Program in Genomics and Ethics
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  2015 Publications

Marcus, R.K., Geurts, J.L., Grzybowski, J.A., Turaga, K.K., Gamblin, T.C., Strong, K.A., Johnston, F.M. Challenges to Clinical Utilization of Hereditary Cancer Gene Panel Testing: Perspectives from the Front Lines. Familial Cancer. (In Press - accepted June 7, 2015)

Strong, K.A., May, T., Levy,S. In sickness and in health: Context matters when considering potential benefits and risks of genome-wide sequencing. Genetics in Medicine. (In Press - accepted May 18, 2015).

Strong, K.A., Becoming the "subject" of my own study. Narrative Inquiry in Bioethics. 2015; 5(3). (In Press - accepted May 5, 2015).

May, T. Strong, K.A., Khoury, M.J., Evans, J.P. Can targeted genetic testing offer useful health information to adoptees? Genetics in Medicine, (2015) 17: 533-535. doi: 10.1038/gim.2015.58.

May, T. An adoptive parental perspective on personal genomic screening. Pediatrics, 2015 Apr; 135(4): e811-4. doi:10.1542/peds.2014-3026.

May, T. On the justifiability of ACMG Recommendations for return of incidental findings from clinical exome and genome sequencing. Journal of Law, Medicine and Ethics. 2015 Mar; 43(1): 134-42. doi: 10.111/jlme.12201.

  2014 Publications

May, T., Zusevics, K.L., Derse, A., Strong, K.A., Jeruzal, J., La Pean Kirschner, A., Farrell, M.H., Spellecy, R. The limits of traditional approaches to informed consent for genomics medicine. Health Care Ethics Committee Forum, 2014 Sep; 26(3): 185-202. doi: 10.1007/s10730-014-9247-3.

Strong, K.A., Zusevics, K.L., Bick, D., Veith, R. Views of non-medical professionals regarding the return of whole genome sequencing incidental findings. Wisconsin Medical Journal, 2014, 113(5): 11-16. doi: 10.1111/cge.12390

Zusevics, K.L., Strong, K.A., Farrell, M., Shimoyama, M.E. Matching the pace of genomic advances through the integration of genomic education in to high school education. Journal of School Health, 2014, 84(6): 351-4. doi: 10.1111/josh.12160.

Strong, K.A., Zusevics, K.L., Bick, D., Veith, R. Views of primary care providers regarding the return of genome sequencing incidental findings. Clinical Genetics, 2014 Nov; 86(5): 461-8. doi: 10.1111/cge.12390.

Strong, K.A., Kerridge, I., Little, J.M. Savior siblings, parenting and the moral valorization of children. Bioethics, 2014, 8(4), 187-193. doi: 10.1111/j.1467-8519.2012.02001

Strong, K.A., Derse, A.R., Dimmock, D.P., Zusevics, K.L., Jeruzal, J., Worthey, E., Bick, D., Scharer, G., La Pean Kirschner, A., Spellecy, R., Farrell, M.H., Geurts, J., Veith, R., May, T. In the absence of evidentiary harm, existing societal norms regarding parental authority should prevail. The American Journal of Bioethics : AJOB, 14(3), 24-6. doi: 10.1080/15265161.2013.879959.

  2013 Publications

Zusevics, K. L. (2013). Public health genomics: A new space for a dialogue on racism through community based participatory research. Public Health, 127(11), 981-983. doi:10.1016/j.puhe.2013.09.011; 10.1016/j.puhe.2013.09.011&

Jacob, H. J., Abrams, K., Bick, D. P., Brodie, K., Dimmock, D. P., Farrell, M., Geurts, J.L., Harris, J., Helbling, D.C., Joers, B.J., Kliegman, R., Kowalski, G., Lazar, J., Margolis, D.A., North, P.E., Northup, J., Roquemore-Goins, A., Scharer, G., Shimoyama, M., Strong, K.A., Tayolor, B.W., Tsaih, S., Tschannen, M.R., Veith, R.L., Wendt, Andre, J., Wilk, B., Worthey, E. A. (2013). Genomics in clinical practice: Lessons from the front lines. Science Translational Medicine,5(194), 194cm5. doi:10.1126/scitranslmed.3006468; 10.1126/scitranslmed.3006468

Lemke, A. A., Bick, D., Dimmock, D., Simpson, P., & Veith, R. (2013). Perspectives of clinical genetics professionals toward genome sequencing and incidental findings: A survey study. Clinical Genetics, 84(3), 230-236. doi:10.1111/cge.12060; 10.1111/cge.12060

May, T., Zusevics, K. L., & Strong, K. A. (2013). On the ethics of clinical whole genome sequencing of children. Pediatrics, 132(2), 207-209. doi:10.1542/peds.2012-3788; 10.1542/peds.2012-3788

Zusevics, K. (2013). Ancillary care, genomics, and the need and opportunity for community-based participatory research. The American Journal of Bioethics : AJOB, 13(2), 54-56. doi:10.1080/15265161.2012.754065; 10.1080/15265161.2012.754065

  2012 Publications

May, T. (2012). Rethinking clinical risk for DNA sequencing. The American Journal of Bioethics: 12 (10), 24-26. doi:10.1080/15265161.2012.699152; 10.1080/15265161.2012.699152

  2006 Publications

May, T. and Spellecy, R. (2006) Autonomy, full information and genetic ignorance in reproductive medicine. The Monist, 89(4): 466-81.: 12 (10), 24-26.