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Author Details

Anya E R Prince
University of Iowa.
2012
45
11
PMIDPaper TitleJournal TitlePublished Year
36260514How should we address the inevitable harms from non-negligent variant reclassification in predictive genetic testing?J Genet Couns2023
37906184The Genetic Information Privacy Act: Drawbacks and Limitations.JAMA2023
37879008The Limits of a Voluntary Framework in an Unethical Data Ecosystem.Am J Bioeth2023
37496383Clinically actionable secondary findings in 130 triads from sub-Saharan African families with non-syndromic orofacial clefts.Mol Genet Genomic Med2023
36919542The Slippery Slope of Prenatal Testing for Social Traits.Am J Bioeth2023
34544841A step forward, but still inadequate: Australian health professionals' views on the genetics and life insurance moratorium.J Med Genet2022
35737492Privacy and the Genetic Community.Am J Bioeth2022
36207733Patient and provider perspectives on polygenic risk scores: implications for clinical reporting and utilization.Genome Med2022
35930740The goldilocks conundrum: Disclosing discrimination risks in informed consent.J Genet Couns2022
36055208Addressing underrepresentation in genomics research through community engagement.Am J Hum Genet2022
35243989Anti-Selection & Genetic Testing in Insurance: An Interdisciplinary Perspective.J Law Med Ethics2022
35058451Voluntary workplace genomic testing: wellness benefit or Pandora's box?NPJ Genom Med2022
33077893Long-awaited progress in addressing genetic discrimination in the United States.Genet Med2021
35663290Genetic testing and insurance implications: Surveying the US general population about discrimination concerns and knowledge of the Genetic Information Nondiscrimination Act (GINA).Risk Manag Insur Rev2021
33815477Employees' Views and Ethical, Legal, and Social Implications Assessment of Voluntary Workplace Genomic Testing.Front Genet2021
34400812The persistent lack of knowledge and misunderstanding of the Genetic Information Nondiscrimination Act (GINA) more than a decade after passage.Genet Med2021
34446926Correction: The persistent lack of knowledge and misunderstanding of the Genetic Information Nondiscrimination Act (GINA) more than a decade after passage.Genet Med2021
34503867The Genetic Discrimination Observatory: confronting novel issues in genetic discrimination.Trends Genet2021
33110270Correction: Long-awaited progress in addressing genetic discrimination in the United States.Genet Med2021
32203466Establishing the International Genetic Discrimination Observatory.Nat Genet2020
34221429What guidance does HIPAA offer to providers considering familial risk notification and cascade genetic testing?J Law Biosci2020
32040382Is Real-Time ELSI Realistic?AJOB Empir Bioeth2020
31850620A survey of U. S. state insurance commissioners concerning genetic testing and life insurance: Redux at 27.J Genet Couns2020
30401960Comparative perspectives: regulating insurer use of genetic information.Eur J Hum Genet2019
31313633Consent for clinical genome sequencing: considerations from the Clinical Sequencing Exploratory Research Consortium.Per Med2019
31068265Shared decision-making in vascular surgery.J Vasc Surg2019
31143452Political economy, stakeholder voices, and saliency: lessons from international policies regulating insurer use of genetic information.J Law Biosci2019
30998825Direct-to-Consumer Genetic Testing and Potential Loopholes in Protecting Consumer Privacy and Nondiscrimination.JAMA2019
29215654Age and perceived risks and benefits of preventive genomic screening.Genet Med2018
30260295Reconceptualizing harms and benefits in the genomic age.Per Med2018
29566453Analysis of state laws on informed consent for clinical genetic testing in the era of genomic sequencing.Am J Med Genet C Semin Med Genet2018
28949901Membership recruitment and training in health care ethics committees: Results from a national pilot survey.AJOB Empir Bioeth2017
31885407Insurance Risk Classification in an Era of Genomics: Is a Rational Discrimination Policy Rational?Neb Law Rev2017
28146641Which Results to Return: Subjective Judgments in Selecting Medically Actionable Genes.Genet Test Mol Biomarkers2017
28260941Is there evidence that we should screen the general population for Lynch syndrome with genetic testing? A systematic review.Pharmgenomics Pers Med2017
27263254TANTAMOUNT TO FRAUD?: EXPLORING NON-DISCLOSURE OF GENETIC INFORMATION IN LIFE INSURANCE APPLICATIONS AS GROUNDS FOR POLICY RESCISSION.Health Matrix Clevel2016
27774243Response to peer commentaries: prevention for those who can pay.J Law Biosci2016
25232850Genomic screening of the general adult population: key concepts for assessing net benefit with systematic evidence reviews.Genet Med2015
26632370Scientific Social Responsibility: Lessons From the Corporate Social Responsibility Movement.Am J Bioeth2015
26339500Prevention for those who can pay: insurance reimbursement of genetic-based preventive interventions in the liminal state between health and disease.J Law Biosci2015
26711421Automatic Placement of Genomic Research Results in Medical Records: Do Researchers Have a Duty? Should Participants Have a Choice?J Law Med Ethics2015
24306140Factors which impact the delivery of genetic risk assessment services focused on inherited cancer genomics: expanding the role and reach of certified genetics professionals.J Genet Couns2014
25325812Beyond social media: inadvertent acquisition of genetic information in medical certifications.Am J Bioeth2014
25063358Genetic information, non-discrimination, and privacy protections in genetic counseling practice.J Genet Couns2014
23061591When does an illness begin: genetic discrimination and disease manifestation.J Law Med Ethics2012
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Collaborators

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McGill University.
Co-authored papers 4
University of North Carolina-Chapel Hill
Co-authored papers 3
University of Washington School of Medicine
Co-authored papers 3
Edmond & Lily Safra Center for Ethics, Harvard University
Co-authored papers 3
Norton Children's Research Institute Affiliated with the University of Louisville
Co-authored papers 3
University of Michigan Medical School.
Co-authored papers 2
University of Edinburgh
Co-authored papers 2
School of Public Health.
Co-authored papers 2
Carlsberg Laboratory, Case Western Reserve University, Johns Hopkins Medicine, Johns Hopkins School of Medicine, Johns Hopkins School of Public Health, Johns Hopkins University, National Academy of Sciences, Pennsylvania State University, Presidential Commission for the Study of Bioethical Issues
Co-authored papers 2
McGill University
Co-authored papers 2
Center for Law, Columbia University Irving Medical Center
Co-authored papers 2
Dartmouth Geisel School of Medicine
Co-authored papers 2
University of North Carolina
Co-authored papers 2
Brigham and Women's Hospital, Broad Institute Ariadne Labs and Harvard Medical School
Co-authored papers 2
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University of North Carolina at Chapel Hill.
Co-authored papers 2
Norton Children's Research Institute, University of Louisville School of Medicine
Co-authored papers 1
Berman Institute of Bioethics, Johns Hopkins University
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USA The Jackson Laboratory Cancer Center
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The First Affiliated Hospital of Xi'an Jiaotong University
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Pennsylvania State University, University Park
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Harvard Medical School and the Harvard Pilgrim Health Care Institute
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University of North Carolina
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Invitae Corporation
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Osaka University
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Case Western Reserve University
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Center for Craniofacial and Dental Genetics, University of Pittsburgh
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Medical Ethics and Health Policy, University of Pennsylvania
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