Abstract
Since the completion of the human genome sequence, the study of common genetic polymorphisms in complex human diseases has become a main activity of human genetics. Employing genome-wide association studies, hundreds of modest genetic risk factors have been identified. In infectious diseases the identification of common risk factors has been varied and as in other common diseases it seems likely that important genetic risk factors remain to be discovered. Nevertheless, the identification of disease-specific genetic risk factors revealed an unexpected overlap in susceptibility genes of diverse inflammatory and infectious diseases. Analysis of the multi-disease susceptibility genes has allowed the definition of shared key pathways of inflammatory dysregulation and suggested unexpected infectious etiologies for other “non-infectious” common diseases.
©2011 by Walter de Gruyter Berlin Boston
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Articles in the same Issue
- Editorial
- Athlete's biological passport: to test or not to test?
- Review
- Prognostic value of cystatin C in acute coronary syndromes: enhancer of atherosclerosis and promising therapeutic target
- Opinion Papers
- The function of oxalic acid in the human metabolism
- Current limitations of the Athlete's Biological Passport use in sports
- Limits and pitfalls of Athlete's Biological Passport
- The Athlete Biological Passport from the perspective of an anti-doping organization
- Perspectives
- Genetics of infectious diseases: hidden etiologies and common pathways
- Guidelines and Recommendations
- IFCC primary reference procedures for the measurement of catalytic activity concentrations of enzymes at 37 °C. Part 9: Reference procedure for the measurement of catalytic concentration of alkaline phosphatase
- Genetics and Molecular Diagnostics
- A template for mutational data analysis of the CFTR gene
- High resolution melting analysis to genotype the most common variants in the HFE gene
- General Clinical Chemistry and Laboratory Medicine
- Bayesian analysis of an international ELISA comparability study
- Inflammatory markers in preeclamptic patients
- Pre-analytical effects of different lithium heparin plasma separation tubes in the routine clinical chemistry laboratory
- Pre-acquisition system assessment of the Sysmex® Coagulation System CS-2100i and comparison with end-user verification; a model for the regional introduction of new analysers and methods
- Evaluation of a commercially available rapid urinary porphobilinogen test
- Reference Values and Biological Variations
- Reference intervals and age and gender dependency for arterial blood gases and electrolytes in adults
- Within-subject biological variation of glucose and HbA1c in healthy persons and in type 1 diabetes patients
- Determinants of oxidative stress related to gender: relevance of age and smoking habit
- Soluble ST2 is not independently associated with androgen and estrogen status in healthy males and females
- Infectious Diseases
- Development of candidate reference reagent for HIV-1 RNA and comparison analysis for different HIV-1 RNA quantitative assay
- Prognostic value of serum angiotensin-converting enzyme activity for outcome of community-acquired pneumonia
- The evaluation of colloidal gold immunochromatographic assay (GICA) for rapid diagnosis of influenza A disease
- Cardiovascular Disease
- N-terminal pro-B-type natriuretic peptide in early and advanced phases of obesity
- Vaspin plasma concentrations and mRNA expressions in patients with stable and unstable angina pectoris
- Prospective study of first stroke in relation to plasma homocysteine and MTHFR 677C>T and 1298A>C genotypes and haplotypes – evidence for an association with hemorrhagic stroke
- Letters to the Editor
- Evaluation of the analytical performance of the Beckman Coulter AU680 automated analytical system based on quality specifications for allowable performance derived from biological variation
- Collagen peptides, interstitial remodelling and sudden cardiac death in hypertrophic cardiomyopathy
- Erratum
- Modified phosphatidylserine-dependent antiprothrombin ELISA enables identification of patients negative for other antiphospholipid antibodies and also detects low avidity antibodies