| 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] |
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| 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
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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
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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
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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
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Ugnė Žulpaitė, Vilma Petrikaitė. Nanosystems for myocardial ischemic injury theranostics. Biochemical Pharmacology 2025; 241 doi: 10.1016/j.bcp.2025.117115
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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
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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
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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
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| 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
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| 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
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| 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
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| 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
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| 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
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| 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
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| 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
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| 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
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| 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
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| 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
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| 19 |
Neda M. Bogari, Samar N. Ekram, Amr A. Amin, Mashhour S. Alotaibi, Naif A. Almalki, Samar A. Amer, Rami Obaid, Reem M. Allam. Evaluating the Role of MIA3 Variant rs17465637 in Coronary Artery Disease: A Comprehensive Case–Control Analysis. Diagnostics 2026; 16(16) doi: 10.3390/diagnostics16162489
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| 20 |
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
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| 21 |
Joana Barbosa Melo. Genetics and myocardial infarction. Revista Portuguesa de Cardiologia 2018; 37(9) doi: 10.1016/j.repc.2018.08.001
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| 22 |
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
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| 23 |
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
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| 24 |
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
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| 25 |
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
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| 26 |
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
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| 27 |
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
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| 28 |
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
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| 29 |
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
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| 30 |
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
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| 31 |
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
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| 32 |
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
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| 33 |
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
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| 34 |
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
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| 35 |
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
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| 36 |
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
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| 37 |
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
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| 38 |
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
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| 39 |
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
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| 40 |
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
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| 41 |
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
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| 42 |
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
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| 43 |
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
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| 44 |
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
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| 45 |
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
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| 46 |
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
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| 47 |
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
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| 48 |
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
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| 49 |
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
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| 50 |
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
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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
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| 52 |
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
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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
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| 54 |
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
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| 55 |
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
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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
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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
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| 58 |
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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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