| 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) doi: 10.1192/bja.2020.60
|
| 3 |
Diane Xue, Anjum Hajat, Alison E. Fohner. Conceptual frameworks for the integration of genetic and social epidemiology in complex diseases. Global Epidemiology 2024; 8 doi: 10.1016/j.gloepi.2024.100156
|
| 4 |
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) doi: 10.1515/jomb-2017-0005
|
| 5 |
Ugnė Žulpaitė, Vilma Petrikaitė. Nanosystems for myocardial ischemic injury theranostics. Biochemical Pharmacology 2025; 241 doi: 10.1016/j.bcp.2025.117115
|
| 6 |
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) doi: 10.1080/08820139.2020.1726382
|
| 7 |
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) doi: 10.1080/00015385.2018.1475093
|
| 8 |
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
|
| 9 |
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) doi: 10.1007/s11033-017-4112-5
|
| 10 |
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 doi: 10.1016/j.genrep.2019.100511
|
| 11 |
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) doi: 10.18087/cardio.2018.11.10195
|
| 12 |
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) doi: 10.33808/clinexphealthsci.953893
|
| 13 |
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) doi: 10.3390/ijms232416127
|
| 14 |
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) doi: 10.4103/ejim.ejim_11_19
|
| 15 |
Chukwuemeka Nwokocha, Javier Palacios, Tolunigba Kolawole, Magdalene Nwokocha, Chinelo Anyaorah, Joel H. Chiroma, Donovan McGrowder, Nelson Orie, Danladi C. Husaini. Toward Precision in Myocardial Injury Management: A Critical Synthesis and the C.A.L.I.B.R.A.T.E. Framework for Biomarker Integration. Clinical Medicine Insights: Cardiology 2026; 20 doi: 10.1177/11795468261454738
|
| 16 |
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
|
| 17 |
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 doi: 10.1016/j.gene.2020.145143
|
| 18 |
Ruikang Liu, Chiyun Sun, Nan Jiang, Yang Liu, Jun Li, Fuyuan Zhang, Cong Chen, Yiying Liu, Xiaodi Qi, Bingting Guo, Kai Yang. Shared Genetic Liability Between Heart Failure and Myocardial Infarction Revealed by Genome-Wide Cross-Trait Analysis. Journal of Cardiovascular Pharmacology and Therapeutics 2026; 31 doi: 10.1177/10742484261452728
|
| 19 |
Svetlana Perovic, Slavica Vujovic, Lejla Kapur-Pojskic, Nemanja Garai, Andjelka Scepanovic. Methylenetetrahydrofolate reductase gene polymorphisms, lipid profiles, and basic renal functional markers as risk for myocardial infarction: A case-control study and haplotype analysis. Archives of Biological Sciences 2024; 76(4) doi: 10.2298/ABS240801035P
|
| 20 |
Joana Barbosa Melo. Genetics and myocardial infarction. Revista Portuguesa de Cardiologia 2018; 37(9) doi: 10.1016/j.repc.2018.08.001
|
| 21 |
Serbulent Yigit, Ayse Feyda Nursal, Atac Celik, Recai Aci, Elgiz Askeroglu. Lack of association between the −2549 insertion/deletion variant of vascular endothelial growth factor and coronary artery disease in the Turkish population. Revista da Associação Médica Brasileira 2024; 70(10) doi: 10.1590/1806-9282.20240333
|
| 22 |
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) doi: 10.3390/genes9120641
|
| 23 |
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
|
| 24 |
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
|
| 25 |
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) doi: 10.1002/jcp.28350
|
| 26 |
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) doi: 10.1097/MD.0000000000023525
|
| 27 |
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 doi: 10.1155/2021/8526144
|
| 28 |
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
|
| 29 |
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) doi: 10.1080/21623945.2019.1595270
|
| 30 |
