Liu H - Search Results

1

An enrichment method to increase cell-free fetal DNA fraction and significantly reduce false negatives and test failures for non-invasive prenatal screening: a feasibility study.

Hu P, Liang D, Chen Y, Lin Y, Qiao F, Li H, Wang T, Peng C, Luo D, Liu H, Xu Z. Hu P, et al. Among authors: liu h. J Transl Med. 2019 Apr 11;17(1):124. doi: 10.1186/s12967-019-1871-x. J Transl Med. 2019. PMID: 30975179 Free PMC article.

2

A prenatal case with discrepant findings between non-invasive prenatal testing and fetal genetic testings.

Pan Q, Sun B, Huang X, Jing X, Liu H, Jiang F, Zhou J, Lin M, Yue H, Hu P, Ning Y. Pan Q, et al. Among authors: liu h. Mol Cytogenet. 2014 Jul 16;7:48. doi: 10.1186/1755-8166-7-48. eCollection 2014. Mol Cytogenet. 2014. PMID: 25478006 Free PMC article.

3

Clinical performance of non-invasive prenatal served as a first-tier screening test for trisomy 21, 18, 13 and sex chromosome aneuploidy in a pilot city in China.

Liu Y, Liu H, He Y, Xu W, Ma Q, He Y, Lei W, Chen G, He Z, Huang J, Liu J, Liu Y, Huang Q, Yu F. Liu Y, et al. Among authors: liu j, liu h. Hum Genomics. 2020 Jun 5;14(1):21. doi: 10.1186/s40246-020-00268-2. Hum Genomics. 2020. PMID: 32503639 Free PMC article.

4

Noninvasive prenatal testing for chromosome aneuploidies and subchromosomal microdeletions/microduplications in a cohort of 8141 single pregnancies.

Hu H, Wang L, Wu J, Zhou P, Fu J, Sun J, Cai W, Liu H, Yang Y. Hu H, et al. Among authors: liu h. Hum Genomics. 2019 Mar 12;13(1):14. doi: 10.1186/s40246-019-0198-2. Hum Genomics. 2019. PMID: 30871627 Free PMC article.

5

Genome-wide profiling reveals alternative polyadenylation of mRNA in human non-small cell lung cancer.

Zhang S, Zhang X, Lei W, Liang J, Xu Y, Liu H, Ma S. Zhang S, et al. Among authors: liu h. J Transl Med. 2019 Aug 7;17(1):257. doi: 10.1186/s12967-019-1986-0. J Transl Med. 2019. PMID: 31391087 Free PMC article.

6

Karyotyping and prenatal diagnosis of 47,XX,+ 8[67]/46,XX [13] Mosaicism: case report and literature review.

Sun S, Zhan F, Jiang J, Zhang X, Yan L, Cai W, Liu H, Cao D. Sun S, et al. Among authors: liu h. BMC Med Genomics. 2019 Dec 21;12(1):197. doi: 10.1186/s12920-019-0639-8. BMC Med Genomics. 2019. PMID: 31864361 Free PMC article.

7

The Gene Mutation Spectrum of Breast Cancer Analyzed by Semiconductor Sequencing Platform.

Liu Y, Yang B, Zhang X, Huang Q, Liu H. Liu Y, et al. Among authors: liu h. Pathol Oncol Res. 2020 Jan;26(1):491-497. doi: 10.1007/s12253-018-0522-5. Epub 2018 Nov 16. Pathol Oncol Res. 2020. PMID: 30443844 Free article.

8

Genetic screening involving 101 hot spots for neonates not passing newborn hearing screening and those random recruited in Dongguan.

Liu Y, Ye L, Zhu P, Wu J, Tan S, Chen J, Wu C, Zhong Y, Wang Y, Li X, Liu H. Liu Y, et al. Among authors: liu h. Int J Pediatr Otorhinolaryngol. 2019 Feb;117:82-87. doi: 10.1016/j.ijporl.2018.11.008. Epub 2018 Nov 22. Int J Pediatr Otorhinolaryngol. 2019. PMID: 30579095

9

Mapping Breakpoints of Complex Chromosome Rearrangements Involving a Partial Trisomy 15q23.1-q26.2 Revealed by Next Generation Sequencing and Conventional Techniques.

Pan Q, Hu H, Han L, Jing X, Liu H, Yang C, Zhang F, Hu Y, Yue H, Ning Y. Pan Q, et al. Among authors: liu h. PLoS One. 2016 May 24;11(5):e0154574. doi: 10.1371/journal.pone.0154574. eCollection 2016. PLoS One. 2016. PMID: 27218255 Free PMC article.

10

Pathogenic variants identified by whole-exome sequencing in 43 patients with epilepsy.

Zhang L, Gao J, Liu H, Tian Y, Zhang X, Lei W, Li Y, Guo Y, Yu H, Yuan E, Liang L, Cui S, Zhang X. Zhang L, et al. Among authors: liu h. Hum Genomics. 2020 Dec 7;14(1):44. doi: 10.1186/s40246-020-00294-0. Hum Genomics. 2020. PMID: 33287870 Free PMC article.

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