Published in Curr Opin Cardiol on May 01, 2010
Evaluation of the left atrial substrate in patients with lone atrial fibrillation using delayed-enhanced MRI: implications for disease progression and response to catheter ablation. Heart Rhythm (2010) 2.42
Differential impact of race and risk factors on incidence of atrial fibrillation. Am Heart J (2011) 0.91
Atrial fibrillation in the elderly. J Geriatr Cardiol (2012) 0.90
Korean Atrial Fibrillation (AF) Network: Genetic Variants for AF Do Not Predict Ablation Success. J Am Heart Assoc (2015) 0.85
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. Nat Genet (2009) 12.19
Variants conferring risk of atrial fibrillation on chromosome 4q25. Nature (2007) 8.03
Common variants in KCNN3 are associated with lone atrial fibrillation. Nat Genet (2010) 3.97
Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy. Nat Genet (2004) 3.88
C/EBPβ controls exercise-induced cardiac growth and protects against pathological cardiac remodeling. Cell (2010) 2.68
High-throughput assay for small molecules that modulate zebrafish embryonic heart rate. Nat Chem Biol (2005) 2.64
Chemical suppression of a genetic mutation in a zebrafish model of aortic coarctation. Nat Biotechnol (2004) 2.57
Familial aggregation in lone atrial fibrillation. Hum Genet (2005) 2.55
Drugs that induce repolarization abnormalities cause bradycardia in zebrafish. Circulation (2003) 2.42
Utility of amino-terminal pro-brain natriuretic peptide, galectin-3, and apelin for the evaluation of patients with acute heart failure. J Am Coll Cardiol (2006) 2.29
Locus for atrial fibrillation maps to chromosome 6q14-16. Circulation (2003) 2.28
Klf2 is an essential regulator of vascular hemodynamic forces in vivo. Dev Cell (2006) 2.26
Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies. J Am Coll Cardiol (2010) 2.17
Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillation. Eur Heart J (2009) 2.06
Notch1b and neuregulin are required for specification of central cardiac conduction tissue. Development (2006) 2.00
RBM20, a gene for hereditary cardiomyopathy, regulates titin splicing. Nat Med (2012) 1.97
Pattern recognition: combining informatics and genetics to re-evaluate conduction disease. Heart (2012) 1.91
Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy. Am J Hum Genet (2013) 1.87
Genetic variation in the alternative splicing regulator RBM20 is associated with dilated cardiomyopathy. Heart Rhythm (2011) 1.85
Echocardiographic evaluation in asymptomatic relatives of patients with dilated cardiomyopathy reveals preclinical disease. Ann Intern Med (2005) 1.85
In vivo recording of adult zebrafish electrocardiogram and assessment of drug-induced QT prolongation. Am J Physiol Heart Circ Physiol (2006) 1.77
Mutant desmocollin-2 causes arrhythmogenic right ventricular cardiomyopathy. Am J Hum Genet (2006) 1.68
C-Reactive protein in lone atrial fibrillation. Am J Cardiol (2006) 1.68
Cardiac sodium channel gene variants and sudden cardiac death in women. Circulation (2007) 1.67
The MedSeq Project: a randomized trial of integrating whole genome sequencing into clinical medicine. Trials (2014) 1.62
Closer look at genetic testing in long-QT syndrome: will DNA diagnostics ever be enough? Circulation (2009) 1.56
ACE I/D polymorphism associated with abnormal atrial and atrioventricular conduction in lone atrial fibrillation and structural heart disease: implications for electrical remodeling. Heart Rhythm (2009) 1.55
Cardiac sodium channel mutation in atrial fibrillation. Heart Rhythm (2007) 1.50
Arterial tortuosity syndrome with multiple intracranial aneurysms: a case report. Arch Neurol (2011) 1.49
Integrin-linked kinase regulates endothelial cell survival and vascular development. Mol Cell Biol (2004) 1.46
Drug-sensitized zebrafish screen identifies multiple genes, including GINS3, as regulators of myocardial repolarization. Circulation (2009) 1.41
Human-zebrafish non-coding conserved elements act in vivo to regulate transcription. Nucleic Acids Res (2005) 1.39
Common variants in cardiac ion channel genes are associated with sudden cardiac death. Circ Arrhythm Electrophysiol (2010) 1.22
Potassium channel gene mutations rarely cause atrial fibrillation. BMC Med Genet (2006) 1.21
A systematic approach to the reporting of medically relevant findings from whole genome sequencing. BMC Med Genet (2014) 1.14
High-resolution cardiovascular function confirms functional orthology of myocardial contractility pathways in zebrafish. Physiol Genomics (2010) 1.10
Notch signaling regulates cardiomyocyte proliferation during zebrafish heart regeneration. Proc Natl Acad Sci U S A (2014) 1.10
