BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Jha CK, Mir R, Elfaki I, Javid J, Babakr AT, Banu S, Chahal SMS. Evaluation of the Association of Omentin 1 rs2274907 A>T and rs2274908 G>A Gene Polymorphisms with Coronary Artery Disease in Indian Population: A Case Control Study. J Pers Med 2019;9:E30. [PMID: 31174318 DOI: 10.3390/jpm9020030] [Cited by in Crossref: 16] [Cited by in F6Publishing: 16] [Article Influence: 5.3] [Reference Citation Analysis]
Number Citing Articles
1 Mir R, Elfaki I, Javid J, Barnawi J, Altayar MA, Albalawi SO, Jalal MM, Tayeb FJ, Yousif A, Ullah MF, Abuduhier FM. Genetic Determinants of Cardiovascular Disease: The Endothelial Nitric Oxide Synthase 3 (eNOS3), Krüppel-Like Factor-14 (KLF-14), Methylenetetrahydrofolate Reductase (MTHFR), MiRNAs27a and Their Association with the Predisposition and Susceptibility to Coronary Artery Disease. Life 2022;12:1905. [DOI: 10.3390/life12111905] [Reference Citation Analysis]
2 Al-Barqaawi MA, Abdul-Jabr T, Mahdi AG, Mirza TJ, Amber KI, Hussain MK. The impact of omentin-1 gene polymorphisms (rs2274907 and rs2274908) on serum lipid concentrations and coronary artery disease in a sample of Iraqi individuals (A pilot study). Clin Biochem 2021:S0009-9120(21)00304-0. [PMID: 34788636 DOI: 10.1016/j.clinbiochem.2021.11.005] [Reference Citation Analysis]
3 Elfaki I, Mir R, Duhier FMA, Alotaibi MA, Alalawy AI, Barnawi J, Babakr AT, Mir MM, Altayeb F, Mirghani H, Frah EAM. Clinical Implications of MiR128, Angiotensin I Converting Enzyme and Vascular Endothelial Growth Factor Gene Abnormalities and Their Association with T2D. Curr Issues Mol Biol 2021;43:1859-75. [PMID: 34889890 DOI: 10.3390/cimb43030130] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
4 Mir R, Elfaki I, Duhier FMA, Alotaibi MA, AlAlawy AI, Barnawi J, Babakr AT, Mir MM, Mirghani H, Hamadi A, Dabla PK. Molecular Determination of mirRNA-126 rs4636297, Phosphoinositide-3-Kinase Regulatory Subunit 1-Gene Variability rs7713645, rs706713 (Tyr73Tyr), rs3730089 (Met326Ile) and Their Association with Susceptibility to T2D. J Pers Med 2021;11:861. [PMID: 34575638 DOI: 10.3390/jpm11090861] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 6.0] [Reference Citation Analysis]
5 Bogari N, Dannoun A, Athar M, Elkhateeb O, Porqueddu M, Allam R, Alamanni F. Genetic Association of rs10757278 on Chromosome 9p21 and Coronary Artery Disease in a Saudi Population. Int J Gen Med 2021;14:1699-707. [PMID: 33981157 DOI: 10.2147/IJGM.S300463] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
6 Mir R, Elfaki I, Khullar N, Waza AA, Jha C, Mir MM, Nisa S, Mohammad B, Mir TA, Maqbool M, Barnawi J, Albalawi SO, Abu-Duhier FM. Role of Selected miRNAs as Diagnostic and Prognostic Biomarkers in Cardiovascular Diseases, Including Coronary Artery Disease, Myocardial Infarction and Atherosclerosis. J Cardiovasc Dev Dis 2021;8:22. [PMID: 33669699 DOI: 10.3390/jcdd8020022] [Cited by in Crossref: 10] [Cited by in F6Publishing: 11] [Article Influence: 10.0] [Reference Citation Analysis]
7 Liu CX, Yin RX, Shi ZH, Zheng PF, Deng GX, Guan YZ, Wei BL. Associations between TUBB-WWOX SNPs, their haplotypes, gene-gene, and gene-environment interactions and dyslipidemia. Aging (Albany NY) 2021;13:5906-27. [PMID: 33612478 DOI: 10.18632/aging.202514] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
8 Jha CK, Mir R, Banu S, Elfaki I, Chahal SMS. Heterozygosity in LDLR rs2228671 and rs72658855 Gene is Associated with Increased Risk of Developing Coronary Artery Disease in India -A Case-Control Study. Endocr Metab Immune Disord Drug Targets 2020;20:388-99. [PMID: 31613733 DOI: 10.2174/1871530319666191015164505] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 5.0] [Reference Citation Analysis]
9 Jha CK, Mir R, Elfaki I, Javid J, Babakr AT, Banu S, Chahal SMS. Reply to Comment: Evaluation of the Association of Omentin 1 rs2274907 A > T and rs2274908 G > A Gene Polymorphisms with Coronary Artery Disease in Indian Population: A Case-Control Study. J Pers Med 2020;10:E194. [PMID: 33114503 DOI: 10.3390/jpm10040194] [Reference Citation Analysis]
10 Vimaleswaran KS. Comment: "Evaluation of the Association of Omentin 1 rs2274907 A>T and rs2274908 G>A Gene Polymorphisms with Coronary Artery Disease in Indian Population: A Case Control Study". J Pers Med 2020;10:E190. [PMID: 33113755 DOI: 10.3390/jpm10040190] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
11 Yan P, Xu Y, Zhang Z, Zhu J, Miao Y, Gao C, Wan Q. Association of Circulating Omentin-1 with Osteoporosis in a Chinese Type 2 Diabetic Population. Mediators Inflamm 2020;2020:9389720. [PMID: 33149724 DOI: 10.1155/2020/9389720] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
12 Askin L, Duman H, Ozyıldız A, Tanriverdi O, Turkmen S. Association between Omentin-1 and Coronary Artery Disease: Pathogenesis and Clinical Research. Curr Cardiol Rev 2020;16:198-201. [PMID: 32392116 DOI: 10.2174/1573403X16666200511085304] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
13 Elfaki I, Mir R, Abu-Duhier FM, Khan R, Sakran M. Phosphatidylinositol 3-kinase Glu545Lys and His1047Tyr Mutations are not Associated with T2D. Curr Diabetes Rev 2020;16:881-8. [PMID: 31749428 DOI: 10.2174/1573399815666191015142201] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 3.0] [Reference Citation Analysis]
14 Elfaki I, Mir R, Mir MM, AbuDuhier FM, Babakr AT, Barnawi J. Potential Impact of MicroRNA Gene Polymorphisms in the Pathogenesis of Diabetes and Atherosclerotic Cardiovascular Disease. J Pers Med 2019;9:E51. [PMID: 31775219 DOI: 10.3390/jpm9040051] [Cited by in Crossref: 22] [Cited by in F6Publishing: 24] [Article Influence: 7.3] [Reference Citation Analysis]
15 K Jha C, Mir R, Elfaki I, Banu S, Chahal SMS. LDLR Gene Polymorphisms (rs5925 and rs1529729) Are Associated with Susceptibility to Coronary Artery Disease in a South Indian Population. Med Sci (Basel) 2019;7:E80. [PMID: 31311124 DOI: 10.3390/medsci7070080] [Cited by in Crossref: 3] [Cited by in F6Publishing: 5] [Article Influence: 1.0] [Reference Citation Analysis]