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Publication
Key informant perspectives on implementing genomic newborn screening: A qualitative study guided by the Action, Actor, Context, Target, Time framework
European Journal of Human Genetics -
Publication
Perceptions and preferences for genetic testing for sickle cell disease or trait: A qualitative study in Cameroon, Ghana and Tanzania
European Journal of Human Genetics -
Publication
Who’s on your genomics research team? Consumer experiences from Australia
Public Health Genomics -
Publication
The biggest struggle: Navigating trust and uncertainty in genetic variant interpretation
Public Health Genomics -
Publication
Co-creating the experience of consent for newborn genome sequencing: The Generation Study
Public Health Genomics -
Publication
Challenges of uncertainty in prenatal decision-making: Skeletal dysplasias
Journal of Law, Medicine & Ethics -
Publication
“A double-edged sword”: A brief history of genomic data governance and genetic researcher perspectives on data sharing
Journal of Law, Medicine & Ethics -
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Publication
Public perspectives on consent for and governance of biobanking in Japan
Journal of Empirical Research on Human Research Ethics