Xu CM - Search Results

1

Associations of Sperm mtDNA Copy Number, DNA Fragmentation Index, and Reactive Oxygen Species With Clinical Outcomes in ART Treatments.

Shi WH, Ye MJ, Qin NX, Zhou ZY, Zhou XY, Xu NX, Chen SC, Li SY, Xu CM. Shi WH, et al. Among authors: xu nx, xu cm. Front Endocrinol (Lausanne). 2022 Mar 23;13:849534. doi: 10.3389/fendo.2022.849534. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 35399940 Free PMC article.

2

Different segregation patterns in five carriers due to a pericentric inversion of chromosome 1.

Luo Y, Xu C, Sun Y, Wang L, Chen S, Jin F. Luo Y, et al. Syst Biol Reprod Med. 2014 Dec;60(6):367-72. doi: 10.3109/19396368.2014.948580. Epub 2014 Aug 6. Syst Biol Reprod Med. 2014. PMID: 25096371

3

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. Among authors: xu cm. Sci Rep. 2015 Dec 3;5:17468. doi: 10.1038/srep17468. Sci Rep. 2015. PMID: 26632257 Free PMC article.

4

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. 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

5

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. Among authors: xu xl, xu cm. Sci Rep. 2016 May 6;6:25488. doi: 10.1038/srep25488. Sci Rep. 2016. PMID: 27150309 Free PMC article.

6

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. Among authors: xu hy, xu cm. Hum Genet. 2017 Feb;136(2):227-239. doi: 10.1007/s00439-016-1752-9. Epub 2016 Nov 28. Hum Genet. 2017. PMID: 27896428

7

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. Prenat Diagn. 2017 Feb;37(2):176-183. doi: 10.1002/pd.4986. Epub 2017 Jan 19. Prenat Diagn. 2017. PMID: 27977861

8

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.

9

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

10

Targeted sequencing identifies a novel SH2D1A pathogenic variant in a Chinese family: Carrier screening and prenatal genetic testing.

Zhang JY, Chen SC, Chen YY, Li SY, Zhang LL, Shen YH, Chang CX, Xiang YQ, Huang HF, Xu CM. Zhang JY, et al. Among authors: xu cm. PLoS One. 2017 Feb 23;12(2):e0172173. doi: 10.1371/journal.pone.0172173. eCollection 2017. PLoS One. 2017. PMID: 28231257 Free PMC article.

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