# | Title | Journal | Year | Citations |
---|
1 | 40-Year Follow-Up After the Fontan Operation | Journal of the American College of Cardiology | 2015 | 484 |
2 | ABCC9 mutations identified in human dilated cardiomyopathy disrupt catalytic KATP channel gating | Nature Genetics | 2004 | 342 |
3 | Mutations in Ribonucleic Acid Binding Protein Gene Cause Familial Dilated Cardiomyopathy | Journal of the American College of Cardiology | 2009 | 299 |
4 | Identification of an angiogenic factor that when mutated causes susceptibility to Klippel–Trenaunay syndrome | Nature | 2004 | 289 |
5 | Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization | Nature Genetics | 2014 | 281 |
6 | Malignant Bileaflet Mitral Valve Prolapse Syndrome in Patients With Otherwise Idiopathic Out-of-Hospital Cardiac Arrest | Journal of the American College of Cardiology | 2013 | 224 |
7 | Characteristics of Premature Ventricular Complexes as Correlates of Reduced Left Ventricular Systolic Function: Study of the Burden, Duration, Coupling Interval, Morphology and Site of Origin of PVCs | Journal of Cardiovascular Electrophysiology | 2011 | 191 |
8 | Prevalence of early-onset atrial fibrillation in congenital long QT syndrome | Heart Rhythm | 2008 | 151 |
9 | Supraventricular tachyarrhythmias in Ebstein anomaly: Management and outcome | Journal of Thoracic and Cardiovascular Surgery | 2004 | 148 |
10 | Liver Disease in Patients After the Fontan Operation | American Journal of Cardiology | 2016 | 147 |
11 | Principles of Percutaneous Paravalvular Leak Closure | JACC: Cardiovascular Interventions | 2012 | 144 |
12 | Institution-Wide QT Alert System Identifies Patients With a High Risk of Mortality | Mayo Clinic Proceedings | 2013 | 133 |
13 | Surgical resection of ventricular cardiac fibromas: early and late results | Annals of Thoracic Surgery | 2003 | 132 |
14 | Characterization of a Phenotype-Based Genetic Test Prediction Score for Unrelated Patients With Hypertrophic Cardiomyopathy | Mayo Clinic Proceedings | 2014 | 131 |
15 | Intraoperative transesophageal echocardiography during surgery for congenital heart defects | Journal of Thoracic and Cardiovascular Surgery | 2002 | 128 |
16 | Transvenous, Antegrade Melody Valve-in-Valve Implantation for Bioprosthetic Mitral and Tricuspid Valve Dysfunction | JACC: Cardiovascular Interventions | 2013 | 128 |
17 | Peripheral artery tonometry demonstrates altered endothelial function in children with type 1 diabetes | Pediatric Diabetes | 2007 | 119 |
18 | Mutation and gender-specific risk in type 2 long QT syndrome: Implications for risk stratification for life-threatening cardiac events in patients with long QT syndrome | Heart Rhythm | 2011 | 117 |
19 | Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study | Cardiovascular Research | 2015 | 108 |
20 | One-Year Follow-Up of the Melody Transcatheter Pulmonary Valve Multicenter Post-Approval Study | JACC: Cardiovascular Interventions | 2014 | 107 |
21 | MYBPC3 mutations are associated with a reduced super-relaxed state in patients with hypertrophic cardiomyopathy | PLoS ONE | 2017 | 106 |
22 | Postural Orthostatic Tachycardia Syndrome: A Clinical Review | Pediatric Neurology | 2010 | 104 |
23 | Magnetic Resonance Elastography | Mayo Clinic Proceedings | 2015 | 103 |
24 | Role of Family History of Sudden Death in Risk Stratification and Prevention of Sudden Death With Implantable Defibrillators in Hypertrophic Cardiomyopathy | American Journal of Cardiology | 2010 | 102 |
25 | Exome Sequencing and Systems Biology Converge to Identify Novel Mutations in the L-Type Calcium Channel, CACNA1C , Linked to Autosomal Dominant Long QT Syndrome | Circulation: Cardiovascular Genetics | 2013 | 102 |
26 | CALM3 mutation associated with long QT syndrome | Heart Rhythm | 2015 | 95 |
