BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Huang Y, Ye H, Hong Q, Xu X, Jiang D, Xu L, Dai D, Sun J, Gao X, Duan S. Association of CDKN2BAS polymorphism rs4977574 with coronary heart disease: a case-control study and a meta-analysis. Int J Mol Sci 2014;15:17478-92. [PMID: 25268619 DOI: 10.3390/ijms151017478] [Cited by in Crossref: 27] [Cited by in F6Publishing: 25] [Article Influence: 3.9] [Reference Citation Analysis]
Number Citing Articles
1 Tang O, Lv J, Cheng Y, Qin F. The Correlation Between 9p21 Chromosome rs4977574 Polymorphism Genotypes and the Development of Coronary Artery Heart Disease. Cardiovasc Toxicol 2017;17:185-9. [DOI: 10.1007/s12012-016-9372-0] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 0.6] [Reference Citation Analysis]
2 Zhao Q, Liao S, Wei H, Liu D, Li J, Zhang X, Yan M, Jin T. CDKN2BAS polymorphisms are associated with coronary heart disease risk a Han Chinese population. Oncotarget 2016;7:82046-54. [PMID: 27741513 DOI: 10.18632/oncotarget.12575] [Cited by in Crossref: 12] [Cited by in F6Publishing: 10] [Article Influence: 4.0] [Reference Citation Analysis]
3 Zhang YN, Qiang B, Fu LJ. Association of ANRIL polymorphisms with coronary artery disease: A systemic meta-analysis. Medicine (Baltimore) 2020;99:e22569. [PMID: 33080691 DOI: 10.1097/MD.0000000000022569] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
4 Temel ŞG, Ergören MÇ. The association between the chromosome 9p21 CDKN2B-AS1 gene variants and the lipid metabolism: A pre-diagnostic biomarker for coronary artery disease. Anatol J Cardiol 2019;21:31-8. [PMID: 30587704 DOI: 10.14744/AnatolJCardiol.2018.90907] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
5 Xiong L, Liu W, Gao L, Mu Q, Liu X, Feng Y, Tang Z, Tang H, Liu H. The ANRIL Genetic Variants and Their Interactions with Environmental Risk Factors on Atherothrombotic Stroke in a Han Chinese Population. J Stroke Cerebrovasc Dis 2018;27:2336-47. [PMID: 29773352 DOI: 10.1016/j.jstrokecerebrovasdis.2018.04.020] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.7] [Reference Citation Analysis]
6 Xu LB, Zhang YQ, Zhang NN, Li B, Weng JY, Li XY, Lu WC, Yu PR, Wang X, Li Y, Han Z, Chen L, He HT, Zhou YF, Ma XX, Xu GD. Rs10757274 gene polymorphisms in coronary artery disease: A systematic review and a meta-analysis. Medicine (Baltimore) 2020;99:e18841. [PMID: 32011499 DOI: 10.1097/MD.0000000000018841] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 4.0] [Reference Citation Analysis]
7 Ou M, Li X, Zhao S, Cui S, Tu J. Long non-coding RNA CDKN2B-AS1 contributes to atherosclerotic plaque formation by forming RNA-DNA triplex in the CDKN2B promoter. EBioMedicine 2020;55:102694. [PMID: 32335370 DOI: 10.1016/j.ebiom.2020.102694] [Cited by in Crossref: 10] [Cited by in F6Publishing: 15] [Article Influence: 10.0] [Reference Citation Analysis]
8 Mehrabi Pour M, Nasiri M, Kamfiroozie H, Zibaeenezhad MJ. Association of the ATG9B gene polymorphisms with coronary artery disease susceptibility: A case-control study. J Cardiovasc Thorac Res 2019;11:109-15. [PMID: 31384404 DOI: 10.15171/jcvtr.2019.19] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
9 Kunnas T, Piesanen J, Nikkari ST. Association of a Chromosome Locus 9p21.3 CDKN2B-AS1 Variant rs4977574 with Hypertension: The TAMRISK Study. Genet Test Mol Biomarkers 2018;22:327-30. [PMID: 29791233 DOI: 10.1089/gtmb.2017.0249] [Cited by in Crossref: 8] [Cited by in F6Publishing: 7] [Article Influence: 2.7] [Reference Citation Analysis]
10 Tsilimigras DI, Bibli SI, Siasos G, Oikonomou E, Perrea DN, Filis K, Tousoulis D, Sigala F. Regulation of Long Non-Coding RNAs by Statins in Atherosclerosis. Biomolecules 2021;11:623. [PMID: 33922114 DOI: 10.3390/biom11050623] [Reference Citation Analysis]
11 Ferreira LE, Secolin R, Lopes-Cendes I, Cabral NL, França PHC. Association and interaction of genetic variants with occurrence of ischemic stroke among Brazilian patients. Gene 2019;695:84-91. [PMID: 30738964 DOI: 10.1016/j.gene.2019.01.041] [Cited by in Crossref: 7] [Cited by in F6Publishing: 5] [Article Influence: 3.5] [Reference Citation Analysis]
12 Wang G, Li Y, Peng Y, Tang J, Li H. Association of polymorphisms in MALAT1 with risk of coronary atherosclerotic heart disease in a Chinese population. Lipids Health Dis 2018;17:75. [PMID: 29631611 DOI: 10.1186/s12944-018-0728-2] [Cited by in Crossref: 27] [Cited by in F6Publishing: 29] [Article Influence: 9.0] [Reference Citation Analysis]
