• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利：CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法，用中文像聊天一样搜索，搜遍4000万医学文献。AI智能推荐，让科研检索更轻松。

立即免费搜索

文件翻译

保留排版，准确专业，支持PDF/Word/PPT等文件格式，支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述，25分钟生成高质量综述，智能提取关键信息，辅助科研写作。

立即免费体验

The Continuing Evolution of Ethical Standards for Genomic Sequencing in Clinical Care: Restoring Patient Choice.

作者信息

Wolf Susan M

机构信息

McKnight Presidential Professor of Law, Medicine & Public Policy; Faegre Baker Daniels Professor of Law; and Professor of Medicine at the University of Minnesota. She is also Chair of the University's Consortium on Law and Values in Health, Environment & the Life Sciences.

出版信息

J Law Med Ethics. 2017 Sep;45(3):333-340. doi: 10.1177/1073110517737531. Epub 2017 Oct 18.

DOI:10.1177/1073110517737531
PMID:30100701
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6085086/
Abstract
摘要

相似文献

1
The Continuing Evolution of Ethical Standards for Genomic Sequencing in Clinical Care: Restoring Patient Choice.临床护理中基因组测序伦理标准的持续演变：恢复患者选择权。
J Law Med Ethics. 2017 Sep;45(3):333-340. doi: 10.1177/1073110517737531. Epub 2017 Oct 18.
2
[Ethical dilemmas in a general practitioner's clinic due to incidental findings resulting from whole genome sequencing].[全科医生诊所中因全基因组测序的偶然发现导致的伦理困境]
Ned Tijdschr Geneeskd. 2018 Jun 15;162:D2087.
3
Factors influencing NCGENES research participants' requests for non-medically actionable secondary findings.影响 NCGENES 研究参与者对非医学可操作性次要发现请求的因素。
Genet Med. 2019 May;21(5):1092-1099. doi: 10.1038/s41436-018-0294-z. Epub 2018 Sep 21.
4
Exome and Genome Sequencing and Parallels in Radiology: Searching for Patient-Centered Management of Incidental and Secondary Findings.外显子组和基因组测序与放射学中的相似之处：探寻以患者为中心的偶然发现和次要发现的管理方法
J Am Coll Radiol. 2016 Dec;13(12 Pt A):1467-1472. doi: 10.1016/j.jacr.2016.06.050. Epub 2016 Aug 29.
5
Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study.临床基因组测序的次要发现：来自多中心研究的患病率、患者观点、家族史评估和医疗保健成本。
Genet Med. 2019 May;21(5):1100-1110. doi: 10.1038/s41436-018-0308-x. Epub 2018 Oct 5.
6
Scanning the body, sequencing the genome: Dealing with unsolicited findings.扫描身体，测序基因组：处理意外发现。
Bioethics. 2017 Nov;31(9):648-656. doi: 10.1111/bioe.12375. Epub 2017 Oct 4.
7
Toward greater understanding of patient decision-making around genome sequencing.旨在更深入了解患者围绕基因组测序的决策过程。
Per Med. 2018 Jan;15(1):57-66. doi: 10.2217/pme-2017-0037.
8
Processes and preliminary outputs for identification of actionable genes as incidental findings in genomic sequence data in the Clinical Sequencing Exploratory Research Consortium.临床测序探索研究联盟中基因组序列数据中可操作基因的识别的过程和初步结果。
Genet Med. 2013 Nov;15(11):860-7. doi: 10.1038/gim.2013.133. Epub 2013 Oct 24.
9
The Legal Dimensions of Genomic Sequencing in Newborn Screening.新生儿筛查中基因组测序的法律维度。
Hastings Cent Rep. 2018 Jul;48 Suppl 2:S39-S41. doi: 10.1002/hast.884.
10
Societal preferences for the return of incidental findings from clinical genomic sequencing: a discrete-choice experiment.临床基因组测序中偶然发现结果反馈的社会偏好：一项离散选择实验
CMAJ. 2015 Apr 7;187(6):E190-E197. doi: 10.1503/cmaj.140697. Epub 2015 Mar 9.

