Xu C - Search Results

1

Chromosomal microarray analysis in fetuses with congenital anomalies of the kidney and urinary tract: A prospective cohort study and meta-analysis.

Li S, Han X, Wang Y, Chen S, Niu J, Qian Z, Li P, Jin L, Xu C. Li S, et al. Among authors: xu c. Prenat Diagn. 2019 Feb;39(3):165-174. doi: 10.1002/pd.5420. Epub 2019 Feb 7. Prenat Diagn. 2019. PMID: 30650192

2

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: xu c. Prenat Diagn. 2014 Apr;34(4):335-40. doi: 10.1002/pd.4303. Epub 2014 Feb 3. Prenat Diagn. 2014. PMID: 24357023

3

Clinical application of noninvasive prenatal testing for the detection of trisomies 21, 18, and 13: a hospital experience.

Zhou Q, Pan L, Chen S, Chen F, Hwang R, Yang X, Wang W, Jiang J, Xu J, Huang H, Xu C. Zhou Q, et al. Among authors: xu c, xu j. Prenat Diagn. 2014 Nov;34(11):1061-5. doi: 10.1002/pd.4428. Epub 2014 Jun 29. Prenat Diagn. 2014. PMID: 24899146

4

Identification of novel PKD1 and PKD2 mutations in a Chinese population with autosomal dominant polycystic kidney disease.

Liu B, Chen SC, Yang YM, Yan K, Qian YQ, Zhang JY, Hu YT, Dong MY, Jin F, Huang HF, Xu CM. Liu B, et al. Sci Rep. 2015 Dec 3;5:17468. doi: 10.1038/srep17468. Sci Rep. 2015. PMID: 26632257 Free PMC article.

5

Association between premature ovarian failure, polymorphisms in MTHFR and MTRR genes and serum homocysteine concentration.

Hou N, Chen S, Chen F, Jiang M, Zhang J, Yang Y, Zhu B, Bai X, Hu Y, Huang H, Xu C. Hou N, et al. Among authors: xu c. Reprod Biomed Online. 2016 Apr;32(4):407-13. doi: 10.1016/j.rbmo.2016.01.009. Epub 2016 Jan 29. Reprod Biomed Online. 2016. PMID: 26874989

6

Identification of PKD2 mutations in human preimplantation embryos in vitro using a combination of targeted next-generation sequencing and targeted haplotyping.

Chen SC, Xu XL, Zhang JY, Ding GL, Jin L, Liu B, Sun DM, Mei CL, Yang XN, Huang HF, Xu CM. Chen SC, et al. Sci Rep. 2016 May 6;6:25488. doi: 10.1038/srep25488. Sci Rep. 2016. PMID: 27150309 Free PMC article.

7

XCI-escaping gene KDM5C contributes to ovarian development via downregulating miR-320a.

Sun YX, Zhang YX, Zhang D, Xu CM, Chen SC, Zhang JY, Ruan YC, Chen F, Zhang RJ, Qian YQ, Liu YF, Jin LY, Yu TT, Xu HY, Luo YQ, Liu XM, Sun F, Sheng JZ, Huang HF. Sun YX, et al. Hum Genet. 2017 Feb;136(2):227-239. doi: 10.1007/s00439-016-1752-9. Epub 2016 Nov 28. Hum Genet. 2017. PMID: 27896428

8

A copy number variation genotyping method for aneuploidy detection in spontaneous abortion specimens.

Chen S, Liu D, Zhang J, Li S, Zhang L, Fan J, Luo Y, Qian Y, Huang H, Liu C, Zhu H, Jiang Z, Xu C. Chen S, et al. Among authors: xu c. Prenat Diagn. 2017 Feb;37(2):176-183. doi: 10.1002/pd.4986. Epub 2017 Jan 19. Prenat Diagn. 2017. PMID: 27977861

9

Prevalence of Prediabetes Risk in Offspring Born to Mothers with Hyperandrogenism.

Tian S, Lin XH, Xiong YM, Liu ME, Yu TT, Lv M, Zhao W, Xu GF, Ding GL, Xu CM, Jin M, Feng C, Wu YT, Tan YJ, Gao Q, Zhang J, Li C, Ren J, Jin LY, Chen B, Zhu H, Zhang XY, Chen SC, Liu XM, Liu Y, Zhang JY, Wang L, Zhang P, Chen XJ, Jin L, Chen X, Meng YC, Wu DD, Lin H, Yang Q, Zhou CL, Li XZ, Wang YY, Xiang YQ, Liu ZW, Gao L, Chen LT, Pan HJ, Li R, Zhang FH, Xing LF, Zhu YM, Klausen C, Leung PCK, Li JX, Sun F, Sheng JZ, Huang HF. Tian S, et al. Among authors: xu gf, xu cm. EBioMedicine. 2017 Feb;16:275-283. doi: 10.1016/j.ebiom.2017.01.011. Epub 2017 Jan 11. EBioMedicine. 2017. PMID: 28111236 Free PMC article.

10

Noninvasive Prenatal Screening of Fetal Aneuploidy without Massively Parallel Sequencing.

Xu C, Wang T, Liu C, Li H, Chen X, Zhu H, Chen S, Xin Q, Tao J, Huang L, Jiang Z. Xu C, et al. Clin Chem. 2017 Apr;63(4):861-869. doi: 10.1373/clinchem.2016.266247. Epub 2017 Feb 14. Clin Chem. 2017. PMID: 28196921

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