Lance A Bare

Summary

Affiliation: Celera Genomics
Country: USA

Publications

  1. ncbi request reprint Five common gene variants identify elevated genetic risk for coronary heart disease
    Lance A Bare
    Celera, Alameda, California 94502, USA
    Genet Med 9:682-9. 2007
  2. pmc Gene variants associated with ischemic stroke: the cardiovascular health study
    May M Luke
    Celera, Alameda, California 94502, USA
    Stroke 40:363-8. 2009
  3. pmc Association of gene variants with incident myocardial infarction in the Cardiovascular Health Study
    Dov Shiffman
    Celera, 1401 Harbor Bay Parkway, Alameda, CA 94502, USA
    Arterioscler Thromb Vasc Biol 28:173-9. 2008
  4. ncbi request reprint Gene variants of VAMP8 and HNRPUL1 are associated with early-onset myocardial infarction
    Dov Shiffman
    Celera Inc, 1401 Harbor Bay Pkwy, Alameda, California 94502, USA
    Arterioscler Thromb Vasc Biol 26:1613-8. 2006
  5. pmc Genetic variants in the KIF6 region and coronary event reduction from statin therapy
    Yonghong Li
    Hum Genet 129:17-23. 2011
  6. ncbi request reprint Prediction of coronary heart disease risk using a genetic risk score: the Atherosclerosis Risk in Communities Study
    Alanna 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
  7. ncbi request reprint Obstetric complications in patients with hereditary thrombophilia identified using the LCx microparticle enzyme immunoassay: a controlled study of 5,000 patients
    Olivier 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
  8. doi request reprint Gene variants associated with deep vein thrombosis
    Irene D Bezemer
    Department of Clinical Epidemiology, Leiden University Medical Center, Leiden, The Netherlands
    JAMA 299:1306-14. 2008

Collaborators

Detail Information

Publications8

  1. ncbi request reprint Five common gene variants identify elevated genetic risk for coronary heart disease
    Lance A Bare
    Celera, Alameda, California 94502, USA
    Genet Med 9:682-9. 2007
    ....
  2. pmc Gene variants associated with ischemic stroke: the cardiovascular health study
    May 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...
  3. pmc Association of gene variants with incident myocardial infarction in the Cardiovascular Health Study
    Dov Shiffman
    Celera, 1401 Harbor Bay Parkway, Alameda, CA 94502, USA
    Arterioscler Thromb Vasc Biol 28:173-9. 2008
    ....
  4. ncbi request reprint Gene variants of VAMP8 and HNRPUL1 are associated with early-onset myocardial infarction
    Dov 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)...
  5. pmc Genetic variants in the KIF6 region and coronary event reduction from statin therapy
    Yonghong 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...
  6. ncbi request reprint Prediction of coronary heart disease risk using a genetic risk score: the Atherosclerosis Risk in Communities Study
    Alanna 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...
  7. ncbi request reprint Obstetric complications in patients with hereditary thrombophilia identified using the LCx microparticle enzyme immunoassay: a controlled study of 5,000 patients
    Olivier 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...
  8. doi request reprint Gene variants associated with deep vein thrombosis
    Irene 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...