Literature DB >> 22200001

Broad consent and biorepositories for molecular epidemiology and genomics research.

Steven S Coughlin.   

Abstract

Year:  2011        PMID： 22200001      PMCID： PMC3243454     

Source DB:  PubMed          Journal:  Int J Mol Epidemiol Genet        ISSN： 1948-1756


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  6 in total

1.  Coding and consent: moral challenges of the database project in Iceland.

Authors:  Vilhjalmur Arnason
Journal:  Bioethics       Date:  2004       Impact factor: 1.898

2.  Can Broad Consent be Informed Consent?

Authors:  Mark Sheehan
Journal:  Public Health Ethics       Date:  2011-08-03       Impact factor: 1.940

Review 3.  Biobanking: international norms.

Authors:  Bartha Maria Knoppers
Journal:  J Law Med Ethics       Date:  2005       Impact factor: 1.718

4.  Informed consent and biobanks.

Authors:  Ellen Wright Clayton
Journal:  J Law Med Ethics       Date:  2005       Impact factor: 1.718

Review 5.  Should donors be allowed to give broad consent to future biobank research?

Authors:  Mats G Hansson; Joakim Dillner; Claus R Bartram; Joyce A Carlson; Gert Helgesson
Journal:  Lancet Oncol       Date:  2006-03       Impact factor: 41.316

6.  Qualitative thematic analysis of consent forms used in cancer genome sequencing.

Authors:  Clarissa Allen; William D Foulkes
Journal:  BMC Med Ethics       Date:  2011-07-19       Impact factor: 2.652
  6 in total
  2 in total

Review 1.  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

2.  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
  2 in total

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