Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Marc Clausen

Showing results (41-50 of 52) with videos related to

Pageof 6
Sort By:
BMJ Open|April 29, 2022
Genetics Adviser: a protocol for a mixed-methods randomised controlled trial evaluating a digital platform for genetics service deliverySalma Shickh, Daena Hirjikaka, Marc Clausen, et al.
Genetics in Medicine Open|December 13, 2024
Genetics Adviser: The development and usability testing of a new patient digital health application to support clinical genomic testingMarc Clausen, Suvetha Krishnapillai, Daena Hirjikaka, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 12, 2019
Effectiveness of the Genomics ADvISER decision aid for the selection of secondary findings from genomic sequencing: a randomized clinical trialYvonne Bombard, Marc Clausen, Salma Shickh, et al.
BMJ Open|October 10, 2019
Health outcomes, utility and costs of returning incidental results from genomic sequencing in a Canadian cancer population: protocol for a mixed-methods randomised controlled trialSalma Shickh, Marc Clausen, Chloe Mighton, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 20, 2024
A Genomic Counseling Model for Population-Based Sequencing: A Pre-Post Intervention StudySelina Casalino, Chloe Mighton, Marc Clausen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 12, 2024
Opportunistic genomic screening has clinical utility: An interventional cohort studyChloe Mighton, Rita Kodida, Salma Shickh, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 17, 2025
Opportunistic screening for broad range of medically relevant secondary findings: Laboratory benefits and burdensChloe Mighton, Emma Reble, Jordan Sam, et al.
BMJ Open|September 4, 2024
Genetics Navigator: protocol for a mixed methods randomized controlled trial evaluating a digital platform to deliver genomic services in Canadian pediatric and adult populationsGuylaine D'Amours, Marc Clausen, Stephanie Luca, et al.
Nature Medicine|October 9, 2025
Feasibility, acceptability and clinical outcomes of the BabyScreen+ genomic newborn screening studySebastian Lunke, Lilian Downie, Jade Caruana, et al.
European Journal of Human Genetics : EJHG|January 29, 2026
Non-invasive screening in hereditary cancer: a randomized controlled trial to test cell-free DNA-based early detection in the CHARM consortiumKirsten M Farncombe, Julia A Sobotka, Melyssa Aronson, et al.
Pageof 6

Showing results (41-50 of 52) with videos related to

Sort By:
Pageof 6
BMJ Open|April 29, 2022
Genetics Adviser: a protocol for a mixed-methods randomised controlled trial evaluating a digital platform for genetics service deliverySalma Shickh, Daena Hirjikaka, Marc Clausen, et al.
Genetics in Medicine Open|December 13, 2024
Genetics Adviser: The development and usability testing of a new patient digital health application to support clinical genomic testingMarc Clausen, Suvetha Krishnapillai, Daena Hirjikaka, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 12, 2019
Effectiveness of the Genomics ADvISER decision aid for the selection of secondary findings from genomic sequencing: a randomized clinical trialYvonne Bombard, Marc Clausen, Salma Shickh, et al.
BMJ Open|October 10, 2019
Health outcomes, utility and costs of returning incidental results from genomic sequencing in a Canadian cancer population: protocol for a mixed-methods randomised controlled trialSalma Shickh, Marc Clausen, Chloe Mighton, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 20, 2024
A Genomic Counseling Model for Population-Based Sequencing: A Pre-Post Intervention StudySelina Casalino, Chloe Mighton, Marc Clausen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 12, 2024
Opportunistic genomic screening has clinical utility: An interventional cohort studyChloe Mighton, Rita Kodida, Salma Shickh, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 17, 2025
Opportunistic screening for broad range of medically relevant secondary findings: Laboratory benefits and burdensChloe Mighton, Emma Reble, Jordan Sam, et al.
BMJ Open|September 4, 2024
Genetics Navigator: protocol for a mixed methods randomized controlled trial evaluating a digital platform to deliver genomic services in Canadian pediatric and adult populationsGuylaine D'Amours, Marc Clausen, Stephanie Luca, et al.
Nature Medicine|October 9, 2025
Feasibility, acceptability and clinical outcomes of the BabyScreen+ genomic newborn screening studySebastian Lunke, Lilian Downie, Jade Caruana, et al.
European Journal of Human Genetics : EJHG|January 29, 2026
Non-invasive screening in hereditary cancer: a randomized controlled trial to test cell-free DNA-based early detection in the CHARM consortiumKirsten M Farncombe, Julia A Sobotka, Melyssa Aronson, et al.
Pageof 6