Perceptions of genetics research as harmful to society: differences among samples of African-Americans and European-Americans.
- Authors
- Furr, L Allen
- Year
- 2002
- Journal
- Genetic testing
- PMID
- 12180073
- DOI
- 10.1089/109065702760093889
Genetics has the potential not only to find cures for diseases, but to possess the mechanisms to change the bio-social make-up of populations. A specific question that has arisen on this issue is how developments in genetic technology may intersect with existing race and ethnic relations. Evidence of the racialization of some genetic disorders has been demonstrated elsewhere. The purpose of this study is to compare and contrast African-American and European-American attitudes on the benefits of genetics research for society. Findings show that African-Americans were more likely to say genetics research is harmful for society. This relationship remained statistically significant after controls were introduced in a regression model. Demographic characteristics and self-rated knowledge of genetics had no effect on attitudes among African-Americans. A willingness to use genetic services correlated with favorable attitudes. Differences in social position may lead some groups to opposing interpretations and symbolic meanings of genetics. This may be true in the context of this study because the social meanings of genetics may be tainted by racialization, historical attempts at eugenics, and the potential abuse of genetics targeting groups partially defined by superficial genetic characteristics.
No figures extracted from this document.
No chunks β full text not yet ingested.
No entities extracted from this document yet.
No uploaded files.
No citations found.
In this knowledge base
External
| Title | Authors | Journal | Year | Link |
|---|---|---|---|---|
| Public Perception of Genetic Research on Sexual Orientation and Gender Identity. | Kunstman BL et al. | β | 2026 | β |
| Influences of race and clinical variables on psychiatric genetic research participation: Results from a schizophrenia sample. | Xavier RM et al. | β | 2023 | β |
| Experiences and practices of key research team members in obtaining informed consent for pharmacogenetic research among people living with HIV: a qualitative study. | Nabukenya S et al. | β | 2022 | β |
| No person left behind: Mapping the health policy landscape for genomics research in the Caribbean. | Bolleddula J et al. | β | 2022 | β |
| A systematic review of gene-by-intervention studies of alcohol and other substance use. | Neale ZE et al. | β | 2021 | β |
| African American mothers' attitudes towards genetic testing in the InterGEN study. | Wright ML et al. | β | 2020 | β |
| Impact of Genetic Testing on Risk-Management Behavior of Black Breast Cancer Survivors: A Longitudinal, Observational Study. | Conley CC et al. | β | 2020 | β |
| Why African Americans say "No": A Study of Pharmacogenomic Research Participation. | Nooruddin M et al. | β | 2020 | β |
| Developing culturally informed genetic services for the Somali immigrants in Minnesota. | Cheung FY et al. | β | 2019 | β |
| Genes, Race, and Causation: US Public Perspectives About Racial Difference. | Outram S et al. | β | 2018 | β |
| Review: Genetic research on alcohol use outcomes in African American populations: A review of the literature, associated challenges, and implications. | Dick DM et al. | β | 2017 | β |
| Predictors of biospecimen donation in the Black Women's Health Study. | Adams-Campbell LL et al. | β | 2016 | β |
| Sociocultural variation in attitudes toward use of genetic information and participation in genetic research by race in the United States: implications for precision medicine. | Dye T et al. | β | 2016 | β |
| "It takes a village": multilevel approaches to recruit African Americans and their families for genetic research. | Ochs-Balcom HM et al. | β | 2015 | β |
| Nonprobability and probability-based sampling strategies in sexual science. | Catania JA et al. | β | 2015 | β |
| Storage and use of Newborn Screening Blood Specimens for Research: Assessing Public Opinion in Illinois. | Hart A et al. | β | 2015 | β |
| Using Public-Private Partnerships to Mitigate Disparities in Access to Genetic Services: Lessons from Wisconsin. | Senier L et al. | β | 2015 | β |
| Factors Associated with African-American Women's Decisions to Participate in Genetic Research. | Still CH et al. | β | 2014 | β |
| Patient characteristics and participation in a genetic study: a type 2 diabetes cohort. | Amiri L et al. | β | 2014 | β |
| Perceptions of African-American health professionals and community members on the participation of children and pregnant women in genetic research. | Ngui EM et al. | β | 2014 | β |
| Attitudes toward Genetic Testing for Hypertension among African American Women and Girls. | Taylor JY et al. | β | 2013 | β |
| Integrating genetic and genomic information into effective cancer care in diverse populations. | Fashoyin-Aje L et al. | β | 2013 | β |
| Ethnic disparities in the perception of ethical risks from psychiatric genetic studies. | Nwulia EA et al. | β | 2011 | β |
| Parents' decisions to screen newborns for FMR1 gene expansions in a pilot research project. | Skinner D et al. | β | 2011 | β |
| Public perspectives on returning genetics and genomics research results. | O'Daniel J et al. | β | 2011 | β |
| Ethical considerations in the collection of genetic data from critically ill patients: what do published studies reveal about potential directions for empirical ethics research? | Freeman BD et al. | β | 2010 | β |
| Public attitudes and beliefs about genetics. | Condit CM | β | 2010 | β |
| The role of race and trust in tissue/blood donation for genetic research. | Bussey-Jones J et al. | β | 2010 | β |
| An exploration of attitudes among black Americans towards psychiatric genetic research. | Murphy E et al. | β | 2009 | β |
| Asking the right questions: views on genetic variation research among black and white research participants. | Bussey-Jones J et al. | β | 2009 | β |
| Decisions to participate in fragile X and other genomics-related research: Native American and African American voices. | Johnson VA et al. | β | 2009 | β |
| Hereditary breast and ovarian cancer syndrome : the impact of race on uptake of genetic counseling and testing. | Simon MS et al. | β | 2009 | β |
| Pharmacogenetics studies in STAR*D: strengths, limitations, and results. | Laje G et al. | β | 2009 | β |
| Racial and ethnic differences in willingness to participate in psychiatric genetic research. | Murphy EJ et al. | β | 2009 | β |
| Great expectations: views of genetic research participants regarding current and future genetic studies. | Henderson G et al. | β | 2008 | β |
| Promotion of cancer family history awareness: Jameslink Cancer Risk Assessment Tool at community health fairs. | Kelly KM et al. | β | 2008 | β |
| Scientific responsibility for the dissemination and interpretation of genetic research: lessons from the "warrior gene" controversy. | Wensley D et al. | β | 2008 | β |
| Applications and implications of advances in human genetics: perspectives from a group of Black Americans. | Sheldon JP et al. | β | 2007 | β |
| Community engagement in genetic research: results of the first public consultation for the Quebec CARTaGENE project. | Godard B et al. | β | 2007 | β |
| Research Participants' Perceptions of the Certificate of Confidentiality's Assurances and Limitations. | Catania JA et al. | β | 2007 | β |
| Genetics, epidemiology, and cancer disparities: is it black and white? | Rebbeck TR et al. | β | 2006 | β |
| Genetic testing for colon cancer among African-Americans in North Carolina. | Satia JA et al. | β | 2006 | β |
| Intentions to participate in genetics research among African American smokers. | Halbert CH et al. | β | 2006 | β |
| Public willingness to participate in and public opinions about genetic variation research: a review of the literature. | Sterling R et al. | β | 2006 | β |
| Recruiting African American women to participate in hereditary breast cancer research. | Halbert CH et al. | β | 2005 | β |
| Warranted concerns, warranted outlooks: a focus group study of public understandings of genetic research. | Bates BR et al. | β | 2005 | β |
| African Americans' opinions about human-genetics research. | Achter P et al. | β | 2004 | β |
| Genetics and public health--evolution, or revolution? | Halliday JL et al. | β | 2004 | β |
| Psychosocial aspects of genetic counseling and testing. | Vadaparampil ST et al. | β | 2004 | β |
| Strategies for consulting with the community: the cases of four large-scale genetic databases. | Godard B et al. | β | 2004 | β |