Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants
Myocardial Infarction Genetics Consortium·2009·Nature Genetics
DOI 10.1038/ng.327
Cited by (1,001)
Items 801–900 of 1,001
- Genetic Risk Prediction for Primary and Secondary Prevention of Atherosclerotic Cardiovascular Disease: an UpdateChristopher Labos, George Thanassoulis · 2018 · Current Cardiology Reports
- AKT and ERK1/2 activation via remote ischemic preconditioning prevents Kcne2 -dependent sudden cardiac deathZhaoyang Hu, Jin Liu, Leng Zhou, Xin Tian, Geoffrey Winston Abbott · 2019 · Physiological Reports
- Polygenic Risk Scores in Familial HypercholesterolemiaDaniel James Rader, Samip Sheth · 2019 · Journal of the American College of Cardiology
- Importance of Thyroid Hormone level and Genetic Variations in Deiodinases for Patients after Acute Myocardial Infarction: A Longitudinal Observational StudyNijolė Kažukauskienė, Daina Skiriutė, Olivija Gustienė, Julius Burkauskas, Violeta Zaliunaite, Narseta Mickuvienė, Julija Brožaitienė · 2020 · Scientific Reports
- Translating Genomic Analyses into Improved Management of Coronary Artery DiseaseChristopher T. Johansen, Matthew Bruce Lanktree, Robert Alexander Hegele · 2010 · Future Cardiology
- Generalidades de la fibrilación auricularLuis Fernando Pava Molano, Pablo E. Perafán-Bautista · 2016 · Revista Colombiana de Cardiología
- Reply to: Hultström et al., Genetic determinants of mannose-binding lectin activity predispose to thromboembolic complications in critical COVID-19. Mannose-binding lectin genetics in COVID-19Rosanna Asselta, Elvezia Maria Paraboschi, Matteo Stravalaci, Pietro Invernizzi, Paolo Bonfanti, Andrea Biondi, Isabel Pagani, Mattia Pedotti, Andrea Doni, Francesco Scavello et al. · 2022 · Nature Immunology
- A Breakthrough in Genetics and its Relevance to Prevention of Coronary Artery Disease in LMICRobert Roberts · 2017 · Global Heart
- The Genetic Basis of Coronary Artery Disease and Atrial Fibrillation: A Search for Disease Mechanisms and Therapeutic TargetsJacques Prince Neelankavil, Christoph D. Rau, Yibin Wang · 2015 · Journal of Cardiothoracic and Vascular Anesthesia
- A comparison of genomic profiles of complex diseases under different modelsVíctor Potenciano, María M. Abad‐Grau, Antonio Alcina, Fuencisla Matesanz · 2015 · BMC Medical Genomics
- Cognitive Phenotypes and Endophenotypes: Concepts and CriteriaCarrie E. Bearden, Anderson M. Winkler, Katherine H. Karlsgodt, Robert M. Bilder · 2016 · Innovations in cognitive neuroscience
- A novel recombinant antibody specific to full-length stromal derived factor-1 for potential application in biomarker studiesDaniel I. Bromage, Staša Taferner, M. Gopala-Krishnan Pillai, Derek M. Yellon, Sean M. Davidson · 2017 · PLoS ONE
- Identification of a single nucleotide polymorphism indicative of high risk in acute myocardial infarctionKavita K. Shalia, Dhananjaya Saranath, Jaipreet Rayar, Vinod K. Shah, Manoj R. Mashru, Surendra L Soneji · 2017 · The Indian Journal of Medical Research
