Academic Content and Language Evaluation of This Article
CrossCheck and Google Search of This Article
Academic Rules and Norms of This Article
Citation of this article
Corresponding Author of This Article
Research Domain of This Article
Article-Type of This Article
Open-Access Policy of This Article
Times Cited Counts in Google of This Article
Number of Hits and Downloads for This Article
- Total Article Views (21998)
All Articles published online
|
Publishing Process of This Article
|
Jan 26, 2016 (publication date) through Jun 17, 2024
Times Cited of This Article
Journal Information of This Article
Publication Name
World Journal of Cardiology
ISSN
1949-8462
Publisher of This Article
Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| For: | Dai X, Wiernek S, Evans JP, Runge MS. Genetics of coronary artery disease and myocardial infarction. World J Cardiol 2016; 8(1): 1-23 [PMID: 26839654 DOI: 10.4330/wjc.v8.i1.1] |
|---|---|
| URL: | https://www.wjgnet.com/1949-8462/full/v8/i1/1.htm |
| Number | Citing Articles |
| 1 |
Na Guo, Peili Wang, Jiaying Yang, Xiaofang Yang, Monique van der Voet, Marjolein Wildwater, Junying Wei, Xuan Tang, Mei Wang, Hongjun Yang. Serum Metabolomic Analysis of Coronary Heart Disease Patients with Stable Angina Pectoris Subtyped by Traditional Chinese Medicine Diagnostics Reveals Biomarkers Relevant to Personalized Treatments. Frontiers in Pharmacology 2021; 12 doi: 10.3389/fphar.2021.664320
|
| 2 |
Andrew M. Novick, David A. Ross. Dualism and the ‘difficult patient’: why integrating neuroscience matters. BJPsych Advances 2020; 26(6): 327 doi: 10.1192/bja.2020.60
|
| 3 |
Maryam Ghaffarzadeh, Hamid Ghaedi, Behnam Alipoor, Mir Davood Omrani, Faranak Kazerouni, Mehrnoosh Shanaki, Afsaneh Labbaf, Hossein Pashaiefar, Ali Rahimipour. Association of miR-149 (RS2292832) Variant with the Risk of Coronary Artery Disease. Journal of Medical Biochemistry 2017; 36(3): 251 doi: 10.1515/jomb-2017-0005
|
| 4 |
Jianwu Zheng, Tielong Chen, Huafang Lin. IL-10, IL-18 Gene Polymorphisms Might Influence Predisposition to Coronary Artery Disease in East Asians: A Meta-Analysis. Immunological Investigations 2021; 50(1): 37 doi: 10.1080/08820139.2020.1726382
|
| 5 |
M. A. Bhat, G. Gandhi. Elevated oxidative DNA damage in patients with coronary artery disease and its association with oxidative stress biomarkers. Acta Cardiologica 2019; 74(2): 153 doi: 10.1080/00015385.2018.1475093
|
| 6 |
Wendong Wang, Zhiwei Xu, Xiaobo Zhu, Xiaotong Chang. Mining the potential therapeutic targets for coronary artery disease by bioinformatics analysis. Molecular Medicine Reports 2018; doi: 10.3892/mmr.2018.9551
|
| 7 |
Boris V. Titov, German J. Osmak, Natalia A. Matveeva, Nino G. Kukava, Roman M. Shakhnovich, Alexander V. Favorov, Mikhail Ya. Ruda, Olga O. Favorova. Genetic risk factors for myocardial infarction more clearly manifest for early age of first onset. Molecular Biology Reports 2017; 44(4): 315 doi: 10.1007/s11033-017-4112-5
|
| 8 |
Nehle Jamali, Mahboobeh Nasiri, Majid Yavarian. Association of the functional genetic variants of TOX3 gene with breast cancer in Iran: A case-control study. Gene Reports 2020; 18: 100511 doi: 10.1016/j.genrep.2019.100511
|
| 9 |
E. Yu. Andreenko, I. S. Yavelov, М. М. Loukianov, A. N. Vernohaeva, O. M. Drapkina, S. A. Boytsov. Ischemic Heart Disease in Subjects of Young Age: Current State of the Problem. Features of Etiology, Clinical Manifestation and Prognosis. Kardiologiia 2018; 58(11): 24 doi: 10.18087/cardio.2018.11.10195
|
| 10 |
Deniz KIRAÇ, Aysun Erdem YAMAN, Hazal GEZMİŞ, Kemal YEŞİLÇİMEN, Tuba AVCILAR, İlter GÜNEY, Elif Çiğdem ALTUNOK, Gülşah KOÇ, Rabican AKKANAT, Turgay İŞBİR. VDBP and VDR Mutations May Cause In-Stent Restenosis. Clinical and Experimental Health Sciences 2022; 12(3): 602 doi: 10.33808/clinexphealthsci.953893
|
| 11 |
Ricardo Pan-Lizcano, Luis Mariñas-Pardo, Lucía Núñez, Fernando Rebollal-Leal, Domingo López-Vázquez, Ana Pereira, Aranzazu Molina-Nieto, Ramón Calviño, Jose Manuel Vázquez-Rodríguez, Manuel Hermida-Prieto. Rare Variants in Genes of the Cholesterol Pathway Are Present in 60% of Patients with Acute Myocardial Infarction. International Journal of Molecular Sciences 2022; 23(24): 16127 doi: 10.3390/ijms232416127
