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Author Details

Benjamin S Wilfond
University of Washington School of Medicine.
1990
315
50
Vardit Ravitsky (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
36660851Incentives in Pediatric Research in Developing Countries: When Are They Too Much?Pediatrics2023
37549363The Moral Value of Telemedicine to the Physician-Patient Relationship.Hastings Cent Rep2023
37607497Refining a Multifaceted Model of Perceived Utility of Genomic Sequencing Results.Public Health Genomics2023
37644850Risk management actions following genetic testing in the Cancer Health Assessments Reaching Many (CHARM) Study: A prospective cohort study.Cancer Med2023
37812093Researcher Obligations to Participants in Novel COVID-19 Vaccine Research.Am J Bioeth2023
37126135Evaluating cancer genetic services in a safety net system: overcoming barriers for a lasting impact beyond the CHARM research project.J Community Genet2023
37421176Most people share genetic test results with relatives even if the findings are normal: Family communication in a diverse population.Genet Med2023
37348312Family-Reflections.com: Creating a parent-to-parent web-based tool regarding pediatric home ventilation.Patient Educ Couns2023
37450523Distinguishing Clinical and Research Risks in Pragmatic Clinical Trials: The Need for Further Stakeholder Engagement.Am J Bioeth2023
37384158Home values and experiences navigation track (HomeVENT): Supporting decisions about pediatric home ventilation.PEC Innov2023
37245030Hyperhydration to Improve Kidney Outcomes in Children with Shiga Toxin-Producing E. coli Infection: a multinational embedded cluster crossover randomized trial (the HIKO STEC trial).Trials2023
37470892Longitudinal adherence to breast cancer surveillance following cancer genetic testing in an integrated health care system.Breast Cancer Res Treat2023
36748334Measuring high-risk parents' opinions about direct-to-consumer genetic testing for adult-onset inherited cancer syndromes in their adolescent and young adult children.J Genet Couns2023
36516964The PrU: Development and validation of a measure to assess personal utility of genomic results.Genet Med2023
36691692Factors That Impact Hospital-Specific Enrollment Rates for a Neonatal Clinical Trial: An Analysis of the HEAL Study.Ethics Hum Res2023
36682451Validation of a Process for Shared Decision-Making in Pediatrics.Acad Pediatr2023
36662553"What Would Give Her the Best Life?": Understanding Why Families Decline Pediatric Home Ventilation.J Palliat Med2023
36938783Medical interpreter-mediated genetic counseling for Spanish preferring adults at risk for a hereditary cancer syndrome.J Genet Couns2023
34302314Barriers to family history knowledge and family communication among LGBTQ+ individuals in the context of hereditary cancer risk assessment.J Genet Couns2022
35676898Family-Assisted Severity of Illness Monitoring for Hospitalized Children in Low-Resource Settings-A Two-Arm Interventional Feasibility Study.Front Pediatr2022
35436948Identifying patients with Lynch syndrome using a universal tumor screening program in an integrated healthcare system.Hered Cancer Clin Pract2022
35763201Toward Meeting the Obligation of Respect for Persons in Pragmatic Clinical Trials.Hastings Cent Rep2022
35664885Ethical Considerations in Ever-Expanding Utilization of ECLS: A Research Agenda.Front Pediatr2022
35689290Literacy-adapted, electronic family history assessment for genetics referral in primary care: patient user insights from qualitative interviews.Hered Cancer Clin Pract2022
35420512Enrolling Adolescents with Rare Disease for Early Phase Clinical Trials While Under the Care of Child Protection Services: Balancing Protection and Access.Am J Bioeth2022
35522237ORCA, a values-based decision aid for selecting additional findings from genomic sequencing in adults: Efficacy results from a randomized trial.Genet Med2022
35933674Engaging Patient Advisory Committees to Inform a Genomic Cancer Risk Study: Lessons for Future Efforts.Perm J2022
36170065To Disclose or Not to Disclose: Secondary Findings of XXY Chromosomes.Am J Bioeth2022
35985537I know Things Now: The Challenges for Genetic Counseling of Adolescents with a Family History of Hereditary Breast Cancer.J Pediatr2022
36053287An accessible, relational, inclusive, and actionable (ARIA) model of genetic counseling compared with usual care: Results of a randomized controlled trial.Genet Med2022
33754278Adaptation and early implementation of the PREdiction model for gene mutations (PREMM<sub>5</sub>â¿¢) for lynch syndrome risk assessment in a diverse population.Fam Cancer2022
35123916Corrigendum 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 Trials2022
35094605Conflicts between parents and clinicians: Tracheotomy decisions and clinical bioethics consultation.Nurs Ethics2022
