Hu H - Search Results

1

Xp22.31 copy number variations in 87 fetuses: refined genotype-phenotype correlations by prenatal and postnatal follow-up.

Hu H, Huang Y, Hou R, Xu H, Liu Y, Liao X, Xu J, Jiang L, Wang D. Hu H, et al. BMC Med Genomics. 2023 Apr 3;16(1):69. doi: 10.1186/s12920-023-01493-z. BMC Med Genomics. 2023. PMID: 37013593 Free PMC article.

2

Prenatal diagnosis of familial submicroscopic duplication at 18q22.3 without phenotypic abnormalities.

Hu H, Ma Y, Zhang R, Xu J, Hu B, Long Y, Xu L, Yao H, Liang Z. Hu H, et al. Among authors: hu b. Taiwan J Obstet Gynecol. 2020 May;59(3):446-450. doi: 10.1016/j.tjog.2020.03.021. Taiwan J Obstet Gynecol. 2020. PMID: 32416897 Free article.

3

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: hu 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

4

Prenatal Diagnosis and Genetic Analysis of 21q21.1-q21.2 Aberrations in Seven Chinese Pedigrees.

Hu H, Zhang R, Ma Y, Luo Y, Pan Y, Xu J, Jiang L, Wang D. Hu H, et al. Front Genet. 2021 Dec 21;12:731815. doi: 10.3389/fgene.2021.731815. eCollection 2021. Front Genet. 2021. PMID: 34992628 Free PMC article.

5

[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: hu h, hu b. 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.

6

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: hu h. 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.

7

A robust approach for blind detection of balanced chromosomal rearrangements with whole-genome low-coverage sequencing.

Dong Z, Jiang L, Yang C, Hu H, Wang X, Chen H, Choy KW, Hu H, Dong Y, Hu B, Xu J, Long Y, Cao S, Chen H, Wang WJ, Jiang H, Xu F, Yao H, Xu X, Liang Z. Dong Z, et al. Among authors: hu h, hu b. Hum Mutat. 2014 May;35(5):625-36. doi: 10.1002/humu.22541. Epub 2014 Apr 9. Hum Mutat. 2014. PMID: 24610732

8

Targeted next-generation sequencing identification of mutations in patients with disorders of sex development.

Dong Y, Yi Y, Yao H, Yang Z, Hu H, Liu J, Gao C, Zhang M, Zhou L, Asan, Yi X, Liang Z. Dong Y, et al. Among authors: hu h. BMC Med Genet. 2016 Mar 15;17:23. doi: 10.1186/s12881-016-0286-2. BMC Med Genet. 2016. PMID: 26980296 Free PMC article.

9

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: hu h, hu b. J Gene Med. 2021 Sep;23(9):e3362. doi: 10.1002/jgm.3362. Epub 2021 Jun 14. J Gene Med. 2021. PMID: 33973298

10

[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: hu 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.

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