• 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 interface of genomic information with the electronic health record: a points to consider statement of the American College of Medical Genetics and Genomics (ACMG).

作者信息

Grebe Theresa A, Khushf George, Chen Margaret, Bailey Dawn, Brenman Leslie Manace, Williams Marc S, Seaver Laurie H

机构信息

Phoenix Children's Hospital, University of Arizona College of Medicine, Phoenix, AZ, USA.

Department of Philosophy, University of South Carolina, Columbia, SC, USA.

出版信息

Genet Med. 2020 Sep;22(9):1431-1436. doi: 10.1038/s41436-020-0841-2. Epub 2020 Jun 1.

DOI:10.1038/s41436-020-0841-2
PMID:32475985
Abstract
摘要

相似文献

1
The interface of genomic information with the electronic health record: a points to consider statement of the American College of Medical Genetics and Genomics (ACMG).基因组信息与电子健康记录的接口：美国医学遗传学与基因组学学会（ACMG）的一份需考虑要点声明
Genet Med. 2020 Sep;22(9):1431-1436. doi: 10.1038/s41436-020-0841-2. Epub 2020 Jun 1.
2
Points to consider to avoid unfair discrimination and the misuse of genetic information: A statement of the American College of Medical Genetics and Genomics (ACMG).避免不公平歧视和基因信息滥用需考虑的要点：美国医学遗传学与基因组学学会（ACMG）声明
Genet Med. 2022 Mar;24(3):512-520. doi: 10.1016/j.gim.2021.11.002. Epub 2021 Dec 16.
3
The designated record set for clinical genetic and genomic testing: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG).临床遗传与基因组检测的指定记录集：美国医学遗传学与基因组学学会（ACMG）的一份考量要点声明
Genet Med. 2023 Mar;25(3):100342. doi: 10.1016/j.gim.2022.11.010. Epub 2022 Dec 22.
4
Stewardship of patient genomic data: A policy statement of the American College of Medical Genetics and Genomics (ACMG).患者基因组数据管理：美国医学遗传学与基因组学学会（ACMG）的政策声明。
Genet Med. 2022 Mar;24(3):509-511. doi: 10.1016/j.gim.2021.11.001. Epub 2021 Dec 16.
5
Patient re-contact after revision of genomic test results: points to consider-a statement of the American College of Medical Genetics and Genomics (ACMG).基因组检测结果修订后的患者重新联系：需考虑的要点——美国医学遗传学与基因组学学会（ACMG）声明
Genet Med. 2019 Apr;21(4):769-771. doi: 10.1038/s41436-018-0391-z. Epub 2018 Dec 22.
6
Incidental detection of acquired variants in germline genetic and genomic testing: a points to consider statement of the American College of Medical Genetics and Genomics (ACMG).生殖系基因和基因组检测中获得性变异的偶然发现：美国医学遗传学与基因组学学会（ACMG）的一份要点声明
Genet Med. 2021 Jul;23(7):1179-1184. doi: 10.1038/s41436-021-01138-5. Epub 2021 Apr 16.
7
Diagnostic testing for uniparental disomy: a points to consider statement from the American College of Medical Genetics and Genomics (ACMG).单亲二体的诊断检测：美国医学遗传学与基因组学学会（ACMG）的一份要点声明
Genet Med. 2020 Jul;22(7):1133-1141. doi: 10.1038/s41436-020-0782-9. Epub 2020 Apr 16.
8
Points to consider when assessing relationships (or suspecting misattributed relationships) during family-based clinical genomic testing: a statement of the American College of Medical Genetics and Genomics (ACMG).基于家庭的临床基因组检测中评估关系（或怀疑关系错误归因）时需考虑的要点：美国医学遗传学与基因组学学会（ACMG）声明
Genet Med. 2020 Aug;22(8):1285-1287. doi: 10.1038/s41436-020-0821-6. Epub 2020 May 14.
9
Points to consider in the reevaluation and reanalysis of genomic test results: a statement of the American College of Medical Genetics and Genomics (ACMG).基因组检测结果重新评估与再分析中需考虑的要点：美国医学遗传学与基因组学学会（ACMG）声明
Genet Med. 2019 Jun;21(6):1267-1270. doi: 10.1038/s41436-019-0478-1. Epub 2019 Apr 24.
10
Clinical, technical, and environmental biases influencing equitable access to clinical genetics/genomics testing: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG).影响临床遗传/基因组检测公平可及性的临床、技术和环境偏倚：美国医学遗传学与基因组学学会（ACMG）的要点声明
Genet Med. 2023 Jun;25(6):100812. doi: 10.1016/j.gim.2023.100812. Epub 2023 Apr 14.

