Published in Proc Natl Acad Sci U S A on May 10, 2010
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Pitx2, an atrial fibrillation predisposition gene, directly regulates ion transport and intercalated disc genes. Circ Cardiovasc Genet (2014) 1.07
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Shox2 mediates Tbx5 activity by regulating Bmp4 in the pacemaker region of the developing heart. Hum Mol Genet (2010) 1.03
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An introduction to murine models of atrial fibrillation. Front Physiol (2012) 0.92
Common variants for atrial fibrillation: results from genome-wide association studies. Hum Genet (2011) 0.92
Pitx2 promotes heart repair by activating the antioxidant response after cardiac injury. Nature (2016) 0.92
Differential impact of race and risk factors on incidence of atrial fibrillation. Am Heart J (2011) 0.91
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Pitx2 confers left morphological, molecular, and functional identity to the sinus venosus myocardium. Cardiovasc Res (2011) 0.88
The role of Shox2 in SAN development and function. Pediatr Cardiol (2012) 0.88
Molecular Basis of Gene-Gene Interaction: Cyclic Cross-Regulation of Gene Expression and Post-GWAS Gene-Gene Interaction Involved in Atrial Fibrillation. PLoS Genet (2015) 0.88
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Long-range regulatory interactions at the 4q25 atrial fibrillation risk locus involve PITX2c and ENPEP. BMC Biol (2015) 0.82
The role of transcription factors in atrial fibrillation. J Thorac Dis (2015) 0.82
A common variant on chromosome 4q25 is associated with prolonged PR interval in subjects with and without atrial fibrillation. Am J Cardiol (2013) 0.81
A common Shox2-Nkx2-5 antagonistic mechanism primes the pacemaker cell fate in the pulmonary vein myocardium and sinoatrial node. Development (2015) 0.81
Genomics of Atrial Fibrillation. Curr Cardiol Rep (2016) 0.80
Transgenic insights linking pitx2 and atrial arrhythmias. Front Physiol (2012) 0.80
Improved understanding of the pathophysiology of atrial fibrillation through the lens of discrete pathological pathways. Glob Cardiol Sci Pract (2014) 0.80
PITX2C loss-of-function mutations responsible for idiopathic atrial fibrillation. Clinics (Sao Paulo) (2014) 0.80
An automated system using spatial oversampling for optical mapping in murine atria. Development and validation with monophasic and transmembrane action potentials. Prog Biophys Mol Biol (2014) 0.80
Electrophysiological mapping of embryonic mouse hearts: mechanisms for developmental pacemaker switch and internodal conduction pathway. J Cardiovasc Electrophysiol (2011) 0.79
Paired-like homeodomain 2: a novel therapeutic target for atrial fibrillation? Front Genet (2014) 0.79
Pitx2c is reactivated in the failing myocardium and stimulates myf5 expression in cultured cardiomyocytes. PLoS One (2014) 0.78
Genetic loci associated with atrial fibrillation: relation to left atrial structure in the Framingham Heart Study. J Am Heart Assoc (2014) 0.78
Genetic Regulation of Sinoatrial Node Development and Pacemaker Program in the Venous Pole. J Cardiovasc Dev Dis (2015) 0.78
Atrial Fibrillation Genetics: Is There a Practical Clinical Value Now or in the Future? Can J Cardiol (2016) 0.78
Cardiovascular pharmacogenomics: the future of cardiovascular therapeutics? Can J Cardiol (2012) 0.77
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PITX2 Modulates Atrial Membrane Potential and the Antiarrhythmic Effects of Sodium-Channel Blockers. J Am Coll Cardiol (2016) 0.77
Coding and non-coding variants in the SHOX2 gene in patients with early-onset atrial fibrillation. Basic Res Cardiol (2016) 0.77
Pleiotropic and isoform-specific functions for Pitx2 in superior colliculus and hypothalamic neuronal development. Mol Cell Neurosci (2012) 0.77
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Genetic Discoveries in Atrial Fibrillation and Implications for Clinical Practice. Arrhythm Electrophysiol Rev (2014) 0.76
The Role of Pharmacogenetics in Atrial Fibrillation Therapeutics: Is Personalized Therapy in Sight? J Cardiovasc Pharmacol (2016) 0.76
PITX2: a master regulator of cardiac channelopathy in atrial fibrillation? Cardiovasc Res (2016) 0.76
ADMIRE: analysis and visualization of differential methylation in genomic regions using the Infinium HumanMethylation450 Assay. Epigenetics Chromatin (2015) 0.76
Association of Single Nucleotide Polymorphisms with Atrial Fibrillation and the Outcome after Catheter Ablation. Acta Cardiol Sin (2016) 0.75
