Wu W - Search Results

1

Application of next-generation sequencing to screen for pathogenic mutations in 123 unrelated Chinese patients with Marfan syndrome or a related disease.

Li J, Lu C, Wu W, Liu Y, Wang R, Si N, Meng X, Zhang S, Zhang X. Li J, et al. Among authors: wu w. Sci China Life Sci. 2019 Dec;62(12):1630-1637. doi: 10.1007/s11427-018-9491-8. Epub 2019 May 15. Sci China Life Sci. 2019. PMID: 31098894

2

Novel Phenotype-Genotype Correlations of Restrictive Cardiomyopathy With Myosin-Binding Protein C (MYBPC3) Gene Mutations Tested by Next-Generation Sequencing.

Wu W, Lu CX, Wang YN, Liu F, Chen W, Liu YT, Han YC, Cao J, Zhang SY, Zhang X. Wu W, et al. J Am Heart Assoc. 2015 Jul 10;4(7):e001879. doi: 10.1161/JAHA.115.001879. J Am Heart Assoc. 2015. PMID: 26163040 Free PMC article.

3

Gross deletions in FBN1 results in variable phenotypes of Marfan syndrome.

Li J, Wu W, Lu C, Liu Y, Wang R, Si N, Liu F, Zhou J, Zhang S, Zhang X. Li J, et al. Among authors: wu w. Clin Chim Acta. 2017 Nov;474:54-59. doi: 10.1016/j.cca.2017.08.023. Epub 2017 Aug 24. Clin Chim Acta. 2017. PMID: 28842177

4

Molecular analysis of inherited cardiomyopathy using next generation semiconductor sequencing technologies.

Lu C, Wu W, Liu F, Yang K, Li J, Liu Y, Wang R, Si N, Gao P, Liu Y, Zhang S, Zhang X. Lu C, et al. Among authors: wu w. J Transl Med. 2018 Aug 30;16(1):241. doi: 10.1186/s12967-018-1605-5. J Transl Med. 2018. PMID: 30165862 Free PMC article.

5

[Screening of LDLR gene mutations in nine patients with familial hypercholesterolemia].

Meng X, Si N, Shen Y, Wang Q, He J, Lu C, Wu W, Zhang S, Zhang X. Meng X, et al. Among authors: wu w. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Dec 10;35(6):783-786. doi: 10.3760/cma.j.issn.1003-9406.2018.06.001. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 30512145 Chinese.

6

[Detection of pathogenic mutations in Marfan syndrome by targeted next-generation semiconductor sequencing].

Lu C, Wu W, Xiao J, Meng Y, Zhang S, Zhang X. Lu C, et al. Among authors: wu w. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013 Jun;30(3):301-4. doi: 10.3760/cma.j.issn.1003-9406.2013.03.011. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013. PMID: 23744319 Chinese.

7

Restrictive Cardiomyopathy Resulting from a Troponin I Type 3 Mutation in a Chinese Family.

Ruan YP, Lu CX, Zhao XY, Liang RJ, Lian H, Routledge M, Wu W, Zhang X, Fan ZJ. Ruan YP, et al. Among authors: wu w. Chin Med Sci J. 2016 Mar 20;31(1):1-7. doi: 10.1016/s1001-9294(16)30015-3. Chin Med Sci J. 2016. PMID: 28031081

8

Analysis of MEF2A mutations in a Chinese population with premature coronary artery disease.

Dai Y, Zhang S, Wu W. Dai Y, et al. Among authors: wu w. Genet Test Mol Biomarkers. 2013 Apr;17(4):352-5. doi: 10.1089/gtmb.2012.0467. Epub 2013 Mar 5. Genet Test Mol Biomarkers. 2013. PMID: 23461724

9

Paradoxical coronary embolisms as a presentation of hereditary hemorrhagic telangiectasia.

Wu W, Lu C, Shen J, Zhang X, Zhang S. Wu W, et al. J Am Coll Cardiol. 2014 Jan 28;63(3):e5. doi: 10.1016/j.jacc.2013.07.114. Epub 2013 Nov 13. J Am Coll Cardiol. 2014. PMID: 24239663 Free article. No abstract available.

10

[Clinical features of patients with premature acute coronary syndrome].

Zhang T, Tian R, Zhang S, Wu W, Liu Z, Fang Q, Xie H, Shen Z, Zeng Y. Zhang T, et al. Among authors: wu w. Zhonghua Xin Xue Guan Bing Za Zhi. 2014 May;42(5):392-5. Zhonghua Xin Xue Guan Bing Za Zhi. 2014. PMID: 25042917 Chinese.

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