Literature DB >> 22046007

Broad consent is informed consent.

Mark Sheehan.   

Abstract

Mesh：

Year:  2011        PMID： 22046007     DOI： 10.1136/bmj.d6900

Source DB:  PubMed          Journal:  BMJ        ISSN： 0959-8138


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  9 in total

Review 1.  The Ethics of Consent in a Shifting Genomic Ecosystem.

Authors:  Sandra Soo-Jin Lee
Journal:  Annu Rev Biomed Data Sci       Date:  2021-07-20

Review 2.  Sharing the Knowledge: Sharing Aggregate Genomic Findings with Research Participants in Developing Countries.

Authors:  Angeliki Kerasidou
Journal:  Dev World Bioeth       Date:  2014-10-08       Impact factor: 2.294

3.  Broad consent versus dynamic consent in biobank research: is passive participation an ethical problem?

Authors:  Kristin Solum Steinsbekk; Bjørn Kåre Myskja; Berge Solberg
Journal:  Eur J Hum Genet       Date:  2013-01-09       Impact factor: 4.246

4.  Emerging ethical issues regarding digital health data. On the World Medical Association Draft Declaration on Ethical Considerations Regarding Health Databases and Biobanks.

Authors:  Christine Aicardi; Lorenzo Del Savio; Edward S Dove; Federica Lucivero; Niccolo Tempini; Barbara Prainsack
Journal:  Croat Med J       Date:  2016-04-28       Impact factor: 1.351

5.  Improving the informed consent process in international collaborative rare disease research: effective consent for effective research.

Authors:  Sabina Gainotti; Cathy Turner; Simon Woods; Anna Kole; Pauline McCormack; Hanns Lochmüller; Olaf Riess; Volker Straub; Manuel Posada; Domenica Taruscio; Deborah Mascalzoni
Journal:  Eur J Hum Genet       Date:  2016-02-10       Impact factor: 4.246

6.  Kenyan health stakeholder views on individual consent, general notification and governance processes for the re-use of hospital inpatient data to support learning on healthcare systems.

Authors:  Daniel Mbuthia; Sassy Molyneux; Maureen Njue; Salim Mwalukore; Vicki Marsh
Journal:  BMC Med Ethics       Date:  2019-01-08       Impact factor: 2.652

7.  Use of broad consent and related procedures in genomics research: Perspectives from research participants in the Genetics of Rheumatic Heart Disease (RHDGen) study in a University Teaching Hospital in Zambia.

Authors:  Oliver Mweemba; John Musuku; Bongani M Mayosi; Michael Parker; Rwamahe Rutakumwa; Janet Seeley; Paulina Tindana; Jantina De Vries
Journal:  Glob Bioeth       Date:  2019-03-24

8.  Hypocrisy Around Medical Patient Data: Issues of Access for Biomedical Research, Data Quality, Usefulness for the Purpose and Omics Data as Game Changer.

Authors:  Erwin Tantoso; Wing-Cheong Wong; Wei Hong Tay; Joanne Lee; Swati Sinha; Birgit Eisenhaber; Frank Eisenhaber
Journal:  Asian Bioeth Rev       Date:  2019-06-01

9.  Ethics review of big data research: What should stay and what should be reformed?

Authors:  Agata Ferretti; Marcello Ienca; Mark Sheehan; Alessandro Blasimme; Edward S Dove; Bobbie Farsides; Phoebe Friesen; Jeff Kahn; Walter Karlen; Peter Kleist; S Matthew Liao; Camille Nebeker; Gabrielle Samuel; Mahsa Shabani; Minerva Rivas Velarde; Effy Vayena
Journal:  BMC Med Ethics       Date:  2021-04-30       Impact factor: 2.652
  9 in total

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