(Q28602677)

6

Stephanie M Fullerton

0 references

Lisa Eckstein

Lisa Eckstein

2

0 references

Henry Greely

7

Hank Greely

0 references

Christine Grady

1

Christine Grady

0 references

Benjamin S Wilfond

15

Benjamin S Wilfond

0 references

David Wendler

16

David Wendler

0 references

Sara Chandros Hull

9

Sara Hull

0 references

Scott Y H Kim

10

Scott Kim

0 references

Rebecca D. Pentz

12

Rebecca Pentz

0 references

author name string

Ben Berkman

3

0 references

Dan Brock

4

0 references

Mats G Hansson

8

0 references

Bernie Lo

11

0 references

Laura Rodriguez

13

0 references

Carol Weil

American Journal of Bioethics

14

0 references

language of work or name

English

0 references

publication date

2015

0 references

number of pages

9

1 reference

based on heuristic

inferred from page(s)

published in

0 references

volume

15

0 references

issue

9

0 references

page(s)

34-42

0 references

cites work

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17 March 2017

1 reference

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From patients to partners: participant-centric initiatives in biomedical research

17 March 2017

1 reference

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Community consultation and communication for a population-based DNA biobank: the Marshfield clinic personalized medicine research project

17 March 2017

1 reference

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Advocacy groups as research organizations: the PXE International example

17 March 2017

1 reference

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The prevalence of hepatitis C virus infection in the United States, 1988 through 1994

17 March 2017

1 reference

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"It's my blood": ethical complexities in the use, storage and export of biological samples: perspectives from South African research participants

7 April 2017

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Biobanks containing clinical specimens: defining characteristics, policies, and practices

29 September 2017

1 reference

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Public attitudes regarding the use of electronic health information and residual clinical tissues for research

29 September 2017

1 reference

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Dynamic consent in the digital age of biology: online initiatives and regulatory considerations

29 September 2017

1 reference

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Broad versus blanket consent for research with human biological samples

29 September 2017

1 reference

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Respecting donors to biobank research

29 September 2017

1 reference

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Parental Perspectives on a Pediatric Human Non-Subjects Biobank

29 September 2017

1 reference

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Community engagement in biobanking: Experiences from the eMERGE Network.

29 September 2017

1 reference

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Publics and biobanks: Pan-European diversity and the challenge of responsible innovation

29 September 2017

1 reference

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Genomic databases access agreements: legal validity and possible sanctions

29 September 2017

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Active choice but not too active: public perspectives on biobank consent models.

29 September 2017

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Autoantibodies predate the onset of systemic lupus erythematosus in northern Sweden

29 September 2017

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Principles of human subjects protections applied in an opt-out, de-identified biobank

29 September 2017

1 reference

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Public attitudes to the storage of blood left over from routine general practice tests and its use in research.

29 September 2017

1 reference

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Participant characteristics that influence consent for genetic research in a population-based survey: the Baltimore epidemiologic catchment area follow-up

29 September 2017

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Consent for genetic research in a general population: an update on the National Health and Nutrition Examination Survey experience

29 September 2017

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One-time general consent for research on biological samples

29 September 2017

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

29 September 2017

1 reference

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Genetic research and donation of tissue samples to biobanks. What do potential sample donors in the Swedish general public think?

29 September 2017

1 reference

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Research with stored biological samples: what do research participants want?

29 September 2017

1 reference

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Informed consent and biobanks: a population-based study of attitudes towards tissue donation for genetic research

29 September 2017

1 reference

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Informed consent for genetic research on blood stored for more than a decade: a population based study

29 September 2017

1 reference

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Public attitudes regarding the donation and storage of blood specimens for genetic research

29 September 2017

1 reference

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Phylogenetic relationships of dengue-2 viruses

29 September 2017

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Long-term mortality after transfusion-associated non-A, non-B hepatitis. The National Heart, Lung, and Blood Institute Study Group

29 September 2017

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Biobanking: shifting the analogy from consent to surrogacy

3 June 2018

1 reference

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Two large-scale surveys on community attitudes toward an opt-out biobank.

27 November 2018

1 reference

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Attitudes towards biomedical use of tissue sample collections, consent, and biobanks among Finns

27 November 2018

1 reference

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Towards an understanding of British public attitudes concerning human cloning.

27 November 2018

1 reference

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Tamoxifen and breast cancer incidence among women with inherited mutations in BRCA1 and BRCA2: National Surgical Adjuvant Breast and Bowel Project (NSABP-P1) Breast Cancer Prevention Trial.

27 November 2018

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Modifications to the HIPAA Privacy, Security, Enforcement, and Breach Notification rules under the Health Information Technology for Economic and Clinical Health Act and the Genetic Information Nondiscrimination Act; other modifications to the HIPAA

27 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26305750

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1080/15265161.2015.1062162

1 reference

1 reference

1 reference

PubMed publication ID

26305750

1 reference