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Impact of a 4q25 genetic variant in atrial flutter and on the risk of atrial fibrillation after cavotricuspid isthmus ablation. J Cardiovasc Electrophysiol (2013) 0.75
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A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke. Nat Genet (2009) 4.11
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Calmodulin kinase II-mediated sarcoplasmic reticulum Ca2+ leak promotes atrial fibrillation in mice. J Clin Invest (2009) 3.45
Increased vulnerability to atrial fibrillation in transgenic mice with selective atrial fibrosis caused by overexpression of TGF-beta1. Circ Res (2004) 3.30
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Atrial natriuretic peptide frameshift mutation in familial atrial fibrillation. N Engl J Med (2008) 2.14
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Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillation. Eur Heart J (2009) 2.06
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Molecular pathway for the localized formation of the sinoatrial node. Circ Res (2007) 1.93
Mutation in the S3 segment of KCNQ1 results in familial lone atrial fibrillation. Heart Rhythm (2009) 1.87
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Regulation of left-right asymmetry by thresholds of Pitx2c activity. Development (2001) 1.77
Targeted mutation reveals essential functions of the homeodomain transcription factor Shox2 in sinoatrial and pacemaking development. Circulation (2007) 1.72
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Pitx2c patterns anterior myocardium and aortic arch vessels and is required for local cell movement into atrioventricular cushions. Development (2002) 1.60
Inter-relationships of atrial fibrillation and atrial flutter mechanisms and clinical implications. J Am Coll Cardiol (2008) 1.52
Cardiac pacemaker function of HCN4 channels in mice is confined to embryonic development and requires cyclic AMP. EMBO J (2008) 1.47
Shox2 is essential for the differentiation of cardiac pacemaker cells by repressing Nkx2-5. Dev Biol (2009) 1.46
A genetic framework for improving arrhythmia therapy. Nature (2008) 1.45
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Nuclear factor 1 and T-cell factor/LEF recognition elements regulate Pitx2 transcription in pituitary development. Mol Cell Biol (2007) 0.94
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Computer-assisted personalized sedation for upper endoscopy and colonoscopy: a comparative, multicenter randomized study. Gastrointest Endosc (2010) 2.96
Bmp2 is essential for cardiac cushion epithelial-mesenchymal transition and myocardial patterning. Development (2005) 2.92
Functional genetic analysis of mouse chromosome 11. Nature (2003) 2.87
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Enhanced sarcoplasmic reticulum Ca2+ leak and increased Na+-Ca2+ exchanger function underlie delayed afterdepolarizations in patients with chronic atrial fibrillation. Circulation (2012) 2.58
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Bmp2 is critical for the murine uterine decidual response. Mol Cell Biol (2007) 2.09
Mutations in BMP4 are associated with subepithelial, microform, and overt cleft lip. Am J Hum Genet (2009) 2.07
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Intracellular calcium leak due to FKBP12.6 deficiency in mice facilitates the inducibility of atrial fibrillation. Heart Rhythm (2008) 2.05
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Calmodulin kinase II is required for fight or flight sinoatrial node physiology. Proc Natl Acad Sci U S A (2009) 1.95
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Stabilization of cardiac ryanodine receptor prevents intracellular calcium leak and arrhythmias. Proc Natl Acad Sci U S A (2006) 1.87
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Pitx2c patterns anterior myocardium and aortic arch vessels and is required for local cell movement into atrioventricular cushions. Development (2002) 1.60
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FRS2α-mediated FGF signals suppress premature differentiation of cardiac stem cells through regulating autophagy activity. Circ Res (2011) 1.52
Threshold-specific requirements for Bmp4 in mandibular development. Dev Biol (2005) 1.50
Bmp signaling regulates myocardial differentiation from cardiac progenitors through a MicroRNA-mediated mechanism. Dev Cell (2010) 1.49
Shox2 is essential for the differentiation of cardiac pacemaker cells by repressing Nkx2-5. Dev Biol (2009) 1.46
Canonical Wnt signaling functions in second heart field to promote right ventricular growth. Proc Natl Acad Sci U S A (2007) 1.46
