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Melissa Basford

Showing results (21-30 of 27) with videos related to

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Journal of the American Medical Informatics Association : JAMIA|August 13, 2024
Empowering the biomedical research community: Innovative SAS deployment on the All of Us Researcher WorkbenchIzabelle Humes, Cathy Shyr, Moira Dillon, et al.
Medrxiv : the Preprint Server for Health Sciences|November 24, 2025
Genome sequencing of 35,024 predominantly African ancestry persons addresses gaps in genomics and healthcareCecile Avery, Mojgan Babanejad, James Baker, et al.
Blood|August 13, 2015
Genetics of glucocorticoid-associated osteonecrosis in children with acute lymphoblastic leukemiaSeth E Karol, Wenjian Yang, Sara L Van Driest, et al.
BMC Medical Research Methodology|November 25, 2016
Conducting a large, multi-site survey about patients' views on broad consent: challenges and solutionsMaureen E Smith, Saskia C Sanderson, Kyle B Brothers, et al.
Clinical and Translational Science|January 25, 2014
The CTSA Consortium's Catalog of Assets for Translational and Clinical Health Research (CATCHR)Jana Shirey-Rice, Brandy Mapes, Melissa Basford, et al.
Patterns (New York, N.Y.)|August 29, 2022
The <i>All of Us</i> Research Program: Data quality, utility, and diversityAndrea H Ramirez, Lina Sulieman, David J Schlueter, et al.
Medrxiv : the Preprint Server for Health Sciences|May 25, 2026
Systematic common and rare variant association testing in 392,030 whole genomes in <i>All of Us</i>Wenhan Lu, Robert J Carroll, Matthew Solomonson, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
Journal of the American Medical Informatics Association : JAMIA|August 13, 2024
Empowering the biomedical research community: Innovative SAS deployment on the All of Us Researcher WorkbenchIzabelle Humes, Cathy Shyr, Moira Dillon, et al.
Medrxiv : the Preprint Server for Health Sciences|November 24, 2025
Genome sequencing of 35,024 predominantly African ancestry persons addresses gaps in genomics and healthcareCecile Avery, Mojgan Babanejad, James Baker, et al.
Blood|August 13, 2015
Genetics of glucocorticoid-associated osteonecrosis in children with acute lymphoblastic leukemiaSeth E Karol, Wenjian Yang, Sara L Van Driest, et al.
BMC Medical Research Methodology|November 25, 2016
Conducting a large, multi-site survey about patients' views on broad consent: challenges and solutionsMaureen E Smith, Saskia C Sanderson, Kyle B Brothers, et al.
Clinical and Translational Science|January 25, 2014
The CTSA Consortium's Catalog of Assets for Translational and Clinical Health Research (CATCHR)Jana Shirey-Rice, Brandy Mapes, Melissa Basford, et al.
Patterns (New York, N.Y.)|August 29, 2022
The <i>All of Us</i> Research Program: Data quality, utility, and diversityAndrea H Ramirez, Lina Sulieman, David J Schlueter, et al.
Medrxiv : the Preprint Server for Health Sciences|May 25, 2026
Systematic common and rare variant association testing in 392,030 whole genomes in <i>All of Us</i>Wenhan Lu, Robert J Carroll, Matthew Solomonson, et al.
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