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For: Huang RT, Wang J, Xue S, Qiu XB, Shi HY, Li RG, Qu XK, Yang XX, Liu H, Li N, Li YJ, Xu YJ, Yang YQ. TBX20 loss-of-function mutation responsible for familial tetralogy of Fallot or sporadic persistent truncus arteriosus. Int J Med Sci 2017;14:323-32. [PMID: 28553164 DOI: 10.7150/ijms.17834] [Cited by in Crossref: 23] [Cited by in F6Publishing: 25] [Article Influence: 4.6] [Reference Citation Analysis]
Number Citing Articles
1 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]
2 Yamamoto H, Inagaki H, Hayano S, Kurahashi H, Kato T. Familial cardiac septal defect due to a novel nine-base deletion in TBX20. Pediatr Int 2022;64:e14995. [PMID: 35298876 DOI: 10.1111/ped.14995] [Reference Citation Analysis]
3 Baban A, Lodato V, Parlapiano G, Drago F. Genetics in Congenital Heart Diseases: Unraveling the Link Between Cardiac Morphogenesis, Heart Muscle Disease, and Electrical Disorders. Heart Fail Clin 2022;18:139-53. [PMID: 34776075 DOI: 10.1016/j.hfc.2021.07.016] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
4 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 F6Publishing: 3] [Reference Citation Analysis]
5 Chen Y, Sun F, Zhang L, Zhou J, Hou J. miR-499a inhibits the proliferation and apoptosis of prostate cancer via targeting UBE2V2. World J Surg Oncol 2021;19:250. [PMID: 34429120 DOI: 10.1186/s12957-021-02371-7] [Cited by in F6Publishing: 4] [Reference Citation Analysis]
6 Hazekamp MG, Barron DJ, Dangel J, Homfray T, Jongbloed MRM, Voges I; ESC Scientific Document Group. Consensus document on optimal management of patients with common arterial trunk. Eur J Cardiothorac Surg 2021;60:7-33. [PMID: 34017991 DOI: 10.1093/ejcts/ezaa423] [Cited by in Crossref: 1] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
7 Hazekamp MG, Barron DJ, Dangel J, Homfray T, Jongbloed MRM, Voges I. Consensus document on optimal management of patients with common arterial trunk. Cardiol Young 2021;:1-25. [PMID: 34016217 DOI: 10.1017/S1047951121001219] [Reference Citation Analysis]
8 Chen Y, Xiao D, Zhang L, Cai CL, Li BY, Liu Y. The Role of Tbx20 in Cardiovascular Development and Function. Front Cell Dev Biol 2021;9:638542. [PMID: 33585493 DOI: 10.3389/fcell.2021.638542] [Cited by in F6Publishing: 3] [Reference Citation Analysis]
9 Nees SN, Chung WK. Genetic Basis of Human Congenital Heart Disease. Cold Spring Harb Perspect Biol 2020;12:a036749. [PMID: 31818857 DOI: 10.1101/cshperspect.a036749] [Cited by in Crossref: 8] [Cited by in F6Publishing: 12] [Article Influence: 4.0] [Reference Citation Analysis]
10 Fang Y, Lai KS, She P, Sun J, Tao W, Zhong TP. Tbx20 Induction Promotes Zebrafish Heart Regeneration by Inducing Cardiomyocyte Dedifferentiation and Endocardial Expansion. Front Cell Dev Biol 2020;8:738. [PMID: 32850848 DOI: 10.3389/fcell.2020.00738] [Cited by in Crossref: 3] [Cited by in F6Publishing: 8] [Article Influence: 1.5] [Reference Citation Analysis]
11 Li W, Li B, Li T, Zhang E, Wang Q, Chen S, Sun K. Identification and analysis of KLF13 variants in patients with congenital heart disease. BMC Med Genet 2020;21:78. [PMID: 32293321 DOI: 10.1186/s12881-020-01009-x] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
12 Nees SN, Chung WK. The genetics of isolated congenital heart disease. Am J Med Genet C Semin Med Genet 2020;184:97-106. [PMID: 31876989 DOI: 10.1002/ajmg.c.31763] [Cited by in Crossref: 5] [Cited by in F6Publishing: 11] [Article Influence: 1.7] [Reference Citation Analysis]
13 Pierpont ME, Brueckner M, Chung WK, Garg V, Lacro RV, McGuire AL, Mital S, Priest JR, Pu WT, Roberts A, Ware SM, Gelb BD, Russell MW; American Heart Association Council on Cardiovascular Disease in the Young; Council on Cardiovascular and Stroke Nursing; and Council on Genomic and Precision Medicine. Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association. Circulation 2018;138:e653-711. [PMID: 30571578 DOI: 10.1161/CIR.0000000000000606] [Cited by in Crossref: 125] [Cited by in F6Publishing: 171] [Article Influence: 41.7] [Reference Citation Analysis]
