(Q57254266)

English

Study newsletters, community and ethics advisory boards, and focus group discussions provide ongoing feedback for a large biobank

scholarly article by Catherine A. McCarty et al published April 2011 in American Journal of Medical Genetics

In more languages

edit

Statements

instance of

scholarly article

0 references

title

Study newsletters, community and ethics advisory boards, and focus group discussions provide ongoing feedback for a large biobank (English)

0 references

0 references

0 references

Catherine A McCarty

1

0 references

author name string

Ann Garber

series ordinal

2

0 references

Jonathan C Reeser

series ordinal

3

0 references

Norman C Fost

series ordinal

4

0 references

language of work or name

English

0 references

publication date

April 2011

0 references

published in

American Journal of Medical Genetics

0 references

volume

155A

0 references

issue

4

0 references

page(s)

737-41

0 references

cites work

Monitoring ethical, legal, and social issues in developing population genetic databases

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FAJMG.A.33896

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FAJMG.A.33896

retrieved

21 January 2018

Research ethics recommendations for whole-genome research: consensus statement

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FAJMG.A.33896

retrieved

21 January 2018

Ethical, legal, and social implications of genomic medicine

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FAJMG.A.33896

retrieved

21 January 2018

Beyond “misunderstanding”: Written information and decisions about taking part in a genetic epidemiology study

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FAJMG.A.33896

retrieved

21 January 2018

Community engagement in genetic research: results of the first public consultation for the Quebec CARTaGENE project.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FAJMG.A.33896

retrieved

21 January 2018

Subjects matter: a survey of public opinions about a large genetic cohort study.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FAJMG.A.33896

retrieved

21 January 2018

Public opinion about the importance of privacy in biobank research

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FAJMG.A.33896

retrieved

21 January 2018

Does waiver of written informed consent from the institutional review board affect response rate in a low-risk research study?

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FAJMG.A.33896

retrieved

21 January 2018

Healthy People 2010 disease prevalence in the Marshfield Clinic Personalized Medicine Research Project cohort: opportunities for public health genomic research

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FAJMG.A.33896

retrieved

21 January 2018

Informed consent and subject motivation to participate in a large, population-based genomics study: the Marshfield Clinic Personalized Medicine Research Project

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FAJMG.A.33896

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FAJMG.A.33896

retrieved

21 January 2018

The Marshfield Clinic Personalized Medicine Research Project: 2008 scientific update and lessons learned in the first 6 years

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FAJMG.A.33896

retrieved

21 January 2018

Public perspectives on informed consent for biobanking

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FAJMG.A.33896

retrieved

21 January 2018

Community engagement and informed consent in the International HapMap project.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FAJMG.A.33896

retrieved

21 January 2018

Marshfield Clinic Personalized Medicine Research Project (PMRP): design, methods and recruitment for a large population-based biobank

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/21572889

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

0 references

0 references

0 references

(Q57254266)

Study newsletters, community and ethics advisory boards, and focus group discussions provide ongoing feedback for a large biobank

Statements

Identifiers

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)