Dong Z - Search Results

1

Low-pass whole-genome sequencing in clinical cytogenetics: a validated approach.

Dong Z, Zhang J, Hu P, Chen H, Xu J, Tian Q, Meng L, Ye Y, Wang J, Zhang M, Li Y, Wang H, Yu S, Chen F, Xie J, Jiang H, Wang W, Choy KW, Xu Z. Dong Z, et al. Genet Med. 2016 Sep;18(9):940-8. doi: 10.1038/gim.2015.199. Epub 2016 Jan 28. Genet Med. 2016. PMID: 26820068 Free article.

2

Low density lipoprotein receptor related protein gene amplification and 766T polymorphism in astrocytomas.

Baum L, Dong ZY, Choy KW, Pang CP, Ng HK. Baum L, et al. Among authors: dong zy. Neurosci Lett. 1998 Oct 30;256(1):5-8. doi: 10.1016/s0304-3940(98)00734-4. Neurosci Lett. 1998. PMID: 9832203

3

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: dong y. Hum Mutat. 2014 May;35(5):625-36. doi: 10.1002/humu.22541. Epub 2014 Apr 9. Hum Mutat. 2014. PMID: 24610732

4

Intragenic and extragenic disruptions of FOXL2 mapped by whole genome low-coverage sequencing in two BPES families with chromosome reciprocal translocation.

Yang Y, Yang C, Zhu Y, Chen H, Zhao R, He X, Tao L, Wang P, Zhou L, Zhao L, Tu M, Dong Z, Chen H, Xie Z. Yang Y, et al. Among authors: dong z. Genomics. 2014 Sep;104(3):170-6. doi: 10.1016/j.ygeno.2014.07.010. Epub 2014 Jul 30. Genomics. 2014. PMID: 25086333 Free article.

5

Copy-Number Variants Detection by Low-Pass Whole-Genome Sequencing.

Dong Z, Xie W, Chen H, Xu J, Wang H, Li Y, Wang J, Chen F, Choy KW, Jiang H. Dong Z, et al. Curr Protoc Hum Genet. 2017 Jul 11;94:8.17.1-8.17.16. doi: 10.1002/cphg.43. Curr Protoc Hum Genet. 2017. PMID: 28696555

6

Identification of balanced chromosomal rearrangements previously unknown among participants in the 1000 Genomes Project: implications for interpretation of structural variation in genomes and the future of clinical cytogenetics.

Dong Z, Wang H, Chen H, Jiang H, Yuan J, Yang Z, Wang WJ, Xu F, Guo X, Cao Y, Zhu Z, Geng C, Cheung WC, Kwok YK, Yang H, Leung TY, Morton CC, Cheung SW, Choy KW. Dong Z, et al. Genet Med. 2018 Jul;20(7):697-707. doi: 10.1038/gim.2017.170. Epub 2017 Nov 2. Genet Med. 2018. PMID: 29095815 Free PMC article.

7

Balanced Chromosomal Rearrangement Detection by Low-Pass Whole-Genome Sequencing.

Dong Z, Ye L, Yang Z, Chen H, Yuan J, Wang H, Guo X, Li Y, Wang J, Chen F, Cheung SW, Morton CC, Jiang H, Choy KW. Dong Z, et al. Curr Protoc Hum Genet. 2018 Jan 24;96:8.18.1-8.18.16. doi: 10.1002/cphg.51. Curr Protoc Hum Genet. 2018. PMID: 29364520 Free PMC article.

8

Development of coupling controlled polymerizations by adapter-ligation in mate-pair sequencing for detection of various genomic variants in one single assay.

Dong Z, Zhao X, Li Q, Yang Z, Xi Y, Alexeev A, Shen H, Wang O, Ruan J, Ren H, Wei H, Qi X, Li J, Zhu X, Zhang Y, Dai P, Kong X, Kirkconnell K, Alferov O, Giles S, Yamtich J, Kermani BG, Dong C, Liu P, Mi Z, Zhang W, Xu X, Drmanac R, Choy KW, Jiang Y. Dong Z, et al. Among authors: dong c. DNA Res. 2019 Aug 1;26(4):313-325. doi: 10.1093/dnares/dsz011. DNA Res. 2019. PMID: 31173071 Free PMC article.

9

Low-pass genome sequencing versus chromosomal microarray analysis: implementation in prenatal diagnosis.

Wang H, Dong Z, Zhang R, Chau MHK, Yang Z, Tsang KYC, Wong HK, Gui B, Meng Z, Xiao K, Zhu X, Wang Y, Chen S, Leung TY, Cheung SW, Kwok YK, Morton CC, Zhu Y, Choy KW. Wang H, et al. Among authors: dong z. Genet Med. 2020 Mar;22(3):500-510. doi: 10.1038/s41436-019-0634-7. Epub 2019 Aug 26. Genet Med. 2020. PMID: 31447483 Free PMC article.

10

Prenatal Diagnosis of Fetuses With Increased Nuchal Translucency by Genome Sequencing Analysis.

Choy KW, Wang H, Shi M, Chen J, Yang Z, Zhang R, Yan H, Wang Y, Chen S, Chau MHK, Cao Y, Chan OYM, Kwok YK, Zhu Y, Chen M, Leung TY, Dong Z. Choy KW, et al. Among authors: dong z. Front Genet. 2019 Aug 16;10:761. doi: 10.3389/fgene.2019.00761. eCollection 2019. Front Genet. 2019. PMID: 31475041 Free PMC article.

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