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For: Lu CX, Wang W, Wang Q, Liu XY, Yang YQ. A Novel MEF2C Loss-of-Function Mutation Associated with Congenital Double Outlet Right Ventricle. Pediatr Cardiol 2018;39:794-804. [PMID: 29468350 DOI: 10.1007/s00246-018-1822-y] [Cited by in Crossref: 17] [Cited by in F6Publishing: 19] [Article Influence: 4.3] [Reference Citation Analysis]
Number Citing Articles
1 Choudhury TZ, Garg V. Molecular genetic mechanisms of congenital heart disease. Curr Opin Genet Dev 2022;75:101949. [PMID: 35816939 DOI: 10.1016/j.gde.2022.101949] [Reference Citation Analysis]
2 Zeng ZH, Chen HX, Liu XC, Yang Q, He GW. Functional significance of novel variants of the MEF2C gene promoter in congenital ventricular septal defects. Am J Med Genet A 2022. [PMID: 35719119 DOI: 10.1002/ajmg.a.62871] [Reference Citation Analysis]
3 Wang E, Fan X, Nie Y, Zheng Z, Hu S. Single-Nucleotide Polymorphisms in Exonic and Promoter Regions of Transcription Factors of Second Heart Field Associated with Sporadic Congenital Cardiac Anomalies. Balkan Journal of Medical Genetics 2021;24:39-47. [DOI: 10.2478/bjmg-2021-0028] [Reference Citation Analysis]
4 Ouyang S, Qin W, Niu Y, Ding Y, Deng Y. An EGFP Knock-in Zebrafish Experimental Model Used in Evaluation of the Amantadine Drug Safety During Early Cardiogenesis. Front Cardiovasc Med 2022;9. [DOI: 10.3389/fcvm.2022.839166] [Reference Citation Analysis]
5 Yu Z, Pek NMQ, Gu M. Delving into the Molecular World of Single Ventricle Congenital Heart Disease. Curr Cardiol Rep 2022. [PMID: 35218503 DOI: 10.1007/s11886-022-01667-8] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
6 Yasuhara J, Garg V. Genetics of congenital heart disease: a narrative review of recent advances and clinical implications. Transl Pediatr 2021;10:2366-86. [PMID: 34733677 DOI: 10.21037/tp-21-297] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 4.0] [Reference Citation Analysis]
7 Cooley Coleman JA, Sarasua SM, Boccuto L, Moore HW, Skinner SA, DeLuca JM. Comprehensive investigation of the phenotype of MEF2C-related disorders in human patients: A systematic review. Am J Med Genet A 2021. [PMID: 34184825 DOI: 10.1002/ajmg.a.62412] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 5.0] [Reference Citation Analysis]
8 Miyamoto M, Gangrade H, Tampakakis E. Understanding Heart Field Progenitor Cells for Modeling Congenital Heart Diseases. Curr Cardiol Rep 2021;23:38. [PMID: 33694131 DOI: 10.1007/s11886-021-01468-5] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 4.0] [Reference Citation Analysis]
9 盛 小. Research Progress of Genes Related to Congenital Heart Disease. ACM 2021;11:2825-2829. [DOI: 10.12677/acm.2021.116410] [Reference Citation Analysis]
10 Corno AF, Durairaj S, Skinner GJ. Narrative review of assessing the surgical options for double outlet right ventricle. Transl Pediatr 2021;10:165-76. [PMID: 33633949 DOI: 10.21037/tp-20-227] [Cited by in Crossref: 2] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
11 Kula-Alwar D, Marber MS, Hughes SM, Hinits Y. Mef2c factors are required for early but not late addition of cardiomyocytes to the ventricle. Dev Biol 2021;470:95-107. [PMID: 33245870 DOI: 10.1016/j.ydbio.2020.11.008] [Cited by in Crossref: 4] [Cited by in F6Publishing: 7] [Article Influence: 2.0] [Reference Citation Analysis]
12 De Ita M, Cisneros B, Rosas-Vargas H. Genetics of Transposition of Great Arteries: Between Laterality Abnormality and Outflow Tract Defect. J Cardiovasc Transl Res 2021;14:390-9. [PMID: 32734553 DOI: 10.1007/s12265-020-10064-x] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 3.5] [Reference Citation Analysis]
13 Suluba E, Shuwei L, Xia Q, Mwanga A. Congenital heart diseases: genetics, non-inherited risk factors, and signaling pathways. Egypt J Med Hum Genet 2020;21. [DOI: 10.1186/s43042-020-0050-1] [Cited by in Crossref: 9] [Cited by in F6Publishing: 10] [Article Influence: 4.5] [Reference Citation Analysis]
14 Wang E, Nie Y, Fan X, Zheng Z, Hu S. Intronic Polymorphisms in Gene of Second Heart Field as Risk Factors for Human Congenital Heart Disease in a Chinese Population. DNA Cell Biol 2019;38:521-31. [PMID: 31013439 DOI: 10.1089/dna.2018.4254] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
15 Clapham KR, Singh I, Capuano IS, Rajagopal S, Chun HJ. MEF2 and the Right Ventricle: From Development to Disease. Front Cardiovasc Med 2019;6:29. [PMID: 30984767 DOI: 10.3389/fcvm.2019.00029] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 3.0] [Reference Citation Analysis]
16 Ma L, Wang J, Li L, Qiao Q, Di RM, Li XM, Xu YJ, Zhang M, Li RG, Qiu XB, Li X, Yang YQ. ISL1 loss-of-function mutation contributes to congenital heart defects. Heart Vessels 2019;34:658-68. [PMID: 30390123 DOI: 10.1007/s00380-018-1289-z] [Cited by in Crossref: 17] [Cited by in F6Publishing: 13] [Article Influence: 4.3] [Reference Citation Analysis]
17 Wang J, Zhang Q, Chen Y, Yu S, Wu X, Bao X, Wen Y. Novel MEF2C point mutations in Chinese patients with Rett (-like) syndrome or non-syndromic intellectual disability: insights into genotype-phenotype correlation. BMC Med Genet 2018;19:191. [PMID: 30376817 DOI: 10.1186/s12881-018-0699-1] [Cited by in Crossref: 19] [Cited by in F6Publishing: 20] [Article Influence: 4.8] [Reference Citation Analysis]