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Dan M Roden

Showing results (401-410 of 593) with videos related to

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Journal of the American College of Cardiology|June 12, 2012
Common variation in the NOS1AP gene is associated with drug-induced QT prolongation and ventricular arrhythmiaYalda Jamshidi, Ilja M Nolte, Chrysoula Dalageorgou, et al.
Journal of the American Medical Informatics Association : JAMIA|March 31, 2016
PheKB: a catalog and workflow for creating electronic phenotype algorithms for transportabilityJacqueline C Kirby, Peter Speltz, Luke V Rasmussen, et al.
HGG Advances|August 29, 2022
Personalized structural biology reveals the molecular mechanisms underlying heterogeneous epileptic phenotypes caused by <i>de novo</i> KCNC2 variantsSouhrid Mukherjee, Thomas A Cassini, Ningning Hu, et al.
Plos One|December 20, 2018
Hypertension genetic risk score is associated with burden of coronary heart disease among patients referred for coronary angiographyMaria Lukács Krogager, Regitze Kuhr Skals, Emil Vincent R Appel, et al.
Immunity, Inflammation and Disease|January 7, 2016
CMTR1 is associated with increased asthma exacerbations in patients taking inhaled corticosteroidsAmber Dahlin, Joshua Denny, Dan M Roden, et al.
Journal of the American Medical Informatics Association : JAMIA|August 8, 2016
Evaluating electronic health record data sources and algorithmic approaches to identify hypertensive individualsPedro L Teixeira, Wei-Qi Wei, Robert M Cronin, et al.
Circulation. Arrhythmia and Electrophysiology|January 9, 2015
Genetic and clinical risk prediction model for postoperative atrial fibrillationMatthew J Kolek, J Daniel Muehlschlegel, William S Bush, et al.
Circulation|December 28, 2018
Phenotypic Refinement of Heart Failure in a National Biobank Facilitates Genetic DiscoveryKrishna G Aragam, Mark Chaffin, Rebecca T Levinson, et al.
Plos One|October 26, 2023
Correction: Hypertension genetic risk score is associated with burden of coronary heart disease among patients referred for coronary angiographyMaria Lukács Krogager, Regitze Kuhr Skals, Emil Vincent R Appel, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 29, 2006
Mice with the R176Q cardiac ryanodine receptor mutation exhibit catecholamine-induced ventricular tachycardia and cardiomyopathyPrince J Kannankeril, Brett M Mitchell, Sanjeewa A Goonasekera, et al.
Pageof 60

Showing results (401-410 of 593) with videos related to

Sort By:
Pageof 60
Journal of the American College of Cardiology|June 12, 2012
Common variation in the NOS1AP gene is associated with drug-induced QT prolongation and ventricular arrhythmiaYalda Jamshidi, Ilja M Nolte, Chrysoula Dalageorgou, et al.
Journal of the American Medical Informatics Association : JAMIA|March 31, 2016
PheKB: a catalog and workflow for creating electronic phenotype algorithms for transportabilityJacqueline C Kirby, Peter Speltz, Luke V Rasmussen, et al.
HGG Advances|August 29, 2022
Personalized structural biology reveals the molecular mechanisms underlying heterogeneous epileptic phenotypes caused by <i>de novo</i> KCNC2 variantsSouhrid Mukherjee, Thomas A Cassini, Ningning Hu, et al.
Plos One|December 20, 2018
Hypertension genetic risk score is associated with burden of coronary heart disease among patients referred for coronary angiographyMaria Lukács Krogager, Regitze Kuhr Skals, Emil Vincent R Appel, et al.
Immunity, Inflammation and Disease|January 7, 2016
CMTR1 is associated with increased asthma exacerbations in patients taking inhaled corticosteroidsAmber Dahlin, Joshua Denny, Dan M Roden, et al.
Journal of the American Medical Informatics Association : JAMIA|August 8, 2016
Evaluating electronic health record data sources and algorithmic approaches to identify hypertensive individualsPedro L Teixeira, Wei-Qi Wei, Robert M Cronin, et al.
Circulation. Arrhythmia and Electrophysiology|January 9, 2015
Genetic and clinical risk prediction model for postoperative atrial fibrillationMatthew J Kolek, J Daniel Muehlschlegel, William S Bush, et al.
Circulation|December 28, 2018
Phenotypic Refinement of Heart Failure in a National Biobank Facilitates Genetic DiscoveryKrishna G Aragam, Mark Chaffin, Rebecca T Levinson, et al.
Plos One|October 26, 2023
Correction: Hypertension genetic risk score is associated with burden of coronary heart disease among patients referred for coronary angiographyMaria Lukács Krogager, Regitze Kuhr Skals, Emil Vincent R Appel, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 29, 2006
Mice with the R176Q cardiac ryanodine receptor mutation exhibit catecholamine-induced ventricular tachycardia and cardiomyopathyPrince J Kannankeril, Brett M Mitchell, Sanjeewa A Goonasekera, et al.
Pageof 60