- The association of polymorphism in PHACTR1 rs9349379 and rs12526453 with coronary artery atherosclerosis or coronary artery calcification. A systematic reviewPavlos G. Koitsopoulos, Simon W. Rabkin · 2020 · Coronary Artery Disease
- Genetics-based risk scores for prediction of premature coronary artery diseaseRajeev Gupta · 2023 · Indian Heart Journal
- Prevalence and risk of cardiovascular risk factors and events in offspring of patients at high vascular risk and effect of location of parental vascular diseaseMaaike Weijmans, Yolanda van der Graaf, Gert Jan de Borst, Folkert Wouter Asselbergs, Maarten Jan Cramer, Ale Algra, Frank L.J. Visseren · 2015 · International Journal of Cardiology
- Genome-Wide Assessment for Genetic Variants Associated with Ventricular Dysfunction after Primary Coronary Artery Bypass Graft SurgeryAmanda A. Fox, Mias Pretorius, Kuang-Yu Liu, Charles D. Collard, Tjörvi E. Perry, Stanton Keith Shernan, Philip L. De Jager, David A. Hafler, Daniel S. Herman, Steven R. DePalma et al. · 2011 · PLoS ONE
- The Relationships Between FAM5C SNP (rs10920501) Variability and Metabolic Syndrome and Inflammation in Women With Coronary Heart DiseaseJennifer L. Cline, Theresa M. Beckie · 2011 · Biological Research For Nursing
- From circulating biomarkers to genomics and imaging in the prediction of cardiovascular events in the general populationCristiano Fava, Martina Montagnana, Gian Cesare Guidi, Olle Melander · 2011 · Annals of Medicine
- The interleukin-1 cluster, dyslipidaemia and risk of myocardial infarctionBernard D. Keavney · 2010 · BMC Medicine
- Association of single-nucleotide polymorphisms on chromosome 1p13 and 9p21 with acute myocardial infarction in a Chinese population: the AMI study in ChinaJin cheng Guo, Wei LI, Xin Liu, Xingyu Wang, Yang Wang, Lisheng Liu · 2011 · Academic Journal of Second Military Medical University
- Association of rs1122608 with Coronary Artery Disease and Lipid Profile: A Meta-analysisShuo Liu, Bingqiu Xiu, Jingdong Liu, Aimin Xue, Qiqun Tang, Yiwen Shen, Jianhui Xie · 2016 · Archives of Medical Research
- Genetics—Current and Future Role in the Prevention and Management of Coronary Artery DiseaseRobert Roberts · 2016 · Current Atherosclerosis Reports
- Implications of Genetic Polymorphisms in Inflammation-Induced Atherosclerosis~!2009-11-03~!2009-12-07~!2010-02-22~!Jayashree Shanker, Vijay Vir Kakkar · 2010 · The Open Cardiovascular Medicine Journal
- Genetic variants of increased waist circumference in psychosisDzana Sudic Hukic, Urban Ösby, Eric Olsson, Agneta Hilding, Claes‐Göran Östenson, Harvest Feng Gu, Ewa Ehrenborg, Gunnar Edman, Martin Schalling, Catharina Lavebratt et al. · 2017 · Psychiatric Genetics
- Epidemiology in Germany—general development and personal experienceH.‐Erich Wichmann · 2017 · European Journal of Epidemiology
- Molecular genetic studies in Saudi population; identified variants from GWAS and meta-analysis in strokeKhalid Khalaf Alharbi, Imran Ali Khan, Mohammad Abdullah Alotaibi, Abdullah Saud Aloyaid, Haifa Abdulaziz Al-Basheer, Naelah Abdullah Alghamdi, Raid Saleem Al-Baradie, Abdulrahman M. Alsulaiman · 2017 · Saudi Journal of Biological Sciences
