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A Template for Authoring and Adapting Genomic Medicine Content in the eMERGE Infobutton Project.电子医疗记录基因组学与环境暴露研究网络（eMERGE）信息按钮项目中用于编写和改编基因组医学内容的模板。
AMIA Annu Symp Proc. 2014 Nov 14;2014:944-53. eCollection 2014.
2
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3
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Integrating genetic information resources with an EHR.将遗传信息资源与电子健康记录相结合。
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7
Integrating Genomic Resources with Electronic Health Records using the HL7 Infobutton Standard.使用HL7信息按钮标准将基因组资源与电子健康记录整合。
Appl Clin Inform. 2016 Aug 31;7(3):817-31. doi: 10.4338/ACI-2016-04-RA-0058.
8
Perspectives on what is needed to implement genomic medicine.关于实施基因组医学所需条件的观点。
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本文引用的文献

1
Incorporation of pharmacogenomics into routine clinical practice: the Clinical Pharmacogenetics Implementation Consortium (CPIC) guideline development process.将药物基因组学纳入常规临床实践：临床药物基因组学实施联盟（CPIC）指南制定过程。
Curr Drug Metab. 2014 Feb;15(2):209-17. doi: 10.2174/1389200215666140130124910.
2
Wikis and collaborative writing applications in health care: a scoping review.医疗保健领域中的维基和协作写作应用：一项范围综述
J Med Internet Res. 2013 Oct 8;15(10):e210. doi: 10.2196/jmir.2787.
3
A survey of informatics approaches to whole-exome and whole-genome clinical reporting in the electronic health record.电子健康记录中全外显子组和全基因组临床报告的信息学方法调查。
Genet Med. 2013 Oct;15(10):824-32. doi: 10.1038/gim.2013.120. Epub 2013 Sep 26.
4
Opportunities for genomic clinical decision support interventions.基因组临床决策支持干预措施的机会。
Genet Med. 2013 Oct;15(10):817-23. doi: 10.1038/gim.2013.128. Epub 2013 Sep 19.
5
Electronic health record design and implementation for pharmacogenomics: a local perspective.电子病历设计与实施中的药物基因组学：本土视角。
Genet Med. 2013 Oct;15(10):833-41. doi: 10.1038/gim.2013.109. Epub 2013 Sep 5.
6
Disseminating context-specific access to online knowledge resources within electronic health record systems.在电子健康记录系统中传播针对特定情境的在线知识资源访问权限。
Stud Health Technol Inform. 2013;192:672-6.
7
PharmGKB: the Pharmacogenomics Knowledge Base.药物基因组学知识库（PharmGKB）
Methods Mol Biol. 2013;1015:311-20. doi: 10.1007/978-1-62703-435-7_20.
8
The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future.电子病历与基因组学（eMERGE）网络：过去、现在和未来。
Genet Med. 2013 Oct;15(10):761-71. doi: 10.1038/gim.2013.72. Epub 2013 Jun 6.
9
The Pharmacogenomics Research Network Translational Pharmacogenetics Program: overcoming challenges of real-world implementation.药物基因组学研究网络转化药物遗传学计划：克服真实世界实施的挑战。
Clin Pharmacol Ther. 2013 Aug;94(2):207-10. doi: 10.1038/clpt.2013.59. Epub 2013 Mar 19.
10
Meeting the electronic health record "meaningful use" criterion for the HL7 infobutton standard using OpenInfobutton and the Librarian Infobutton Tailoring Environment (LITE).使用OpenInfobutton和图书馆员信息按钮定制环境（LITE）满足HL7信息按钮标准的电子健康记录“有意义使用”标准。
AMIA Annu Symp Proc. 2012;2012:112-20. Epub 2012 Nov 3.

电子医疗记录基因组学与环境暴露研究网络（eMERGE）信息按钮项目中用于编写和改编基因组医学内容的模板。

A Template for Authoring and Adapting Genomic Medicine Content in the eMERGE Infobutton Project.

作者信息

Overby Casey L, Rasmussen Luke V, Hartzler Andrea, Connolly John J, Peterson Josh F, Hedberg RoseMary E, Freimuth Robert R, Shirts Brian H, Denny Joshua C, Larson Eric B, Chute Christopher G, Jarvik Gail P, Ralston James D, Shuldiner Alan R, Starren Justin, Kullo Iftikhar J, Tarczy-Hornoch Peter, Williams Marc S

机构信息

Program for Personalized and Genomic Medicine and Department of Medicine, University of Maryland, Baltimore, MD ; Center for Health-related Informatics and Bioimaging, University of Maryland, Baltimore, MD.

Department of Preventive Medicine, The Children's Hospital of Philadelphia, Philadelphia, PA.

出版信息

AMIA Annu Symp Proc. 2014 Nov 14;2014:944-53. eCollection 2014.

PMID:25954402
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4419923/
Abstract

The Electronic Medical Records and Genomics (eMERGE) Network is a national consortium that is developing methods and best practices for using the electronic health record (EHR) for genomic medicine and research. We conducted a multi-site survey of information resources to support integration of pharmacogenomics into clinical care. This work aimed to: (a) characterize the diversity of information resource implementation strategies among eMERGE institutions; (b) develop a master template containing content topics of important for genomic medicine (as identified by the DISCERN-Genetics tool); and (c) assess the coverage of content topics among information resources developed by eMERGE institutions. Given that a standard implementation does not exist and sites relied on a diversity of information resources, we identified a need for a national effort to efficiently produce sharable genomic medicine resources capable of being accessed from the EHR. We discuss future areas of work to prepare institutions to use infobuttons for distributing standardized genomic content.

摘要

电子病历与基因组学（eMERGE）网络是一个全国性联盟，正在开发将电子健康记录（EHR）用于基因组医学和研究的方法及最佳实践。我们开展了一项信息资源的多中心调查，以支持将药物基因组学整合到临床护理中。这项工作旨在：（a）描述eMERGE机构间信息资源实施策略的多样性；（b）开发一个包含对基因组医学重要的内容主题的主模板（由DISCERN-遗传学工具确定）；（c）评估eMERGE机构开发的信息资源中内容主题的覆盖范围。鉴于不存在标准实施方法且各机构依赖多种信息资源，我们确定需要开展一项全国性工作，以高效生产能够从电子健康记录中获取的可共享基因组医学资源。我们讨论了未来的工作领域，以使各机构做好使用信息按钮来分发标准化基因组内容的准备。