Published in Cardiovasc Res on October 01, 2004
Genetic causes of human heart failure. J Clin Invest (2005) 2.79
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Genetic origins of pediatric heart disease. Pediatr Cardiol (2009) 0.92
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Somatic mutations in cardiac malformations. J Med Genet (2006) 0.78
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Investigation of association between PFO complicated by cryptogenic stroke and a common variant of the cardiac transcription factor GATA4. PLoS One (2011) 0.75
Molecular basis of AV block and cardiac malformations. Cardiovasc Res (2004) 0.75
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Point mutations in murine Nkx2-5 phenocopy human congenital heart disease and induce pathogenic Wnt signaling. JCI Insight (2017) 0.75
Inherited arrhythmias in children. Indian Pacing Electrophysiol J (2008) 0.75
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Atenolol versus losartan in children and young adults with Marfan's syndrome. N Engl J Med (2014) 5.11
Comparison of magnetic resonance feature tracking for strain calculation with harmonic phase imaging analysis. JACC Cardiovasc Imaging (2010) 3.50
Constitutively active AMP kinase mutations cause glycogen storage disease mimicking hypertrophic cardiomyopathy. J Clin Invest (2002) 3.33
Extracellular matrix remodeling and organization in developing and diseased aortic valves. Circ Res (2006) 2.91
Calmodulin mutations associated with recurrent cardiac arrest in infants. Circulation (2013) 2.66
Hypoplastic left heart syndrome is heritable. J Am Coll Cardiol (2007) 2.24
Bicuspid aortic valve is heritable. J Am Coll Cardiol (2004) 2.18
Hypoplastic left heart syndrome: current considerations and expectations. J Am Coll Cardiol (2012) 2.10
NKX2.5 mutations in patients with congenital heart disease. J Am Coll Cardiol (2003) 2.09
Hypoplastic left heart syndrome links to chromosomes 10q and 6q and is genetically related to bicuspid aortic valve. J Am Coll Cardiol (2009) 1.88
Electrocardiographic features in Andersen-Tawil syndrome patients with KCNJ2 mutations: characteristic T-U-wave patterns predict the KCNJ2 genotype. Circulation (2005) 1.77
Circumferential strain analysis identifies strata of cardiomyopathy in Duchenne muscular dystrophy: a cardiac magnetic resonance tagging study. J Am Coll Cardiol (2009) 1.74
Spectrum of heart disease associated with murine and human GATA4 mutation. J Mol Cell Cardiol (2007) 1.71
Polymorphic ventricular tachycardia and KCNJ2 mutations. Heart Rhythm (2004) 1.68
Transcription factors and congenital heart defects. Annu Rev Physiol (2006) 1.66
Clinical, genetic, and biophysical characterization of SCN5A mutations associated with atrioventricular conduction block. Circulation (2002) 1.65
KCNJ2 mutation results in Andersen syndrome with sex-specific cardiac and skeletal muscle phenotypes. Am J Hum Genet (2002) 1.60
Risk factors for aortic valve disease in bicuspid aortic valve: a family-based study. Am J Med Genet A (2011) 1.55
Genetic variants in SCN5A promoter are associated with arrhythmia phenotype severity in patients with heterozygous loss-of-function mutation. Heart Rhythm (2012) 1.51
ACC/AHA/AAP recommendations for training in pediatric cardiology. Pediatrics (2005) 1.46
A common SCN5A polymorphism modulates the biophysical effects of an SCN5A mutation. J Clin Invest (2003) 1.41
Mouse heart valve structure and function: echocardiographic and morphometric analyses from the fetus through the aged adult. Am J Physiol Heart Circ Physiol (2008) 1.40
Outpatient continuous inotrope infusion as an adjunct to heart failure therapy in Duchenne muscular dystrophy. Neuromuscul Disord (2006) 1.40
Magnetic resonance derived myocardial strain assessment using feature tracking. J Vis Exp (2011) 1.32
Evidence in favor of linkage to human chromosomal regions 18q, 5q and 13q for bicuspid aortic valve and associated cardiovascular malformations. Hum Genet (2007) 1.28
Fetal heart rate predictors of long QT syndrome. Circulation (2012) 1.24
Prevalence and distribution of late gadolinium enhancement in a large population of patients with Duchenne muscular dystrophy: effect of age and left ventricular systolic function. J Cardiovasc Magn Reson (2013) 1.18
Characteristics of children and young adults with Marfan syndrome and aortic root dilation in a randomized trial comparing atenolol and losartan therapy. Am Heart J (2013) 1.14
Analysis of Ellis van Creveld syndrome gene products: implications for cardiovascular development and disease. Hum Mol Genet (2009) 1.13
Developmentally regulated SCN5A splice variant potentiates dysfunction of a novel mutation associated with severe fetal arrhythmia. Heart Rhythm (2011) 1.11
Arrhythmia phenotype during fetal life suggests long-QT syndrome genotype: risk stratification of perinatal long-QT syndrome. Circ Arrhythm Electrophysiol (2013) 1.11
Prenatal head growth and white matter injury in hypoplastic left heart syndrome. Pediatr Res (2008) 1.09
