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Cited by in F6Publishing
For: 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]
Number Citing Articles
1 Shi HY, Xie MS, Yang CX, Huang RT, Xue S, Liu XY, Xu YJ, Yang YQ. Identification of SOX18 as a New Gene Predisposing to Congenital Heart Disease. Diagnostics (Basel) 2022;12. [PMID: 36010266 DOI: 10.3390/diagnostics12081917] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]
2 Vastrad B, Vastrad C. Bioinformatics Analysis of next generation sequencing data for Risk Prediction in Patients with Type 1 diabetes mellitus.. [DOI: 10.1101/2022.03.17.484749] [Reference Citation Analysis]
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