Early-Onset Atrial Fibrillation and the Prevalence of Rare Variants in Cardiomyopathy and Arrhythmia Genes
Published 2021 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Early-Onset Atrial Fibrillation and the Prevalence of Rare Variants in Cardiomyopathy and Arrhythmia Genes
Authors
Keywords
-
Journal
JAMA Cardiology
Volume -, Issue -, Pages -
Publisher
American Medical Association (AMA)
Online
2021-09-08
DOI
10.1001/jamacardio.2021.3370
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Association of Rare Genetic Variants and Early-Onset Atrial Fibrillation in Ethnic Minority Individuals
- (2021) Brandon Chalazan et al. JAMA Cardiology
- Reevaluating the Genetic Contribution of Monogenic Dilated Cardiomyopathy
- (2020) Francesco Mazzarotto et al. CIRCULATION
- How Will Genetics Inform the Clinical Care of Atrial Fibrillation?
- (2020) M. Benjamin Shoemaker et al. CIRCULATION RESEARCH
- Frequency of genomic secondary findings among 21,915 eMERGE network participants
- (2020) GENETICS IN MEDICINE
- Exome sequencing and characterization of 49,960 individuals in the UK Biobank
- (2020) Cristopher V. Van Hout et al. NATURE
- Enrichment of loss-of-function and copy number variants in ventricular cardiomyopathy genes in ‘lone’ atrial fibrillation
- (2020) Julieta Lazarte et al. EUROPACE
- Monogenic and Polygenic Contributions to Atrial Fibrillation Risk: Results from a National Biobank
- (2019) Seung Hoan Choi et al. CIRCULATION RESEARCH
- 2019 HRS expert consensus statement on evaluation, risk stratification, and management of arrhythmogenic cardiomyopathy: Executive summary
- (2019) Jeffrey A. Towbin et al. HEART RHYTHM
- Broad Genetic Testing in a Clinical Setting Uncovers a High Prevalence of Titin Loss-of-Function Variants in Very Early Onset Atrial Fibrillation
- (2019) William R. Goodyer et al. Circulation-Genomic and Precision Medicine
- Re-analysis of whole-exome sequencing data uncovers novel diagnostic variants and improves molecular diagnostic yields for sudden death and idiopathic diseases
- (2019) Elias L. Salfati et al. Genome Medicine
- Incidental and clinically actionable genetic variants in 1005 whole exomes and genomes from Qatar
- (2018) Abhinav Jain et al. MOLECULAR GENETICS AND GENOMICS
- Unknown
- (2018) HUMAN MUTATION
- Association Between Titin Loss-of-Function Variants and Early-Onset Atrial Fibrillation
- (2018) Seung Hoan Choi et al. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
- EHRA/HRS/APHRS/SOLAECE expert consensus on atrial cardiomyopathies: Definition, characterization, and clinical implication
- (2017) Andreas Goette et al. HEART RHYTHM
- Actionable secondary findings from whole-genome sequencing of 954 East Asians
- (2017) Clara Sze-man Tang et al. HUMAN GENETICS
- A Missense Variant in PLEC Increases Risk of Atrial Fibrillation
- (2017) Rosa B. Thorolfsdottir et al. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
- Association of Arrhythmia-Related Genetic Variants With Phenotypes Documented in Electronic Medical Records
- (2016) Sara L. Van Driest et al. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
- Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies
- (2016) Martín F. Ortiz-Genga et al. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
- Aggregate penetrance of genomic variants for actionable disorders in European and African Americans
- (2016) P. Natarajan et al. Science Translational Medicine
- Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology
- (2015) Sue Richards et al. GENETICS IN MEDICINE
- Actionable exomic incidental findings in 6503 participants: challenges of variant classification
- (2015) Laura M. Amendola et al. GENOME RESEARCH
- ClinGen — The Clinical Genome Resource
- (2015) Heidi L. Rehm et al. NEW ENGLAND JOURNAL OF MEDICINE
- Comparison and integration of deleteriousness prediction methods for nonsynonymous SNVs in whole exome sequencing studies
- (2015) C. Dong et al. HUMAN MOLECULAR GENETICS
- 2014 AHA/ACC/HRS Guideline for the Management of Patients With Atrial Fibrillation: Executive Summary
- (2014) Craig T. January et al. CIRCULATION
- A common genetic variant within SCN10A modulates cardiac SCN5A expression
- (2014) Malou van den Boogaard et al. JOURNAL OF CLINICAL INVESTIGATION
- HRS/EHRA/APHRS Expert Consensus Statement on the Diagnosis and Management of Patients with Inherited Primary Arrhythmia Syndromes
- (2013) Silvia G. Priori et al. HEART RHYTHM
- Very early-onset lone atrial fibrillation patients have a high prevalence of rare variants in genes previously associated with atrial fibrillation
- (2013) Morten S. Olesen et al. HEART RHYTHM
- Genetic variation in T-box binding element functionally affects SCN5A/SCN10A enhancer
- (2012) Malou van den Boogaard et al. JOURNAL OF CLINICAL INVESTIGATION
- HRS/EHRA Expert Consensus Statement on the State of Genetic Testing for the Channelopathies and Cardiomyopathies
- (2011) Michael J. Ackerman et al. HEART RHYTHM
- A rare variant in MYH6 is associated with high risk of sick sinus syndrome
- (2011) Hilma Holm et al. NATURE GENETICS
- Several common variants modulate heart rate, PR interval and QRS duration
- (2010) Hilma Holm et al. NATURE GENETICS
- Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction
- (2010) Nona Sotoodehnia et al. NATURE GENETICS
- Genome-wide association study of PR interval
- (2010) Arne Pfeufer et al. NATURE GENETICS
- Genetic variation in SCN10A influences cardiac conduction
- (2010) John C Chambers et al. NATURE GENETICS
- A novel mutation in LAMIN A/C is associated with isolated early-onset atrial fibrillation and progressive atrioventricular block followed by cardiomyopathy and sudden cardiac death
- (2009) Hubert Pan et al. HEART RHYTHM
- The non-synonymous coding IKr-channel variant KCNH2-K897T is associated with atrial fibrillation: results from a systematic candidate gene-based analysis of KCNH2 (HERG)
- (2008) Moritz F. Sinner et al. EUROPEAN HEART JOURNAL
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExplorePublish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn More