• 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

Educating patients and providers through comprehensive pharmacogenetic test reports.

作者信息

Haga Susanne B

机构信息

Center for Applied Genomics & Precision Medicine, Duke School of Medicine, 304 Research Drive, Box 90141, Durham, NC 27708, USA.

出版信息

Pharmacogenomics. 2017 Jul;18(11):1047-1050. doi: 10.2217/pgs-2017-0088. Epub 2017 Jul 7.

DOI:10.2217/pgs-2017-0088
PMID:28686141
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5591460/
Abstract
摘要

相似文献

1
Educating patients and providers through comprehensive pharmacogenetic test reports.通过全面的药物遗传学检测报告对患者和医疗服务提供者进行教育。
Pharmacogenomics. 2017 Jul;18(11):1047-1050. doi: 10.2217/pgs-2017-0088. Epub 2017 Jul 7.
2
Managing Increased Accessibility to Pharmacogenomic Data.应对药物基因组学数据可及性增加的问题。
Clin Pharmacol Ther. 2019 Nov;106(5):922-924. doi: 10.1002/cpt.1602. Epub 2019 Sep 3.
3
Stakeholder perspectives of the clinical utility of pharmacogenomic testing in solid organ transplantation.利益相关者对临床实用型药物基因组检测在实体器官移植中的看法。
Pharmacogenomics. 2019 Dec;20(18):1291-1302. doi: 10.2217/pgs-2019-0129. Epub 2019 Nov 22.
4
Medical education in pharmacogenomics-results from a survey on pharmacogenetic knowledge in healthcare professionals within the European pharmacogenomics clinical implementation project Ubiquitous Pharmacogenomics (U-PGx).药物基因组学中的医学教育——欧洲药物基因组学临床实施项目“泛在药物基因组学（U-PGx）”中医疗保健专业人员药物遗传学知识调查结果
Eur J Clin Pharmacol. 2017 Oct;73(10):1247-1252. doi: 10.1007/s00228-017-2292-5. Epub 2017 Jul 2.
5
Precision Medicine: Lessons Learned From Implementation of a Pharmacogenetics-Based Patient Care Program in a Real-World Setting.精准医学：在实际环境中实施基于药物遗传学的患者护理计划所汲取的经验教训。
Clin Pharmacol Ther. 2019 Nov;106(5):933-935. doi: 10.1002/cpt.1611. Epub 2019 Sep 13.
6
Facilitators and Barriers to the Adoption of Pharmacogenetic Testing in an Inner-City Population.促进和阻碍在城市内人群中采用药物遗传学检测的因素。
Pharmacotherapy. 2018 Feb;38(2):205-216. doi: 10.1002/phar.2077. Epub 2018 Jan 21.
7
Primary care providers' use of pharmacist support for delivery of pharmacogenetic testing.初级保健提供者利用药剂师支持进行药物基因检测。
Pharmacogenomics. 2017 Mar;18(4):359-367. doi: 10.2217/pgs-2016-0177. Epub 2017 Feb 22.
8
Implementation of wide-scale pharmacogenetic testing in primary care.在基层医疗中实施广泛的药物遗传学检测。
Pharmacogenomics. 2019 Aug;20(12):903-913. doi: 10.2217/pgs-2019-0043.
9
A stepwise approach to implementing pharmacogenetic testing in the primary care setting.在初级保健环境中逐步实施药物遗传学检测的方法。
Pharmacogenomics. 2019 Oct;20(15):1103-1112. doi: 10.2217/pgs-2019-0053.
10
Pharmacogenomics education, research and clinical implementation in the state of Minnesota.明尼苏达州的药物基因组学教育、研究和临床实施。
Pharmacogenomics. 2021 Jul;22(11):681-691. doi: 10.2217/pgs-2021-0058. Epub 2021 Jun 17.

引用本文的文献

1
The Intersection between Pharmacogenomics and Health Equity: A Case Example.药物基因组学与健康公平性的交叉点：一个案例
Pharmacy (Basel). 2023 Dec 5;11(6):186. doi: 10.3390/pharmacy11060186.
2
Pharmacogenomics in practice: a review and implementation guide.实践中的药物基因组学：综述与实施指南。
Front Pharmacol. 2023 May 18;14:1189976. doi: 10.3389/fphar.2023.1189976. eCollection 2023.
3
Pharmacogenomics and health disparities, are we helping?药物基因组学与健康差异，我们是否有所助益？
Front Genet. 2023 Jan 23;14:1099541. doi: 10.3389/fgene.2023.1099541. eCollection 2023.
4
Investigating the presentation of uncertainty in an icon array: A randomized trial.探究图标阵列中不确定性的呈现方式：一项随机试验。
PEC Innov. 2022 Dec;1:None. doi: 10.1016/j.pecinn.2021.100003.
5
Integrating pharmacogenetic testing into primary care.将药物遗传学检测纳入初级保健。
Expert Rev Precis Med Drug Dev. 2017;2(6):327-336. doi: 10.1080/23808993.2017.1398046. Epub 2017 Nov 3.
6
Pharmacogenomic Testing In Pediatrics: Navigating The Ethical, Social, And Legal Challenges.儿科药物基因组学检测：应对伦理、社会和法律挑战
Pharmgenomics Pers Med. 2019 Oct 14;12:273-285. doi: 10.2147/PGPM.S179172. eCollection 2019.
7
A stepwise approach to implementing pharmacogenetic testing in the primary care setting.在初级保健环境中逐步实施药物遗传学检测的方法。
Pharmacogenomics. 2019 Oct;20(15):1103-1112. doi: 10.2217/pgs-2019-0053.
8
First Responder to Genomic Information: A Guide for Primary Care Providers.基因组信息的第一响应者：初级保健提供者指南。
Mol Diagn Ther. 2019 Aug;23(4):459-466. doi: 10.1007/s40291-019-00407-z.
9
Opportunities to implement a sustainable genomic medicine program: lessons learned from the IGNITE Network.实施可持续基因组医学计划的机会：来自 IGNITE 网络的经验教训。
Genet Med. 2019 Mar;21(3):743-747. doi: 10.1038/s41436-018-0080-y. Epub 2018 Jul 12.

本文引用的文献

1
Expanding access to high-quality plain-language patient education information through context-specific hyperlinks.通过特定情境超链接扩大获取高质量通俗易懂的患者教育信息的途径。
AMIA Annu Symp Proc. 2017 Feb 10;2016:277-284. eCollection 2016.
2
Participant-perceived understanding and perspectives on pharmacogenomics: the Mayo Clinic RIGHT protocol (Right Drug, Right Dose, Right Time).参与者对药物基因组学的理解和看法：梅奥诊所 RIGHT 方案（正确的药物、正确的剂量、正确的时间）。
Genet Med. 2017 Jul;19(7):819-825. doi: 10.1038/gim.2016.192. Epub 2017 Jan 5.
3
Infographics: Healthcare Communication for the Digital Age.信息图表：数字时代的医疗沟通
Ulster Med J. 2016 May;85(2):71-5.
4
Pharmacogenetic allele nomenclature: International workgroup recommendations for test result reporting.药物遗传学等位基因命名法：检测结果报告的国际工作组建议
Clin Pharmacol Ther. 2016 Feb;99(2):172-85. doi: 10.1002/cpt.280. Epub 2015 Nov 20.
5
Public preferences for communicating personal genomic risk information: a focus group study.公众对传达个人基因组风险信息的偏好：一项焦点小组研究。
Health Expect. 2016 Dec;19(6):1203-1214. doi: 10.1111/hex.12406. Epub 2015 Sep 1.
6
Informing the Design of Direct-to-Consumer Interactive Personal Genomics Reports.为直接面向消费者的交互式个人基因组学报告设计提供信息。
J Med Internet Res. 2015 Jun 12;17(6):e146. doi: 10.2196/jmir.4415.
7
Presenting Numeric Information with Percentages and Descriptive Risk Labels: A Randomized Trial.使用百分比和描述性风险标签呈现数值信息：一项随机试验。
Med Decis Making. 2015 Nov;35(8):937-47. doi: 10.1177/0272989X15584922. Epub 2015 May 7.
8
Developing patient-friendly genetic and genomic test reports: formats to promote patient engagement and understanding.制定患者友好型遗传和基因组检测报告：促进患者参与和理解的格式。
Genome Med. 2014 Jul 31;6(7):58. doi: 10.1186/s13073-014-0058-6. eCollection 2014.
9
Refining the structure and content of clinical genomic reports.优化临床基因组报告的结构与内容。
Am J Med Genet C Semin Med Genet. 2014 Mar;166C(1):85-92. doi: 10.1002/ajmg.c.31395. Epub 2014 Mar 10.
10
Communicating genetic risk information for common disorders in the era of genomic medicine.在基因组医学时代传播常见疾病的遗传风险信息。
Annu Rev Genomics Hum Genet. 2013;14:491-513. doi: 10.1146/annurev-genom-092010-110722.