Masanori Aikawa, Abhijeet R. Sonawane, Sarvesh Chelvanambi, Takaharu Asano, Arda Halu, Joan T. Matamalas, Sasha A. Singh, Shizuka Uchida, Elena Aikawa, Alex Arenas, Jean-Luc Balligand, Chiara Giannarelli, Calum A. MacRae, Neil V. Morgan, Cécile Oury, Hendrik Tevaearai Stahel, Joseph Loscalzo. Precision cardiovascular medicine: shifting the innovation paradigm. Frontiers in Science 2025; 3 doi: 10.3389/fsci.2025.1474469
|
| 31 |
Arzu Ay, Nevra Alkanli, Gokay Taylan, Esra Ergin. Inflammatory Cytokine Genetics and Coronary Artery Disease: Pathogenetic and Protective Analysis of IL-18 (−607 C/A, −137 G/C) and IL-8 (+781 C/T) Gene Variations. Current Issues in Molecular Biology 2026; 48(6) doi: 10.3390/cimb48060589
|
| 32 |
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
|
| 33 |
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) doi: 10.1007/s11033-020-05585-2
|
| 34 |
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
|
| 35 |
Sonja Rajić, Thomas Delerue, Justiina Ronkainen, Ruiyuan Zhang, Joanna Ciantar, Daria Kostiniuk, Pashupati P. Mishra, Leo-Pekka Lyytikäinen, Nina Mononen, Laura Kananen, Annette Peters, Juliane Winkelmann, Marcus E. Kleber, Stefan Lorkowski, Mika Kähönen, Terho Lehtimäki, Olli Raitakari, Melanie Waldenberger, Christian Gieger, Winfried März, Emily W. Harville, Sylvain Sebert, Saara Marttila, Emma Raitoharju. Regulation of nc886 (vtRNA2-1) RNAs is associated with cardiometabolic risk factors and diseases. Clinical Epigenetics 2025; 17(1) doi: 10.1186/s13148-025-01871-7
|
| 36 |
Nurdaulet Tasmurzayev, Baglan Imanbek, Assiya Boltaboyeva, Gulmira Dikhanbayeva, Sarsenbek Zhussupbekov, Qarlygash Saparbayeva, Gulshat Amirkhanova. Explainable AI for Coronary Artery Disease Stratification Using Routine Clinical Data. Algorithms 2025; 18(11) doi: 10.3390/a18110693
|
| 37 |
Prosenjit Saha Apu, Md. Arju Hossain, Md. Shakil, Md. Selim Reza, Siddique Akber Ansari, Irfan Aamer Ansari, Mahammad Humayoo, Md Habibur Rahman. Single-Cell RNA Sequencing to Identify Natural Killer Cell-Linked Genetic Markers and Regulatory Biomolecules in Coronary Heart Disease. Current Bioinformatics 2026; 21(3) doi: 10.2174/0115748936362436250417105150
|
| 38 |
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) doi: 10.1080/10641963.2021.1969660
|
| 39 |
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 doi: 10.1155/2021/8832478
|
| 40 |
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) doi: 10.1177/2047487318780748
|
| 41 |
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) doi: 10.1016/j.tracli.2021.12.008
|
| 42 |
Rui Vitorino. Minimally Invasive Versus Invasive Proteomics: Urine and Blood Biomarkers in Coronary Artery Disease. PROTEOMICS – Clinical Applications 2025; 19(1) doi: 10.1002/prca.202400062
|
| 43 |
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 doi: 10.1016/j.ienj.2020.100855
|
| 44 |
Kamna Srivastava, Kirti Tyagi. Single nucleotide polymorphisms of microRNA in cardiovascular diseases. Clinica Chimica Acta 2018; 478 doi: 10.1016/j.cca.2017.12.037
|
| 45 |
L. Maximilian Buja, Michelle M. McDonald, Bihong Zhao, Navneet Narula, Jagat Narula, Rolf F. Barth. Insights from autopsy-initiated pathological studies of the pathogenesis and clinical manifestations of atherosclerosis and ischemic heart disease: Part II. Ischemic heart disease. Cardiovascular Pathology 2025; 76 doi: 10.1016/j.carpath.2025.107727
|
| 46 |
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) doi: 10.1016/j.ygeno.2020.09.004
|
| 47 |
Xiaoxu Wang, Yaxin Luan, Chengsen Zhang. A meta‐analysis on correlations of OX40L variants with atherosclerotic disorders. Journal of Cellular Biochemistry 2019; 120(6) doi: 10.1002/jcb.28240
|
| 48 |
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
|
| 49 |
