Chen W - Search Results

1

Non-pathological complete paternal uniparental isodisomy of chromosome 2 revealed in a maternity testing case.

Chen M, Jiang J, Li C, Ren H, Chen W, Liu Z, Cheng F, Zhao J, Chen T, Chen C, Yan J. Chen M, et al. Among authors: chen c, chen t, chen w. Int J Legal Med. 2019 Jul;133(4):993-997. doi: 10.1007/s00414-018-1857-x. Epub 2018 May 25. Int J Legal Med. 2019. PMID: 29802460

2

Concurrent copy number variations on chromosome 8 and 22 combined with mutation at FGA locus revealed in a parentage testing case.

Yang Y, Ren H, Chen W, Xie B, Wang Y, Shi Y, Chen C, Li C, Yi L, Fang X, Yan J. Yang Y, et al. Among authors: chen c, chen w. Forensic Sci Int Genet. 2015 Nov;19:81-85. doi: 10.1016/j.fsigen.2015.07.002. Epub 2015 Jul 8. Forensic Sci Int Genet. 2015. PMID: 26186693

3

Genetic variants of TREML2 are associated with HLA-B27-positive ankylosing spondylitis.

Feng Y, Hong Y, Zhang X, Cao C, Yang X, Lai S, Fan C, Cheng F, Yan M, Li C, Huang W, Chen W, Zhu P, Zeng C. Feng Y, et al. Among authors: chen w. Gene. 2018 Aug 20;668:121-128. doi: 10.1016/j.gene.2018.05.057. Epub 2018 May 17. Gene. 2018. PMID: 29778423

4

Four-Generation Pedigree of Monozygotic Female Twins Reveals Genetic Factors in Twinning Process by Whole-Genome Sequencing.

Liu S, Hong Y, Cui K, Guan J, Han L, Chen W, Xu Z, Gong K, Ou Y, Zeng C, Li S, Zhang D, Hu D. Liu S, et al. Among authors: chen w. Twin Res Hum Genet. 2018 Oct;21(5):361-368. doi: 10.1017/thg.2018.41. Epub 2018 Aug 1. Twin Res Hum Genet. 2018. PMID: 30064533

5

Whole Genome Analyses of Chinese Population and De Novo Assembly of A Northern Han Genome.

Du Z, Ma L, Qu H, Chen W, Zhang B, Lu X, Zhai W, Sheng X, Sun Y, Li W, Lei M, Qi Q, Yuan N, Shi S, Zeng J, Wang J, Yang Y, Liu Q, Hong Y, Dong L, Zhang Z, Zou D, Wang Y, Song S, Liu F, Fang X, Chen H, Liu X, Xiao J, Zeng C. Du Z, et al. Among authors: chen w, chen h. Genomics Proteomics Bioinformatics. 2019 Jun;17(3):229-247. doi: 10.1016/j.gpb.2019.07.002. Epub 2019 Sep 5. Genomics Proteomics Bioinformatics. 2019. PMID: 31494266 Free PMC article.

6

Novel and functional DNA sequence variants within the GATA6 gene promoter in ventricular septal defects.

Li C, Li X, Pang S, Chen W, Qin X, Huang W, Zeng C, Yan B. Li C, et al. Among authors: chen w. Int J Mol Sci. 2014 Jul 17;15(7):12677-87. doi: 10.3390/ijms150712677. Int J Mol Sci. 2014. PMID: 25036032 Free PMC article.

7

Noninvasive chimeric DNA profiling identifies tumor-originated HBV integrants contributing to viral antigen expression in liver cancer.

Chen W, Zhang K, Dong P, Fanning G, Tao C, Zhang H, Guo S, Wang Z, Hong Y, Yang X, Lai S, Ding H, Zhao H, Zeng C, Protzer U, Zhang D. Chen W, et al. Hepatol Int. 2020 May;14(3):326-337. doi: 10.1007/s12072-020-10016-2. Epub 2020 Feb 25. Hepatol Int. 2020. PMID: 32100258

8

Genetic flux between h1 and h2 haplotypes of the 17q21.31 inversion in European population.

Deng L, Tang X, Hao X, Chen W, Lin J, Yu Y, Zhang D, Zeng C. Deng L, et al. Among authors: chen w. Genomics Proteomics Bioinformatics. 2011 Jun;9(3):113-8. doi: 10.1016/S1672-0229(11)60014-4. Genomics Proteomics Bioinformatics. 2011. PMID: 21802048 Free PMC article.

9

Hepatic stellate cells-specific LOXL1 deficiency abrogates hepatic inflammation, fibrosis, and corrects lipid metabolic abnormalities in non-obese NASH mice.

Yang A, Yan X, Fan X, Shi Y, Huang T, Li W, Chen W, Jia J, You H. Yang A, et al. Among authors: chen w. Hepatol Int. 2021 Oct;15(5):1122-1135. doi: 10.1007/s12072-021-10210-w. Epub 2021 May 20. Hepatol Int. 2021. PMID: 34014450

10

In vitro transcriptome analysis of two Chinese isolates of Streptococcus suis serotype 2.

Zhang D, Du N, Ma S, Hu Q, Lu G, Chen W, Zeng C. Zhang D, et al. Among authors: chen w. Genomics Proteomics Bioinformatics. 2014 Dec;12(6):266-75. doi: 10.1016/j.gpb.2014.11.001. Epub 2014 Dec 16. Genomics Proteomics Bioinformatics. 2014. PMID: 25526982 Free PMC article.

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