Deletion of ETS-1, a gene in the Jacobsen syndrome critical region, causes ventricular septal defects and abnormal ventricular morphology in mice. Hum Mol Genet (2009) 1.09
Elastin haploinsufficiency results in progressive aortic valve malformation and latent valve disease in a mouse model. Circ Res (2010) 1.02
Detection of progressive cardiac dysfunction by serial evaluation of circumferential strain in patients with Duchenne muscular dystrophy. Am J Cardiol (2010) 1.00
An intronic mutation causes long QT syndrome. J Am Coll Cardiol (2004) 0.97
BMP and FGF regulatory pathways in semilunar valve precursor cells. Dev Dyn (2007) 0.97
Abnormal circumferential strain is present in young Duchenne muscular dystrophy patients. Pediatr Cardiol (2013) 0.96
Patterns of left ventricular remodeling in patients with Duchenne Muscular Dystrophy: a cardiac MRI study of ventricular geometry, global function, and strain. Int J Cardiovasc Imaging (2011) 0.95
The role of mitochondrial genome in essential hypertension in a Chinese Han population. Eur J Hum Genet (2009) 0.95
Abnormalities of diastolic function precede dilated cardiomyopathy associated with Duchenne muscular dystrophy. J Am Soc Echocardiogr (2006) 0.95
Clinical, genetic, and biophysical characterization of a homozygous HERG mutation causing severe neonatal long QT syndrome. Pediatr Res (2003) 0.93
Left ventricular T2 distribution in Duchenne muscular dystrophy. J Cardiovasc Magn Reson (2010) 0.93
Trafficking-competent and trafficking-defective KCNJ2 mutations in Andersen syndrome. Hum Mutat (2006) 0.92
Regional circumferential strain is a biomarker for disease severity in duchenne muscular dystrophy heart disease: a cross-sectional study. Pediatr Cardiol (2014) 0.89
Effects of steroids and angiotensin converting enzyme inhibition on circumferential strain in boys with Duchenne muscular dystrophy: a cross-sectional and longitudinal study utilizing cardiovascular magnetic resonance. J Cardiovasc Magn Reson (2011) 0.88
Bidirectional ventricular tachycardia and channelopathy. Am J Cardiol (2003) 0.88
Differentiation of cardiac Purkinje fibers requires precise spatiotemporal regulation of Nkx2-5 expression. Dev Dyn (2006) 0.88
Autonomic dysfunction: a driving force for myocardial fibrosis in young Duchenne muscular dystrophy patients? Pediatr Cardiol (2014) 0.87
Highly sensitive noninvasive cardiac transplant rejection monitoring using targeted quantification of donor-specific cell-free deoxyribonucleic acid. J Am Coll Cardiol (2013) 0.85
Genetic analyses in two extended families with deletion 22q11 syndrome: importance of extracardiac manifestations. J Pediatr (2005) 0.84
The presence of bicuspid aortic valve does not predict ventricular septal defect type. Am J Med Genet A (2008) 0.83
Bilateral semilunar valve disease in a child with partial deletion of the Williams-Beuren syndrome region is associated with elastin haploinsufficiency. J Heart Valve Dis (2006) 0.83
Genetic characterization of familial CPVT after 30 years. Biol Res Nurs (2009) 0.83
Aorta Measurements are Heritable and Influenced by Bicuspid Aortic Valve. Front Genet (2011) 0.83
Spontaneous rupture of atrioventricular valve tensor apparatus as late manifestation of anti-Ro/SSA antibody-mediated cardiac disease. Am J Cardiol (2011) 0.82
Electrocardiographic abnormalities in very young Duchenne muscular dystrophy patients precede the onset of cardiac dysfunction. Neuromuscul Disord (2011) 0.81
Magnetic resonance imaging assessment of cardiac dysfunction in δ-sarcoglycan null mice. Neuromuscul Disord (2010) 0.80
A management strategy for fetal immune-mediated atrioventricular block. J Matern Fetal Neonatal Med (2010) 0.80
Left ventricular noncompaction in Duchenne muscular dystrophy. J Cardiovasc Magn Reson (2013) 0.79
Looking down the atrioventricular canal. Cardiovasc Res (2010) 0.78
Neonatal long QT syndrome due to a de novo dominant negative hERG mutation. Am J Crit Care (2007) 0.78
Compound heterozygous SCN5A mutations: does the sum of the parts equal the whole? Heart Rhythm (2009) 0.78
TBX5: a developmental key that fits many locks. J Mol Cell Cardiol (2003) 0.77
Complex story of the genetic origins of pediatric heart disease. Circulation (2010) 0.77
Thar's tendons in them thar valves! Circ Res (2008) 0.77
Structure-function relationships in myosin binding protein-C: taking off the blinders and collaring hypertrophic cardiomyopathy. Circ Res (2002) 0.76
Pulmonary vascular resistance in repaired congenital diaphragmatic hernia vs. age-matched controls. Pediatr Res (2012) 0.76
Genetics of sick sinus syndrome. Card Electrophysiol Clin (2010) 0.76
Sudden infant death syndrome and long QT syndrome: the zealots versus the naysayers. Heart Rhythm (2006) 0.75
A candidate locus approach identifies a long QT syndrome gene mutation. Biol Res Nurs (2003) 0.75
ACCF/AHA/AAP recommendations for training in pediatric cardiology. Task force 7: training guidelines for research in pediatric cardiology. J Am Coll Cardiol (2005) 0.75
Congenital sick sinus syndrome with atrial inexcitability and coronary sinus flutter. Circ Arrhythm Electrophysiol (2011) 0.75