27 | Immediate Outcomes of Covered Stent Placement for Treatment or Prevention of Aortic Wall Injury Associated With Coarctation of the Aorta (COAST II) | JACC: Cardiovascular Interventions | 2016 | 94 |
28 | Competitive Sports Participation in Athletes With Congenital Long QT Syndrome | JAMA - Journal of the American Medical Association | 2012 | 93 |
29 | Feasibility of identifying amyloid and hypertrophic cardiomyopathy with the use of computerized quantitative texture analysis of clinical echocardiographic data | Journal of the American College of Cardiology | 1989 | 89 |
30 | Intrinsic Endocardial Defects Contribute to Hypoplastic Left Heart Syndrome | Cell Stem Cell | 2020 | 89 |
31 | Identifying predictors of hepatic disease in patients after the Fontan operation: A postmortem analysis | Journal of Thoracic and Cardiovascular Surgery | 2013 | 87 |
32 | Whole-Exome Molecular Autopsy After Exertion-Related Sudden Unexplained Death in the Young | Circulation: Cardiovascular Genetics | 2016 | 87 |
33 | Long-Term Results of the Fontan Operation | Pediatric Cardiology | 2007 | 84 |
34 | Biomedicine and diseases: the Klippel-Trenaunay syndrome, vascular anomalies and vascular morphogenesis | Cellular and Molecular Life Sciences | 2005 | 83 |
35 | Infective Endocarditis in the Pediatric Patient: A 60-Year Single-Institution Review | Mayo Clinic Proceedings | 2012 | 83 |
36 | Improving Results of Surgery for Ebstein Anomaly: Where Are We After 235 Cone Repairs? | Annals of Thoracic Surgery | 2018 | 81 |
37 | Sudden cardiac death and late arrhythmias after the Fontan operation | Congenital Heart Disease | 2017 | 78 |
38 | Implantable cardioverter-defibrillator use in catecholaminergic polymorphic ventricular tachycardia: A systematic review | Heart Rhythm | 2018 | 77 |
39 | Electrocardiographic and oximetric changes during partial complex and generalized seizures | Epilepsy Research | 2011 | 76 |
40 | Unexplained Drownings and the Cardiac Channelopathies: A Molecular Autopsy Series | Mayo Clinic Proceedings | 2011 | 75 |
41 | Thrombotic and Embolic Complications Associated With Atrial Arrhythmia After Fontan Operation | Journal of the American College of Cardiology | 2016 | 75 |
42 | Modeling structural and functional deficiencies ofRBM20familial dilated cardiomyopathy using human induced pluripotent stem cells | Human Molecular Genetics | 2016 | 75 |
43 | Life-Threatening Event Risk in Children With Wolff-Parkinson-White Syndrome | JACC: Clinical Electrophysiology | 2018 | 75 |
44 | Artificial Intelligence–Enabled Assessment of the Heart Rate Corrected QT Interval Using a Mobile Electrocardiogram Device | Circulation | 2021 | 75 |
45 | Mexiletine Shortens the QT Interval in Patients With Potassium Channel–Mediated Type 2 Long QT Syndrome | Circulation: Arrhythmia and Electrophysiology | 2019 | 74 |
46 | Recessive MYH6 Mutations in Hypoplastic Left Heart With Reduced Ejection Fraction | Circulation: Cardiovascular Genetics | 2015 | 72 |
47 | Compound heterozygous NOTCH1 mutations underlie impaired cardiogenesis in a patient with hypoplastic left heart syndrome | Human Genetics | 2015 | 71 |
48 | Late outcome of repair of congenital coronary artery fistulas—a word of caution | Journal of Thoracic and Cardiovascular Surgery | 2013 | 69 |
49 | Relationships Among Conduit Type, Pre-Stenting, and Outcomes in Patients Undergoing Transcatheter Pulmonary Valve Replacement in the Prospective North American and European Melody Valve Trials | JACC: Cardiovascular Interventions | 2017 | 68 |
50 | Role of Transvenous Implantable Cardioverter-Defibrillators in Preventing Sudden Cardiac Death in Children, Adolescents, and Young Adults | Mayo Clinic Proceedings | 2002 | 67 |