Zhou X - Search Results

1

Analysis of complex chromosomal rearrangement involving chromosome 6 via the integration of optical genomic mapping and molecular cytogenetic methodologies.

Hao N, Lou H, Li M, Zhang H, Chang J, Qi Q, Zhou X, Bai J, Guo J, Wang Y, Zhang Y, Jiang Y. Hao N, et al. Among authors: zhou x. J Hum Genet. 2024 Jan;69(1):3-11. doi: 10.1038/s10038-023-01197-3. Epub 2023 Oct 11. J Hum Genet. 2024. PMID: 37821671

2

A rare de novo duplication of chromosome 21q22.12 → q22.3 with other concomitant deletion and duplication of small fragments in 21q associated with Down syndrome: Prenatal diagnosis, molecular cytogenetic characterization.

Qi Q, Zhou X, Jiang Y, Hao N, Zhou J, Zhang L. Qi Q, et al. Among authors: zhou x, zhou j. Mol Cytogenet. 2013 Mar 6;6(1):11. doi: 10.1186/1755-8166-6-11. Mol Cytogenet. 2013. PMID: 23497671 Free PMC article.

3

Genetic counseling, prenatal screening and diagnosis of Down syndrome in the second trimester in women of advanced maternal age: a prospective study.

Qi QW, Jiang YL, Zhou XY, Liu JT, Yin J, Bian XM. Qi QW, et al. Chin Med J (Engl). 2013;126(11):2007-10. Chin Med J (Engl). 2013. PMID: 23769548

4

[Value of second trimester maternal serum sFlt-1, PlGF and their ratio in the prediction of preeclampsia].

Gao J, Shen J, Jiang Y, Zhou X, Qi H, Liu X, Liu J, Yang J, Bian X. Gao J, et al. Among authors: zhou x. Zhonghua Fu Chan Ke Za Zhi. 2014 Jan;49(1):22-5. Zhonghua Fu Chan Ke Za Zhi. 2014. PMID: 24694913 Chinese.

5

Quantitation of fetal DNA fraction in maternal plasma using circulating single molecule amplification and re-sequencing technology (cSMART).

Song Y, Zhou X, Huang S, Li X, Qi Q, Jiang Y, Liu Y, Ma C, Li Z, Xu M, Cram DS, Liu J. Song Y, et al. Among authors: zhou x. Clin Chim Acta. 2016 May 1;456:151-156. doi: 10.1016/j.cca.2016.03.005. Epub 2016 Mar 15. Clin Chim Acta. 2016. PMID: 26993877

6

Copy number variation sequencing-based prenatal diagnosis using cell-free fetal DNA in amniotic fluid.

Qi Q, Lu S, Zhou X, Yao F, Hao N, Yin G, Li W, Bai J, Li N, Cram DS. Qi Q, et al. Among authors: zhou x. Prenat Diagn. 2016 Jun;36(6):576-83. doi: 10.1002/pd.4830. Epub 2016 May 17. Prenat Diagn. 2016. PMID: 27084671

7

Contribution of maternal copy number variations to false-positive fetal trisomies detected by noninvasive prenatal testing.

Zhou X, Sui L, Xu Y, Song Y, Qi Q, Zhang J, Zhu H, Sun H, Tian F, Xu M, Cram DS, Liu J. Zhou X, et al. Prenat Diagn. 2017 Apr;37(4):318-322. doi: 10.1002/pd.5014. Epub 2017 Feb 24. Prenat Diagn. 2017. PMID: 28152582

8

Pregnancy Combined with Epilepsy and Cerebral Cavernous Malformation.

Xu YL, Liu JT, Song YJ, Zhou XY, Qi QW, Bian XM, Xu ZQ, Li L. Xu YL, et al. Chin Med J (Engl). 2017 Mar 5;130(5):619-620. doi: 10.4103/0366-6999.200533. Chin Med J (Engl). 2017. PMID: 28229997 Free PMC article. No abstract available.

9

High levels of circulating cell-free DNA are a biomarker of active SLE.

Xu Y, Song Y, Chang J, Zhou X, Qi Q, Tian X, Li M, Zeng X, Xu M, Zhang W, Cram DS, Liu J. Xu Y, et al. Among authors: zhou x. Eur J Clin Invest. 2018 Nov;48(11):e13015. doi: 10.1111/eci.13015. Epub 2018 Aug 23. Eur J Clin Invest. 2018. PMID: 30079480

10

Simultaneous Detection of CNVs and SNVs Improves the Diagnostic Yield of Fetuses with Ultrasound Anomalies and Normal Karyotypes.

Qi Q, Jiang Y, Zhou X, Meng H, Hao N, Chang J, Bai J, Wang C, Wang M, Guo J, Ouyang Y, Xu Z, Xiao M, Zhang VW, Liu J. Qi Q, et al. Among authors: zhou x. Genes (Basel). 2020 Nov 25;11(12):1397. doi: 10.3390/genes11121397. Genes (Basel). 2020. PMID: 33255631 Free PMC article.

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