Literature DB >> 20818551

Managing patient expectations about deidentification.

Shawneequa L Callier1, Harald Schmidt.   

Abstract

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Year:  2010        PMID： 20818551      PMCID： PMC3380536          DOI： 10.1080/15265161.2010.494222

Source DB:  PubMed          Journal:  Am J Bioeth        ISSN： 1526-5161            Impact factor:   11.229


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  9 in total

1.  Electronic health records and research: privacy versus scientific priorities.

Authors:  Sharona Hoffman
Journal:  Am J Bioeth       Date:  2010-09       Impact factor: 11.229

2.  Ethics. Identifiability in genomic research.

Authors:  William W Lowrance; Francis S Collins
Journal:  Science       Date:  2007-08-03       Impact factor: 47.728

3.  Genomes for all.

Authors:  George M Church
Journal:  Sci Am       Date:  2006-01       Impact factor: 2.142

4.  Research on medical records without informed consent.

Authors:  Franklin G Miller
Journal:  J Law Med Ethics       Date:  2008       Impact factor: 1.718

5.  Tailoring the process of informed consent in genetic and genomic research.

Authors:  Charles N Rotimi; Patricia A Marshall
Journal:  Genome Med       Date:  2010-03-24       Impact factor: 11.117

6.  Anonymization of electronic medical records for validating genome-wide association studies.

Authors:  Grigorios Loukides; Aris Gkoulalas-Divanis; Bradley Malin
Journal:  Proc Natl Acad Sci U S A       Date:  2010-04-12       Impact factor: 11.205

7.  How anonymous is 'anonymous'? Some suggestions towards a coherent universal coding system for genetic samples.

Authors:  Harald Schmidt; Shawneequa Callier
Journal:  J Med Ethics       Date:  2012-02-16       Impact factor: 2.903

8.  Is deidentification sufficient to protect health privacy in research?

Authors:  Mark A Rothstein
Journal:  Am J Bioeth       Date:  2010-09       Impact factor: 11.229

9.  Patients' views on identifiability of samples and informed consent for genetic research.

Authors:  Sara Chandros Hull; Richard R Sharp; Jeffrey R Botkin; Mark Brown; Mark Hughes; Jeremy Sugarman; Debra Schwinn; Pamela Sankar; Dragana Bolcic-Jankovic; Brian R Clarridge; Benjamin S Wilfond
Journal:  Am J Bioeth       Date:  2008-10       Impact factor: 11.229
  9 in total
  1 in total

1.  Balancing Benefits and Risks of Immortal Data: Participants' Views of Open Consent in the Personal Genome Project.

Authors:  Oscar A Zarate; Julia Green Brody; Phil Brown; Mónica D Ramirez-Andreotta; Laura Perovich; Jacob Matz
Journal:  Hastings Cent Rep       Date:  2015-12-17       Impact factor: 2.683
  1 in total

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