34998990Responding to signals of mental and behavioral health risk in pragmatic clinical trials: Ethical obligations in a healthcare ecosystem.Contemp Clin Trials2022
34908169Allocation of Opportunities to Participate in Clinical Trials during the Covid-19 Pandemic and Other Public Health Emergencies.Hastings Cent Rep2022
35176501Ethical and epistemic issues in the design and conduct of pragmatic stepped-wedge cluster randomized clinical trials.Contemp Clin Trials2022
34906471Motivations and concerns of patients considering participation in an implementation study of a hereditary cancer risk assessment program in diverse primary care settings.Genet Med2022
35171038Development and evaluation of an exome sequencing training course for medical interpreters.Per Med2022
35080259Home mechanical ventilation for children with severe neurological impairment: Parents' perspectives on clinician counselling.Dev Med Child Neurol2022
34738745Parent perspectives on facilitating decision-making around pediatric home ventilation.Pediatr Pulmonol2022
34551279From Monochromatic to Technicolor: Parent Perspectives on Challenges and Approaches to Seeing Children with Severe Neurological Impairment Holistically.J Palliat Med2022
34658003Perceived Utility of Genomic Sequencing: Qualitative Analysis and Synthesis of a Conceptual Model to Inform Patient-Centered Instrument Development.Patient2022
32981477Participant Reactions to a Literacy-Focused, Web-Based Informed Consent Approach for a Genomic Implementation Study.AJOB Empir Bioeth2021
33853890Presymptomatic Detection and Intervention for Autism Spectrum Disorder.Pediatrics2021
33719913Reframing Recruitment: Evaluating Framing in Authorization for Research Contact Programs.AJOB Empir Bioeth2021
33825623Supporting Investigators in Challenging Cases: Unease in the Face of an Ethically Appropriate Action.Am J Bioeth2021
33825622Conjoined Consent: Informed Consent When Donor and Recipient Are Both Research Participants.Am J Bioeth2021
33811178A 2020 Executive Order That Threatens Progress in Shared Decision-Making.Pediatrics2021
33530721An ethics framework for consolidating and prioritizing COVID-19 clinical trials.Clin Trials2021
33914815Patient perspectives on how to demonstrate respect: Implications for clinicians and healthcare organizations.PLoS One2021
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Collaborators

Center for Health Research, Kaiser Permanente Northwest
Co-authored papers 45
University of Washington School of Medicine
Co-authored papers 39
Kaiser Permanente Center for Health Research
Co-authored papers 36
Seattle Children's Hospital
Co-authored papers 31
Clinical Center, National Institutes of Health
Co-authored papers 29
University of Washington Medical Center
Co-authored papers 26
Center for Biomedical Ethics, Stanford University School of Medicine
Co-authored papers 20
Illumina Inc.
Co-authored papers 20
and Translational Research Center
Co-authored papers 19
Stanford Center for Biomedical Ethics, Stanford University
Co-authored papers 18
Seattle Children's Hospital, University of Washington School of Medicine
Co-authored papers 15
University of California-San Francisco.
Co-authored papers 14
University of North Carolina-Chapel Hill
Co-authored papers 13
Norton Children's Research Institute Affiliated with the University of Louisville
Co-authored papers 13
Harvard Medical School, Vanderbilt University, Yale University Yale Law School
Co-authored papers 12
Division of Ethics, Department of Medical Humanities and Ethics, Columbia University
Co-authored papers 12
Medical Ethics and Health Policy, University of Pennsylvania
Co-authored papers 12
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 12
The Heart Institute, Cincinnati Children's Hospital Medical Center
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Seattle Children's Research Institute
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Oregon Health & Science University (OHSU)
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Vanderbilt-Ingram Cancer Center, Vanderbilt University Medical Center
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University of North Carolina
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Biomedical Ethics, Mayo Clinic and Foundation
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Johns Hopkins School of Medicine
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Law School and Medical School, University of Minnesota
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Brigham and Women's Hospital, Broad Institute Ariadne Labs and Harvard Medical School
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NIH Clinical Center
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Johns Hopkins University, Berman Institute of Bioethics
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Baylor College of Medicine.
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