Результаты поиска - D M Roden
- Отображение 1 - 13 результаты of 13
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Genetics of acquired long QT syndrome по D M Roden
Опубликовано 2005Revisão -
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Genomic Medicine, Precision Medicine, Personalized Medicine: What’s in a Name? по D M Roden, Rachel F. Tyndale
Опубликовано 2013Editorial -
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Clinical Pharmacogenetics Implementation Consortium Guidelines for Cytochrome P450-2C19 (CYP2C19) Genotype and Clopidogrel Therapy по 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
Опубликовано 2011Artigo -
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Detecting Drug Interactions From Adverse-Event Reports: Interaction Between Paroxetine and Pravastatin Increases Blood Glucose Levels по 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
Опубликовано 2011Artigo -
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Clinical Pharmacogenetics Implementation Consortium Guidelines for CYP2C19 Genotype and Clopidogrel Therapy: 2013 Update по 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
Опубликовано 2013Artigo -
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Optimizing Drug Outcomes Through Pharmacogenetics: A Case for Preemptive Genotyping по 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
Опубликовано 2012Artigo -
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The Clinical Pharmacogenetics Implementation Consortium Guideline for SLCO1B1 and Simvastatin-Induced Myopathy: 2014 Update по 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
Опубликовано 2014Artigo -
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Operational Implementation of Prospective Genotyping for Personalized Medicine: The Design of the Vanderbilt PREDICT Project по 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
Опубликовано 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 по 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
Опубликовано 2015Artigo -
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Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillation по 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
Опубликовано 2008Revisão
Инструменты поиска:
Связанные темы
Medicine
Internal medicine
Biology
Gene
Pharmacology
Genetics
Genotype
Pharmacogenetics
Adverse effect
Bioinformatics
Cardiology
Clopidogrel
Pathology
Aspirin
Biochemistry
Drug
Atrial fibrillation
CYP2C19
Computer science
Confidence interval
Conventional PCI
Cytochrome P450
Disease
Genotyping
Guideline
Intensive care medicine
Long QT syndrome
Metabolism
Mutation
Myocardial infarction