Literature DB >> 17575464

Community engagement and informed consent in the International HapMap project.

Charles Rotimi1, Mark Leppert, Ichiro Matsuda, Changqing Zeng, Houcan Zhang, Clement Adebamowo, Ike Ajayi, Toyin Aniagwu, Missy Dixon, Yoshimitsu Fukushima, Darryl Macer, Patricia Marshall, Chibuzor Nkwodimmah, Andy Peiffer, Charmaine Royal, Eiko Suda, Hui Zhao, Vivian Ota Wang, Jean McEwen.   

Abstract

The International HapMap Consortium has developed the HapMap, a resource that describes the common patterns of human genetic variation (haplotypes). Processes of community/public consultation and individual informed consent were implemented in each locality where samples were collected to understand and attempt to address both individual and group concerns. Perceptions about the research varied, but we detected no critical opposition to the research. Incorporating community input and responding to concerns raised was challenging. However, the experience suggests that approaching genetic variation research in a spirit of openness can help investigators better appreciate the views of the communities whose samples they seek to study and help communities become more engaged in the science. Copyright 2007 S. Karger AG, Basel.

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Year:  2007        PMID: 17575464     DOI: 10.1159/000101761

Source DB:  PubMed          Journal:  Community Genet        ISSN: 1422-2795


  31 in total

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Authors:  Alice K Hawkins
Journal:  J Genet Couns       Date:  2010-08-03       Impact factor: 2.537

2.  Structuring public engagement for effective input in policy development on human tissue biobanking.

Authors:  Kieran C O'Doherty; A Hawkins
Journal:  Public Health Genomics       Date:  2010-04-15       Impact factor: 2.000

Review 3.  A HapMap harvest of insights into the genetics of common disease.

Authors:  Teri A Manolio; Lisa D Brooks; Francis S Collins
Journal:  J Clin Invest       Date:  2008-05       Impact factor: 14.808

4.  Community engagement about genetic variation research.

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Review 5.  African genetic diversity and adaptation inform a precision medicine agenda.

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Journal:  Nat Rev Genet       Date:  2021-01-11       Impact factor: 53.242

6.  Ethical, Legal, and Social Issues (ELSI) in Clinical Genetics Research.

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Journal:  Methods Mol Biol       Date:  2021

7.  Diversity and inclusion in genomic research: why the uneven progress?

Authors:  Amy R Bentley; Shawneequa Callier; Charles N Rotimi
Journal:  J Community Genet       Date:  2017-07-18

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

Authors:  Catherine A McCarty; Ann Garber; Jonathan C Reeser; Norman C Fost
Journal:  Am J Med Genet A       Date:  2011-03-15       Impact factor: 2.802

9.  Engaging rural communities in genetic research: challenges and opportunities.

Authors:  Caress Dean; Amanda J Fogleman; Whitney E Zahnd; Alexander E Lipka; Ripan Singh Malhi; Kristin R Delfino; Wiley D Jenkins
Journal:  J Community Genet       Date:  2017-05-05

10.  Views on personalized medicine: do the attitudes of African American and white prescription drug consumers differ?

Authors:  M De Marco; S Cykert; N Coad; K Doost; J Schaal; B White; D Young; M R Isler; G Corbie-Smith
Journal:  Public Health Genomics       Date:  2009-09-23       Impact factor: 2.000

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