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Christopher G Chute

Showing results (241-250 of 286) with videos related to

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Journal of the American Medical Informatics Association : JAMIA|December 7, 2022
Characterizing variability of electronic health record-driven phenotype definitionsPascal S Brandt, Abel Kho, Yuan Luo, et al.
Journal of the American Medical Informatics Association : JAMIA|November 22, 2011
Use of diverse electronic medical record systems to identify genetic risk for type 2 diabetes within a genome-wide association studyAbel N Kho, M Geoffrey Hayes, Laura Rasmussen-Torvik, et al.
Academic Medicine : Journal of the Association of American Medical Colleges|June 25, 2009
Synergies and distinctions between computational disciplines in biomedical research: perspective from the Clinical andTranslational Science Award programsElmer V Bernstam, William R Hersh, Stephen B Johnson, et al.
American Journal of Human Genetics|May 11, 2020
Predictive Utility of Polygenic Risk Scores for Coronary Heart Disease in Three Major Racial and Ethnic GroupsOzan Dikilitas, Daniel J Schaid, Matthew L Kosel, et al.
Mayo Clinic Proceedings|November 6, 2018
The Return of Actionable Variants Empirical (RAVE) Study, a Mayo Clinic Genomic Medicine Implementation Study: Design and Initial ResultsIftikhar J Kullo, Janet Olson, Xiao Fan, et al.
Journal of the American Medical Informatics Association : JAMIA|April 18, 2022
Harmonizing units and values of quantitative data elements in a very large nationally pooled electronic health record (EHR) datasetKatie R Bradwell, Jacob T Wooldridge, Benjamin Amor, et al.
Circulation. Cardiovascular Genetics|April 19, 2017
Investigating the Genetic Architecture of the PR Interval Using Clinical PhenotypesJonathan D Mosley, M Benjamin Shoemaker, Quinn S Wells, et al.
Journal of the American Medical Informatics Association : JAMIA|June 4, 2018
Empowering genomic medicine by establishing critical sequencing result data flows: the eMERGE exampleSamuel Aronson, Lawrence Babb, Darren Ames, et al.
Medrxiv : the Preprint Server for Health Sciences|June 6, 2022
Generalizable Long COVID Subtypes: Findings from the NIH N3C and RECOVER ProgramsJustin T Reese, Hannah Blau, Timothy Bergquist, et al.
Journal of the American Medical Informatics Association : JAMIA|July 5, 2015
CSER and eMERGE: current and potential state of the display of genetic information in the electronic health recordBrian H Shirts, Joseph S Salama, Samuel J Aronson, et al.
Pageof 29

Showing results (241-250 of 286) with videos related to

Sort By:
Pageof 29
Journal of the American Medical Informatics Association : JAMIA|December 7, 2022
Characterizing variability of electronic health record-driven phenotype definitionsPascal S Brandt, Abel Kho, Yuan Luo, et al.
Journal of the American Medical Informatics Association : JAMIA|November 22, 2011
Use of diverse electronic medical record systems to identify genetic risk for type 2 diabetes within a genome-wide association studyAbel N Kho, M Geoffrey Hayes, Laura Rasmussen-Torvik, et al.
Academic Medicine : Journal of the Association of American Medical Colleges|June 25, 2009
Synergies and distinctions between computational disciplines in biomedical research: perspective from the Clinical andTranslational Science Award programsElmer V Bernstam, William R Hersh, Stephen B Johnson, et al.
American Journal of Human Genetics|May 11, 2020
Predictive Utility of Polygenic Risk Scores for Coronary Heart Disease in Three Major Racial and Ethnic GroupsOzan Dikilitas, Daniel J Schaid, Matthew L Kosel, et al.
Mayo Clinic Proceedings|November 6, 2018
The Return of Actionable Variants Empirical (RAVE) Study, a Mayo Clinic Genomic Medicine Implementation Study: Design and Initial ResultsIftikhar J Kullo, Janet Olson, Xiao Fan, et al.
Journal of the American Medical Informatics Association : JAMIA|April 18, 2022
Harmonizing units and values of quantitative data elements in a very large nationally pooled electronic health record (EHR) datasetKatie R Bradwell, Jacob T Wooldridge, Benjamin Amor, et al.
Circulation. Cardiovascular Genetics|April 19, 2017
Investigating the Genetic Architecture of the PR Interval Using Clinical PhenotypesJonathan D Mosley, M Benjamin Shoemaker, Quinn S Wells, et al.
Journal of the American Medical Informatics Association : JAMIA|June 4, 2018
Empowering genomic medicine by establishing critical sequencing result data flows: the eMERGE exampleSamuel Aronson, Lawrence Babb, Darren Ames, et al.
Medrxiv : the Preprint Server for Health Sciences|June 6, 2022
Generalizable Long COVID Subtypes: Findings from the NIH N3C and RECOVER ProgramsJustin T Reese, Hannah Blau, Timothy Bergquist, et al.
Journal of the American Medical Informatics Association : JAMIA|July 5, 2015
CSER and eMERGE: current and potential state of the display of genetic information in the electronic health recordBrian H Shirts, Joseph S Salama, Samuel J Aronson, et al.
Pageof 29