引用本文的文献

1
Insights into the Molecular Genetic of Hemophilia A and Hemophilia B: The Relevance of Genetic Testing in Routine Clinical Practice.血友病 A 和血友病 B 的分子遗传学研究进展：遗传检测在常规临床实践中的相关性。
Hamostaseologie. 2022 Dec;42(6):390-399. doi: 10.1055/a-1945-9429. Epub 2022 Dec 22.
2
Whole-genome sequencing.全基因组测序
Pract Neurol. 2021 May 10;21(4):322-7. doi: 10.1136/practneurol-2020-002561.
3
Predictive Analytics and the Return of "Research" Information to Participants.预测性分析与“研究”信息向参与者的反馈
Appl Hum Factors Ergon Conf. 2020 Jul;1208:138-145. doi: 10.1007/978-3-030-51057-2_20. Epub 2020 Jul 10.
4
Integrating Rules for Genomic Research, Clinical Care, Public Health Screening and DTC Testing: Creating Translational Law for Translational Genomics.整合基因组研究、临床护理、公共卫生筛查和 DTC 检测的规则：为转化基因组学制定转化法。
J Law Med Ethics. 2020 Mar;48(1):69-86. doi: 10.1177/1073110520916996.
5
Return of individual genomic research results: are laws and policies keeping step?个体基因组研究结果的返还：法律法规是否跟上步伐？
Eur J Hum Genet. 2019 Apr;27(4):535-546. doi: 10.1038/s41431-018-0311-3. Epub 2019 Jan 8.

本文引用的文献

1
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.临床外显子组和基因组测序中次要发现报告的建议，2016年更新版（美国医学遗传学与基因组学学会次要发现v2.0）：美国医学遗传学与基因组学学会政策声明
Genet Med. 2017 Feb;19(2):249-255. doi: 10.1038/gim.2016.190. Epub 2016 Nov 17.
2
Genetic Misdiagnoses and the Potential for Health Disparities.基因误诊与健康差异的可能性。
N Engl J Med. 2016 Aug 18;375(7):655-65. doi: 10.1056/NEJMsa1507092.
3
Unequal representation of genetic variation across ancestry groups creates healthcare inequality in the application of precision medicine.遗传变异在不同祖先群体中的分布不均，导致了精准医学应用中的医疗保健不平等。
Genome Biol. 2016 Jul 14;17(1):157. doi: 10.1186/s13059-016-1016-y.
4
Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.临床测序探索性研究联盟：加速基于证据的基因组医学实践。
Am J Hum Genet. 2016 Jun 2;98(6):1051-1066. doi: 10.1016/j.ajhg.2016.04.011. Epub 2016 May 12.
5
Parental Views on Expanded Newborn Screening Using Whole-Genome Sequencing.父母对使用全基因组测序进行扩大新生儿筛查的看法。
Pediatrics. 2016 Jan;137 Suppl 1(Suppl 1):S36-46. doi: 10.1542/peds.2015-3731H.
6
Mapping the Ethics of Translational Genomics: Situating Return of Results and Navigating the Research-Clinical Divide.绘制转化基因组学的伦理图谱：定位结果反馈并跨越研究与临床的鸿沟
J Law Med Ethics. 2015 Fall;43(3):486-501. doi: 10.1111/jlme.12291.
7
Returning a Research Participant's Genomic Results to Relatives: Analysis and Recommendations.向研究参与者的亲属反馈基因组结果：分析与建议。
J Law Med Ethics. 2015 Fall;43(3):440-63. doi: 10.1111/jlme.12288.
8
Identification of Medically Actionable Secondary Findings in the 1000 Genomes.在千人基因组计划中对具有医学可操作性的次要发现进行鉴定。
PLoS One. 2015 Sep 2;10(9):e0135193. doi: 10.1371/journal.pone.0135193. eCollection 2015.
9
Looking for Trouble: Preventive Genomic Sequencing in the General Population and the Role of Patient Choice.自找麻烦：普通人群中的预防性基因组测序与患者选择的作用
Am J Bioeth. 2015;15(7):3-14. doi: 10.1080/15265161.2015.1039721.
10
Points to Consider: Ethical, Legal, and Psychosocial Implications of Genetic Testing in Children and Adolescents.需考虑的要点：儿童和青少年基因检测的伦理、法律及社会心理影响
Am J Hum Genet. 2015 Jul 2;97(1):6-21. doi: 10.1016/j.ajhg.2015.05.022.