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A Novel Spatial Position Prediction Navigation System Makes Surgery More Accurate

IEEE transactions on medical imaging, 2023-12, Vol.42 (12), p.3614-3624

2023

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GATA4 Loss-of-Function Mutation and the Congenitally Bicuspid Aortic Valve

The American journal of cardiology, 2018-02, Vol.121 (4), p.469-474

2018

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GATA4 Loss-of-Function Mutations Underlie Familial Tetralogy of Fallot

Human mutation, 2013-12, Vol.34 (12), p.1662-1671

2013

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A Novel NKX2.5 Loss-of-Function Mutation Associated With Congenital Bicuspid Aortic Valve

The American journal of cardiology, 2014-12, Vol.114 (12), p.1891-1895

2014

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TBX5 loss-of-function mutation contributes to familial dilated cardiomyopathy

Biochemical and biophysical research communications, 2015-03, Vol.459 (1), p.166-171

2015

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MEF2C loss-of-function mutation associated with familial dilated cardiomyopathy

Clinical chemistry and laboratory medicine, 2018-02, Vol.56 (3), p.502-511

2018

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GATA4 loss-of-function mutation underlies familial dilated cardiomyopathy

Biochemical and biophysical research communications, 2013-10, Vol.439 (4), p.591-596

2013

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Prevalence and Spectrum of NKX2-5 Mutations Associated With Sporadic Adult-Onset Dilated Cardiomyopathy

International Heart Journal, 2017, Vol.58(4), pp.521-529

2017

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GATA6 loss-of-function mutations contribute to familial dilated cardiomyopathy

International journal of molecular medicine, 2014-11, Vol.34 (5), p.1315-1322

2014

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A novel NR2F2 loss-of-function mutation predisposes to congenital heart defect

European journal of medical genetics, 2018-04, Vol.61 (4), p.197-203

2018

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CASZ1 loss-of-function mutation contributes to familial dilated cardiomyopathy

Clinical chemistry and laboratory medicine, 2017, Vol.55 (9), p.1417

2017

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ZBTB17 loss-of-function mutation contributes to familial dilated cardiomyopathy

Heart and vessels, 2018-07, Vol.33 (7), p.722-732

2018

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HAND2 loss-of-function mutation causes familial dilated cardiomyopathy

European journal of medical genetics, 2019-09, Vol.62 (9), p.103540-103540, Article 103540

2019

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A HAND2 Loss-of-Function Mutation Causes Familial Ventricular Septal Defect and Pulmonary Stenosis

G3 : genes - genomes - genetics, 2016-04, Vol.6 (4), p.987-992

2016

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Prevalence and spectrum of Nkx2.5 mutations associated with idiopathic atrial fibrillation

Clinics (São Paulo, Brazil), 2013-06, Vol.68 (6), p.777-784

2013

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Impact of prior permanent pacemaker on long‐term clinical outcomes of patients undergoing percutaneous coronary intervention

Clinical cardiology (Mahwah, N.J.), 2017-04, Vol.40 (4), p.205-209

2017

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A novel NKX2-5 loss-of-function mutation predisposes to familial dilated cardiomyopathy and arrhythmias

International journal of molecular medicine, 2015-02, Vol.35 (2), p.478-486

2015

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GATA5 loss-of-function mutation in familial dilated cardiomyopathy

International journal of molecular medicine, 2015-03, Vol.35 (3), p.763-770

2015

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NKX2-6 mutation predisposes to familial atrial fibrillation

International journal of molecular medicine, 2014-12, Vol.34 (6), p.1581-1590

2014

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PITX2C loss-of-function mutations responsible for idiopathic atrial fibrillation

Clinics (São Paulo, Brazil), 2014-01, Vol.69 (1), p.15-22

2014

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TBX5 loss-of-function mutation contributes to atrial fibrillation and atypical Holt-Oram syndrome

Molecular medicine reports, 2016-05, Vol.13 (5), p.4349-4356

2016

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CASZ1 loss-of-function mutation associated with congenital heart disease

Gene, 2016-12, Vol.595 (1), p.62-68

2016

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PITX2 loss-of-function mutation contributes to tetralogy of Fallot

Gene, 2016-02, Vol.577 (2), p.258-264

2016

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Efficacy and safety of a novel multi-electrode radiofrequency ablation catheter for renal sympathetic denervation in pigs

Journal of geriatric cardiology : JGC, 2015-11, Vol.12 (6), p.618-625

2015

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HAND1 loss-of-function mutation associated with familial dilated cardiomyopathy

Clinical chemistry and laboratory medicine, 2016-07, Vol.54 (7), p.1161-1167

2016

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A Novel Spatial Position Prediction Navigation System Makes Surgery More Accurate

GATA4 Loss-of-Function Mutation and the Congenitally Bicuspid Aortic Valve

GATA4 Loss-of-Function Mutations Underlie Familial Tetralogy of Fallot

A Novel NKX2.5 Loss-of-Function Mutation Associated With Congenital Bicuspid Aortic Valve

TBX5 loss-of-function mutation contributes to familial dilated cardiomyopathy

MEF2C loss-of-function mutation associated with familial dilated cardiomyopathy

GATA4 loss-of-function mutation underlies familial dilated cardiomyopathy

Prevalence and Spectrum of NKX2-5 Mutations Associated With Sporadic Adult-Onset Dilated Cardiomyopathy

GATA6 loss-of-function mutations contribute to familial dilated cardiomyopathy

A novel NR2F2 loss-of-function mutation predisposes to congenital heart defect

CASZ1 loss-of-function mutation contributes to familial dilated cardiomyopathy

ZBTB17 loss-of-function mutation contributes to familial dilated cardiomyopathy

HAND2 loss-of-function mutation causes familial dilated cardiomyopathy

A HAND2 Loss-of-Function Mutation Causes Familial Ventricular Septal Defect and Pulmonary Stenosis

Prevalence and spectrum of Nkx2.5 mutations associated with idiopathic atrial fibrillation

Impact of prior permanent pacemaker on long‐term clinical outcomes of patients undergoing percutaneous coronary intervention

A novel NKX2-5 loss-of-function mutation predisposes to familial dilated cardiomyopathy and arrhythmias

GATA5 loss-of-function mutation in familial dilated cardiomyopathy

NKX2-6 mutation predisposes to familial atrial fibrillation

PITX2C loss-of-function mutations responsible for idiopathic atrial fibrillation

TBX5 loss-of-function mutation contributes to atrial fibrillation and atypical Holt-Oram syndrome

CASZ1 loss-of-function mutation associated with congenital heart disease

PITX2 loss-of-function mutation contributes to tetralogy of Fallot

Efficacy and safety of a novel multi-electrode radiofrequency ablation catheter for renal sympathetic denervation in pigs

HAND1 loss-of-function mutation associated with familial dilated cardiomyopathy

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