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Author Details
Full Name
Anya E R Prince
Affiliation
University of Iowa.
ORCID
Career Start Year
2012
Papers
45
H Index
11
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36260514
How should we address the inevitable harms from non-negligent variant reclassification in predictive genetic testing?
J Genet Couns
2023
37906184
The Genetic Information Privacy Act: Drawbacks and Limitations.
JAMA
2023
37879008
The Limits of a Voluntary Framework in an Unethical Data Ecosystem.
Am J Bioeth
2023
37496383
Clinically actionable secondary findings in 130 triads from sub-Saharan African families with non-syndromic orofacial clefts.
Mol Genet Genomic Med
2023
36919542
The Slippery Slope of Prenatal Testing for Social Traits.
Am J Bioeth
2023
34544841
A step forward, but still inadequate: Australian health professionals' views on the genetics and life insurance moratorium.
J Med Genet
2022
35737492
Privacy and the Genetic Community.
Am J Bioeth
2022
36207733
Patient and provider perspectives on polygenic risk scores: implications for clinical reporting and utilization.
Genome Med
2022
35930740
The goldilocks conundrum: Disclosing discrimination risks in informed consent.
J Genet Couns
2022
36055208
Addressing underrepresentation in genomics research through community engagement.
Am J Hum Genet
2022
35243989
Anti-Selection & Genetic Testing in Insurance: An Interdisciplinary Perspective.
J Law Med Ethics
2022
35058451
Voluntary workplace genomic testing: wellness benefit or Pandora's box?
NPJ Genom Med
2022
33077893
Long-awaited progress in addressing genetic discrimination in the United States.
Genet Med
2021
35663290
Genetic testing and insurance implications: Surveying the US general population about discrimination concerns and knowledge of the Genetic Information Nondiscrimination Act (GINA).
Risk Manag Insur Rev
2021
33815477
Employees' Views and Ethical, Legal, and Social Implications Assessment of Voluntary Workplace Genomic Testing.
Front Genet
2021
34400812
The persistent lack of knowledge and misunderstanding of the Genetic Information Nondiscrimination Act (GINA) more than a decade after passage.
Genet Med
2021
34446926
Correction: The persistent lack of knowledge and misunderstanding of the Genetic Information Nondiscrimination Act (GINA) more than a decade after passage.
Genet Med
2021
34503867
The Genetic Discrimination Observatory: confronting novel issues in genetic discrimination.
Trends Genet
2021
33110270
Correction: Long-awaited progress in addressing genetic discrimination in the United States.
Genet Med
2021
32203466
Establishing the International Genetic Discrimination Observatory.
Nat Genet
2020
34221429
What guidance does HIPAA offer to providers considering familial risk notification and cascade genetic testing?
J Law Biosci
2020
32040382
Is Real-Time ELSI Realistic?
AJOB Empir Bioeth
2020
31850620
A survey of U. S. state insurance commissioners concerning genetic testing and life insurance: Redux at 27.
J Genet Couns
2020
30401960
Comparative perspectives: regulating insurer use of genetic information.
Eur J Hum Genet
2019
31313633
Consent for clinical genome sequencing: considerations from the Clinical Sequencing Exploratory Research Consortium.
Per Med
2019
31068265
Shared decision-making in vascular surgery.
J Vasc Surg
2019
31143452
Political economy, stakeholder voices, and saliency: lessons from international policies regulating insurer use of genetic information.
J Law Biosci
2019
30998825
Direct-to-Consumer Genetic Testing and Potential Loopholes in Protecting Consumer Privacy and Nondiscrimination.
JAMA
2019
29215654
Age and perceived risks and benefits of preventive genomic screening.
Genet Med
2018
30260295
Reconceptualizing harms and benefits in the genomic age.
Per Med
2018
29566453
Analysis of state laws on informed consent for clinical genetic testing in the era of genomic sequencing.
Am J Med Genet C Semin Med Genet
2018
28949901
Membership recruitment and training in health care ethics committees: Results from a national pilot survey.
AJOB Empir Bioeth
2017
31885407
Insurance Risk Classification in an Era of Genomics: Is a Rational Discrimination Policy Rational?
Neb Law Rev
2017
28146641
Which Results to Return: Subjective Judgments in Selecting Medically Actionable Genes.
Genet Test Mol Biomarkers
2017
28260941
Is there evidence that we should screen the general population for Lynch syndrome with genetic testing? A systematic review.
Pharmgenomics Pers Med
2017
27263254
TANTAMOUNT TO FRAUD?: EXPLORING NON-DISCLOSURE OF GENETIC INFORMATION IN LIFE INSURANCE APPLICATIONS AS GROUNDS FOR POLICY RESCISSION.
Health Matrix Clevel
2016
27774243
Response to peer commentaries: prevention for those who can pay.
J Law Biosci
2016
25232850
Genomic screening of the general adult population: key concepts for assessing net benefit with systematic evidence reviews.
Genet Med
2015
26632370
Scientific Social Responsibility: Lessons From the Corporate Social Responsibility Movement.
Am J Bioeth
2015
26339500
Prevention for those who can pay: insurance reimbursement of genetic-based preventive interventions in the liminal state between health and disease.
J Law Biosci
2015
26711421
Automatic Placement of Genomic Research Results in Medical Records: Do Researchers Have a Duty? Should Participants Have a Choice?
J Law Med Ethics
2015
24306140
Factors 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 Couns
2014
25325812
Beyond social media: inadvertent acquisition of genetic information in medical certifications.
Am J Bioeth
2014
25063358
Genetic information, non-discrimination, and privacy protections in genetic counseling practice.
J Genet Couns
2014
23061591
When does an illness begin: genetic discrimination and disease manifestation.
J Law Med Ethics
2012
1 - 45 of 45
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