Chen F - Search Results

1

Noninvasive prenatal paternity testing using targeted massively parallel sequencing.

Qu N, Xie Y, Li H, Liang H, Lin S, Huang E, Gao J, Chen F, Shi Y, Ou X. Qu N, et al. Among authors: chen f. Transfusion. 2018 Jul;58(7):1792-1799. doi: 10.1111/trf.14577. Epub 2018 Mar 13. Transfusion. 2018. PMID: 29536546

2

Transcriptome and network changes in climbers at extreme altitudes.

Chen F, Zhang W, Liang Y, Huang J, Li K, Green CD, Liu J, Zhang G, Zhou B, Yi X, Wang W, Liu H, Xu X, Shen F, Qu N, Wang Y, Gao G, San A, JiangBai L, Sang H, Fang X, Kristiansen K, Yang H, Wang J, Han JD, Wang J. Chen F, et al. PLoS One. 2012;7(2):e31645. doi: 10.1371/journal.pone.0031645. Epub 2012 Feb 29. PLoS One. 2012. PMID: 22393366 Free PMC article.

3

Clinical application of massively parallel sequencing-based prenatal noninvasive fetal trisomy test for trisomies 21 and 18 in 11,105 pregnancies with mixed risk factors.

Dan S, Wang W, Ren J, Li Y, Hu H, Xu Z, Lau TK, Xie J, Zhao W, Huang H, Xie J, Sun L, Zhang X, Wang W, Liao S, Qiang R, Cao J, Zhang Q, Zhou Y, Zhu H, Zhong M, Guo Y, Lin L, Gao Z, Yao H, Zhang H, Zhao L, Jiang F, Chen F, Jiang H, Li S, Li Y, Wang J, Wang J, Duan T, Su Y, Zhang X. Dan S, et al. Among authors: chen f. Prenat Diagn. 2012 Dec;32(13):1225-32. doi: 10.1002/pd.4002. Epub 2012 Nov 9. Prenat Diagn. 2012. PMID: 23138752 Clinical Trial.

4

Massively parallel sequencing for chromosomal abnormality testing in trophectoderm cells of human blastocysts.

Yin X, Tan K, Vajta G, Jiang H, Tan Y, Zhang C, Chen F, Chen S, Zhang C, Pan X, Gong C, Li X, Lin C, Gao Y, Liang Y, Yi X, Mu F, Zhao L, Peng H, Xiong B, Zhang S, Cheng D, Lu G, Zhang X, Lin G, Wang W. Yin X, et al. Among authors: chen s, chen f. Biol Reprod. 2013 Mar 21;88(3):69. doi: 10.1095/biolreprod.112.106211. Print 2013 Mar. Biol Reprod. 2013. PMID: 23349234

5

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: chen s, chen f. PLoS One. 2013;8(1):e54236. doi: 10.1371/journal.pone.0054236. Epub 2013 Jan 23. PLoS One. 2013. PMID: 23372689 Free PMC article.

6

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: chen f. Prenat Diagn. 2013 Jun;33(6):584-90. doi: 10.1002/pd.4110. Prenat Diagn. 2013. PMID: 23592436

7

Noninvasive prenatal detection for pathogenic CNVs: the application in α-thalassemia.

Ge H, Huang X, Li X, Chen S, Zheng J, Jiang H, Zhang C, Pan X, Guo J, Chen F, Chen N, Fang Q, Jiang H, Wang W. Ge H, et al. Among authors: chen n, chen s, chen f. PLoS One. 2013 Jun 28;8(6):e67464. doi: 10.1371/journal.pone.0067464. Print 2013. PLoS One. 2013. PMID: 23840709 Free PMC article.

8

Noninvasive prenatal testing of trisomies 21 and 18 by massively parallel sequencing of maternal plasma DNA in twin pregnancies.

Huang X, Zheng J, Chen M, Zhao Y, Zhang C, Liu L, Xie W, Shi S, Wei Y, Lei D, Xu C, Wu Q, Guo X, Shi X, Zhou Y, Liu Q, Gao Y, Jiang F, Zhang H, Su F, Ge H, Li X, Pan X, Chen S, Chen F, Fang Q, Jiang H, Lau TK, Wang W. Huang X, et al. Among authors: chen m, chen s, chen f. Prenat Diagn. 2014 Apr;34(4):335-40. doi: 10.1002/pd.4303. Epub 2014 Feb 3. Prenat Diagn. 2014. PMID: 24357023

9

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: chen m, chen s, chen f. Gene. 2014 Jul 10;544(2):252-8. doi: 10.1016/j.gene.2014.04.055. Epub 2014 Apr 24. Gene. 2014. PMID: 24768736

10

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: chen s, chen f. 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.

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 Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

26,982 results

Search Page

Filters