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Cited by in F6Publishing
For: Ke Z, Zhang G, Guo Y, Sun Y, Wang J, Li N, Qiu X, Xu Y, Yang Y. A novel PRRX1 loss-of-function variation contributing to familial atrial fibrillation and congenital patent ductus arteriosus. Genet Mol Biol 2022;45:e20210378. [DOI: 10.1590/1678-4685-gmb-2021-0378] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
Number Citing Articles
1 Wang Y, Xu YJ, Yang CX, Huang RT, Xue S, Yuan F, Yang YQ. SMAD4 loss-of-function mutation predisposes to congenital heart disease. Eur J Med Genet 2022;66:104677. [PMID: 36496093 DOI: 10.1016/j.ejmg.2022.104677] [Reference Citation Analysis]
2 Shi H, Xie M, Yang C, Huang R, Xue S, Liu X, Xu Y, Yang Y. Identification of SOX18 as a New Gene Predisposing to Congenital Heart Disease. Diagnostics 2022;12:1917. [DOI: 10.3390/diagnostics12081917] [Reference Citation Analysis]