Work

“I don’t want to be Henrietta Lacks”: diverse patient perspectives on donating biospecimens for precision medicine research

Year: 2018

Type: article

Source: Genetics in Medicine

DOI: 10.1038/s41436-018-0032-6

Authors: Sandra S.-J. Lee, Mildred K. Cho, Stephanie A. Kraft, Nina Varsava, Katie Gillespie, Kelly E. Ormond, Benjamin S. Wilfond, David Magnus

Institutions: Stanford Medicine, Stanford University, Seattle Children's Hospital, University of Washington, Seattle Children's Research Institute, Treuman Katz Center for Pediatric Bioethics and Palliative Care, Palo Alto Medical Foundation

Language: English

Topic: Ethics in Clinical Research

Subfield: Public Health, Environmental and Occupational Health

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: bronze

Funders: National Institutes of Health, Palo Alto Medical Foundation, U.S. National Library of Medicine

Award: Beyond Consent: Patient Preferences for Governance of Use of Clinical Data and Samples

OpenAlex ID: W2805736463

FWCI: 8.753

Cites: 29

Cited by: 129

Related to: 10