Liu P - Search Results

1

A method for noninvasive detection of fetal large deletions/duplications by low coverage massively parallel sequencing.

Chen S, Lau TK, Zhang C, Xu C, Xu Z, Hu P, Xu J, Huang H, Pan L, Jiang F, Chen F, Pan X, Xie W, Liu P, Li X, Zhang L, Li S, Li Y, Xu X, Wang W, Wang J, Jiang H, Zhang X. Chen S, et al. Among authors: liu p. Prenat Diagn. 2013 Jun;33(6):584-90. doi: 10.1002/pd.4110. Prenat Diagn. 2013. PMID: 23592436

2

Noninvasive prenatal testing for autosomal recessive conditions by maternal plasma sequencing in a case of congenital deafness.

Meng M, Li X, Ge H, Chen F, Han M, Zhang Y, Kang D, Xie W, Gao Z, Pan X, Dai P, Chi F, Chen S, Liu P, Zhang C, Cao J, Jiang H, Xu X, Wang W, Duan T. Meng M, et al. Among authors: liu p. Genet Med. 2014 Dec;16(12):972-6. doi: 10.1038/gim.2014.51. Epub 2014 May 15. Genet Med. 2014. PMID: 24830326 Free article.

3

Isolation and whole genome sequencing of fetal cells from maternal blood towards the ultimate non-invasive prenatal testing.

Chen F, Liu P, Gu Y, Zhu Z, Nanisetti A, Lan Z, Huang Z, Liu JS, Kang X, Deng Y, Luo L, Jiang D, Qiu Y, Pan J, Xia J, Xiong K, Liu C, Xie L, Shi Q, Li J, Zhang X, Wang W, Drmanac S, Bolund L, Jiang H, Drmanac R, Xu X. Chen F, et al. Among authors: liu c, liu js, liu p. Prenat Diagn. 2017 Dec;37(13):1311-1321. doi: 10.1002/pd.5186. Prenat Diagn. 2017. PMID: 29144536 Clinical Trial.

4

Haplotype-based approach for noninvasive prenatal tests of Duchenne muscular dystrophy using cell-free fetal DNA in maternal plasma.

Xu Y, Li X, Ge HJ, Xiao B, Zhang YY, Ying XM, Pan XY, Wang L, Xie WW, Ni L, Chen SP, Jiang WT, Liu P, Ye H, Cao Y, Zhang JM, Liu Y, Yang ZJ, Chen YW, Chen F, Jiang H, Ji X. Xu Y, et al. Among authors: liu y, liu p. Genet Med. 2015 Nov;17(11):889-96. doi: 10.1038/gim.2014.207. Epub 2015 Feb 5. Genet Med. 2015. PMID: 25654318 Free article.

5

An Advanced Model to Precisely Estimate the Cell-Free Fetal DNA Concentration in Maternal Plasma.

Kang X, Xia J, Wang Y, Xu H, Jiang H, Xie W, Chen F, Zeng P, Li X, Xie Y, Liu H, Huang G, Chen D, Liu P, Jiang H, Zhang X. Kang X, et al. Among authors: liu h, liu p. PLoS One. 2016 Sep 23;11(9):e0161928. doi: 10.1371/journal.pone.0161928. eCollection 2016. PLoS One. 2016. PMID: 27662469 Free PMC article.

6

A whole-genome sequencing-based novel preimplantation genetic testing method for de novo mutations combined with chromosomal balanced translocations.

Yuan P, Xia J, Ou S, Liu P, Du T, Zheng L, Yin X, Xie L, Zhang S, Yan H, Gao Y, Zhang Q, Jiang H, Chen F, Wang W. Yuan P, et al. Among authors: liu p. J Assist Reprod Genet. 2020 Oct;37(10):2525-2533. doi: 10.1007/s10815-020-01921-4. Epub 2020 Aug 11. J Assist Reprod Genet. 2020. PMID: 32783137 Free PMC article.

7

Non-targeted metabolomics and lipidomics LC-MS data from maternal plasma of 180 healthy pregnant women.

Luan H, Meng N, Liu P, Fu J, Chen X, Rao W, Jiang H, Xu X, Cai Z, Wang J. Luan H, et al. Among authors: liu p. Gigascience. 2015 Apr 9;4:16. doi: 10.1186/s13742-015-0054-9. eCollection 2015. Gigascience. 2015. PMID: 25859341 Free PMC article.

8

Pregnancy-induced metabolic phenotype variations in maternal plasma.

Luan H, Meng N, Liu P, Feng Q, Lin S, Fu J, Davidson R, Chen X, Rao W, Chen F, Jiang H, Xu X, Cai Z, Wang J. Luan H, et al. Among authors: liu p. J Proteome Res. 2014 Mar 7;13(3):1527-36. doi: 10.1021/pr401068k. Epub 2014 Jan 27. J Proteome Res. 2014. PMID: 24450375

9

Simultaneous detection of genomic imbalance in patients receiving preimplantation genetic testing for monogenic diseases (PGT-M).

Yang L, Xu Y, Xia J, Yan H, Ding C, Shi Q, Wu Y, Liu P, Pan J, Zeng Y, Zhang Y, Chen F, Jiang H, Xu Y, Li W, Zhou C, Gao Y. Yang L, et al. Among authors: liu p. Front Genet. 2022 Sep 29;13:976131. doi: 10.3389/fgene.2022.976131. eCollection 2022. Front Genet. 2022. PMID: 36246639 Free PMC article.

10

A novel method for noninvasive diagnosis of monogenic diseases from circulating fetal cells.

Chang L, Zhu X, Li R, Wu H, Chen W, Chen J, Liu H, Li S, Liu P. Chang L, et al. Among authors: liu h, liu p. Prenat Diagn. 2021 Mar;41(4):400-408. doi: 10.1002/pd.5796. Epub 2020 Nov 4. Prenat Diagn. 2021. PMID: 32673403

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