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For: Wang J, Hu X, Guo Y, Gu J, Xu J, Li Y, Li N, Yang X, Yang Y. HAND1 Loss-of-Function Mutation Causes Tetralogy of Fallot. Pediatr Cardiol 2017;38:547-57. [DOI: 10.1007/s00246-016-1547-8] [Cited by in Crossref: 11] [Cited by in F6Publishing: 9] [Article Influence: 1.8] [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 Yang L, Yang Y, Liu X, Chen Y, Chen Y, Lin Y, Sun Y, Shen B. CHDGKB: a knowledgebase for systematic understanding of genetic variations associated with non-syndromic congenital heart disease. Database (Oxford) 2020;2020:baaa048. [PMID: 32608479 DOI: 10.1093/database/baaa048] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
3 Vincentz JW, Firulli BA, Toolan KP, Osterwalder M, Pennacchio LA, Firulli AB. HAND transcription factors cooperatively specify the aorta and pulmonary trunk. Dev Biol 2021;476:1-10. [PMID: 33757801 DOI: 10.1016/j.ydbio.2021.03.011] [Reference Citation Analysis]
4 Presta I, Donato A, Chirchiglia D, Malara N, Donato G. Cardiac myxoma and neural crests: a tense relationship. Cardiovasc Pathol 2020;44:107163. [PMID: 31760243 DOI: 10.1016/j.carpath.2019.107163] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.7] [Reference Citation Analysis]
5 Liu H, Xu Y, Li R, Wang Z, Zhang M, Qu X, Qiao Q, Li X, Di R, Qiu X, Yang Y. HAND2 loss-of-function mutation causes familial dilated cardiomyopathy. European Journal of Medical Genetics 2019;62:103540. [DOI: 10.1016/j.ejmg.2018.09.007] [Cited by in Crossref: 12] [Cited by in F6Publishing: 10] [Article Influence: 4.0] [Reference Citation Analysis]
6 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: 2] [Article Influence: 1.0] [Reference Citation Analysis]
7 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: 6] [Article Influence: 2.8] [Reference Citation Analysis]
8 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: 11] [Article Influence: 2.5] [Reference Citation Analysis]
9 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: 10] [Article Influence: 3.0] [Reference Citation Analysis]
10 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: 12] [Article Influence: 3.4] [Reference Citation Analysis]