Short QT syndrome
Data up to Jan 2025
Total Citations Per Year
Abstract
References (74)
An analysis of the time-relations of electrocardiograms
1920 • 3,889 citations
A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome
1995 • 2,263 citations
Genetic basis and molecular mechanism for idiopathic ventricular fibrillation
1998 • 1,803 citations
Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval, and sudden death
1957 • 1,593 citations
Diagnostic criteria for the long QT syndrome. An update.
1993 • 1,160 citations
Cellular Basis for the Brugada Syndrome and Other Mechanisms of Arrhythmogenesis Associated With ST-Segment Elevation
1999 • 1,122 citations
KCNQ1 Gain-of-Function Mutation in Familial Atrial Fibrillation
2003 • 975 citations
Recommendations for competitive sports participation in athletes with cardiovascular disease: A consensus document from the Study Group of Sports Cardiology of the Working Group of Cardiac Rehabilitation and Exercise Physiology and the Working Group of Myocardial and Pericardial Diseases of the European Society of Cardiology
2005 • 965 citations
Sudden Death Associated With Short-QT Syndrome Linked to Mutations in HERG
2003 • 846 citations
Mutations of the Cardiac Ryanodine Receptor (RyR2) Gene in Familial Polymorphic Ventricular Tachycardia
2001 • 726 citations
Short QT Syndrome
2003 • 706 citations
Idiopathic Short QT Interval:A New Clinical Syndrome?
2000 • 659 citations
Sex differences in the evolution of the electrocardiographic QT interval with age.
1992 • 634 citations
The Measurement of the Q-T Interval of the Electrocardiogram
1952 • 630 citations
A Novel Form of Short QT Syndrome (SQT3) Is Caused by a Mutation in the KCNJ2 Gene
2005 • 615 citations
Mutation in the KCNQ1 Gene Leading to the Short QT-Interval Syndrome
2004 • 615 citations
The M Cell:
1999 • 606 citations
Macropinocytosis in phagocytes: regulation of MHC class-II-restricted antigen presentation in dendritic cells
2015 • 540 citations
Linkage of a Cardiac Arrhythmia, the Long QT Syndrome, and the Harvey ras -1 Gene
1991 • 526 citations
Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome)
2002 • 526 citations
The Brugada syndrome: clinical, electrophysiologic and genetic aspects
1999 • 510 citations
A subpopulation of cells with unique electrophysiological properties in the deep subepicardium of the canine ventricle. The M cell.
1991 • 499 citations
Cellular Basis for the ECG Features of the LQT1 Form of the Long-QT Syndrome
1998 • 499 citations
Identification of a KCNE2 Gain-of-Function Mutation in Patients with Familial Atrial Fibrillation
2004 • 387 citations
Short QT syndrome: pharmacological treatment
2004 • 359 citations
Short QT syndrome: A case report and review of literature
2006 • 341 citations
Short QT syndrome: clinical findings and diagnostic-therapeutic implications
2006 • 325 citations
Unique Topographical Distribution of M Cells Underlies Reentrant Mechanism of Torsade de Pointes in the Long-QT Syndrome
2002 • 305 citations
Short QT Syndrome and Atrial Fibrillation Caused by Mutation in KCNH2
2005 • 303 citations
Reinduction of Atrial Fibrillation Immediately After Termination of the Arrhythmia Is Mediated by Late Phase 3 Early Afterdepolarization–Induced Triggered Activity
2003 • 302 citations
De novo KCNQ1 mutation responsible for atrial fibrillation and short QT syndrome in utero
2005 • 298 citations
Genomic Structure of Three Long QT Syndrome Genes:KVLQT1, HERG,andKCNE1
1998 • 225 citations
Carnitine Deficiency Disorders in Children
2004 • 223 citations
Amplified Transmural Dispersion of Repolarization as the Basis for Arrhythmogenesis in a Canine Ventricular-Wedge Model of Short-QT Syndrome
2004 • 212 citations
Further Insights into the Effect of Quinidine in Short QT Syndrome Caused by a Mutation in HERG
2005 • 193 citations
Congenital Short QT Syndrome and Implantable Cardioverter Defibrillator Treatment:
2003 • 180 citations
QT interval variables from 24 hour electrocardiography and the two year risk of sudden death.
