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Author Details
Full Name
Colin Halverson
Affiliation
Indiana University Center for Bioethics.
ORCID
Career Start Year
2012
Papers
23
H Index
10
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36595008
What is "Personal" About Personal Experience? A Call to Reflexivity for All.
Am J Bioeth
2023
34779299
Biobank Participants' Attitudes Toward Data Sharing and Privacy: The Role of Trust in Reducing Perceived Risks.
J Empir Res Hum Res Ethics
2022
34936236
Biobank Participants' Attitudes toward Requiring Understanding for Biobank Consent.
Ethics Hum Res
2022
34307413
Adolescent Assent and Reconsent for Biobanking: Recent Developments and Emerging Ethical Issues.
Front Med (Lausanne)
2021
36046768
Returning negative results from large-scale genomic screening: Experiences from the eMERGE III network.
Am J Med Genet A
2021
33622053
Ending the pharmacogenomic gag rule: the imperative to report all results.
Pharmacogenomics
2021
34558037
Assessing parental understanding of variant reclassification in pediatric neurology and developmental pediatrics clinics.
J Community Genet
2021
31432391
Patients' views on variants of uncertain significance across indications.
J Community Genet
2020
32555418
Ethical conflicts in translational genetic research: lessons learned from the eMERGE-III experience.
Genet Med
2020
32121581
What Results Should Be Returned from Opportunistic Screening in Translational Research?
J Pers Med
2020
32413979
Understanding the Return of Genomic Sequencing Results Process: Content Review of Participant Summary Letters in the eMERGE Research Network.
J Pers Med
2020
32329193
Patient perspectives on variant reclassification after cancer susceptibility testing.
Mol Genet Genomic Med
2020
31553110
Patients' willingness to reconsider cancer genetic testing after initially declining: Mention it again.
J Genet Couns
2020
29110969
How do patients describe their disabilities? A coding system for categorizing patients' descriptions.
Disabil Health J
2018
29895237
Unspoken ambivalence in kinship obligation in living donation.
Prog Transplant
2018
30379944
A systematic literature review of individuals' perspectives on privacy and genetic information in the United States.
PLoS One
2018
26860291
Was it worth it? Patients' perspectives on the perceived value of genomic-based individualized medicine.
J Community Genet
2016
27222023
Living Kidney Donors Who Develop Kidney Failure: Excerpts of Their Thoughts.
Am J Nephrol
2016
26937348
Patients' views on incidental findings from clinical exome sequencing.
Appl Transl Genom
2015
22261760
Incidental findings of therapeutic misconception in biobank-based research.
Genet Med
2012
22573882
Attitudes of African-American parents about biobank participation and return of results for themselves and their children.
J Med Ethics
2012
22438108
Biobank participation and returning research results: perspectives from a deliberative engagement in South Side Chicago.
Am J Med Genet A
2012
22454259
Engaging African-Americans about biobanks and the return of research results.
J Community Genet
2012
1 - 23 of 23
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