Yasushi Imai, Kengo Kusano, Takeshi Aiba, Junya Ako, Yoshihiro Asano, Mariko Harada-Shiba, Masaharu Kataoka, Tomoki Kosho, Toru Kubo, Takayoshi Matsumura, Tetsuo Minamino, Kenji Minatoya, Hiroyuki Morita, Masakazu Nishigaki, Seitaro Nomura, Hitoshi Ogino, Seiko Ohno, Masayuki Takamura, Toshihiro Tanaka, Kenichi Tsujita, Tetsuro Uchida, Hiroyuki Yamagishi, Yusuke Ebana, Kanna Fujita, Kazufumi Ida, Shunsuke Inoue, Kaoru Ito, Yuki Kuramoto, Jun Maeda, Keiji Matsunaga, Reiko Neki, Kenta Sugiura, Hayato Tada, Akihiro Tsuji, Takanobu Yamada, Tomomi Yamaguchi, Eiichiro Yamamoto, Akinori Kimura, Koichiro Kuwahara, Koji Maemura, Tohru Minamino, Hiroko Morisaki, Katsushi Tokunaga. JCS/JCC/JSPCCS 2024 Guideline on Genetic Testing and Counseling in Cardiovascular Disease. Journal of Cardiology 2025; 85(2) doi: 10.1016/j.jjcc.2024.10.002
|
| 50 |
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) doi: 10.1177/1470320316655037
|
| 51 |
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) doi: 10.3390/jcdd9090295
|
| 52 |
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 doi: 10.1016/j.gene.2018.05.117
|
| 53 |
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
|
| 54 |
Majid Kadhum Hussain, Ibrahem Rahem J. Al-Aadily, Alhan Abdulmohsin A. Al-Rashid, Abdol Hussein A. Algenabi, Ahmed Naseer Kaftan, Muna Abdulridha Al-Barqaawi, Layth Ahmed A. Al-Fahham, Teba Jaber Merza, Iman Jabbar Kadhim, Mohammed Ali Abdulameer Khikani. Insight into adiponectin gene impact on coronary artery disease from a polymorphism case-control study in Iraqi individuals. Gene Reports 2024; 36 doi: 10.1016/j.genrep.2024.101996
|
| 55 |
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) doi: 10.23950/jcmk/13918
|
| 56 |
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) doi: 10.1159/000499866
|
| 57 |
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
|
| 58 |
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) doi: 10.2174/1389450123666220811101032
|
| 59 |
A. R. Sidko, B. V. Titov, T. S. Sukhinina, L. O. Minushkina, I. S. Kiselev, Ye. V. Parfyonova, O. O. Favorova. Search for Age-Dependent Genetic Risk Factors for Predicting Early Myocardial Infarction in Men And Women. Kardiologiia 2025; 65(7) doi: 10.18087/cardio.2025.7.n2909
|
| 60 |
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
|
| 61 |
S. M Shiraz Rizvi, Farzana Mahdi, Jyoti Dwivedi, Bashir Ahmad Mir, Zeashan H Zaidi, Namakkal Soorappan Rajasekaran. Association of NOS3 (rs1799983) and DDAH2 (rs805305) Gene Polymorphisms With Coronary Artery Disease in the Northern Indian Cohort. Cureus 2025; doi: 10.7759/cureus.79546
|
| 62 |
Asma Amrani-Midoun, Nadia Laredj, Taki Djebaili, Djelti Mounia, Abdelkader Djelloul, Lilia Zouli, Hamid Aoumeur, Nachi Mourad. Association of insertion/deletion (I/D) polymorphism of angiotensin-converting enzyme gene (ACE) with ST segment elevation myocardial infarction and factors risk in Western Algeria: case-control study. Cor et Vasa 2025; 67(5) doi: 10.33678/cor.2025.027
|
| 63 |
Duy Cong Tran, Minh Duc Do, Linh Hoang Gia Le, Truc Thanh Thai, Sy Van Hoang, Binh Quang Truong. Relationship between the AGT M235T genetic variant and the characteristics and prognosis of coronary atherosclerosis in patients with acute myocardial infarction. Molecular Biology Reports 2024; 51(1) doi: 10.1007/s11033-024-09986-5
|
| 64 |
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) doi: 10.1172/JCI129203
|
| 65 |
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) doi: 10.1177/0003319717696622
|
| 66 |
Nidhi P. Kulkarni, Clement C. Zai, Mikaela K. Dimick, Alysha A. Sultan, L. Trevor Young, Benjamin I. Goldstein. Greater polygenic risk for cardiovascular disease is associated with reduced executive function among youth with bipolar disorder. Journal of Affective Disorders 2026; 397 doi: 10.1016/j.jad.2025.120926
|
| 67 |
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) doi: 10.36740/WLek202001138
|
| 68 |
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
|
| 69 |
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 doi: 10.1016/j.gene.2018.01.036
|
| 70 |
