Center for Bioethics and Medical Humanities

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Program in Genomics and Ethics Related Publications


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.
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