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Ron Do

Showing results (31-40 of 171) with videos related to

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Genome Biology|March 11, 2025
Trans-ancestral rare variant association study with machine learning-based phenotyping for metabolic dysfunction-associated steatotic liver diseaseRobert Chen, Ben Omega Petrazzini, Áine Duffy, et al.
European Journal of Heart Failure|March 12, 2022
Genetic and phenotypic profiling of supranormal ejection fraction reveals decreased survival and underdiagnosed heart failureIain S Forrest, Ghislain Rocheleau, Shantanu Bafna, et al.
Infection|June 5, 2021
Non-invasive ventilation versus mechanical ventilation in hypoxemic patients with COVID-19Iain S Forrest, Suraj K Jaladanki, Ishan Paranjpe, et al.
Genome Medicine|June 12, 2026
Genetically supported drug target prioritization for rare diseasesRobert Chen, Áine Duffy, Matthew Mort, et al.
European Heart Journal|July 2, 2025
Gene therapy and genome editing for lipoprotein disordersChen Gurevitz, Archna Bajaj, Amit V Khera, et al.
BMC Medicine|August 22, 2023
An atlas of associations between 14 micronutrients and 22 cancer outcomes: Mendelian randomization analysesJong Yeob Kim, Minku Song, Min Seo Kim, et al.
Nature Genetics|June 23, 2025
Using large-scale population-based data to improve disease risk assessment of clinical variantsIain S Forrest, Kuan-Lin Huang, Julie M Eggington, et al.
Biotechniques|March 30, 2006
Deoxynucleotides can replace dideoxynucleotides in minisequencing by arrayed primer extensionScott J Tebbutt, Gareth D Mercer, Ron Do, et al.
Cell Reports Methods|December 10, 2024
Ensemble and consensus approaches to prediction of recessive inheritance for missense variants in human diseaseBen O Petrazzini, Daniel J Balick, Iain S Forrest, et al.
European Heart Journal. Digital Health|March 12, 2026
Three-year risk prediction of aortic stenosis using routine medical records: derivation and validation in 919 954 individuals from two cohortsBen O Petrazzini, Waqas A Malick, Stamatios Lerakis, et al.
Pageof 18

Showing results (31-40 of 171) with videos related to

Sort By:
Pageof 18
Genome Biology|March 11, 2025
Trans-ancestral rare variant association study with machine learning-based phenotyping for metabolic dysfunction-associated steatotic liver diseaseRobert Chen, Ben Omega Petrazzini, Áine Duffy, et al.
European Journal of Heart Failure|March 12, 2022
Genetic and phenotypic profiling of supranormal ejection fraction reveals decreased survival and underdiagnosed heart failureIain S Forrest, Ghislain Rocheleau, Shantanu Bafna, et al.
Infection|June 5, 2021
Non-invasive ventilation versus mechanical ventilation in hypoxemic patients with COVID-19Iain S Forrest, Suraj K Jaladanki, Ishan Paranjpe, et al.
Genome Medicine|June 12, 2026
Genetically supported drug target prioritization for rare diseasesRobert Chen, Áine Duffy, Matthew Mort, et al.
European Heart Journal|July 2, 2025
Gene therapy and genome editing for lipoprotein disordersChen Gurevitz, Archna Bajaj, Amit V Khera, et al.
BMC Medicine|August 22, 2023
An atlas of associations between 14 micronutrients and 22 cancer outcomes: Mendelian randomization analysesJong Yeob Kim, Minku Song, Min Seo Kim, et al.
Nature Genetics|June 23, 2025
Using large-scale population-based data to improve disease risk assessment of clinical variantsIain S Forrest, Kuan-Lin Huang, Julie M Eggington, et al.
Biotechniques|March 30, 2006
Deoxynucleotides can replace dideoxynucleotides in minisequencing by arrayed primer extensionScott J Tebbutt, Gareth D Mercer, Ron Do, et al.
Cell Reports Methods|December 10, 2024
Ensemble and consensus approaches to prediction of recessive inheritance for missense variants in human diseaseBen O Petrazzini, Daniel J Balick, Iain S Forrest, et al.
European Heart Journal. Digital Health|March 12, 2026
Three-year risk prediction of aortic stenosis using routine medical records: derivation and validation in 919 954 individuals from two cohortsBen O Petrazzini, Waqas A Malick, Stamatios Lerakis, et al.
Pageof 18