Zhang Y - Search Results

1

Multiple approaches for massively parallel sequencing of SARS-CoV-2 genomes directly from clinical samples.

Xiao M, Liu X, Ji J, Li M, Li J, Yang L, Sun W, Ren P, Yang G, Zhao J, Liang T, Ren H, Chen T, Zhong H, Song W, Wang Y, Deng Z, Zhao Y, Ou Z, Wang D, Cai J, Cheng X, Feng T, Wu H, Gong Y, Yang H, Wang J, Xu X, Zhu S, Chen F, Zhang Y, Chen W, Li Y, Li J. Xiao M, et al. Among authors: zhang y. Genome Med. 2020 Jun 30;12(1):57. doi: 10.1186/s13073-020-00751-4. Genome Med. 2020. PMID: 32605661 Free PMC article.

2

A metagenome-wide association study of gut microbiota in type 2 diabetes.

Qin J, Li Y, Cai Z, Li S, Zhu J, Zhang F, Liang S, Zhang W, Guan Y, Shen D, Peng Y, Zhang D, Jie Z, Wu W, Qin Y, Xue W, Li J, Han L, Lu D, Wu P, Dai Y, Sun X, Li Z, Tang A, Zhong S, Li X, Chen W, Xu R, Wang M, Feng Q, Gong M, Yu J, Zhang Y, Zhang M, Hansen T, Sanchez G, Raes J, Falony G, Okuda S, Almeida M, LeChatelier E, Renault P, Pons N, Batto JM, Zhang Z, Chen H, Yang R, Zheng W, Li S, Yang H, Wang J, Ehrlich SD, Nielsen R, Pedersen O, Kristiansen K, Wang J. Qin J, et al. Among authors: zhang m, zhang f, zhang w, zhang d, zhang z, zhang y. Nature. 2012 Oct 4;490(7418):55-60. doi: 10.1038/nature11450. Epub 2012 Sep 26. Nature. 2012. PMID: 23023125

3

Non-invasive fetal sex determination by maternal plasma sequencing and application in X-linked disorder counseling.

Pan X, Zhang C, Li X, Chen S, Ge H, Zhang Y, Chen F, Jiang H, Jiang F, Zhang H, Wang W, Zhang X. Pan X, et al. Among authors: zhang c, zhang h, zhang x, zhang y. J Matern Fetal Neonatal Med. 2014 Dec;27(18):1829-33. doi: 10.3109/14767058.2014.885942. Epub 2014 Feb 20. J Matern Fetal Neonatal Med. 2014. PMID: 24444365

4

Haplotype-based approach for noninvasive prenatal diagnosis of congenital adrenal hyperplasia by maternal plasma DNA sequencing.

Ma D, Ge H, Li X, Jiang T, Chen F, Zhang Y, Hu P, Chen S, Zhang J, Ji X, Xu X, Jiang H, Chen M, Wang W, Xu Z. Ma D, et al. Among authors: zhang j, zhang y. Gene. 2014 Jul 10;544(2):252-8. doi: 10.1016/j.gene.2014.04.055. Epub 2014 Apr 24. Gene. 2014. PMID: 24768736

5

Noninvasive prenatal testing for autosomal recessive conditions by maternal plasma sequencing in a case of congenital deafness.

Meng M, Li X, Ge H, Chen F, Han M, Zhang Y, Kang D, Xie W, Gao Z, Pan X, Dai P, Chi F, Chen S, Liu P, Zhang C, Cao J, Jiang H, Xu X, Wang W, Duan T. Meng M, et al. Among authors: zhang c, zhang y. Genet Med. 2014 Dec;16(12):972-6. doi: 10.1038/gim.2014.51. Epub 2014 May 15. Genet Med. 2014. PMID: 24830326 Free article.

6

Noninvasive prenatal paternity testing by maternal plasma DNA sequencing in twin pregnancies.

Xie Y, Qu N, Lin S, Jiang H, Zhang Y, Zhang X, Liang H, Chen F, Ou X. Xie Y, et al. Among authors: zhang x, zhang y. Electrophoresis. 2020 Jun;41(12):1095-1102. doi: 10.1002/elps.202000036. Epub 2020 May 14. Electrophoresis. 2020. PMID: 32249439

7

Simultaneous detection of fetal aneuploidy, de novo FGFR3 mutations and paternally derived β-thalassemia by a novel method of noninvasive prenatal testing.

Yang L, Wu Y, Hu Z, Zhang H, Pu D, Yan H, Zhang S, Jiang H, Liu Q, Yuan Y, Zhang Y, Chen F, Lu Y, Pan S, Lin L, Gao Y. Yang L, et al. Among authors: zhang s, zhang h, zhang y. Prenat Diagn. 2021 Mar;41(4):440-448. doi: 10.1002/pd.5879. Epub 2021 Jan 21. Prenat Diagn. 2021. PMID: 33340121 Free PMC article.

8

Influence of low tumor content on tumor mutational burden estimation by whole-exome sequencing and targeted panel sequencing.

Zhang W, Wang R, Fang H, Ma X, Li D, Liu T, Chen Z, Wang K, Hao S, Yu Z, Chang Z, Na C, Wang Y, Bai J, Zhang Y, Chen F, Li M, Chen C, Wei L, Li J, Chang X, Qu S, Yang L, Huang J. Zhang W, et al. Among authors: zhang y. Clin Transl Med. 2021 May;11(5):e415. doi: 10.1002/ctm2.415. Clin Transl Med. 2021. PMID: 34047470 Free PMC article.

9

Identification of novel bat coronaviruses sheds light on the evolutionary origins of SARS-CoV-2 and related viruses.

Zhou H, Ji J, Chen X, Bi Y, Li J, Wang Q, Hu T, Song H, Zhao R, Chen Y, Cui M, Zhang Y, Hughes AC, Holmes EC, Shi W. Zhou H, et al. Among authors: zhang y. Cell. 2021 Aug 19;184(17):4380-4391.e14. doi: 10.1016/j.cell.2021.06.008. Epub 2021 Jun 9. Cell. 2021. PMID: 34147139 Free PMC article.

10

Simultaneous detection of genomic imbalance in patients receiving preimplantation genetic testing for monogenic diseases (PGT-M).

Yang L, Xu Y, Xia J, Yan H, Ding C, Shi Q, Wu Y, Liu P, Pan J, Zeng Y, Zhang Y, Chen F, Jiang H, Xu Y, Li W, Zhou C, Gao Y. Yang L, et al. Among authors: zhang y. Front Genet. 2022 Sep 29;13:976131. doi: 10.3389/fgene.2022.976131. eCollection 2022. Front Genet. 2022. PMID: 36246639 Free PMC article.

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