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1081 - 1090 of 3992 Topics
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Publication
Ethics of the new biology and genetic medicine (molecular ethics): Brief (re)view from the USA
Pathology InternationalDigital citation created by the Bioethics Research Library, Georgetown University, for the National Information Resource on Ethics and Human Genetics, a project funded by the United States National… -
Research Tool
Codebook: Assessment of a Video and Survey about Expanded Carrier Screening
This study assessed the impact of a video and survey about expanded carrier screening on patient knowledge and decision making. The REDCap codebook for this study outlines each data element of the… -
Research Tool
Codebook: The Influence of Genetic Testing on Redirection of Care in the NICU
Mowery and colleagues conducted a descriptive study characterizing the influence of genetic testing on redirecting care for neo-nates. The REDCap codebook for this study outlines each data element of… -
Research Tool
Codebook: Newborn Screening Residuals
This study evaluated public opinion about the policies and practices relevant to the retention and use of residual bloodspots for biomedical research. The REDCap codebook for this study outlines each… -
Additional Resource
Accessibility, Inclusion, and Action in Medical Education
This report by the Association of American Medical Colleges (AAMC) and the University of California, San Francisco, School of Medicine (UCSF) shares the day-to-day experiences of learners and…- accessibility
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Publication
Categorizing genetic tests to identify their ethical, legal, and social implications
Am J Med Genet A -
Publication
Patients' perceptions of pharmacogenetic testing and access to their results: State of the art in Spain and systematic review
Journal of Personalized Medicine -
Publication
Is there evidence that we should screen the general population for lynch syndrome with genetic testing? A systematic review
Pharmacogenomics and Personalized Medicine