Chen F - Search Results

1

Genome-wide detection of additional fetal chromosomal abnormalities by cell-free DNA testing of 15,626 consecutive pregnant women.

Yao H, Gao Y, Zhao J, Zhang R, Xu H, Hu H, Luo Y, Yuan Y, Fu M, Zhang H, Jiang H, Wang W, Yang H, Wang J, Liang Z, Chen F. Yao H, et al. Among authors: chen f. Sci China Life Sci. 2019 Feb;62(2):215-224. doi: 10.1007/s11427-017-9344-7. Epub 2018 Aug 2. Sci China Life Sci. 2019. PMID: 30076564

2

Noninvasive prenatal test for FGFR3-related skeletal dysplasia based on next-generation sequencing and plasma cell-free DNA: Test performance analysis and feasibility exploration.

Ren Y, Zhao J, Li R, Xie Y, Jiang S, Zhou H, Liu H, You Y, Chen F, Wang W, Gao Y, Meng Y, Lu Y. Ren Y, et al. Among authors: chen f. Prenat Diagn. 2018 Oct;38(11):821-828. doi: 10.1002/pd.5334. Epub 2018 Aug 19. Prenat Diagn. 2018. PMID: 30048571

3

Copy number variation profile in noninvasive prenatal testing (NIPT) can identify co-existing maternal malignancies: Case reports and a literature review.

Ji X, Chen F, Zhou Y, Li J, Yuan Y, Mo Y, Liu Q, Tseng JY, Shih-Chieh Lin D, Shen SH, Liu Y, Ye W, Cheung YN, Yuen KY, Lin S, Fu M, Zhang H, Liu N, Wang J, Yang H, Wang Y, Li S, Fan S, Jin X, Mao M, Sung PL. Ji X, et al. Among authors: chen f. Taiwan J Obstet Gynecol. 2018 Dec;57(6):871-877. doi: 10.1016/j.tjog.2018.10.032. Taiwan J Obstet Gynecol. 2018. PMID: 30545544 Free article. Review.

4

Identifying occult maternal malignancies from 1.93 million pregnant women undergoing noninvasive prenatal screening tests.

Ji X, Li J, Huang Y, Sung PL, Yuan Y, Liu Q, Chen Y, Ju J, Zhou Y, Huang S, Chen F, Han Y, Yuan W, Fan C, Zhao Q, Wu H, Feng S, Liu W, Li Z, Chen J, Chen M, Yao H, Zeng L, Ma T, Fan S, Zhang J, Yuen KY, Cheng SH, Chik IWS, Liu NT, Zhu J, Lin S, Cao J, Tong S, Shan Z, Li W, Hekmat MR, Garshasbi M, Suela J, Torres Y, Cigudosa JC, Ruiz FJP, Rodríguez L, García M, Bernik J, Traven E, Reš U, Tul N, Tseng CF, Zhao D, Sun L, Pan Q, Shen L, Dai M, Wang Y, Wang J, Yang H, Yin Y, Duan T, Zhu B, Choolani M, Jin X, Chen Y, Mao M. Ji X, et al. Among authors: chen j, chen m, chen f, chen y. Genet Med. 2019 Oct;21(10):2293-2302. doi: 10.1038/s41436-019-0510-5. Epub 2019 Apr 12. Genet Med. 2019. PMID: 30976098 Free article.

5

Detection of fetal trisomy and single gene disease by massively parallel sequencing of extracellular vesicle DNA in maternal plasma: a proof-of-concept validation.

Zhang W, Lu S, Pu D, Zhang H, Yang L, Zeng P, Su F, Chen Z, Guo M, Gu Y, Luo Y, Hu H, Lu Y, Chen F, Gao Y. Zhang W, et al. Among authors: chen z, chen f. BMC Med Genomics. 2019 Nov 4;12(1):151. doi: 10.1186/s12920-019-0590-8. BMC Med Genomics. 2019. PMID: 31684971 Free PMC article.

6

FF-QuantSC: accurate quantification of fetal fraction by a neural network model.

Yuan Y, Chai X, Liu N, Gu B, Li S, Gao Y, Zhou L, Liu Q, Yang F, Liu J, Qiu J, Zhang J, Hou Y, Cen M, Tian Z, Tang W, Zhang H, Chen F, Yin Y, Wang W. Yuan Y, et al. Among authors: chen f. Mol Genet Genomic Med. 2020 Jun;8(6):e1232. doi: 10.1002/mgg3.1232. Epub 2020 Apr 13. Mol Genet Genomic Med. 2020. PMID: 32281746 Free PMC article.

7

[Positive maternal blood cfDNA test caused by confined placental mosaicism in a case].

Gao Y, Yao H, Su F, Zhang R, Hu H, Xu J, Xu L, Zhao L, Chen F, Liang Z. Gao Y, et al. Among authors: chen f. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Jun 10;37(6):627-628. doi: 10.3760/cma.j.issn.1003-9406.2020.06.007. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 32472538 Chinese. No abstract available.

8

Simultaneous detection of fetal aneuploidy, de novo FGFR3 mutations and paternally derived β-thalassemia by a novel method of noninvasive prenatal testing.

Yang L, Wu Y, Hu Z, Zhang H, Pu D, Yan H, Zhang S, Jiang H, Liu Q, Yuan Y, Zhang Y, Chen F, Lu Y, Pan S, Lin L, Gao Y. Yang L, et al. Among authors: chen f. Prenat Diagn. 2021 Mar;41(4):440-448. doi: 10.1002/pd.5879. Epub 2021 Jan 21. Prenat Diagn. 2021. PMID: 33340121 Free PMC article.

9

Temporal persistence of residual fetal cell-free DNA from a deceased cotwin after selective fetal reduction in dichorionic diamniotic twin pregnancies.

Chen M, Su F, Wang J, Zhou L, Liu Q, Chai X, Yuan Y, Cen M, Wu Y, Wang Y, Chen F, Zhang Y, Chen D, Gao Y. Chen M, et al. Among authors: chen d, chen f. Prenat Diagn. 2021 Nov;41(12):1602-1610. doi: 10.1002/pd.5898. Epub 2021 Feb 8. Prenat Diagn. 2021. PMID: 33555061

10

Comparison of single cell sequencing data between two whole genome amplification methods on two sequencing platforms.

Chen D, Zhen H, Qiu Y, Liu P, Zeng P, Xia J, Shi Q, Xie L, Zhu Z, Gao Y, Huang G, Wang J, Yang H, Chen F. Chen D, et al. Among authors: chen f. Sci Rep. 2018 Mar 21;8(1):4963. doi: 10.1038/s41598-018-23325-2. Sci Rep. 2018. PMID: 29563514 Free PMC article.

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