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Recontacting in clinical genetics and genomic medicine? We need to talk about it.在临床遗传学和基因组医学中重新联系?我们需要谈谈这个问题。
Eur J Hum Genet. 2017 May;25(5):520-521. doi: 10.1038/ejhg.2017.8. Epub 2017 Feb 8.
2
Recontacting in medical genetics: the implications of a broadening knowledge base.医学遗传学中的再联系:拓宽知识库的影响。
Hum Genet. 2022 May;141(5):1045-1051. doi: 10.1007/s00439-021-02353-5. Epub 2021 Aug 30.
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A 'joint venture' model of recontacting in clinical genomics: challenges for responsible implementation.临床基因组学中重新联系的“合资企业”模式:负责任实施面临的挑战
Eur J Med Genet. 2017 Jul;60(7):403-409. doi: 10.1016/j.ejmg.2017.05.001. Epub 2017 May 10.
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Experts reflecting on the duty to recontact patients and research participants; why professionals should take the lead in developing guidelines.专家们对再次联系患者和研究参与者的职责进行反思;为何专业人士应带头制定指导方针。
Eur J Med Genet. 2020 Feb;63(2):103642. doi: 10.1016/j.ejmg.2019.03.006. Epub 2019 Mar 20.
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Recontacting or not recontacting? A survey of current practices in clinical genetics centres in Europe.是否重新联系?欧洲临床遗传中心当前实践情况调查。
Eur J Hum Genet. 2018 Jul;26(7):946-954. doi: 10.1038/s41431-018-0131-5. Epub 2018 Apr 23.
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Recontact in clinical practice: a survey of clinical genetics services in the United Kingdom.临床实践中的再次接触:英国临床遗传学服务调查
Genet Med. 2016 Sep;18(9):876-81. doi: 10.1038/gim.2015.194. Epub 2016 Feb 18.
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Recontacting patients in clinical genetics services: recommendations of the European Society of Human Genetics.临床遗传学服务中患者的再联系:欧洲人类遗传学会的建议。
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Recontact practices of cancer genetic counselors and an exploration of professional, legal, and ethical duty.癌症遗传咨询师的再次接触实践以及对专业、法律和道德责任的探讨。
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Recontacting in light of new genetic diagnostic techniques for patients with intellectual disability: Feasibility and parental perspectives.鉴于针对智力残疾患者的新基因诊断技术进行再次联系:可行性及家长观点。
Eur J Med Genet. 2018 Apr;61(4):213-218. doi: 10.1016/j.ejmg.2017.11.017. Epub 2017 Nov 27.
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Recontacting clinical genetics patients with reclassified results: equity and policy challenges.向临床遗传学患者重新传达重新分类的结果:公平性与政策挑战
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"Your cancer is no longer considered cancer": Psychological reactions to reclassification information and communication preferences.“您的癌症不再被视为癌症”:对重新分类信息的心理反应及沟通偏好
PEC Innov. 2023 May 10;2:100165. doi: 10.1016/j.pecinn.2023.100165. eCollection 2023 Dec.
2
Cases in Precision Medicine: Is There an Obligation to Return Reinterpreted Genetic Results to Former Patients?精准医学案例:是否有义务将重新解读的遗传结果告知以前的患者?
Ann Intern Med. 2023 Apr;176(4):563-567. doi: 10.7326/M22-3682. Epub 2023 Mar 28.
3
Evaluating the Integration of Genomics into Cancer Screening Programmes: Challenges and Opportunities.评估基因组学融入癌症筛查项目:挑战与机遇
Curr Genet Med Rep. 2019;7(2):63-74. doi: 10.1007/s40142-019-00162-x. Epub 2019 May 18.
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Is there a duty to reinterpret genetic data? The ethical dimensions.是否有义务重新解释基因数据?伦理维度。
Genet Med. 2020 Mar;22(3):633-639. doi: 10.1038/s41436-019-0679-7. Epub 2019 Oct 15.
5
Recontacting patients in clinical genetics services: recommendations of the European Society of Human Genetics.临床遗传学服务中患者的再联系:欧洲人类遗传学会的建议。
Eur J Hum Genet. 2019 Feb;27(2):169-182. doi: 10.1038/s41431-018-0285-1. Epub 2018 Oct 11.
6
Recontacting or not recontacting? A survey of current practices in clinical genetics centres in Europe.是否重新联系?欧洲临床遗传中心当前实践情况调查。
Eur J Hum Genet. 2018 Jul;26(7):946-954. doi: 10.1038/s41431-018-0131-5. Epub 2018 Apr 23.
7
Paediatric genomics: diagnosing rare disease in children.儿科基因组学:诊断儿童罕见病。
Nat Rev Genet. 2018 May;19(5):253-268. doi: 10.1038/nrg.2017.116. Epub 2018 Feb 5.
8
The challenges of the expanded availability of genomic information: an agenda-setting paper.基因组信息可及性扩大带来的挑战:一篇议程设定文件。
J Community Genet. 2018 Apr;9(2):103-116. doi: 10.1007/s12687-017-0331-7. Epub 2017 Sep 26.
9
Recontacting in clinical practice: the views and expectations of patients in the United Kingdom.临床实践中的再次联系:英国患者的观点与期望
Eur J Hum Genet. 2017 Oct;25(10):1106-1112. doi: 10.1038/ejhg.2017.122. Epub 2017 Aug 2.

