Publications
Interpreting Complexity, ed. M. Feldman, S.S. Lee, and J. McCormick. in preparation, Oxford: Oxford University Press.
Brown T. and K. Lowenberg. Biobanks, privacy, and the subpoena power. Stanford Journal of Science Policy and Law, forthcoming.
Brown T. and E. Murphy. Through A Scanner Darkly – functional neuroimaging as evidence of a criminal defendant’s past mental states. Stanford Law Review, 2009. 15.
Butte A.J. and I.S. Kohane. Creation and implications of a phenome-genome network. Nat Biotechnol, 2006. 24(1):55-62.
Caulfield T., Fullerton S.M., Ali-Khan S.E., Arbour L., Burchard E.G., Cooper R.S., et al. Race and ancestry in biomedical research: exploring the challenges. Genome Med, 2009. 1:8.
Caulfield T., McGuire A.L., Cho M., Buchanan J.A., Burgess M.M., Danilczyk U., et al. Research ethics recommendations for whole genome research: consensus statement. PLoS Biol, 2008.6(3):e73.
Cho M.K., Sabeti P.C. and S.A. Tishkoff. Ethical and social implications of research on natural selection in humans. Trends Genet, in press.
Cho M.K. Understanding incidental findings in the context of genetics and genomics. J Law Med Ethics, 2008. 36(2):280-25.
Cho M.K. Translating genomics into the clinic: moving to the post-Mendelian world. Genome Med, 2009. 1:7.
Cho M.K., Tobin S.L., Greely H.T., McCormick J., Boyce A. and D. Magnus. Research ethics consultation: the Stanford experience. IRB: Ethics & Human Research, 2008. 30(6):1-6.
Cho M.K., Tobin S.L., Greely H.T., McCormick J., Boyce A. and D. Magnus. Response to open peer commentaries on "Strangers at the benchside: research ethics consultation." Am J Bioeth, 2008. 8:4-6.
Cho M.K., Tobin S.L., Greely H.T., McCormick J., Boyce A. and D. Magnus. Strangers at the benchside: research ethics consultation. Am J Bioeth, 2008. 8(3): 4-13.
Cho M.K. Racial and ethnic categories in biomedical research: There is no baby in the bathwater. Am J Law Med Ethics, 2006. 34(3):497-9.
Cho M., McGee G., and D. Magnus, Lessons of the stem cell scandal. Science, 2006. 311:614-5.
Crawley L.M., Ahn D.K. and M.A. Winkleby. Perceived medical discrimination and cancer screening behaviors of racial and ethnic inority adults. Cancer Epidemiol Biomarkers Prev, 2008. 17(8):1937-44.
Crawley L. The paradox of race in the Bidil® debate. J Natl Med Assoc, 2007. 99(7):821-2.
Greely H.T. "Who Knows What Evil Lurks in the Hearts of Men?": Behavioral Genomics, Neuroscience, Criminal Law, and the Search for Hidden Knowledge, in The Impact of Behavioral Sciences on the Criminal Law, N. Farahany, Editor. 2009, Oxford University Press.
Greely H.T. Genetic Genealogy: Genetics Meets the Marketplace, in Revisiting Race in a Genomic Age, B.A. Koenig, S.S. Lee, and S.S. Richardson, Editors. 2008, Rutgers University Press: New Brunswick. p. 271-99.
Greely H. The genetics of fear. Democracy, Summer 2008: p. 55-60. 19.
Greely H.T. Within You, Without You, in Imagining Science. T. Caulfield and S. Caulfield, Editors. 2008, Alberta University Press.
Greely H.T. The uneasy ethical and legal underpinnings of large-scale genomic biobanks. Annu Rev Genomics Hum Genet, 2007. 8:343-64.
Greely H., Cho M., Hogle L., and D. Satz. Thinking about the human neuron mouse. American Journal of Bioethics: Neuroscience. 2007 May/June. 7(5): p. 27-40. 20.
Greely H., Cho M., Hogle L., and D. Satz. Response to peer commentaries. American Journal of Bioethics: Neuroscience, 2007 May/June. 7(5): p. W4-6.
