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For: Radhakrishna U, Vishweswaraiah S, Veerappa AM, Zafra R, Albayrak S, Sitharam PH, Saiyed NM, Mishra NK, Guda C, Bahado-Singh R. Newborn blood DNA epigenetic variations and signaling pathway genes associated with Tetralogy of Fallot (TOF). PLoS One 2018;13:e0203893. [PMID: 30212560 DOI: 10.1371/journal.pone.0203893] [Cited by in Crossref: 16] [Cited by in F6Publishing: 17] [Article Influence: 4.0] [Reference Citation Analysis]
Number Citing Articles
1 Nelson JS, Kwok C, Braganca NE, Lopez DL, Espina Rey AP, Robinson M, Ebert SN. Comparison of DNA methylation patterns across tissue types in infants with tetralogy of Fallot. Birth Defects Research. [DOI: 10.1002/bdr2.2090] [Reference Citation Analysis]
2 Morton SU, Pereira AC, Quiat D, Richter F, Kitaygorodsky A, Hagen J, Bernstein D, Brueckner M, Goldmuntz E, Kim RW, Lifton RP, Porter GA Jr, Tristani-Firouzi M, Chung WK, Roberts A, Gelb BD, Shen Y, Newburger JW, Seidman JG, Seidman CE. Genome-Wide De Novo Variants in Congenital Heart Disease Are Not Associated With Maternal Diabetes or Obesity. Circ Genom Precis Med 2022;15:e003500. [PMID: 35130025 DOI: 10.1161/CIRCGEN.121.003500] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
3 Wang G, Wang B, Yang P. Epigenetics in Congenital Heart Disease. JAHA. [DOI: 10.1161/jaha.121.025163] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
4 Joshi RO, Kukshal P, Chellappan S, Guhathakurta S. "The study of expression levels of DNA methylation regulators in patients affected with congenital heart defects (CHDs)". Birth Defects Res 2022. [PMID: 35191222 DOI: 10.1002/bdr2.1988] [Reference Citation Analysis]
5 Ducreux B, Frappier J, Bruno C, Doukani A, Guilleman M, Simon E, Martinaud A, Bourc'his D, Barberet J, Fauque P. Genome-Wide Analysis of DNA Methylation in Buccal Cells of Children Conceived through IVF and ICSI. Genes (Basel) 2021;12:1912. [PMID: 34946866 DOI: 10.3390/genes12121912] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
6 Cao J, Wu Q, Huang Y, Wang L, Su Z, Ye H. The role of DNA methylation in syndromic and non-syndromic congenital heart disease. Clin Epigenetics 2021;13:93. [PMID: 33902696 DOI: 10.1186/s13148-021-01077-7] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 9.0] [Reference Citation Analysis]
7 Lim TB, Foo SYR, Chen CK. The Role of Epigenetics in Congenital Heart Disease. Genes (Basel) 2021;12:390. [PMID: 33803261 DOI: 10.3390/genes12030390] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 9.0] [Reference Citation Analysis]
8 Joshi RO, Chellappan S, Kukshal P. Exploring the Role of Maternal Nutritional Epigenetics in Congenital Heart Disease. Curr Dev Nutr 2020;4:nzaa166. [PMID: 33294766 DOI: 10.1093/cdn/nzaa166] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 4.5] [Reference Citation Analysis]
9 Xiaodi L, Ming Y, Hongfei X, Yanjie Z, Ruoyi G, Ma X, Wei S, Guoying H. DNA methylation at CpG island shore and RXRα regulate NR2F2 in heart tissues of tetralogy of Fallot patients. Biochem Biophys Res Commun 2020;529:1209-15. [PMID: 32819587 DOI: 10.1016/j.bbrc.2020.06.110] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
10 Bahado-Singh RO, Vishweswaraiah S, Aydas B, Yilmaz A, Saiyed NM, Mishra NK, Guda C, Radhakrishna U. Precision cardiovascular medicine: artificial intelligence and epigenetics for the pathogenesis and prediction of coarctation in neonates. J Matern Fetal Neonatal Med 2020;:1-8. [PMID: 32019381 DOI: 10.1080/14767058.2020.1722995] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 3.5] [Reference Citation Analysis]
11 Meisner JK, Martin DM. Congenital heart defects in CHARGE: The molecular role of CHD7 and effects on cardiac phenotype and clinical outcomes. Am J Med Genet C Semin Med Genet 2020;184:81-9. [PMID: 31833191 DOI: 10.1002/ajmg.c.31761] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 2.7] [Reference Citation Analysis]
12 Šutić M, Motzek A, Bubanović G, Linke M, Sabol I, Vugrek O, Ozretić P, Brčić L, Seiwerth S, Debeljak Ž, Jakovčević A, Janevski Z, Stančić-Rokotov D, Vukić-Dugac A, Jakopović M, Samaržija M, Zechner U, Knežević J. Promoter methylation status of ASC/TMS1/PYCARD is associated with decreased overall survival and TNM status in patients with early stage non-small cell lung cancer (NSCLC). Transl Lung Cancer Res 2019;8:1000-15. [PMID: 32010578 DOI: 10.21037/tlcr.2019.12.08] [Cited by in Crossref: 7] [Cited by in F6Publishing: 8] [Article Influence: 2.3] [Reference Citation Analysis]
13 Keir M, Ebert P, Kovacs AH, Smith JM, Kwan E, Field TS, Brossard-racine M, Marelli A. Neurocognition in Adult Congenital Heart Disease: How to Monitor and Prevent Progressive Decline. Canadian Journal of Cardiology 2019;35:1675-85. [DOI: 10.1016/j.cjca.2019.06.020] [Cited by in Crossref: 13] [Cited by in F6Publishing: 14] [Article Influence: 4.3] [Reference Citation Analysis]
14 Bahado-singh RO, Vishweswaraiah S, Aydas B, Mishra NK, Yilmaz A, Guda C, Radhakrishna U. Artificial intelligence analysis of newborn leucocyte epigenomic markers for the prediction of autism. Brain Research 2019;1724:146457. [DOI: 10.1016/j.brainres.2019.146457] [Cited by in Crossref: 14] [Cited by in F6Publishing: 9] [Article Influence: 4.7] [Reference Citation Analysis]
15 Jarrell DK, Lennon ML, Jacot JG. Epigenetics and Mechanobiology in Heart Development and Congenital Heart Disease. Diseases 2019;7:E52. [PMID: 31480510 DOI: 10.3390/diseases7030052] [Cited by in Crossref: 31] [Cited by in F6Publishing: 33] [Article Influence: 10.3] [Reference Citation Analysis]
16 Smith JMC, Andrade JG, Human D, Field TS. Adults With Complex Congenital Heart Disease: Cerebrovascular Considerations for the Neurologist. Front Neurol 2019;10:329. [PMID: 31019488 DOI: 10.3389/fneur.2019.00329] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.7] [Reference Citation Analysis]