All Stories

  1. Revisions to the Common Rule: A proposal in search of evidence
  2. The Human Genome Project, and recent advances in personalized genomics
  3. Education and Parental Involvement in Decision-Making About Newborn Screening: Understanding Goals to Clarify Content
  4. Personalized medicine and genome-based treatments: Why personalized medicine ≠ individualized treatments
  5. Stakeholder attitudes towards the role and application of informed consent for newborn bloodspot screening: a study protocol
  6. Benefits and burdens of newborn screening: public understanding and decision-making
  7. Too many crying babies: a systematic review of pain management practices during immunizations on YouTube
  8. Schools and Childhood Obesity
  9. Childhood Obesity
  10. Childhood Obesity and Parental Responsibility
  11. Childhood Obesity Interventions, Equity, and Social Justice
  12. Childhood Obesity and the “Obesogenic Environment”
  13. Introduction
  14. Empirical Uncertainty
  15. Normative Uncertainty
  16. Stigma and Weight Bias
  17. Conclusion
  18. Price Policies as Strategies for Obesity Prevention
  19. Responding to Food Marketing Targeted at Children
  20. Impact of stated barriers on proposed warfarin prescription for atrial fibrillation: a survey of Canadian physicians
  21. Parental Decision-Making and Acceptance of Newborn Bloodspot Screening: An Exploratory Study
  22. Public attitudes towards genomic risk profiling as a component of routine population screening 1
  23. Considering consent: a structural equation modelling analysis of factors influencing decisional quality when accepting newborn screening
  24. Standards and classification: A perspective on the ‘obesity epidemic’
  25. Informed Choice for Newborn Blood Spot Screening in the United Kingdom: A Survey of Parental Perceptions
  26. Informed Choice for Newborn Blood Spot Screening in the United Kingdom: A Survey of Parental Perceptions
  27. Social science and ethics review: A question of practice not principle
  28. Parental information use in the context of newborn bloodspot screening. An exploratory mixed methods study
  29. Public Perceptions of Genomic Risk Profiling for Assessing Risk of Colorectal Cancer
  30. Proceduralisation, choice and parental reflections on decisions to accept newborn bloodspot screening
  31. Fiscal food policy: Equity and practice
  32. Knowledge or Understanding? Informed Choice in the Context of Newborn Bloodspot Screening
  33. Patient Empowerment in Clinical Genetics Services
  34. What process attributes of clinical genetics services could maximise patient benefits?
  35. Outcome Measurement in Clinical Genetics Services: A Systematic Review of Validated Measures
  36. Outcome measures for clinical genetics services: A comparison of genetics healthcare professionals and patients’ views
  37. Improving Service Evaluation in Clinical Genetics: Identifying Effects of Genetic Diseases on Individuals and Families
  38. The emotional effects of genetic diseases: Implications for clinical genetics