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Author Details
Full Name
Stephanie A Kraft
Affiliation
University of Washington School of Medicine
ORCID
Career Start Year
2015
Papers
60
H Index
16
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37442368
Equity Concerns Across Pediatric Research Recruitment: An Analysis of Research Staff Interviews.
Acad Pediatr
2024
36341765
Conducting clinical genomics research during the COVID-19 pandemic: Lessons learned from the CSER consortium experience.
Am J Med Genet A
2023
37667436
Conducting inclusive research in genetics for transgender, gender-diverse, and sex-diverse individuals: Case analyses and recommendations from a clinical genomics study.
J Genet Couns
2023
37735658
Patient priorities for fulfilling the principle of respect in research: findings from a modified Delphi study.
BMC Med Ethics
2023
37607497
Refining a Multifaceted Model of Perceived Utility of Genomic Sequencing Results.
Public Health Genomics
2023
37450523
Distinguishing Clinical and Research Risks in Pragmatic Clinical Trials: The Need for Further Stakeholder Engagement.
Am J Bioeth
2023
36926958
Centering Patients' Voices in Artificial Intelligenceâ¿¿Based Telemedicine.
Am J Public Health
2023
34658003
Perceived Utility of Genomic Sequencing: Qualitative Analysis and Synthesis of a Conceptual Model to Inform Patient-Centered Instrument Development.
Patient
2022
35763201
Toward Meeting the Obligation of Respect for Persons in Pragmatic Clinical Trials.
Hastings Cent Rep
2022
35689290
Literacy-adapted, electronic family history assessment for genetics referral in primary care: patient user insights from qualitative interviews.
Hered Cancer Clin Pract
2022
36590359
Relationship building in pediatric research recruitment: Insights from qualitative interviews with research staff.
J Clin Transl Sci
2022
35933674
Engaging Patient Advisory Committees to Inform a Genomic Cancer Risk Study: Lessons for Future Efforts.
Perm J
2022
35123916
Corrigendum to "Cancer Health Assessments Reaching Many (CHARM): A clinical trial assessing a multimodal cancer genetics services delivery program and its impact on diverse populations" [Contemporary Clinical Trials 106 (2021) 106432].
Contemp Clin Trials
2022
34906471
Motivations and concerns of patients considering participation in an implementation study of a hereditary cancer risk assessment program in diverse primary care settings.
Genet Med
2022
32981477
Participant Reactions to a Literacy-Focused, Web-Based Informed Consent Approach for a Genomic Implementation Study.
AJOB Empir Bioeth
2021
33719913
Reframing Recruitment: Evaluating Framing in Authorization for Research Contact Programs.
AJOB Empir Bioeth
2021
33825652
Fostering Relationships in Pediatric Oncology Research: A Relational Ethics Approach to Clinically Integrated Research.
Am J Bioeth
2021
33825630
Respecting Donor-Recipient Relationships in Research Decision-Making Commentary on: <i>When Living Donor and Kidney Transplant Recipient Are Both Research Subjects</i>.
Am J Bioeth
2021
33914815
Patient perspectives on how to demonstrate respect: Implications for clinicians and healthcare organizations.
PLoS One
2021
34888063
Examining access to care in clinical genomic research and medicine: Experiences from the CSER Consortium.
J Clin Transl Sci
2021
34778694
Systemic Barriers to Risk-Reducing Interventions for Hereditary Cancer Syndromes: Implications for Health Care Inequities.
JCO Precis Oncol
2021
33984519
Cancer Health Assessments Reaching Many (CHARM): A clinical trial assessing a multimodal cancer genetics services delivery program and its impact on diverse populations.
Contemp Clin Trials
2021
33984463
Pediatric Death by Neurologic Criteria: The Ever-Changing Landscape and the Expanding Role of Palliative Care Professionals.
J Pain Symptom Manage
2021
34192059
Informed consent: Old and new challenges in the context of the COVID-19 pandemic.
J Clin Transl Sci
2021
33945415
Promoting Disclosure and Understanding in Informed Consent: Optimizing the Impact of the Common Rule "Key Information" Requirement.
Am J Bioeth
2021
33150424
Public attitudes toward an authorization for contact program for clinical research.
J Am Med Inform Assoc
2021
32220905
Can a Parent Refuse the Brain Death Examination?
Pediatrics
2020
32089547
Integrating stakeholder feedback in translational genomics research: an ethnographic analysis of a study protocol's evolution.
Genet Med
2020
33103984
Respect and Trustworthiness in the Patient-Provider-Machine Relationship: Applying a Relational Lens to Machine Learning Healthcare Applications.
Am J Bioeth
2020
32735337
Assessing Parent Decisions About Child Participation in a Behavioral Health Intervention Study and Utility of Informed Consent Forms.
JAMA Netw Open
2020
33023975
Demonstrating 'respect for persons' in clinical research: findings from qualitative interviews with diverse genomics research participants.
J Med Ethics
2020
32364474
Bridging the Researcher-Participant Gap: A Research Agenda to Build Effective Research Relationships.
Am J Bioeth
2020
30585505
Exploring Ethical Concerns About Human Challenge Studies: A Qualitative Study of Controlled Human Malaria Infection Study Participants' Motivations and Attitudes.
J Empir Res Hum Res Ethics
2019
29887604
"I don't want to be Henrietta Lacks": diverse patient perspectives on donating biospecimens for precision medicine research.
Genet Med
2019
30245516
The evolving landscape of expanded carrier screening: challenges and opportunities.
Genet Med
2019
31544678
An Ethical Case for Dual-Role Consent: Increasing Research Diversity as a Matter of Respect and Justice.
Am J Bioeth
2019
31090520
Understanding as an Ethical Aspiration in an Era of Digital Technology-Based Communication: An Analysis of Informed Consent Functions.
Am J Bioeth
2019
30585833
What Does the Word "Treatable" Mean? Implications for Communication and Decision-Making in Critical Illness.
Crit Care Med
2019
29293279
Patient actions and reactions after receiving negative results from expanded carrier screening.
Clin Genet
2018
29697352
Trustworthiness in Untrustworthy Times: Response to Open Peer Commentaries on Beyond Consent.
Am J Bioeth
2018
29512940
Engaging populations underrepresented in research through novel approaches to consent.
Am J Med Genet C Semin Med Genet
2018
29733724
Lessons Learned From A Study Of Genomics-Based Carrier Screening For Reproductive Decision Making.
Health Aff (Millwood)
2018
29621457
Beyond Consent: Building Trusting Relationships With Diverse Populations in Precision Medicine Research.
Am J Bioeth
2018
29250907
Patient perspectives on the use of categories of conditions for decision making about genomic carrier screening results.
Am J Med Genet A
2018
29267267
Metaphors matter: from biobank to a library of medical information.
Genet Med
2018
27625314
A randomized study of multimedia informational aids for research on medical practices: Implications for informed consent.
Clin Trials
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
29148942
Attending to the Interrelatedness of the Functions of Consent.
Am J Bioeth
2017
28661747
Comprehension and Choice Under the Revised Common Rule: Improving Informed Consent by Offering Reasons Why Some Enroll in Research and Others Do Not.
Am J Bioeth
2017
1 - 50 of 60
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Kelly J Shipman
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Alexander M Capron
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Barbara B Biesecker
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