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Clinical Chemistry and Laboratory Medicine
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May 16, 2003
The use of denaturing high-performance liquid chromatography (DHPLC) for the analysis of genetic variations: impact for diagnostics and pharmacogenetics
Felix W Frueh, Mario Noyer-Weidner
Drug Discovery Today. Technologies
|
July 2, 2014
Questions and answers about the Pilot Process for Biomarker Qualification at the FDA
Federico M Goodsaid, Felix W Frueh
Personalized Medicine
|
May 24, 2018
Pharmacogenomics steps toward personalized medicine
Hong-Guang Xie, Felix W Frueh
Drug Discovery Today. Technologies
|
July 2, 2014
The Predictive Safety Testing Consortium: A synthesis of the goals, challenges and accomplishments of the Critical Path
Federico M Goodsaid, Felix W Frueh, William Mattes
Toxicology
|
February 19, 2008
Strategic paths for biomarker qualification
Federico M Goodsaid, Felix W Frueh, William Mattes
Journal of Personalized Medicine
|
January 7, 2015
Physician Awareness and Utilization of Food and Drug Administration (FDA)-Approved Labeling for Pharmacogenomic Testing Information
Eric J Stanek, Christopher L Sanders, Felix W Frueh
Biomarkers in Medicine
|
May 19, 2010
Integration and use of biomarkers in drug development, regulation and clinical practice: a US regulatory perspective
Shashi Amur, Felix W Frueh, Lawrence J Lesko, et al.
Pharmacogenomics
|
December 24, 2008
4th US FDA-Drug Information Association pharmacogenomics workshop, held 10-12 December, 2007
Felix W Frueh, Ronald A Salerno, Lawrence J Lesko, et al.
Nature Reviews. Genetics
|
June 2, 2011
The future of direct-to-consumer clinical genetic tests
Felix W Frueh, Henry T Greely, Robert C Green, et al.
Drug Discovery Today. Technologies
|
July 2, 2014
An integrated bioinformatics infrastructure essential for advancing pharmacogenomics and personalized medicine in the context of the FDA's Critical Path Initiative
Weida Tong, Stephen C Harris, Hong Fang, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 30) with videos related to
Sort By:
Page
of 3
Clinical Chemistry and Laboratory Medicine
|
May 16, 2003
The use of denaturing high-performance liquid chromatography (DHPLC) for the analysis of genetic variations: impact for diagnostics and pharmacogenetics
Felix W Frueh, Mario Noyer-Weidner
Drug Discovery Today. Technologies
|
July 2, 2014
Questions and answers about the Pilot Process for Biomarker Qualification at the FDA
Federico M Goodsaid, Felix W Frueh
Personalized Medicine
|
May 24, 2018
Pharmacogenomics steps toward personalized medicine
Hong-Guang Xie, Felix W Frueh
Drug Discovery Today. Technologies
|
July 2, 2014
The Predictive Safety Testing Consortium: A synthesis of the goals, challenges and accomplishments of the Critical Path
Federico M Goodsaid, Felix W Frueh, William Mattes
Toxicology
|
February 19, 2008
Strategic paths for biomarker qualification
Federico M Goodsaid, Felix W Frueh, William Mattes
Journal of Personalized Medicine
|
January 7, 2015
Physician Awareness and Utilization of Food and Drug Administration (FDA)-Approved Labeling for Pharmacogenomic Testing Information
Eric J Stanek, Christopher L Sanders, Felix W Frueh
Biomarkers in Medicine
|
May 19, 2010
Integration and use of biomarkers in drug development, regulation and clinical practice: a US regulatory perspective
Shashi Amur, Felix W Frueh, Lawrence J Lesko, et al.
Pharmacogenomics
|
December 24, 2008
4th US FDA-Drug Information Association pharmacogenomics workshop, held 10-12 December, 2007
Felix W Frueh, Ronald A Salerno, Lawrence J Lesko, et al.
Nature Reviews. Genetics
|
June 2, 2011
The future of direct-to-consumer clinical genetic tests
Felix W Frueh, Henry T Greely, Robert C Green, et al.
Drug Discovery Today. Technologies
|
July 2, 2014
An integrated bioinformatics infrastructure essential for advancing pharmacogenomics and personalized medicine in the context of the FDA's Critical Path Initiative
Weida Tong, Stephen C Harris, Hong Fang, et al.
Page
of 3