Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Cathy Shyr

Showing results (11-20 of 23) with videos related to

Pageof 3
Sort By:
Medrxiv : the Preprint Server for Health Sciences|April 3, 2026
Diagnostic Accuracy of Large Language Models for Rare Diseases: A Systematic Review and Meta-AnalysisMinh-Ha Nguyen, Chih-Ting Yang, Thomas A Cassini, et al.
Studies in Health Technology and Informatics|August 8, 2025
Accuracy of Large Language Models in Generating Rare Disease Differential Diagnosis Using Key Clinical FeaturesCathy Shyr, Rory J Tinker, Paul A Harris, et al.
Medrxiv : the Preprint Server for Health Sciences|November 24, 2025
A statistical framework for evaluating the repeatability and reproducibility of large language modelsCathy Shyr, Boyu Ren, Chih-Yuan Hsu, et al.
Journal of Clinical and Translational Science|January 10, 2025
Expert advice from ResearchMatch volunteers: Recruitment Innovation Center use cases and innovationMaeve Tischbein, Sarah K Cook, Cathy Shyr, et al.
Journal of the American Medical Informatics Association : JAMIA|January 14, 2026
Information extraction from clinical notes: are we ready to switch to large language models?Yan Hu, Xu Zuo, Yujia Zhou, et al.
Journal of the American Medical Informatics Association : JAMIA|July 15, 2024
Leveraging artificial intelligence to summarize abstracts in lay language for increasing research accessibility and transparencyCathy Shyr, Randall W Grout, Nan Kennedy, et al.
Public Health Genomics|February 17, 2026
Sex-Specific Diagnostic Inequality in Fabry Disease: Lessons Learned from Analysis of Newborn Screening and Cascade Testing in Tennessee from 2017 to 2024Yutaka Furuta, Neena S Agrawal, Natalie N Owen, et al.
Public Health Genomics|May 21, 2026
Sex-Based Disparities in Fabry Disease Cause Challenges in Newborn ScreeningYutaka Furuta, Neena S Agrawal, Natalie N Owen, et al.
Research Square|April 10, 2026
Reframing AI for Rare Disease RecognitionWei-Qi Wei, Chao Yan, Wu-Chen Su, et al.
American Journal of Human Genetics|September 5, 2025
All of Us Research Program year in review: 2024Tara Dutka, Erika J Faust, C Scott Gallagher, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
Medrxiv : the Preprint Server for Health Sciences|April 3, 2026
Diagnostic Accuracy of Large Language Models for Rare Diseases: A Systematic Review and Meta-AnalysisMinh-Ha Nguyen, Chih-Ting Yang, Thomas A Cassini, et al.
Studies in Health Technology and Informatics|August 8, 2025
Accuracy of Large Language Models in Generating Rare Disease Differential Diagnosis Using Key Clinical FeaturesCathy Shyr, Rory J Tinker, Paul A Harris, et al.
Medrxiv : the Preprint Server for Health Sciences|November 24, 2025
A statistical framework for evaluating the repeatability and reproducibility of large language modelsCathy Shyr, Boyu Ren, Chih-Yuan Hsu, et al.
Journal of Clinical and Translational Science|January 10, 2025
Expert advice from ResearchMatch volunteers: Recruitment Innovation Center use cases and innovationMaeve Tischbein, Sarah K Cook, Cathy Shyr, et al.
Journal of the American Medical Informatics Association : JAMIA|January 14, 2026
Information extraction from clinical notes: are we ready to switch to large language models?Yan Hu, Xu Zuo, Yujia Zhou, et al.
Journal of the American Medical Informatics Association : JAMIA|July 15, 2024
Leveraging artificial intelligence to summarize abstracts in lay language for increasing research accessibility and transparencyCathy Shyr, Randall W Grout, Nan Kennedy, et al.
Public Health Genomics|February 17, 2026
Sex-Specific Diagnostic Inequality in Fabry Disease: Lessons Learned from Analysis of Newborn Screening and Cascade Testing in Tennessee from 2017 to 2024Yutaka Furuta, Neena S Agrawal, Natalie N Owen, et al.
Public Health Genomics|May 21, 2026
Sex-Based Disparities in Fabry Disease Cause Challenges in Newborn ScreeningYutaka Furuta, Neena S Agrawal, Natalie N Owen, et al.
Research Square|April 10, 2026
Reframing AI for Rare Disease RecognitionWei-Qi Wei, Chao Yan, Wu-Chen Su, et al.
American Journal of Human Genetics|September 5, 2025
All of Us Research Program year in review: 2024Tara Dutka, Erika J Faust, C Scott Gallagher, et al.
Pageof 3