|
| 12 |
Nashwa S. Ghanem, Naglaa M. El-Sayed, Ahmed K. Abbas, Ollfat G. Shaker. Adiponectin and its polymorphism: relation to coronary artery disease. The Egyptian Journal of Internal Medicine 2019; 31(3): 376 doi: 10.4103/ejim.ejim_11_19
|
| 13 |
Ye Yao, Weidong Sun, Qingfeng Sun, Bao Jing, Siqi Liu, Xinyu Liu, Guanghui Shen, Ru Chen, Haiyang Wang. RETRACTED: Platelet-Derived Exosomal MicroRNA-25-3p Inhibits Coronary Vascular Endothelial Cell Inflammation Through Adam10 via the NF-κB Signaling Pathway in ApoE−/− Mice. Frontiers in Immunology 2019; 10 doi: 10.3389/fimmu.2019.02205
|
| 14 |
Yingxue Li, Aijun Liu, Jidong Song, Zhiyong Zhang, Qi Zhang. Association of genetic defects in the apelin-AGTRL1 system with myocardial infarction risk in Han Chinese. Gene 2021; 766: 145143 doi: 10.1016/j.gene.2020.145143
|
| 15 |
Joana Barbosa Melo. Genetics and myocardial infarction. Revista Portuguesa de Cardiologia 2018; 37(9): 737 doi: 10.1016/j.repc.2018.08.001
|
| 16 |
Meeshanthini V. Dogan, Steven R. H. Beach, Ronald L. Simons, Amaury Lendasse, Brandan Penaluna, Robert A. Philibert. Blood-Based Biomarkers for Predicting the Risk for Five-Year Incident Coronary Heart Disease in the Framingham Heart Study via Machine Learning. Genes 2018; 9(12): 641 doi: 10.3390/genes9120641
|
| 17 |
Salma Younes, Zumin Shi, Hatem Zayed. Genetic variations associated with coronary artery disease and myocardial infarction in the Arab world: a systematic review and meta-analysis. Highlights in BioScience 2020; doi: 10.36462/H.BioSci.20213
|
| 18 |
Peilin Xiao, Jianli Shi, Xiaoli Liu. Associations of leptin and leptin receptor genetic variants with coronary artery disease: a meta-analysis. Bioscience Reports 2019; 39(6) doi: 10.1042/BSR20190466
|
| 19 |
Arup Kr. Malakar, Debashree Choudhury, Binata Halder, Prosenjit Paul, Arif Uddin, Supriyo Chakraborty. A review on coronary artery disease, its risk factors, and therapeutics. Journal of Cellular Physiology 2019; 234(10): 16812 doi: 10.1002/jcp.28350
|
| 20 |
Fei Wang, Xiaoqing Cai, Piqi Jiao, Yan Liu, Bin Yuan, Peng Zhang, Hongbin Liu, Ling Ma. Relationship between long non-coding RNA and prognosis of patients with coronary heart disease after percutaneous coronary intervention. Medicine 2020; 99(51): e23525 doi: 10.1097/MD.0000000000023525
|
| 21 |
Miaomiao Liu, Ying Zhang, Xiantong Cao, Xue Wang, Francesco Busard?. Serum Levels of lncRNA CCHE1 and TCF21 in Patients with Coronary Artery Disease and Their Clinical Significances. Disease Markers 2021; 2021: 1 doi: 10.1155/2021/8526144
|
| 22 |
Shuhong Dai, Mei Ding, Na Liang, Zhuo Li, Daqing Li, Lianyue Guan, Hongyu Liu. Associations of ACE I/D polymorphism with the levels of ACE, kallikrein, angiotensin II and interleukin-6 in STEMI patients. Scientific Reports 2019; 9(1) doi: 10.1038/s41598-019-56263-8
|
| 23 |
Zhiyuan Wang, Jinglan Diao, Xin Yue, Jingquan Zhong. Effects of ADIPOQ polymorphisms on individual susceptibility to coronary artery disease: a meta-analysis. Adipocyte 2019; 8(1): 137 doi: 10.1080/21623945.2019.1595270
|
| 24 |
Yi-Dan Hao, Bright Eric Ohene, Shi-Wei Yang, Yu-Jie Zhou. First-degree relatives with similar phenotypic characterisation of acute myocardial infarction: a case report and review of the literature. BMC Cardiovascular Disorders 2019; 19(1) doi: 10.1186/s12872-019-01303-4
|
| 25 |
Gholamreza Shahsavari, Negar Nouryazdan, Glavizh Adibhesami, Mehdi Birjandi. Genetic associations and serum paraoxonase levels with atherosclerosis in western Iranian patients. Molecular Biology Reports 2020; 47(7): 5137 doi: 10.1007/s11033-020-05585-2
|
| 26 |
Yupeng Huang, Hongyan Jin, Guokang Yang. WITHDRAWN: A meta-analysis on associations of CDKN2B-AS variants with atherosclerotic cardio-cerebral vascular diseases. Life Sciences 2018; doi: 10.1016/j.lfs.2018.12.047
|
| 27 |
Rui-Bing Niu, Xiao-Xian Dong, Li-Ping Guo, Li Pan, Yue-Qin Hai, Xiao-Xiao Chen, Bao-Sheng Duan. Study on the relationship between SLCO1B1 and ApoE gene polymorphisms and the risk of coronary heart disease in the Mongolian population. Clinical and Experimental Hypertension 2021; 43(8): 788 doi: 10.1080/10641963.2021.1969660
