An LRP8 Variant Is Associated with Familial and Premature Coronary Artery Disease and Myocardial Infarction
- 31 October 2007
- journal article
- research article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 81 (4) , 780-791
- https://doi.org/10.1086/521581
Abstract
No abstract availableKeywords
This publication has 31 references indexed in Scilit:
- Peakwide Mapping on Chromosome 3q13 Identifies the Kalirin Gene as a Novel Candidate Gene for Coronary Artery DiseaseAmerican Journal of Human Genetics, 2007
- Genetic susceptibility to myocardial infarction and coronary artery diseaseHuman Molecular Genetics, 2006
- GATA2 Is Associated with Familial Early-Onset Coronary Artery DiseasePLoS Genetics, 2006
- Heart Disease and Stroke Statistics—2006 UpdateCirculation, 2006
- Platelets in AtherothrombosisMayo Clinic Proceedings, 2006
- Joint analysis is more efficient than replication-based analysis for two-stage genome-wide association studiesNature Genetics, 2006
- Role of p38 MAP kinase in postcapillary venule leukocyte adhesion induced by ischemia/reperfusion injuryPharmacological Research, 2005
- Association between the Gene Encoding 5-Lipoxygenase–Activating Protein and Stroke Replicated in a Scottish PopulationAmerican Journal of Human Genetics, 2005
- Binding of Low Density Lipoprotein to Platelet Apolipoprotein E Receptor 2′ Results in Phosphorylation of p38MAPKPublished by Elsevier ,2004
- Monte Carlo tests for associations between disease and alleles at highly polymorphic lociAnnals of Human Genetics, 1995