GATA5 loss-of-function mutation in familial dilated cardiomyopathy

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

(2014) Xin-Kai Qu et al.   AMERICAN JOURNAL OF CARDIOLOGY

SPEG Interacts with Myotubularin, and Its Deficiency Causes Centronuclear Myopathy with Dilated Cardiomyopathy

(2014) Pankaj B. Agrawal et al.   AMERICAN JOURNAL OF HUMAN GENETICS

New-onset left bundle branch block independently predicts long-term mortality in patients with idiopathic dilated cardiomyopathy: data from the Trieste Heart Muscle Disease Registry

(2014) A. Aleksova et al.   EUROPACE

NKX2.5 mutation identification on exome sequencing in a patient with heterotaxy

(2014) Kosuke Izumi et al.   European Journal of Medical Genetics

Endothelin 1 gene as a modifier in dilated cardiomyopathy

(2014) Lova Satyanarayna Matsa et al.   GENE

Prevalence and spectrum of GATA4 mutations associated with sporadic dilated cardiomyopathy

(2014) Jian Li et al.   GENE

Mutational Spectrum of the NKX2-5 Gene in Patients with Lone Atrial Fibrillation

(2014) Hong Yu et al.   International Journal of Medical Sciences

GATA5 loss-of-function mutations associated with congenital bicuspid aortic valve

(2014) LIN-MEI SHI et al.   INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE

Increased circulating T-helper 22 cells in patients with dilated cardiomyopathy

(2014) QING KONG et al.   Molecular Medicine Reports

Identification of two novel GATA6 mutations in patients with nonsyndromic conotruncal heart defects

(2014) XIKE WANG et al.   Molecular Medicine Reports

Coxsackievirus B detection in cases of myocarditis, myopericarditis, pericarditis and dilated cardiomyopathy in hospitalized patients

(2014) IMED GAALOUL et al.   Molecular Medicine Reports

RAF1 mutations in childhood-onset dilated cardiomyopathy

(2014) Perundurai S Dhandapany et al.   NATURE GENETICS

Novel and Highly Lethal NKX2.5 Missense Mutation in a Family With Sudden Death and Ventricular Arrhythmia

(2014) Jennifer L. Perera et al.   PEDIATRIC CARDIOLOGY

Nucleocytoplasmic Shuttling of a GATA Transcription Factor Functions as a Development Timer

(2014) H. Cai et al.   SCIENCE

Perturbation of NCOA6 Leads to Dilated Cardiomyopathy

(2014) Jae-il Roh et al.   Cell Reports

Mutation spectrum of GATA4 associated with congenital atrial septal defects

(2013) Yi-Qing Yang et al.   Archives of Medical Science

GATA4 loss-of-function mutation underlies familial dilated cardiomyopathy

(2013) Ruo-Gu Li et al.   BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS

Functional Characterization of a Novel Mutation in NKX2-5 Associated With Congenital Heart Disease and Adult-Onset Cardiomyopathy

(2013) Mauro W. Costa et al.   Circulation-Cardiovascular Genetics

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

(2013) WH Xie et al.   Clinics

The need to modify patient selection to improve the benefits of implantable cardioverter-defibrillator for primary prevention of sudden death in non-ischaemic dilated cardiomyopathy

(2013) M. Disertori et al.   EUROPACE

The HLA class II allele DQB1*0309 is associated with dilated cardiomyopathy

(2013) Sabine Pankuweit et al.   GENE

A novel mutation of GATA4 (K319E) is responsible for familial atrial septal defect and pulmonary valve stenosis

(2013) Rong Xiang et al.   GENE

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

(2013) Yi-Qing Yang et al.   HUMAN MUTATION

GATA5 loss-of-Function Mutations Underlie Tetralogy of Fallot

(2013) Dong Wei et al.   International Journal of Medical Sciences

A novel GATA4 loss-of-function mutation responsible for familial dilated cardiomyopathy

(2013) LAN ZHAO et al.   INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE

Genetic mutations and mechanisms in dilated cardiomyopathy

(2013) Elizabeth M. McNally et al.   JOURNAL OF CLINICAL INVESTIGATION

Identification of Functional Mutations in GATA4 in Patients with Congenital Heart Disease

(2013) Erli Wang et al.   PLoS One

Mitochondrial Fusion Directs Cardiomyocyte Differentiation via Calcineurin and Notch Signaling

