| scholarly article | Q13442814 |
| P50 | author | Anuj Goel | Q57551348 |
| P2860 | cites work | Potential etiologic and functional implications of genome-wide association loci for human diseases and traits | Q22066284 |
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| A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease | Q29417111 | ||
| Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes | Q29417138 | ||
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| Genome-wide association study identifies eight loci associated with blood pressure | Q29614414 | ||
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| Genetic variants influencing circulating lipid levels and risk of coronary artery disease | Q37477713 | ||
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| Association of the 9p21.3 locus with risk of first-ever myocardial infarction in Pakistanis: case-control study in South Asia and updated meta-analysis of Europeans | Q37731775 | ||
| Plasma interleukin-5 levels are related to antibodies binding to oxidized low-density lipoprotein and to decreased subclinical atherosclerosis. | Q43607095 | ||
| Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease | Q43617306 | ||
| Cholesteryl Ester Storage Disease (CESD) due to novel mutations in the LIPA gene | Q46078301 | ||
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 9 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | coronary artery disease | Q844935 |
| P304 | page(s) | e1002260 | |
| P577 | publication date | 2011-09-01 | |
| P1433 | published in | PLOS Genetics | Q1893441 |
| P1476 | title | Large-scale gene-centric analysis identifies novel variants for coronary artery disease | |
| P478 | volume | 7 |
| Q28267020 | A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease |
| Q33585301 | A genetic risk score for CAD, psychological stress, and their interaction as predictors of CAD, fatal MI, non-fatal MI and cardiovascular death |
| Q40817564 | A genetic risk score is associated with statin-induced low-density lipoprotein cholesterol lowering |
| Q38466780 | A study in familial hypercholesterolemia suggests reduced methylomic plasticity in men with coronary artery disease |
| Q35058865 | Analysis of gene-gene interactions among common variants in candidate cardiovascular genes in coronary artery disease |
| Q37701906 | Association of non-synonymous variants in WIPF3 and LIPA genes with abdominal aortic aneurysm: an autopsy study |
| Q30544909 | Association of the rs7395662 SNP in the MADD-FOLH1 and several environmental factors with serum lipid levels in the Mulao and Han populations |
| Q50318400 | Atherosclerosis Is an Inflammatory Disease which Lacks a Common Anti-inflammatory Therapy: How Human Genetics Can Help to This Issue. A Narrative Review |
| Q35127516 | Atherosclerosis and Alzheimer--diseases with a common cause? Inflammation, oxysterols, vasculature |
| Q33789638 | B cells and humoral immunity in atherosclerosis |
| Q57315137 | Bedeutung moderner Genomstudien für das Herzinfarktrisiko |
| Q47838511 | CRISPR/Cas9-Mediated Gene Editing in Human iPSC-Derived Macrophage Reveals Lysosomal Acid Lipase Function in Human Macrophages-Brief Report |
| Q96022738 | CYP17A1 deficient XY mice display susceptibility to atherosclerosis, altered lipidomic profile and atypical sex development |
| Q37636600 | Candidate gene association study of coronary artery calcification in chronic kidney disease: findings from the CRIC study (Chronic Renal Insufficiency Cohort). |
| Q30411394 | Causal effects of body mass index on cardiometabolic traits and events: a Mendelian randomization analysis |
| Q38026701 | Clinical validation of genetic markers for improved risk estimation |
| Q33837769 | Coherent somatic mutation in autoimmune disease |
| Q27321601 | Complex genetic architecture of cardiac disease in a wild type inbred strain of Drosophila melanogaster |
| Q33727315 | Coronary Artery Disease-Associated LIPA Coding Variant rs1051338 Reduces Lysosomal Acid Lipase Levels and Activity in Lysosomes. |
| Q27024688 | Coronary artery disease in Bangladesh: a review |
| Q58563912 | DNA methylation in blood as a mediator of the association of mid-childhood body mass index with cardio-metabolic risk score in early adolescence |
| Q35786681 | Discovering Genetic Interactions in Large-Scale Association Studies by Stage-wise Likelihood Ratio Tests |
