Things I finished reading in February 2023:
Books and dissertations
- Boyle, Philip J., ed. Getting doctors to listen: ethics and outcomes data in context. Georgetown University Press, 1998.
- Camfield, Laura Emma Lilian. Measuring quality of life in dystonia: an ethnography of contested representations. Diss. Goldsmiths, University of London, 2002.
- Cunningham III, Robert and Robert Cunningham Jr. The Blues: A History of the Blue Cross and Blue Shield System. Northern Illinois University Press, 1997.
- Dawkins, Holly V., and Annetine C. Gelijns, eds. Adopting new medical technology. National Academies Press, 1994.
- Elkins, James. The object stares back: On the nature of seeing. Houghton Mifflin Harcourt, 1997.
- Engebretsen, Eivind, and Mona Baker. Rethinking Evidence in the Time of Pandemics. Cambridge University Press, 2022.
- Galindo Salazar, Nicolás. “Lives made viable: trans possibilities and regulation in the context of Mexican mental healthcare institutions.” (2022).
- Gelijns, Annetine C., ed. Modern methods of clinical investigation. Institute of Medicine, 1990.
- Gelijns, Annetine C., ed. Technology and health care in an era of limits. National Academies Press, 1992.
- Gilman, Sander L. Making the Body Beautiful: A Cultural History of Aesthetic Surgery. Princeton University Press, 1999.
- Goodwin, Jeff, James M. Jasper, and Francesca Polletta, eds. Passionate politics: Emotions and social movements. University of Chicago Press, 2001.
- Gordon, Colin. Dead on arrival: The politics of health care in twentieth-century America. Vol. 18. Princeton University Press, 2009.
- Haider, Asad. Mistaken identity: race and class in the age of Trump. Verso Books, 2018.
- Nickerson, Michelle M. Mothers of conservatism: Women and the postwar right. Princeton University Press, 2012.
- Scott, William. Urology at Hopkins: a chronicle 1889-1986. James Buchanan Brady Urological Institute, 1987.
- Rappaport, Joanne. The politics of memory: Native historical interpretation in the Colombian Andes. Vol. 70. CUP Archive, 1990.
- Richardson, Henry S. Moral entanglements: the ancillary-care obligations of medical researchers. Oxford University Press, 2012.
- Ricoeur, Paul. Oneself as another. University of Chicago Press, 1992.
- Unger, Roberto Mangabeira. Politics: Volume 3, Social Theory: Its Situation and Its Task. Columbia University Press, 1987.
- Volf, Miroslav. The end of memory: Remembering rightly in a violent world. Wm. B. Eerdmans Publishing, 2021.
- Walsh, Patrick, and Janet Worthington. The Brady-100 years., James Buchanan Brady Urological Institute, 2015.
- Ziegler, Mary. Roe: The History of a National Obsession. Yale University Press, 2023.
Papers and Chapters
- Adair, Cassius, and Aren Aizura. ““The Transgender Craze Seducing Our [Sons]”; or, All the Trans Guys Are Just Dating Each Other.” Transgender Studies Quarterly 9.1 (2022): 44-64.
- Ahmed, Sara. “Who knows? Knowing strangers and strangerness.” Australian feminist studies 15.31 (2000): 49-68.
- Bal, P. Matthijs. “Why we should stop measuring performance and well-being.” Zeitschrift für Arbeits-und Organisationspsychologie (2020).
- Baldwin, Melinda. “Scientific autonomy, public accountability, and the rise of “peer review” in the Cold War United States.” Isis 109.3 (2018): 538-558.
- Barkun, Jeffrey S., et al. “Evaluation and stages of surgical innovations.” The Lancet 374.9695 (2009): 1089-1096.
- Bell, Kirsten. “Cochrane reviews and the behavioural turn in evidence-based medicine.” Health Sociology Review 21.3 (2012): 313-321.
- Berkwits, Michael. “From practice to research: the case for criticism in an age of evidence.” Social science & medicine 47.10 (1998): 1539-1545.
- Berenstain, Nora. “Cis Feminist Moves to Innocence” Hypatia (2023).
- Bluhm, Robyn. “Evidence-based medicine and patient autonomy.” IJFAB: International Journal of Feminist Approaches to Bioethics 2.2 (2009): 134-151.
- Bonchek, Lawrence I. “The role of the randomized clinical trial in the evaluation of new operations.” The Surgical clinics of North America 62.4 (1982): 761-769.
- Burke, Kelsy, et al. “LG but Not T: Opposition to Transgender Rights Amidst Gay and Lesbian Acceptance.” The Sociological Quarterly (2023): 1-22.
- Chaplyn, Georgia, et al. “Experiences of parents of trans young people accessing Australian health services for their child: Findings from Trans Pathways.” International Journal of Transgender Health (2023): 1-17.
- Cline, James S., and Keith A. Rosten. “The Effect of Policy Language on the Containment of Health Care Cost.” Tort & Insurance Law Journal (1985): 120-136.