BMP4 is required in the anterior heart field and its derivatives for endocardial cushion remodeling, outflow tract septation, and semilunar valve development. Dev Dyn (2008) 1.44
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Mouse hesr1 and hesr2 genes are redundantly required to mediate Notch signaling in the developing cardiovascular system. Dev Biol (2005) 1.42
Non-equilibrium gating in cardiac Na+ channels: an original mechanism of arrhythmia. Circulation (2003) 1.42
Bmp4 in limb bud mesoderm regulates digit pattern by controlling AER development. Dev Biol (2004) 1.41
Role of RyR2 phosphorylation at S2814 during heart failure progression. Circ Res (2012) 1.41
Fine mapping of a seizure susceptibility locus on mouse Chromosome 1: nomination of Kcnj10 as a causative gene. Mamm Genome (2004) 1.39
Accelerated development of pressure overload-induced cardiac hypertrophy and dysfunction in an RyR2-R176Q knockin mouse model. Hypertension (2010) 1.39
Serum response factor orchestrates nascent sarcomerogenesis and silences the biomineralization gene program in the heart. Proc Natl Acad Sci U S A (2008) 1.39
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System for tamoxifen-inducible expression of cre-recombinase from the Foxa2 locus in mice. Dev Dyn (2008) 1.37
Heart-specific overexpression of CUGBP1 reproduces functional and molecular abnormalities of myotonic dystrophy type 1. Hum Mol Genet (2010) 1.35
The LIM-homeodomain transcription factor Lmx1b plays a crucial role in podocytes. J Clin Invest (2002) 1.32
Pitx2 regulates cardiac left-right asymmetry by patterning second cardiac lineage-derived myocardium. Dev Biol (2006) 1.32
Junctophilin-2 expression silencing causes cardiocyte hypertrophy and abnormal intracellular calcium-handling. Circ Heart Fail (2011) 1.32
Pitx2 promotes development of splanchnic mesoderm-derived branchiomeric muscle. Development (2006) 1.31
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Inhibition of CaMKII phosphorylation of RyR2 prevents induction of atrial fibrillation in FKBP12.6 knockout mice. Circ Res (2011) 1.29
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Mice lacking central serotonergic neurons show enhanced inflammatory pain and an impaired analgesic response to antidepressant drugs. J Neurosci (2007) 1.26
Runx1 and Runx2 cooperate during sternal morphogenesis. Development (2010) 1.24
Junctophilin-2 is necessary for T-tubule maturation during mouse heart development. Cardiovasc Res (2013) 1.22
Bmp signaling regulates a dose-dependent transcriptional program to control facial skeletal development. Development (2012) 1.22
Hippo signaling regulates pancreas development through inactivation of Yap. Mol Cell Biol (2012) 1.21
Lmx1b is essential for Fgf8 and Wnt1 expression in the isthmic organizer during tectum and cerebellum development in mice. Development (2006) 1.20
BMP receptor type IA in limb bud mesenchyme regulates distal outgrowth and patterning. Dev Biol (2006) 1.20
Genetic inhibition of PKA phosphorylation of RyR2 prevents dystrophic cardiomyopathy. Proc Natl Acad Sci U S A (2010) 1.20
PKC inhibition ameliorates the cardiac phenotype in a mouse model of myotonic dystrophy type 1. J Clin Invest (2009) 1.19
GGAPs, a new family of bifunctional GTP-binding and GTPase-activating proteins. Mol Cell Biol (2003) 1.18
Defects in ankyrin-based membrane protein targeting pathways underlie atrial fibrillation. Circulation (2011) 1.18
Phosphorylation of RyR2 and shortening of RyR2 cluster spacing in spontaneously hypertensive rat with heart failure. Am J Physiol Heart Circ Physiol (2007) 1.17
Frs2alpha-deficiency in cardiac progenitors disrupts a subset of FGF signals required for outflow tract morphogenesis. Development (2008) 1.16
Hesr1 and Hesr3 are essential to generate undifferentiated quiescent satellite cells and to maintain satellite cell numbers. Development (2011) 1.16
Targeted disruption of hesr2 results in atrioventricular valve anomalies that lead to heart dysfunction. Circ Res (2004) 1.16
Pitx2 is functionally important in the early stages of vascular smooth muscle cell differentiation. J Cell Biol (2008) 1.14
Exercise training during diabetes attenuates cardiac ryanodine receptor dysregulation. J Appl Physiol (1985) (2009) 1.14
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Lmx1b controls the differentiation and migration of the superficial dorsal horn neurons of the spinal cord. Development (2004) 1.12
Epac2 mediates cardiac β1-adrenergic-dependent sarcoplasmic reticulum Ca2+ leak and arrhythmia. Circulation (2013) 1.12