Meta-analysis identifies six new susceptibility loci for atrial fibrillation

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3. Multilocus Genetic Risk Score Associates With Ischemic Stroke in Case–Control and Prospective Cohort Studies
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4. Common variation in atrial fibrillation: navigating the path from genetic association to mechanism
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5. Genetic Control of Left Atrial Gene Expression Yields Insights into the Genetic Susceptibility for Atrial Fibrillation
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6. Proteomics Profiling and Risk of New‐Onset Atrial Fibrillation: Framingham Heart Study
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7. Long-range regulatory interactions at the 4q25 atrial fibrillation risk locus involve PITX2c and ENPEP
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8. Hypercoagulability, D-dimer and atrial fibrillation: an overview of biological and clinical evidence
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9. Polygenic Risk Scores for Kidney Function and Their Associations with Circulating Proteome, and Incident Kidney Diseases
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10. Cardiovascular Pharmacogenomics: Expectations and Practical Benefits
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11. Very early-onset lone atrial fibrillation patients have a high prevalence of rare variants in genes previously associated with atrial fibrillation
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12. Korean Atrial Fibrillation (AF) Network: Genetic Variants for AF Do Not Predict Ablation Success
    Eue‐Keun Choi, Jae Hyung Park, Ji‐Young Lee, Chung Mo Nam, Min Ki Hwang, Jae‐Sun Uhm, Boyoung Joung, Young‐Guk Ko, Moon‐Hyoung Lee, Steven A. Lubitz et al. · 2015 · Journal of the American Heart Association
13. Atrial Fibrillation Associated Chromosome 4q25 Variants Are Not Associated with PITX2c Expression in Human Adult Left Atrial Appendages
    Shamone R. Gore-Panter, Jeffery Hsu, Peter Hanna, Alan Marc Gillinov, Gösta Pettersson, David W. Newton, Christine Schomisch Moravec, David R. Van Wagoner, Mina K. Chung, John Barnard et al. · 2014 · PLoS ONE
14. PANCR, the PITX2 Adjacent Noncoding RNA, Is Expressed in Human Left Atria and Regulates PITX2c Expression
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15. Methylome-wide Association Study of Atrial Fibrillation in Framingham Heart Study
    Honghuang Lin, Xiaoyan Yin, Zhijun Xie, Kathryn L. Lunetta, Steven A. Lubitz, Martin G. Larson, Darae Ko, Jared W. Magnani, Michael Mendelson, Chunyu Liu et al. · 2017 · Scientific Reports
16. Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases
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17. Genomic variant in CAV1 increases susceptibility to coronary artery disease and myocardial infarction
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18. Integrative Omics Approach to Identifying Genes Associated With Atrial Fibrillation
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19. Molecular Basis of Gene-Gene Interaction: Cyclic Cross-Regulation of Gene Expression and Post-GWAS Gene-Gene Interaction Involved in Atrial Fibrillation
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20. Genetic and Clinical Risk Prediction Model for Postoperative Atrial Fibrillation
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21. SK channels and ventricular arrhythmias in heart failure
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22. Funny channel gene mutations associated with arrhythmias
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23. Atrial Fibrillation and Race – A Contemporary Review
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24. Proteins Associated with Risk of Kidney Function Decline in the General Population
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25. Clonal haematopoiesis of indeterminate potential and atrial fibrillation: an east Asian cohort study
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26. Coding and non-coding variants in the SHOX2 gene in patients with early-onset atrial fibrillation
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27. Homeobox transcription factor Pitx2: The rise of an asymmetry gene in cardiogenesis and arrhythmogenesis
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28. Novel Loci Associated With PR Interval in a Genome-Wide Association Study of 10 African American Cohorts
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29. Genetic variants associated with risk of atrial fibrillation regulate expression of PITX2, CAV1, MYOZ1, C9orf3 and FANCC
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30. Genetic Susceptibility for Atrial Fibrillation in Patients Undergoing Atrial Fibrillation Ablation
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31. TBX5mutations contribute to early-onset atrial fibrillation in Chinese and Caucasians
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33. Genetic Investigation Into the Differential Risk of Atrial Fibrillation Among Black and White Individuals
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34. Differentially expressed genes for atrial fibrillation identified by RNA sequencing from paired human left and right atrial appendages
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36. Functional modeling in zebrafish demonstrates that the atrial-fibrillation-associated geneGREM2regulates cardiac laterality, cardiomyocyte differentiation and atrial rhythm
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37. Molecular mechanisms of atrial fibrosis: implications for the clinic
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45. Identification of Functional Variant Enhancers Associated With Atrial Fibrillation
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48. Early sarcomere and metabolic defects in a zebrafish pitx2c cardiac arrhythmia model
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49. Genome-Wide Identification of Expression Quantitative Trait Loci (eQTLs) in Human Heart
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50. A truncating SCN5A mutation combined with genetic variability causes sick sinus syndrome and early atrial fibrillation
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51. Weighted Gene Coexpression Network Analysis of Human Left Atrial Tissue Identifies Gene Modules Associated With Atrial Fibrillation
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