1. A novel de novoTBX5mutation in a patient with Holt-Oram syndrome leading to a dramatically reduced biological function
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2. Sinus node dysfunction and atrial fibrillation—Relationships, clinical phenotypes, new mechanisms, and treatment approaches
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3. TBX5 variant with the novel phenotype of mixed‑type total anomalous pulmonary venous return in Holt‑Oram Syndrome and variable intrafamilial heart defects
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4. Interrogating the Interplay between Cardiac Transcription Factors and Non-Coding RNAs in Atrial Fibrillation
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5. TBX5 variants and cardiac phenotype: A systematic review of the literature and a novel variant
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6. Genetics of sinoatrial node function and heart rate disorders
   Lieve E. van der Maarel et al, 2023, Disease Models & Mechanisms CrossRef
7. Afterdepolarizations and abnormal calcium handling in atrial myocytes with modulated SERCA uptake: a sensitivity analysis of calcium handling channels
   Andy C. Y. Lo et al, 2020, Philosophical Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences CrossRef
8. Effect of hyperglycemia on tbx5a and nppa gene expression and its correlation to structural and functional changes in developing zebrafish heart
   Suruthi Sankar et al, 2022, Cell Biology International CrossRef
9. An update on the molecular diagnosis of congenital heart disease: focus on loss-of-function mutations
   Yan-Jie Li et al, 2017, Expert Review of Molecular Diagnostics CrossRef
10. A Novel MEF2C Loss-of-Function Mutation Associated with Congenital Double Outlet Right Ventricle
    Cai-Xia Lu et al, 2018, Pediatric Cardiology CrossRef
11. Familial dilated cardiomyopathy associated with pathogenic TBX5 variants: Expanding the cardiac phenotype associated with Holt–Oram syndrome
    Jenny Patterson et al, 2020, American Journal of Medical Genetics Part A CrossRef
12. Molecular Basis of Atrial Fibrillation Initiation and Maintenance
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13. Interplay between cardiac transcription factors and non-coding RNAs in predisposing to atrial fibrillation
    Alexander T. Mikhailov et al, 2018, Journal of Molecular Medicine CrossRef
14. Genetic and non-genetic risk factors associated with atrial fibrillation
    Lindsay J. Young et al, 2022, Life Sciences CrossRef
15. ISL1 loss-of-function mutation contributes to congenital heart defects
    Lan Ma et al, 2019, Heart and Vessels CrossRef
16. The Atrium in Atrial Fibrillation – A Clinical Review on How to Manage Atrial Fibrotic Substrates
    Pedro Silva Cunha et al, 2022, Frontiers in Cardiovascular Medicine CrossRef
17. In Vivo Dissection of Chamber-Selective Enhancers Reveals Estrogen-Related Receptor as a Regulator of Ventricular Cardiomyocyte Identity
    Yangpo Cao et al, 2023, Circulation CrossRef
18. Investigating the role connective tissue fibroblasts play in the altered muscle anatomy associated with the limb abnormality, Radial Dysplasia
    George R. F. Murphy et al, 2024, Journal of Anatomy CrossRef
19. Nr2f1a maintains atrial nkx2.5 expression to repress pacemaker identity within venous atrial cardiomyocytes of zebrafish
    Kendall E Martin et al, 2023, eLife CrossRef
20. TBX5 R264K acts as a modifier to develop dilated cardiomyopathy in mice independently of T-box pathway
    Nariaki Miyao et al, 2020, PLOS ONE CrossRef
21. A novel TBX5 mutation predisposes to familial cardiac septal defects and atrial fibrillation as well as bicuspid aortic valve
    Wei-Feng Jiang et al, 2020, Genetics and Molecular Biology CrossRef
22. Atrial Fibrillation: Focus on Myocardial Connexins and Gap Junctions
    Yu-Han Guo et al, 2022, Biology CrossRef