Wu Y - Search Results

1

Genome-wide copy number variant analysis for congenital ventricular septal defects in Chinese Han population.

An Y, Duan W, Huang G, Chen X, Li L, Nie C, Hou J, Gui Y, Wu Y, Zhang F, Shen Y, Wu B, Wang H. An Y, et al. Among authors: wu y, wu b. BMC Med Genomics. 2016 Jan 8;9:2. doi: 10.1186/s12920-015-0163-4. BMC Med Genomics. 2016. PMID: 26742958 Free PMC article.

2

Analysis of CGG repeats in FMR1 in Chinese women with idiopathic premature ovarian failure.

Ye Y, Lan X, Cong J, Li N, Wu Y, Zhang M, Liu J, Cui Y, Wu BL, An Y, Wu J. Ye Y, et al. Among authors: wu y, wu bl, wu j. Reprod Biomed Online. 2014 Sep;29(3):382-7. doi: 10.1016/j.rbmo.2014.05.004. Epub 2014 May 15. Reprod Biomed Online. 2014. PMID: 24912415

3

Genetic architecture, epigenetic influence and environment exposure in the pathogenesis of Autism.

Yu L, Wu Y, Wu BL. Yu L, et al. Among authors: wu y, wu bl. Sci China Life Sci. 2015 Oct;58(10):958-67. doi: 10.1007/s11427-015-4941-1. Sci China Life Sci. 2015. PMID: 26490976 Review.

4

Developing a one-step triplet-repeat primed PCR assay for diagnosing myotonic dystrophy.

Lan X, Li N, Wan H, Luo L, Wu Y, Li S, An Y, Wu BL. Lan X, et al. Among authors: wu y, wu bl. J Genet Genomics. 2018 Oct 20;45(10):549-552. doi: 10.1016/j.jgg.2018.06.008. Epub 2018 Sep 8. J Genet Genomics. 2018. PMID: 30297192 No abstract available.

5

LHCGR and ALMS1 defects likely cooperate in the development of polycystic ovary syndrome indicated by double-mutant mice.

Yu L, Wang L, Tao W, Zhang W, Yang S, Wang J, Fei J, Peng R, Wu Y, Zhen X, Shao H, Gu W, Li R, Wu BL, Wang H. Yu L, et al. Among authors: wu y, wu bl. J Genet Genomics. 2021 May 20;48(5):384-395. doi: 10.1016/j.jgg.2021.03.014. Epub 2021 May 1. J Genet Genomics. 2021. PMID: 34147365

6

Integrative preimplantation genetic testing analysis for a Chinese family with hereditary spherocytosis caused by a novel splicing variant of SPTB.

Tian Y, Wang Y, Yang J, Gao P, Xu H, Wu Y, Li M, Chen H, Lu D, Yan H. Tian Y, et al. Among authors: wu y. Front Genet. 2023 Sep 18;14:1221853. doi: 10.3389/fgene.2023.1221853. eCollection 2023. Front Genet. 2023. PMID: 37795245 Free PMC article.

7

Study on the prevention of infection in terminal cancer patients applying epidural analgesia by adding cefazolin to anesthetics: a randomized controlled trial.

Xie P, Li Z, Yang J, Wu Y. Xie P, et al. Among authors: wu y. Jpn J Clin Oncol. 2020 Aug 4;50(8):867-872. doi: 10.1093/jjco/hyaa060. Jpn J Clin Oncol. 2020. PMID: 32409838 Clinical Trial.

8

A feasibility study of noninvasive prenatal diagnosis in facioscapulohumeral muscular dystrophy type 1 in a Chinese family.

Qin Y, Xu H, Yang J, Wu Y, Li H, Wang B, Liu L, Ren D, Xu R, Li M, Zhang C, Song J. Qin Y, et al. Among authors: wu y. Front Genet. 2022 Oct 25;13:1046096. doi: 10.3389/fgene.2022.1046096. eCollection 2022. Front Genet. 2022. PMID: 36386852 Free PMC article.

9

Insight of novel biomarkers for papillary thyroid carcinoma through multiomics.

Liu W, Zhu J, Wu Z, Yin Y, Wu Q, Wu Y, Zheng J, Wang C, Chen H, Qazi TJ, Wu J, Zhang Y, Liu H, Yang J, Lu D, Zhang X, Ai Z. Liu W, et al. Among authors: wu y, wu q, wu z, wu j. Front Oncol. 2023 Sep 19;13:1269751. doi: 10.3389/fonc.2023.1269751. eCollection 2023. Front Oncol. 2023. PMID: 37795451 Free PMC article.

10

A novel noninvasive prenatal testing method for chromosomal rearrangements using maternal circulating cell-free foetal DNA.

Zhang S, Pei Z, Lei C, Bai Y, Wu J, Xiao M, Zhou J, Hu B, Chen S, Wu Y, Yang J, Sun X, Lu D, Xu C, Xu C. Zhang S, et al. Among authors: wu y, wu j. Clin Transl Med. 2023 Jan;13(1):e1160. doi: 10.1002/ctm2.1160. Clin Transl Med. 2023. PMID: 36610059 Free PMC article. No abstract available.

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