Kyle B. Brothers

University of North Carolina at Chapel Hill — United States

Medicine · Health Sciences

35h-index5.0kcitations150works5.02yr avg
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Research Topics

Ethics in Clinical Research(59), Genomics and Rare Diseases(57), BRCA gene mutations in cancer(43), Biomedical Ethics and Regulation(30), Ethics and Legal Issues in Pediatric Healthcare(17)

Publications148 total

Genetic counselors’ perspectives and experiences with workplace genetic testing: Results of a national survey
Genetics in Medicine Open·2025Open Access
Should a Genomic Diagnosis be a Ticket or a Roadmap? Threats to Equity in the Pursuit of Developmental Services in Early Childhood
The American Journal of Bioethics·2025· 9 cited
Medical vs Nonmedical Immunization Exemptions for Child Care and School Attendance: Policy Statement
PEDIATRICS·2025· 6 citedOpen Access
Motivations for participation in a spinal cord epidural stimulation study: Perspectives of individuals with spinal cord injury and their caregivers
2025Open Access
Correction: Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study
UNC Libraries·2025Open Access
Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study
UNC Libraries·2025Open Access
ACMG SF v3.3 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG)
Genetics in Medicine·2025· 24 cited
Genomic Sequencing in Pediatric Oncology: Perspectives of Parents and Adolescents on Ethical Issues
Journal of Pediatric Hematology/Oncology·2025
Moving to the Middle Ground: Redefining Genomic Utility to Expand Understanding of Familial Benefit
UNC Libraries·2025Open Access
Genomic sequencing in diverse and underserved pediatric populations: Parent perspectives on understanding, uncertainty, psychosocial impact, and personal utility of results
Genetics in Medicine·2025
Early Intervention services in the era of genomic medicine: setting a research agenda
Pediatric Research·2024· 6 citedOpen Access
Supporting Stewardship: Funding, Utilization, and Sustainability as Ethical Concerns in Networked Biobanking
AJOB Empirical Bioethics·2024· 2 citedOpen Access
Measuring perceived utility of genomic sequencing: Development and validation of the GENEtic Utility (GENE-U) scale for adult screening
Genetics in Medicine·2024· 7 citedOpen Access
Perspectives of paediatric providers on antibiotic stewardship in a high‐prescribing rural region
Journal of Evaluation in Clinical Practice·2024
Consideration of disease penetrance in the selection of secondary findings gene-disease pairs: A policy statement of the American College of Medical Genetics and Genomics (ACMG)
Genetics in Medicine·2024· 10 citedOpen Access
Measuring perceived utility of genomic sequencing: Development and validation of the GENEtic Utility (GENE-U) scale for pediatric diagnostic testing
Genetics in Medicine·2024· 13 citedOpen Access
Expanding Applications of Clinical Genetic Testing — Ethical Challenges
New England Journal of Medicine·2024· 7 citedOpen Access
Ethical and Legal Issues Surrounding Genetic Testing in the NICU
NeoReviews·2024· 7 citedOpen Access
Moving to the Middle Ground: Redefining Genomic Utility to Expand Understanding of Familial Benefit
Ethics & Human Research·2024· 7 citedOpen Access
Frequency and reasons that parents decline genetic testing for critically ill neonates
Genetics in Medicine Open·2024· 1 citedOpen Access
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Frequent Co-authors

Ellen Wright Clayton(15), Kevin M. Bowling(12), Gregory M. Cooper(12), Wendy K. Chung(11), Stacy W. Gray(10), Kelly M. East(10), Gregory S. Barsh(9), Gail P. Jarvik(8), Laura M. Amendola(8), Ingrid A. Holm(8), Amy L. McGuire(8), Michelle D. Amaral(8), Whitley V. Kelley(8), R Myers(8), Leslie G. Biesecker(8), Barbara A. Koenig(8), Benjamin S. Wilfond(8), Nanibaa’ A. Garrison(7), Michelle L. Thompson(7), Candice R. Finnila(7)