Anya E.R. Prince, "The Genetic Information Nondiscrimination Act (GINA) of 2008," with M. Waterstone and others, in Genetic Discrimination: Transatlantic Perspectives on the Case for a European-level Legal Response, edited by Gerard Quinn, Aisling de Paor, and Peter Blanck. NY: Routledge, 2015, at 114, 14 pages.
Anya E.R. Prince, "Proxy Discrimination in the Age of Artificial Intelligence and Big Data," with Daniel Schwarcz, 105 Iowa Law Review 1257 (2020), 62 pages.
Anya E.R. Prince, "The Problems with Patchwork: State Approaches to Regulating Insurer Use of Genetic Information," with Jarrod O. Anderson and Anna C.F. Lewis, 22 DePaul J. Health Care L. 1 (2021), 41 pages.
Anya E.R Prince, "Is Real-Time ELSI Realistic?" with John M. Conley, Arlene M. Davis, Jean Cadigan & Gabriel Lazaro-Munoz, 11 AJOB Empirical Bioethics 134 (2020),11 pages. (DOI: 10.1080/23294515.2020.1722289)
Anya E.R. Prince, "Referencing BRCA in Hereditary Cancer Risk Discussions: In Search of an Anchor in a Sea of Uncertainty," with Margaret Waltz, Julianne M. O'Daniel, Ann Katherine M. Foreman, Bradford C. Powell, and Jonathan S. Berg, Journal of Genetic Counseling, January, 2020, 11 pages. (DOI: 10.1002/jgc4.1219)
Anya E.R. Prince, "Potential (Mis)use of Epigenetic Age Estimators by Private Companies and Public Agencies: Human Rights Law Should Provide Ethical Guidance," with Charles Dupras, Stephan Beck, Mark A. Rothstein, Alison Berner, Katie M. Saulnier, Miriam Pinkesz, Stamatina Liosi, Lingqiao Song, and Yann Joly, 5 Environmental Epigenetics 1 (2019), 12 pages. (https://doi.org/10.1093/eep/dvz018)
Anya E.R. Prince, "A survey of U. S. state insurance commissioners concerning genetic testing and life insurance: Redux at 27," with Dexter R. Golinghorst, Journal of Genetic Counseling (December 18, 2019), 8 pages. (DOI: 10.1002/jgc4.1197)
Anya E.R. Prince, "Shared Decision-making in Vascular Surgery," with Jun Xu, 70 Journal of Vascular Surgery 1711 (2019), 5 pages.
Anya E.R. Prince, "Consent for Clinical Genome Sequencing: Considerations from the Clinical Sequencing Exploratory Research Consortium," with Joon-Ho Yu, et.al.,16 Personalized Medicine 325 (2019), 11 pages.
Anya E.R. Prince, "Gene Therapy's Field of Dreams: If you Build it, Will we Pay?" with Laura Hercher, 97 North Carolina Law Review 1463 (2019), 32 pages.
Anya E.R. Prince, "Political Economy, Stakeholder Voices, and Saliency: Lessons from International Policies Regulating Insurer Use of Genetic Information," 6 Journal of Law and the Biosciences 461 (2019), 34 pages.
Anya E.R. Prince, "Comparative Perspectives: Regulating Insurer Use of Genetic Information," European Journal of Human Genetics 1 (Nov. 6, 2018), 9 pages.
Anya E.R. Prince, "Reconceptualizing Harms and Benefits in the Genomic Age," with Benjamin E. Berkman, Personalized Medicine (2018), 10 pages.
Anya E.R. Prince, “Analysis of State Laws on Informed Consent for Clinical Genetic Testing in the Era of Genomic Sequencing,” with Kayte Spector-Bagdady and others, 178C American Journal of Medical Genetics, Part C, Seminars in Medical Genetics 81 (2018), 8 pages.
Anya E.R. Prince, "Insurance Risk Classification in an Era of Genomics: Is a Rational Discrimination Policy Rational?" 96 Nebraska Law Review 624 (2018), 64 pages.
Anya E.R. Prince, "Age and Perceived Risks and Benefits of Preventive Genomic Screening," with Margaret Waltz and others, Genetics in Medicine (online version), (2017), 7 pages.
Anya E.R. Prince, "Is there Evidence that we should Screen the General Population for Lynch Syndrome with Genetic Testing? A Systematic Review," with R.J. Cadigan and others. 10 Pharmacogenomics and Personalized Medicine 49 (2017), 12 pages.
Anya E.R. Prince, "Membership Recruitment and Training in Health Care Ethics Committees: Results from a National Pilot Survey," with R.J. Cadigan, and others, 8 AJOB Empirical Bioethics 161 (2017), 9 pages.
Anya E.R. Prince, "Which Results to Return: Subjective Judgments in Selecting Medically Actionable Genes," with G. Lázaro-Muñoz, and others, 21 Genetic Testing and Molecular Biomarkers 184 (2017), 11 pages.
Anya E.R. Prince, "Navigating Professional Norms in an Inter-Professional Environment: The 'Practice' of Healthcare Ethics Committees," 15 Connecticut Public Interest Law Journal 115 (2016), 42 pages.
Anya E.R. Prince, "Tantamount to Fraud? Exploring Non-Disclosure of Genetic Information in Life Insurance Applications as Grounds for Policy Rescission," 26 Case Western Reserve Health Matrix: Journal of Law-Medicine 255 (2016), 52 pages.
Anya E.R. Prince, "Automatic Placement of Genomic Research Results in Medical Records: Do Researchers have a Duty? Should Participants have a Choice?" with J.M. Conley and others, 43 Journal of Law, Medicine & Ethics 827 (2015), 16 pages.
Anya E.R. Prince, "Prevention for those who can Pay: Insurance Reimbursement of Genetic-based Preventive Interventions in the Liminal State between Health and Disease," 2 Journal of Law and the Biosciences 365 (2015), 31 pages.
Anya E.R. Prince, "Scientific Social Responsibility: Lessons from the Corporate Social Responsibility Movement," with J. Conley and others, 15 American Journal of Bioethics 64 (2015), 3 pages.
Anya E.R. Prince, "Factors which Impact the Delivery of Genetic Risk Assessment Services Focused on Inherited Cancer Genomics: Expanding the Role and Reach of Certified Genetics Professionals," with C. Radford and T. Pal, 23 Journal of Genetic Counseling 522 (2014), 9 pages.
Anya E.R. Prince, "Genetic Information, Non-discrimination, and Privacy Protections in Genetic Counseling Practice," with M.I. Roche, 23 Journal of Genetic Counseling 891 (2014), 12 pages.
Anya E.R. Prince, "Genomic Screening of the General Adult Population: Key Concepts for Assessing Net Benefit with Systematic Evidence Reviews," with J.S. Berg and others. 17 Genetics in Medicine 441 (2014), 3 pages.
Anya E.R. Prince, "Comprehensive Protection of Genetic Information: One Size Privacy or Property Models may not Fit All," 79 Brooklyn Law Review 175 (2013), 52 pages.
Anya E.R. Prince, "When does an Illness begin: Genetic Discrimination and Disease Manifestation," with B.E. Berkman, 40 Journal of Law, Medicine & Ethics 655 (2012), 10 pages.
Anya E.R. Prince, "Direct-to-Consumer Genetic Testing and Potential Loopholes in Protecting Consumer Privacy and Nondiscrimination," with Rachele M. Hendricks-Sturrup and Christine Y. Lu, 321 JAMA 1869 (2019), 2 pages.