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Author Details
Full Name
Diane M Korngiebel
Affiliation
Google
ORCID
Career Start Year
2012
Papers
24
H Index
11
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36228119
AMIA's code of professional and ethical conduct 2022.
J Am Med Inform Assoc
2022
37725563
Patient Recommendations for the Content and Design of Electronic Returns of Genetic Test Results: Interview Study Among Patients Who Accessed Their Genetic Test Results via the Internet.
JMIRx Med
2022
34083689
Considering the possibilities and pitfalls of Generative Pre-trained Transformer 3 (GPT-3) in healthcare delivery.
NPJ Digit Med
2021
30676118
Practice Implications of Expanded Genetic Testing in Oncology.
Cancer Invest
2019
31160753
Improving recommendations for genomic medicine: building an evolutionary process from clinical practice advisory documents to guidelines.
Genet Med
2019
29159545
Clinician-Stakeholders' Perspectives on Using Patient Portals to Return Lynch Syndrome Screening Results.
J Genet Couns
2018
27939182
Implementing Precision Medicine: The Ethical Challenges.
Trends Pharmacol Sci
2017
30146866
Research on Medical Practices (ROMP): Attitudes of IRB Personnel about Randomization and Informed Consent.
IRB
2017
30387977
Research on Medical Practices: Why Patients Consider Participating and the Investigational Misconception.
IRB
2017
28471433
Identifying "ownership" through role descriptions to support implementing universal colorectal cancer tumor screening for Lynch syndrome.
Genet Med
2017
27011058
Patient safety in genomic medicine: an exploratory study.
Genet Med
2016
27653592
Participants' Role Expectations in Genetics Research and Re-consent: Revising the Theory and Methods of Mental Models Research Relating to Roles.
J Health Commun
2016
27257125
A comparison of institutional review board professionals' and patients' views on consent for research on medical practices.
Clin Trials
2016
26889673
Generating a taxonomy for genetic conditions relevant to reproductive planning.
Am J Med Genet A
2016
26832115
The Role of Patient Perspectives in Clinical Research Ethics and Policy: Response to Open Peer Commentaries on "Patient Perspectives on the Learning Health System".
Am J Bioeth
2016
26801345
Participant views on consent in cancer genetics research: preparing for the precision medicine era.
J Community Genet
2016
25719903
Closing the gap between knowledge and clinical application: challenges for genomic translation.
PLoS Genet
2015
26305741
Patient Perspectives on the Learning Health System: The Importance of Trust and Shared Decision Making.
Am J Bioeth
2015
26331187
What Should Be the Character of the Researcher- Participant Relationship? Views of Participants in a Long-standing Cancer Genetic Registry.
IRB
2015
26180955
Addressing the Challenges of Research With Small Populations.
Am J Public Health
2015
25868119
Attitudes Toward Risk and Informed Consent for Research on Medical Practices: A Cross-sectional Survey.
Ann Intern Med
2015
25717404
Developing Governance for Federated Community-based EHR Data Sharing.
AMIA Jt Summits Transl Sci Proc
2014
24004706
Barriers and facilitators to evidence-based blood pressure control in community practice.
J Am Board Fam Med
2013
22779052
LC Data QUEST: A Technical Architecture for Community Federated Clinical Data Sharing.
AMIA Jt Summits Transl Sci Proc
2012
1 - 24 of 24
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