1993 • 180 citations
A common polymorphism in KCNH2 (HERG) hastens cardiac repolarization
2003 • 162 citations
Survivors of out-of-hospital cardiac arrest with apparently normal heart: Need for definition and standardized clinical evaluation
1997 • 160 citations
Modulation of inactivation by mutation N588K in KCNH2: A link to arrhythmogenesis in short QT syndrome
2005 • 151 citations
Carnitine transport: Pathophysiology and metabolism of known molecular defects
2003 • 136 citations
Quality of Life and Psychological Status of Patients With Implantable Cardioverter Defibrillators
2006 • 131 citations
Sudden death in patients without structural heart disease
2004 • 130 citations
The N588K-HERG K+ channel mutation in the ‘short QT syndrome’: Mechanism of gain-in-function determined at 37 °C
2005 • 127 citations
Pharmacogenetics and drug-induced arrhythmias
2001 • 127 citations
Is idiopathic ventricular fibrillation a short QT syndrome? Comparison of QT intervals of patients with idiopathic ventricular fibrillation and healthy controls
2004 • 126 citations
Late‐Phase 3 EAD. A Unique Mechanism Contributing to Initiation of Atrial Fibrillation
2006 • 125 citations
Distribution and Prognostic Significance of QT Intervals in the Lowest Half Centile in 12,012 Apparently Healthy Persons
2006 • 119 citations
Short QT syndrome: Successful prevention of sudden cardiac death in an adolescent by implantable cardioverter-defibrillator treatment for primary prophylaxis
2005 • 93 citations
Disopyramide is an effective inhibitor of mutant HERG K+ channels involved in variant 1 short QT syndrome
2006 • 82 citations
Differences between Ventricular Repolarization in Men and Women: Description, Mechanism and Implications
2003 • 79 citations
Cellular basis and mechanism underlying normal and abnormal myocardial repolarization and arrhythmogenesis
2004 • 73 citations
Short QT syndrome: mechanisms, diagnosis and treatment
2005 • 67 citations
ECG phenomenon of idiopathic and paradoxical short QT intervals.
2002 • 62 citations
Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome)
2002 • 60 citations
Temperature modulation of ventricular arrhythmogenicity in a canine tissue model of Brugada syndrome
2006 • 59 citations
Cellular and ionic basis for the sex-related difference in the manifestation of the Brugada syndrome and progressive conduction disease phenotypes
2003 • 57 citations
Molecular Genetics of Arrhythmias and Cardiovascular Conditions Associated with Arrhythmias
2003 • 54 citations
Short QT Syndrome
2005 • 52 citations
Self‐terminating idiopathic ventricular fibrillation presenting as syncope: a 40‐year follow‐up report
1990 • 49 citations
KCNQ1 gain-of-function mutation in familial atrial fibrillation
2003 • 47 citations
Short QT syndrome. a familial cause of sudden death
2004 • 45 citations
Is acquired short QT due to digitalis intoxication responsible for malignant venticular arrhythmias?
2006 • 39 citations
Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia
2001 • 39 citations
The kangaroo as a model for the study of hypertrophic cardiomyopathy in man
1986 • 30 citations
Deceleration‐dependent shortening of the qt interval: A new electrocardiographic phenomenon?
1999 • 29 citations
Linkage of Cardiac Arrhythmia, Long QT Syndrome, and the Harvey ras-1 Gene
1992 • 25 citations
Short QT syndrome: Should we push the frontier forward?
2005 • 25 citations
Imaging Single Cardiac Ryanodine Receptor Ca2+ Fluxes in Lipid Bilayers
2004 • 23 citations
Shortening of the QT interval immediately preceding the onset of idiopathic spontaneous ventricular tachycardia
1995 • 20 citations
Characteristics of cardiac action potentials in marsupials
1989 • 18 citations
Short QT syndrome
2006 • 14 citations
Echocardiographic and electrocardiographic study of the normal kangaroo heart
1990 • 14 citations
The electrocardiogram of the eastern grey kangaroo (Macropus giganteus)
1986 • 10 citations