Greely H.T., Knowing Sin: Making Sure Good Science Doesn't Go Bad, in Cerebrum 2007: Emerging Ideas in Brain Science, C.A. Read, Editor. 2007, Dana Press: New York.
Greely H.T. Stanford symposium on preimplantation genetic diagnosis: an introduction - and some conclusions. Fertil Steril, 2006. 85:1631-2. (and edited the four article symposium)
Greely H.T. Neuroethics and ELSI: similarities and differences. Minn J L Sci & Tech, 2006. 7:599-637.
Greely H.T. Electronic transfer of medical records in clinical care and research: an irresistible force meets a moveable object in Biological Material and Electronic Data: Much Ado About Nothing?, B.M. Knoppers and C. Hervé, Editors. 2006, Les Études Hospitalières: Bordeaux. p. 35-50.
Greely H.T., Riordan D.P., Garrison N.A. and J. L. Mountain. Family ties: the use of DNA offender databases to catch offenders' kin. J Law Med Ethics, 2006. 34:248-62.
Greely H.T. Regulating human biological enhancements: questionable justifications and international complications. The Mind, The Body and the Law: University of Technology, Sydney, Law Review. 2005. 7:87-110./Santa Clara J Int'l L, 2006. 4:87-110. (joint issue)
Greely H.T. Banning genetic discrimination. N Engl J Med, 2005. 353(9):865-7.
Greely H.T. Population participation and other factors that impact the compilation and the utility of resulting databases. LA L Rev, 2005. 66:79-90.
Greely H.T. Disabilities, enhancements, and the meanings of sports. Stanford Law & Policy Review, 2004 Spring. 15(2): p. 99-132.
Greely H.T. Genetic modification, review of Designing Our Descendants: The Promises and Perils of Genetic Modifications, Audry R. Chapman, Mark S. Frankel, ed. JAMA, 2004 Sept. 292: p. 1374-5. 23.
Greely H.T. Human genetic enhancement: a lawyer's view, review of Wondergenes: Genetic Enhancement and the Future of Society by Maxwell J. Mehlman. Med Humanit Rev, 2003 Fall. 17(No. 2): p. 42-6. 22.
Illes J., Kirschen M.P., Edwards E., Bandettini P., Cho M.K., Ford, P.J., et al. Practical approaches to incidental findings in brain imaging research. Neurology, 2008. 70:384-90.
Illes J., Kirschen M.P., Edwards E., Stanford L.R., Bandettini P., Cho M.K., et al. Ethics: Incidental findings in brain imaging research. Science, 2006. 311:783-4.
Illes J., De Vries R., Cho M. and P. Schraedley-Desmond. From genetics to neuroethics: ELSI priorities for brain imaging. Am J Bioeth, 2006. 6(2):W24-31.
Karp D.R., Carlin S., Cook-Deegan R., Ford D.E., Geller G., Glass D.N., et al. Ethical and practical issues associated with aggregating databases. PLoS Med, 2008. 5(9): p. e190.
Koenig B., Lee S.S. and S.S. Richardson. Introduction, in Revisiting Race in a Genomic Age, B.A. Koenig, S.S. Lee and S.S. Richardson, Editors. 2008, Rutgers University Press: New Brunswick.
Lee S.S. In Search of Difference in the New Genetics: Race, Science and Justice. in preparation, New York: Routledge Press. (book length manuscript)
Lee S.S. and L. Crawley. Response to open peer commentaries on "Research 2.0: social networking and DTC genomics." Am J Bioeth. 2009;9(6):W1-W3.
Lee S.S., Bolnick D.A., Duster T., Ossorio P. and K. Tallbear. Genetics: The illusive gold standard in genetic ancestry testing. Science. 2009;325(5936):38-39.
Lee S.S. and L. Crawley. Research 2.0: social networking and DTC genomics. Am J Bioeth. 2009;9(6):35-44.
Lee S.S. and A. Mudaliar. Racing forward: the Genomics and Personalized Medicine Act. Science, 2009. 323(6912):342.