|
| 28 |
Martyna Fronczek, Joanna Katarzyna Strzelczyk, Tadeusz Osadnik, Krzysztof Biernacki, Zofia Ostrowska, Silvia Angeletti. VDR Gene Polymorphisms in Healthy Individuals with Family History of Premature Coronary Artery Disease. Disease Markers 2021; 2021: 1 doi: 10.1155/2021/8832478
|
| 29 |
Xiaoqing Li, Yong Lin, Ruizhi Zhang. Associations between endothelial nitric oxide synthase gene polymorphisms and the risk of coronary artery disease: A systematic review and meta-analysis of 132 case-control studies. European Journal of Preventive Cardiology 2019; 26(2): 160 doi: 10.1177/2047487318780748
|
| 30 |
Raj Bharath, Krishna Kumar Mohanan Nair, Debasish Gupta, Reshma Vijayan. Assessment of Lewis negative phenotype as a risk factor for multivessel disease in patients with acute coronary syndrome. Transfusion Clinique et Biologique 2022; 29(2): 129 doi: 10.1016/j.tracli.2021.12.008
|
| 31 |
Saban Mor, Zaretsky Lev-RN, Shachar Tal. Is family history of coronary artery disease important in the emergency department triage?. International Emergency Nursing 2020; 50: 100855 doi: 10.1016/j.ienj.2020.100855
|
| 32 |
Kamna Srivastava, Kirti Tyagi. Single nucleotide polymorphisms of microRNA in cardiovascular diseases. Clinica Chimica Acta 2018; 478: 101 doi: 10.1016/j.cca.2017.12.037
|
| 33 |
Abdulrahman Mujalli, Babajan Banaganapalli, Nuha Mohammad Alrayes, Noor A. Shaik, Ramu Elango, Jumana Y. Al-Aama. Myocardial infarction biomarker discovery with integrated gene expression, pathways and biological networks analysis. Genomics 2020; 112(6): 5072 doi: 10.1016/j.ygeno.2020.09.004
|
| 34 |
Xiaoxu Wang, Yaxin Luan, Chengsen Zhang. A meta‐analysis on correlations of OX40L variants with atherosclerotic disorders. Journal of Cellular Biochemistry 2019; 120(6): 9624 doi: 10.1002/jcb.28240
|
| 35 |
Zijiang Zhu, Yuhan Geng, Long Ma, Keying Yao, Ruitong Chang, Yongming Ma, Jialong Li. Association between CBS gene T833C, G919A and 844ins68 polymorphisms in the 8th exon region and coronary artery disease: a meta-analysis. Clinical and Experimental Hypertension 2024; 46(1) doi: 10.1080/10641963.2024.2328147
|
| 36 |
Shu-hong Dai, Ji-fu Li, Jin-bo Feng, Rui-jian Li, Chuan-bao Li, Zhuo Li, Yun Zhang, Da-qing Li. Association of serum levels of AngII, KLK1, andACE/KLK1polymorphisms with acute myocardial infarction induced by coronary artery stenosis. Journal of the Renin-Angiotensin-Aldosterone System 2016; 17(2): 147032031665503 doi: 10.1177/1470320316655037
|
| 37 |
Nayla Nasr, Beáta Soltész, János Sándor, Róza Adány, Szilvia Fiatal. Prognostic Modelling Studies of Coronary Heart Disease—A Systematic Review of Conventional and Genetic Risk Factor Studies. Journal of Cardiovascular Development and Disease 2022; 9(9): 295 doi: 10.3390/jcdd9090295
|
| 38 |
M. Nasiri, M. Rauf, H. Kamfiroozie, M.J. Zibaeenezhad, Z. Jamali. SIRT1 gene polymorphisms associated with decreased risk of atherosclerotic coronary artery disease. Gene 2018; 672: 16 doi: 10.1016/j.gene.2018.05.117
|
| 39 |
Panagiota Kontou, Athanasia Pavlopoulou, Georgia Braliou, Spyridoula Bogiatzi, Niki Dimou, Sripal Bangalore, Pantelis Bagos. Identification of gene expression profiles in myocardial infarction: a systematic review and meta-analysis. BMC Medical Genomics 2018; 11(1) doi: 10.1186/s12920-018-0427-x
|
| 40 |
Askhat Myngbay, Serik Alibekov. CDKN2B-AS1 gene rs4977574 polymorphism in the severity of coronary artery disease in the Kazakh population. Journal of Clinical Medicine of Kazakhstan 2023; 20(6): 23 doi: 10.23950/jcmk/13918
|
| 41 |
Yan Long, Xiao-Tao Zhao, Chang Liu, Yuan-Yuan Sun, Yin-Ting Ma, Xin-Yu Liu, Ji-Xuan Liu. A Case-Control Study of the Association of the Polymorphisms of <b><i>MTHFR</i></b> and <b><i>APOE</i></b> with Risk Factors and the Severity of Coronary Artery Disease. Cardiology 2019; 142(3): 149 doi: 10.1159/000499866
|
| 42 |
Hongling Su, Yunshan Cao, Jing Li, Yan Zhu, Xuming Ma. GST null polymorphisms may affect the risk of coronary artery disease: evidence from a meta-analysis. Thrombosis Journal 2020; 18(1) doi: 10.1186/s12959-020-00234-x
|
| 43 |