14 Shi Y, Li Y, Wang Y, Zhuang J, Wang H, Hu M, Mo X, Yue S, Chen Y, Fan X, Chen J, Cai W, Zhu X, Wan Y, Zhong Y, Ye X, Li F, Zhou Z, Dai G, Luo R, Ocorr K, Jiang Z, Li X, Zhu P, Wu X, Yuan W. The Functional Polymorphism R129W in the BVES Gene Is Associated with Sporadic Tetralogy of Fallot in the Han Chinese Population. Genet Test Mol Biomarkers 2019;23:601-9. [PMID: 31386585 DOI: 10.1089/gtmb.2019.0085] [Cited by in Crossref: 1] [Article Influence: 0.3] [Reference Citation Analysis]
15 Gong J, Sheng W, Ma D, Huang G, Liu F. DNA methylation status of TBX20 in patients with tetralogy of Fallot. BMC Med Genomics 2019;12:75. [PMID: 31138201 DOI: 10.1186/s12920-019-0534-3] [Cited by in Crossref: 6] [Cited by in F6Publishing: 8] [Article Influence: 2.0] [Reference Citation Analysis]
16 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: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
17 Luyckx I, Kumar AA, Reyniers E, Dekeyser E, Vanderstraeten K, Vandeweyer G, Wünnemann F, Preuss C, Mazzella JM, Goudot G, Messas E, Albuisson J, Jeunemaitre X, Eriksson P, Mohamed SA, Kempers M, Salemink S, Duijnhouwer A, Andelfinger G, Dietz HC, Verstraeten A, Van Laer L, Loeys BL; MIBAVA Leducq Consortium. Copy number variation analysis in bicuspid aortic valve-related aortopathy identifies TBX20 as a contributing gene. Eur J Hum Genet 2019;27:1033-43. [PMID: 30820038 DOI: 10.1038/s41431-019-0364-y] [Cited by in Crossref: 8] [Cited by in F6Publishing: 14] [Article Influence: 2.7] [Reference Citation Analysis]
18 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: 11] [Cited by in F6Publishing: 13] [Article Influence: 2.8] [Reference Citation Analysis]
19 Li N, Wang ZS, Wang XH, Xu YJ, Qiao Q, Li XM, Di RM, Guo XJ, Li RG, Zhang M, Qiu XB, Yang YQ. A SHOX2 loss-of-function mutation underlying familial atrial fibrillation. Int J Med Sci 2018;15:1564-72. [PMID: 30443179 DOI: 10.7150/ijms.27424] [Cited by in Crossref: 15] [Cited by in F6Publishing: 16] [Article Influence: 3.8] [Reference Citation Analysis]
20 Rakhmanov Y, Maltese PE, Marinelli C, Beccari T, Dundar M, Bertelli M. Genetic testing for tetralogy of Fallot. The EuroBiotech Journal 2018;2:71-3. [DOI: 10.2478/ebtj-2018-0043] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
21 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: 10] [Cited by in F6Publishing: 16] [Article Influence: 2.5] [Reference Citation Analysis]
22 Yang X, Kong Q, Li Z, Xu M, Cai Z, Zhao C. Association between the promoter methylation of the TBX20 gene and tetralogy of fallot. Scand Cardiovasc J 2018;52:287-91. [PMID: 30084275 DOI: 10.1080/14017431.2018.1499955] [Cited by in Crossref: 3] [Cited by in F6Publishing: 5] [Article Influence: 0.8] [Reference Citation Analysis]
23 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: 12] [Cited by in F6Publishing: 15] [Article Influence: 3.0] [Reference Citation Analysis]
24 Qiao XH, Wang Q, Wang J, Liu XY, Xu YJ, Huang RT, Xue S, Li YJ, Zhang M, Qu XK, Li RG, Qiu XB, Yang YQ. A novel NR2F2 loss-of-function mutation predisposes to congenital heart defect. Eur J Med Genet 2018;61:197-203. [PMID: 29222010 DOI: 10.1016/j.ejmg.2017.12.003] [Cited by in Crossref: 17] [Cited by in F6Publishing: 14] [Article Influence: 3.4] [Reference Citation Analysis]
25 Qiao XH, Wang F, Zhang XL, Huang RT, Xue S, Wang J, Qiu XB, Liu XY, Yang YQ. MEF2C loss-of-function mutation contributes to congenital heart defects. Int J Med Sci 2017;14:1143-53. [PMID: 29104469 DOI: 10.7150/ijms.21353] [Cited by in Crossref: 17] [Cited by in F6Publishing: 19] [Article Influence: 3.4] [Reference Citation Analysis]