- Joint analysis of multiple phenotypes for extremely unbalanced case‐control association studiesHongjing Xie, Xuewei Cao, Shuanglin Zhang, Qiuying Sha · 2023 · Genetic Epidemiology
- Genome-Wide Methylation Profiling in Archival Formalin-Fixed Paraffin-Embedded Tissue SamplesJonathan Keith Killian, Robert L. Walker, Sven Bilke, Yidong Chen, Sean R. Davis, Robert Cornelison, William I. Smith, Paul S. Meltzer · 2011 · Methods in molecular biology
- Variants in the CXCL12 gene was associated with coronary artery disease susceptibility in Chinese Han populationJunbo Zhang, Huijun Ma, Jie Gao, Shu Kong, Jiangtao You, Ying Sheng · 2017 · Oncotarget
- Genome-wide association studies in myocardial infarction and coronary artery disease.Pier Mannuccio Mannucci, Luca Andrea Lotta, Flora Peyvandi · 2010 · Europe PMC (PubMed Central)
- Editorial: The CXCR4 Ligand/Receptor Family and the DPP4 Protease in High-Risk Cardiovascular PatientsHeidi Noels, Jürgen Bernhagen · 2016 · Frontiers in Immunology
- Rare Variants in Genes of the Cholesterol Pathway Are Present in 60% of Patients with Acute Myocardial InfarctionRicardo Pan-Lizcano, Luis Mariñas‐Pardo, Lucía Núñez, Fernando Rebollal-Leal, Domingo López Vázquez, Ana Pereira, Aranzazu Molina-Nieto, Ramón Calviño, José Manuel Vázquez‐Rodríguez, Manuel Hermida‐Prieto · 2022 · International Journal of Molecular Sciences
- New insights on genetic background of major diabetic vascular complicationsZuira Tariq, Salah Abusnana, Bashair M. Mussa, Hala Zakaria · 2024 · Diabetology & Metabolic Syndrome
- Genome-Wide Association Studies Complemented with Mechanistic Biological Studies Identify Sortilin 1 as a Novel Regulator of Cholesterol TraffickingAli J. Marian · 2011 · Current Atherosclerosis Reports
- Single Nucleotide Polymorphisms and PharmacogenomicsAzher Mustafa Arafah, Shafat Ali, Sabhiya Majid, Samia Rashid, Shabhat Rasool, Hilal Ahmad Wani, Iyman Rasool, Muneeb U. Rehman · 2021 · Springer eBooks
- A Missense Variation in PHACTR2 Associates with Impaired Actin Dynamics, Dilated Cardiomyopathy, and Left Ventricular Non-Compaction in HumansPierre Majdalani, Aviva Levitas, Hanna Krymko, Leonel Slanovic, Alex Braiman, Uzi Hadad, Salam Dabsan, Amir Horev, Raz Zarivach, Ruti Parvari · 2023 · International Journal of Molecular Sciences
- Current Genomics in Cardiovascular MedicineVinit Sawhney, Scott Brouilette, Dominic James Abrams, RICHARD JOHN SCHILLING, Benjamin O’Brien · 2012 · Current Genomics
- Clinical applications of molecular genetic discoveriesAli J. Marian · 2015 · Translational research
- Multiomics Analysis Coupled with Text Mining Identify Novel Biomarker Candidates for Recurrent Cardiovascular EventsConstantina Chalikiopoulou, Barbara Jenko Bizjan, Georgios Leventopoulos, Kalliopi Smaili, Tanja Blagus, Ariadni Menti, John Liopetas, Anne John, Bassam R. Ali, Vita Dolžan et al. · 2020 · OMICS A Journal of Integrative Biology
- Genomic Strategies Toward Identification of Novel Therapeutic TargetsThorsten Kessler, Heribert Schunkert · 2020 · Handbook of experimental pharmacology
- Functional geneticsGiovanna Marchetti, Mirko Pinotti, Barbara Lunghi, Caterina Casari, Francesco Bernardi · 2011 · Thrombosis Research
