|
Voices of Women With Lived Experience of Substance Use During Pregnancy : A Qualitative Study of Motivators and Barriers to Recruitment and Retention in Research |
2023 |
Journal Article |
|
Ethical Responsibilities for Companies That Process Personal Data |
2023 |
Journal Article |
|
No person left behind: Mapping the health policy landscape for genomics research in the Caribbean |
2022 |
Journal Article |
|
Polygenic risk in a diverse world |
2021-02-05 |
Journal Article |
|
Integrating Rules for Genomic Research, Clinical Care, Public Health Screening and DTC Testing: Creating Translational Law for Translational Genomics |
2021-01-01 |
Journal Article |
|
A Socioecological Framework for Engaging Pregnant Substance-Using Women in Research: Multi-Stakeholder Perspectives |
2021 |
Journal Article |
|
FMT and Microbial Medical Products: Generating High-Quality Evidence through Good Governance |
2020 |
Journal Article |
|
How Can Law and Policy Advance Quality in Genomic Analysis and Interpretation for Clinical Care |
2020 |
Journal Article |
|
Inclusion of American Indians and Alaskan Natives in Large National Studies: Ethical Considerations and Implications for Biospecimen Collection in the HEALthy Brain and Child Development Study |
2020 |
Journal Article |
|
Regulating stool for microbiota transplantation |
2019 |
Journal Article |
|
Do No Harm – A Roadmap for Responsible Machine Learning for Healthcare |
2019 |
Journal Article |
|
The Challenge of Regulating Clinical Decision Support Software After 21st Century Cures |
2018 |
Journal Article |
|
Fairness in Manufacturing Cellular Therapies |
2018 |
Journal Article |
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Genotype-Driven Recruitment Without Deception |
2017 |
Journal Article |
|
Why we Should Not Use the Affordable Care Act to Encourage Widespread Whole Genome Sequencing |
2014 |
Journal Article |
|
The Ethics of Translating High-Throughput Science into Clinical Practice |
2014 |
Journal Article |
|
Clines Without Classes: How to Make Sense of Human Variation |
2014 |
Journal Article |
|
Repositories for Sharing Human Data in Stem Cell Research |
2014 |
Book Section |
|
Reflections on the Cost of "Low-Cost" Whole Genome Sequencing: Framing the Health Policy Debate |
2013-11 |
Journal Article |
|
Regulation of Online Social Network Studies |
2013-01 |
Journal Article |
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Managing Incidental Findings and Research Results in Genomic Research Involving Biobanks and Archived Data Sets |
2012 |
Journal Article |
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Taking Aims Seriously: Repository Research and Limits on Duty to Return Individual Research Findings |
2012 |
Journal Article |
|
Bodies of Data: Genomic Data and Bioscience Data Sharing |
2011 |
Journal Article |
|
Myth and Mystification |
2011 |
Book Section |
|
Race, Genes and Intelligence |
2010 |
Journal Article |
