Lessons from HeLa Cells: The Ethics and Policy of Biospecimens

von Beskow, Laura M.
Veröffentlicht in Annu Rev Genomics Hum Genet (2016)

Offering Individual Genetic Research Results: Context Matters

von Beskow, Laura M., Burke, Wylie
Veröffentlicht 2010

PROSPECTIVE BIOREPOSITORY PARTICIPANTS’ PERSPECTIVES ON ACCESS TO RESEARCH RESULTS

von Beskow, Laura M., Smolek, Sondra J.
Veröffentlicht 2009

Epilepsy Patient-Participants and Genetic Research Results as “Answers”

von Namey, Emily E., Beskow, Laura M.
Veröffentlicht 2011

New and Improved? 21st Century Cures Act Revisions to Certificates of Confidentiality

von Wolf, Leslie E., Beskow, Laura M.
Veröffentlicht in Am J Law Med (2018)

Exploring understanding of “understanding”: The paradigm case of biobank consent comprehension

von Beskow, Laura M., Weinfurt, Kevin P.
Veröffentlicht in Am J Bioeth (2019)

Genomic databases, subpoenas, and Certificates of Confidentiality

von Wolf, Leslie E., Beskow, Laura M.
Veröffentlicht in Genet Med (2019)

Research Recruitment Through US Central Cancer Registries: Balancing Privacy and Scientific Issues

von Beskow, Laura M., Sandler, Robert S., Weinberger, Morris
Veröffentlicht 2006

INFORMED CONSENT IN GENOMICS AND GENETIC RESEARCH

von McGuire, Amy L., Beskow, Laura M.
Veröffentlicht 2010

Return of Genetic Research Results to Participants and Families: IRB Perspectives and Roles

von Beskow, Laura M., O’Rourke, P. Pearl
Veröffentlicht in J Law Med Ethics (2015)

Developing informed consent materials for non-English-speaking participants: An analysis of four professional firm translations from English to Spanish

von Brelsford, Kathleen Marie, Ruiz, Ernesto, Beskow, Laura
Veröffentlicht in Clin Trials (2018)

Certificates of Confidentiality and the Compelled Disclosure of Research Data

von Beskow, Laura M., Dame, Lauren, Costello, E. Jane
Veröffentlicht 2008

Research Participants’ Understanding of and Reactions to Certificates of Confidentiality

von Beskow, Laura M., Check, Devon K., Ammarell, Natalie
Veröffentlicht 2014

Research use of electronic health records: patients’ perspectives on contact by researchers

von Brelsford, Kathleen M, Spratt, Susan E, Beskow, Laura M
Veröffentlicht in J Am Med Inform Assoc (2018)

Thought leader perspectives on benefits and harms in precision medicine research

von Beskow, Laura M., Hammack, Catherine M., Brelsford, Kathleen M.
Veröffentlicht in PLoS One (2018)

Patient perspectives on use of electronic health records for research recruitment

von Beskow, Laura M., Brelsford, Kathleen M., Hammack, Catherine M.
Veröffentlicht in BMC Med Res Methodol (2019)

Thought Leader Perspectives on Participant Protections in Precision Medicine Research

von Hammack, Catherine M., Brelsford, Kathleen M., Beskow, Laura M.
Veröffentlicht in J Law Med Ethics (2019)

Consent for acute care research and the regulatory “gray zone”

von Beskow, Laura M., Lindsell, Christopher J., Rice, Todd W.
Veröffentlicht in Am J Bioeth (2020)

Am I a control?: Genotype-driven research recruitment and self-understandings of study participants

von Michie, Marsha, Cadigan, R. Jean, Henderson, Gail, Beskow, Laura M.
Veröffentlicht 2012

Canadian Research Ethics Board Leadership Attitudes to the Return of Genetic Research Results to Individuals and their Families

von Fernandez, Conrad V., O'Rourke, P. Pearle, Beskow, Laura M.
Veröffentlicht in J Law Med Ethics (2015)