Agnieszka Pietruszyńska-Reszetarska, Robert Pietruszyński, Robert Irzmański. The Significance of Genetically Determined Methylation and Folate Metabolism Disorders in the Pathogenesis of Coronary Artery Disease: A Target for New Therapies?. International Journal of Molecular Sciences 2024; 25(13) doi: 10.3390/ijms25136924
|
| 71 |
An Viet Tran, Anh Phuong Nguyen, Phat Tan Tran, Khue Duy Nguyen, Thuan Tuan Nguyen, Bao Lam Thai Tran, Cao Thi Tai Nguyen. The prognostic value of AGTR1 A1166C gene polymorphism in all-cause mortality and heart failure in patients with acute myocardial infarction. Journal of the Renin-Angiotensin-Aldosterone System 2025; 26 doi: 10.1177/14703203241312627
|
| 72 |
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) doi: 10.1016/j.yexmp.2016.12.003
|
| 73 |
Emin Grbić, Jernej Letonja, Danijel Petrovič. The VEGFA rs2010963 Gene Polymorphism Is a Potential Genetic Risk Factor for Myocardial Infarction in Slovenian Subjects with Type 2 Diabetes Mellitus. Biomolecules 2024; 14(12) doi: 10.3390/biom14121584
|
| 74 |
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) doi: 10.1016/j.arcmed.2019.12.017
|
| 75 |
Yu Xuan Jin, David Alexandru Anton, Ming Yuan Zhou, Amir Pourghadiri, Chaocheng Liu. Dermatogenomic Insights into Systemic Diseases: Implications for Primary and Preventive Medicine. DNA 2026; 6(1) doi: 10.3390/dna6010002
|
| 76 |
天雨 高. Gene Screening for Familial Hypercholesterolemia-Related Coronary Heart Disease in Patients from Inner Mongolia. Advances in Clinical Medicine 2025; 15(03) doi: 10.12677/acm.2025.153721
|
| 77 |
Zhipeng Song, Rui Gao, Bo Yan. Potential roles of microRNA-1 and microRNA-133 in cardiovascular disease. Reviews in Cardiovascular Medicine 2020; 21(1) doi: 10.31083/j.rcm.2020.01.577
|
| 78 |
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) doi: 10.1016/j.ygeno.2020.01.019
|
| 79 |
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)) doi: 10.25557/IGPP.2017.4.8527
|
| 80 |
Léo Henches, Jihye Kim, Zhiyu Yang, Simone Rubinacci, Gabriel Pires, Clara Albiñana, Christophe Boetto, Hanna Julienne, Arthur Frouin, Antoine Auvergne, Yuka Suzuki, Sarah Djebali, Olivier Delaneau, Andrea Ganna, Bjarni Vilhjálmsson, Florian Privé, Hugues Aschard. Polygenic risk score prediction accuracy convergence. Human Genetics and Genomics Advances 2025; 6(3) doi: 10.1016/j.xhgg.2025.100457
|
| 81 |
Marisa Cañadas-Garre, Joaquín J. Maqueda, Blanca Baños-Jaime, Claire Hill, Ryan Skelly, Ruaidhri Cappa, Eoin Brennan, Ross Doyle, Catherine Godson, Alexander P. Maxwell, Amy Jayne McKnight. Mitochondrial related variants associated with cardiovascular traits. Frontiers in Physiology 2024; 15 doi: 10.3389/fphys.2024.1395371
|
| 82 |
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 doi: 10.1016/j.ijbiomac.2018.11.021
|
| 83 |
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) doi: 10.1161/CIRCULATIONAHA.121.053730
|
| 84 |
Joana Barbosa Melo. Genetics and myocardial infarction. Revista Portuguesa de Cardiologia (English Edition) 2018; 37(9) doi: 10.1016/j.repce.2018.09.002
|
| 85 |
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) doi: 10.29296/25877305-2023-04-09
|
| 86 |
AS Arthi Sri, VP Veeraraghavan, S Patil, AT Raj. Long Non-Coding RNA as a Potential Diagnostic Tool in Coronary Artery Diseases - A Systematic Review. Nigerian Journal of Clinical Practice 2025; 28(1) doi: 10.4103/njcp.njcp_256_24
|
| 87 |
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
|
| 88 |
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) doi: 10.1097/MD.0000000000025146
|
| 89 |
Junyu Zhou, Meiling Liu, Sunmin Park. Association of Metabolic Diseases and Moderate Fat Intake with Myocardial Infarction Risk. Nutrients 2024; 16(24) doi: 10.3390/nu16244273
|
| 90 |
Kun Feng, Jinyue Yang, Kai Liu. Shared genetic associations and aetiology between obstructive sleep apnoea and cardiovascular diseases: a genome-wide cross-trait analysis and bidirectional Mendelian randomization analysis. European Journal of Preventive Cardiology 2025; 32(15) doi: 10.1093/eurjpc/zwae347