- Induced pluripotent stem cell modeling of complex genetic diseasesJohn Travis Hinson, Kenta Nakamura, Sean M. Wu · 2012 · Drug Discovery Today Disease Models
- The Relationship Between Gene Polymorphisms and Dipping Profile in Patients With Coronary Heart DiseaseMarcin Wirtwein, Olle Melander, Marketa Sjögren, Michał Hoffmann, Krzysztof Narkiewicz, Marcin Gruchała, Wojciech Sobiczewski · 2016 · American Journal of Hypertension
- “My Parents Died of Myocardial Infarction: Is that My Destiny?”Nupoor Narula, Claudio Rapezzi, Luigi Tavazzi, Eloisa Arbustini · 2012 · Medical Clinics of North America
- Common genetic variants do not associate with CAD in familial hypercholesterolemiaErik P.A. van Iperen, Suthesh Sivapalaratnam, S. Matthijs Boekholdt, G. Kees Hovingh, Stephanie Maiwald, Michael W.T. Tanck, Nicole Soranzo, Jonathan C. Stephens, Jennifer G. Sambrook, Marcel M Levi et al. · 2013 · European Journal of Human Genetics
- The 9p21 coronary artery disease locus and kidney dysfunction in patients with Type 2 diabetes mellitusSalvatore De Cosmo, Sabrina Prudente, Olga Lamacchia, Daniela Lucchesi, Hetal Shah, Christine Mendonça, Laura Pucci, Luana Mercuri, Ernest V. Gervino, Thomas H. Hauser et al. · 2012 · Nephrology Dialysis Transplantation
- Genomic Medicine in the Prevention and Treatment of Atherosclerotic Cardiovascular DiseaseSony Tuteja, Daniel James Rader · 2012 · Personalized Medicine
- Value of Chromosome 9p21 Polymorphism for Prediction of Cardiovascular Mortality in Han Chinese Without Coronary LesionsI‐Te Lee, Kae‐Woei Liang, Jun‐Sing Wang, Wen‐Jane Lee, Yii-Der Ida Chen, Shih-Yi Lin, Wen-Lieng Lee, Wayne Huey‐Herng Sheu · 2015 · Medicine
- PharmacogeneticsJanice Y. Chyou, Jessica L. Mega, Marc Steven Sabatine · 2012 · Elsevier eBooks
- Commentary: The Year in Endocrine Genetics for Basic ScientistsWilliam F. Crowley · 2011 · Molecular Endocrinology
- Atherosclerosis: Pathogenesis, Genetics and Experimental ModelsJonathon W. Homeister, Monte S. Willis · 2010 · Wiley eBooks
- PHACTR1 and Atherosclerosis: It’s ComplicatedAmir Rezvan · 2023 · Arteriosclerosis Thrombosis and Vascular Biology
- Acute Myocardial Infarction Incidence, Mortality and Case Fatality in Santa Clara, Cuba, 2007–2008Alberto Morales, Yuri Madrazo, José I Ramírez, Luis Cofiño Castañeda, Wilfredo de J. Machín Cabrera, Licet Álvarez, R. Cañas Angulo, Raúl Dueñas Fernández, Roberto Bermúdez · 2011 · MEDICC Review
- Mapping the knowledge of omics in myocardial infarction: A scientometric analysis in R Studio, VOSviewer, Citespace, and SciMATXuan Wei, Min Wang, Shengnan Yu, Zhengqi Han, Chang Li, Yue Qi Zhong, Mengzhou Zhang, Tiantong Yang · 2025 · Medicine
- The APOB polymorphism rs1801701 A/G (p.R3638Q) is an independent risk factor for early-onset coronary artery disease: Data from a Spanish cohortEliécer Coto, Rebeca Lorca, Julián Rodríguez-Reguero, Marı́a Martı́n, Isaac Pascual, Pablo Avanzas y, Elías Cuesta‐Llavona, Daniel Vázquez‐Coto, Carmen Díaz‐Corte, Salvador Tranche et al. · 2021 · Nutrition Metabolism and Cardiovascular Diseases
