Yao H - Search Results

1

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: yao h. 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.

2

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. 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

3

Clinical application of massively parallel sequencing-based prenatal noninvasive fetal trisomy test for trisomies 21 and 18 in 11,105 pregnancies with mixed risk factors.

Dan S, Wang W, Ren J, Li Y, Hu H, Xu Z, Lau TK, Xie J, Zhao W, Huang H, Xie J, Sun L, Zhang X, Wang W, Liao S, Qiang R, Cao J, Zhang Q, Zhou Y, Zhu H, Zhong M, Guo Y, Lin L, Gao Z, Yao H, Zhang H, Zhao L, Jiang F, Chen F, Jiang H, Li S, Li Y, Wang J, Wang J, Duan T, Su Y, Zhang X. Dan S, et al. Among authors: yao h. Prenat Diagn. 2012 Dec;32(13):1225-32. doi: 10.1002/pd.4002. Epub 2012 Nov 9. Prenat Diagn. 2012. PMID: 23138752 Clinical Trial.

4

A retrospective analysis the clinic data and follow-up of non-invasive prenatal test in detection of fetal chromosomal aneuploidy in more than 40,000 cases in a single prenatal diagnosis center.

Luo Y, Hu H, Jiang L, Ma Y, Zhang R, Xu J, Pan Y, Long Y, Yao H, Liang Z. Luo Y, et al. Among authors: yao h. Eur J Med Genet. 2020 Sep;63(9):104001. doi: 10.1016/j.ejmg.2020.104001. Epub 2020 Jul 2. Eur J Med Genet. 2020. PMID: 32622960

5

An assessment of the analytical performance of non-invasive prenatal testing (NIPT) in detecting sex chromosome aneuploidies: 34,717-patient sample in a single prenatal diagnosis Centre in China.

Luo Y, Hu H, Zhang R, Ma Y, Pan Y, Long Y, Hu B, Yao H, Liang Z. Luo Y, et al. Among authors: yao h. J Gene Med. 2021 Sep;23(9):e3362. doi: 10.1002/jgm.3362. Epub 2021 Jun 14. J Gene Med. 2021. PMID: 33973298

6

[Factors affecting the failure of non-invasive prenatal testing and the feasibility analysis of retesting].

Luo Y, Hu H, Zhang R, Pan Y, Ma Y, Long Y, Xu J, Xu L, Hu B, Yao H, Chang Q. Luo Y, et al. Among authors: yao h. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Jun 10;37(6):603-608. doi: 10.3760/cma.j.issn.1003-9406.2020.06.002. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 32472533 Chinese.

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: yao h. 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

Noninvasive prenatal genetic testing for fetal aneuploidy detects maternal trisomy X.

Yao H, Zhang L, Zhang H, Jiang F, Hu H, Chen F, Jiang H, Mu F, Zhao L, Liang Z, Wang W. Yao H, et al. Prenat Diagn. 2012 Nov;32(11):1114-6. doi: 10.1002/pd.3946. Epub 2012 Aug 18. Prenat Diagn. 2012. PMID: 22903289 No abstract available.

9

Distinct karyotypes in two offspring of a man with jumping translocation karyotype 45,XY,der(16)t(16;22)(q24;q11.2), -22 [59]/45,XY,der(1)t(1;22)(p36;q11.2), -22 [11]/45,XY,der(22)t(22;22)(p13;q11.2), -22 [10].

Hu H, Yao H, Dong Y, Long Y, Xu L, Hu B, Xu G, Liang Z. Hu H, et al. Among authors: yao h. Am J Med Genet A. 2014 Aug;164A(8):2048-53. doi: 10.1002/ajmg.a.36560. Epub 2014 Apr 15. Am J Med Genet A. 2014. PMID: 24737738

10

Karyotypic and molecular genetic changes associated with fetal cardiovascular abnormalities: results of a retrospective 4-year ultrasonic diagnosis study.

Bao B, Wang Y, Hu H, Yao H, Li Y, Tang S, Zheng L, Xu Y, Liang Z. Bao B, et al. Among authors: yao h. Int J Biol Sci. 2013 May 9;9(5):463-71. doi: 10.7150/ijbs.5404. Print 2013. Int J Biol Sci. 2013. PMID: 23678296 Free PMC article.

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