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

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

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

Incomplete right bundle branch block: a novel electrocardiographic marker for lone atrial fibrillation

(2010) J. B. Nielsen et al.   EUROPACE

Gating-Related Molecular Motions in the Extracellular Domain of the IKs Channel: Implications for IKs Channelopathy

(2010) Yu Hong Wang et al.   JOURNAL OF MEMBRANE BIOLOGY

QTc: how long is too long?

(2009) J N Johnson et al.   BRITISH JOURNAL OF SPORTS MEDICINE

Structural basis for KV7.1–KCNEx interactions in the IKs channel complex

(2009) Alicia Lundby et al.   HEART RHYTHM

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

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

Augmented potassium current is a shared phenotype for two genetic defects associated with familial atrial fibrillation

(2009) Robert L. Abraham et al.   JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY

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

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

DNA Methylation Analysis of Chromosome 21 Gene Promoters at Single Base Pair and Single Allele Resolution

(2009) Yingying Zhang et al.   PLoS Genetics

Structure of KCNE1 and Implications for How It Modulates the KCNQ1 Potassium Channel†‡

(2008) Congbao Kang et al.   BIOCHEMISTRY

Prevalence of early-onset atrial fibrillation in congenital long QT syndrome

(2008) Jonathan N. Johnson et al.   HEART RHYTHM

Differential Allelic Expression in the Human Genome: A Robust Approach To Identify Genetic and Epigenetic Cis-Acting Mechanisms Regulating Gene Expression

(2008) David Serre et al.   PLoS Genetics