Jie Yang, Xue-Song Yang, Qian Zhang, Xin Zhuang, Xiao-Kang Dong, Yue-Hua Jiang, Yan-Nan Tao, Chuan-Hua Yang. Downregulated LINC01614 Ameliorates Hypoxia/Reoxygenation-Stimulated Myocardial Injury by Directly Sponging microRNA-138-5p. Dose-Response 2020; 18(1): 155932582091378 doi: 10.1177/1559325820913786
|
| 44 |
Tanja Rouhani Rankouhi, Daniëlle van Keulen, Dennie Tempel, Jennifer Venhorst. Oncostatin M: Risks and Benefits of a Novel Therapeutic Target for Atherosclerosis. Current Drug Targets 2022; 23(14): 1345 doi: 10.2174/1389450123666220811101032
|
| 45 |
Amein K. Al-Ali, Abdullah M. Al-Rubaish, Rudaynah A. Alali, Mohammed S. Almansori, Mohammed A. Al-Jumaan, Abdullah M. Alshehri, Mohammed S. Al-Madan, ChittiBabu Vatte, Tess Cherlin, Sylvia Young, Shefali S. Verma, Grant Morahan, Bobby P. C. Koeleman, Brendan J. Keating. Uncovering myocardial infarction genetic signatures using GWAS exploration in Saudi and European cohorts. Scientific Reports 2023; 13(1) doi: 10.1038/s41598-023-49105-1
|
| 46 |
Jane A. Leopold, Bradley A. Maron, Joseph Loscalzo. The application of big data to cardiovascular disease: paths to precision medicine. Journal of Clinical Investigation 2020; 130(1): 29 doi: 10.1172/JCI129203
|
| 47 |
Weiming Li, Yingxue Li, Zhiyong Zhang, Kun Xia, Xiaoming Shang, Xinchun Yang, Lefeng Wang, Qi Zhang. Predictive Nomogram of RAGE Genetic Polymorphisms and Metabolic Risk Factors for Myocardial Infarction Risk in a Han Chinese Population. Angiology 2017; 68(10): 877 doi: 10.1177/0003319717696622
|
| 48 |
Adam Kern, Krystian Bojko, Ewa Sienkiewicz, Artur Zarzecki, Jacek Bil. NON-ST-ELEVATION ACUTE CORONARY SYNDROME DUE TO A TOTALLY OCCLUDED CORONARY ARTERY: A HISTORY OF TWO TWIN BROTHERS. Wiadomości Lekarskie 2020; 73(1): 201 doi: 10.36740/WLek202001138
|
| 49 |
Hua Chen, Shifang Ding, Mi Zhou, Xiayin Wu, Xi Liu, Yun Wu, Dechao Liu. Association of rs662799 in APOA5 with CAD in Chinese Han population. BMC Cardiovascular Disorders 2018; 18(1) doi: 10.1186/s12872-017-0735-7
|
| 50 |
German J. Osmak, Boris V. Titov, Natalia A. Matveeva, Vitalina V. Bashinskaya, Roman M. Shakhnovich, Tatiana S. Sukhinina, Nino G. Kukava, Mikhail Ya. Ruda, Olga O. Favorova. Impact of 9p21.3 region and atherosclerosis-related genes' variants on long-term recurrent hard cardiac events after a myocardial infarction. Gene 2018; 647: 283 doi: 10.1016/j.gene.2018.01.036
|
| 51 |
Rosalinda Posadas-Sánchez, Javier Ángeles-Martínez, Nonanzit Pérez-Hernández, José Manuel Rodríguez-Pérez, Fabiola López-Bautista, Teresa Villarreal-Molina, José Manuel Fragoso, Carlos Posadas-Romero, Gilberto Vargas-Alarcón. Receptor-interacting protein 2 (RIP2) gene polymorphisms are associated with increased risk of subclinical atherosclerosis and clinical and metabolic parameters. The Genetics of Atherosclerotic Disease (GEA) Mexican study. Experimental and Molecular Pathology 2017; 102(1): 1 doi: 10.1016/j.yexmp.2016.12.003
|
| 52 |
Teresita De Jesús Hernández Flores, Juan Ramón González García, Yoaly Josefina Sánchez López, Norma Alejandra Vázquez Cárdenas, Ana Gabriela Colima Fausto, Sergio Yair Rodríguez Preciado, María Teresa Magaña Torres. LDLR Gene Mutation p.Asp360His and Familial Hypercholesterolemia in a Mexican Community. Archives of Medical Research 2020; 51(2): 153 doi: 10.1016/j.arcmed.2019.12.017
|
| 53 |
Jianhong Yu, Xiuping Wu, Jianchao Ni, Jianhai Zhang. RETRACTED: Relationship between common eNOS gene polymorphisms and predisposition to coronary artery disease: Evidence from a meta-analysis of 155 published association studies. Genomics 2020; 112(3): 2452 doi: 10.1016/j.ygeno.2020.01.019
|
| 54 |
Г.А. Березовская, Е.С. Клокова, Н.Н. Петрищев. Genetic predictors for symptoms recurrenсe in coronary artery disease after percutaneous coronary intervention. ZHurnal «Patologicheskaia fiziologiia i eksperimental`naia terapiia» 2017; (4(61)): 81 doi: 10.25557/IGPP.2017.4.8527
|
| 55 |
Sehime Gulsun Temel, Mahmut Cerkez Ergoren, Izel Yilmaz, Haluk Barbaros Oral. The use of ACE INDEL polymorphism as a biomarker of coronary artery disease (CAD) in humans with Mediterranean-style diet. International Journal of Biological Macromolecules 2019; 123: 576 doi: 10.1016/j.ijbiomac.2018.11.021
|
| 56 |
