Suppr超能文献

Incomplete knowledge of the clinical context as a barrier to interpreting incidental genetic research findings.

作者信息

Costain Gregory, Bassett Anne S

机构信息

University of Toronto, Toronto, Canada.

出版信息

Am J Bioeth. 2013;13(2):58-60. doi: 10.1080/15265161.2012.754063.

Abstract
摘要

相似文献

2
Managing incidental findings: lessons from neuroimaging.
Am J Bioeth. 2013;13(2):46-7. doi: 10.1080/15265161.2012.754069.
3
Reframing the ethical debate regarding incidental findings in genetic research.
Am J Bioeth. 2013;13(2):44-6. doi: 10.1080/15265161.2013.757972.
4
Genomic incidental findings: reducing the burden to be fair.
Am J Bioeth. 2013;13(2):52-4. doi: 10.1080/15265161.2012.754066.
5
Legal implications of an ethical duty to search for genetic incidental findings.
Am J Bioeth. 2013;13(2):48-9. doi: 10.1080/15265161.2012.754068.
6
The duty to rescue in genomic research.
Am J Bioeth. 2013;13(2):50-1. doi: 10.1080/15265161.2012.754067.
7
The Nirvana fallacy and the return of results.
Am J Bioeth. 2013;13(2):43-4. doi: 10.1080/15265161.2013.755826.
10

引用本文的文献

1
Incidental findings of uncertain significance: To know or not to know--that is not the question.
BMC Med Ethics. 2016 Feb 13;17:13. doi: 10.1186/s12910-016-0096-2.
3
The Human Genome Project, and recent advances in personalized genomics.
Risk Manag Healthc Policy. 2015 Feb 16;8:9-20. doi: 10.2147/RMHP.S58728. eCollection 2015.
4
Attitudes of genetics professionals toward the return of incidental results from exome and whole-genome sequencing.
Am J Hum Genet. 2014 Jul 3;95(1):77-84. doi: 10.1016/j.ajhg.2014.06.004. Epub 2014 Jun 26.
5
ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
Genet Med. 2013 Jul;15(7):565-74. doi: 10.1038/gim.2013.73. Epub 2013 Jun 20.

本文引用的文献

1
Do researchers have an obligation to actively look for genetic incidental findings?
Am J Bioeth. 2013;13(2):32-42. doi: 10.1080/15265161.2012.754062.
4
Incidental medical information in whole-exome sequencing.
Pediatrics. 2012 Jun;129(6):e1605-11. doi: 10.1542/peds.2011-0080. Epub 2012 May 14.
5
INTERIM guidelines for the diagnosis and management of familial hypercholesterolaemia.
Heart Lung Circ. 2012 Mar;21(3):159-62. doi: 10.1016/j.hlc.2011.11.006. Epub 2012 Jan 30.
6
Offering individual genetic research results: context matters.
Sci Transl Med. 2010 Jun 30;2(38):38cm20. doi: 10.1126/scitranslmed.3000952.
7
Familial hypercholesterolaemia: summary of NICE guidance.
BMJ. 2008 Aug 27;337:a1095. doi: 10.1136/bmj.a1095.
8
Update and analysis of the University College London low density lipoprotein receptor familial hypercholesterolemia database.
Ann Hum Genet. 2008 Jul;72(Pt 4):485-98. doi: 10.1111/j.1469-1809.2008.00436.x. Epub 2008 Mar 5.
9
The family history--more important than ever.
N Engl J Med. 2004 Nov 25;351(22):2333-6. doi: 10.1056/NEJMsb042979.
10
Location of a major susceptibility locus for familial schizophrenia on chromosome 1q21-q22.
Science. 2000 Apr 28;288(5466):678-82. doi: 10.1126/science.288.5466.678.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验