about
Immortal Life of the Common Rule: Ethics, Consent, and the Future of Cancer ResearchConsumer Perspectives on Access to Direct-to-Consumer Genetic Testing: Role of Demographic Factors and the Testing Experience."The Google of Healthcare": enabling the privatization of genetic bio/databanking.Public health service research in guatemala: toward new scholarship.Inpatient Postpartum Long-Acting Reversible Contraception: Care That Promotes Reproductive Justice.Revisiting Expectations in an Era of Precision Oncology."Something of an adventure": postwar NIH research ethos and the Guatemala STD experiments.Stemming the Standard-of-Care SPRAWL: Clinician Self-Interest and the Case of Electronic Fetal Monitoring.Exome and Genome Sequencing and Parallels in Radiology: Searching for Patient-Centered Management of Incidental and Secondary Findings.Reg-ent within the Learning Health System.Analysis of state laws on informed consent for clinical genetic testing in the era of genomic sequencing.Broad Consent for Head and Neck Cancer Research.From in vivo to in vitro: How the Guatemala STD Experiments Transformed Bodies Into Biospecimens.Big data, ethics, and regulations: Implications for consent in the learning health systemRECONCEPTUALIZING CONSENT FOR DIRECT-TO-CONSUMER HEALTH SERVICESEncouraging Participation And Transparency In Biobank Research
P50
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P50
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Kayte Spector-Bagdady
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Kayte Spector-Bagdady
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