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BMJ Open|July 8, 2021
Coached, Coordinated, Enhanced Neonatal Transition (CCENT): protocol for a multicentre pragmatic randomised controlled trial of transition-to-home support for parents of high-risk infantsJulia Orkin, Nathalie Major, Kayla Esser, 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 Paediatrics Open|April 12, 2018
Appendectomy versus non-operative treatment for acute uncomplicated appendicitis in children: study protocol for a multicentre, open-label, non-inferiority, randomised controlled trialNigel J Hall, Simon Eaton, Olivier Abbo, 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.Plos Biology|November 14, 2013
Reflections on the cost of "low-cost" whole genome sequencing: framing the health policy debateTimothy Caulfield, Jim Evans, Amy McGuire, et al.JAMA|December 13, 2022
Guidelines for Reporting Outcomes in Trial Reports: The CONSORT-Outcomes 2022 ExtensionNancy J Butcher, Andrea Monsour, Emma J Mew, et al.JAMA|December 13, 2022
Guidelines for Reporting Outcomes in Trial Protocols: The SPIRIT-Outcomes 2022 ExtensionNancy J Butcher, Andrea Monsour, Emma J Mew, et al.Genetics in Medicine Open|October 15, 2025
How does personal utility depend on clinical setting? Evidence from 3 cohortsElise Poole, Stephanie Luca, Daniel Assamad, et al.BMJ Open|March 27, 2026
Understanding the impact of genomic secondary findings on clinical care and patient experience: a protocol for a prospective observational studyDaniel Assamad, Abigail Hansen, Katharine Fooks, et al.Journal of Genetic Counseling|May 5, 2026
Understanding the decision of parents to opt-out of medically actionable secondary findings offered through genome sequencingAbigail Hansen, Stephanie Luca, Olivia Moran, et al.Pageof 32