Variation in inflammation-related genes and risk of incident nonfatal myocardial infarction or ischemic stroke
- 5 November 2007
- journal article
- research article
- Published by Elsevier BV in Atherosclerosis
- Vol. 198 (1), 166-173
- https://doi.org/10.1016/j.atherosclerosis.2007.09.031
Abstract
No abstract availableKeywords
This publication has 31 references indexed in Scilit:
- Copy Number Variation in the Human Genome and Its Implications for Cardiovascular DiseaseCirculation, 2007
- Global variation in copy number in the human genomeNature, 2006
- Lymphotoxin-α Gene and Risk of Myocardial Infarction in 6,928 Cases and 2,712 Controls in the ISIS Case-Control StudyPLoS Genetics, 2006
- Simple estimates of haplotype relative risks in case‐control dataGenetic Epidemiology, 2006
- Sequence Variations inPCSK9,Low LDL, and Protection against Coronary Heart DiseaseNew England Journal of Medicine, 2006
- Whole-genome genotyping with the single-base extension assayNature Methods, 2005
- Inflammatory markers and cardiovascular health in older adultsCardiovascular Research, 2005
- Series of Monographs on Venous Thromboembolic DiseaseCirculation, 2004
- Functional SNPs in the lymphotoxin-α gene that are associated with susceptibility to myocardial infarctionNature Genetics, 2002
- Score Tests for Association between Traits and Haplotypes when Linkage Phase Is AmbiguousAmerican Journal of Human Genetics, 2002