Atrial Fibrillation Is a Complex Trait

Identification of Functional Variant Enhancers Associated with Atrial Fibrillation

(2020) Antoinette Felicia van Ouwerkerk et al.   CIRCULATION RESEARCH

Monogenic and Polygenic Contributions to Atrial Fibrillation Risk: Results from a National Biobank

(2019) Seung Hoan Choi et al.   CIRCULATION RESEARCH

Generation and primary characterization of iAM-1, a versatile new line of conditionally immortalized atrial myocytes with preserved cardiomyogenic differentiation capacity

(2018) Jia Liu et al.   CARDIOVASCULAR RESEARCH

Multi-ethnic genome-wide association study for atrial fibrillation

(2018) Carolina Roselli et al.   NATURE GENETICS

A promoter interaction map for cardiovascular disease genetics

(2018) Lindsey E Montefiori et al.   eLife

Association of of Atrial Fibrillation Clinical Phenotypes With Treatment Patterns and Outcomes

(2018) Taku Inohara et al.   JAMA Cardiology

Biobank-driven genomic discovery yields new insight into atrial fibrillation biology

(2018) Jonas B. Nielsen et al.   NATURE GENETICS

Pitx2 promotes heart repair by activating the antioxidant response after cardiac injury

(2016) Ge Tao et al.   NATURE

Massively parallel quantification of the regulatory effects of noncoding genetic variation in a human cohort

(2015) Christopher M. Vockley et al.   GENOME RESEARCH

Global epidemiology of atrial fibrillation

(2014) Faisal Rahman et al.   Nature Reviews Cardiology

Genome-Wide Quantitative Enhancer Activity Maps Identified by STARR-seq

(2013) C. D. Arnold et al.   SCIENCE

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

Atrial Natriuretic Peptide Frameshift Mutation in Familial Atrial Fibrillation

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