| The Opioid Crisis in Black Communities |
28 |
| Health Research with Big Data: Time for Systemic Oversight |
17 |
| The EU General Data Protection Regulation: Implications for International Scientific Research in the Digital Era |
13 |
| Design Issues in E-Consent |
12 |
| State Responses to the Opioid Crisis |
9 |
| Broadband Access as a Public Health Issue: The Role of Law in Expanding Broadband Access and Connecting Underserved Communities for Better Health Outcomes |
8 |
| Civil Litigation and the Opioid Epidemic: The Role of Courts in a National Health Crisis |
8 |
| The Opioid Epidemic in Indian Country |
7 |
| The Impact of Prescription Drug Monitoring Programs on US Opioid Prescriptions |
7 |
| Time to End the Use of Genetic Test Results in Life Insurance Underwriting |
7 |
| Determination of Death by Neurologic Criteria in the United States: The Case for Revising the Uniform Determination of Death Act |
7 |
| Capacity, Vulnerability, and Informed Consent for Research |
6 |
| Health Equity, School Discipline Reform, and Restorative Justice |
5 |
| Situated Prevention: Framing the New Dementia |
5 |
| Seeing Beyond the Margins: Challenges to Informed Inclusion of Vulnerable Populations in Research |
5 |
| Alzheimer Disease: Perspectives from Epidemiology and Genetics |
4 |
| Pragmatic Tools for Sharing Genomic Research Results with the Relatives of Living and Deceased Research Participants |
4 |
| Fentanyl: A Whole New World? |
4 |
| The Role of Civil Commitment in the Opioid Crisis |
4 |
| Big Data and the Opioid Crisis: Balancing Patient Privacy with Public Health |
4 |
| Genomic Data-Sharing Practices |
4 |
| Importance of Participant-Centricity and Trust for a Sustainable Medical Information Commons |
3 |
| The Reasonable Person Standard for Research Disclosure: A Reasonable Addition to the Common Rule |
3 |
| Implementing Regulatory Broad Consent Under the Revised Common Rule: Clarifying Key Points and the Need for Evidence |
3 |
| Breastfeeding with HIV: An Evidence-Based Case for New Policy |
3 |
| Considering Quality of Life while Repudiating Disability Injustice: A Pathways Approach to Setting Priorities |
3 |
| Antibiotic Pipeline Coordinators |
3 |
| A Grant Framework as a Push Incentive to Stimulate Research and Development of New Antibiotics |
3 |
| Moral Limits of Brain Organoid Research |
3 |
| Cross Sector Data Sharing: Necessity, Challenge, and Hope |
3 |
| Informed Consent in Translational Genomics: Insufficient Without Trustworthy Governance |
3 |
| Bundling Justice: Medicaid's Support for Housing |
3 |
| The Role of Community Health Needs Assessments in Medicalizing Poverty |
3 |
| Dementia, Healthcare Decision Making, and Disability Law |
2 |
| The Impact of Regulatory Policies on the Future of Fecal Microbiota Transplantation |
2 |
| Vaginal Microbiota Transplantation: The Next Frontier |
2 |
| Public Health Surveillance: Electronic Reporting as a Point of Reference |
2 |
| Medical-Legal Partnership: Lessons from Five Diverse MLPs in New Haven, Connecticut |
2 |
| Healthy People: The Role of Law and Policy in the Nation's Public Health Agenda |
2 |
| Where Did Informed Consent for Research Come From? |
2 |
| Avoiding Exploitation in Phase I Clinical Trials: More than (Un)Just Compensation |
2 |
| Striving for Health Equity through Medical, Public Health, and Legal Collaboration |
2 |
| Emergency Declarations for Public Health Issues: Expanding Our Definition of Emergency |
2 |
| The Ethical and Public Health Implications of Family Separation |
2 |
| A Genomically Informed Education System? Challenges for Behavioral Genetics |
2 |
| Opening Closed Doors: Promoting IRB Transparency |
2 |
| Child Trafficking: Issues for Policy and Practice |
2 |
| Opioid Crisis in the US - Lessons from Western Europe |
2 |
| Privacy Risks of Interoperable Electronic Health Records: Segmentation of Sensitive Information Will Help |
2 |
| Pain and Addiction in Specialty and Primary Care: The Bookends of a Crisis |
2 |
