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

GATA4 loss-of-function mutation underlies familial dilated cardiomyopathy

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

Sequencing of NOTCH1, GATA5, TGFBR1 and TGFBR2genes in familial cases of bicuspid aortic valve

(2013) Ilenia Foffa et al.   BMC Medical Genetics

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

Factors Related to the Need for Surgery after the Diagnosis of Bicuspid Aortic Valve: One Center´s Experience under a Conservative Approach

(2013) Josep M. Alegret et al.   International Journal of Medical Sciences

Novel GATA4 mutations in patients with congenital ventricular septal defects

(2013) Yi-Qing Yang et al.   MEDICAL SCIENCE MONITOR

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

(2013) Erli Wang et al.   PLoS One

Heart Disease and Stroke Statistics—2013 Update

(2012) Alan S. Go et al.   CIRCULATION

Novel GATA5 loss-of-function mutations underlie familial atrial fibrillation

(2012) JY Gu et al.   Clinics

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

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

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

R25C mutation in the NKX2.5 gene in Italian patients affected with non-syndromic and syndromic congenital heart disease

(2012) Giorgia Beffagna et al.   Journal of Cardiovascular Medicine

Rare non-synonymous variations in the transcriptional activation domains of GATA5 in bicuspid aortic valve disease

(2012) Ratnasari Padang et al.   JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY

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

Transforming Growth Factor-Beta Receptor Type II Mutation in a Patient With Bicuspid Aortic Valve Disease and Intraoperative Aortic Dissection

(2011) Evaldas Girdauskas et al.   ANNALS OF THORACIC SURGERY

GATA4 loss-of-function mutations in familial atrial fibrillation

(2011) Yi-Qing Yang et al.   CLINICA CHIMICA ACTA

GATA5 interacts with GATA4 and GATA6 in outflow tract development

(2011) Brigitte Laforest et al.   DEVELOPMENTAL BIOLOGY

Search of somatic GATA4 and NKX2.5 gene mutations in sporadic septal heart defects

(2011) Marleny Salazar et al.   European Journal of Medical Genetics

Incidence of Aortic Complications in Patients With Bicuspid Aortic Valves

(2011) Hector I. Michelena et al.   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

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

Combined Mutation Screening of NKX2-5, GATA4, and TBX5 in Congenital Heart Disease: Multiple Heterozygosity and Novel Mutations

(2011) Javier T. Granados-Riveron et al.   Congenital Heart Disease

A novel mutation of GATA4 in a familial atrial septal defect

(2010) Ying Chen et al.   CLINICA CHIMICA ACTA

GATA4 Mutations in 357 Unrelated Patients with Congenital Heart Malformation

(2010) Tanya L. Butler et al.   Genetic Testing and Molecular Biomarkers

Endocarditis on the bicuspid aortic valve: what's the risk?

(2010) W. Baig   HEART

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

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

Bicuspid Aortic Valve Disease

(2010) Samuel C. Siu et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Identification of GATA6 Sequence Variants in Patients With Congenital Heart Defects

(2010) Meenakshi Maitra et al.   PEDIATRIC RESEARCH

Genetic screening of 104 patients with congenitally malformed hearts revealed a fresh mutation of GATA4 in those with atrial septal defects

(2009) Haruka Hamanoue et al.   CARDIOLOGY IN THE YOUNG

Ascending Aortic Dilatation Associated With Bicuspid Aortic Valve

(2009) Thomas M. Tadros et al.   CIRCULATION

Heart Valve Development

(2009) Michelle D. Combs et al.   CIRCULATION RESEARCH

Gata4andGata5Cooperatively Regulate Cardiac Myocyte Proliferation in Mice

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

GATA4 Mutations in Chinese Patients with Congenital Cardiac Septal Defects

(2009) Ming-wu Chen et al.   PEDIATRIC CARDIOLOGY

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

GATA4 mutations in 486 Chinese patients with congenital heart disease

(2008) Weimin Zhang et al.   European Journal of Medical Genetics