307 results on '"Parker, Lisa S."'
Search Results
2. Responsible Adoption of Generative AI in Higher Education: Developing a 'Points to Consider' Approach Based on Faculty Perspectives
3. Genetic and Genomics Research
4. The Immortal Life of Henrietta Lacks , Feminist Themes, and Research Ethics
5. Social Justice, Federal Paternalism, and Feminism: Breast Implants in the Cultural Context of Female Beauty
6. 5. Genetic Research With Minority Populations
7. Ethical considerations in precision medicine
8. List of contributors
9. A new paradigm for investigating real-world social behavior and its neural underpinnings
10. Responsible Adoption of Generative AI in Higher Education: Developing a “Points to Consider” Approach Based on Faculty Perspectives
11. ‘Recurrent losers unite’: Online forums, evidence-based activism, and pregnancy loss
12. Breast Cancer Genetic Screening and Critical Bioethics’ Gaze 1
13. Narrative methods for assessing “quality of life” in hand transplantation: five case studies with bioethical commentary
14. Normative and conceptual ELSI research: what it is, and why it’s important
15. Chapter 7 - Ethical considerations in precision medicine
16. Answers to Questions that Weren’t Asked: The Ethical Complexities of Identifying Misattributed Paternity During the Transplant Evaluation Process
17. Advancing Pharmacogenomics Education in the Core PharmD Curriculum through Student Personal Genomic Testing
18. A new paradigm for investigating real-world social behavior and its neural underpinnings.
19. Preventive Ethics in the Management of Ophthalmic Genetic Disorders
20. Introduction
21. Autonomy's Limits: Living Donation and Health-Related Harm
22. Ethics of Organ Transplants
23. Ethical Expertise, Maternal Thinking, and the Work of Clinical Ethicists
24. Sickle Cell Trait Screening of Collegiate Athletes: Ethical Reasons for Program Reform
25. Incidental findings in the use of DNA to identify human remains: An ethical assessment
26. DNA Identification After Conflict or Disaster
27. Subtle Psychosocial Sequelae of Genetic Test Results
28. Answers to Questions that Weren’t Asked: The Ethical Complexities of Identifying Misattributed Paternity During the Transplant Evaluation Process
29. List of contributors
30. A New Paradigm for Investigating Real-World Social Behavior and its Neural Underpinnings
31. Caregivers as Subjects of Clinical Drug Trials: A Review of Human Subjects Protection Practices in Published Studies of Alzheimer's Disease Pharmacotherapies
32. Prenatal whole-exome sequencing: parental attitudes
33. Bioethics in the United States: 1989–1991
34. Practices and Attitudes toward Returning Genomic Research Results to Low-Resource Research Participants
35. Developing a Community-Academic Partnership to Improve Recognition and Treatment of Depression in Underserved African American and White Elders
36. Familial Coercion to Participate in Genetic Family Studies: Is There Cause for IRB Intervention?
37. Beauty and Breast Implantation: How Candidate Selection Affects Autonomy and Informed Consent
38. In Sport and Social Justice, Is Genetic Enhancement a Game Changer?
39. The Ethics of Tobacco Harm Reduction: An Analysis of E-Cigarette Availability From the Perspectives of Utilitarianism, Bioethics, and Public Health Ethics
40. Ethical dimensions of disparities in depression research and treatment in the pharmacogenomic era
41. Flattening the Rationing Curve: The Need for Explicit Guidelines for Implicit Rationing during the COVID-19 Pandemic
42. Ethical Practices and Legal Challenges in Mental Health Research
43. Research Use of Ecological Momentary Assessment for Adverse Event Monitoring Following Amyloid-β Results Disclosure
44. Susan M. Wolf (ed.): Feminism and Bioethics: Beyond Reproduction
45. The future of incidental findings: should they be viewed as benefits?
46. Managing incidental findings in human subjects research: analysis and recommendations.
47. The Consortium Ethics Program: An approach to establishing a permanent regional ethics network
48. Fulfilling the Underlying Purpose of Informed Consent to Research
49. An Agenda for the Future
50. Exceptions to the Legal Requirements: Emergency, Waiver, Therapeutic Privilege, and Compulsory Treatment
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