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June C Carroll

Showing results (91-100 of 108) 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.
Annals of Family Medicine|September 22, 2025
An Innovative Strategy for Collecting Family Health History: An Effectiveness-Implementation Trial in Primary Care ClinicsJune C Carroll, Michelle Greiver, Sahana Kukan, et al.
BJGP Open|November 14, 2025
Family physicians' experiences with an electronic medical record-integrated family history collection strategy: a qualitative studySakina Walji, Tutsirai Makuwaza, Erin Bearss, et al.
BMJ Open|April 28, 2018
Evaluation of a decision aid for incidental genomic results, the Genomics ADvISER: protocol for a mixed methods randomised controlled trialSalma Shickh, Marc Clausen, Chloe Mighton, et al.
European Journal of Human Genetics : EJHG|March 3, 2026
"Where do I go from here?" Navigating a lifelong road without a map: the care experiences of hereditary cancer patientsCarly Butkowsky, June C Carroll, Melyssa Aronson, et al.
European Journal of Human Genetics : EJHG|March 9, 2019
Development of patient "profiles" to tailor counseling for incidental genomic sequencing resultsChloe Mighton, Lindsay Carlsson, Marc Clausen, et al.
Human Genetics|June 23, 2022
A comprehensive genomic reporting structure for communicating all clinically significant primary and secondary findingsJordan Sam, Emma Reble, Rita Kodida, et al.
Journal of Medical Genetics|May 22, 2023
A model for the return and referral of all clinically significant secondary findings of genomic sequencingRita Kodida, Emma Reble, Marc Clausen, 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.
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.
Pageof 11

Showing results (91-100 of 108) 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.
Annals of Family Medicine|September 22, 2025
An Innovative Strategy for Collecting Family Health History: An Effectiveness-Implementation Trial in Primary Care ClinicsJune C Carroll, Michelle Greiver, Sahana Kukan, et al.
BJGP Open|November 14, 2025
Family physicians' experiences with an electronic medical record-integrated family history collection strategy: a qualitative studySakina Walji, Tutsirai Makuwaza, Erin Bearss, et al.
BMJ Open|April 28, 2018
Evaluation of a decision aid for incidental genomic results, the Genomics ADvISER: protocol for a mixed methods randomised controlled trialSalma Shickh, Marc Clausen, Chloe Mighton, et al.
European Journal of Human Genetics : EJHG|March 3, 2026
"Where do I go from here?" Navigating a lifelong road without a map: the care experiences of hereditary cancer patientsCarly Butkowsky, June C Carroll, Melyssa Aronson, et al.
European Journal of Human Genetics : EJHG|March 9, 2019
Development of patient "profiles" to tailor counseling for incidental genomic sequencing resultsChloe Mighton, Lindsay Carlsson, Marc Clausen, et al.
Human Genetics|June 23, 2022
A comprehensive genomic reporting structure for communicating all clinically significant primary and secondary findingsJordan Sam, Emma Reble, Rita Kodida, et al.
Journal of Medical Genetics|May 22, 2023
A model for the return and referral of all clinically significant secondary findings of genomic sequencingRita Kodida, Emma Reble, Marc Clausen, 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.
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.
Pageof 11