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Genetics of Atrial Fibrillation in 2020: GWAS, Genome Sequencing, Polygenic Risk, and Beyond.
Roselli, Carolina; Rienstra, Michiel; Ellinor, Patrick T.
Affiliation
  • Roselli C; From the Cardiovascular Disease Initiative, Broad Institute of MIT and Harvard, Cambridge, MA (C.R., P.T.E.).
  • Rienstra M; Department of Cardiology, University of Groningen, University Medical Center Groningen, the Netherlands (C.R., M.R.).
  • Ellinor PT; Department of Cardiology, University of Groningen, University Medical Center Groningen, the Netherlands (C.R., M.R.).
Circ Res ; 127(1): 21-33, 2020 06 19.
Article in En | MEDLINE | ID: mdl-32716721
ABSTRACT
Atrial fibrillation is a common heart rhythm disorder that leads to an increased risk for stroke and heart failure. Atrial fibrillation is a complex disease with both environmental and genetic risk factors that contribute to the arrhythmia. Over the last decade, rapid progress has been made in identifying the genetic basis for this common condition. In this review, we provide an overview of the primary types of genetic analyses performed for atrial fibrillation, including linkage studies, genome-wide association studies, and studies of rare coding variation. With these results in mind, we aim to highlighting the existing knowledge gaps and future directions for atrial fibrillation genetics research.
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Full text: 1 Database: MEDLINE Main subject: Atrial Fibrillation / Genetic Predisposition to Disease Type of study: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Limits: Animals / Humans Language: En Journal: Circ Res Year: 2020 Type: Article

Full text: 1 Database: MEDLINE Main subject: Atrial Fibrillation / Genetic Predisposition to Disease Type of study: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Limits: Animals / Humans Language: En Journal: Circ Res Year: 2020 Type: Article