(Q51813875)

13 April 2018

title

Patients' attitudes to informed consent for genomic research with donated samples. (English)

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13 April 2018

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2

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13 April 2018

Daniel Sulmasy

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3

object named as

Daniel P Sulmasy

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13 April 2018

author name string

J Ignacio Valle-Mansilla

series ordinal

1

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13 April 2018

publication date

1 August 2010

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13 April 2018

published in

Cancer Investigation

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13 April 2018

volume

28

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13 April 2018

issue

7

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13 April 2018

page(s)

726-734

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13 April 2018

Biobanking for epidemiological research and public health

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https://api.crossref.org/works/10.3109%2F07357907.2010.494320

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One-time general consent for research on biological samples

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

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

21 January 2018

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Consent for genetic research in a general population: the NHANES experience

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

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

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Consent for long-term storage of blood samples by Indigenous Australian research participants: the DRUID Study experience

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Consent and anonymization in research involving biobanks: differing terms and norms present serious barriers to an international framework

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21 January 2018

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Informed consent, participation in, and withdrawal from a population based cohort study involving genetic analysis

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Attitudes towards clinical research among cancer trial participants and non-participants: an interview study using a Grounded Theory approach.

21 January 2018

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Attitudes toward research participation and investigator conflicts of interest among advanced cancer patients participating in early phase clinical trials.

21 January 2018

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Informed consent for biorepositories: assessing prospective participants' understanding and opinions

21 January 2018

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Participation in clinical trials as viewed by the patient: understanding cultural and emotional aspects which influence choice.

21 January 2018

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Consent for use of personal information for health research: do people with potentially stigmatizing health conditions and the general public differ in their opinions?

21 January 2018

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Why the use of anonymous samples for research matters

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Perceptions of potential donors in the Swedish public towards information and consent procedures in relation to use of human tissue samples in biobanks: a population-based study

21 January 2018

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10.3109/07357907.2010.494320

21 January 2018

Identifiers

DOI

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13 April 2018

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13 April 2018