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Author Details

Kyle B Brothers
Norton Children's Research Institute Affiliated with the University of Louisville
2002
96
26
PMIDPaper TitleJournal TitlePublished Year
36524987Words matter: The language of difference in human genetics.Genet Med2023
37511639Parents' Perspectives on the Utility of Genomic Sequencing in the Neonatal Intensive Care Unit.J Pers Med2023
37347242ACMG SF v3.2 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).Genet Med2023
37245625Concordance of International Regulation of Pediatric Health Research.J Pediatr2023
34799539Attention-Deficit/Hyperactivity Disorder Practice Patterns: A Survey of Kentucky Pediatric Providers.J Dev Behav Pediatr2022
35802134ACMG SF v3.1 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).Genet Med2022
35838066Newborn screening for neurodevelopmental diseases: Are we there yet?Am J Med Genet C Semin Med Genet2022
35657379Challenges for precision public health communication in the era of genomic medicine.Genet Med2022
36414972Return of non-ACMG recommended incidental genetic findings to pediatric patients: considerations and opportunities from experiences in genomic sequencing.Genome Med2022
36227983Data sharing and community-engaged research.Science2022
36055208Addressing underrepresentation in genomics research through community engagement.Am J Hum Genet2022
35201881Streamlining ethics review for international health research.Science2022
34930662Genome sequencing as a first-line diagnostic test for hospitalized infants.Genet Med2022
34658003Perceived Utility of Genomic Sequencing: Qualitative Analysis and Synthesis of a Conceptual Model to Inform Patient-Centered Instrument Development.Patient2022
33972721Genomic medicine implementation protocols in the PhenX Toolkit: tools for standardized data collection.Genet Med2021
33649579Taking an antiracist posture in scientific publications in human genetics and genomics.Genet Med2021
33843487The Therapeutic Odyssey: Positioning Genomic Sequencing in the Search for a Child's Best Possible Life.AJOB Empir Bioeth2021
33815477Employees' Views and Ethical, Legal, and Social Implications Assessment of Voluntary Workplace Genomic Testing.Front Genet2021
34888063Examining access to care in clinical genomic research and medicine: Experiences from the CSER Consortium.J Clin Transl Sci2021
34806961"If It's Ethical During a Pandemic⿦": Lessons from COVID-19 for Post-Pandemic Biobanking.Am J Bioeth2021
34687653Conceptualization of utility in translational clinical genomics research.Am J Hum Genet2021
32342752Unregulated Health Research Using Mobile Devices: Ethical Considerations and Policy Recommendations.J Law Med Ethics2020
32075871A Process-Based Approach to Responding to Parents or Guardians Who Hope for a Miracle.Pediatrics2020
33253510Banning Genetic Discrimination in Life Insurance - Time to Follow Florida's Lead.N Engl J Med2020
33157006Analogies in Genomics Policymaking: Debates and Drawbacks.Am J Hum Genet2020
32763189Fostering Responsible Research on Ancient DNA.Am J Hum Genet2020
32342755Online Pediatric Research: Addressing Consent, Assent, and Parental Permission.J Law Med Ethics2020
30611438Reconciling Opportunistic and Population Screening in Clinical Genomics.Mayo Clin Proc2019
31957580Legal and Ethical Challenges of International Direct-to-Participant Genomic Research: Conclusions and Recommendations.J Law Med Ethics2019
29904163Physicians' perspectives on receiving unsolicited genomic results.Genet Med2019
29976988Developing a conceptual, reproducible, rubric-based approach to consent and result disclosure for genetic testing by clinicians with minimal genetics background.Genet Med2019
31313633Consent for clinical genome sequencing: considerations from the Clinical Sequencing Exploratory Research Consortium.Per Med2019
31541538Participant Engagement in Translational Genomics Research: Respect for Persons-and Then Some.Ethics Hum Res2019
30951675The Responsibility to Recontact Research Participants after Reinterpretation of Genetic and Genomic Research Results.Am J Hum Genet2019
30894702Rethinking the "open future" argument against predictive genetic testing of children.Genet Med2019
31152729Bespoke Babies: Genome Editing in Cystic Fibrosis Embryos.Ann Thorac Surg2019
30994072A Belmont Reboot: Building a Normative Foundation for Human Research in the 21st Century.J Law Med Ethics2019
30676903Genomic Contextualism: Shifting the Rhetoric of Genetic Exceptionalism.Am J Bioeth2019
30287922Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study.Genet Med2019
30670880Correction: Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study.Genet Med2019
30590688Enrichment sampling for a multi-site patient survey using electronic health records and census data.J Am Med Inform Assoc2019
29260321Efficacy of an Internet-based depression intervention to improve rates of treatment in adolescent mothers.Arch Womens Ment Health2018
30242811How Should Primary Care Physicians Respond to Direct-to-Consumer Genetic Test Results?AMA J Ethics2018
30240342Parents' attitudes toward consent and data sharing in biobanks: A multisite experimental survey.AJOB Empir Bioeth2018
29980585Research Consent at the Age of Majority: Preferable but not Obligatory.Pediatrics2018
28364300Providers' Behaviors and Beliefs on Prescribing Antipsychotic Medication to Children: A Qualitative Study.Community Ment Health J2018
29665847Tensions in ethics and policy created by National Precision Medicine Programs.Hum Genomics2018
29790872Genomic sequencing identifies secondary findings in a cohort of parent study participants.Genet Med2018
29655271Correction to: PUGS: A novel scale to assess perceptions of uncertainties in genome sequencing.Clin Genet2018
29652076Systematic reanalysis of genomic data improves quality of variant interpretation.Clin Genet2018
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Collaborators

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Co-authored papers 24
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University of Washington Medical Center
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Harvard Medical School
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University of Louisville
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University of California-San Francisco.
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National Human Genome Research Institute, National Institutes of Health
Co-authored papers 7
Illumina Inc.
Co-authored papers 7
University of Washington School of Medicine
Co-authored papers 7
University of Washington School of Medicine
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Norton Children's Research Institute, University of Louisville School of Medicine
Co-authored papers 7
Penn State College of Medicine
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HudsonAlpha Institute for Biotechnology
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University of North Carolina
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Genomic Medicine Institute
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