Research Topics
Genomes and Genes | Lance A BareSummaryAffiliation: Celera Genomics Country: USA Publications
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Detail Information
Publications
Five common gene variants identify elevated genetic risk for coronary heart diseaseLance A Bare
Celera, Alameda, California 94502, USA
Genet Med 9:682-9. 2007....
Gene variants associated with ischemic stroke: the cardiovascular health studyMay M Luke
Celera, Alameda, California 94502, USA
Stroke 40:363-8. 2009..The purpose of this study was to determine whether 74 single nucleotide polymorphisms (SNPs), which had been associated with coronary heart disease, are associated with incident ischemic stroke...
Association of gene variants with incident myocardial infarction in the Cardiovascular Health StudyDov Shiffman
Celera, 1401 Harbor Bay Parkway, Alameda, CA 94502, USA
Arterioscler Thromb Vasc Biol 28:173-9. 2008....
Gene variants of VAMP8 and HNRPUL1 are associated with early-onset myocardial infarctionDov Shiffman
Celera Inc, 1401 Harbor Bay Pkwy, Alameda, California 94502, USA
Arterioscler Thromb Vasc Biol 26:1613-8. 2006..Identify gene variants associated with early-onset myocardial infarction (MI)...
Genetic variants in the KIF6 region and coronary event reduction from statin therapyYonghong Li
Hum Genet 129:17-23. 2011..These three SNPs are in high linkage disequilibrium with one another (r (2) > 0.84). Functional studies of these variants may help to understand the role of KIF6 in the pathogenesis of CHD and differential response to statin therapy...
Prediction of coronary heart disease risk using a genetic risk score: the Atherosclerosis Risk in Communities StudyAlanna C Morrison
Human Genetics Center and Division of Epidemiology, University of Texas Health Science Center at Houston, Houston, TX 77030, USA
Am J Epidemiol 166:28-35. 2007..This study demonstrates the concept of aggregating information from multiple single nucleotide polymorphisms into a risk score and indicates that it can improve prediction of incident CHD in the ARIC study...
Obstetric complications in patients with hereditary thrombophilia identified using the LCx microparticle enzyme immunoassay: a controlled study of 5,000 patientsOlivier Kocher
Department of Pathology, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA 02215, USA
Am J Clin Pathol 127:68-75. 2007..These results confirm the association between genetic thrombophilia and selected obstetric complications...
Gene variants associated with deep vein thrombosisIrene D Bezemer
Department of Clinical Epidemiology, Leiden University Medical Center, Leiden, The Netherlands
JAMA 299:1306-14. 2008..The genetic causes of deep vein thrombosis (DVT) are not fully understood...