本文引用的文献

1
Recontacting in clinical practice: an investigation of the views of healthcare professionals and clinical scientists in the United Kingdom.临床实践中的再次联系:对英国医疗保健专业人员和临床科学家观点的调查。
Eur J Hum Genet. 2017 Feb;25(3):275-279. doi: 10.1038/ejhg.2016.188. Epub 2017 Jan 4.
2
Am I My Family's Keeper? Disclosure Dilemmas in Next-Generation Sequencing.我是家人的守护者吗?下一代测序中的信息披露困境
Hum Mutat. 2016 Dec;37(12):1257-1262. doi: 10.1002/humu.23118.
3
Recontact in clinical practice: a survey of clinical genetics services in the United Kingdom.临床实践中的再次接触:英国临床遗传学服务调查
Genet Med. 2016 Sep;18(9):876-81. doi: 10.1038/gim.2015.194. Epub 2016 Feb 18.
4
Legal, ethical issues loom over topic of recontacting patients: advances in research, next-generation sequencing lead geneticists to consider approaching former patients with results about genetic variants.再次联系患者的话题面临法律和伦理问题:研究进展、新一代测序技术促使遗传学家考虑将基因变异结果告知以前的患者。
Am J Med Genet A. 2015 Apr;167A(4):vii-viii. doi: 10.1002/ajmg.a.37059.
5
Is there a duty to recontact in light of new genetic technologies? A systematic review of the literature.鉴于新的基因技术,是否有再次联系的义务?文献系统综述。
Genet Med. 2015 Aug;17(8):668-78. doi: 10.1038/gim.2014.173. Epub 2014 Dec 11.
6
Provision of genetic services in Europe: current practices and issues.欧洲遗传服务的提供:当前实践与问题
Eur J Hum Genet. 2003 Dec;11 Suppl 2:S13-48. doi: 10.1038/sj.ejhg.5201111.
7
The duty to recontact: attitudes of genetics service providers.再次联系的义务:遗传学服务提供者的态度
Am J Hum Genet. 1999 Mar;64(3):852-60. doi: 10.1086/302293.
8
Risk reversals in predictive testing for Huntington disease.亨廷顿病预测性检测中的风险逆转
Am J Hum Genet. 1997 Oct;61(4):945-52. doi: 10.1086/514873.

Recontacting in clinical genetics and genomic medicine? We need to talk about it.

作者信息

Carrieri Daniele, Dheensa Sandi, Doheny Shane, Clarke Angus J, Turnpenny Peter D, Lucassen Anneke M, Kelly Susan E

机构信息

Egenis, University of Exeter,Exeter, UK.

Faculty of Medicine, University of Southampton, Southampton, UK.

出版信息

Eur J Hum Genet. 2017 May;25(5):520-521. doi: 10.1038/ejhg.2017.8. Epub 2017 Feb 8.

DOI:10.1038/ejhg.2017.8
PMID:28176765
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5437914/
Abstract
摘要