Wang J - Search Results

1

Identification of a de novo fetal variant in osteogenesis imperfecta by targeted sequencing-based noninvasive prenatal testing.

Yin X, Du Y, Zhang H, Wang Z, Wang J, Fu X, Cui Y, Chen C, Liang J, Xuan Z, Zhang X. Yin X, et al. Among authors: wang z, wang j. J Hum Genet. 2018 Nov;63(11):1129-1137. doi: 10.1038/s10038-018-0489-9. Epub 2018 Aug 21. J Hum Genet. 2018. PMID: 30131598

2

High resolution global chromosomal aberrations from spontaneous miscarriages revealed by low coverage whole genome sequencing.

Qi H, Xuan ZL, Du Y, Cai LR, Zhang H, Wen XH, Kong XD, Yang K, Mi Y, Fu XX, Cao SB, Wang J, Chen CJ, Liang JB. Qi H, et al. Among authors: wang j. Eur J Obstet Gynecol Reprod Biol. 2018 May;224:21-28. doi: 10.1016/j.ejogrb.2018.03.008. Epub 2018 Mar 8. Eur J Obstet Gynecol Reprod Biol. 2018. PMID: 29525519

3

Pilot study of a novel multi-functional noninvasive prenatal test on fetus aneuploidy, copy number variation, and single-gene disorder screening.

Luo Y, Jia B, Yan K, Liu S, Song X, Chen M, Jin F, Du Y, Wang J, Hong Y, Cao S, Li D, Dong M. Luo Y, et al. Among authors: wang j. Mol Genet Genomic Med. 2019 Apr;7(4):e00597. doi: 10.1002/mgg3.597. Epub 2019 Feb 14. Mol Genet Genomic Med. 2019. PMID: 30767419 Free PMC article.

4

Noninvasive prenatal testing for fetal subchromosomal copy number variations and chromosomal aneuploidy by low-pass whole-genome sequencing.

Yu D, Zhang K, Han M, Pan W, Chen Y, Wang Y, Jiao H, Duan L, Zhu Q, Song X, Hong Y, Chen C, Wang J, Hui F, Huang L, Chen C, Du Y. Yu D, et al. Among authors: wang j, wang y. Mol Genet Genomic Med. 2019 Jun;7(6):e674. doi: 10.1002/mgg3.674. Epub 2019 Apr 19. Mol Genet Genomic Med. 2019. PMID: 31004415 Free PMC article.

5

Detection of a rare de novo 18p terminal deletion with inverted duplication in a Chinese pregnant woman.

Zhu J, Qi H, Cao S, Cai L, Wen X, Tang G, Wan Q, Chen C, Wang J, Zeng W, Luo Y. Zhu J, et al. Among authors: wang j. Mol Genet Genomic Med. 2019 Sep;7(9):e868. doi: 10.1002/mgg3.868. Epub 2019 Jul 17. Mol Genet Genomic Med. 2019. PMID: 31317671 Free PMC article. Review.

6

A proof-of-concept study on the effects of low total cfDNA content and solutions to increase the NIPT trisomy 21 detection rate.

Du Y, Chen A, Yang R, Zhou T, Zhou Q, Yang L, Wang J, Hong Y, Chen C, Wan Q, Yang L, Chen Y. Du Y, et al. Among authors: wang j. J Clin Lab Anal. 2020 Feb;34(2):e23035. doi: 10.1002/jcla.23035. Epub 2019 Sep 30. J Clin Lab Anal. 2020. PMID: 31568605 Free PMC article.

7

Characteristics and prognostic significance of genetic mutations in acute myeloid leukemia based on a targeted next-generation sequencing technique.

Wang RQ, Chen CJ, Jing Y, Qin JY, Li Y, Chen GF, Zhou W, Li YH, Wang J, Li DW, Zhao HM, Wang BH, Wang LL, Wang H, Wang MZ, Gao XN, Yu L. Wang RQ, et al. Among authors: wang h, wang mz, wang ll, wang j, wang bh. Cancer Med. 2020 Nov;9(22):8457-8467. doi: 10.1002/cam4.3467. Epub 2020 Sep 24. Cancer Med. 2020. PMID: 32970934 Free PMC article.

8

A rare case of NIPT discrepancy caused by the placental mosaicism of three different karyotypes, 47,XXX, 47,XX,+21, and 48,XXX,+21.

Li J, Xie M, Wang F, Ma J, Li J, Chen C, Li Z, Wang J, Zhang Y, Li Y. Li J, et al. Among authors: wang f, wang j. Mol Genet Genomic Med. 2020 Aug;8(8):e1279. doi: 10.1002/mgg3.1279. Epub 2020 May 28. Mol Genet Genomic Med. 2020. PMID: 32463164 Free PMC article.

9

The Comprehensive Comparison of Bacterial Artificial Chromosomes (BACs)-on-Beads Assay and Copy Number Variation Sequencing in Prenatal Diagnosis of Southern Chinese Women.

Xu L, Zhang M, Huang H, Wang Y, Chen L, Chen M, Wang J, Chen C, Li B, Li Z. Xu L, et al. Among authors: wang j, wang y. J Mol Diagn. 2020 Nov;22(11):1324-1332. doi: 10.1016/j.jmoldx.2020.07.005. Epub 2020 Aug 26. J Mol Diagn. 2020. PMID: 32858251 Free article.

10

Is an SV caller compatible with sequencing data? An online recommendation tool to automatically recommend the optimal caller based on data features.

Wang S, Liu Y, Wang J, Zhu X, Shi Y, Wang X, Liu T, Xiao X, Wang J. Wang S, et al. Among authors: wang x, wang j. Front Genet. 2023 Jan 6;13:1096797. doi: 10.3389/fgene.2022.1096797. eCollection 2022. Front Genet. 2023. PMID: 36685885 Free PMC article.

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