Select Faculty Publications Prior to WSU Appointment

Pandemic Preparedness and Response

  • Nature, “Isolation is not the answer: International scientific collaboration is the best defence against bioterror,” vol. 429, no. 6992 (10 June, 2004).
  • Science, “Bioterrorism Defense Priorities,” 301 (4 July, 2003).
  • Science, “Wrong Turns from Worst Worries,” (invited book review essay) 329 (24 Sept. 2010).
  • JAMA, “Bioethics and Armed Conflict,” (invited book review essay), 298, no. 5 (Aug. 1, 2007).
  • JAMA,“Biological Weapons,” (invited book review essay), 294, no. 22 (Dec. 14, 2005).
  • American Journal of Public Health “Expanding Bioshield: A Call for Caution,” vol. 97, no. S1 (2007).
  • Vaccine, “‘Clustering of Exemptions’ as a Collective Action Threat to Herd Immunity,” vol. 21, nos. 11&12 (2003).
  • Human Vaccines, “Free-Riding, Fairness, and the Rights of Minority Groups in Exemption from Mandatory Childhood Vaccination,” vol. 1, no. 1 (2005).
  • Expert Review of Vaccines, “Vaccines as Community-Oriented Therapy,” vol. 2, no. 3 (2003).
  • American Journal of Bioethics. Ethics, Pandemics, and the Duty to Treat. vol. 8, no. 8, (2008).
  • Hastings Center Report, “The Smallpox Vaccination of Healthcare Workers: Professional Obligations and Defense Against Bioterrorism,” vol. 33, no. 5 (2003).

Clinical and Research Ethics

  • Encyclopedia of Bioethics, 4th Edition (MacMillan Publishers, 2014). “Rights of Conscience”.
  • Encyclopedia of Bioethics, 3rd Edition (MacMillan Publishers, 2003). “Rights of Conscience”.
  • American Philosophical Quarterly vol.31, no.2 (1994). “The Concept of Autonomy”.
  • Academic Medicine, “IRBs, Hospital Ethics Committees, and the Need for ‘Translational Informed Consent’,” vol. 82, no. 7 (2007).
  • Journal of Clinical Ethics “Evaluating the Outcomes of Ethics Consultation,” vol. 17, no. 2 (2006)
  • Journal of Law, Medicine and Ethics, More Than Cheating: Deception, IRB Shopping, and the Normative Legitimacy of IRBs,” vol. 40, no. 4 (2012).
  • Milbank Quarterly “Patients, Families and Organ Donation: Who Should Decide?” vol.78, no.2 (2000).
  • Perspectives in Biology and Medicine “Personal Morality and Professional Obligations: Rights of Conscience and Informed Consent,” vol. 52 no. 1 (2009).

Genetics

  • Monist, “Autonomy, Full Information, and Genetic Ignorance in Reproductive Medicine,” 89(4), (2006).
  • American Journal of Bioethics, “Does lack of ‘Genetic relative Family Health History’ represent a potentially avoidable health disparity for adoptees?” vol. 16, no. 12 (2016).
  • Pediatrics, “An Adoptive Parental Perspective on Personal Genomic Screening,” vol. 135, no. 5 (2015).
  • Genetics in Medicine, “In sickness and in health: Context matters when considering potential benefits and risks of genome-wide sequencing,” vol. 17, no. 8 (2015).
  • Journal of Law, Medicine and Ethics, “On the Justifiability of ACMG Recommendations for Reporting of Incidental Findings in Clinical Exome and Genome Sequencing,” vol. 43, no. 1 (Spring, 2015).
  • American Journal of Bioethics, “Re-Thinking Clinical Risk for DNA Sequencing,” vol. 12, no. 10 (2012).
  • Pediatrics, “On the Ethics of Whole Genome Sequencing of Children,” vol. 132, no. 2 (2013).