|
| 91 |
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 doi: 10.1016/j.gene.2017.04.045
|
| 92 |
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
|
| 93 |
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) doi: 10.1097/MBC.0000000000000714
|
| 94 |
Enrico Maiorino, Joseph Loscalzo. Phenomics and Robust Multiomics Data for Cardiovascular Disease Subtyping. Arteriosclerosis, Thrombosis, and Vascular Biology 2023; 43(7) doi: 10.1161/ATVBAHA.122.318892
|
| 95 |
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) doi: 10.34172/jcvtr.2020.49
|
| 96 |
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) doi: 10.1007/s12350-020-02403-x
|
| 97 |
Hare Krishna, Ajay Kumar, Shalabh Agarwal, Sanjeev Kumar Jain. A Meta-analysis on Molecular Gene Expression Profiles in Coronary Artery Disease. Journal of Cardiac Critical Care TSS 2026; 10 doi: 10.25259/JCCC_64_2025
|
| 98 |
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 doi: 10.1155/2017/9548612
|
| 99 |
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) doi: 10.1111/cge.14491
|
| 100 |
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
|
| 101 |
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
|
| 102 |
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 doi: 10.1155/2021/5662080
|
| 103 |
R. Jasmine, Sowmiya Soundararajan, A. Sherlin Rosita, H. Deena Priscilla. Systems Biology Approaches: Prevention, Diagnosis, and Understanding Mechanisms of Complex Diseases. 2024; doi: 10.1007/978-981-99-9462-5_2
|
| 104 |
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) doi: 10.21518/2079-701X-2018-12-196-200
|
| 105 |
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
|
| 106 |
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
|
| 107 |
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 doi: 10.1016/j.atherosclerosis.2019.01.027
|
| 108 |
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) doi: 10.29252/ijcp-25001
|
| 109 |
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 doi: 10.1155/2020/9738567
|
| 110 |
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
|
| 111 |
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) doi: 10.1007/s00439-020-02250-3
|
| 112 |
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) doi: 10.1002/gepi.22446
|
| 113 |
Yupeng Huang, Hongyan Jin, Guokang Yang. Associations Between Common Polymorphisms of CDKN2B-AS and Susceptibility to ASCVD. Angiology 2020; 71(10) doi: 10.1177/0003319720941387
|
| 114 |
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) doi: 10.1371/journal.pone.0230035
|
| 115 |
Kathleen T. Hickey, Amir Elzomor. Cardiac Channelopathies: Recognition, Treatment, Management. AACN Advanced Critical Care 2018; 29(1) doi: 10.4037/aacnacc2018664
|
| 116 |
Xiaojun Bi, Ze Wang, Jingteng He. Recent advances in biomimetic nanodelivery systems for the treatment of myocardial ischemia reperfusion injury. Colloids and Surfaces B: Biointerfaces 2025; 247 doi: 10.1016/j.colsurfb.2024.114414
|
| 117 |
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) doi: 10.4103/rcm.rcm_15_20
|
| 118 |
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) doi: 10.29252//ijcp-25001
|
| 119 |
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) doi: 10.1266/ggs.21-00073
|
| 120 |
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) doi: 10.2174/1871530319666190417111940
|
| 121 |
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) doi: 10.3390/life12060865
|
| 122 |
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) doi: 10.1007/s10557-019-06926-5
|
| 123 |
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) doi: 10.1093/trstmh/trab018
|
| 124 |
Michael Fossel, Joe Bean, Nina Khera, Mikhail G. Kolonin. A Unified Model of Age-Related Cardiovascular Disease. Biology 2022; 11(12) doi: 10.3390/biology11121768
|
| 125 |
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) doi: 10.4103/jpcs.jpcs_70_23
