Jiang Z - Search Results

1

AccuCopy quantification combined with pre-amplification of long-distance PCR for fast analysis of intron 22 inversion in haemophilia A.

Ding Q, Wu X, Lu Y, Chen C, Shen R, Zhang X, Jiang Z, Wang X. Ding Q, et al. Among authors: jiang z. Clin Chim Acta. 2016 Jul 1;458:78-83. doi: 10.1016/j.cca.2016.04.015. Epub 2016 Apr 19. Clin Chim Acta. 2016. PMID: 27101812

2

A capillary electrophoresis-based variant hotspot genotyping method for rapid and reliable analysis of the phenylalanine hydroxylase gene in the Chinese Han population.

Shao B, Liu A, Zhang J, Wang Y, Qiao F, Zhang C, Zhu Y, Lin Y, Hu P, Tao T, Jiang Z, Tan J, Xu Z. Shao B, et al. Among authors: jiang z. Clin Chim Acta. 2021 Dec;523:267-272. doi: 10.1016/j.cca.2021.10.009. Epub 2021 Oct 12. Clin Chim Acta. 2021. PMID: 34653385

3

Noninvasive fetal genotyping of single nucleotide variants and linkage analysis for prenatal diagnosis of monogenic disorders.

Wu W, Zhou X, Jiang Z, Zhang D, Yu F, Zhang L, Wang X, Chen S, Xu C. Wu W, et al. Among authors: jiang z. Hum Genomics. 2022 Jul 27;16(1):28. doi: 10.1186/s40246-022-00400-4. Hum Genomics. 2022. PMID: 35897115 Free PMC article.

4

A modified multiplex ligation-dependent probe amplification method for the detection of 22q11.2 copy number variations in patients with congenital heart disease.

Zhang X, Xu Y, Liu D, Geng J, Chen S, Jiang Z, Fu Q, Sun K. Zhang X, et al. Among authors: jiang z. BMC Genomics. 2015 May 8;16(1):364. doi: 10.1186/s12864-015-1590-5. BMC Genomics. 2015. PMID: 25952753 Free PMC article.

5

Noninvasive Prenatal Screening of Fetal Aneuploidy without Massively Parallel Sequencing.

Xu C, Wang T, Liu C, Li H, Chen X, Zhu H, Chen S, Xin Q, Tao J, Huang L, Jiang Z. Xu C, et al. Among authors: jiang z. Clin Chem. 2017 Apr;63(4):861-869. doi: 10.1373/clinchem.2016.266247. Epub 2017 Feb 14. Clin Chem. 2017. PMID: 28196921

6

Identification of Chromosomal Abnormalities in Early Pregnancy Loss Using a High-Throughput Ligation-Dependent Probe Amplification-Based Assay.

Wang Y, Zhou R, Jiang L, Meng L, Tan J, Qiao F, Wang Y, Zhang C, Cheng Q, Jiang Z, Hu P, Xu Z. Wang Y, et al. Among authors: jiang l, jiang z. J Mol Diagn. 2021 Jan;23(1):38-45. doi: 10.1016/j.jmoldx.2020.10.002. Epub 2020 Oct 15. J Mol Diagn. 2021. PMID: 33069876 Free article.

7

A copy number variation genotyping method for aneuploidy detection in spontaneous abortion specimens.

Chen S, Liu D, Zhang J, Li S, Zhang L, Fan J, Luo Y, Qian Y, Huang H, Liu C, Zhu H, Jiang Z, Xu C. Chen S, et al. Among authors: jiang z. Prenat Diagn. 2017 Feb;37(2):176-183. doi: 10.1002/pd.4986. Epub 2017 Jan 19. Prenat Diagn. 2017. PMID: 27977861

8

Comprehensive copy number analysis of Y chromosome-linked loci for detection of structural variations and diagnosis of male infertility.

Chen S, Zhang Q, Chu L, Chang C, Chen Y, Bao Z, Peng W, Zhang L, Li S, Liu C, Zhu H, Yu F, Chen X, Jiang L, Lu D, Jiang Z, Jin L, Xu C. Chen S, et al. Among authors: jiang l, jiang z. J Hum Genet. 2022 Feb;67(2):107-114. doi: 10.1038/s10038-021-00973-3. Epub 2021 Aug 31. J Hum Genet. 2022. PMID: 34462535

9

A capillary electrophoresis-based multiplex PCR assay for expanded carrier screening in the eastern Han Chinese population.

Hu P, Tan J, Yu F, Shao B, Zhang F, Zhang J, Lin Y, Tao T, Jiang L, Jiang Z, Xu Z. Hu P, et al. Among authors: jiang l, jiang z. NPJ Genom Med. 2022 Jan 25;7(1):6. doi: 10.1038/s41525-021-00280-y. NPJ Genom Med. 2022. PMID: 35079019 Free PMC article.

10

Efficient typing of copy number variations in a segmental duplication-mediated rearrangement hotspot using multiplex competitive amplification.

Du R, Lu C, Jiang Z, Li S, Ma R, An H, Xu M, An Y, Xia Y, Jin L, Wang X, Zhang F. Du R, et al. Among authors: jiang z. J Hum Genet. 2012 Aug;57(8):545-51. doi: 10.1038/jhg.2012.66. Epub 2012 Jun 7. J Hum Genet. 2012. PMID: 22673690

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