| Q38723704 | Experimental Biology for the Identification of Causal Pathways in Atherosclerosis |
| Q46406593 | Experimental Evolution and Heart Function in Drosophila. |
| Q40191164 | Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms |
| Q36948239 | Frequency of the cholesteryl ester storage disease common LIPA E8SJM mutation (c.894G>A) in various racial and ethnic groups. |
| Q36467059 | Gene-centric meta-analyses of 108 912 individuals confirm known body mass index loci and reveal three novel signals |
| Q37634121 | Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci |
| Q30423388 | Gene-centric meta-analysis of lipid traits in African, East Asian and Hispanic populations |
| Q37682697 | Genetic Risk, Adherence to a Healthy Lifestyle, and Coronary Disease |
| Q27315831 | Genetic loci on chromosome 5 are associated with circulating levels of interleukin-5 and eosinophil count in a European population with high risk for cardiovascular disease |
| Q36609691 | Genetic predisposition to coronary heart disease and stroke using an additive genetic risk score: a population-based study in Greece |
| Q26866396 | Genetics of coronary artery disease |
| Q26769994 | Genetics of coronary artery disease and myocardial infarction |
| Q38101513 | Genetics of coronary artery disease and myocardial infarction--2013. |
| Q38010348 | Genetics of coronary artery disease in the 21st century. |
| Q33732873 | Genetics of coronary artery disease: an update |
| Q34553141 | Genetics of coronary artery disease: discovery, biology and clinical translation |
| Q34261931 | Genetics of human cardiovascular disease |
| Q28066981 | Genetics of the acute coronary syndrome |
| Q57315135 | Genetische Analysen als Basis einer individualisierten Medizin bei koronarer Herzkrankheit |
| Q33906092 | Genome-Wide Linkage Analysis of Large Multiple Multigenerational Families Identifies Novel Genetic Loci for Coronary Artery Disease |
| Q58800768 | Global genetic diversity of human apolipoproteins and effects on cardiovascular disease risk |
| Q34344282 | Identification of CAD candidate genes in GWAS loci and their expression in vascular cells |
| Q38851472 | Immune-mediated mechanisms of atherosclerosis and implications for the clinic |
| Q87799091 | Impact of Apolipoprotein(a) Isoform Size on Lipoprotein(a) Lowering in the HPS2-THRIVE Study |
| Q30663945 | Information and Risk Modification Trial (INFORM): design of a randomised controlled trial of communicating different types of information about coronary heart disease risk, alongside lifestyle advice, to achieve change in health-related behaviour |
| Q35859582 | Inheritance of coronary artery disease in men: an analysis of the role of the Y chromosome |
| Q55346354 | Integrative Bioinformatics Approaches for Identification of Drug Targets in Hypertension. |
| Q35863952 | Interleukin-6 receptor pathways in coronary heart disease: a collaborative meta-analysis of 82 studies |
| Q55230011 | LIPA Variants in Genome-Wide Association Studies of Coronary Artery Diseases: Loss-of-Function or Gain-of-Function? |
| Q36921066 | Large-scale association analysis identifies new risk loci for coronary artery disease |
| Q30419436 | Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci |
| Q30425020 | Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci |
| Q38639815 | Lipoprotein(a) and Arterial Stiffness Parameters |
| Q38213476 | Lipoprotein(a) as a therapeutic target in cardiovascular disease |
| Q36853815 | Loci influencing blood pressure identified using a cardiovascular gene-centric array |
| Q59128283 | Long Noncoding RNA : Lnc-ing Genetic Variation at the Chromosome 9p21 Locus to Molecular Mechanisms of Atherosclerosis |
| Q28596209 | Low eosinophil and low lymphocyte counts and the incidence of 12 cardiovascular diseases: a CALIBER cohort study |
| Q92336069 | Lysosomal Acid Lipase in Lipid Metabolism and Beyond |
| Q52652320 | Lysosomal acid lipase and lipid metabolism: new mechanisms, new questions, and new therapies. |
| Q39371640 | Lysosomal acid lipase deficiency: a form of non-obese fatty liver disease (NOFLD). |
| Q34463784 | Lysosomal acid lipase: at the crossroads of normal and atherogenic cholesterol metabolism |
| Q34317404 | Meta-analyses of KIF6 Trp719Arg in coronary heart disease and statin therapeutic effect |
