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Cited by in F6Publishing
For: Sheng YR, Hou SY, Hu WT, Wei CY, Liu YK, Liu YY, Jiang L, Xiang JJ, Sun XX, Lei CX, Wang HL, Zhu XY. Characterization of Copy-Number Variations and Possible Candidate Genes in Recurrent Pregnancy Losses. Genes (Basel) 2021;12:141. [PMID: 33499090 DOI: 10.3390/genes12020141] [Cited by in Crossref: 1] [Cited by in F6Publishing: 5] [Article Influence: 1.0] [Reference Citation Analysis]
Number Citing Articles
1 Nikitina TV, Lebedev IN. Stem Cell-Based Trophoblast Models to Unravel the Genetic Causes of Human Miscarriages. Cells 2022;11:1923. [PMID: 35741051 DOI: 10.3390/cells11121923] [Reference Citation Analysis]
2 Gu C, Li K, Li L, Gao H, Li R, He Y. Genomic imbalance in euploid pregnancy loss. J Assist Reprod Genet 2022. [PMID: 35666339 DOI: 10.1007/s10815-022-02527-8] [Reference Citation Analysis]
3 Khamees DA, Al-ouqaili MTS. Cross-sectional study of chromosomal aberrations and immunologic factors in Iraqi couples with recurrent pregnancy loss. PeerJ 2022;10:e12801. [DOI: 10.7717/peerj.12801] [Reference Citation Analysis]
4 Wu H, Huang Q, Zhang X, Yu Z, Zhong Z. Analysis of Genomic Copy Number Variation in Miscarriages During Early and Middle Pregnancy. Front Genet 2021;12:732419. [PMID: 34603391 DOI: 10.3389/fgene.2021.732419] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
5 Zhang X, Huang Q, Yu Z, Wu H. Copy number variation characterization and possible candidate genes in miscarriage and stillbirth by next-generation sequencing analysis. J Gene Med 2021;:e3383. [PMID: 34342101 DOI: 10.1002/jgm.3383] [Cited by in F6Publishing: 1] [Reference Citation Analysis]