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Author Details
Full Name
Wylie Burke
Affiliation
The Heart Institute, Cincinnati Children's Hospital Medical Center
ORCID
Career Start Year
1975
Papers
314
H Index
62
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37268102
Repair of truncus arteriosus and atrioventricular septal defect: A value of virtual reality.
J Thorac Cardiovasc Surg
2024
36166685
Measuring Attitudes About Alcohol Misuse and Dependence Among Alaska Native People Within a Tribal Health Care System.
J Addict Med
2023
37526719
Genetic Architecture of Dilated Cardiomyopathy in Individuals of African and European Ancestry.
JAMA
2023
37348094
Executive Summary of the Ovarian Cancer Evidence Review Conference.
Obstet Gynecol
2023
37348095
Health Disparities in Ovarian Cancer: Report From the Ovarian Cancer Evidence Review Conference.
Obstet Gynecol
2023
36972543
Cases in Precision Medicine: Is There an Obligation to Return Reinterpreted Genetic Results to Former Patients?
Ann Intern Med
2023
36748709
Practical considerations for reinterpretation of individual genetic variants.
Genet Med
2023
36938756
Effectiveness of the <i>Family Heart Talk</i> Communication Tool in Improving Family Member Screening for Dilated Cardiomyopathy: Results of a Randomized Trial.
Circulation
2023
35103767
Prevalence and Cumulative Risk of Familial Idiopathic Dilated Cardiomyopathy.
JAMA
2022
35436152
The Challenge of Genetic Variants of Uncertain Clinical Significance : A Narrative Review.
Ann Intern Med
2022
35536229
Communal Coping as a Strategy to Enhance Family Engagement in Dilated Cardiomyopathy.
Circ Genom Precis Med
2022
35659933
Is there a way to reduce the inequity in variant interpretation on the basis of ancestry?
Am J Hum Genet
2022
36533507
Values and Practices to Strengthen Genetic Research Partnerships with Indigenous Communities.
Prog Community Health Partnersh
2022
35998578
Communicating Precision Medicine Research: Multidisciplinary Teams and Diverse Communities.
Public Health Genomics
2022
35878403
Ethical Considerations in Precision Medicine and Genetic Testing in Internal Medicine Practice: A Position Paper From the American College of Physicians.
Ann Intern Med
2022
35225705
Tribal Deliberations about Precision Medicine Research: Addressing Diversity and Inequity in Democratic Deliberation Design and Evaluation.
J Empir Res Hum Res Ethics
2022
35245474
2021 McKusick Leadership Award: Learning from communities.
Am J Hum Genet
2022
34906504
Precision medicine research with American Indian and Alaska Native communities: Results of a deliberative engagement with tribal leaders.
Genet Med
2022
35272301
Health Disparities in Uterine Cancer: Report From the Uterine Cancer Evidence Review Conference.
Obstet Gynecol
2022
34870514
Stakeholder Perspectives on Returning Nonactionable Apolipoprotein L1 (APOL1) Genetic Results to African American Research Participants.
J Empir Res Hum Res Ethics
2022
32873931
Response to Faulkner et al.
Genet Med
2021
36303973
Explaining the Black-White Disparity in Preterm Birth: A Consensus Statement From a Multi-Disciplinary Scientific Work Group Convened by the March of Dimes.
Front Reprod Health
2021
33853887
Diagnosis, Education, and Care of Patients with <i>APOL1</i>-Associated Nephropathy: A Delphi Consensus and Systematic Review.
J Am Soc Nephrol
2021
33792358
Utility and Diversity: Challenges for Genomic Medicine.
Annu Rev Genomics Hum Genet
2021
34554063
Solidarity: A Missing Component of Research Ethics.
Am J Bioeth
2021
33414545
Toward better governance of human genomic data.
Nat Genet
2021
30714494
Perceptions of alcohol misuse among Alaska native health care system stakeholders: A qualitative exploration.
J Ethn Subst Abuse
2020
31843866
Predictive and Precision Medicine with Genomic Data.
Clin Chem
2020
31728919
Correction to: Native Hawaiian Views on Biobanking.
J Cancer Educ
2020
32041801
At the Research-Clinical Interface: Returning Individual Genetic Results to Research Participants.
Clin J Am Soc Nephrol
2020
31916645
Exploring relatives' perceptions of participation, ethics, and communication in a patient-driven study for hereditary cancer variant reclassification.
J Genet Couns
2020
33416640
"You Actually View Us as the Experts in Our Own System": Indigenous-Academic Community Partnership.
Prog Community Health Partnersh
2020
32895299
Preimplantation Genetic Testing for Genetic Kidney Disease: Addressing Moral Uncertainties and Access Inequity.
Clin J Am Soc Nephrol
2020
32160020
Variant Interpretation for Dilated Cardiomyopathy: Refinement of the American College of Medical Genetics and Genomics/ClinGen Guidelines for the DCM Precision Medicine Study.
Circ Genom Precis Med
2020
31616070
Is there a duty to reinterpret genetic data? The ethical dimensions.
Genet Med
2020
30676118
Practice Implications of Expanded Genetic Testing in Oncology.
Cancer Invest
2019
31889772
Can Precision Medicine Reduce the Burden of Diabetes?
Ethn Dis
2019
31889771
Access and Management: Indigenous Perspectives on Genomic Data Sharing.
Ethn Dis
2019
31649725
Data Management in Health-Related Research Involving Indigenous Communities in the United States and Canada: A Scoping Review.
Front Genet
2019
30027524
Experiences of patients seeking to participate in variant of uncertain significance reclassification research.
J Community Genet
2019
31217590
ADDENDUM: Genetic counseling and testing for Alzheimer disease: joint practice guidelines of the American College of Medical Genetics and the National Society of Genetic Counselors.
Genet Med
2019
31400517
Clinical exome sequencing vs. usual care for hereditary colorectal cancer diagnosis: A pilot comparative effectiveness study.
Contemp Clin Trials
2019
31279488
Precision medicine and health disparities: The case of pediatric acute lymphoblastic leukemia.
Nurs Outlook
2019
31480040
Apolipoprotein L1 Testing in African Americans: Involving the Community in Policy Discussions.
Am J Nephrol
2019
31307368
Genomes in Context.
Am J Bioeth
2019
30858224
You Are Just Now Telling Us About This? African American Perspectives of Testing for Genetic Susceptibility to Kidney Disease.
J Am Soc Nephrol
2019
31163102
Patient goals, motivations, and attitudes in a patient-driven variant reclassification study.
J Genet Couns
2019
30964586
The Feelings About genomiC Testing Results (FACToR) Questionnaire: Development and Preliminary Validation.
J Genet Couns
2019
31048483
Consent insufficient for data release.
Science
2019
31160753
Improving recommendations for genomic medicine: building an evolutionary process from clinical practice advisory documents to guidelines.
Genet Med
2019
1 - 50 of 314
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