Purification of hearts from zebrafish embryos. Biotechniques (2006) 1.07
Defining the pathogenicity of DNA sequence variation. Circ Cardiovasc Genet (2009) 1.07
Human amyloidogenic light chain proteins result in cardiac dysfunction, cell death, and early mortality in zebrafish. Am J Physiol Heart Circ Physiol (2013) 1.06
Animal models for arrhythmias. Cardiovasc Res (2005) 1.05
Human cardiomyopathy mutations induce myocyte hyperplasia and activate hypertrophic pathways during cardiogenesis in zebrafish. Dis Model Mech (2011) 1.03
Carotid intima-media thickness is associated with premature parental coronary heart disease: the Framingham Heart Study. Circulation (2003) 1.02
In vivo natriuretic peptide reporter assay identifies chemical modifiers of hypertrophic cardiomyopathy signalling. Cardiovasc Res (2011) 1.01
Ion channel mutations in AF: signal or noise? Heart Rhythm (2008) 0.99
Aging syndrome genes and premature coronary artery disease. BMC Med Genet (2005) 0.95
Techniques for the in vivo assessment of cardio-renal function in zebrafish (Danio rerio) larvae. J Physiol (2012) 0.94
A novel locus for dilated cardiomyopathy, diffuse myocardial fibrosis, and sudden death on chromosome 10q25-26. J Am Coll Cardiol (2006) 0.92
A one-page summary report of genome sequencing for the healthy adult. Public Health Genomics (2015) 0.92
Hedgehog signaling via angiopoietin1 is required for developmental vascular stability. Mech Dev (2010) 0.91
Arrhythmogenic right ventricular cardiomyopathy. Heart Fail Clin (2010) 0.89
Genetics of atrial fibrillation. Med Clin North Am (2008) 0.88
Next-generation genome-wide association studies: time to focus on phenotype? Circ Cardiovasc Genet (2011) 0.88
Genetic testing in cardiovascular diseases. Curr Opin Cardiol (2014) 0.88
Adrenergic-receptor polymorphisms and heart failure. N Engl J Med (2002) 0.87
Chemical and metabolomic screens identify novel biomarkers and antidotes for cyanide exposure. FASEB J (2013) 0.86
Myocardial blood flow and oxygen consumption in patients with Friedreich's ataxia prior to the onset of cardiomyopathy. Coron Artery Dis (2007) 0.86
The zebrafish: scalable in vivo modeling for systems biology. Wiley Interdiscip Rev Syst Biol Med (2010) 0.85
Eya4 regulation of Na+/K+-ATPase is required for sensory system development in zebrafish. Development (2008) 0.85
Differential activation of natriuretic peptide receptors modulates cardiomyocyte proliferation during development. Development (2013) 0.84
Acquisition, Analysis, and Sharing of Data in 2015 and Beyond: A Survey of the Landscape: A Conference Report From the American Heart Association Data Summit 2015. J Am Heart Assoc (2015) 0.84
Novel cardiovascular gene functions revealed via systematic phenotype prediction in zebrafish. Development (2014) 0.84
Prioritizing causal disease genes using unbiased genomic features. Genome Biol (2014) 0.82
Comparison of echocardiographic and cardiac magnetic resonance imaging in hypertrophic cardiomyopathy sarcomere mutation carriers without left ventricular hypertrophy. Circ Cardiovasc Genet (2013) 0.81
Future translational applications from the contemporary genomics era: a scientific statement from the American Heart Association. Circulation (2015) 0.81
Action and the actionability in exome variation. Circ Cardiovasc Genet (2012) 0.79
Symptoms in atrial fibrillation: why keep score? Circ Arrhythm Electrophysiol (2009) 0.78
Growth arrest specific gene (GAS) 6 modulates platelet thrombus formation and vascular wall homeostasis and represents an attractive drug target. Curr Pharm Des (2007) 0.78
Clinical screening and genetic testing. Clin Lab Med (2010) 0.77
Lysosomal dysfunction and impaired autophagy underlie the pathogenesis of amyloidogenic light chain-mediated cardiotoxicity. EMBO Mol Med (2015) 0.76
Genetic screening and risk assessment in hypertrophic cardiomyopathy. J Am Coll Cardiol (2004) 0.76
Sequential effects of spadetail, one-eyed pinhead and no tail on midline convergence of nephric primordia during zebrafish embryogenesis. Dev Biol (2013) 0.76
Clinical screening and genetic testing. Heart Fail Clin (2010) 0.75
Risk stratification in the long-QT syndrome. N Engl J Med (2003) 0.75
Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function. J Clin Invest (2017) 0.75
The genetics of cardiomyopathies: what clinicians should know. Curr Heart Fail Rep (2007) 0.75
A dream, a journey, and a promise: the inauguration of Circulation: Cardiovascular Genetics. Circ Cardiovasc Genet (2008) 0.75
Management strategy in 249 consecutive patients with obstructive hypertrophic cardiomyopathy referred to a dedicated program. Am J Cardiol (2012) 0.75