- Genetics of spontaneous cervical and coronary artery dissectionsIsabel Rada, Juan F. Calderón, Gonzalo Martínez, Paula Muñoz Venturelli · 2023 · Frontiers in Global Women s Health
- Comparison of atherosclerotic cardiovascular disease (ASCVD) and Framingham risk scores (FRS) in an Iranian populationMatin Sepehrinia, Hossein Pourmontaseri, Mehrab Sayadi, Mohammad Mehdi Naghizadeh, Reza Homayounfar, Mojtaba Farjam, Azizallah Dehghan, Abdulhakim Alkamel · 2024 · International Journal of Cardiology Cardiovascular Risk and Prevention
- The Role of Preventive Health Care in Preventing Chronic DiseasesGudeta D. Fufaa · 2024 · IntechOpen eBooks
- Polygenic Prediction of Recurrent Events After Early-Onset Myocardial InfarctionMaddalena Ardissino, Elvezia Maria Paraboschi, Samuel A. Lambert, Lois G. Kim, Martin Kelemen, Giuseppe Maglietta, Antonio Crocamo, Giulia Magnani, S Bricoli, Luigi Vignali et al. · 2024 · Circulation Genomic and Precision Medicine
- Assessing Consistency Between Versions of Genotype-Calling Algorithm Birdseed for the Genome-Wide Human SNP Array 6.0 Using HapMap SamplesHuixiao Hong, Lei Xu, Weida Tong · 2010 · Advances in experimental medicine and biology
- Genetic Association Analysis and Meta‐Analysis of Imputed SNPs in Longitudinal StudiesIsaac Subirana, Juan R. González · 2013 · Genetic Epidemiology
- Synergistic Effect between BRAP Polymorphism and Diabetes on the Extent of Coronary Atherosclerosis in the Chinese PopulationPo‐Chao Hsu, Tsung‐Hsien Lin, Ho‐Ming Su, Suh‐Hang Hank Juo, Wen‐Ter Lai, Sheng‐Hsiung Sheu · 2011 · Cardiology
- Genetic Risk Score Does Not Correlate with Body Mass Index of Latina Women in a Clinical TrialKimberly R. Coenen, Sharon M. Karp, Sabina B. Gesell, Mary S. Dietrich, Thomas M. Morgan, Shari L. Barkin · 2011 · Clinical and Translational Science
- Family History of Myocardial Infarction Increases Risk of Renal Dysfunction in Middle AgeAnders G. Christensson, Olle Melander, Erik Fjellstedt, Maria Ohlson-Andersson · 2014 · American Journal of Nephrology
- The Relationship Between Coronary Artery Disease and Genetic Polymorphisms of Melanoma Inhibitory Activity 3Hooshang Zaimkohan, Mohammad Keramatipour, Seyed Reza Mirhafez, Javad Tavakkoly‐Bazzaz, Azadeh Tahooni, Mohammad Piryaei, Majid Ghayour‐Mobarhan, Seyed Mohamad Hossein Ghaderian · 2016 · Iranian Red Crescent Medical Journal
- Genetics in the prevention and management of coronary artery diseaseRobert Roberts · 2018 · Current Opinion in Cardiology
- Integrating external controls in case–control studies improves power for rare‐variant testsYatong Li, Seunggeun Lee · 2022 · Genetic Epidemiology
- Genetic Variants, Cardiovascular Risk and Genome-Wide Association StudiesOsmel Companioni, Francisco Rodríguez‐Esparragón, Alfonso Medina Fernández‐Aceytuno, José Carlos Rodríguez Pérez · 2011 · Revista Española de Cardiología (English Edition)
- PHACTR1 haplotypes are associated with carotid plaque presence and affect PHACTR1 mRNA expression in carotid plaque tissueJovana Kuveljić, Tamara Djurić, Aleksandra Stanković, Igor B. KONCAR, Dragan Alavantić, Maja Živković · 2019 · Gene
