Rezultaty - D M Roden
- Rezultaty 1 - 13 Rezultaty od 13
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Genetics of acquired long QT syndrome od D M Roden
Wydane 2005Revisão -
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Clinical Pharmacogenetics Implementation Consortium Guidelines for Cytochrome P450-2C19 (CYP2C19) Genotype and Clopidogrel Therapy od Stuart A. Scott, Katrin Sangkuhl, E E Gardner, Catherine M. Stein, Jean‐Sébastien Hulot, J. A. Johnson, D M Roden, Teri E. Klein, Alan R. Shuldiner
Wydane 2011Artigo -
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Detecting Drug Interactions From Adverse-Event Reports: Interaction Between Paroxetine and Pravastatin Increases Blood Glucose Levels od Nicholas P. Tatonetti, Joshua C. Denny, S. Murphy, G H Fernald, G. Krishnan, Vı́ctor Castro, Patrick Yue, P S Tsau, Isaac S. Kohane, D M Roden, Russ B. Altman
Wydane 2011Artigo -
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Clinical Pharmacogenetics Implementation Consortium Guidelines for CYP2C19 Genotype and Clopidogrel Therapy: 2013 Update od Stuart A. Scott, Katrin Sangkuhl, Catherine M. Stein, Jean‐Sébastien Hulot, Jessica L. Mega, D M Roden, Teri E. Klein, Marc S. Sabatine, Julie A. Johnson, Alan R. Shuldiner
Wydane 2013Artigo -
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Optimizing Drug Outcomes Through Pharmacogenetics: A Case for Preemptive Genotyping od Jonathan S. Schildcrout, Joshua C. Denny, Erica Bowton, W. Gregg, Jill M. Pulley, Melissa Basford, James D. Cowan, Hai-liang Xu, Andrea H. Ramirez, Dana C. Crawford, Marylyn D. Ritchie, Josh F. Peterson, Daniel R. Masys, Russell A. Wilke, D M Roden
Wydane 2012Artigo -
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The Clinical Pharmacogenetics Implementation Consortium Guideline for SLCO1B1 and Simvastatin-Induced Myopathy: 2014 Update od Laura B. Ramsey, Samuel G. Johnson, Kelly E. Caudle, Cyrine E. Haidar, Deepak Voora, Russell A. Wilke, Whitney D. Maxwell, Howard L. McLeod, Ronald M. Krauss, D M Roden, QiPing Feng, Rhonda M. Cooper‐DeHoff, Li Gong, Teri E. Klein, Mia Wadelius, Mikko Niemi
Wydane 2014Artigo -
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Operational Implementation of Prospective Genotyping for Personalized Medicine: The Design of the Vanderbilt PREDICT Project od Jill M. Pulley, Joshua C. Denny, JF Peterson, Gordon R. Bernard, C. L. Vnencak-Jones, Andrea H. Ramirez, Jessica Delaney, Erica Bowton, Kevin B. Johnson, Dana C. Crawford, J. Schildcrout, Daniel R. Masys, Holli H. Dilks, Russell A. Wilke, Ellen Wright Clayton, E. Shultz, Michael Laposata, John McPherson, Jim Jirjis, D M Roden
Wydane 2012Artigo -
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Role of common and rare variants in <i>SCN10A</i>: results from the Brugada syndrome QRS locus gene discovery collaborative study od Elijah R. Behr, Eleonora Savio‐Galimberti, Julien Barc, Anders G. Holst, Evmorfia Petropoulou, Bram P. Prins, Javad Jabbari, Margherita Torchio, Myriam Berthet, Yuka Mizusawa, Tao Yang, Eline A. Nannenberg, Federica Dagradi, Peter Weeke, Rachel Bastiaenan, Michael J. Ackerman, Stig Haunsø, Antoine Leenhardt, Stefan Kääb, Vincent Probst, Richard Redon, Sanjay Sharma, Arthur A.M. Wilde, Jacob Tfelt‐Hansen, Peter J. Schwartz, D M Roden, Connie R. Bezzina, Morten S. Olesen, Dawood Darbar, Pascale Guicheney, Lia Crotti, Yalda Jamshidi
Wydane 2015Artigo -
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Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillation od Stefan Kääb, Dawood Darbar, Charlotte van Noord, Josée Dupuis, Arne Pfeufer, Chris Newton-Cheh, Renate B. Schnabel, S Makino, Moritz F. Sinner, Prince J. Kannankeril, Britt Maria Beckmann, Subbarao Choudry, Brian S. Donahue, Jan Heeringa, Siegfried Perz, Kathryn L. Lunetta, Martin G. Larson, Daniel Levy, Calum A. MacRae, Jeremy N. Ruskin, A. Wacker, Albert Schömig, H.‐Erich Wichmann, Gerhard Steinbeck, Thomas Meitinger, André G. Uitterlinden, Jacqueline C.M. Witteman, D M Roden, Emelia J. Benjamin, Patrick T. Ellinor
Wydane 2008Revisão
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Computer science
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