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BMJ Open
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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 infants
Julia 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 reliability
Robin 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 trial
Nigel 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 geneticist
Kaitlin 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 debate
Timothy Caulfield, Jim Evans, Amy McGuire, et al.
JAMA
|
December 13, 2022
Guidelines for Reporting Outcomes in Trial Reports: The CONSORT-Outcomes 2022 Extension
Nancy J Butcher, Andrea Monsour, Emma J Mew, et al.
JAMA
|
December 13, 2022
Guidelines for Reporting Outcomes in Trial Protocols: The SPIRIT-Outcomes 2022 Extension
Nancy 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 cohorts
Elise 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 study
Daniel 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 sequencing
Abigail Hansen, Stephanie Luca, Olivia Moran, et al.
Page
of 32
Search research articles
Search
Showing results (301-310 of 311) with videos related to
Sort By:
Page
of 32
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 infants
Julia 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 reliability
Robin 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 trial
Nigel 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 geneticist
Kaitlin 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 debate
Timothy Caulfield, Jim Evans, Amy McGuire, et al.
JAMA
|
December 13, 2022
Guidelines for Reporting Outcomes in Trial Reports: The CONSORT-Outcomes 2022 Extension
Nancy J Butcher, Andrea Monsour, Emma J Mew, et al.
JAMA
|
December 13, 2022
Guidelines for Reporting Outcomes in Trial Protocols: The SPIRIT-Outcomes 2022 Extension
Nancy 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 cohorts
Elise 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 study
Daniel 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 sequencing
Abigail Hansen, Stephanie Luca, Olivia Moran, et al.
Page
of 32