|
| 126 |
Ming Lu, Bin Lu, Le Wang. Temporal Decomposition Analysis of Noncommunicable Disease Burden: The Interplay of Population Aging, Population Growth, and Low Physical Activity, 2010–2019. Journal of Physical Activity and Health 2025; 22(3) doi: 10.1123/jpah.2024-0201
|
| 127 |
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
|
| 128 |
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 doi: 10.1016/j.gene.2018.06.040
|
| 129 |
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) doi: 10.1002/jcb.27898
|
| 130 |
Maxwell Quinn, Richard Y. K. Zhang, Idris Bello, Kerry-Anne Rye, Shane R. Thomas. Myeloperoxidase as a Promising Therapeutic Target after Myocardial Infarction. Antioxidants 2024; 13(7) doi: 10.3390/antiox13070788
|
| 131 |
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 doi: 10.1063/5.0067563
|
| 132 |
Ishu Garg, Harish Kumar, Madhu Verma, Iti Chauhan, Vishal Panwar. Treating Cardiovascular Disorders with Personalized Medicine. Cardiovascular & Hematological Disorders-Drug Targets 2025; 25(2) doi: 10.2174/011871529X361429250215190129
|
| 133 |
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
|
| 134 |
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) doi: 10.2174/1874609815666220304193925
|
| 135 |
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
|
| 136 |
Nidhi P. Kulkarni, Clement C. Zai, Kody G. Kennedy, Megan Mio, L. Trevor Young, Bradley J. MacIntosh, Benjamin I. Goldstein. Higher polygenic risk for cardiovascular disease is associated with lower cerebral blood flow in youth with bipolar disorder. Neurobiology of Disease 2026; 221 doi: 10.1016/j.nbd.2026.107347
|
| 137 |
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 doi: 10.1155/2020/8183420
|
| 138 |
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) doi: 10.1159/000504752
|
| 139 |
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) doi: 10.1371/journal.pone.0237074
|
| 140 |
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) doi: 10.1111/sji.12560
|
| 141 |
Yasushi Imai, Kengo Kusano, Takeshi Aiba, Junya Ako, Yoshihiro Asano, Mariko Harada-Shiba, Masaharu Kataoka, Tomoki Kosho, Toru Kubo, Takayoshi Matsumura, Tetsuo Minamino, Kenji Minatoya, Hiroyuki Morita, Masakazu Nishigaki, Seitaro Nomura, Hitoshi Ogino, Seiko Ohno, Masayuki Takamura, Toshihiro Tanaka, Kenichi Tsujita, Tetsuro Uchida, Hiroyuki Yamagishi, Yusuke Ebana, Kanna Fujita, Kazufumi Ida, Shunsuke Inoue, Kaoru Ito, Yuki Kuramoto, Jun Maeda, Keiji Matsunaga, Reiko Neki, Kenta Sugiura, Hayato Tada, Akihiro Tsuji, Takanobu Yamada, Tomomi Yamaguchi, Eiichiro Yamamoto, Akinori Kimura, Koichiro Kuwahara, Koji Maemura, Tohru Minamino, Hiroko Morisaki, Katsushi Tokunaga. JCS/JCC/JSPCCS 2024 Guideline on Genetic Testing and Counseling in Cardiovascular Disease. Circulation Journal 2024; 88(12) doi: 10.1253/circj.CJ-23-0926
|
| 142 |
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
|
| 143 |
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) doi: 10.1371/journal.pone.0248203
|
| 144 |
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 doi: 10.1016/j.mgene.2020.100738
|
| 145 |
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
|
| 146 |
Zh. Y. Baigarayeva, A. K. Boltaboyeva, B. T. Imanbek, M. I. Kozhamberdiyeva, Zh. K. Zholdybayeva. COMPARATIVE ANALYSIS OF MACHINE LEARNING METHODS FOR PREDICTING CORONARY HEART DISEASE: EVIDENCE FROM THE UCI HEART DISEASE DATASET. Bulletin of Shakarim University. Technical Sciences 2026; 1(4(20)) doi: 10.53360/2788-7995-2025-4(20)-6
|
| 147 |
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) doi: 10.1080/14737159.2017.1311208
|
| 148 |
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) doi: 10.1016/j.mayocp.2019.03.005
|
| 149 |
Liyuan Zhu, Shuiping Zhao, Wang Zhao. Potential Regulatory Role of lncRNA-miRNA-mRNA in Coronary Artery Disease (CAD). International Heart Journal 2021; 62(6) doi: 10.1536/ihj.21-156
|