Whole-exome sequencing in familial atrial fibrillation

Exome Sequencing and Systems Biology Converge to Identify Novel Mutations in the L-Type Calcium Channel, CACNA1C , Linked to Autosomal Dominant Long QT Syndrome

(2013) Nicole J. Boczek et al.   Circulation-Cardiovascular Genetics

Whole Exome Sequencing Identifies a Causal RBM20 Mutation in a Large Pedigree With Familial Dilated Cardiomyopathy

(2013) Quinn S. Wells et al.   Circulation-Cardiovascular Genetics

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

(2013) Peter Weeke et al.   HEART RHYTHM

Evaluating Pathogenicity of Rare Variants From Dilated Cardiomyopathy in the Exome Era

(2012) Nadine Norton et al.   Circulation-Cardiovascular Genetics

Chromosome 4q25 Variants Are Genetic Modifiers of Rare Ion Channel Mutations Associated With Familial Atrial Fibrillation

(2012) Marylyn D. Ritchie et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Differential confounding of rare and common variants in spatially structured populations

(2012) Iain Mathieson et al.   NATURE GENETICS

Meta-analysis identifies six new susceptibility loci for atrial fibrillation

(2012) Patrick T Ellinor et al.   NATURE GENETICS

Exome sequencing as a tool for Mendelian disease gene discovery

(2011) Michael J. Bamshad et al.   NATURE REVIEWS GENETICS

Systems Pharmacology of Arrhythmias

(2010) S. I. Berger et al.   Science Signaling

Transgenic simulation of human heart failure-like L-type Ca2+-channels: implications for fibrosis and heart rate in mice

(2009) Nadine Beetz et al.   CARDIOVASCULAR RESEARCH

Accelerated inactivation of the L-type calcium current due to a mutation in CACNB2b underlies Brugada syndrome

(2009) Jonathan M. Cordeiro et al.   JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY

Finding the missing heritability of complex diseases

(2009) Teri A. Manolio et al.   NATURE

Targeted capture and massively parallel sequencing of 12 human exomes

(2009) Sarah B. Ng et al.   NATURE

Exome sequencing identifies the cause of a mendelian disorder

(2009) Sarah B Ng et al.   NATURE GENETICS

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