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Communicating genetic risk information for common disorders in the era of genomic medicine.
Annual Review of Genomics and Human Genetics ( IF 7.7 ) Pub Date : 2013-01-01 , DOI: 10.1146/annurev-genom-092010-110722
Denise M Lautenbach 1 , Kurt D Christensen , Jeffrey A Sparks , Robert C Green
Affiliation  

Communicating genetic risk information in ways that maximize understanding and promote health is increasingly important given the rapidly expanding availability and capabilities of genomic technologies. A well-developed literature on risk communication in general provides guidance for best practices, including presentation of information in multiple formats, attention to framing effects, use of graphics, sensitivity to the way numbers are presented, parsimony of information, attentiveness to emotions, and interactivity as part of the communication process. Challenges to communicating genetic risk information include deciding how best to tailor it, streamlining the process, deciding what information to disclose, accepting that communications may have limited influence, and understanding the impact of context. Meeting these challenges has great potential for empowering individuals to adopt healthier lifestyles and improve public health, but will require multidisciplinary approaches and collaboration.

中文翻译:

交流基因组医学时代常见疾病的遗传风险信息。

鉴于基因组技术的可用性和能力迅速扩大,以最大限度地了解和促进健康的方式交流遗传风险信息变得越来越重要。完善的风险交流文献总体上为最佳实践提供了指导,包括以多种格式呈现信息、注意框架效果、图形的使用、对数字呈现方式的敏感性、信息的简洁性、对情绪的关注以及交互性作为沟通过程的一部分。遗传风险信息交流面临的挑战包括决定如何最好地调整信息、简化流程、决定披露哪些信息、接受交流可能影响有限以及了解背景的影响。
更新日期:2013-09-04
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