Zhang J - Search Results

1

Confined placental origin of the circulating cell free fetal DNA revealed by a discordant non-invasive prenatal test result in a trisomy 18 pregnancy.

Mao J, Wang T, Wang BJ, Liu YH, Li H, Zhang J, Cram D, Chen Y. Mao J, et al. Among authors: zhang j. Clin Chim Acta. 2014 Jun 10;433:190-3. doi: 10.1016/j.cca.2014.03.011. Epub 2014 Mar 22. Clin Chim Acta. 2014. PMID: 24667696

2

A pregnancy with discordant fetal and placental chromosome 18 aneuploidies revealed by invasive and noninvasive prenatal diagnosis.

Chen C, Cram DS, Xie F, Wang P, Xu X, Li H, Song Z, Chen D, Zhang J, Tang S. Chen C, et al. Among authors: zhang j. Reprod Biomed Online. 2014 Jul;29(1):136-9. doi: 10.1016/j.rbmo.2014.03.017. Epub 2014 Apr 4. Reprod Biomed Online. 2014. PMID: 24797099

3

Maternal X chromosome copy number variations are associated with discordant fetal sex chromosome aneuploidies detected by noninvasive prenatal testing.

Wang S, Huang S, Ma L, Liang L, Zhang J, Zhang J, Cram DS. Wang S, et al. Among authors: zhang j. Clin Chim Acta. 2015 Apr 15;444:113-6. doi: 10.1016/j.cca.2015.02.014. Epub 2015 Feb 14. Clin Chim Acta. 2015. PMID: 25689220

4

Maternal mosaicism is a significant contributor to discordant sex chromosomal aneuploidies associated with noninvasive prenatal testing.

Wang Y, Chen Y, Tian F, Zhang J, Song Z, Wu Y, Han X, Hu W, Ma D, Cram D, Cheng W. Wang Y, et al. Among authors: zhang j. Clin Chem. 2014 Jan;60(1):251-9. doi: 10.1373/clinchem.2013.215145. Epub 2013 Nov 5. Clin Chem. 2014. PMID: 24193117

5

Copy number variation sequencing for comprehensive diagnosis of chromosome disease syndromes.

Liang D, Peng Y, Lv W, Deng L, Zhang Y, Li H, Yang P, Zhang J, Song Z, Xu G, Cram DS, Wu L. Liang D, et al. Among authors: zhang j, zhang y. J Mol Diagn. 2014 Sep;16(5):519-526. doi: 10.1016/j.jmoldx.2014.05.002. Epub 2014 Jul 3. J Mol Diagn. 2014. PMID: 24998187 Free article.

6

A PGD pregnancy achieved by embryo copy number variation sequencing with confirmation by non-invasive prenatal diagnosis.

Wang H, Wang L, Ma M, Song Z, Zhang J, Xu G, Fan J, Li N, Cram DS, Yao Y. Wang H, et al. Among authors: zhang j. J Genet Genomics. 2014 Aug 20;41(8):453-6. doi: 10.1016/j.jgg.2014.06.007. Epub 2014 Jul 17. J Genet Genomics. 2014. PMID: 25160978 No abstract available.

7

Noninvasive prenatal testing for Wilson disease by use of circulating single-molecule amplification and resequencing technology (cSMART).

Lv W, Wei X, Guo R, Liu Q, Zheng Y, Chang J, Bai T, Li H, Zhang J, Song Z, Cram DS, Liang D, Wu L. Lv W, et al. Among authors: zhang j. Clin Chem. 2015 Jan;61(1):172-81. doi: 10.1373/clinchem.2014.229328. Epub 2014 Nov 6. Clin Chem. 2015. PMID: 25376582

8

The Performance of Whole Genome Amplification Methods and Next-Generation Sequencing for Pre-Implantation Genetic Diagnosis of Chromosomal Abnormalities.

Li N, Wang L, Wang H, Ma M, Wang X, Li Y, Zhang W, Zhang J, Cram DS, Yao Y. Li N, et al. Among authors: zhang w, zhang j. J Genet Genomics. 2015 Apr 20;42(4):151-9. doi: 10.1016/j.jgg.2015.03.001. Epub 2015 Mar 14. J Genet Genomics. 2015. PMID: 25953353

9

The clinical utility of next-generation sequencing for identifying chromosome disease syndromes in human embryos.

Fan J, Wang L, Wang H, Ma M, Wang S, Liu Z, Xu G, Zhang J, Cram DS, Yao Y. Fan J, et al. Among authors: zhang j. Reprod Biomed Online. 2015 Jul;31(1):62-70. doi: 10.1016/j.rbmo.2015.03.010. Epub 2015 Apr 9. Reprod Biomed Online. 2015. PMID: 25985995

10

Contribution of maternal copy number variations to false-positive fetal trisomies detected by noninvasive prenatal testing.

Zhou X, Sui L, Xu Y, Song Y, Qi Q, Zhang J, Zhu H, Sun H, Tian F, Xu M, Cram DS, Liu J. Zhou X, et al. Among authors: zhang j. Prenat Diagn. 2017 Apr;37(4):318-322. doi: 10.1002/pd.5014. Epub 2017 Feb 24. Prenat Diagn. 2017. PMID: 28152582

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