Lee S.S., Mountain J., Koenig B., Altman R., Brown M., Camarillo A., et al. The ethics of characterizing difference: guiding principles on using racial categories in human genetics. Genome Biol, 2008. 9(7): 404.
Lee S.S. Racial Realism: Reframing Disparity into Difference, in Revisiting Race in a Genomic Age, B.A. Koenig, S.S. Lee, and S.S. Richardson, Editors. 2008, Rutgers University Press: New Brunswick.
Lee S.S. The ethical implications of stratifying by race in pharmacogenomics. Clin Pharmacol Ther, 2006. 81(1):122-5.
Lee S.S. The politics of hope: dreaming in a genomic age. Science, 2006. 313:1888-9. (Invited Review).
Lee S.S. Identifying "race" in the new genetics: bio-banks of a kind. Patterns Prejudice. Editor: Sander L. Gilman., 2006. 40(Nos 4, 5):443-60.
Lee S.S., Mountain J. and B.A. Koenig, The Meanings of Race in the New Genomics, in The Social Contributions to Health, Difference and Inequality: The Social Medicine Reader 2nd Edition, Volume II, G.E. Henderson, et al., Editors. 2005, Duke University Press.
Lee S.S. "Racializing drug design”: pharmacogenomics and implications for health disparities. Am J Public Health, 2005. 95(12):2133-8.
Lee S.S. Personalized medicine and pharmacogenomics: ethical and social challenges. Per Med, 2005. 2(1):29-35.
Liu Y.I., Wise P.H. and A.J. Butte. The "etiome": identification and clustering of human disease etiological factors. BMC Bioinformatics, 2009. 10(Suppl 2):S14.
Magnus D., Cho M.K. and R. Cook-Deegan. Direct-to-consumer genetic tests: beyond medical regulation? Genome Med, 2009. 1:17.
Magnus D. The ethics of preimplantation genetic diagnosis. Fertility Today, 2005. 1(1).
McCormick J. and S.S. Lee, eds. Capturing complexity: the scientific, societal and ethical meanings of "environment" in genetic research. BMC Genet, Special issue, in press.
McCormick J.B., Boyce A.M. and M.K. Cho. Biomedical scientists' perceptions of ethical and social implications: is there a role for research ethics consultation? PLoS ONE, 2009. 4(3): e4659.
McGuire A., Caulfield T. and M. Cho. Research ethics and the challenge of whole genome sequencing. Nat Rev Genet, 2007. 9:152-56.
McGuire A.L., Cho M.K., McGuire S.E. and T. Caulfield. The future of personal genomics. Science, 2007. 317(5845):1687.
Ormond K.E., Cirino A.L, Helenowski I.B., Chisholm R.L. and W.A. Wolf. Assessing the understanding of biobank participants. Am J Med Genet A, 2009. 149A(2):188-98.
Ormond K.E., Banuvar S., Daly A., Iris M., Minogue J., and S. Elias. Information preferences of high literacy pregnant women regarding informed consent models for genetic carrier screening. Patient Educ Couns. 2009;75(2):244-250.
Sankar P., Cho M.K. and J. Mountain. Race and ethnicity in genetic research. Am J Med Genet, 2007. 143A(9):961-70.
Singh J., Illes J., Lazzeroni L. and J. Hallmayer. Trends in US autism research funding. J Autism Dev Disord, 2009. [Epub aead of print]
Singh J., Hallmayer J. and J. Illes. Interacting and paradoxical forces in neuroscience and society. Nat Rev Neurosci, 2007. 8(2):153-60.
Tabor H.K. and M.K. Cho. Ethical implications of array comparative genomic hybridization in complex phenotypes: points to consider in research. Genet Med, 2007. 9(9):626-31.
Wolf S.M., Lawrenz F.P., Nelson C.A., Kahn J.P., Cho M.K., Clayton E.W., et al. Managing incidental findings in human subjects research: analysis and recommendations. J Law Med Ethics, 2008. 36(2): 219-48.
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