Li W - Search Results

1

Single-cell RNA sequencing identifies an Il1rn⁺/Trem1⁺ macrophage subpopulation as a cellular target for mitigating the progression of thoracic aortic aneurysm and dissection.

Liu X, Chen W, Zhu G, Yang H, Li W, Luo M, Shu C, Zhou Z. Liu X, et al. Among authors: li w. Cell Discov. 2022 Feb 8;8(1):11. doi: 10.1038/s41421-021-00362-2. Cell Discov. 2022. PMID: 35132073 Free PMC article.

2

Genetic testing of 248 Chinese aortopathy patients using a panel assay.

Yang H, Luo M, Fu Y, Cao Y, Yin K, Li W, Meng C, Ma Y, Zhang J, Fan Y, Shu C, Chang Q, Zhou Z. Yang H, et al. Among authors: li w. Sci Rep. 2016 Sep 9;6:33002. doi: 10.1038/srep33002. Sci Rep. 2016. PMID: 27611364 Free PMC article.

3

Common Variant in Glycoprotein Ia Increases Long-Term Adverse Events Risk After Coronary Artery Bypass Graft Surgery.

Liu H, Xu Z, Gu H, Li W, Chen W, Sun C, Zhao K, Teng X, Zhang H, Jiang L, Hu S, Zhou Z, Zheng Z. Liu H, et al. Among authors: li w. J Am Heart Assoc. 2016 Nov 23;5(12):e004496. doi: 10.1161/JAHA.116.004496. J Am Heart Assoc. 2016. PMID: 27881421 Free PMC article.

4

Genetic analyses in a cohort of 191 pulmonary arterial hypertension patients.

Yang H, Zeng Q, Ma Y, Liu B, Chen Q, Li W, Xiong C, Zhou Z. Yang H, et al. Among authors: li w. Respir Res. 2018 May 9;19(1):87. doi: 10.1186/s12931-018-0789-9. Respir Res. 2018. PMID: 29743074 Free PMC article.

5

Two common mutations within CYP2C19 affected platelet aggregation in Chinese patients undergoing PCI: a one-year follow-up study.

Wang Z, Liu Z, Wang W, Fu Y, Chen W, Li W, Zhang X, Tang Y, Zhou Z. Wang Z, et al. Among authors: li w. Pharmacogenomics J. 2019 Apr;19(2):157-163. doi: 10.1038/s41397-018-0036-2. Epub 2018 Jul 31. Pharmacogenomics J. 2019. PMID: 30061570

6

Secondary findings in 421 whole exome-sequenced Chinese children.

Chen W, Li W, Ma Y, Zhang Y, Han B, Liu X, Zhao K, Zhang M, Mi J, Fu Y, Zhou Z. Chen W, et al. Among authors: li w. Hum Genomics. 2018 Sep 14;12(1):42. doi: 10.1186/s40246-018-0174-2. Hum Genomics. 2018. PMID: 30217213 Free PMC article.

7

The co-segregation of the MYL2 R58Q mutation in Chinese hypertrophic cardiomyopathy family and its pathological effect on cardiomyopathy disarray.

Yin K, Ma Y, Cui H, Sun Y, Han B, Liu X, Zhao K, Li W, Wang J, Wang H, Wang S, Zhou Z. Yin K, et al. Among authors: li w. Mol Genet Genomics. 2019 Oct;294(5):1241-1249. doi: 10.1007/s00438-019-01578-4. Epub 2019 May 18. Mol Genet Genomics. 2019. PMID: 31104103

8

Long non-coding and coding RNA profiling using strand-specific RNA-seq in human hypertrophic cardiomyopathy.

Liu X, Ma Y, Yin K, Li W, Chen W, Zhang Y, Zhu C, Li T, Han B, Liu X, Wang S, Zhou Z. Liu X, et al. Among authors: li t, li w. Sci Data. 2019 Jun 13;6(1):90. doi: 10.1038/s41597-019-0094-6. Sci Data. 2019. PMID: 31197155 Free PMC article.

9

Single-Cell RNA-Seq of the Developing Cardiac Outflow Tract Reveals Convergent Development of the Vascular Smooth Muscle Cells.

Liu X, Chen W, Li W, Li Y, Priest JR, Zhou B, Wang J, Zhou Z. Liu X, et al. Among authors: li y, li w. Cell Rep. 2019 Jul 30;28(5):1346-1361.e4. doi: 10.1016/j.celrep.2019.06.092. Cell Rep. 2019. PMID: 31365875 Free article.

10

Exome-Based Case-Control Analysis Highlights the Pathogenic Role of Ciliary Genes in Transposition of the Great Arteries.

Liu X, Chen W, Li W, Priest JR, Fu Y, Pang K, Ma B, Han B, Liu X, Hu S, Zhou Z. Liu X, et al. Among authors: li w. Circ Res. 2020 Mar 27;126(7):811-821. doi: 10.1161/CIRCRESAHA.119.315821. Epub 2020 Feb 11. Circ Res. 2020. PMID: 32078439 Free article.

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