(2013) A. Kasahara et al.   SCIENCE

Wenckebach Periodicity at Rest That Normalizes With Tachycardia in a Family With a NKX2.5 Mutation

(2012) Warren Guntheroth et al.   AMERICAN JOURNAL OF CARDIOLOGY

Novel GATA6 Mutations Associated with Congenital Ventricular Septal Defect or Tetralogy of Fallot

(2012) Juan Wang et al.   DNA AND CELL BIOLOGY

GATA6 loss-of-function mutation in atrial fibrillation

(2012) Yi-Qing Yang et al.   European Journal of Medical Genetics

Identification of a missense mutation in the melusin-encoding ITGB1BP2 gene in a patient with dilated cardiomyopathy

(2012) Volker Ruppert et al.   GENE

Prevalence and spectrum of GATA6 mutations associated with familial atrial fibrillation

(2012) Yi-Qing Yang et al.   INTERNATIONAL JOURNAL OF CARDIOLOGY

Mutational spectrum of the GATA5 gene associated with familial atrial fibrillation

(2012) Yi-Qing Yang et al.   INTERNATIONAL JOURNAL OF CARDIOLOGY

Prevalence and spectrum of GATA5 mutations associated with congenital heart disease

(2012) Jin-Qi Jiang et al.   INTERNATIONAL JOURNAL OF CARDIOLOGY

Dilated cardiomyopathy in patients with mutations in anoctamin 5

(2012) K. Wahbi et al.   INTERNATIONAL JOURNAL OF CARDIOLOGY

Sudden cardiac death in non-ischemic dilated cardiomyopathy: A critical appraisal of existing and potential risk stratification tools

(2012) Emmanuel Koutalas et al.   INTERNATIONAL JOURNAL OF CARDIOLOGY

Novel GATA6 loss-of-function mutation responsible for familial atrial fibrillation

(2012) JIAN LI et al.   INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE

A novel GATA5 loss-of-function mutation underlies lone atrial fibrillation

(2012) XIN-HUA WANG et al.   INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE

Mutation spectrum of the GATA4 gene in patients with idiopathic atrial fibrillation

(2012) Jun Wang et al.   MOLECULAR BIOLOGY REPORTS

GATA5 Loss-of-Function Mutation Responsible for the Congenital Ventriculoseptal Defect

(2012) Dong Wei et al.   PEDIATRIC CARDIOLOGY

Contribution of Acquired Factors to the Pathogenesis of Dilated Cardiomyopathy

(2011) Tsutomu Yoshikawa   CIRCULATION JOURNAL

GATA5 interacts with GATA4 and GATA6 in outflow tract development

(2011) Brigitte Laforest et al.   DEVELOPMENTAL BIOLOGY

The genetics of dilated cardiomyopathy

(2011) English Flack et al.   HEART RHYTHM

Loss of Gata5 in mice leads to bicuspid aortic valve

(2011) Brigitte Laforest et al.   JOURNAL OF CLINICAL INVESTIGATION

A Novel GATA4 Loss-of-Function Mutation Associated With Congenital Ventricular Septal Defect

(2011) Yi-Qing Yang et al.   PEDIATRIC CARDIOLOGY

Dilated Cardiomyopathy and Role of Antithrombotic Therapy

(2010) Ashraf S. Abdo et al.   AMERICAN JOURNAL OF THE MEDICAL SCIENCES

Prevalence of Desmosomal Protein Gene Mutations in Patients With Dilated Cardiomyopathy

(2010) Perry Elliott et al.   Circulation-Cardiovascular Genetics

Mutations in the cardiac transcription factor GATA4 in patients with lone atrial fibrillation

(2010) Maximilian G. Posch et al.   European Journal of Medical Genetics

A novel GATA6 mutation in patients with tetralogy of Fallot or atrial septal defect

(2010) Xiaoping Lin et al.   JOURNAL OF HUMAN GENETICS

Primary contribution to zebrafish heart regeneration by gata4 + cardiomyocytes

(2010) Kazu Kikuchi et al.   NATURE

Gata4andGata5Cooperatively Regulate Cardiac Myocyte Proliferation in Mice

(2009) Manvendra K. Singh et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

GATA6 mutations cause human cardiac outflow tract defects by disrupting semaphorin-plexin signaling

(2009) K. Kodo et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

GATA4 and GATA5 are essential for heart and liver development in Xenopus embryos

(2008) Kim E Haworth et al.   BMC DEVELOPMENTAL BIOLOGY