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Cited by in F6Publishing
For: Zhao L, Jiang WF, Yang CX, Qiao Q, Xu YJ, Shi HY, Qiu XB, Wu SH, Yang YQ. SOX17 loss-of-function variation underlying familial congenital heart disease. Eur J Med Genet 2021;64:104211. [PMID: 33794346 DOI: 10.1016/j.ejmg.2021.104211] [Cited by in Crossref: 6] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
Number Citing Articles
1 Shi HY, Xie MS, Guo YH, Yang CX, Gu JN, Qiao Q, Di RM, Qiu XB, Xu YJ, Yang YQ. VEZF1 loss-of-function mutation underlying familial dilated cardiomyopathy. Eur J Med Genet 2023;66:104705. [PMID: 36657711 DOI: 10.1016/j.ejmg.2023.104705] [Reference Citation Analysis]
2 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]
3 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]
4 Wang Z, Qiao X, Xu Y, Liu X, Huang R, Xue S, Qiu H, Yang Y, Aga SS. SMAD1 Loss-of-Function Variant Responsible for Congenital Heart Disease. BioMed Research International 2022;2022:1-8. [DOI: 10.1155/2022/9916325] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
5 Shen L, Yu J, Ge Y, Li H, Li Y, Cao Z, Luan P, Xiao F, Gao H, Zhang H. Associations of Transcription Factor 21 Gene Polymorphisms with the Growth and Body Composition Traits in Broilers. Animals 2022;12:393. [DOI: 10.3390/ani12030393] [Reference Citation Analysis]
6 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]
7 Vastrad B, Vastrad C. Bioinformatics analysis of differentially expressed genes in non alcoholic fatty liver disease using next generation sequencing data.. [DOI: 10.1101/2021.12.16.472893] [Reference Citation Analysis]