JOURNAL ARTICLES

• Meyer, M. N., Heck, P. R., Holtzman, G. S., Anderson, S. M., Cai, W., Watts, D. J., & Chabris, C. F. (2019) Objecting to experiments that compare two unobjectionable policies or treatments. Proceedings of the National Academy of Sciences, 116(22), 10723-10728
  
  COVERAGE: Cass Sunstein at Bloomberg; Alex Tabarrok at Marginal Revoution; Kelsey Piper at Vox; Kevin Drum at Mother Jones; Jesse Singal for British Psychological Society; Oral Argument podcast; Scott Koenig for Naut​ilus; Tom Chivers at UnHerd
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• Heck, P. R. & Meyer, M. N. (2019). Information avoidance in genetic health: Perceptions, norms, and preferences. Social Cognition, 37(3), 266-293 (preprint)
• Heck, P.R. & Meyer, M. N. Population whole exome screening: Primary care provider attitudes about preparedness, information avoidance, and nudging. Medical Clinics (in press)
• Linnér, R. K., et al. (2019). Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences. Nature Genetics (online first https://doi.org/10.1z038/s41588-018-0309-3)
• Lynch, H. F., Nicholls, S., Meyer, M. N., & Taylor, H. A. (2018). Of parachutes and participant protection: Advancing effective research ethics oversight. Journal of Empirical Research on Human Research Ethics, https://doi.org/10.1177/1556264618812625, 1-7
• Lee, J. L., et al. (2018). Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. Nature Genetics, 50(8), 1112-1121
• ​Marc S. Williams, et al. (2018). Implementation of patient-centered precision health in a learning healthcare system: the Geisinger experience with genomic medicine, Health Affairs, 37(5), 757-764
• Meyer, M. N. (2018). Practical tips for ethical data sharing. Advances in Methods and Practices in Psychological Science, 1(1), 131-144
• Buchanan, A. H., Manickam, K., Meyer, M. N., et al. (2018). Early cancer diagnoses through BRCA1/2 screening of unselected adult biobank participants. Genetics in Medicine, 20(5), 554-558
• Meyer, M. N. (2016). Pregnancy exclusions, posthumous pregnancy, and the Constitution. Lahey Health Journal of Medical Ethics, Spring, 6-7
• Aysu Okbay, et al. (2016). Genome-wide association study identifies 74 loci associated with educational attainment. Nature, 533(7604), 539-542
• Aysu Okbay, et al. (2016). Genetic variants associated with subjective well-being, depressive symptoms and neuroticism identified through genome-wide analyses. Nature Genetics, 48(6), 624-633
• Meyer, M. N. (2015). Above the (public health) law?: Healthcare worker deception & disobedience in a time of distrust. Journal of Law, 5(1), 121-136
• Meyer, M. N. (2015). Two cheers for corporate experimentation: The A/B illusion and the virtues of data-driven innovation. Colorado Technology Law Journal, 13(2), 273-331 (slides)
• Meyer, M. N., Lantos, J., London, A. J., McGuire, A. L., Schuklenk, U. & Stell, L. (2014). Misjudgements will drive social trials underground. Nature, 511(7509), 265 (list of 28 additional signatories)
• Meyer, M. N. (2013). Regulating the production of knowledge: Research risk-benefit analysis and the heterogeneity problem. Administrative Law Review, 65(2), 237-298
• Meyer, M. N. (2013). Are you ready for some...research? Uncertain diagnoses, research data privacy, & preference heterogeneity. Journal of Law, 3(1), 99-110
• Niels A. Rietveld, et al. (2013). GWAS of 126,559 individuals identifies genetic variants associated with educational attainment. Science, 340(6139), 1467-1471 (AAAS); see also FAQs (authored first draft) 
• Meyer, M. N. (2013). From evidence-based medicine to evidence-based practice. Hastings Center Report, 43(2), 11-12
• Meyer, M. N. (2011). The subject-researcher relationship: In defense of contracting around default rules. American Journal of Bioethics, 11(4), 27-30 
• Meyer, M. N. (2010). Against one-size-fits-all research ethics. Hastings Center Report, 40(5), 10-11
• Meyer, M. N. & Fossett, J. F. (2009). The more things change: The new NIH guidelines on human stem cell research. Kennedy Institute of Ethics Journal, 19(3), 289-307 
• Meyer, M. N. (2008). The kindness of strangers: The donative contract between subjects and researchers and the non-obligation to return individual results of genetic research. American Journal of Bioethics, 8(11), 44-50
• Meyer, M. N. (2006). Note, The plaintiff as person: Cause lawyering, human subject research, and the secret agent problem. Harvard Law Review 119: 1510-1531
• Meyer, M. N. (2004). Comment, Icelandic Supreme Court holds that inclusion of an individual's genetic information in a national database infringes on the privacy interests of his child: Guomundsdottir v. Iceland. Harvard Law Review, 118, 810-817
• Fletcher, J. C., Meyer, M. N., Benson, J. M. & Denk, C. E. (1998). When and why do Virginians choose to terminate treatment? Virginia Medical Quarterly, 125(2), 112-116, 119 (PubMed)