(Q46491407)

22 December 2017

title

Consent for biobanking: assessing the understanding and views of cancer patients (English)

1 reference

22 December 2017

0 references

0 references

1

1 reference

22 December 2017

author name string

Isabelle Pellegrini

2

1 reference

22 December 2017

Frédéric Viret

3

1 reference

22 December 2017

Norbert Vey

4

1 reference

22 December 2017

Lise-Marie Daufresne

5

1 reference

22 December 2017

Christian Chabannon

6

1 reference

22 December 2017

Claire Julian-Reynier

7

1 reference

22 December 2017

language of work or name

English

0 references

publication date

20 December 2010

1 reference

22 December 2017

Journal of the National Cancer Institute

published in

1 reference

22 December 2017

volume

103

1 reference

22 December 2017

issue

2

1 reference

22 December 2017

page(s)

154-157

1 reference

22 December 2017

Why might people donate tissue for cancer research? Insights from organ/tissue/blood donation and clinical research.

cites work

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2FDJQ498

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2FDJQ498

"Broad" consent, exceptions to consent and the question of using biological samples for research purposes different from the initial collection purpose.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2FDJQ498

Research on stored biological samples: views of African American and White American cancer patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2FDJQ498

Views of female breast cancer patients who donated biologic samples regarding storage and use of samples for genetic research.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2FDJQ498

A trial of consent procedures for future research with clinically derived biological samples

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2FDJQ498

Opt-out plus, the patients' choice: preferences of cancer patients concerning information and consent regimen for future research with biological samples archived in the context of treatment

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2FDJQ498

The debate over research on stored biological samples: what do sources think?

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2FDJQ498

How will GINA influence participation in pharmacogenomics research and clinical testing?

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2FDJQ498

High rate of consent to bank biologic samples for future research: the Eastern Cooperative Oncology Group experience

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2FDJQ498

Use of archived specimens in evaluation of prognostic and predictive biomarkers

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2FDJQ498

Sources of bias in specimens for research about molecular markers for cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2FDJQ498

Assessing the understanding of biobank participants.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2FDJQ498

The ethics of research using biobanks: reason to question the importance attributed to informed consent

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2FDJQ498

Waiting is the hardest part: anticipating medical test results affects processing and recall of important information.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2FDJQ498

Timing of consent for the research use of surgically removed tissue: is postoperative consenting acceptable?

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2FDJQ498

21 January 2018

Identifiers

DOI

10.1093/JNCI/DJQ498

1 reference

22 December 2017

1 reference

22 December 2017