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Medrxiv : the Preprint Server for Health Sciences
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September 4, 2024
Leveraging Generative AI to Accelerate Biocuration of Medical Actions for Rare Disease
Enock Niyonkuru, J Harry Caufield, Leigh C Carmody, et al.
Translational Psychiatry
|
June 8, 2024
Association of post-COVID phenotypic manifestations with new-onset psychiatric disease
Ben Coleman, Elena Casiraghi, Tiffany J Callahan, et al.
Bioinformatics Advances
|
April 5, 2024
Node-degree aware edge sampling mitigates inflated classification performance in biomedical random walk-based graph representation learning
Luca Cappelletti, Lauren Rekerle, Tommaso Fontana, et al.
American Journal of Human Genetics
|
August 30, 2016
A Whole-Genome Analysis Framework for Effective Identification of Pathogenic Regulatory Variants in Mendelian Disease
Damian Smedley, Max Schubach, Julius O B Jacobsen, et al.
European Journal of Human Genetics : EJHG
|
February 24, 2026
Systematic benchmarking demonstrates large language models have not reached the diagnostic accuracy of traditional rare-disease decision support tools
Justin T Reese, Leonardo Chimirri, Yasemin Bridges, et al.
Medrxiv : the Preprint Server for Health Sciences
|
April 28, 2021
NSAID use and clinical outcomes in COVID-19 patients: A 38-center retrospective cohort study
Justin T Reese, Ben Coleman, Lauren Chan, et al.
Virology Journal
|
May 15, 2022
NSAID use and clinical outcomes in COVID-19 patients: a 38-center retrospective cohort study
Justin T Reese, Ben Coleman, Lauren Chan, et al.
Journal of Biomedical Informatics
|
January 30, 2023
A method for comparing multiple imputation techniques: A case study on the U.S. national COVID cohort collaborative
Elena Casiraghi, Rachel Wong, Margaret Hall, 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.
Ebiomedicine
|
December 23, 2022
Generalisable long COVID subtypes: findings from the NIH N3C and RECOVER programmes
Justin T Reese, Hannah Blau, Elena Casiraghi, et al.
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of 9
Search research articles
Search
Showing results (71-80 of 84) with videos related to
Sort By:
Page
of 9
Medrxiv : the Preprint Server for Health Sciences
|
September 4, 2024
Leveraging Generative AI to Accelerate Biocuration of Medical Actions for Rare Disease
Enock Niyonkuru, J Harry Caufield, Leigh C Carmody, et al.
Translational Psychiatry
|
June 8, 2024
Association of post-COVID phenotypic manifestations with new-onset psychiatric disease
Ben Coleman, Elena Casiraghi, Tiffany J Callahan, et al.
Bioinformatics Advances
|
April 5, 2024
Node-degree aware edge sampling mitigates inflated classification performance in biomedical random walk-based graph representation learning
Luca Cappelletti, Lauren Rekerle, Tommaso Fontana, et al.
American Journal of Human Genetics
|
August 30, 2016
A Whole-Genome Analysis Framework for Effective Identification of Pathogenic Regulatory Variants in Mendelian Disease
Damian Smedley, Max Schubach, Julius O B Jacobsen, et al.
European Journal of Human Genetics : EJHG
|
February 24, 2026
Systematic benchmarking demonstrates large language models have not reached the diagnostic accuracy of traditional rare-disease decision support tools
Justin T Reese, Leonardo Chimirri, Yasemin Bridges, et al.
Medrxiv : the Preprint Server for Health Sciences
|
April 28, 2021
NSAID use and clinical outcomes in COVID-19 patients: A 38-center retrospective cohort study
Justin T Reese, Ben Coleman, Lauren Chan, et al.
Virology Journal
|
May 15, 2022
NSAID use and clinical outcomes in COVID-19 patients: a 38-center retrospective cohort study
Justin T Reese, Ben Coleman, Lauren Chan, et al.
Journal of Biomedical Informatics
|
January 30, 2023
A method for comparing multiple imputation techniques: A case study on the U.S. national COVID cohort collaborative
Elena Casiraghi, Rachel Wong, Margaret Hall, 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.
Ebiomedicine
|
December 23, 2022
Generalisable long COVID subtypes: findings from the NIH N3C and RECOVER programmes
Justin T Reese, Hannah Blau, Elena Casiraghi, et al.
Page
of 9