Zhengfeng Xu[Author] - Search Results

Year	Number of Results
2003	1
2004	3
2006	3
2007	2
2008	4
2009	3
2010	1
2011	5
2012	7
2013	10
2014	7
2015	6
2016	7
2017	7
2018	13
2019	11
2020	9
2021	15
2022	16
2023	15
2024	18
2025	4

1

Transcriptomic Profiling of Human Placenta in Gestational Diabetes Mellitus at the Single-Cell Level.

Yang Y, Guo F, Peng Y, Chen R, Zhou W, Wang H, OuYang J, Yu B, Xu Z. Yang Y, et al. Among authors: xu z. Front Endocrinol (Lausanne). 2021 May 7;12:679582. doi: 10.3389/fendo.2021.679582. eCollection 2021. Front Endocrinol (Lausanne). 2021. PMID: 34025588 Free PMC article.

2

Whole genome sequencing vs chromosomal microarray analysis in prenatal diagnosis.

Hu P, Zhang Q, Cheng Q, Luo C, Zhang C, Zhou R, Meng L, Huang M, Wang Y, Wang Y, Qiao F, Xu Z. Hu P, et al. Among authors: xu z. Am J Obstet Gynecol. 2023 Sep;229(3):302.e1-302.e18. doi: 10.1016/j.ajog.2023.03.005. Epub 2023 Mar 11. Am J Obstet Gynecol. 2023. PMID: 36907537

3

Comprehensive genetic analysis of facioscapulohumeral muscular dystrophy by Nanopore long-read whole-genome sequencing.

Huang M, Zhang Q, Jiao J, Shi J, Xu Y, Zhang C, Zhou R, Liu W, Liang Y, Chen H, Wang Y, Xu Z, Hu P. Huang M, et al. Among authors: xu z. J Transl Med. 2024 May 13;22(1):451. doi: 10.1186/s12967-024-05259-8. J Transl Med. 2024. PMID: 38741136 Free PMC article.

4

Copy number variations and fetal ventriculomegaly.

Wang Y, Hu P, Xu Z. Wang Y, et al. Among authors: xu z. Curr Opin Obstet Gynecol. 2018 Apr;30(2):104-110. doi: 10.1097/GCO.0000000000000439. Curr Opin Obstet Gynecol. 2018. PMID: 29356709 Review.

5

A new strategy for prenatal genetic screening of copy number variations in the DMD gene: A large cohort study based on NIPT analysis.

Wang Y, Sun Y, Meng L, He Q, Zhao J, Zhou R, Wang Z, Tan J, Ma D, Fan L, Chen Y, Wang Y, Jiang Z, Qiao Z, Wu X, Shao B, Xue Y, Song L, Wang T, Hu P, Xu Z. Wang Y, et al. Among authors: xu z. Clin Transl Med. 2024 May;14(5):e1706. doi: 10.1002/ctm2.1706. Clin Transl Med. 2024. PMID: 38797938 Free PMC article. No abstract available.

6

DNA sequencing versus standard prenatal aneuploidy screening.

Liao C, Zhengfeng X, Zhang K. Liao C, et al. Among authors: zhengfeng x. N Engl J Med. 2014 Aug 7;371(6):577-8. doi: 10.1056/NEJMc1405486. N Engl J Med. 2014. PMID: 25099588 No abstract available.

7

Application of next generation sequencing in the screening of monogenic diseases in China, 2021: a consensus among Chinese newborn screening experts.

Tong F, Wang J, Xiao R, Wu BB, Zou CC, Wu DW, Wang H, Zou H, Han LS, Yang L, Zou L, Hei MY, Yang RL, Yuan TM, Wen W, Huang XW, Gu XF, Yang YL, Huang YL, Zhang YJ, Yu YG, Xu ZF, Zhou WH, Zhao ZY. Tong F, et al. World J Pediatr. 2022 Apr;18(4):235-242. doi: 10.1007/s12519-022-00522-8. Epub 2022 Mar 15. World J Pediatr. 2022. PMID: 35292922 No abstract available.

8

Cadherin-18 loss in prospermatogonia and spermatogonial stem cells enhances cell adhesion through a compensatory mechanism.

Li XX, Zhang DC, Wang Y, Wen J, Wang XJ, Cao YL, Jiang R, Li JR, Li YN, Liu HH, Xie WH, Xu ZF, Hu P, Zou K. Li XX, et al. Zool Res. 2024 Sep 18;45(5):1048-1060. doi: 10.24272/j.issn.2095-8137.2023.373. Zool Res. 2024. PMID: 39147719 Free PMC article.

9

Correction of a homoplasmic mitochondrial tRNA mutation in patient-derived iPSCs via a mitochondrial base editor.

Chen X, Chen M, Zhu Y, Sun H, Wang Y, Xie Y, Ji L, Wang C, Hu Z, Guo X, Xu Z, Zhang J, Yang S, Liang D, Shen B. Chen X, et al. Among authors: xu z. Commun Biol. 2023 Nov 3;6(1):1116. doi: 10.1038/s42003-023-05500-y. Commun Biol. 2023. PMID: 37923818 Free PMC article.

10

Application of next-generation sequencing for the diagnosis of fetuses with congenital heart defects.

Qiao F, Hu P, Xu Z. Qiao F, et al. Among authors: xu z. Curr Opin Obstet Gynecol. 2019 Apr;31(2):132-138. doi: 10.1097/GCO.0000000000000520. Curr Opin Obstet Gynecol. 2019. PMID: 30608255 Review.

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