13 Huang X, Zhang W, Shao Z. Association between long non-coding RNA polymorphisms and cancer risk: a meta-analysis. Biosci Rep 2018;38:BSR20180365. [PMID: 29802154 DOI: 10.1042/BSR20180365] [Cited by in Crossref: 25] [Cited by in F6Publishing: 15] [Article Influence: 8.3] [Reference Citation Analysis]
14 Liu D, Song J, Ji X, Liu Z, Cong M, Hu B. Association of Genetic Polymorphisms on VEGFA and VEGFR2 With Risk of Coronary Heart Disease. Medicine (Baltimore) 2016;95:e3413. [PMID: 27175642 DOI: 10.1097/MD.0000000000003413] [Cited by in Crossref: 15] [Cited by in F6Publishing: 11] [Article Influence: 3.8] [Reference Citation Analysis]
15 Zhao J, Wu X, Nie S, Gao X, Sun J, Li K, Zhang T, Huang Y. Association of CDKN2B-AS1 rs1333049 with Brain Diseases: A Case-control Study and a Meta-analysis. Clin Psychopharmacol Neurosci 2017;15:53-8. [PMID: 28138111 DOI: 10.9758/cpn.2017.15.1.53] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 1.5] [Reference Citation Analysis]
16 Deng Y, Huang J, Zhang H, Zhu X, Gong Q. Association of expression of DRD2 rs1800497 polymorphism with migraine risk in Han Chinese individuals. J Pain Res 2018;11:763-9. [PMID: 29695928 DOI: 10.2147/JPR.S151350] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 1.3] [Reference Citation Analysis]
17 AbdulAzeez S, Al-Nafie AN, Al-Shehri A, Borgio JF, Baranova EV, Al-Madan MS, Al-Ali RA, Al-Muhanna F, Al-Ali A, Al-Mansori M, Ibrahim MF, Asselbergs FW, Keating B, Koeleman BP, Al-Ali AK. Intronic Polymorphisms in the CDKN2B-AS1 Gene Are Strongly Associated with the Risk of Myocardial Infarction and Coronary Artery Disease in the Saudi Population. Int J Mol Sci 2016;17:395. [PMID: 26999117 DOI: 10.3390/ijms17030395] [Cited by in Crossref: 21] [Cited by in F6Publishing: 21] [Article Influence: 4.2] [Reference Citation Analysis]
18 Li YY, Wang H, Zhang YY. CDKN2B-AS1 gene rs4977574 A/G polymorphism and coronary heart disease: A meta-analysis of 40,979 subjects. J Cell Mol Med 2021;25:8877-89. [PMID: 34418317 DOI: 10.1111/jcmm.16849] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
19 Zhang L, Ji H, Huang Y, Hu H, Li B, Yang Y, Yu H, Chen X, Li W, Liu F, Wang S, Wang C, Chen K, Bao Y, Liu H, Duan S. Association of BAX hypermethylation with coronary heart disease is specific to individuals aged over 70. Medicine (Baltimore) 2019;98:e14130. [PMID: 30681575 DOI: 10.1097/MD.0000000000014130] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
20 Khorshidi HR, Taheri M, Noroozi R, Sarrafzadeh S, Sayad A, Ghafouri-Fard S. ANRIL Genetic Variants in Iranian Breast Cancer Patients. Cell J 2017;19:72-8. [PMID: 28580310 DOI: 10.22074/cellj.2017.4496] [Cited by in F6Publishing: 15] [Reference Citation Analysis]
21 Xu B, Fang Z, He S, Wang J, Yang X. ANRIL polymorphism rs4977574 is associated with increased risk of coronary artery disease in Asian populations: A meta-analysis of 12,005 subjects. Medicine (Baltimore) 2018;97:e12641. [PMID: 30278588 DOI: 10.1097/MD.0000000000012641] [Cited by in Crossref: 8] [Cited by in F6Publishing: 4] [Article Influence: 2.7] [Reference Citation Analysis]
22 Chen L, Qu H, Guo M, Zhang Y, Cui Y, Yang Q, Bai R, Shi D. ANRIL and atherosclerosis. J Clin Pharm Ther 2020;45:240-8. [PMID: 31703157 DOI: 10.1111/jcpt.13060] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
23 Zhong J, Chen X, Ye H, Wu N, Chen X, Duan S. CDKN2A and CDKN2B methylation in coronary heart disease cases and controls. Exp Ther Med 2017;14:6093-8. [PMID: 29285163 DOI: 10.3892/etm.2017.5310] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
24 Xu X, Li Y, Huang Y, Ye H, Han L, Ji H, Chen X, Wu N, Jiang D, Xu L, Dai D, Duan S, Chen X. Impact of gender and age on the association of the BUD13-ZNF259 rs964184 polymorphism with coronary heart disease. Anatol J Cardiol 2018;19:42-9. [PMID: 29339699 DOI: 10.14744/AnatolJCardiol.2017.8002] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
25 Wang Z, Zhao J, Sun J, Nie S, Li K, Gao F, Zhang T, Duan S, Di Y, Huang Y, Gao X. Sex-dichotomous effects of NOS1AP promoter DNA methylation on intracranial aneurysm and brain arteriovenous malformation. Neurosci Lett 2016;621:47-53. [PMID: 27080431 DOI: 10.1016/j.neulet.2016.04.016] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 1.4] [Reference Citation Analysis]