• 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

相似文献

1
Translational research is a key to nongeneticist physicians' genomics education.转化研究是帮助非遗传学医生进行基因组学教育的关键。
Genet Med. 2014 Dec;16(12):871-3. doi: 10.1038/gim.2014.67. Epub 2014 May 29.
2
Framework for development of physician competencies in genomic medicine: report of the Competencies Working Group of the Inter-Society Coordinating Committee for Physician Education in Genomics.基因组医学中医师能力发展框架:基因组学医师教育跨学会协调委员会能力工作组报告
Genet Med. 2014 Nov;16(11):804-9. doi: 10.1038/gim.2014.35. Epub 2014 Apr 24.
3
Patient-centered communication in the era of electronic health records: What does the evidence say?电子健康记录时代以患者为中心的沟通:证据表明了什么?
Patient Educ Couns. 2017 Jan;100(1):50-64. doi: 10.1016/j.pec.2016.07.031. Epub 2016 Jul 25.
4
Professional medical education and genomics.专业医学教育与基因组学
Annu Rev Genomics Hum Genet. 2014;15:507-16. doi: 10.1146/annurev-genom-090413-025522. Epub 2014 Mar 12.
5
Realizing the potential of genomics: translation is not translational research.认识到基因组学的潜力:转化并非转化研究。
Genet Med. 2009 Dec;11(12):898-9; author reply 899. doi: 10.1097/GIM.0b013e3181c20bd2.
6
The National Institutes of Health's Biomedical Translational Research Information System (BTRIS): design, contents, functionality and experience to date.美国国立卫生研究院的生物医学转化研究信息系统(BTRIS):设计、内容、功能及目前的经验。
J Biomed Inform. 2014 Dec;52:11-27. doi: 10.1016/j.jbi.2013.11.004. Epub 2013 Nov 19.
7
A randomized trial to improve patient-centered care and hypertension control in underserved primary care patients.一项旨在改善服务不足的初级保健患者以患者为中心的护理和高血压控制的随机试验。
J Gen Intern Med. 2011 Nov;26(11):1297-304. doi: 10.1007/s11606-011-1794-6. Epub 2011 Jul 6.
8
University of Florida Clinical and Translational Science Institute: transformation and translation in personalized medicine.佛罗里达大学临床与转化科学研究所:个性化医疗中的转化与应用
Clin Transl Sci. 2011 Dec;4(6):400-2. doi: 10.1111/j.1752-8062.2011.00348.x. Epub 2011 Nov 9.
9
Physician-related barriers to communication and patient- and family-centred decision-making towards the end of life in intensive care: a systematic review.重症监护室临终阶段医生在沟通以及以患者和家庭为中心的决策方面存在的相关障碍:一项系统综述
Crit Care. 2014 Nov 18;18(6):604. doi: 10.1186/s13054-014-0604-z.
10
Provider interaction with the electronic health record: the effects on patient-centered communication in medical encounters.医疗服务提供者与电子健康记录的交互:对医疗问诊中以患者为中心的沟通的影响。
Patient Educ Couns. 2014 Sep;96(3):315-9. doi: 10.1016/j.pec.2014.05.004. Epub 2014 May 14.

