| scholarly article | Q13442814 |
| P819 | ADS bibcode | 2006PLoSO...1...64L |
| P356 | DOI | 10.1371/JOURNAL.PONE.0000064 |
| P8608 | Fatcat ID | release_p6uxmnerr5gr3pn5pxnhn5h7jm |
| P932 | PMC publication ID | 1762368 |
| P698 | PubMed publication ID | 17183695 |
| P5875 | ResearchGate publication ID | 6616148 |
| P50 | author | Leif Groop | Q27214742 |
| Olle Melander | Q28050435 | ||
| Eero Lindholm | Q55437843 | ||
| Peter Almgren | Q87790487 | ||
| Goran Berglund | Q114314386 | ||
| Marju Orho-Melander | Q30432345 | ||
| P2093 | author name string | Carl-David Agardh | |
| P2860 | cites work | Molecular genetics of coronary artery disease | Q24674808 |
| Metabolic consequences of a family history of NIDDM (the Botnia study): evidence for sex-specific parental effects. | Q51000283 | ||
| Genetic variance of SGK-1 is associated with blood pressure, blood pressure change over time and strength of the insulin-diastolic blood pressure relationship. | Q51509291 | ||
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| Classifying diabetes according to the new WHO clinical stages | Q57655935 | ||
| Microalbuminuria: An Early Marker of Renal Involvement in Diabetes | Q60218076 | ||
| The Malmo Diet and Cancer Study. Design and feasibility | Q70551410 | ||
| Site of intimal rupture or erosion of thrombosed coronary atherosclerotic plaques is characterized by an inflammatory process irrespective of the dominant plaque morphology | Q72708405 | ||
| MHC2TA is associated with differential MHC molecule expression and susceptibility to rheumatoid arthritis, multiple sclerosis and myocardial infarction | Q28581447 | ||
| Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits | Q29614876 | ||
| Functional variation in LGALS2 confers risk of myocardial infarction and regulates lymphotoxin-alpha secretion in vitro | Q33292125 | ||
| Single nucleotide polymorphisms in multiple novel thrombospondin genes may be associated with familial premature myocardial infarction | Q34103271 | ||
| Pathophysiology of coronary artery disease | Q34429470 | ||
| Report of the adult treatment panel III: the 2001 National Cholesterol Education Program guidelines on the detection, evaluation and treatment of elevated cholesterol in adults | Q35585953 | ||
| Genetics of diabetic nephropathy in type 2 DM: candidate gene analysis for the pathogenic role of inflammation | Q36262400 | ||
| Cardiovascular morbidity and mortality associated with the metabolic syndrome | Q39513407 | ||
| Microalbuminuria and potential confounders. A review and some observations on variability of urinary albumin excretion. | Q40382042 | ||
| A prospective study of parental history of myocardial infarction and coronary heart disease in women | Q41491315 | ||
| Microalbuminuria as predictor of vascular disease in non-diabetic subjects. Islington Diabetes Survey | Q41914147 | ||
| Functional SNPs in the lymphotoxin-alpha gene that are associated with susceptibility to myocardial infarction | Q44212606 | ||
| Major risk factors as antecedents of fatal and nonfatal coronary heart disease events | Q44556056 | ||
| Coagulation and inflammation in overt diabetic nephropathy: association with hyperhomocysteinemia | Q45060599 | ||
| Prevalence of conventional risk factors in patients with coronary heart disease | Q47677468 | ||
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | metabolic syndrome | Q657193 |
| P304 | page(s) | e64 | |
| P577 | publication date | 2006-12-20 | |
| P1433 | published in | PLOS One | Q564954 |
| P1476 | title | Polymorphism in the MHC2TA gene is associated with features of the metabolic syndrome and cardiovascular mortality | |
| P478 | volume | 1 |
| Q51371611 | A polymorphism of the interferon-gamma-inducible protein 30 gene is associated with hyperglycemia in severely obese individuals. |
| Q37700366 | Challenges and standards in reporting diagnostic and prognostic biomarker studies |
| Q44088455 | Complexity of factors related to outcome of neuropathic and neuroischaemic/ischaemic diabetic foot ulcers: a cohort study |
| Q81044319 | Ischaemic stroke in hypertensive patients is associated with variations in the PDE4D genome region |
| Q33717534 | Lack of association of the CIITA -168A→G promoter SNP with myasthenia gravis and its role in autoimmunity |
| Q50457965 | Molecular characterization of chicken class II transactivator gene. |
| Q37419122 | Molecular genetics of atherosclerosis |
| Q34469229 | Polymorphisms in the inflammatory genes CIITA, CLEC16A and IFNG influence BMD, bone loss and fracture in elderly women |
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