De novo KCNQ1 mutation responsible for atrial fibrillation and short QT syndrome in utero

Atrial Fibrillation Begets Atrial Fibrillation

1995 • 3,388 citations

Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

1996 • 1,746 citations

Coassembly of KVLQT1 and minK (IsK) proteins to form cardiac IKS potassium channel

1996 • 1,741 citations

KvLQT1 and IsK (minK) proteins associate to form the IKS cardiac potassium current

1996 • 1,585 citations

KCNQ1 Gain-of-Function Mutation in Familial Atrial Fibrillation

2003 • 975 citations

Sudden Death Associated With Short-QT Syndrome Linked to Mutations in HERG

2003 • 846 citations

Mutations in the hminK gene cause long QT syndrome and suppress lKs function

1997 • 763 citations

Mutation in the KCNQ1 Gene Leading to the Short QT-Interval Syndrome

2004 • 615 citations

Identification of a Genetic Locus for Familial Atrial Fibrillation

1997 • 559 citations

A constitutively open potassium channel formed by KCNQ1 and KCNE3

2000 • 481 citations

Identification of a KCNE2 Gain-of-Function Mutation in Patients with Familial Atrial Fibrillation

2004 • 387 citations

[16] Electrophysiologic recordings from Xenopus oocytes

1998 • 361 citations

New normal limits for the paediatric electrocardiogram

2001 • 360 citations

Mathematical models of action potentials in the periphery and center of the rabbit sinoatrial node

2000 • 347 citations

Familial atrial fibrillation is a genetically heterogeneous disorder

2003 • 331 citations

A Computational Model of the Human Left-Ventricular Epicardial Myocyte

2004 • 282 citations

Targeted disruption of the Kcnq1 gene produces a mouse model of Jervell and Lange– Nielsen Syndrome

2001 • 244 citations

KCNE2 confers background current characteristics to the cardiac KCNQ1 potassium channel

2000 • 239 citations

Short- and Long-Term Outcome of Children With Congenital Complete Heart Block Diagnosed In Utero or as a Newborn

2000 • 238 citations

Rapid and slow components of delayed rectifier current in human atrial myocytes

1994 • 236 citations

[19] Electrophysiological recording from Xenopus oocytes

1992 • 236 citations

Atrial electrophysiological remodeling caused by rapid atrial activation: underlying mechanisms and clinical relevance to atrial fibrillation

1999 • 147 citations

Genome-Wide Linkage Scan Identifies a Novel Genetic Locus on Chromosome 5p13 for Neonatal Atrial Fibrillation Associated With Sudden Death and Variable Cardiomyopathy

2004 • 122 citations

A superfamily of small potassium channel subunits: form and function of the MinK-related peptides (MiRPs)

1998 • 113 citations

Delayed Rectifier Channels in Human Ventricular Myocytes

1995 • 74 citations

KCNQ1 gain-of-function mutation in familial atrial fibrillation

2003 • 47 citations

Familial atrial fibrillation

2020 • 19 citations

Estimation of outward currents in isolated human atrial myocytes using inactivation time course analysis

1998 • 17 citations

Familial atrial fibrillation: simulation of the mechanisms and effects of a slow rectifier potassium channel mutation in human atrial tissue

2005 • 6 citations