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Robin Z Hayeems

Showing results (81-90 of 106) with videos related to

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Pediatrics|August 4, 2016
Parent Experience With False-Positive Newborn Screening Results for Cystic FibrosisRobin Z Hayeems, Fiona A Miller, Carolyn J Barg, et al.
The Journal of Pediatrics|March 11, 2017
Psychosocial Response to Uncertain Newborn Screening Results for Cystic FibrosisRobin Z Hayeems, Fiona A Miller, Carolyn J Barg, et al.
Clinical Therapeutics|July 15, 2023
Protocol for a Prospective, Observational Cost-effectiveness Analysis of Returning Secondary Findings of Genome Sequencing for Unexplained Suspected Genetic ConditionsWendy J Ungar, Robin Z Hayeems, Christian R Marshall, et al.
American Journal of Human Genetics|March 29, 2023
Trio RNA sequencing in a cohort of medically complex childrenAshish R Deshwar, Kyoko E Yuki, Huayun Hou, et al.
CMAJ Open|May 24, 2022
Comparing genome sequencing technologies to improve rare disease diagnostics: a protocol for the evaluation of a pilot project, Genome-wide Sequencing OntarioRobin Z Hayeems, Christian R Marshall, Meredith K Gillespie, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 25, 2025
A Microcosting and Cost Consequence Analysis from a Randomized Controlled Trial Comparing Genome Sequencing to Exome Sequencing for Genetic DiagnosisWendy J Ungar, Vercancy Wu, Christian R Marshall, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 14, 2025
Comparing the performance of exome and genome sequencing for rare disease diagnostics: A randomized implementation effectiveness trialRobin Z Hayeems, Wendy J Ungar, Christian R Marshall, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 9, 2018
De novo missense variants in RAC3 cause a novel neurodevelopmental syndromeGregory Costain, Bert Callewaert, Heinz Gabriel, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
The Clinician-reported Genetic testing Utility InDEx (C-GUIDE): Preliminary evidence of validity and reliabilityRobin Z Hayeems, Stephanie Luca, Wendy J Ungar, et al.
BMJ Open|August 10, 2025
TRIAGE-GS: protocol for a randomised controlled trial of a genomics-first approach to rare disease diagnosis for patients awaiting assessment by a clinical geneticistKaitlin J Stanley, Caitlin Chisholm, Meredith K Gillespie, et al.
Pageof 11

Showing results (81-90 of 106) with videos related to

Sort By:
Pageof 11
Pediatrics|August 4, 2016
Parent Experience With False-Positive Newborn Screening Results for Cystic FibrosisRobin Z Hayeems, Fiona A Miller, Carolyn J Barg, et al.
The Journal of Pediatrics|March 11, 2017
Psychosocial Response to Uncertain Newborn Screening Results for Cystic FibrosisRobin Z Hayeems, Fiona A Miller, Carolyn J Barg, et al.
Clinical Therapeutics|July 15, 2023
Protocol for a Prospective, Observational Cost-effectiveness Analysis of Returning Secondary Findings of Genome Sequencing for Unexplained Suspected Genetic ConditionsWendy J Ungar, Robin Z Hayeems, Christian R Marshall, et al.
American Journal of Human Genetics|March 29, 2023
Trio RNA sequencing in a cohort of medically complex childrenAshish R Deshwar, Kyoko E Yuki, Huayun Hou, et al.
CMAJ Open|May 24, 2022
Comparing genome sequencing technologies to improve rare disease diagnostics: a protocol for the evaluation of a pilot project, Genome-wide Sequencing OntarioRobin Z Hayeems, Christian R Marshall, Meredith K Gillespie, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 25, 2025
A Microcosting and Cost Consequence Analysis from a Randomized Controlled Trial Comparing Genome Sequencing to Exome Sequencing for Genetic DiagnosisWendy J Ungar, Vercancy Wu, Christian R Marshall, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 14, 2025
Comparing the performance of exome and genome sequencing for rare disease diagnostics: A randomized implementation effectiveness trialRobin Z Hayeems, Wendy J Ungar, Christian R Marshall, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 9, 2018
De novo missense variants in RAC3 cause a novel neurodevelopmental syndromeGregory Costain, Bert Callewaert, Heinz Gabriel, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
The Clinician-reported Genetic testing Utility InDEx (C-GUIDE): Preliminary evidence of validity and reliabilityRobin Z Hayeems, Stephanie Luca, Wendy J Ungar, et al.
BMJ Open|August 10, 2025
TRIAGE-GS: protocol for a randomised controlled trial of a genomics-first approach to rare disease diagnosis for patients awaiting assessment by a clinical geneticistKaitlin J Stanley, Caitlin Chisholm, Meredith K Gillespie, et al.
Pageof 11