Natalie R. Hasbani, Symen Ligthart, Michael R. Brown, Adam S. Heath, Allison Bebo, Kellan E. Ashley, Eric Boerwinkle, Alanna C. Morrison, Aaron R. Folsom, David Aguilar, Paul S. de Vries. American Heart Association’s Life’s Simple 7: Lifestyle Recommendations, Polygenic Risk, and Lifetime Risk of Coronary Heart Disease. Circulation 2022; 145(11): 808 doi: 10.1161/CIRCULATIONAHA.121.053730
|
| 57 |
Joana Barbosa Melo. Genetics and myocardial infarction. Revista Portuguesa de Cardiologia (English Edition) 2018; 37(9): 737 doi: 10.1016/j.repce.2018.09.002
|
| 58 |
G. Roytberg, S. Prozorov, N. Kondratova, D. Sokolov. STENTING OF CORONARY ARTERIES IN ACUTE MYOCARDIAL INFARCTION IN FIRST DEGREE RELATIVES WITH FAMILIAL ATHEROSCLEROSIS. Vrach 2024; 34(4): 48 doi: 10.29296/25877305-2023-04-09
|
| 59 |
Szilvia Fiatal, Róza Ádány. Application of Single-Nucleotide Polymorphism-Related Risk Estimates in Identification of Increased Genetic Susceptibility to Cardiovascular Diseases: A Literature Review. Frontiers in Public Health 2018; 5 doi: 10.3389/fpubh.2017.00358
|
| 60 |
Bolin Wang, Zhihui Su, Lijun Wan, Tao He. Relationship between long non-coding RNA polymorphism and the risk of coronary artery disease. Medicine 2021; 100(12): e25146 doi: 10.1097/MD.0000000000025146
|
| 61 |
Kun Xia, Rongjing Ding, Zhiyong Zhang, Weiming Li, Xiaoming Shang, Xinchun Yang, Lefeng Wang, Qi Zhang. The association of eight potentially functional polymorphisms in five adrenergic receptor-encoding genes with myocardial infarction risk in Han Chinese. Gene 2017; 624: 43 doi: 10.1016/j.gene.2017.04.045
|
| 62 |
Lina Hu, Guoyi Su, Xia Wang. The roles of ANRIL polymorphisms in coronary artery disease: a meta-analysis. Bioscience Reports 2019; 39(12) doi: 10.1042/BSR20181559
|
| 63 |
Irma Isordia-Salas, José A. Alvarado-Moreno, Rosa M. Jiménez-Alvarado, Jesús Hernández-Juárez, David Santiago-Germán, Alfredo Leaños-Miranda, Abraham Majluf-Cruz. Association of renin–angiotensin system genes polymorphisms and risk of premature ST elevation myocardial infarction in young Mexican population. Blood Coagulation & Fibrinolysis 2018; 29(3): 267 doi: 10.1097/MBC.0000000000000714
|
| 64 |
Enrico Maiorino, Joseph Loscalzo. Phenomics and Robust Multiomics Data for Cardiovascular Disease Subtyping. Arteriosclerosis, Thrombosis, and Vascular Biology 2023; 43(7): 1111 doi: 10.1161/ATVBAHA.122.318892
|
| 65 |
Najmeh Ramezanpour, Mahboobeh Nasiri, Omid Reza Akbarpour. Association of rs4618210A>G variant in PLCL2 gene with myocardial infarction: A case-control study in Iran. Journal of Cardiovascular and Thoracic Research 2020; 12(4): 303 doi: 10.34172/jcvtr.2020.49
|
| 66 |
G. Angelidis, V. Valotassiou, M. Satra, D. Psimadas, J. Koutsikos, J. Skoularigis, P. Kollia, P. Georgoulias. Investigating the genetic characteristics of CAD: Is there a role for myocardial perfusion imaging techniques?. Journal of Nuclear Cardiology 2022; 29(6): 2909 doi: 10.1007/s12350-020-02403-x
|
| 67 |
Zsolt Bagyura, Loretta Kiss, Kristóf Hirschberg, Balázs Berta, Gábor Széplaki, Árpád Lux, Zsolt Szelid, Pál Soós, Béla Merkely. Association between VEGF Gene Polymorphisms and In-Stent Restenosis after Coronary Intervention Treated with Bare Metal Stent. Disease Markers 2017; 2017: 1 doi: 10.1155/2017/9548612
|
| 68 |
Sepideh Mehvari, Nahid Karimian Fathi, Sara Saki, Maryam Asadnezhad, Sanaz Arzhangi, Fatemeh Ghodratpour, Marzieh Mohseni, Farzane Zare Ashrafi, Saeed Sadeghian, Mohammadali Boroumand, Fatemeh Shokohizadeh, Elham Rostami, Rahnama Boroumand, Reza Najafipour, Reza Malekzadeh, Yasser Riazalhosseini, Mohammadreza Akbari, Mark Lathrop, Hossein Najmabadi, Kaveh Hosseini, Kimia Kahrizi. Contribution of genetic variants in the development of familial premature coronary artery disease in a cohort of cardiac patients. Clinical Genetics 2024; 105(6): 611 doi: 10.1111/cge.14491
|
| 69 |
Xiao Miao, Xinlin Chen, Zhijun Xie, Honghuang Lin. Tissue-specific Network Analysis of Genetic Variants Associated with Coronary Artery Disease. Scientific Reports 2018; 8(1) doi: 10.1038/s41598-018-29904-7
|
| 70 |
