NKX2-6 mutation predisposes to familial atrial fibrillation

Gain-of-function mutations in potassium channel subunit KCNE2 associated with early-onset lone atrial fibrillation

(2014) Jonas Bille Nielsen et al.   Biomarkers in Medicine

The Clinical Profile and Pathophysiology of Atrial Fibrillation

(2014) Jason Andrade et al.   CIRCULATION RESEARCH

Changes in Left Ventricular Filling in Patients with Persistent Atrial Fibrillation

(2014) Franjo Naji et al.   International Journal of Medical Sciences

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

Conotruncal malformations and absent thymus due to a deleterious NKX2-6 mutation

(2014) Asaf Ta-Shma et al.   JOURNAL OF MEDICAL GENETICS

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

Transcription factors and atrial fibrillation

(2013) S. Mahida   CARDIOVASCULAR RESEARCH

A novel KCND3 gain-of-function mutation associated with early-onset of persistent lone atrial fibrillation

(2013) Morten Salling Olesen et al.   CARDIOVASCULAR RESEARCH

Causes of Death and Influencing Factors in Patients With Atrial Fibrillation

(2013) Eloi Marijon et al.   CIRCULATION

Heart Disease and Stroke Statistics—2014 Update

(2013) Alan S. Go et al.   CIRCULATION

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

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

(2013) XB Qiu et al.   Clinics

Prevalence and Spectrum of PITX2c Mutations Associated with Congenital Heart Disease

(2013) Juan Wang et al.   DNA AND CELL BIOLOGY

A novel PITX2c loss-of-function mutation associated with familial atrial fibrillation

(2013) Jun Wang et al.   European Journal of Medical Genetics

Candidate gene approach to identifying rare genetic variants associated with lone atrial fibrillation

(2013) Peter Weeke et al.   HEART RHYTHM

Very early-onset lone atrial fibrillation patients have a high prevalence of rare variants in genes previously associated with atrial fibrillation

(2013) Morten S. Olesen et al.   HEART RHYTHM

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

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

Atrial Fibrillation reduces the Functional REServe of the Heart by a fifth: A pilot FRESH-AF study

(2013) Muzahir H. Tayebjee et al.   INTERNATIONAL JOURNAL OF CARDIOLOGY

Atrial fibrillation: Profile and burden of an evolving epidemic in the 21st century

(2013) Jocasta Ball et al.   INTERNATIONAL JOURNAL OF CARDIOLOGY

Prevalence and spectrum of PITX2c mutations associated with familial atrial fibrillation

(2013) Yi-Qing Yang et al.   INTERNATIONAL JOURNAL OF CARDIOLOGY

The association between hyperuricemia, left atrial size and new-onset atrial fibrillation

(2013) Tze-Fan Chao et al.   INTERNATIONAL JOURNAL OF CARDIOLOGY

Impact of atrial fibrillation-induced tachycardiomyopathy in patients undergoing pulmonary vein isolation

(2013) Naiara Calvo et al.   INTERNATIONAL JOURNAL OF CARDIOLOGY

GATA5 loss-of-Function Mutations Underlie Tetralogy of Fallot

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

PITX2c Loss-of-Function Mutations Responsible for Congenital Atrial Septal Defects

(2013) Fang Yuan et al.   International Journal of Medical Sciences

Mutations of the SCN4B-encoded sodium channel β4 subunit in familial atrial fibrillation

(2013) RUO-GU LI et al.   INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE

A novel PITX2c loss-of-function mutation underlies lone atrial fibrillation

(2013) YI-MENG ZHOU et al.   INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE

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

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

Novel GATA4 mutations in patients with congenital ventricular septal defects

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

High Familial Risk of Atrial Fibrillation/Atrial Flutter in Multiplex Families: A Nationwide Family Study in Sweden

(2013) Bengt Zöller et al.   Journal of the American Heart Association

Atrial Fibrillation and the Risk of Myocardial Infarction

(2013) Elsayed Z. Soliman et al.   JAMA Internal Medicine

Crystal Structure of the Human NKX2.5 Homeodomain in Complex with DNA Target

(2012) Lagnajeet Pradhan et al.   BIOCHEMISTRY

Mutations in the potassium channel subunit KCNE1 are associated with early-onset familial atrial fibrillation

(2012) Morten S Olesen et al.   BMC Medical Genetics

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

A KCNJ8 mutation associated with early repolarization and atrial fibrillation

(2012) J. T. Delaney et al.   EUROPACE

Genetic variation in KCNA5: impact on the atrial-specific potassium current IKur in patients with lone atrial fibrillation

