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In the Media
Exploring the Ethics of Genetic Testing: Where Does Duty Begin and End?
Technology Networks |Holly Large- genetic testing
- Ethics
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In the Media
Citizen jury will deliberate on gene-editing regulation and ethics
Mirage News |- Gene Editing
- Regulation
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In the Media
‘It Will Consume Your Life’: 4 Families Take on Rare Diseases
The New York Times |Gina Kolata- Rare Diseases
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In the Media
The Ethics of Genetics Testing: “Duty of Care”, Consent and Data Security PODCAST Opinionated Science: Episode 9
Technology Networks |Laura Elizabeth Lansdowne, Ruairi J MacKenzie, Molly Campbell, Holly Large- Ethics
- genetic testing
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In the Media
The Wilderness of Rare Genetic Diseases and the Parents Navigating It
The New York Times |Brendan Borrell- Genetic Diseases
- Parents
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In the Media
We need to talk about big data and genomics. Here's why – and how
The European Sting |Anna Middleton- Genomics
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Grant Abstract
Implementation and Implications of Sickle Cell Trait Screening in the NCAA
PROJECT NARRATIVE The sickle cell trait (SCT) screening program of the National Collegiate Athletic Association (NCAA) is regarded as one of the largest mandated genetic screening programs in the…- Address
- Adopted
- Affect
- African American student
- Area
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Grant Abstract
Genomics, Biometrics and Identity
Public Health Relevance Section Policies in the U.S. increasingly rely upon genomic information as a biometric to inform visa application processes, by verifying biological relationship claims or…- Advocate
- Affect
- Attention
- authority
- base
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Grant Abstract
The Stanford Training Program in ELSI Research
PUBLIC HEALTH RELEVANCE The proposed research training program at Stanford University is to create independent scholars who can conduct rigorous research on ethical, legal and social implications…- Research
- Training Programs