引用本文的文献

1
Implementation of a culturally competent genetic testing programme into living donor evaluation: A two-site, non-randomised, pre-post trial design.将文化能力纳入活体供者评估的基因检测项目的实施:一项两站点、非随机、前后试验设计。
BMJ Open. 2023 May 15;13(5):e067657. doi: 10.1136/bmjopen-2022-067657.
2
Informing Integration of Genomic Medicine Into Primary Care: An Assessment of Current Practice, Attitudes, and Desired Resources.告知将基因组医学纳入初级保健:对当前实践、态度和所需资源的评估。
Front Genet. 2019 Nov 21;10:1189. doi: 10.3389/fgene.2019.01189. eCollection 2019.
3
Preparing Medical Specialists to Practice Genomic Medicine: Education an Essential Part of a Broader Strategy.培养医学专家以开展基因组医学实践:教育是更广泛战略的重要组成部分。
Front Genet. 2019 Sep 11;10:789. doi: 10.3389/fgene.2019.00789. eCollection 2019.
4
Impact of SLCO1B1 Pharmacogenetic Testing on Patient and Healthcare Outcomes: A Systematic Review.SLCO1B1 药物遗传学检测对患者和医疗保健结果的影响:系统评价。
Clin Pharmacol Ther. 2019 Aug;106(2):360-373. doi: 10.1002/cpt.1223. Epub 2018 Oct 18.
5
A collaborative translational research framework for evaluating and implementing the appropriate use of human genome sequencing to improve health.评估和实施人类基因组测序以改善健康的适当应用的合作转化研究框架。
PLoS Med. 2018 Aug 2;15(8):e1002631. doi: 10.1371/journal.pmed.1002631. eCollection 2018 Aug.
6
Impacts of incorporating personal genome sequencing into graduate genomics education: a longitudinal study over three course years.将个人基因组测序纳入研究生基因组学教育的影响:一项为期三个学年的纵向研究。
BMC Med Genomics. 2018 Jan 30;11(1):5. doi: 10.1186/s12920-018-0319-0.
7
Benefit of Preemptive Pharmacogenetic Information on Clinical Outcome.预先获取遗传药理学信息对临床结果的益处。
Clin Pharmacol Ther. 2018 May;103(5):787-794. doi: 10.1002/cpt.1035. Epub 2018 Mar 13.
8
How Primary Care Providers Talk to Patients about Genome Sequencing Results: Risk, Rationale, and Recommendation.初级保健提供者如何与患者讨论基因组测序结果:风险、原理和建议。
J Gen Intern Med. 2018 Jun;33(6):877-885. doi: 10.1007/s11606-017-4295-4. Epub 2018 Jan 26.
9
The Impact of Whole-Genome Sequencing on the Primary Care and Outcomes of Healthy Adult Patients: A Pilot Randomized Trial.全基因组测序对健康成年患者的初级保健和结局的影响:一项先导随机试验。
Ann Intern Med. 2017 Jun 27;167(3):159-169. doi: 10.7326/M17-0188. Print 2017 Aug 1.
10
Challenges and strategies for implementing genomic services in diverse settings: experiences from the Implementing GeNomics In pracTicE (IGNITE) network.在不同环境中实施基因组服务的挑战与策略:来自“实践中实施基因组学(IGNITE)”网络的经验
BMC Med Genomics. 2017 May 22;10(1):35. doi: 10.1186/s12920-017-0273-2.

本文引用的文献

1
Clinical interpretation and implications of whole-genome sequencing.全基因组测序的临床解读及意义。
JAMA. 2014 Mar 12;311(10):1035-45. doi: 10.1001/jama.2014.1717.
2
The growing role of professional societies in educating clinicians in genomics.专业学会在为临床医生提供基因组学教育方面日益重要的作用。
Genet Med. 2014 Aug;16(8):571-2. doi: 10.1038/gim.2014.6. Epub 2014 Feb 6.
3
Six components necessary for effective public health program implementation.有效实施公共卫生项目的六个必要组成部分。
Am J Public Health. 2014 Jan;104(1):17-22. doi: 10.2105/AJPH.2013.301608. Epub 2013 Nov 14.
4
Clinical whole-exome sequencing for the diagnosis of mendelian disorders.临床全外显子测序用于孟德尔疾病的诊断。
N Engl J Med. 2013 Oct 17;369(16):1502-11. doi: 10.1056/NEJMoa1306555. Epub 2013 Oct 2.
5
Special report: exome sequencing for clinical diagnosis of patients with suspected genetic disorders.特别报告:外显子组测序用于疑似遗传性疾病患者的临床诊断
Technol Eval Cent Assess Program Exec Summ. 2013 Aug;28(3):1-4.
6
Diagnostic exome sequencing in persons with severe intellectual disability.对严重智力障碍者进行外显子组诊断测序。
N Engl J Med. 2012 Nov 15;367(20):1921-9. doi: 10.1056/NEJMoa1206524. Epub 2012 Oct 3.
7
GenetiKit: a randomized controlled trial to enhance delivery of genetics services by family physicians.GenetiKit:一项通过家庭医生增强遗传服务提供的随机对照试验。
Fam Pract. 2011 Dec;28(6):615-23. doi: 10.1093/fampra/cmr040. Epub 2011 Jul 10.
8
Bringing genetics into primary care: findings from a national evaluation of pilots in England.将遗传学引入初级医疗保健:英国全国性试点评估结果
J Health Serv Res Policy. 2009 Oct;14(4):204-11. doi: 10.1258/jhsrp.2009.008158.
9
Shattuck lecture--clinical research to clinical practice--lost in translation?沙塔克讲座——从临床研究到临床实践——迷失在翻译中了吗?
N Engl J Med. 2003 Aug 28;349(9):868-74. doi: 10.1056/NEJMsa035507.

Translational research is a key to nongeneticist physicians' genomics education.

作者信息

Feero W Gregory, Manolio Teri A, Khoury Muin J

机构信息

Maine Dartmouth Family Medicine Residency Program, Augusta, Maine, USA.

Division of Genomic Medicine, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA.

出版信息

Genet Med. 2014 Dec;16(12):871-3. doi: 10.1038/gim.2014.67. Epub 2014 May 29.

DOI:10.1038/gim.2014.67
PMID:24875299
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4697936/
Abstract
摘要