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Author Details
Full Name
Benjamin S Wilfond
Affiliation
University of Washington School of Medicine.
ORCID
Career Start Year
1990
Papers
315
H Index
50
Expertise
CM4AI Collaborator
Vardit Ravitsky (CM4AI)
PMID
Paper Title
Journal Title
Published Year
36660851
Incentives in Pediatric Research in Developing Countries: When Are They Too Much?
Pediatrics
2023
37549363
The Moral Value of Telemedicine to the Physician-Patient Relationship.
Hastings Cent Rep
2023
37607497
Refining a Multifaceted Model of Perceived Utility of Genomic Sequencing Results.
Public Health Genomics
2023
37644850
Risk management actions following genetic testing in the Cancer Health Assessments Reaching Many (CHARM) Study: A prospective cohort study.
Cancer Med
2023
37812093
Researcher Obligations to Participants in Novel COVID-19 Vaccine Research.
Am J Bioeth
2023
37126135
Evaluating cancer genetic services in a safety net system: overcoming barriers for a lasting impact beyond the CHARM research project.
J Community Genet
2023
37421176
Most people share genetic test results with relatives even if the findings are normal: Family communication in a diverse population.
Genet Med
2023
37348312
Family-Reflections.com: Creating a parent-to-parent web-based tool regarding pediatric home ventilation.
Patient Educ Couns
2023
37450523
Distinguishing Clinical and Research Risks in Pragmatic Clinical Trials: The Need for Further Stakeholder Engagement.
Am J Bioeth
2023
37384158
Home values and experiences navigation track (HomeVENT): Supporting decisions about pediatric home ventilation.
PEC Innov
2023
37245030
Hyperhydration to Improve Kidney Outcomes in Children with Shiga Toxin-Producing E. coli Infection: a multinational embedded cluster crossover randomized trial (the HIKO STEC trial).
Trials
2023
37470892
Longitudinal adherence to breast cancer surveillance following cancer genetic testing in an integrated health care system.
Breast Cancer Res Treat
2023
36748334
Measuring 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 Couns
2023
36516964
The PrU: Development and validation of a measure to assess personal utility of genomic results.
Genet Med
2023
36691692
Factors That Impact Hospital-Specific Enrollment Rates for a Neonatal Clinical Trial: An Analysis of the HEAL Study.
Ethics Hum Res
2023
36682451
Validation of a Process for Shared Decision-Making in Pediatrics.
Acad Pediatr
2023
36662553
"What Would Give Her the Best Life?": Understanding Why Families Decline Pediatric Home Ventilation.
J Palliat Med
2023
36938783
Medical interpreter-mediated genetic counseling for Spanish preferring adults at risk for a hereditary cancer syndrome.
J Genet Couns
2023
34302314
Barriers to family history knowledge and family communication among LGBTQ+ individuals in the context of hereditary cancer risk assessment.
J Genet Couns
2022
35676898
Family-Assisted Severity of Illness Monitoring for Hospitalized Children in Low-Resource Settings-A Two-Arm Interventional Feasibility Study.
Front Pediatr
2022
35436948
Identifying patients with Lynch syndrome using a universal tumor screening program in an integrated healthcare system.
Hered Cancer Clin Pract
2022
35763201
Toward Meeting the Obligation of Respect for Persons in Pragmatic Clinical Trials.
Hastings Cent Rep
2022
35664885
Ethical Considerations in Ever-Expanding Utilization of ECLS: A Research Agenda.
Front Pediatr
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
35420512
Enrolling Adolescents with Rare Disease for Early Phase Clinical Trials While Under the Care of Child Protection Services: Balancing Protection and Access.
Am J Bioeth
2022
35522237
ORCA, a values-based decision aid for selecting additional findings from genomic sequencing in adults: Efficacy results from a randomized trial.
Genet Med
2022
35933674
Engaging Patient Advisory Committees to Inform a Genomic Cancer Risk Study: Lessons for Future Efforts.
Perm J
2022
36170065
To Disclose or Not to Disclose: Secondary Findings of XXY Chromosomes.
Am J Bioeth
2022
35985537
I know Things Now: The Challenges for Genetic Counseling of Adolescents with a Family History of Hereditary Breast Cancer.
J Pediatr
2022
36053287
An accessible, relational, inclusive, and actionable (ARIA) model of genetic counseling compared with usual care: Results of a randomized controlled trial.
Genet Med
2022
33754278
Adaptation 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 Cancer
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
35094605
Conflicts between parents and clinicians: Tracheotomy decisions and clinical bioethics consultation.
Nurs Ethics
2022
34998990
Responding to signals of mental and behavioral health risk in pragmatic clinical trials: Ethical obligations in a healthcare ecosystem.
Contemp Clin Trials
2022
34908169
Allocation of Opportunities to Participate in Clinical Trials during the Covid-19 Pandemic and Other Public Health Emergencies.
Hastings Cent Rep
2022
35176501
Ethical and epistemic issues in the design and conduct of pragmatic stepped-wedge cluster randomized clinical trials.
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
35171038
Development and evaluation of an exome sequencing training course for medical interpreters.
Per Med
2022
35080259
Home mechanical ventilation for children with severe neurological impairment: Parents' perspectives on clinician counselling.
Dev Med Child Neurol
2022
34738745
Parent perspectives on facilitating decision-making around pediatric home ventilation.
Pediatr Pulmonol
2022
34551279
From Monochromatic to Technicolor: Parent Perspectives on Challenges and Approaches to Seeing Children with Severe Neurological Impairment Holistically.
J Palliat Med
2022
34658003
Perceived Utility of Genomic Sequencing: Qualitative Analysis and Synthesis of a Conceptual Model to Inform Patient-Centered Instrument Development.
Patient
2022
32981477
Participant Reactions to a Literacy-Focused, Web-Based Informed Consent Approach for a Genomic Implementation Study.
AJOB Empir Bioeth
2021
33853890
Presymptomatic Detection and Intervention for Autism Spectrum Disorder.
Pediatrics
2021
33719913
Reframing Recruitment: Evaluating Framing in Authorization for Research Contact Programs.
AJOB Empir Bioeth
2021
33825623
Supporting Investigators in Challenging Cases: Unease in the Face of an Ethically Appropriate Action.
Am J Bioeth
2021
33825622
Conjoined Consent: Informed Consent When Donor and Recipient Are Both Research Participants.
Am J Bioeth
2021
33811178
A 2020 Executive Order That Threatens Progress in Shared Decision-Making.
Pediatrics
2021
33530721
An ethics framework for consolidating and prioritizing COVID-19 clinical trials.
Clin Trials
2021
33914815
Patient perspectives on how to demonstrate respect: Implications for clinicians and healthcare organizations.
PLoS One
2021
1 - 50 of 315
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E Clayton
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