| Q38074824 | Meta-analyses of four eosinophil related gene variants in coronary heart disease |
| Q54977501 | Metformin and AMP Kinase Activation Increase Expression of the Sterol Transporters ABCG5/8 (ATP-Binding Cassette Transporter G5/G8) With Potential Antiatherogenic Consequences. |
| Q34583994 | Mixed modeling of meta-analysis P-values (MixMAP) suggests multiple novel gene loci for low density lipoprotein cholesterol |
| Q38541814 | Molecular genetics of coronary artery disease |
| Q35069996 | NEXN is a novel susceptibility gene for coronary artery disease in Han Chinese |
| Q33991765 | No large-effect low-frequency coding variation found for myocardial infarction |
| Q36822328 | Physiological difference in autophagic flux in macrophages from 2 mouse strains regulates cholesterol ester metabolism |
| Q35122015 | Plasma IL-5 concentration and subclinical carotid atherosclerosis |
| Q55395813 | Plasma cytokines and risk of coronary heart disease in the PROCARDIS study. |
| Q92281052 | Polygenetic risk for coronary artery disease increases hospitalization burden and mortality |
| Q89010113 | Polygenic Risk Score for Coronary Heart Disease Modifies the Elevated Risk by Cigarette Smoking for Disease Incidence |
| Q34020610 | Polymorphism of 9p21.3 locus is associated with 5-year survival in high-risk patients with myocardial infarction |
| Q55061762 | Pooled genetic analysis reveals an association of SNPs of only a few genes with risk predisposition to ischemic stroke in a Chinese population. |
| Q37048550 | Positive correlation between variants of lipid metabolism‑related genes and coronary heart disease |
| Q35176614 | Relationship between CYP17A1 genetic polymorphism and coronary artery disease in a Chinese Han population |
| Q55691982 | Retracted: Polymorphism of 9p21.3 Locus Is Associated with 5-Year Survival in High-Risk Patients with Myocardial Infarction |
| Q38359111 | Shared genetic aetiology of coronary artery disease and atherosclerotic stroke - 2015. |
| Q34999265 | Single nucleotide polymorphisms within LIPA (Lysosomal Acid Lipase A) gene are associated with susceptibility to premature coronary artery disease. a replication in the genetic of atherosclerotic disease (GEA) Mexican study. |
| Q61447675 | Stigmasterol accumulation causes cardiac injury and promotes mortality |
| Q37576928 | The Association between KIF6 Single Nucleotide Polymorphism rs20455 and Serum Lipids in Filipino-American Women |
| Q35894608 | The Bangladesh Risk of Acute Vascular Events (BRAVE) Study: objectives and design |
| Q55318081 | The Contribution of Autoantibodies to Inflammatory Cardiovascular Pathology. |
| Q28080690 | The Genetic Basis of Coronary Artery Disease and Atrial Fibrillation: A Search for Disease Mechanisms and Therapeutic Targets |
| Q35849271 | The endothelial protein C receptor (PROCR) Ser219Gly variant and risk of common thrombotic disorders: a HuGE review and meta-analysis of evidence from observational studies. |
| Q37995873 | The enigma of genetics etiology of atherosclerosis in the post-GWAS era. |
| Q37201894 | The genetic basis for survivorship in coronary artery disease |
| Q37983699 | The genetics of familial combined hyperlipidaemia |
| Q39230390 | The immunology of atherosclerosis |
| Q26748869 | The impact of genome-wide association studies on the pathophysiology and therapy of cardiovascular disease |
| Q27002724 | The mammalian tribbles homolog TRIB3, glucose homeostasis, and cardiovascular diseases |
| Q27000791 | The role of T and B cells in human atherosclerosis and atherothrombosis |
| Q38201295 | The role of genetic risk factors in coronary artery disease |
| Q36225325 | The rs10757278 polymorphism of the 9p21.3 locus is associated with premature coronary artery disease in Polish patients |
| Q42598795 | The shared allelic architecture of adiponectin levels and coronary artery disease |
| Q26823146 | Toward individualized cholesterol-lowering treatment in end-stage renal disease |
| Q34180975 | Validated context-dependent associations of coronary heart disease risk with genotype variation in the chromosome 9p21 region: the Atherosclerosis Risk in Communities study |
| Q36170750 | c.*84G>A Mutation in CETP Is Associated with Coronary Artery Disease in South Indians |
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