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  • Print publication year: 2017
  • Online publication date: October 2017


Andrews, L. B. (1992). Torts and the double helix: Malpractice liability for failure to warn of genetic risks. Houston Law Review, 29, 149184.
Ansari, D., De Smedt, B., & Grabner, R. H. (2012). Neuroeducation: A critical overview of an emerging field. Neuroethics, 5, 105117. doi:10.1007/s12152-011-9119-3
Bowling, B. V., Huether, C. A., Wang, L., Myers, M. F., Markle, G. C., Dean, G. E., et al. (2008). Genetic literacy of undergraduate non-science majors and the impact of introductoy biology and genetics courses. BioScience, 58, 654660.
Buchanan, A. (2011). Cognitive enhancement and education. Theory and Research in Education, 2, 145162.
Buchanan, A., Brock, D., Daniels, N., & Wikler, D. (2000). From chance to choice: Genetics and justice. New York, NY: Cambridge.
Burton, A. (2009). Should patient confidentiality come second to the prevention of disease in others? The Lancet Oncology, 10, 210211.
Carew, T. J., & Magsamen, S. H. (2010). Neuroscience and education: An ideal partnership for producing evidence-based solutions to guide 21st century learning. Neuron, 67, 685688. doi:10.1016/j.neuron.2010.08.028
Clayton, E. W. (1997). Genetic testing in children. Journal of Medicine & Philosophy, 22, 233251.
Collier, R. (2012). Genetic tests for athletic ability: Science or snake oil? Canadian Medical Association Journal, 184, E43E44.
Davies, K. (2010). The $1,000 genome: The revolution in DNA sequencing and the new era of personalized medicine. New York, NY: Free Press.
Devonshire, I. M., & Dommett, E. J. (2010). Neuroscience: Viable applications in education? The Neuroscientist, 16, 349356. doi:10.1177/1073858410370900
Dickens, B. M., Pei, N., & Taylor, K. M. (1996). Legal and ethical issues in genetic testing and counseling for susceptibility to breast, ovarian and colon cancer. CMAJ Canadian Medical Association Journal, 154, 813818.
Dougherty, M. J., Pleasants, C., Solow, L., Wong, A., & Zhang, H. (2011). A comprehensive analysis of high school genetics standards: Are states keeping pace with modern genetics? CBE Life Sciences Education, 10, 318327. doi:10.1187/cbe.10-09-0122
Feero, W., & Green, E. D. (2011). Genomics education for health care professionals in the 21st century. JAMA, 306, 989990. doi:10.1001/jama.2011.1245
Fischer, K. W., Goswami, U., Geake, J., & the Task Force on the Future of Educational Neuroscience. (2010). The future of educational neuroscience. Mind, Brain, and Education, 4, 6880. doi:10.1111/j.1751-228X.2010.01086.x
Fisher, C. B., & Harrington McCarthy, E. L. (2013). Ethics in prevention science involving genetic testing. Prevention Science, 14, 310318. doi:10.1007/s11121-012-0318-x
Gollust, S. E., Hull, S. C., & Wilfond, B. S. (2002). Limitations of direct-to-consumer advertising for clinical genetic testing. JAMA, 288, 17621767.
Greenbaum, D. (2012). Introducing personal genomics to college athletes: Potentials and pitfalls. The American Journal of Bioethics, 12, 4547. doi:10.1080/15265161.2012.656811
Greenbaum, D., Sboner, A., Mu, X. J., & Gerstein, M. (2011). Genomics and privacy: Implications of the new reality of closed data for the field. PLoS Computational Biology, 7, e1002278.
Grigorenko, E. L. (2004). Genetic bases of developmental dyslexia: A capsule review of heritability estimates. Enfance, 3, 273287.
Grigorenko, E. L. (2005). A conservative meta-analysis of linkage and linkage-association studies of developmental dyslexia. Scientific Studies of Reading, 9, 285316.
Grigorenko, E. L. (2007a). Bridging genomics and education. Retrieved from
Grigorenko, E. L. (2007b). How can genomics inform education? Mind, Brain, and Education, 1, 2027.
Grigorenko, E. L. (2010). Bringing genomic sciences to the classroom. Science. Retrieved from
Grigorenko, E. L. (2015). Genomic sciences for developmentalists: A merge of science and practice. New Directions in Child and Adolescent Development, 147.
Gurwitz, D., & Bregman-Eschet, Y. (2009). Personal genomics services: Whose genomes? European Journal of Human Genetics, 17, 883889.
Guttmacher, A. E., Porteous, M. E., & McInerney, J. D. (2007). Educating health-care professionals about genetics and genomics. Nature Reviews Genetics, 8, 151157.
Gymrek, M., McGuire, A. L., Golan, D., Halperin, E., & Erlich, Y. (2013). Identifying personal genomes by surname inference. Science, 339, 321324. doi:10.1126/science.1229566
Hanson, J. W., & Thomson, E. J. (2000). Genetic testing in children: Ethical and social points to consider. Pediatric Annals, 29, 285291.
Hardiman, M., Rinne, L., Gregory, E., & Yarmolinskaya, J. (2012). Neuroethics, neuroeducation, and classroom teaching: Where the brain sciences meet pedagogy. Neuroethics(2), 135143. doi:10.1007/s12152-011-9116-6
Harris, J. (2007). Enhancing evolution: The ethical case for making better people. Princeton, NJ: Princeton University Press.
Henderson, B. J., & Maguire, B. T. (2000). Three lay mental models of disease inheritance. Social Science & Medicine, 50, 293301.
Hensley Alford, S., McBride, C. M., Reid, R. J., Larson, E. B., Baxevanis, A. D., & Brody, L. C. (2011). Participation in genetic testing research varies by social group. Public Health Genomics, 14, 8593.
