Ou X - Search Results

1

Mosaic duplication of 8q24.1q24.3 detected by chromosomal microarray but not karyotyping in two unrelated fetuses with cardiac defects.

Lin S, Huang S, Ou X, Gu H, Wang Y, Li P, Zhou Y. Lin S, et al. Among authors: ou x. Mol Cytogenet. 2021 May 18;14(1):26. doi: 10.1186/s13039-021-00544-3. Mol Cytogenet. 2021. PMID: 34006293 Free PMC article.

2

Noninvasive fetal genotyping of paternally inherited alleles using targeted massively parallel sequencing in parentage testing cases.

Yang D, Liang H, Gao Y, Lin S, He Z, Gao J, Sun H, Li Q, Ma X, Ou X. Yang D, et al. Among authors: ou x. Transfusion. 2017 Jun;57(6):1505-1514. doi: 10.1111/trf.14077. Epub 2017 Mar 10. Transfusion. 2017. PMID: 28295384

3

An SNP panel for the analysis of paternally inherited alleles in maternal plasma using ion Torrent PGM.

Yang D, Liang H, Lin S, Li Q, Ma X, Gao J, Sun H, Chen Q, Wu J, Ou X. Yang D, et al. Among authors: ou x. Int J Legal Med. 2018 Mar;132(2):343-352. doi: 10.1007/s00414-017-1594-6. Epub 2017 Apr 20. Int J Legal Med. 2018. PMID: 28429088

4

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: ou x. Transfusion. 2018 Jul;58(7):1792-1799. doi: 10.1111/trf.14577. Epub 2018 Mar 13. Transfusion. 2018. PMID: 29536546

5

A microhap panel for kinship analysis through massively parallel sequencing technology.

Qu N, Lin S, Gao Y, Liang H, Zhao H, Ou X. Qu N, et al. Among authors: ou x. Electrophoresis. 2020 Feb;41(3-4):246-253. doi: 10.1002/elps.201900337. Epub 2019 Dec 19. Electrophoresis. 2020. PMID: 31816113

6

Noninvasive prenatal paternity testing by maternal plasma DNA sequencing in twin pregnancies.

Xie Y, Qu N, Lin S, Jiang H, Zhang Y, Zhang X, Liang H, Chen F, Ou X. Xie Y, et al. Among authors: ou x. Electrophoresis. 2020 Jun;41(12):1095-1102. doi: 10.1002/elps.202000036. Epub 2020 May 14. Electrophoresis. 2020. PMID: 32249439

7

Evaluation of a Microhaplotype-Based Noninvasive Prenatal Test in Twin Gestations: Determination of Paternity, Zygosity, and Fetal Fraction.

Bai Z, Zhao H, Lin S, Huang L, He Z, Wang H, Ou X. Bai Z, et al. Among authors: ou x. Genes (Basel). 2020 Dec 27;12(1):26. doi: 10.3390/genes12010026. Genes (Basel). 2020. PMID: 33375453 Free PMC article.

8

Application of SNPs with low minor allele frequencies in missing person identification (MPI) through kinship analysis of DNA mixtures.

Zhang N, Shi S, Lin S, Bai Z, Ling X, Gao J, Yan R, Ou X. Zhang N, et al. Among authors: ou x. Electrophoresis. 2023 Oct;44(19-20):1569-1578. doi: 10.1002/elps.202300111. Epub 2023 Jul 16. Electrophoresis. 2023. PMID: 37454302

9

Null alleles of the X and Y chromosomal amelogenin gene in a Chinese population.

Ou X, Chen W, Chen H, Zhao F, Zheng J, Tong D, Chen Y, Chen A, Sun H. Ou X, et al. Int J Legal Med. 2012 Jul;126(4):513-8. doi: 10.1007/s00414-011-0594-1. Epub 2011 Jul 7. Int J Legal Med. 2012. PMID: 21735294

10

Complete paternal uniparental isodisomy for Chromosome 2 revealed in a parentage testing case.

Ou X, Liu C, Chen S, Yu J, Zhang Y, Liu S, Sun H. Ou X, et al. Transfusion. 2013 Jun;53(6):1266-9. doi: 10.1111/j.1537-2995.2012.03863.x. Epub 2012 Aug 23. Transfusion. 2013. PMID: 22924962

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