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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
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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 TreatmentsFrontiers 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 mattersBJPsych Advances 2020; 26(6): 327 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 diseasesGlobal Epidemiology 2024; 8: 100156 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 DiseaseJournal of Medical Biochemistry 2017; 36(3): 251 doi: 10.1515/jomb-2017-0005
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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-AnalysisImmunological Investigations 2021; 50(1): 37 doi: 10.1080/08820139.2020.1726382
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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 biomarkersActa Cardiologica 2019; 74(2): 153 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 analysisMolecular Medicine Reports 2018;  doi: 10.3892/mmr.2018.9551
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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 onsetMolecular Biology Reports 2017; 44(4): 315 doi: 10.1007/s11033-017-4112-5
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Nehle Jamali, Mahboobeh Nasiri, Majid Yavarian. Association of the functional genetic variants of TOX3 gene with breast cancer in Iran: A case-control studyGene Reports 2020; 18: 100511 doi: 10.1016/j.genrep.2019.100511
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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 PrognosisKardiologiia 2018; 58(11): 24 doi: 10.18087/cardio.2018.11.10195
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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 RestenosisClinical and Experimental Health Sciences 2022; 12(3): 602 doi: 10.33808/clinexphealthsci.953893
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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 InfarctionInternational Journal of Molecular Sciences 2022; 23(24): 16127 doi: 10.3390/ijms232416127
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Nashwa S. Ghanem, Naglaa M. El-Sayed, Ahmed K. Abbas, Ollfat G. Shaker. Adiponectin and its polymorphism: relation to coronary artery diseaseThe Egyptian Journal of Internal Medicine 2019; 31(3): 376 doi: 10.4103/ejim.ejim_11_19
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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−/− MiceFrontiers in Immunology 2019; 10 doi: 10.3389/fimmu.2019.02205
15
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 ChineseGene 2021; 766: 145143 doi: 10.1016/j.gene.2020.145143
16
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 analysisArchives of Biological Sciences 2024; 76(4): 455 doi: 10.2298/ABS240801035P
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Joana Barbosa Melo. Genetics and myocardial infarctionRevista Portuguesa de Cardiologia 2018; 37(9): 737 doi: 10.1016/j.repc.2018.08.001
18
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 populationRevista da Associação Médica Brasileira 2024; 70(10) doi: 10.1590/1806-9282.20240333
19
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 LearningGenes 2018; 9(12): 641 doi: 10.3390/genes9120641
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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-analysisHighlights in BioScience 2020;  doi: 10.36462/H.BioSci.20213
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Peilin Xiao, Jianli Shi, Xiaoli Liu. Associations of leptin and leptin receptor genetic variants with coronary artery disease: a meta-analysisBioscience Reports 2019; 39(6) doi: 10.1042/BSR20190466
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Arup Kr. Malakar, Debashree Choudhury, Binata Halder, Prosenjit Paul, Arif Uddin, Supriyo Chakraborty. A review on coronary artery disease, its risk factors, and therapeuticsJournal of Cellular Physiology 2019; 234(10): 16812 doi: 10.1002/jcp.28350
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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 interventionMedicine 2020; 99(51): e23525 doi: 10.1097/MD.0000000000023525
24
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 SignificancesDisease Markers 2021; 2021: 1 doi: 10.1155/2021/8526144
25
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 patientsScientific Reports 2019; 9(1) doi: 10.1038/s41598-019-56263-8
26
Zhiyuan Wang, Jinglan Diao, Xin Yue, Jingquan Zhong. Effects of ADIPOQ polymorphisms on individual susceptibility to coronary artery disease: a meta-analysisAdipocyte 2019; 8(1): 137 doi: 10.1080/21623945.2019.1595270
27
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 literatureBMC Cardiovascular Disorders 2019; 19(1) doi: 10.1186/s12872-019-01303-4
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Gholamreza Shahsavari, Negar Nouryazdan, Glavizh Adibhesami, Mehdi Birjandi. Genetic associations and serum paraoxonase levels with atherosclerosis in western Iranian patientsMolecular Biology Reports 2020; 47(7): 5137 doi: 10.1007/s11033-020-05585-2
