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Expertise in Coronary Artery Disease: HELP
Rasika A. Mathias
Based on 6 articles published since 2008
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Expertise Level
The expertise of Rasika A. Mathias ranks in the Graphical view (beta)
Uncounted papers?
Aliases Mathias, Rasika A   ·   Mathias, Rasika
Work Locations
Details
Most likely:    Johns Hopkins University   Contact    
2010
  • Genometrics Section, Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore, MD, USA. · Pubmed 20529293
2011
  • Department of Anesthesiology and Critical Care Medicine,J ohns Hopkins University School of Medicine, Baltimore, MD, USA. · Pubmed 21791418
  • Department of Medicine, The Johns Hopkins GeneSTAR Research Program, The Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA. · Pubmed 21270820
2010
  • Department of Medicine, Division of General Internal Medicine, Johns Hopkins Medical Institutions, Baltimore, Maryland, USA. · Pubmed 20299483
Probable:    National Institutes of Health      
2010
  • Genometrics Section, Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore, MD, USA. · Pubmed 20529293
Possible:    Stanford University   Contact    
2010
  • Department of Medicine, Stanford University School of Medicine, Stanford, California 94304-1334, USA. · Pubmed 20933357
Specific Interests

In the titles of their published articles, experts often reveal their very specific interests.

Here are the titles of all articles written by Rasika A. Mathias in 2008-2019 about Coronary Artery Disease:

  • Multiethnic Exome-Wide Association Study of Subclinical Atherosclerosis. 2016
  • Identification of a specific intronic PEAR1 gene variant associated with greater platelet aggregability and protein expression. 2011
  • A common variant in the CDKN2B gene on chromosome 9p21 protects against coronary artery disease in Americans of African ancestry. 2011
  • Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies. 2010
  • A combined genome-wide linkage and association approach to find susceptibility loci for platelet function phenotypes in European American and African American families with coronary artery disease. 2010
  • Independent metabolic syndrome variants predict new-onset coronary artery disease. 2010
Show List of Full Article Records
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Johns Hopkins University
2010
  • Genometrics Section, Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore, MD, USA. · Pubmed 20529293
2011
  • Department of Anesthesiology and Critical Care Medicine,J ohns Hopkins University School of Medicine, Baltimore, MD, USA. · Pubmed 21791418
  • Department of Medicine, The Johns Hopkins GeneSTAR Research Program, The Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA. · Pubmed 21270820
2010
  • Department of Medicine, Division of General Internal Medicine, Johns Hopkins Medical Institutions, Baltimore, Maryland, USA. · Pubmed 20299483
National Institutes of Health
2010
  • Genometrics Section, Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore, MD, USA. · Pubmed 20529293
Stanford University
2010
  • Department of Medicine, Stanford University School of Medicine, Stanford, California 94304-1334, USA. · Pubmed 20933357
Yearly article counts 000100002300
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