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Dan M Roden

Showing results (461-470 of 593) with videos related to

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Journal of the American Medical Informatics Association : JAMIA|August 21, 2018
A case study evaluating the portability of an executable computable phenotype algorithm across multiple institutions and electronic health record environmentsJennifer A Pacheco, Luke V Rasmussen, Richard C Kiefer, et al.
Circulation. Genomic and Precision Medicine|February 3, 2022
Rare Variation in Drug Metabolism and Long QT Genes and the Genetic Susceptibility to Acquired Long QT SyndromeBelinda Gray, Alban-Elouen Baruteau, Albert A Antolin, et al.
Plos One|December 19, 2013
Mechanistic phenotypes: an aggregative phenotyping strategy to identify disease mechanisms using GWAS dataJonathan D Mosley, Sara L Van Driest, Emma K Larkin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 12, 2013
Implementing genomic medicine in the clinic: the future is hereTeri A Manolio, Rex L Chisholm, Brad Ozenberger, et al.
The Journal of Pediatrics|June 27, 2020
Variants in ADRB1 and CYP2C9: Association with Response to Atenolol and Losartan in Marfan SyndromeSara L Van Driest, Lynn A Sleeper, Bruce D Gelb, et al.
Circulation. Cardiovascular Genetics|December 25, 2009
Variation in the 4q25 chromosomal locus predicts atrial fibrillation after coronary artery bypass graft surgerySimon C Body, Charles D Collard, Stanton K Shernan, et al.
Nature Genetics|July 13, 2010
Genome-wide association study identifies a susceptibility locus at 21q21 for ventricular fibrillation in acute myocardial infarctionConnie R Bezzina, Raha Pazoki, Abdennasser Bardai, et al.
Heart Rhythm|May 10, 2023
Multicenter clinical and functional evidence reclassifies a recurrent noncanonical filamin C splice-altering variantMatthew J O'Neill, Suet Nee Chen, Lynne Rumping, et al.
European Heart Journal|June 25, 2022
Polygenic risk score for ACE-inhibitor-associated cough based on the discovery of new genetic lociJonas Ghouse, Vinicius Tragante, Ayesha Muhammad, et al.
Genome Medicine|January 16, 2024
The impact of damaging epilepsy and cardiac genetic variant burden in sudden death in the youngMegan J Puckelwartz, Lorenzo L Pesce, Edgar J Hernandez, et al.
Pageof 60

Showing results (461-470 of 593) with videos related to

Sort By:
Pageof 60
Journal of the American Medical Informatics Association : JAMIA|August 21, 2018
A case study evaluating the portability of an executable computable phenotype algorithm across multiple institutions and electronic health record environmentsJennifer A Pacheco, Luke V Rasmussen, Richard C Kiefer, et al.
Circulation. Genomic and Precision Medicine|February 3, 2022
Rare Variation in Drug Metabolism and Long QT Genes and the Genetic Susceptibility to Acquired Long QT SyndromeBelinda Gray, Alban-Elouen Baruteau, Albert A Antolin, et al.
Plos One|December 19, 2013
Mechanistic phenotypes: an aggregative phenotyping strategy to identify disease mechanisms using GWAS dataJonathan D Mosley, Sara L Van Driest, Emma K Larkin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 12, 2013
Implementing genomic medicine in the clinic: the future is hereTeri A Manolio, Rex L Chisholm, Brad Ozenberger, et al.
The Journal of Pediatrics|June 27, 2020
Variants in ADRB1 and CYP2C9: Association with Response to Atenolol and Losartan in Marfan SyndromeSara L Van Driest, Lynn A Sleeper, Bruce D Gelb, et al.
Circulation. Cardiovascular Genetics|December 25, 2009
Variation in the 4q25 chromosomal locus predicts atrial fibrillation after coronary artery bypass graft surgerySimon C Body, Charles D Collard, Stanton K Shernan, et al.
Nature Genetics|July 13, 2010
Genome-wide association study identifies a susceptibility locus at 21q21 for ventricular fibrillation in acute myocardial infarctionConnie R Bezzina, Raha Pazoki, Abdennasser Bardai, et al.
Heart Rhythm|May 10, 2023
Multicenter clinical and functional evidence reclassifies a recurrent noncanonical filamin C splice-altering variantMatthew J O'Neill, Suet Nee Chen, Lynne Rumping, et al.
European Heart Journal|June 25, 2022
Polygenic risk score for ACE-inhibitor-associated cough based on the discovery of new genetic lociJonas Ghouse, Vinicius Tragante, Ayesha Muhammad, et al.
Genome Medicine|January 16, 2024
The impact of damaging epilepsy and cardiac genetic variant burden in sudden death in the youngMegan J Puckelwartz, Lorenzo L Pesce, Edgar J Hernandez, et al.
Pageof 60