Literature DB >> 10878695

Genetic association studies in complex diseases.

B Keavney1.   

Abstract

Genetic association studies are the most frequent type of study performed in the investigation of the genetic basis of complex cardiovascular conditions. While relatively easy to perform, and having previously correctly identified genetic effects subsequently proven to be due to genetic linkage, interpretation of the results of these studies is not always straightforward. Issues such as population stratification, data-driven subgroup analysis, possible absence of linkage disequilibrium between marker and disease locus, and testing of multiple hypotheses are discussed and the likely place for association studies in a strategy involving studies of a variety of designs geared to finding genetic determinants of disease susceptibility is addressed. Journal of Human Hypertension (2000) 14, 361-367

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Year:  2000        PMID: 10878695     DOI: 10.1038/sj.jhh.1001020

Source DB:  PubMed          Journal:  J Hum Hypertens        ISSN: 0950-9240            Impact factor:   3.012


  3 in total

Review 1.  Using single nucleotide polymorphisms as a means to understanding the pathophysiology of asthma.

Authors:  L J Palmer; W O Cookson
Journal:  Respir Res       Date:  2001-03-08

2.  The mitochondrial DNA T16189C polymorphism and HIV-associated cardiomyopathy: a genotype-phenotype association study.

Authors:  Gasnat Shaboodien; Mark E Engel; Faisal F Syed; Joanna Poulton; Motasim Badri; Bongani M Mayosi
Journal:  BMC Med Genet       Date:  2009-04-27       Impact factor: 2.103

3.  Common variation neighbouring micro-RNA 22 is associated with increased left ventricular mass.

Authors:  Andrew R Harper; Bongani M Mayosi; Antony Rodriguez; Thahira Rahman; Darroch Hall; Chrysovalanto Mamasoula; Peter J Avery; Bernard D Keavney
Journal:  PLoS One       Date:  2013-01-25       Impact factor: 3.240

  3 in total

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