journal Article
Topology and its Applications, ISSN 0166-8641, 04/2017, Volume 221, pp. 715 - 736
A handlebody-link is a disjoint union of embeddings of handlebodies in and an HL-homotopy is an equivalence relation on handlebody-links generated by... 
Milnor's [formula omitted]-invariant | Tensor | Clasper | Handlebody-link | Hypermatrix | Milnor's μ‾-invariant | MOVES | MATHEMATICS, APPLIED | CLASSIFICATION | KNOTTED HANDLEBODIES | EQUIVALENCE | MATHEMATICS | SPATIAL GRAPHS | HOMOLOGY | Milnor's (mu)over-bar-invariant
Journal Article
Cardiac electrophysiology clinics, ISSN 1877-9182, 2014, Volume 6, Issue 4, pp. 819 - 824
The mechanism of sodium current disorders remains largely unknown. Recent research results have shown the complexity of sodium current disorders but at the... 
Cardiac conduction disturbance | Brugada syndrome | Dilated cardiomyopathy | Atrial fibrillation | Sodium current disorder | Long QT syndrome | Sick sinus syndrome
Journal Article