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Pharmacogenomics
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July 17, 2009
Back to the future: why randomized controlled trials cannot be the answer to pharmacogenomics and personalized medicine
Felix W Frueh
Drug Discovery Today
|
October 4, 2011
Considerations for safety pharmacogenetics in clinical practice
Felix W Frueh
Trends in Molecular Medicine
|
March 3, 2012
On rat poison and human medicines: personalizing warfarin therapy
Felix W Frueh
Pharmacogenomics
|
April 27, 2010
Real-world clinical effectiveness, regulatory transparency and payer coverage: three ingredients for translating pharmacogenomics into clinical practice
Felix W Frueh
Personalized Medicine
|
May 24, 2018
Considerations for a business model for the effective integration of novel biomarkers into drug development
Felix W Frueh
Nature Biotechnology
|
September 12, 2006
Impact of microarray data quality on genomic data submissions to the FDA
Felix W Frueh
Value in Health : the Journal of the International Society for Pharmacoeconomics and Outcomes Research
|
September 17, 2013
Regulation, reimbursement, and the long road of implementation of personalized medicine--a perspective from the United States
Felix W Frueh
Pharmacogenomics
|
June 24, 2004
From pharmacogenetics to personalized medicine: a vital need for educating health professionals and the community
Felix W Frueh, David Gurwitz
Expert Review of Molecular Diagnostics
|
August 12, 2014
Molecular diagnostics clinical utility strategy: a six-part framework
Felix W Frueh, Bruce Quinn
Environmental and Molecular Mutagenesis
|
June 15, 2007
Implementing the U.S. FDA guidance on pharmacogenomic data submissions
Federico Goodsaid, Felix W Frueh
Page
of 3
Search research articles
Search
Showing results (1-10 of 30) with videos related to
Sort By:
Page
of 3
Pharmacogenomics
|
July 17, 2009
Back to the future: why randomized controlled trials cannot be the answer to pharmacogenomics and personalized medicine
Felix W Frueh
Drug Discovery Today
|
October 4, 2011
Considerations for safety pharmacogenetics in clinical practice
Felix W Frueh
Trends in Molecular Medicine
|
March 3, 2012
On rat poison and human medicines: personalizing warfarin therapy
Felix W Frueh
Pharmacogenomics
|
April 27, 2010
Real-world clinical effectiveness, regulatory transparency and payer coverage: three ingredients for translating pharmacogenomics into clinical practice
Felix W Frueh
Personalized Medicine
|
May 24, 2018
Considerations for a business model for the effective integration of novel biomarkers into drug development
Felix W Frueh
Nature Biotechnology
|
September 12, 2006
Impact of microarray data quality on genomic data submissions to the FDA
Felix W Frueh
Value in Health : the Journal of the International Society for Pharmacoeconomics and Outcomes Research
|
September 17, 2013
Regulation, reimbursement, and the long road of implementation of personalized medicine--a perspective from the United States
Felix W Frueh
Pharmacogenomics
|
June 24, 2004
From pharmacogenetics to personalized medicine: a vital need for educating health professionals and the community
Felix W Frueh, David Gurwitz
Expert Review of Molecular Diagnostics
|
August 12, 2014
Molecular diagnostics clinical utility strategy: a six-part framework
Felix W Frueh, Bruce Quinn
Environmental and Molecular Mutagenesis
|
June 15, 2007
Implementing the U.S. FDA guidance on pharmacogenomic data submissions
Federico Goodsaid, Felix W Frueh
Page
of 3