Manal S. Fawzy, Eman A. Toraih, Nagwa M. Aly, Abeer Fakhr-Eldeen, Dahlia I. Badran, Mohammad H. Hussein. Atherosclerotic and thrombotic genetic and environmental determinants in Egyptian coronary artery disease patients: a pilot study. BMC Cardiovascular Disorders 2017; 17(1) doi: 10.1186/s12872-016-0456-3
|
| 71 |
Zhenying Zhang, Sushuang Nan, Xiujuan Duan, Lizhong Wang, Xiaojing Sun, Haiying Zheng, Simona Pichini. Relationship between Expression of Plasma lncRNA-HEIH and Prognosis in Patients with Coronary Artery Disease. Disease Markers 2021; 2021: 1 doi: 10.1155/2021/5662080
|
| 72 |
R. Jasmine, Sowmiya Soundararajan, A. Sherlin Rosita, H. Deena Priscilla. Systems Biology Approaches: Prevention, Diagnosis, and Understanding Mechanisms of Complex Diseases. 2024; : 27 doi: 10.1007/978-981-99-9462-5_2
|
| 73 |
T. A. Degaeva, L. N. Goncharova, I. V. Sychev. Development of additional criteria for development of complications in patients with arterial hypertension who are carriers of the methylenetetrahydrofolate reductase gene polymorphism. Medical Council 2018; (12): 196 doi: 10.21518/2079-701X-2018-12-196-200
|
| 74 |
Ameen M. Mohammad, Galawezh O. Othman, Chiman H. Saeed, Sarah Al Allawi, George S. Gedeon, Shatha M. Qadir, Nasir Al-Allawi. Genetic polymorphisms in early-onset myocardial infarction in a sample of Iraqi patients: a pilot study. BMC Research Notes 2020; 13(1) doi: 10.1186/s13104-020-05367-w
|
| 75 |
Abhijeet Rajendra Sonawane, Elena Aikawa, Masanori Aikawa. Connections for Matters of the Heart: Network Medicine in Cardiovascular Diseases. Frontiers in Cardiovascular Medicine 2022; 9 doi: 10.3389/fcvm.2022.873582
|
| 76 |
Giovanni Mario Pes, Guido Parodi, Maria Pina Dore. Glucose-6-phosphate dehydrogenase deficiency and risk of cardiovascular disease: A propensity score-matched study. Atherosclerosis 2019; 282: 148 doi: 10.1016/j.atherosclerosis.2019.01.027
|
| 77 |
Soodeh Omidi, Fatemeh Ebrahimzadeh, Samira Kalayinia. 9P21.3 locus; An Important Region in Coronary Artery Disease: A Panel Approach to Investigation of the Coronary Artery Disease Etiology. International Journal of Cardiovascular Practice 2019; 4(2): 21 doi: 10.29252/ijcp-25001
|
| 78 |
Asma Naseer Cheema, Dilek Pirim, Xingbin Wang, Jabar Ali, Attya Bhatti, Peter John, Eleanor Feingold, F. Yesim Demirci, M. Ilyas Kamboh. Association Study of Coronary Artery Disease-Associated Genome-Wide Significant SNPs with Coronary Stenosis in Pakistani Population. Disease Markers 2020; 2020: 1 doi: 10.1155/2020/9738567
|
| 79 |
Yahuan Xu, Bibo Shao. Circulating lncRNA IFNG‐AS1 expression correlates with increased disease risk, higher disease severity and elevated inflammation in patients with coronary artery disease. Journal of Clinical Laboratory Analysis 2018; 32(7) doi: 10.1002/jcla.22452
|
| 80 |
Antonio Di Narzo, Itziar Frades, Heidi M. Crane, Paul K. Crane, Jean-Sebastian Hulot, Andrew Kasarskis, Amy Hart, Carmen Argmann, Marla Dubinsky, Inga Peter, Ke Hao. Meta-analysis of sample-level dbGaP data reveals novel shared genetic link between body height and Crohn’s disease. Human Genetics 2021; 140(6): 865 doi: 10.1007/s00439-020-02250-3
|
| 81 |
Yunfeng Huang, Qin Hui, Marta Gwinn, Yi‐Juan Hu, Arshed A. Quyyumi, Viola Vaccarino, Yan V. Sun. Interaction between genetics and smoking in determining risk of coronary artery diseases. Genetic Epidemiology 2022; 46(3-4): 199 doi: 10.1002/gepi.22446
|
| 82 |
Yupeng Huang, Hongyan Jin, Guokang Yang. Associations Between Common Polymorphisms of CDKN2B-AS and Susceptibility to ASCVD. Angiology 2020; 71(10): 934 doi: 10.1177/0003319720941387
|
| 83 |
Julie Hahn, Yi-Ping Fu, Michael R. Brown, Joshua C. Bis, Paul S. de Vries, Mary F. Feitosa, Lisa R. Yanek, Stefan Weiss, Franco Giulianini, Albert Vernon Smith, Xiuqing Guo, Traci M. Bartz, Diane M. Becker, Lewis C. Becker, Eric Boerwinkle, Jennifer A. Brody, Yii-Der Ida Chen, Oscar H. Franco, Megan Grove, Tamara B. Harris, Albert Hofman, Shih-Jen Hwang, Brian G. Kral, Lenore J. Launer, Marcello R. P. Markus, Kenneth M. Rice, Stephen S. Rich, Paul M. Ridker, Fernando Rivadeneira, Jerome I. Rotter, Nona Sotoodehnia, Kent D. Taylor, André G. Uitterlinden, Uwe Völker, Henry Völzke, Jie Yao, Daniel I. Chasman, Marcus Dörr, Vilmundur Gudnason, Rasika A. Mathias, Wendy Post, Bruce M. Psaty, Abbas Dehghan, Christopher J. O’Donnell, Alanna C. Morrison, Marie-Pierre Dubé. Genetic loci associated with prevalent and incident myocardial infarction and coronary heart disease in the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium. PLOS ONE 2020; 15(11): e0230035 doi: 10.1371/journal.pone.0230035
