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Author Details

Stephanie M Fullerton
University of Washington School of Medicine
1994
134
39
Vardit Ravitsky (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
37771152Conflating race and ancestry: Tracing decision points about population descriptors over the precision medicine research life course.HGG Adv2024
37962912Interrogating the Value of Return of Results for Diverse Populations: Perspectives from Precision Medicine Researchers.AJOB Empir Bioeth2024
37771152Conflating race and ancestry: Tracing decision points about population descriptors over the precision medicine research life course.HGG Adv2024
37752309Risk perception and intended behavior change after uninformative genetic results for adult-onset hereditary conditions in unselected patients.Eur J Hum Genet2024
37962912Interrogating the Value of Return of Results for Diverse Populations: Perspectives from Precision Medicine Researchers.AJOB Empir Bioeth2024
37752309Risk perception and intended behavior change after uninformative genetic results for adult-onset hereditary conditions in unselected patients.Eur J Hum Genet2024
36547466The designated record set for clinical genetic and genomic testing: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG).Genet Med2023
37755714An Ethical Framework for Research Using Genetic Ancestry.Perspect Biol Med2023
37604133Factors Influencing Genetic Screening Enrollment among a Diverse, Community-Ascertained Cohort.Public Health Genomics2023
37491393Pangenomics: prioritize diversity in collaborations.Nature2023
37442104Rethinking Benefit and Responsibility in the Context of Diversity: Perspectives from the Front Lines of Precision Medicine Research.Public Health Genomics2023
37343562Studying the impact of translational genomic research: Lessons from eMERGE.Am J Hum Genet2023
37181330Cloud-based biomedical data storage and analysis for genomic research: Landscape analysis of data governance in emerging NIH-supported platforms.HGG Adv2023
37126431Community Engagement in Precision Medicine Research: Organizational Practices and Their Impacts for Equity.AJOB Empir Bioeth2023
37069702Diagnostic yield of genetic screening in a diverse, community-ascertained cohort.Genome Med2023
37058144Clinical, technical, and environmental biases influencing equitable access to clinical genetics/genomics testing: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG).Genet Med2023
36724788Trustworthiness matters: Building equitable and ethical science.Cell2023
36621880Returning integrated genomic risk and clinical recommendations: The eMERGE study.Genet Med2023
36547466The designated record set for clinical genetic and genomic testing: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG).Genet Med2023
37491393Pangenomics: prioritize diversity in collaborations.Nature2023
37755714An Ethical Framework for Research Using Genetic Ancestry.Perspect Biol Med2023
37604133Factors Influencing Genetic Screening Enrollment among a Diverse, Community-Ascertained Cohort.Public Health Genomics2023
37126431Community Engagement in Precision Medicine Research: Organizational Practices and Their Impacts for Equity.AJOB Empir Bioeth2023
37058144Clinical, technical, and environmental biases influencing equitable access to clinical genetics/genomics testing: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG).Genet Med2023
37343562Studying the impact of translational genomic research: Lessons from eMERGE.Am J Hum Genet2023
37181330Cloud-based biomedical data storage and analysis for genomic research: Landscape analysis of data governance in emerging NIH-supported platforms.HGG Adv2023
37442104Rethinking Benefit and Responsibility in the Context of Diversity: Perspectives from the Front Lines of Precision Medicine Research.Public Health Genomics2023
37069702Diagnostic yield of genetic screening in a diverse, community-ascertained cohort.Genome Med2023
36724788Trustworthiness matters: Building equitable and ethical science.Cell2023
36621880Returning integrated genomic risk and clinical recommendations: The eMERGE study.Genet Med2023
34870514Stakeholder Perspectives on Returning Nonactionable Apolipoprotein L1 (APOL1) Genetic Results to African American Research Participants.J Empir Res Hum Res Ethics2022
36119389Recommendations on the use and reporting of race, ethnicity, and ancestry in genetic research: Experiences from the NHLBI TOPMed program.Cell Genom2022
36055210Social and scientific motivations to move beyond groups in allele frequencies: The TOPMed experience.Am J Hum Genet2022
36035175Environmental scan of family chart linking for genetic cascade screening in a U.S. integrated health system.Front Genet2022
35945632Feasibility, acceptability, and limited efficacy of health system-led familial risk notification: protocol for a mixed-methods evaluation.Pilot Feasibility Stud2022
35728460Strategies of inclusion: The tradeoffs of pursuing "baked in" diversity through place-based recruitment.Soc Sci Med2022
35707062Lessons learned and recommendations for data coordination in collaborative research: The CSER consortium experience.HGG Adv2022
35430888Polygenic risk, population structure and ongoing difficulties with race in human genetics.Philos Trans R Soc Lond B Biol Sci2022
35420968Getting genetic ancestry right for science and society.Science2022
35216680Family secrets: Experiences and outcomes of participating in direct-to-consumer genetic relative-finder services.Am J Hum Genet2022
35130331Beyond inclusion: Enacting team equity in precision medicine research.PLoS One2022
34870514Stakeholder Perspectives on Returning Nonactionable Apolipoprotein L1 (APOL1) Genetic Results to African American Research Participants.J Empir Res Hum Res Ethics2022
36267415Population genomic screening: Ethical considerations to guide age at implementation.Front Genet2022
36187415Targeting Representation: Interpreting Calls for Diversity in Precision Medicine Research.Yale J Biol Med2022
35707062Lessons learned and recommendations for data coordination in collaborative research: The CSER consortium experience.HGG Adv2022
35728460Strategies of inclusion: The tradeoffs of pursuing "baked in" diversity through place-based recruitment.Soc Sci Med2022
35430888Polygenic risk, population structure and ongoing difficulties with race in human genetics.Philos Trans R Soc Lond B Biol Sci2022
35420968Getting genetic ancestry right for science and society.Science2022
36035175Environmental scan of family chart linking for genetic cascade screening in a U.S. integrated health system.Front Genet2022
36267415Population genomic screening: Ethical considerations to guide age at implementation.Front Genet2022
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Collaborators

University of Washington Medical Center
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The Heart Institute, Cincinnati Children's Hospital Medical Center
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University of Washington
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University of Washington
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Illumina Inc.
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University of California-San Francisco.
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Baylor College of Medicine.
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University of Washington
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University of Washington
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Center for Genetic Medicine, Feinberg School of Medicine, Northwestern University
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Kaiser Permanente Washington
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University of Minnesota Medical School, 1035 University Drive duluth
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University of Washington.
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University of Washington School of Medicine.
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Harvard Medical School
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University of Washington Medical Center
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Institute for Society and Genetics, University of California los angeles
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Norton Children's Research Institute Affiliated with the University of Louisville
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Biomedical Ethics, Mayo Clinic and Foundation
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University of Washington School of Medicine, University of Washington
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National Human Genome Research Institute, National Institutes of Health
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Boston Children's Hospital, Harvard Medical School
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University College London
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Institute for Health Equity Research, Icahn School of Medicine at Mount Sinai
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Kaiser Permanente Washington Health Research Institute
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Center for Biomedical Ethics and Society, Vanderbilt University Medical Center
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