Hook, C. C., DiMagno, E. P., & Tefferi, A. (2004). Primer on medical genomics, Part XIII: Ethical and regulatory issues. Mayo Clinic Proceedings, 79, 645650.
Hoppe, N. (2013). From omics to etics to policy and ethics: Regulating evolution. Frontiers in Genetics, 4, 12.
Howard-Jones, P. A., & Fenton, K. D. (2012). The need for interdisciplinary dialogue in developing ethical approaches to neuroeducational research. Neuroethics, 5, 119134. doi:10.1007/s12152-011-9101-0
Howard, H. C., Avard, D., & Borry, P. (2011). Are the kids really all right? Direct-to-consumer genetic testing in children: Are company policies clashing with professional norms? European Journal of Human Genetics, 19, 11221126. doi:10.1038/ejhg.2011.94
Jin, J. (2000). An evaluation of the Ethical, Legal and Social Implications program of the U.S. Human Genome Project. Princeton Journal of Bioethics, 3, 3550.
Kaye, J. (2008). The regulation of direct-to-consumer genetic tests. Human Molecular Genetics, 17(R2), 15.
Kegley, J. A. (1996). Using genetic information: The individual and the community. Medicine and Law, 15, 377389.
Khoury, M. J., McBride, C. M., Schully, S. D., Ioannidis, J. P. A., Feero, W. G., Janssens, A. C. J. W., et al. (2009). The Scientific Foundation for Personal Genomics: Recommendations from a National Institutes of Health-Centers for Disease Control and Prevention Multidisciplinary Workshop. Genetics in Medicine, 11(8), 559567.
Kingsberry, S. Q., Mickel, E., Wartel, S. G., & Holmes, V. (2011). An education model for integrating genetics and genomics into social work practice. Social Work in Public Health, 26, 392404. doi:10.1080/10911350902990924
Korf, B. R. (2011). Genetics and genomics education: The next generation. Genetics in Medicine, 13, 201202.
Kung, J. T., & Gelbart, M. E. (2012). Getting a head start: The importance of personal genetics education in high schools. Yale Journal of Biology & Medicine, 85, 8792.
Lacroix, M., Nycum, G., Godard, B., & Knoppers, B. M. (2008). Should physicians warn patients’ relatives of genetic risks? CMAJ Canadian Medical Association Journal, 178, 593595.
Lanie, A. D., Jayaratne, T. E., Sheldon, J. P., Kardia, S. L., Anderson, E. S., Feldbaum, M., et al. (2004). Exploring the public understanding of basic genetic concepts. Journal of Genetic Counseling, 13, 305320.
Lucassen, A., & Montgomery, J. (2010). Predictive genetic testing in children: Where are we now? An overview and a UK perspective. Familial Cancer, 9, 37.
Madsen, A. (2010, October 1). Peeking at “the cards you were dealt.” Quest, 17.
Maher, B. S. (2011). Human genetics: Genomes on prescription. Nature, 478, 2224. doi:10.1038/478022a
McConkie-Rosell, A., & Spiridigliozzi, G. A. (2004). “Family matters”: A conceptual framework for genetic testing in children. Journal of Genetic Counseling, 13, 929.
McGuire, A. L., & Burke, W. (2008). An unwelcome side effect of direct-to-consumer personal genome testing: Raiding the medical commons. JAMA, 300, 26692671.
Meslin, E. M., Thomson, E. J., & Boyer, J. T. (1997). The Ethical, Legal, and Social Implications Research Program at the National Human Genome Research Institute. Kennedy Institute of Ethics Journal, 7, 291298.
Middleton, A., Hewison, J., & Mueller, R. F. (1998). Attitudes of deaf adults toward genetic testing for hereditary deafness. American Journal of Human Genetics, 63, 11751180.
Mills Shaw, K. R., Van Horne, K., Zhang, H., & Boughman, J. (2008). Essay contest reveals misconceptions of high school students in genetics content. Genetics, 178, 11571168.
The National Cancer Institute. (2013). HINTS briefs: Public awareness of direct-to-consumer genetic tests. Washington, DC: The National Cancer Institute.
Nelkin, D., & Tancredi, L. (1991). Classify and control: Genetic information in the schools. American Journal of Law & Medicine, 17, 51.
Parker, M. (2010). Genetic testing in children and young people. Familial Cancer, 9, 1518.
Rodriguez, L. L., Brooks, L. D., Greenber, J. H., & Green, E. D. (2013). The complexities of genomic identifiability. Science, 339, 275276. doi:10.1126/science.1234593
Savulescu, J., & Bostrom, N. (Eds.). (2009). Human enhancement. New York, NY: Oxford University Press.
Serpati, L., & Loughan, A. R. (2012). Teacher perceptions of neuroeducation: A mixed methods survey of teachers in the United States. Mind, Brain & Education, 6, 174176. doi:10.1111/j.1751-228X.2012.01153.x
Skiba, T., Landi, N., Wagner, R., & Grigorenko, E. L. (2011). In search of the perfect phenotype: An analysis of linkage and association studies of reading and reading-related processes. Behavior Genetics, 41, 630.
Su, P. (2013). Direct-to-consumer genetic testing: A comprehensive view. Yale Journal of Biology and Medicine, 86, 359365.
Taylor, J., Roehrig, A. D., Soden Hensler, B., Connor, C. M., & Schatschneider, C. (2010). Teacher quality moderates the genetic effects on early reading. Science, 328, 512514.
Watson, J. D. (1990). The Human Genome Project: past, present, and future. Science, 248, 4449.
Wright, C. F., Hall, A., & Zimmern, R. L. (2011). Regulating direct-to-consumer genetic tests: What is all the fuss about? Genetics in Medicine, 13(4), 295300.