|
| 84 |
Kathleen T. Hickey, Amir Elzomor. Cardiac Channelopathies: Recognition, Treatment, Management. AACN Advanced Critical Care 2018; 29(1): 43 doi: 10.4037/aacnacc2018664
|
| 85 |
RahulS Patil, CM Satvic, LaxmiH Shetty, HS Natraj Setty, Spandana Komma, AneshRajesh Jain, TR Raghu, CN Manjunath. Clinical and angiographic profile of premature heart attack in patients with family history of premature coronary heart disease: A substudy of the PCAD registry (Registered under the Clinical Trials Registry of India [CTRI/2018/03/012544]). Research in Cardiovascular Medicine 2020; 9(2): 42 doi: 10.4103/rcm.rcm_15_20
|
| 86 |
Soodeh Omidi, Fatemeh Ebrahimzadeh, Samira Kalayinia. 9P21.3 locus; An Important Region in Coronary Artery Disease: A Panel Approach to Investigation of the Coronary Artery Disease Etiology. International Journal of Cardiovascular Practice 2019; 4(2): 21 doi: 10.29252//ijcp-25001
|
| 87 |
Ze-Liang Lin, Yan-Cun Liu, Yu-Lei Gao, Xin-Sen Chen, Chao-Lan Wang, Song-Tao Shou, Yan-Fen Chai. S100A9 and SOCS3 as diagnostic biomarkers of acute myocardial infarction and their association with immune infiltration. Genes & Genetic Systems 2022; 97(2): 67 doi: 10.1266/ggs.21-00073
|
| 88 |
Rashid Mir, Chandan k Jha, Imadeldin Elfaki, Jamsheed Javid, Suriya Rehman, Naina Khullar, Shaheena Banu, S. M. S. Chahal. Incidence of MicroR-4513C/T Gene Variability in Coronary Artery Disease - A case-Control Study. Endocrine, Metabolic & Immune Disorders - Drug Targets 2019; 19(8): 1216 doi: 10.2174/1871530319666190417111940
|
| 89 |
Lăcrămioara Ionela Butnariu, Laura Florea, Minerva Codruta Badescu, Elena Țarcă, Irina-Iuliana Costache, Eusebiu Vlad Gorduza. Etiologic Puzzle of Coronary Artery Disease: How Important Is Genetic Component?. Life 2022; 12(6): 865 doi: 10.3390/life12060865
|
| 90 |
Giuseppe Lippi, Fabian Sanchis-Gomar. An Estimation of the Worldwide Epidemiologic Burden of Physical Inactivity-Related Ischemic Heart Disease. Cardiovascular Drugs and Therapy 2020; 34(1): 133 doi: 10.1007/s10557-019-06926-5
|
| 91 |
Samar M Alhusseiny, Nora E Saleh, Wafaa M El-Zayady, Mohammed S Hussein, Samar N El-Beshbishi. Association between Toxoplasma gondii infection and coronary atherosclerosis. Transactions of The Royal Society of Tropical Medicine and Hygiene 2021; 115(10): 1190 doi: 10.1093/trstmh/trab018
|
| 92 |
Michael Fossel, Joe Bean, Nina Khera, Mikhail G. Kolonin. A Unified Model of Age-Related Cardiovascular Disease. Biology 2022; 11(12): 1768 doi: 10.3390/biology11121768
|
| 93 |
Ram Kumar Garg. To Fight Noncommunicable Diseases, We Need to Understand Risk Factors, Health Results, and Intervention Methods. Journal of the Practice of Cardiovascular Sciences 2023; 9(3): 237 doi: 10.4103/jpcs.jpcs_70_23
|
| 94 |
Natalie N. Khalil, Megan L. McCain. Engineering the Cellular Microenvironment of Post-infarct Myocardium on a Chip. Frontiers in Cardiovascular Medicine 2021; 8 doi: 10.3389/fcvm.2021.709871
|
| 95 |
Yu Liu, Jianxin Cheng, Xiangyi Guo, Jingjing Mo, Beibei Gao, Huiyuan Zhou, Yixin Wu, Zhijuan Li. The roles of PAI-1 gene polymorphisms in atherosclerotic diseases: A systematic review and meta-analysis involving 149,908 subjects. Gene 2018; 673: 167 doi: 10.1016/j.gene.2018.06.040
|
| 96 |
Yingli Xie, Di Zhao, Pingshuan Dong, Honglei Wang, Daolin Li, Lihong Lai. Effects of ANRIL polymorphisms on the likelihood of coronary artery disease: A meta‐analysis. Journal of Cellular Biochemistry 2019; 120(4): 6113 doi: 10.1002/jcb.27898
|
| 97 |
Dunia Tahseen Nema Al-Aridhi, Khalid I. H. Allehibi, Zainab A. Razak Al-Sharifi, Muthanna Al Quraishi. Prediction of coronary artery disease by determining serum level of Galectin-3 as a novel biochemical marker and its correlation with the number of coronary arteries occlusion in Iraqi patients with type 2 diabetes mellitus. PROCEEDINGS OF THE III INTERNATIONAL CONFERENCE ON ADVANCED TECHNOLOGIES IN MATERIALS SCIENCE, MECHANICAL AND AUTOMATION ENGINEERING: MIP: Engineering-III – 2021 2021; 2402: 030001 doi: 10.1063/5.0067563
