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For: Zhao X, Fu L. Efficacy of copy-number variation sequencing technology in prenatal diagnosis. J Perinat Med 2019;47:651-5. [PMID: 31287799 DOI: 10.1515/jpm-2019-0005] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]
Number Citing Articles
1 Zhang S, Xu Y, Lu D, Fu D, Zhao Y. Combined use of karyotyping and copy number variation sequencing technology in prenatal diagnosis. PeerJ 2022;10:e14400. [PMID: 36523456 DOI: 10.7717/peerj.14400] [Reference Citation Analysis]
2 Xue H, Yu A, Lin M, Chen X, Guo Q, Xu L, Huang H. Efficiency of expanded noninvasive prenatal testing in the detection of fetal subchromosomal microdeletion and microduplication in a cohort of 31,256 single pregnancies. Sci Rep 2022;12:19750. [PMID: 36396840 DOI: 10.1038/s41598-022-24337-9] [Reference Citation Analysis]
3 Bu X, Zhou S, Li X, Li S, Li H, Ding S, He J, Linpeng S. A retrospective single-center analysis of prenatal diagnosis and follow-up of 626 chinese patients with positive non-invasive prenatal screening results. Front Genet 2022;13:965106. [DOI: 10.3389/fgene.2022.965106] [Reference Citation Analysis]
4 Zhang X, Wu H, Gu Z, Yu Z, Lan L, Huang Q. Chromosomal Copy Number Variation Analysis in Pregnancy Products from Recurrent and Sporadic Miscarriage Using Next-Generation Sequencing. Reprod Sci 2022. [PMID: 35578104 DOI: 10.1007/s43032-022-00969-0] [Reference Citation Analysis]
5 Qiao J, Yuan J, Hu W, Li Q, Fang H, Xu Y, Dai Y. Combined diagnosis of QF-PCR and CNV-Seq in fetal chromosomal abnormalities: A new perspective on prenatal diagnosis. J Clin Lab Anal 2022;:e24311. [PMID: 35195919 DOI: 10.1002/jcla.24311] [Reference Citation Analysis]
6 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 Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
7 Ye X, Lin S, Song X, Tan M, Li J, Wang J, Yan H, Zhang H, Li S, Chen D, Chen M. Identification of copy number variants by NGS-based NIPT at low sequencing depth. Eur J Obstet Gynecol Reprod Biol 2021;256:297-301. [PMID: 33310305 DOI: 10.1016/j.ejogrb.2020.11.026] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 2.7] [Reference Citation Analysis]
8 Hu X, Guo R, Guo J, Qi Z, Li W, Hao C. Parallel Tests of Whole Exome Sequencing and Copy Number Variant Sequencing Increase the Diagnosis Yields of Rare Pediatric Disorders. Front Genet 2020;11:473. [PMID: 32595695 DOI: 10.3389/fgene.2020.00473] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 1.3] [Reference Citation Analysis]