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GATA6 loss-of-function mutation contributes to congenital bicuspid aortic valve

Gene, 2018-07, Vol.663, p.115-120

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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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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A New ISL1 Loss-of-Function Mutation Predisposes to Congenital Double Outlet Right Ventricle

International Heart Journal, 2019/09/27, Vol.60(5), pp.1113-1122

2019

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NR2F2 loss‑of‑function mutation is responsible for congenital bicuspid aortic valve

International journal of molecular medicine, 2019-04, Vol.43 (4), p.1839-1846

2019

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Discovery of GJC1 (Cx45) as a New Gene Underlying Congenital Heart Disease and Arrhythmias

Biology (Basel, Switzerland), 2023-02, Vol.12 (3), p.346

2023

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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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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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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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HAND1 loss-of-function mutation contributes to congenital double outlet right ventricle

International journal of molecular medicine, 2017-03, Vol.39 (3), p.711-718

2017

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Identification of SOX18 as a New Gene Predisposing to Congenital Heart Disease

Diagnostics (Basel), 2022-08, Vol.12 (8), p.1917

2022

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MESP1 loss-of-function mutation contributes to double outlet right ventricle

Molecular medicine reports, 2017-09, Vol.16 (3), p.2747-2754

2017

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SMAD4 loss-of-function mutation predisposes to congenital heart disease

European journal of medical genetics, 2023-01, Vol.66 (1), p.104677-104677, Article 104677

2023

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Use of human aortic extracellular matrix as a scaffold for construction of a patient-specific tissue engineered vascular patch

Biomedical materials (Bristol), 2017-10, Vol.12 (6), p.065006-065006

2017

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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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Meta-analysis of clinical studies comparing coronary artery bypass grafting with percutaneous coronary intervention in patients with end-stage renal disease

European journal of cardio-thoracic surgery, 2013-03, Vol.43 (3), p.459-467

2013

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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

2016

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A novel TBX20 loss-of-function mutation contributes to adult-onset dilated cardiomyopathy or congenital atrial septal defect

Molecular medicine reports, 2016-10, Vol.14 (4), p.3307-3314

2016

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Prevalence and spectrum of NKX2.5 mutations in patients with congenital atrial septal defect and atrioventricular block

Molecular medicine reports, 2017-04, Vol.15 (4), p.2247-2254

2017

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A Novel NKX2.6 Mutation Associated with Congenital Ventricular Septal Defect

Pediatric cardiology, 2015-03, Vol.36 (3), p.646-656

2015

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TBX20 loss-of-function mutation responsible for familial tetralogy of Fallot or sporadic persistent truncus arteriosus

International journal of medical sciences, 2017-01, Vol.14 (4), p.323-332

2017

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MEF2C loss-of-function mutation contributes to congenital heart defects

International journal of medical sciences, 2017-01, Vol.14 (11), p.1143-1153

2017

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A novel NKX2.5 loss-of-function mutation responsible for familial atrial fibrillation

International journal of molecular medicine, 2013-05, Vol.31 (5), p.1119-1126

2013

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A novel HAND2 loss-of-function mutation responsible for tetralogy of Fallot

International journal of molecular medicine, 2016-02, Vol.37 (2), p.445-451

2016

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GATA6 loss-of-function mutation contributes to congenital bicuspid aortic valve

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

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

A New ISL1 Loss-of-Function Mutation Predisposes to Congenital Double Outlet Right Ventricle

NR2F2 loss‑of‑function mutation is responsible for congenital bicuspid aortic valve

Discovery of GJC1 (Cx45) as a New Gene Underlying Congenital Heart Disease and Arrhythmias

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

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

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

HAND1 loss-of-function mutation contributes to congenital double outlet right ventricle

Identification of SOX18 as a New Gene Predisposing to Congenital Heart Disease

MESP1 loss-of-function mutation contributes to double outlet right ventricle

SMAD4 loss-of-function mutation predisposes to congenital heart disease

Use of human aortic extracellular matrix as a scaffold for construction of a patient-specific tissue engineered vascular patch

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

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

Meta-analysis of clinical studies comparing coronary artery bypass grafting with percutaneous coronary intervention in patients with end-stage renal disease

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

A novel TBX20 loss-of-function mutation contributes to adult-onset dilated cardiomyopathy or congenital atrial septal defect

Prevalence and spectrum of NKX2.5 mutations in patients with congenital atrial septal defect and atrioventricular block

A Novel NKX2.6 Mutation Associated with Congenital Ventricular Septal Defect

TBX20 loss-of-function mutation responsible for familial tetralogy of Fallot or sporadic persistent truncus arteriosus

MEF2C loss-of-function mutation contributes to congenital heart defects

A novel NKX2.5 loss-of-function mutation responsible for familial atrial fibrillation

A novel HAND2 loss-of-function mutation responsible for tetralogy of Fallot

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