1. The Role of Transposable Elements in Congenital Malformations with Notes on Their Potential Implications for Morphological Evolution in Mammals
   Fabio Barteri et al, 2020, Current Molecular Biology Reports CrossRef
2. Gene‐by‐gene interactions associated with the risk of conotruncal heart defects
   Chen Lyu et al, 2020, Molecular Genetics & Genomic Medicine CrossRef
3. CpG island shore methylation of ZFPM2 is identified in tetralogy of fallot samples
   Wei Sheng et al, 2016, Pediatric Research CrossRef
4. The role of DNA methylation in syndromic and non-syndromic congenital heart disease
   Jiali Cao et al, 2021, Clinical Epigenetics CrossRef
5. Epigenetic determinants and non-myocardial signaling pathways contributing to heart growth and regeneration
   Jihyun Jang et al, 2024, Pharmacology & Therapeutics CrossRef
6. High CpG island methylation of p16 gene and loss of p16 protein expression associate with the development and progression of tetralogy of Fallot
   SI-JU GAO et al, 2016, Journal of Genetics CrossRef
7. Genomics and Epigenomics of Congenital Heart Defects: Expert Review and Lessons Learned in Africa
   Nicholas Ekow Thomford et al, 2018, OMICS: A Journal of Integrative Biology CrossRef
8. Myocardial tissue-specific Dnmt1 knockout in rats protects against pathological injury induced by Adriamycin
   Tong-Tong Wu et al, 2020, Laboratory Investigation CrossRef
9. Targeting DNA Hypomethylation in Malignancy by Epigenetic Therapies
   Niaz Mahmood et al, 2019, Human Cell Transformation CrossRef
10. Altered expression of DNA methyltransferases and methylation status of the TLR4 and TNF-α promoters in COVID-19
    Sohair Salem et al, 2023, Archives of Virology CrossRef
11. The Role of Epigenetics in Congenital Heart Disease
    Tingsen Benson Lim et al, 2021, Genes CrossRef
12. The Role of Clonal Hematopoiesis of Indeterminant Potential and DNA (Cytosine-5)-Methyltransferase Dysregulation in Pulmonary Arterial Hypertension and Other Cardiovascular Diseases
    Isaac M. Emon et al, 2023, Cells CrossRef
13. Association of DNMT1 Gene Polymorphisms with Congenital Heart Disease in Child Patients
    FengYu Wang et al, 2015, Pediatric Cardiology CrossRef
14. The study of expression levels of DNA methylation regulators in patients affected with congenital heart defects (CHDs)
    Radha O. Joshi et al, 2022, Birth Defects Research CrossRef
15. Epigenetic effects of (nano)materials in environmental species – Cu case study in Enchytraeus crypticus
    Rita C. Bicho et al, 2020, Environment International CrossRef
16. Rs4841587 in GATA4 and rs6999593 in DNMT1 gene associated with congenital heart diseases in the southeast of Iran
    Noor Mohammad Noori et al, 2020, Meta Gene CrossRef
17. LINE-1 retrotransposon methylation in chorionic villi of first trimester miscarriages with aneuploidy
    Stanislav A. Vasilyev et al, 2021, Journal of Assisted Reproduction and Genetics CrossRef
18. Association between the promoter methylation of the TBX20 gene and tetralogy of fallot
    Xiaofei Yang et al, 2018, Scandinavian Cardiovascular Journal CrossRef
19. Epigenetics of Aberrant Cardiac Wound Healing
    Adam Russell‐Hallinan et al, 2018, Comprehensive Physiology CrossRef
20. Mending a broken heart: In vitro, in vivo and in silico models of congenital heart disease
    Abdul Jalil Rufaihah et al, 2021, Disease Models & Mechanisms CrossRef
21. Knockdown of DNA methyltransferase 3a alters gene expression and inhibits function of embryonic cardiomyocytes
    Xiefan Fang et al, 2016, The FASEB Journal CrossRef
22. CTLA-4 methylation regulates the pathogenesis of myasthenia gravis and the expression of related cytokines
    Ti-Kun Fang et al, 2018, Medicine CrossRef
23. DNMT3B rs2424913 as a Risk Factor for Congenital Heart Defects in Down Syndrome
    Dijana Majstorović et al, 2023, Genes CrossRef
24. Human fetal hearts with tetralogy of Fallot have altered fluid dynamics and forces
    Hadi Wiputra et al, 2018, American Journal of Physiology-Heart and Circulatory Physiology CrossRef