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

J Scott Roberts

Showing results (91-100 of 174) with videos related to

Pageof 18
Sort By:
Glomerular Diseases|October 30, 2023
Assessment of the Needs of Nephrology Divisions to Implement Return of Clinically Significant Research Genetic Results: A Survey of Nephrotic Syndrome Study Network (NEPTUNE) InvestigatorsJennifer E Fishbein, Loryn Wilson Dass, Chrysta Lienczewski, et al.
Journal of Alzheimer'S Disease Reports|April 3, 2026
Qualitative insights into participant and care partner perspectives on research-based Alzheimer's disease biomarker testing and disclosureAnnalise Rahman-Filipiak, Mary Lesniak, Alicia Burgei, et al.
Public Health Genomics|September 11, 2025
Employee Perspectives on Genetic Testing in the Workplace: Results from a National SurveyJ Scott Roberts, Wendy R Uhlmann, Drew Blasco, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 23, 2016
Prescription medication changes following direct-to-consumer personal genomic testing: findings from the Impact of Personal Genomics (PGen) StudyDeanna Alexis Carere, Tyler J VanderWeele, Jason L Vassy, et al.
Genome Medicine|August 14, 2015
Explaining, not just predicting, drives interest in personal genomicsSusanne F Meisel, Deanna Alexis Carere, Jane Wardle, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|November 18, 2008
Comparing test-specific distress of susceptibility versus deterministic genetic testing for Alzheimer's diseaseMichael R Cassidy, J Scott Roberts, Thomas D Bird, et al.
Annals of Internal Medicine|March 2, 2016
Consumer Perceptions of Interactions With Primary Care Providers After Direct-to-Consumer Personal Genomic TestingCathelijne H van der Wouden, Deanna Alexis Carere, Anke H Maitland-van der Zee, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 5, 2018
Patient understanding of, satisfaction with, and perceived utility of whole-genome sequencing: findings from the MedSeq ProjectJ Scott Roberts, Jill O Robinson, Pamela M Diamond, et al.
Patient Education and Counseling|December 26, 2016
Disclosing genetic risk of Alzheimer's disease to cognitively impaired patients and visit companions: Findings from the REVEAL StudyYue Guan, Debra L Roter, Lori H Erby, et al.
Journal of Health Communication|October 17, 2018
Communication Predictors of Patient and Companion Satisfaction with Alzheimer's Genetic Risk DisclosureYue Guan, Debra L Roter, Lori H Erby, et al.
Pageof 18

Showing results (91-100 of 174) with videos related to

Sort By:
Pageof 18
Glomerular Diseases|October 30, 2023
Assessment of the Needs of Nephrology Divisions to Implement Return of Clinically Significant Research Genetic Results: A Survey of Nephrotic Syndrome Study Network (NEPTUNE) InvestigatorsJennifer E Fishbein, Loryn Wilson Dass, Chrysta Lienczewski, et al.
Journal of Alzheimer'S Disease Reports|April 3, 2026
Qualitative insights into participant and care partner perspectives on research-based Alzheimer's disease biomarker testing and disclosureAnnalise Rahman-Filipiak, Mary Lesniak, Alicia Burgei, et al.
Public Health Genomics|September 11, 2025
Employee Perspectives on Genetic Testing in the Workplace: Results from a National SurveyJ Scott Roberts, Wendy R Uhlmann, Drew Blasco, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 23, 2016
Prescription medication changes following direct-to-consumer personal genomic testing: findings from the Impact of Personal Genomics (PGen) StudyDeanna Alexis Carere, Tyler J VanderWeele, Jason L Vassy, et al.
Genome Medicine|August 14, 2015
Explaining, not just predicting, drives interest in personal genomicsSusanne F Meisel, Deanna Alexis Carere, Jane Wardle, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|November 18, 2008
Comparing test-specific distress of susceptibility versus deterministic genetic testing for Alzheimer's diseaseMichael R Cassidy, J Scott Roberts, Thomas D Bird, et al.
Annals of Internal Medicine|March 2, 2016
Consumer Perceptions of Interactions With Primary Care Providers After Direct-to-Consumer Personal Genomic TestingCathelijne H van der Wouden, Deanna Alexis Carere, Anke H Maitland-van der Zee, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 5, 2018
Patient understanding of, satisfaction with, and perceived utility of whole-genome sequencing: findings from the MedSeq ProjectJ Scott Roberts, Jill O Robinson, Pamela M Diamond, et al.
Patient Education and Counseling|December 26, 2016
Disclosing genetic risk of Alzheimer's disease to cognitively impaired patients and visit companions: Findings from the REVEAL StudyYue Guan, Debra L Roter, Lori H Erby, et al.
Journal of Health Communication|October 17, 2018
Communication Predictors of Patient and Companion Satisfaction with Alzheimer's Genetic Risk DisclosureYue Guan, Debra L Roter, Lori H Erby, et al.
Pageof 18