- Genetic Markers of Myocardial InfarctionStojan Kariž · 2012 · Journal of Clinical & Experimental Cardiology
- Mutation detection in Chinese patients with familial hypercholesterolemiaRan Du, Liang‐Liang Fan, Minjie Lin, Zhijian He, Hao Huang, Yaqin Chen, Jingjing Li, Kun Xia, Shui‐Ping Zhao, Rong Xiang · 2016 · SpringerPlus
- The genetics of epigenetics: is there a link with cardiovascular diseaseQingzhong Xiao, Shu Ye · 2010 · Heart
- Genetic Variants on Chromosome 10q11.21 are Associated with Ischemic Stroke in the Northern Chinese Han PopulationRuixia Zhu, Xu Liu, Zhiyi He · 2013 · Journal of Molecular Neuroscience
- Genetische Diagnostik polygener ErkrankungenTeresa Trenkwalder, Thorsten Kessler, Heribert Schunkert · 2017 · Herz
- The Multifunctional Role of KCNE2: From Cardiac Arrhythmia to Multisystem DisordersSong Ming, Yixin Zhuge, Yuqi Tu, Jie Liu, Wenjuan Liu · 2024 · Cells
- Cohort Profile: The Girona Heart RegistryIrene Roman Degano, Nuria Herrera-Marín, Isaac Subirana, Anna Camps-Vilaró, Álvaro Hernáez, Joan Sala, Rafael Masiá, Rafel Ramos, Roberto Elosúa, Jaume Marrugat · 2025 · International Journal of Epidemiology
- Perfil genómico de riesgo en la práctica clínicaVíctor E. Raggio, Leda Roche · 2009 · DOAJ (DOAJ: Directory of Open Access Journals)
- Investigation ofKIF6Trp719Arg gene polymorphism in a case-control study of coronary artery disease and non-fatal myocardial infarction in the Eastern Province of Saudi ArabiaChittibabu Vatte, Cyril Cyrus, Abdullah M. Al Shehri, Shahanas Chathoth, Mohammed Almansori, Awatif Al-Nafaie, Rudaynah A. Alali, Fahad Al‐Muhanna, Folkert Wouter Asselbergs, Amein Al Ali · 2016 · Annals of Saudi Medicine
- Genetics of Atherosclerotic Cardiovascular DiseaseAtif Qasim, Muredach P. Reilly · 2013 · Elsevier eBooks
- Genetic Variants in Immune Related Genes as Predictors of Responsiveness to BCG Immunotherapy in Metastatic Melanoma PatientsRomela Irene Ramos, Misa A. Shaw, Leland Jay Foshag, Stacey L. Stern, Negin Rahimzadeh, David A. Elashoff, Dave S.�B. Hoon · 2020 · Cancers
- Association of PHACTR1 intronic variants with the first myocardial infarction and their effect on PHACTR1 mRNA expression in PBMCsJovana Kuveljić, Tamara Djurić, Goran R. Stankovic, Milica Dekleva, Aleksandra Stanković, Dragan Alavantić, Maja Živković · 2021 · Gene
- Polygenic risk scores for dyslipidemia and atherosclerotic cardiovascular disease: progress toward clinical implementationM. Levin, D. Rader · 2022 · Best Practice & Research Clinical Endocrinology & Metabolism
- Systems biomedicine: It’s your turn —Recent progress in systems biomedicineZhuqin Zhang, Zhiguo Zhao, Bing Liu, Dongguo Li, Dandan Zhang, Hou‐Zao Chen, De‐Pei Liu · 2013 · Quantitative Biology
- Genomics relevant to the neuroanaesthesiologistVidya Chidambaran · 2016 · Journal of Neuroanaesthesiology and Critical Care
- The KCNE Family of Ion Channel Regulatory SubunitsGeoffrey Winston Abbott · 2016 · Elsevier eBooks
