New susceptibility locus for coronary artery disease on chromosome 3q22.3

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Items 101–200 of 485

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13. Genetics of Coronary Artery Disease and Myocardial Infarction - 2013
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17. Genetic Architecture of Coronary Artery Disease in the Genome-Wide Era: Implications for the Emerging “Golden Dozen” Loci
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18. Association of SNP rs17465637 on Chromosome 1q41 and rs599839 on 1p13.3 with Myocardial Infarction in an American Caucasian Population
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19. Association of a polymorphism of BTN2A1 with myocardial infarction in East Asian populations
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20. Association of Genetic Variants Influencing Lipid Levels with Coronary Artery Disease in Japanese Individuals
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23. Genetics of coronary artery disease in the light of genome-wide association studies
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24. Literature-Based Genetic Risk Scores for Coronary Heart Disease
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25. Genome-Wide Association and Functional Studies Identify SCML4 and THSD7A as Novel Susceptibility Genes for Coronary Artery Disease
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29. BDgene: A Genetic Database for Bipolar Disorder and Its Overlap With Schizophrenia and Major Depressive Disorder
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30. Association of a Genetic Risk Score With Prevalent and Incident Myocardial Infarction in Subjects Undergoing Coronary Angiography
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31. Incremental predictive value of 152 single nucleotide polymorphisms in the 10-year risk prediction of incident coronary heart disease: the Rotterdam Study
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32. Transcriptome-wide association study of coronary artery disease identifies novel susceptibility genes
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33. A study of the role of GATA2 gene polymorphism in coronary artery disease risk traits
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34. Common Coding Variants of the HNF1A Gene Are Associated With Multiple Cardiovascular Risk Phenotypes in Community-Based Samples of Younger and Older European-American Adults
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35. Utility of genetic determinants of lipids and cardiovascular events in assessing risk
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36. Genome-wide association study in takotsubo syndrome — Preliminary results and future directions
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37. Runs of Homozygosity: Association with Coronary Artery Disease and Gene Expression in Monocytes and Macrophages
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38. Association of CDKN2BAS Polymorphism rs4977574 with Coronary Heart Disease: A Case-Control Study and a Meta-Analysis
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39. Associations of the ATP-binding cassette transporter A1 R219K polymorphism with HDL-C level and coronary artery disease risk: A meta-analysis
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40. Strategies Beyond Genome-Wide Association Studies for Atherosclerosis
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41. Polygenic risk scores outperform machine learning methods in predicting coronary artery disease status
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42. Association Tests for X-Chromosomal Markers – A Comparison of Different Test Statistics
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43. Population Genomics of Cardiometabolic Traits: Design of the University College London-London School of Hygiene and Tropical Medicine-Edinburgh-Bristol (UCLEB) Consortium
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44. Genotype-informed estimation of risk of coronary heart disease based on genome-wide association data linked to the electronic medical record
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45. Risk loci for coronary artery calcification replicated at 9p21 and 6q24 in the Heinz Nixdorf Recall Study
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46. Genomic Risk Variants at 1p13.3, 1q41, and 3q22.3 Are Associated With Subsequent Cardiovascular Outcomes in Healthy Controls and in Established Coronary Artery Disease
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47. Could Artificial Intelligence/Machine Learning and Inclusion of Diet-Gut Microbiome Interactions Improve Disease Risk Prediction? Case Study: Coronary Artery Disease
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48. The ENPP1 Q121 Variant Predicts Major Cardiovascular Events in High-Risk Individuals
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50. Replication and Meta‐analysis of Genome‐Wide Association Studies
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52. Genetic Causes of Myocardial Infarction
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55. Association of genetic variants in SEMA3F, CLEC16A, LAMA3, and PCSK2 with myocardial infarction in Japanese individuals
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56. The Genome-Wide Association Study—A New Era for Common Polygenic Disorders
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57. The impact of susceptibility loci for coronary artery disease on other vascular domains and recurrence risk
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59. SH2B3 Is a Genetic Determinant of Cardiac Inflammation and Fibrosis
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