Challenges in the phenotypic characterisation of patients in genetic studies of coronary artery disease
- 8 December 2006
- journal article
- review article
- Published by BMJ in Journal of Medical Genetics
- Vol. 44 (3) , 161-165
- https://doi.org/10.1136/jmg.2006.045732
Abstract
Coronary artery disease and acute myocardial infarction are complex traits in which there has been recent research to identify the principal genes that engender susceptibility or provide protection. Although there has been exceptional progress in the technology, which now allows genotyping of hundreds of thousands of single-nucleotide polymorphisms in each individual, there remains a pattern of inconsistency in the studies performed to date, in part owing to the difficulties in defining cases and controls. In this paper, salient issues to facilitate research in this important field are reviewed.Keywords
This publication has 40 references indexed in Scilit:
- Genetic susceptibility to myocardial infarction and coronary artery diseaseHuman Molecular Genetics, 2006
- GATA2 Is Associated with Familial Early-Onset Coronary Artery DiseasePLoS Genetics, 2006
- Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetesNature Genetics, 2006
- Characterization of Coronary Atherosclerotic Plaques by Multidetector Computed TomographyPublished by Elsevier ,2006
- Complement Factor H Polymorphism in Age-Related Macular DegenerationScience, 2005
- ALOX5AP Gene and the PDE4D Gene in a Central European Population of Stroke PatientsStroke, 2005
- Large scale association analysis for identification of genes underlying premature coronary heart disease: cumulative perspective from analysis of 111 candidate genesJournal of Medical Genetics, 2004
- Replication of the association between the thrombospondin-4 A387P polymorphism and myocardial infarctionAmerican Heart Journal, 2004
- Functional SNPs in the lymphotoxin-α gene that are associated with susceptibility to myocardial infarctionNature Genetics, 2002
- Two Loci on Chromosomes 2 and X for Premature Coronary Heart Disease Identified in Early- and Late-Settlement Populations of FinlandAmerican Journal of Human Genetics, 2000