- An Integrative Co-localization (INCO) Analysis for SNV and CNV Genomic Features With an Application to Taiwan Biobank DataQi-You Yu, Tzu‐Pin Lu, Tzu-Hung Hsiao, Ching‐Heng Lin, Chi-Yun Wu, Jung‐Ying Tzeng, Chuhsing Kate Hsiao · 2021 · Frontiers in Genetics
- Genomics and Pharmacogenomics of Lipid-Lowering TherapiesKieran F. Docherty, Sandosh Padmanabhan · 2014 · Elsevier eBooks
- Genetic Risk Factors for Type 2 Diabetes and Related TraitsJens Kristoffer Hertel · 2012 · NORA - Norwegian Open Research Archives
- Coronary Artery Disease and Myocardial InfarctionSamir B. Damani, Eric J. Topol · 2012 · Elsevier eBooks
- Antisense Oligonucleotide Targeting Sortilin Reduces Vascular Calcification in Mice in a Sex-Dependent MannerAdrien Lupieri, DAKOTA R. BECKER-GREENE, Thanh-Dat Le, Marina Marangoni Roschel, Prabhash Kumar Jha, Abhijeet R. Sonawane, Adam E. Mullick, Sotirios Tsimikas, Shiori Kuraoka, Sasha A. Singh et al. · 2025 · Arteriosclerosis Thrombosis and Vascular Biology
- Platelet GenomicsPaul F. Bray, Chris Ian Jones, Nicole Soranzo, Willem Hendrik Ouwehand · 2012 · Elsevier eBooks
- The T Allele of rs8075977 in the 5′-Flanking Region of the PEDF Gene Is Associated with Reduced Risk of Coronary Artery Disease in Elderly Chinese MenShouyuan Ma, Yuanyuan Guo, Shuxia Wang, Jinxin Shi, Jie Liu, Jianfeng Liu, Ping Zhu · 2017 · The Tohoku Journal of Experimental Medicine
- PHACTRing in actin: actin deregulation in genetic epilepsiesLara Eid, Praveen K. Raju, Elsa Rossignol · 2018 · Brain
- Identification of Genetic Variants Associated With Myocardial Infarction in Saudi ArabiaKamal Waheeb Alghalayini, Mohammed A. Salama, Hadiah Bassam Al Mahdi, Sameer Alharthi, Wesam Awad Alhejily, Mirvat A. Alasnag, Noura O Tasbhji, Diana A. H. Al-Quwaie, Panos Deloukas, Sherif Edris · 2020 · The Heart Surgery Forum
- Association of CELSR2, APOB100, ABCG5/8, LDLR, and APOE polymorphisms and their genetic risks with lipids among the Thai subjectsManit Nuinoon, Wutthichai Saiphak, Nantiya Nawaka, Chutima Rattanawan, Burabha Pussadhamma, Nutjaree Jeenduang · 2022 · Saudi Journal of Biological Sciences
- Analysis of the Association between Copy Number Variation and Ventricular Fibrillation in ST-Elevation Acute Myocardial InfarctionRoberto Lorente-Bermúdez, Ricardo Pan-Lizcano, Lucía Núñez, Domingo López Vázquez, Fernando Rebollal-Leal, José Manuel Vázquez‐Rodríguez, Manuel Hermida‐Prieto · 2024 · International Journal of Molecular Sciences
- Associations of Blood Lipid-Related Polygenic Scores, Lifestyle Factors and Their Combined Effects with Risk of Coronary Artery Disease in the UK Biobank CohortJungyoon Choi, Wanqing Wen, Guochong Jia, Ran Tao, Jirong Long, Xiao‐Ou Shu, Wei Zheng · 2024 · Journal of Cardiovascular Translational Research
- Analysis of rs6725887 in the WD Repeat Protein 12 in Association with Coronary Artery Disease in Iranian Patients.Mohammad Piryaei, Sayyed Mohammad Hossein Ghaderian, Hossein Vakili, Hooshang Zaimkohan, Nastaran Mohammadi Ghahhari, Maryam Mafi Golchin · 2015 · PubMed Central
- Genetische Analysen als Basis einer individualisierten Medizin bei koronarer HerzkrankheitThorsten Kessler, Bernhard M. Kaess, Felix J. Bourier, Jeanette Erdmann, Heribert Schunkert · 2014 · Herz