- Eckert, Claudia, and Rafaela Hillerbrand. “Models in Engineering Design as Decision-Making Aids.” Engineering Studies 14.2 (2022): 134-157.
- Eddy, David M. “Investigational treatments: how strict should we be?.” JAMA 278.3 (1997): 179-185.
- Gilbert, John P., Bucknam McPeek, and Frederick Mosteller. “Statistics and ethics in surgery and anesthesia.” Science 198.4318 (1977): 684-689.
- Gill, Virginia Teas, and Douglas W. Maynard. “On “labeling” in actual interaction: Delivering and receiving diagnoses of developmental disabilities.” Social problems 42.1 (1995): 11-37.
- Gill, Virginia Teas. “Doing attributions in medical interaction: Patients’ explanations for illness and doctors’ responses.” Social Psychology Quarterly (1998): 342-360.
- Gill, Virginia Teas. “Patient” demand” for medical interventions: exerting pressure for an offer in a primary care clinic visit.” Research on Language and Social Interaction 38.4 (2005): 451-479.
- Gill, Virginia Teas, Anita Pomerantz, and Paul Denvir. “Pre‐emptive resistance: patients’ participation in diagnostic sense‐making activities.” Sociology of health & illness 32.1 (2010): 1-20.
- Gupta, M. “A critical appraisal of evidence‐based medicine: some ethical considerations.” Journal of evaluation in clinical practice 9.2 (2003): 111-121.
- Hanemaayer, Ariane. “Evidence-based medicine: a genealogy of the dominant science of medical education.” Journal of Medical Humanities 37 (2016): 449-473.
- Hutton, John, Paul Trueman, and Christopher Henshall. “Coverage with evidence development: an examination of conceptual and policy issues.” International journal of technology assessment in health care 23.4 (2007): 425-432.
- Kane, Bridget, and Saturnino Luz. “Achieving diagnosis by consensus.” Computer Supported Cooperative Work (CSCW) 18 (2009): 357-392.
- Lambert, Helen. “Accounting for EBM: notions of evidence in medicine.” Social science & medicine 62.11 (2006): 2633-2645.
- Livingstone, J. Leslie, and K. R. Balachandran. “Cost and effectiveness of physician peer review in reducing medicare overutilization.” Accounting, Organizations and Society 2.2 (1977): 153-164.
- Malterud, Kirsti. “The legitimacy of clinical knowledge: towards a medical epistemology embracing the art of medicine.” Theoretical medicine 16 (1995): 183-198.
- Miller, Franklin G., and Steven D. Pearson. “Coverage with Evidence Development Ethical Issues and Policy Implications.” Medical care (2008): 746-751.
- Molewijk, Albert C., et al. “Implicit normativity in evidence-based medicine: a plea for integrated empirical ethics research.” Health Care Analysis 11 (2003): 69-92.
- Pillow, Wanda. “Confession, catharsis, or cure? Rethinking the uses of reflexivity as methodological power in qualitative research.” International journal of qualitative studies in education 16.2 (2003): 175-196.
- Pushkar, Piyush, and Louise Tomkow. “Clinician-led evidence-based activism: a critical analysis.” Critical Public Health 31.2 (2021): 235-244.
- Reiser, Stanley Joel. “Criteria for standard versus experimental therapy.” Health Affairs 13.3 (1994): 127-136.
- Roberts, Derek J., et al. “Challenges and potential solutions to the evaluation, monitoring, and regulation of surgical innovations.” BMC surgery 19.1 (2019): 1-9.
- Sanabria, Emilia. “Circulating ignorance: Complexity and agnogenesis in the obesity “epidemic”.” Cultural Anthropology 31.1 (2016): 131-158.
- Sánchez-Holgado, Patricia, Carlos Arcila-Calderón, and Marcos Gomes-Barbosa. “Hate Speech and Polarization Around the “Trans Law” in Spain.” Politics and Governance 11.2 (2023).
- Schüklenk, Udo, et al. “The ethics of genetic research on sexual orientation.” Hastings Center Report 27.4 (1997): 6-13.
- Schüklenk, Udo, and Christopher Lowry. “Terminal illness and access to phase 1 experimental agents, surgeries and devices: reviewing the ethical arguments.” British medical bulletin 89.1 (2009): 7-22.
- Steinberg, Earl P., Sean Tunis, and David Shapiro. “Insurance coverage for experimental technologies.” Health Affairs 14.4 (1995): 143-158.
- Stradling, J. R., and R. J. O. Davies. “The unacceptable face of evidence‐based medicine.” Journal of Evaluation in Clinical Practice 3.2 (1997).
- Turowetz, Jason, Lucas Z. Wiscons, and Douglas W. Maynard. “Disorder or difference? How clinician‐patient interaction and patient age shape the process and meaning of autism diagnosis.” Sociology of Health & Illness (2023).