Xu X - Search Results

1

Genomic architecture of fetal central nervous system anomalies using whole-genome sequencing.

Yang Y, Zhao S, Sun G, Chen F, Zhang T, Song J, Yang W, Wang L, Zhan N, Yang X, Zhu X, Rao B, Yin Z, Zhou J, Yan H, Huang Y, Ye J, Huang H, Cheng C, Zhu S, Guo J, Xu X, Chen X. Yang Y, et al. Among authors: xu x. NPJ Genom Med. 2022 May 13;7(1):31. doi: 10.1038/s41525-022-00301-4. NPJ Genom Med. 2022. PMID: 35562572 Free PMC article.

2

A single cell level based method for copy number variation analysis by low coverage massively parallel sequencing.

Zhang C, Zhang C, Chen S, Yin X, Pan X, Lin G, Tan Y, Tan K, Xu Z, Hu P, Li X, Chen F, Xu X, Li Y, Zhang X, Jiang H, Wang W. Zhang C, et al. Among authors: xu x, xu z. PLoS One. 2013;8(1):e54236. doi: 10.1371/journal.pone.0054236. Epub 2013 Jan 23. PLoS One. 2013. PMID: 23372689 Free PMC article.

3

A method for noninvasive detection of fetal large deletions/duplications by low coverage massively parallel sequencing.

Chen S, Lau TK, Zhang C, Xu C, Xu Z, Hu P, Xu J, Huang H, Pan L, Jiang F, Chen F, Pan X, Xie W, Liu P, Li X, Zhang L, Li S, Li Y, Xu X, Wang W, Wang J, Jiang H, Zhang X. Chen S, et al. Among authors: xu c, xu x, xu z, xu j. Prenat Diagn. 2013 Jun;33(6):584-90. doi: 10.1002/pd.4110. Prenat Diagn. 2013. PMID: 23592436

4

Effective noninvasive zygosity determination by maternal plasma target region sequencing.

Zheng J, Xu C, Guo J, Wei Y, Ge H, Li X, Zhang C, Jiang H, Pan L, Tang W, Xie W, Zhang H, Zhao Y, Jiang F, Chen S, Wang W, Xu X, Chen F, Huang H, Jiang H. Zheng J, et al. Among authors: xu c, xu x. PLoS One. 2013 Jun 10;8(6):e65050. doi: 10.1371/journal.pone.0065050. Print 2013. PLoS One. 2013. PMID: 23762285 Free PMC article.

5

HIVID: an efficient method to detect HBV integration using low coverage sequencing.

Li W, Zeng X, Lee NP, Liu X, Chen S, Guo B, Yi S, Zhuang X, Chen F, Wang G, Poon RT, Fan ST, Mao M, Li Y, Li S, Wang J, Jianwang, Xu X, Jiang H, Zhang X. Li W, et al. Among authors: xu x. Genomics. 2013 Oct;102(4):338-44. doi: 10.1016/j.ygeno.2013.07.002. Epub 2013 Jul 15. Genomics. 2013. PMID: 23867110 Free article.

6

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: xu x, xu z. Gene. 2014 Jul 10;544(2):252-8. doi: 10.1016/j.gene.2014.04.055. Epub 2014 Apr 24. Gene. 2014. PMID: 24768736

7

Embryo genome profiling by single-cell sequencing for preimplantation genetic diagnosis in a β-thalassemia family.

Xu Y, Chen S, Yin X, Shen X, Pan X, Chen F, Jiang H, Liang Y, Wang W, Xu X, Wang J, Zhang X, Zhou C, Wang J. Xu Y, et al. Among authors: xu x. Clin Chem. 2015 Apr;61(4):617-26. doi: 10.1373/clinchem.2014.228569. Epub 2015 Feb 26. Clin Chem. 2015. PMID: 25722458

8

Genome-wide characteristics of de novo mutations in autism.

Yuen RK, Merico D, Cao H, Pellecchia G, Alipanahi B, Thiruvahindrapuram B, Tong X, Sun Y, Cao D, Zhang T, Wu X, Jin X, Zhou Z, Liu X, Nalpathamkalam T, Walker S, Howe JL, Wang Z, MacDonald JR, Chan A, D'Abate L, Deneault E, Siu MT, Tammimies K, Uddin M, Zarrei M, Wang M, Li Y, Wang J, Wang J, Yang H, Bookman M, Bingham J, Gross SS, Loy D, Pletcher M, Marshall CR, Anagnostou E, Zwaigenbaum L, Weksberg R, Fernandez BA, Roberts W, Szatmari P, Glazer D, Frey BJ, Ring RH, Xu X, Scherer SW. Yuen RK, et al. Among authors: xu x. NPJ Genom Med. 2016 Aug 3;1:160271-1602710. doi: 10.1038/npjgenmed.2016.27. NPJ Genom Med. 2016. PMID: 27525107 Free PMC article.

9

Isolation and whole genome sequencing of fetal cells from maternal blood towards the ultimate non-invasive prenatal testing.

Chen F, Liu P, Gu Y, Zhu Z, Nanisetti A, Lan Z, Huang Z, Liu JS, Kang X, Deng Y, Luo L, Jiang D, Qiu Y, Pan J, Xia J, Xiong K, Liu C, Xie L, Shi Q, Li J, Zhang X, Wang W, Drmanac S, Bolund L, Jiang H, Drmanac R, Xu X. Chen F, et al. Among authors: xu x. Prenat Diagn. 2017 Dec;37(13):1311-1321. doi: 10.1002/pd.5186. Prenat Diagn. 2017. PMID: 29144536 Clinical Trial.

10

Single-cell RNA-seq reveals dynamic transcriptome profiling in human early neural differentiation.

Shang Z, Chen D, Wang Q, Wang S, Deng Q, Wu L, Liu C, Ding X, Wang S, Zhong J, Zhang D, Cai X, Zhu S, Yang H, Liu L, Fink JL, Chen F, Liu X, Gao Z, Xu X. Shang Z, et al. Among authors: xu x. Gigascience. 2018 Nov 1;7(11):giy117. doi: 10.1093/gigascience/giy117. Gigascience. 2018. PMID: 30239706 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

54,219 results

Search Page