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Yupeng Huang, Hongyan Jin, Guokang Yang. WITHDRAWN: A meta-analysis on associations of CDKN2B-AS variants with atherosclerotic cardio-cerebral vascular diseasesLife Sciences 2018;  doi: 10.1016/j.lfs.2018.12.047
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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 populationClinical and Experimental Hypertension 2021; 43(8): 788 doi: 10.1080/10641963.2021.1969660
31
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 DiseaseDisease Markers 2021; 2021: 1 doi: 10.1155/2021/8832478
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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 studiesEuropean Journal of Preventive Cardiology 2019; 26(2): 160 doi: 10.1177/2047487318780748
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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 syndromeTransfusion Clinique et Biologique 2022; 29(2): 129 doi: 10.1016/j.tracli.2021.12.008
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Rui Vitorino. Minimally Invasive Versus Invasive Proteomics: Urine and Blood Biomarkers in Coronary Artery DiseasePROTEOMICS – Clinical Applications 2025; 19(1) doi: 10.1002/prca.202400062
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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
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Kamna Srivastava, Kirti Tyagi. Single nucleotide polymorphisms of microRNA in cardiovascular diseasesClinica Chimica Acta 2018; 478: 101 doi: 10.1016/j.cca.2017.12.037
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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 diseaseCardiovascular Pathology 2025; 76: 107727 doi: 10.1016/j.carpath.2025.107727
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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 analysisGenomics 2020; 112(6): 5072 doi: 10.1016/j.ygeno.2020.09.004
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Xiaoxu Wang, Yaxin Luan, Chengsen Zhang. A meta‐analysis on correlations of OX40L variants with atherosclerotic disordersJournal of Cellular Biochemistry 2019; 120(6): 9624 doi: 10.1002/jcb.28240
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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-analysisClinical and Experimental Hypertension 2024; 46(1) doi: 10.1080/10641963.2024.2328147
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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 DiseaseJournal of Cardiology 2025; 85(2): 115 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, and ACE/KLK1 polymorphisms with acute myocardial infarction induced by coronary artery stenosisJournal of the Renin-Angiotensin-Aldosterone System 2016; 17(2) doi: 10.1177/1470320316655037
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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 StudiesJournal of Cardiovascular Development and Disease 2022; 9(9): 295 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 diseaseGene 2018; 672: 16 doi: 10.1016/j.gene.2018.05.117
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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-analysisBMC Medical Genomics 2018; 11(1) doi: 10.1186/s12920-018-0427-x
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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 individualsGene Reports 2024; 36: 101996 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 populationJournal of Clinical Medicine of Kazakhstan 2023; 20(6): 23 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 DiseaseCardiology 2019; 142(3): 149 doi: 10.1159/000499866
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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-analysisThrombosis 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 AtherosclerosisCurrent Drug Targets 2022; 23(14): 1345 doi: 10.2174/1389450123666220811101032
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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 cohortsScientific 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 CohortCureus 2025;  doi: 10.7759/cureus.79546
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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 infarctionMolecular 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 medicineJournal of Clinical Investigation 2020; 130(1): 29 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 PopulationAngiology 2017; 68(10): 877 doi: 10.1177/0003319717696622
