Tan Y - Search Results

1

A single cell level based method for copy number variation analysis by low coverage massively parallel sequencing.

Zhang C, Zhang C, Chen S, Yin X, Pan X, Lin G, Tan Y, Tan K, Xu Z, Hu P, Li X, Chen F, Xu X, Li Y, Zhang X, Jiang H, Wang W. Zhang C, et al. Among authors: tan y, tan k. PLoS One. 2013;8(1):e54236. doi: 10.1371/journal.pone.0054236. Epub 2013 Jan 23. PLoS One. 2013. PMID: 23372689 Free PMC article.

2

[Chromosome copy analysis by single-cell comparative genomic hybridization technique based on primer extension preamplification and degenerate oligonucleotide primed-PCR].

Tan K, Di YF, Cheng DH, Xu F, Lu GX, Tan YQ. Tan K, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010 Aug;27(4):387-92. doi: 10.3760/cma.j.issn.1003-9406.2010.04.006. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010. PMID: 20677142 Chinese.

3

Massively parallel sequencing for chromosomal abnormality testing in trophectoderm cells of human blastocysts.

Yin X, Tan K, Vajta G, Jiang H, Tan Y, Zhang C, Chen F, Chen S, Zhang C, Pan X, Gong C, Li X, Lin C, Gao Y, Liang Y, Yi X, Mu F, Zhao L, Peng H, Xiong B, Zhang S, Cheng D, Lu G, Zhang X, Lin G, Wang W. Yin X, et al. Among authors: tan y, tan k. Biol Reprod. 2013 Mar 21;88(3):69. doi: 10.1095/biolreprod.112.106211. Print 2013 Mar. Biol Reprod. 2013. PMID: 23349234

4

Rapid detection of aneuploidies on a benchtop sequencing platform.

Xie W, Tan Y, Li X, Lin G, Jiang H, Chen F, Zhang C, Gong F, Pan X, Chen S, Lu G, Wang W, Zhang X. Xie W, et al. Among authors: tan y. Prenat Diagn. 2013 Mar;33(3):232-7. doi: 10.1002/pd.4049. Epub 2013 Jan 28. Prenat Diagn. 2013. PMID: 23359364

5

[A de novo partial 5p deletion and cryptic 18p duplication detected by SNP-Array in a boy featuring Cri du Chat syndrome].

Hu JC, Tan K, Cheng DH, Li LY, Lu GX, Tan YQ. Hu JC, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013 Feb;30(1):87-90. doi: 10.3760/cma.j.issn.1003-9406.2013.01.021. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013. PMID: 23450488 Chinese.

6

Karyotype determination and reproductive guidance for short stature women with a hidden Y chromosome fragment.

Cheng DH, Gong F, Tan K, Lu CF, Lin G, Lu GX, Tan YQ. Cheng DH, et al. Reprod Biomed Online. 2013 Jul;27(1):89-95. doi: 10.1016/j.rbmo.2013.03.015. Epub 2013 Apr 6. Reprod Biomed Online. 2013. PMID: 23664816

7

Identification of proteins related to epigenetic regulation in the malignant transformation of aberrant karyotypic human embryonic stem cells by quantitative proteomics.

Sun Y, Yang Y, Zeng S, Tan Y, Lu G, Lin G. Sun Y, et al. Among authors: tan y. PLoS One. 2014 Jan 17;9(1):e85823. doi: 10.1371/journal.pone.0085823. eCollection 2014. PLoS One. 2014. PMID: 24465727 Free PMC article.

8

The first patient with a pure 1p36 microtriplication associated with severe clinical phenotypes.

Xu F, Zhang YN, Cheng DH, Tan K, Zhong CG, Lu GX, Lin G, Tan YQ. Xu F, et al. Mol Cytogenet. 2014 Oct 3;7(1):64. doi: 10.1186/s13039-014-0064-9. eCollection 2014. Mol Cytogenet. 2014. PMID: 25324898 Free PMC article.

9

Blastocysts can be rebiopsied for preimplantation genetic diagnosis and screening.

Zhang S, Tan K, Gong F, Gu Y, Tan Y, Lu C, Luo K, Lu G, Lin G. Zhang S, et al. Among authors: tan y, tan k. Fertil Steril. 2014 Dec;102(6):1641-5. doi: 10.1016/j.fertnstert.2014.09.018. Epub 2014 Oct 22. Fertil Steril. 2014. PMID: 25439805

10

Clinical outcome of preimplantation genetic diagnosis and screening using next generation sequencing.

Tan Y, Yin X, Zhang S, Jiang H, Tan K, Li J, Xiong B, Gong F, Zhang C, Pan X, Chen F, Chen S, Gong C, Lu C, Luo K, Gu Y, Zhang X, Wang W, Xu X, Vajta G, Bolund L, Yang H, Lu G, Du Y, Lin G. Tan Y, et al. Among authors: tan k. Gigascience. 2014 Dec 4;3(1):30. doi: 10.1186/2047-217X-3-30. eCollection 2014. Gigascience. 2014. PMID: 25685330 Free PMC article.

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