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Robin Z Hayeems

Showing results (51-60 of 106) with videos related to

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European Journal of Human Genetics : EJHG|October 4, 2022
Applying the Clinician-reported Genetic testing Utility InDEx (C-GUIDE) to genome sequencing: further evidence of validityRobin Z Hayeems, Stephanie Luca, Anna C E Hurst, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 27, 2026
Development and content validation of the Clinician-reported Genetic testing Utility InDEx for genomic newborn screening (C-GUIDE NBS)Salma Shickh, Stephanie Luca, Katharine Fooks, et al.
NPJ Genomic Medicine|December 15, 2020
Clinical utility of genomic sequencing: a measurement toolkitRobin Z Hayeems, David Dimmock, David Bick, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 13, 2026
A comprehensive approach to evaluating the clinical utility of genome sequencing in rare disease: A large prospective Canadian cohortSalma Shickh, Katharine Fooks, Viji Venkataramanan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
The complexity of diagnosing rare disease: An organizing framework for outcomes research and health economics based on real-world evidenceRobin Z Hayeems, Christine Michaels-Igbokwe, Viji Venkataramanan, et al.
Pediatrics|January 18, 2012
Citizens' values regarding research with stored samples from newborn screening in CanadaYvonne Bombard, Fiona A Miller, Robin Z Hayeems, et al.
Pediatrics|July 15, 2015
Public Perceptions of the Benefits and Risks of Newborn ScreeningFiona A Miller, Robin Z Hayeems, Yvonne Bombard, et al.
European Journal of Human Genetics : EJHG|January 10, 2026
Experiencing acute genomic care: perspectives from parents in the neonatal and paediatric intensive care units towards rapid genomic sequencingMichael P Mackley, Megan A Dickson, Anna Szuto, et al.
Pediatrics|June 1, 2016
Using Newborn Screening Bloodspots for Research: Public Preferences for Policy OptionsRobin Z Hayeems, Fiona A Miller, Carolyn J Barg, et al.
Applied Health Economics and Health Policy|December 31, 2024
Exome Sequencing in the Diagnostic Pathway for Suspected Rare Genetic Diseases: Does the Order of Testing Affect its Cost-Effectiveness?Koen Degeling, Toni Tagimacruz, Karen V MacDonald, et al.
Pageof 11

Showing results (51-60 of 106) with videos related to

Sort By:
Pageof 11
European Journal of Human Genetics : EJHG|October 4, 2022
Applying the Clinician-reported Genetic testing Utility InDEx (C-GUIDE) to genome sequencing: further evidence of validityRobin Z Hayeems, Stephanie Luca, Anna C E Hurst, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 27, 2026
Development and content validation of the Clinician-reported Genetic testing Utility InDEx for genomic newborn screening (C-GUIDE NBS)Salma Shickh, Stephanie Luca, Katharine Fooks, et al.
NPJ Genomic Medicine|December 15, 2020
Clinical utility of genomic sequencing: a measurement toolkitRobin Z Hayeems, David Dimmock, David Bick, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 13, 2026
A comprehensive approach to evaluating the clinical utility of genome sequencing in rare disease: A large prospective Canadian cohortSalma Shickh, Katharine Fooks, Viji Venkataramanan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
The complexity of diagnosing rare disease: An organizing framework for outcomes research and health economics based on real-world evidenceRobin Z Hayeems, Christine Michaels-Igbokwe, Viji Venkataramanan, et al.
Pediatrics|January 18, 2012
Citizens' values regarding research with stored samples from newborn screening in CanadaYvonne Bombard, Fiona A Miller, Robin Z Hayeems, et al.
Pediatrics|July 15, 2015
Public Perceptions of the Benefits and Risks of Newborn ScreeningFiona A Miller, Robin Z Hayeems, Yvonne Bombard, et al.
European Journal of Human Genetics : EJHG|January 10, 2026
Experiencing acute genomic care: perspectives from parents in the neonatal and paediatric intensive care units towards rapid genomic sequencingMichael P Mackley, Megan A Dickson, Anna Szuto, et al.
Pediatrics|June 1, 2016
Using Newborn Screening Bloodspots for Research: Public Preferences for Policy OptionsRobin Z Hayeems, Fiona A Miller, Carolyn J Barg, et al.
Applied Health Economics and Health Policy|December 31, 2024
Exome Sequencing in the Diagnostic Pathway for Suspected Rare Genetic Diseases: Does the Order of Testing Affect its Cost-Effectiveness?Koen Degeling, Toni Tagimacruz, Karen V MacDonald, et al.
Pageof 11