Kuo Y - Search Results

1

A novel pathogenic mutation in FBN2 associated with congenital contractural arachnodactyly for preimplantation genetic diagnosis.

Li J, Wang Y, Zhu X, Nie Y, Kuo Y, Guan S, Huang J, Lian Y, Zhao Y, Li R, Wei Y, Qiao J, Yan L. Li J, et al. Among authors: kuo y. J Genet Genomics. 2020 May 20;47(5):281-284. doi: 10.1016/j.jgg.2020.03.007. Epub 2020 May 8. J Genet Genomics. 2020. PMID: 32747207 No abstract available.

2

Identifying normal embryos from reciprocal translocation carriers by whole chromosome haplotyping.

Yan Z, Wang Y, Nie Y, Zhi X, Zhu X, Qin M, Guan S, Ren Y, Kuo Y, Chang D, Chen W, Yuan P, Yan L, Qiao J. Yan Z, et al. Among authors: kuo y. J Genet Genomics. 2018 Sep 20;45(9):505-508. doi: 10.1016/j.jgg.2018.05.006. Epub 2018 Jul 11. J Genet Genomics. 2018. PMID: 30287172 No abstract available.

3

Genetic testing and PGD for unexplained recurrent fetal malformations with MAGEL2 gene mutation.

Guo W, Nie Y, Yan Z, Zhu X, Wang Y, Guan S, Kuo Y, Zhang W, Zhi X, Wei Y, Yan L, Qiao J. Guo W, et al. Among authors: kuo y. Sci China Life Sci. 2019 Jul;62(7):886-894. doi: 10.1007/s11427-019-9541-0. Epub 2019 May 30. Sci China Life Sci. 2019. PMID: 31152388

4

Trio-whole-exome sequencing and preimplantation genetic diagnosis for unexplained recurrent fetal malformations.

Guo W, Lai Y, Yan Z, Wang Y, Nie Y, Guan S, Kuo Y, Zhang W, Zhu X, Peng M, Zhi X, Wei Y, Yan L, Qiao J. Guo W, et al. Among authors: kuo y. Hum Mutat. 2020 Feb;41(2):432-448. doi: 10.1002/humu.23935. Epub 2019 Nov 11. Hum Mutat. 2020. PMID: 31680349

5

scHaplotyper: haplotype construction and visualization for genetic diagnosis using single cell DNA sequencing data.

Yan Z, Zhu X, Wang Y, Nie Y, Guan S, Kuo Y, Chang D, Li R, Qiao J, Yan L. Yan Z, et al. Among authors: kuo y. BMC Bioinformatics. 2020 Feb 1;21(1):41. doi: 10.1186/s12859-020-3381-5. BMC Bioinformatics. 2020. PMID: 32007105 Free PMC article.

6

Novel PGD strategy based on single sperm linkage analysis for carriers of single gene pathogenic variant and chromosome reciprocal translocation.

Wang Y, Zhu X, Yan Z, Zhi X, Guan S, Kuo Y, Nie Y, Lian Y, Huang J, Wei Y, Liu P, Li R, Qiao J, Yan L. Wang Y, et al. Among authors: kuo y. J Assist Reprod Genet. 2020 May;37(5):1239-1250. doi: 10.1007/s10815-020-01753-2. Epub 2020 Apr 29. J Assist Reprod Genet. 2020. PMID: 32350783 Free PMC article.

7

A strategy using SNP linkage analysis for monogenic diseases PGD combined with HLA typing.

Wang Y, Qin M, Yan Z, Guan S, Kuo Y, Kong S, Nie Y, Zhu X, Zhi X, Qiao J, Yan L. Wang Y, et al. Among authors: kuo y. Clin Genet. 2020 Aug;98(2):138-146. doi: 10.1111/cge.13770. Epub 2020 May 25. Clin Genet. 2020. PMID: 32378203

8

Single-cell DNA methylation sequencing reveals epigenetic alterations in mouse oocytes superovulated with different dosages of gonadotropins.

Huo Y, Yan ZQ, Yuan P, Qin M, Kuo Y, Li R, Yan LY, Feng HL, Qiao J. Huo Y, et al. Among authors: kuo y. Clin Epigenetics. 2020 Jun 1;12(1):75. doi: 10.1186/s13148-020-00866-w. Clin Epigenetics. 2020. PMID: 32487258 Free PMC article.

9

Effects of oocyte vitrification on the behaviors and physiological indexes of aged first filial generation mice.

Huo Y, Qin Q, Zhang L, Kuo Y, Wang H, Yan L, Li R, Zhang X, Yan J, Qiao J. Huo Y, et al. Among authors: kuo y. Cryobiology. 2020 Aug;95:20-28. doi: 10.1016/j.cryobiol.2020.06.012. Epub 2020 Jun 26. Cryobiology. 2020. PMID: 32598946 Free article.

10

Clinical application of an NGS-based method in the preimplantation genetic testing for Duchenne muscular dystrophy.

Ren Y, Lian Y, Yan Z, Zhai F, Yang M, Zhu X, Wang Y, Nie Y, Guan S, Kuo Y, Huang J, Shi X, Jia J, Qiao J, Yan L. Ren Y, et al. Among authors: kuo y. J Assist Reprod Genet. 2021 Aug;38(8):1979-1986. doi: 10.1007/s10815-021-02126-z. Epub 2021 Mar 15. J Assist Reprod Genet. 2021. PMID: 33719023 Free PMC article.

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