|
| 98 |
Shivan Barungi, Pablo Hernández-Camarero, Gerardo Moreno-Terribas, Rafael Villalba-Montoro, Juan Antonio Marchal, Elena López-Ruiz, Macarena Perán. Clinical implications of inflammation in atheroma formation and novel therapies in cardiovascular diseases. Frontiers in Cell and Developmental Biology 2023; 11 doi: 10.3389/fcell.2023.1148768
|
| 99 |
Santhi Priya Sobha, Kumar Ebenezar Kesavarao. Contribution of Glutathione-S-Transferases Polymorphism and Risk of
Coronary Artery Diseases: A Meta-Analysis. Current Aging Science 2022; 15(3): 282 doi: 10.2174/1874609815666220304193925
|
| 100 |
Xia Zhang, Yan Jun Cao, Hong Yu Zhang, Hongliang Cong, Jian Zhang. Associations between ADIPOQ polymorphisms and coronary artery disease: a meta-analysis. BMC Cardiovascular Disorders 2019; 19(1) doi: 10.1186/s12872-019-1041-3
|
| 101 |
Lang Wang, Jun Hu, Jiali Zhou, Fan Guo, Tan Yao, Liang Zhang. Weighed Gene Coexpression Network Analysis Screens the Potential Long Noncoding RNAs and Genes Associated with Progression of Coronary Artery Disease. Computational and Mathematical Methods in Medicine 2020; 2020: 1 doi: 10.1155/2020/8183420
|
| 102 |
Pan Yang, Junli Liu, Jinqiu Xiao, Huagang Jian, Hao Chen. Associations between Seven Common Cytokine Gene Polymorphisms and Coronary Artery Disease: Evidence from a Meta-Analysis. International Archives of Allergy and Immunology 2020; 181(4): 301 doi: 10.1159/000504752
|
| 103 |
Delicia Shu Qin Ooi, Sze Min Ong, Ming Hui Eng, Yiong Huak Chan, Yung Seng Lee, Adrian Fatt Hoe Low, Mark Yan-Yee Chan, Chew-Kiat Heng, Johnson Rajasingh. Detection of ADTRP in circulation and its role as a novel biomarker for coronary artery disease. PLOS ONE 2020; 15(8): e0237074 doi: 10.1371/journal.pone.0237074
|
| 104 |
X. Xie, X. Shi, M. Liu. The Roles of TLR Gene Polymorphisms in Atherosclerosis: A Systematic Review and Meta‐Analysis of 35,317 Subjects. Scandinavian Journal of Immunology 2017; 86(1): 50 doi: 10.1111/sji.12560
|
| 105 |
Ping Li, Xinxin Yan, Guidong Xu, Zhi Pang, Jiayi Weng, Juan Yin, Meifen Li, Lan Yu, Qian Chen, Kangyun Sun. A novel plasma lncRNA ENST00000416361 is upregulated in coronary artery disease and is related to inflammation and lipid metabolism. Molecular Medicine Reports 2020; doi: 10.3892/mmr.2020.11067
|
| 106 |
Zhipeng Song, Lu Chen, Shuchao Pang, Bo Yan, Katriina Aalto-Setala. Molecular genetic study on GATA5 gene promoter in acute myocardial infarction. PLOS ONE 2021; 16(3): e0248203 doi: 10.1371/journal.pone.0248203
|
| 107 |
Alireza Bahiraee, Azim Nejatizadeh, Hossein Farshidi, Keyanoosh Malekzadeh, Solaleh Emamgholipour, Reyhane Ebrahimi, Amirsaeed Sabeti Aghabozorgi, Mahdy Yazdany, Mohammad Shekari. Association analysis of premature coronary artery disease and cytochrome P450 2D6 (CYP2D6) C100T and G1846A genetic variants and haplotypes in Iranian population. Meta Gene 2020; 25: 100738 doi: 10.1016/j.mgene.2020.100738
|
| 108 |
Yoshiji Yamada, Yoshiki Yasukochi, Kimihiko Kato, Mitsutoshi Oguri, Hideki Horibe, Tetsuo Fujimaki, Ichiro Takeuchi, Jun Sakuma. Identification of 26 novel loci that confer susceptibility to early‑onset coronary artery disease in a Japanese population. Biomedical Reports 2018; doi: 10.3892/br.2018.1152
|
| 109 |
Dolores Corella, Oscar Coltell, George Mattingley, José V. Sorlí, Jose M. Ordovas. Utilizing nutritional genomics to tailor diets for the prevention of cardiovascular disease: a guide for upcoming studies and implementations. Expert Review of Molecular Diagnostics 2017; 17(5): 495 doi: 10.1080/14737159.2017.1311208
|
| 110 |
Subramanian Senthilkumaran, Ramachandran Meenakshisundaram, Wedatallah Osman, Ponniah Thirumalaikolundusubramanian. Acute Myocardial Infarction During Pregnancy and the Puerperium: Experiences and Challenges From Southern India. Mayo Clinic Proceedings 2019; 94(5): 918 doi: 10.1016/j.mayocp.2019.03.005
|
| 111 |
Liyuan Zhu, Shuiping Zhao, Wang Zhao. Potential Regulatory Role of lncRNA-miRNA-mRNA in Coronary Artery Disease (CAD). International Heart Journal 2021; 62(6): 1369 doi: 10.1536/ihj.21-156
|