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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 BROTHERSWiadomości Lekarskie 2020; 73(1): 201 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 populationBMC 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 infarctionGene 2018; 647: 283 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): 6924 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 infarctionJournal 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 studyExperimental and Molecular Pathology 2017; 102(1): 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 MellitusBiomolecules 2024; 14(12): 1584 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 CommunityArchives of Medical Research 2020; 51(2): 153 doi: 10.1016/j.arcmed.2019.12.017
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天雨 高. Gene Screening for Familial Hypercholesterolemia-Related Coronary Heart Disease in Patients from Inner MongoliaAdvances in Clinical Medicine 2025; 15(03): 1133 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 diseaseReviews 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 studiesGenomics 2020; 112(3): 2452 doi: 10.1016/j.ygeno.2020.01.019
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Г.А. Березовская, Е.С. Клокова, Н.Н. Петрищев. Genetic predictors for symptoms recurrenсe in coronary artery disease after percutaneous coronary interventionZHurnal «Patologicheskaia fiziologiia i eksperimental`naia terapiia» 2017; (4(61)): 81 doi: 10.25557/IGPP.2017.4.8527
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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 traitsFrontiers in Physiology 2024; 15 doi: 10.3389/fphys.2024.1395371
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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 dietInternational Journal of Biological Macromolecules 2019; 123: 576 doi: 10.1016/j.ijbiomac.2018.11.021
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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 DiseaseCirculation 2022; 145(11): 808 doi: 10.1161/CIRCULATIONAHA.121.053730
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Joana Barbosa Melo. Genetics and myocardial infarctionRevista Portuguesa de Cardiologia (English Edition) 2018; 37(9): 737 doi: 10.1016/j.repce.2018.09.002
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G. Roytberg, S. Prozorov, N. Kondratova, D. Sokolov. STENTING OF CORONARY ARTERIES IN ACUTE MYOCARDIAL INFARCTION IN FIRST DEGREE RELATIVES WITH FAMILIAL ATHEROSCLEROSISVrach 2024; 34(4): 48 doi: 10.29296/25877305-2023-04-09
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AS Arthi Sri, VP Veeraraghavan, S Patil, AT Raj. Long Non-Coding RNA as a Potential Diagnostic Tool in Coronary Artery Diseases - A Systematic ReviewNigerian Journal of Clinical Practice 2025; 28(1): 1 doi: 10.4103/njcp.njcp_256_24
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Szilvia Fiatal, Róza Ádány. Application of Single-Nucleotide Polymorphism-Related Risk Estimates in Identification of Increased Genetic Susceptibility to Cardiovascular Diseases: A Literature ReviewFrontiers in Public Health 2018; 5 doi: 10.3389/fpubh.2017.00358
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Bolin Wang, Zhihui Su, Lijun Wan, Tao He. Relationship between long non-coding RNA polymorphism and the risk of coronary artery diseaseMedicine 2021; 100(12): e25146 doi: 10.1097/MD.0000000000025146
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Junyu Zhou, Meiling Liu, Sunmin Park. Association of Metabolic Diseases and Moderate Fat Intake with Myocardial Infarction RiskNutrients 2024; 16(24): 4273 doi: 10.3390/nu16244273
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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 analysisEuropean Journal of Preventive Cardiology 2024;  doi: 10.1093/eurjpc/zwae347
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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 ChineseGene 2017; 624: 43 doi: 10.1016/j.gene.2017.04.045
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Lina Hu, Guoyi Su, Xia Wang. The roles of ANRIL polymorphisms in coronary artery disease: a meta-analysisBioscience Reports 2019; 39(12) doi: 10.1042/BSR20181559
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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 populationBlood Coagulation & Fibrinolysis 2018; 29(3): 267 doi: 10.1097/MBC.0000000000000714
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Enrico Maiorino, Joseph Loscalzo. Phenomics and Robust Multiomics Data for Cardiovascular Disease SubtypingArteriosclerosis, Thrombosis, and Vascular Biology 2023; 43(7): 1111 doi: 10.1161/ATVBAHA.122.318892
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Najmeh Ramezanpour, Mahboobeh Nasiri, Omid Reza Akbarpour. Association of rs4618210A>G variant in PLCL2 gene with myocardial infarction: A case-control study in IranJournal of Cardiovascular and Thoracic Research 2020; 12(4): 303 doi: 10.34172/jcvtr.2020.49
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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
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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 StentDisease Markers 2017; 2017: 1 doi: 10.1155/2017/9548612
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