Wu Y - Search Results

1

Xu L, Wen W, Yang Y, Xie J, Li R, Wu Y, Hu Y, Wang L, Chong M. Xu L, et al. Among authors: wu y. Am J Cardiol. 2020 May 1;125(9):1312-1316. doi: 10.1016/j.amjcard.2020.01.048. Epub 2020 Feb 8. Am J Cardiol. 2020. PMID: 32143815

2

A case of sitosterolemia misdiagnosed as familial hypercholesterolemia: A 4-year follow-up.

Wang W, Jiang L, Chen PP, Wu Y, Su PY, Wang LY. Wang W, et al. Among authors: wu y. J Clin Lipidol. 2018 Jan-Feb;12(1):236-239. doi: 10.1016/j.jacl.2017.10.008. Epub 2017 Nov 11. J Clin Lipidol. 2018. PMID: 29246730

3

Genetically confirmed familial hypercholesterolemia in outpatients with hypercholesterolemia.

Wang X, Jiang L, Sun LY, Wu Y, Wen WH, Wang XF, Liu W, Zhou YJ, Wang LY. Wang X, et al. Among authors: wu y. J Geriatr Cardiol. 2018 Jun;15(6):434-440. doi: 10.11909/j.issn.1671-5411.2018.06.006. J Geriatr Cardiol. 2018. PMID: 30108616 Free PMC article.

4

Comparison of long-term outcomes of young patients after a coronary event associated with familial hypercholesterolemia.

Wang X, Cai G, Wang Y, Liu R, Xi Z, Li G, Wen W, Wu Y, Wang C, Ji Q, Wang X, Zhang Q, Zeng Y, Wang L, Liu W, Zhou Y. Wang X, et al. Among authors: wu y. Lipids Health Dis. 2019 Jun 1;18(1):131. doi: 10.1186/s12944-019-1074-8. Lipids Health Dis. 2019. PMID: 31153370 Free PMC article.

5

Independent Severe Cases of Heterozygous Familial Hypercholesterolemia Caused by the W483X and Novel W483G Mutations in the Low-Density Lipoprotein Receptor Gene That Were Clinically Diagnosed as Homozygous Cases.

Cheng S, Wu Y, Wen W, An M, Gao Y, Wang L, Han X, Shang H. Cheng S, et al. Among authors: wu y. Genet Test Mol Biomarkers. 2019 Jun;23(6):401-408. doi: 10.1089/gtmb.2019.0012. Genet Test Mol Biomarkers. 2019. PMID: 31161821

6

An interspecies study of lipid profiles and atherosclerosis in familial hypercholesterolemia animal models with low-density lipoprotein receptor deficiency.

He K, Wang J, Shi H, Yu Q, Zhang X, Guo M, Sun H, Lin X, Wu Y, Wang L, Wang Y, Xian X, Liu G. He K, et al. Among authors: wu y. Am J Transl Res. 2019 May 15;11(5):3116-3127. eCollection 2019. Am J Transl Res. 2019. PMID: 31217881 Free PMC article.

7

Supravalvular Aortic Stenosis and the Risk of Premature Death Among Patients With Homozygous Familial Hypercholesterolemia.

Zhang R, Xie J, Zhou J, Xu L, Pan Y, Qu Y, Li R, Chong M, Song L, Wen W, Wu Y, Li J, Wang L, Yang Y. Zhang R, et al. Among authors: wu y. Am J Cardiol. 2021 Apr 15;145:58-63. doi: 10.1016/j.amjcard.2020.12.080. Epub 2021 Jan 14. Am J Cardiol. 2021. PMID: 33454344

8

Integrated analysis of microRNA and mRNA expression profiles in homozygous familial hypercholesterolemia patients and validation of atherosclerosis associated critical regulatory network.

Wu Y, Jiang L, Zhang H, Cheng S, Wen W, Xu L, Zhang F, Yang Y, Wang L, Chen J. Wu Y, et al. Genomics. 2021 Jul;113(4):2572-2582. doi: 10.1016/j.ygeno.2021.05.036. Epub 2021 May 28. Genomics. 2021. PMID: 34052320 Free article.

9

Prognostic value of coronary flow velocity reserve in patients with homozygous familial hypercholesterolemia.

Xie J, Yang Y, Wang L, Pan Y, Zhang R, Qu Y, Li R, Wen W, Wu Y, Li J, Ma X. Xie J, et al. Among authors: wu y. Echocardiography. 2021 Sep;38(9):1489-1495. doi: 10.1111/echo.15147. Epub 2021 Aug 26. Echocardiography. 2021. PMID: 34448504

10

Global perspective of familial hypercholesterolaemia: a cross-sectional study from the EAS Familial Hypercholesterolaemia Studies Collaboration (FHSC).

EAS Familial Hypercholesterolaemia Studies Collaboration (FHSC). EAS Familial Hypercholesterolaemia Studies Collaboration (FHSC). Lancet. 2021 Nov 6;398(10312):1713-1725. doi: 10.1016/S0140-6736(21)01122-3. Epub 2021 Sep 7. Lancet. 2021. PMID: 34506743

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