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The Yale Journal of Biology and Medicine
|
October 3, 2022
Targeting Representation: Interpreting Calls for Diversity in Precision Medicine Research
Sandra Soo-Jin Lee, Stephanie M Fullerton, Caitlin E McMahon, et al.
Pilot and Feasibility Studies
|
August 9, 2022
Feasibility, acceptability, and limited efficacy of health system-led familial risk notification: protocol for a mixed-methods evaluation
Paula R Blasi, Aaron Scrol, Melissa L Anderson, et al.
Patient Education and Counseling
|
January 18, 2021
What improves the likelihood of people receiving genetic test results communicating to their families about genetic risk?
Deborah J Bowen, Sukh Makhnoon, Brian H Shirts, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 1, 2013
Return of incidental findings in genomic medicine: measuring what patients value--development of an instrument to measure preferences for information from next-generation testing (IMPRINT)
Caroline Savage Bennette, Susan Brown Trinidad, Stephanie M Fullerton, et al.
Journal of Personalized Medicine
|
July 2, 2021
Patient and Family Preferences on Health System-Led Direct Contact for Cascade Screening
Nora B Henrikson, Paula Blasi, Marlaine Figueroa Gray, et al.
Health Affairs (Project Hope)
|
August 10, 2016
Using Genetic Technologies To Reduce, Rather Than Widen, Health Disparities
Caren E Smith, Stephanie M Fullerton, Keith A Dookeran, et al.
Genome Medicine
|
April 18, 2023
Diagnostic yield of genetic screening in a diverse, community-ascertained cohort
Nandana D Rao, Jailanie Kaganovsky, Emily A Malouf, et al.
Cancer Causes & Control : CCC
|
February 16, 2021
The FamilyTalk randomized controlled trial: patient-reported outcomes in clinical genetic sequencing for colorectal cancer
Sukh Makhnoon, Deborah J Bowen, Brian H Shirts, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
March 12, 2014
Refining the structure and content of clinical genomic reports
Michael O Dorschner, Laura M Amendola, Brian H Shirts, et al.
American Journal of Nephrology
|
September 4, 2019
Apolipoprotein L1 Testing in African Americans: Involving the Community in Policy Discussions
Bessie A Young, Erika Blacksher, Kerri L Cavanaugh, et al.
Page
of 12
Search research articles
Search
Showing results (61-70 of 118) with videos related to
Sort By:
Page
of 12
The Yale Journal of Biology and Medicine
|
October 3, 2022
Targeting Representation: Interpreting Calls for Diversity in Precision Medicine Research
Sandra Soo-Jin Lee, Stephanie M Fullerton, Caitlin E McMahon, et al.
Pilot and Feasibility Studies
|
August 9, 2022
Feasibility, acceptability, and limited efficacy of health system-led familial risk notification: protocol for a mixed-methods evaluation
Paula R Blasi, Aaron Scrol, Melissa L Anderson, et al.
Patient Education and Counseling
|
January 18, 2021
What improves the likelihood of people receiving genetic test results communicating to their families about genetic risk?
Deborah J Bowen, Sukh Makhnoon, Brian H Shirts, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 1, 2013
Return of incidental findings in genomic medicine: measuring what patients value--development of an instrument to measure preferences for information from next-generation testing (IMPRINT)
Caroline Savage Bennette, Susan Brown Trinidad, Stephanie M Fullerton, et al.
Journal of Personalized Medicine
|
July 2, 2021
Patient and Family Preferences on Health System-Led Direct Contact for Cascade Screening
Nora B Henrikson, Paula Blasi, Marlaine Figueroa Gray, et al.
Health Affairs (Project Hope)
|
August 10, 2016
Using Genetic Technologies To Reduce, Rather Than Widen, Health Disparities
Caren E Smith, Stephanie M Fullerton, Keith A Dookeran, et al.
Genome Medicine
|
April 18, 2023
Diagnostic yield of genetic screening in a diverse, community-ascertained cohort
Nandana D Rao, Jailanie Kaganovsky, Emily A Malouf, et al.
Cancer Causes & Control : CCC
|
February 16, 2021
The FamilyTalk randomized controlled trial: patient-reported outcomes in clinical genetic sequencing for colorectal cancer
Sukh Makhnoon, Deborah J Bowen, Brian H Shirts, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
March 12, 2014
Refining the structure and content of clinical genomic reports
Michael O Dorschner, Laura M Amendola, Brian H Shirts, et al.
American Journal of Nephrology
|
September 4, 2019
Apolipoprotein L1 Testing in African Americans: Involving the Community in Policy Discussions
Bessie A Young, Erika Blacksher, Kerri L Cavanaugh, et al.
Page
of 12