引用本文的文献

1
Finding buried genetic test results in the electronic health record is inefficient and variable across institutions.在电子健康记录中查找隐藏的基因检测结果效率低下，且各机构之间存在差异。
Ther Adv Rare Dis. 2025 Jul 11;6:26330040251356521. doi: 10.1177/26330040251356521. eCollection 2025 Jan-Dec.
2
Low frequency of structured documentation for cancer genetic testing in a large electronic health record dataset: A brief report using All of Us Research data.大型电子健康记录数据集中癌症基因检测结构化文档的低频率：使用“我们所有人”研究数据的简要报告
J Genet Couns. 2025 Apr;34(2):e2011. doi: 10.1002/jgc4.2011.
3
A Comprehensive Approach to Clinical Decision Support in the Return of Genome Informed Risk Assessments to Primary Care Pediatricians.
将基因组信息风险评估反馈给基层医疗儿科医生的临床决策支持综合方法。
Appl Clin Inform. 2025 Jan;16(1):193-204. doi: 10.1055/a-2445-9185. Epub 2025 Feb 26.
4
Misattributed paternity discovery: A critique of medical organizations' recommendations.错误认定亲子关系的发现：对医学组织建议的批判
Am J Hum Genet. 2025 Mar 6;112(3):492-507. doi: 10.1016/j.ajhg.2025.01.006. Epub 2025 Feb 3.
5
Protocol for a type 3 hybrid implementation cluster randomized clinical trial to evaluate the effect of patient and clinician nudges to advance the use of genomic medicine across a diverse health system.一种 3 型混合实施集群随机临床试验的方案，旨在评估患者和临床医生提示在多样化医疗体系中推进基因组医学应用的效果。
Implement Sci. 2024 Aug 19;19(1):61. doi: 10.1186/s13012-024-01385-5.
6
Enabling the clinical application of artificial intelligence in genomics: a perspective of the AMIA Genomics and Translational Bioinformatics Workgroup.推动人工智能在基因组学中的临床应用：AMIA 基因组学和转化生物信息学工作组的观点。
J Am Med Inform Assoc. 2024 Jan 18;31(2):536-541. doi: 10.1093/jamia/ocad211.
7
Do genomic passports leave us more vulnerable or less vulnerable? Perspectives from an online citizen engagement.基因护照会让我们变得更易受伤害还是更不易受伤害？来自在线公民参与的观点。
Humanit Soc Sci Commun. 2023;10(1):83. doi: 10.1057/s41599-023-01580-7. Epub 2023 Mar 4.
8
Impact of integrating genomic data into the electronic health record on genetics care delivery.将基因组数据整合到电子健康记录中对遗传护理服务的影响。
Genet Med. 2022 Nov;24(11):2338-2350. doi: 10.1016/j.gim.2022.08.009. Epub 2022 Sep 15.
9
Variation among DNA banking consent forms: points for clinicians to bank on.DNA库同意书之间的差异：临床医生可依赖的要点。
J Community Genet. 2022 Aug;13(4):389-397. doi: 10.1007/s12687-022-00601-3. Epub 2022 Jul 14.
10
Genomic medicine for liver disease.肝病的基因组医学
Hepatology. 2022 Sep;76(3):860-868. doi: 10.1002/hep.32364. Epub 2022 Feb 21.