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Publication
Knowledge and attitudes about privacy and secondary data use among African-Americans using direct-to-consumer genetic testing
Public Health GenomicsParticipants in this study by Ziegler and colleagues found secondary research use of their data acceptable depending on the type of research being pursued. However, about half stated that use by law… -
Publication
Diverse parental perspectives of the social and educational needs for expanding newborn screening through genomic sequencing
Public Health GenomicsTimmins and colleagues find that mothers are supportive of expanding newborn screening for both medical and personal utility and express a desire for more education and control of the process. -
Publication
Data sharing and community-engaged research
ScienceSabatello and colleagues discuss areas of tension between the community-engaged research and data sharing movements including incentives and benefit sharing; group harm and power structures; and… -
Publication
Racial and ethnic disparities among participants in precision oncology clinical studies
JAMA Network Open -
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Publication
Next-generation sequencing in precision oncology: Patient understanding and expectations
Cancer Medicine -
Publication
Immortal life of the common rule: Ethics, consent, and the future of cancer research
Journal of Clinical Oncology -