A KCNQ1 mutation causes age-dependant bradycardia and persistent atrial fibrillation

Overlapping Cardiac Phenotype Associated with a Familial Mutation in the Voltage Sensor of the KCNQ1 Channel

(2013) Ulrike Henrion et al.   CELLULAR PHYSIOLOGY AND 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

AKCNQ1Mutation Causes a High Penetrance for Familial Atrial Fibrillation

(2012) DANIEL C. BARTOS et al.   JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY

Pro-arrhythmogenic effects of the S140GKCNQ1mutation in human atrial fibrillation - insights from modelling

(2012) Sanjay Kharche et al.   JOURNAL OF PHYSIOLOGY-LONDON

Tachybradycardia in the isolated canine right atrium induced by chronic sympathetic stimulation and pacemaker current inhibition

(2010) Boyoung Joung et al.   AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY

Mutations in sodium channel β-subunit SCN3B are associated with early-onset lone atrial fibrillation

(2010) Morten S. Olesen et al.   CARDIOVASCULAR RESEARCH

Monogenic atrial fibrillation as pathophysiological paradigms

(2010) S. Mahida et al.   CARDIOVASCULAR RESEARCH

Complex Interactions Between the Sinoatrial Node and Atrium During Reentrant Arrhythmias in the Canine Heart

(2010) Vadim V. Fedorov et al.   CIRCULATION

R231C mutation in KCNQ1 causes long QT syndrome type 1 and familial atrial fibrillation

(2010) Daniel C. Bartos et al.   HEART RHYTHM

Cholesterol Inhibits M-type K+Channels via Protein Kinase C-dependent Phosphorylation in Sympathetic Neurons

(2010) Seul-Yi Lee et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Mutation in the S3 segment of KCNQ1 results in familial lone atrial fibrillation

(2009) Saumya Das et al.   HEART RHYTHM

Common variants at ten loci influence QT interval duration in the QTGEN Study

(2009) Christopher Newton-Cheh et al.   NATURE GENETICS

Atrial fibrillation: evidence for genetically determined disease

(2008) Ali Andalib et al.   CURRENT OPINION IN CARDIOLOGY

Kv7.1 (KCNQ1) properties and channelopathies

(2008) David Peroz et al.   JOURNAL OF PHYSIOLOGY-LONDON

Mechanisms by which atrial fibrillation-associated mutations in the S1 domain of KCNQ1 slow deactivation of IKs channels

(2008) Lioara Restier et al.   JOURNAL OF PHYSIOLOGY-LONDON

Molecular Genetics of Atrial Fibrillation

(2008) Chia-Ti Tsai et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY