AMA Code of Medical Ethics' Opinion on Population-Based Genomic Research
Bibliographic Data
| ID | 15746296 |
|---|---|
| Authors | AMA Council on Ethical and Judicial Affairs (corresponding author) |
| Year | 2011 |
| Volume | 13 |
| Issue | 2 |
| Pages | 100-101 |
| Publication date | 2011-02-01 |
| Open Access | Yes |
| Type | ARTICLE |
| Venue | The AMA Journal of Ethic (JOURNAL) |
| Journal identifiers | ISSN: 2376-6980 • E-ISSN: 2376-6980 |
| Publisher | American Medical Association (PUBLISHER • US) |
| DOI | 10.1001/virtualmentor.2011.13.2.coet1-1102 |
| PMID | 23121847 |
| OpenAlex | W4238172972 |
| Language | EN |
Opinion 2.079 - Safeguards in the Use of DNA Databanks in Genomic Research The following safeguards should be applied to the use of databases for the purpose of population-based genomic research: (1) Physicians who participate as investigators in genomic research should have adequate training in genomic research and related ethical issues so as to be able to discuss these issues with patients and/or potential research subjects
Biology · Computational biology · DNA · Engineering ethics · Environmental health · Ethical issues · genomic DNA · Genomic medicine · Population · Research ethics · Biomedical Ethics and Regulation · BRCA gene mutations in cancer · Engineering · Ethics in Clinical Research · Medicine · Genetics
| Highly cited | No |
|---|