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Journal of the American Medical Informatics Association : JAMIA
|
December 7, 2022
Characterizing variability of electronic health record-driven phenotype definitions
Pascal 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 study
Abel 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 programs
Elmer 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 Groups
Ozan 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 Results
Iftikhar 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) dataset
Katie 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 Phenotypes
Jonathan 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 example
Samuel 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 Programs
Justin 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 record
Brian H Shirts, Joseph S Salama, Samuel J Aronson, et al.
Page
of 29
Search research articles
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Showing results (241-250 of 286) with videos related to
Sort By:
Page
of 29
Journal of the American Medical Informatics Association : JAMIA
|
December 7, 2022
Characterizing variability of electronic health record-driven phenotype definitions
Pascal 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 study
Abel 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 programs
Elmer 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 Groups
Ozan 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 Results
Iftikhar 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) dataset
Katie 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 Phenotypes
Jonathan 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 example
Samuel 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 Programs
Justin 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 record
Brian H Shirts, Joseph S Salama, Samuel J Aronson, et al.
Page
of 29