(2012) Ingrid E. Christophersen et al.   EUROPEAN HEART JOURNAL

GATA6 loss-of-function mutation in atrial fibrillation

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

Patients originally diagnosed with idiopathic atrial fibrillation more often suffer from insidious coronary artery disease compared to healthy sinus rhythm controls

(2012) Bob Weijs et al.   HEART RHYTHM

Renal dysfunction and the risk of thromboembolic events in patients with atrial fibrillation after catheter ablation—The potential role beyond the CHA2DS2-VASc score

(2012) Tze-Fan Chao et al.   HEART RHYTHM

Atrial fibrillation and the risk of incident dementia: A meta-analysis

(2012) Pasquale Santangeli et al.   HEART RHYTHM

Concomitant obstructive sleep apnea increases the recurrence of atrial fibrillation following radiofrequency catheter ablation of atrial fibrillation: Clinical impact of continuous positive airway pressure therapy

(2012) Yoshihisa Naruse et al.   HEART RHYTHM

Obesity results in progressive atrial structural and electrical remodeling: Implications for atrial fibrillation

(2012) Hany S. Abed et al.   HEART RHYTHM

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

Familial Aggregation of Lone Atrial Fibrillation in Young Persons

(2012) Nina Øyen et al.   JOURNAL OF THE AMERICAN COLLEGE OF 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

2011 ACCF/AHA/HRS Focused Updates Incorporated Into the ACC/AHA/ESC 2006 Guidelines for the Management of Patients With Atrial Fibrillation

(2011) Valentin Fuster et al.   CIRCULATION

SCN1Bb R214Q found in 3 patients: 1 with Brugada syndrome and 2 with lone atrial fibrillation

(2011) Morten S. Olesen et al.   HEART RHYTHM

Functional dominant-negative mutation of sodium channel subunit gene SCN3B associated with atrial fibrillation in a Chinese GeneID population

(2010) Pengyun Wang et al.   BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS

Paradigm of Genetic Mosaicism and Lone Atrial Fibrillation

(2010) Isabelle L. Thibodeau et al.   CIRCULATION

NKX2-5: an update on this hypermutable homeodomain protein and its role in human congenital heart disease (CHD)

(2010) Stella Marie Reamon-Buettner et al.   HUMAN MUTATION

Familial Aggregation of Lone atrial Fibrillation in the Chinese Population

(2010) Yi-Qing Yang et al.   INTERNAL MEDICINE

Association Between Familial Atrial Fibrillation and Risk of New-Onset Atrial Fibrillation

(2010) Steven A. Lubitz et al.   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

Familial Aggregation of Atrial Fibrillation

(2009) Ingrid Elisabeth Christophersen et al.   Circulation-Arrhythmia and Electrophysiology

Mutations in Sodium Channel β1- and β2-Subunits Associated With Atrial Fibrillation

(2009) Hiroshi Watanabe et al.   Circulation-Arrhythmia and Electrophysiology

Atrial fibrillation: A developmental point of view

(2009) Mathilda T.M. Mommersteeg et al.   HEART RHYTHM

Novel KCNA5 loss-of-function mutations responsible for atrial fibrillation

(2009) Yiqing Yang et al.   JOURNAL OF HUMAN GENETICS

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

KCNE3 Mutation V17M Identified in a Patient with Lone Atrial Fibrillation

(2008) Alicia Lundby et al.   CELLULAR PHYSIOLOGY AND BIOCHEMISTRY

Cardiac Sodium Channel ( SCN5A ) Variants Associated with Atrial Fibrillation

(2008) Dawood Darbar et al.   CIRCULATION

The non-synonymous coding IKr-channel variant KCNH2-K897T is associated with atrial fibrillation: results from a systematic candidate gene-based analysis of KCNH2 (HERG)

(2008) Moritz F. Sinner et al.   EUROPEAN HEART JOURNAL

Gain of function in IKs secondary to a mutation in KCNE5 associated with atrial fibrillation

(2008) Lasse S. Ravn et al.   HEART RHYTHM

Prolonged Signal-Averaged P-Wave Duration as an Intermediate Phenotype for Familial Atrial Fibrillation

(2008) Dawood Darbar et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Atrial Natriuretic Peptide Frameshift Mutation in Familial Atrial Fibrillation

(2008) Denice M. Hodgson-Zingman et al.   NEW ENGLAND JOURNAL OF MEDICINE