• 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

Research to reduce inequities in cancer risk services: Insights for remote genetic counseling in a pandemic and beyond.

作者信息

Lee Robin, Frick Miya, Joseph Galen, Guerra Claudia, Stewart Susan, Kaplan Celia, Dixit Niharika, Tsoh Janice Y, Flores Selena, Pasick Rena J

机构信息

University of California, San Francisco, San Francisco, California, USA.

University of California, Davis, Davis, California, USA.

出版信息

J Genet Couns. 2021 Oct;30(5):1292-1297. doi: 10.1002/jgc4.1525. Epub 2021 Oct 23.

DOI:10.1002/jgc4.1525
PMID:34687478
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8657358/
Abstract
摘要

相似文献

1
Research to reduce inequities in cancer risk services: Insights for remote genetic counseling in a pandemic and beyond.减少癌症风险服务不平等现象的研究：大流行及以后远程遗传咨询的见解
J Genet Couns. 2021 Oct;30(5):1292-1297. doi: 10.1002/jgc4.1525. Epub 2021 Oct 23.
2
Telegenetics: Remote Counseling During the COVID-19 Pandemic.远程遗传学：COVID-19大流行期间的远程咨询
Clin J Oncol Nurs. 2020 Jun 1;24(3):244-248. doi: 10.1188/20.CJON.244-248.
3
Transition to telephone genetic counseling services during the COVID-19 pandemic.在 COVID-19 大流行期间向电话遗传咨询服务过渡。
J Genet Couns. 2021 Aug;30(4):984-988. doi: 10.1002/jgc4.1365. Epub 2020 Dec 4.
4
Utilizing Remote Real-Time Videoconferencing to Expand Access to Cancer Genetic Services in Community Practices: A Multicenter Feasibility Study.利用远程实时视频会议扩大社区医疗机构癌症基因检测服务的可及性：一项多中心可行性研究
J Med Internet Res. 2016 Feb 1;18(2):e23. doi: 10.2196/jmir.4564.
5
Acceptability of telemedicine and other cancer genetic counseling models of service delivery in geographically remote settings.远程医疗及其他癌症遗传咨询服务模式在地理偏远地区的可接受性。
J Genet Couns. 2014 Apr;23(2):221-8. doi: 10.1007/s10897-013-9652-9. Epub 2013 Sep 8.
6
Telemedicine for contraceptive counseling: An exploratory survey of US family planning providers following rapid adoption of services during the COVID-19 pandemic.远程避孕咨询服务：在 COVID-19 大流行期间迅速采用该服务后，对美国计划生育服务提供者的探索性调查。
Contraception. 2021 Mar;103(3):157-162. doi: 10.1016/j.contraception.2020.11.006. Epub 2020 Nov 17.
7
Reaching high-risk underserved individuals for cancer genetic counseling by video-teleconferencing.通过视频电话会议为高风险的医疗服务不足人群提供癌症遗传咨询。
J Community Support Oncol. 2016 Apr;14(4):162-8. doi: 10.12788/jcso.0247.
8
Telehealth genetic services during the COVID-19 Pandemic: Implementation and patient experiences across multiple specialties in Nebraska.新冠肺炎疫情期间的远程医疗遗传服务：内布拉斯加州多个专业的实施情况和患者体验。
J Genet Couns. 2021 Oct;30(5):1233-1243. doi: 10.1002/jgc4.1507. Epub 2021 Oct 7.
9
Benefits and limitations of telegenetics: A literature review.远程遗传学的优缺点：文献综述。
J Genet Couns. 2021 Aug;30(4):924-937. doi: 10.1002/jgc4.1418. Epub 2021 Apr 4.
10
The COVID-19 pandemic and reproductive genetic counseling: Changes in access and service delivery at an academic medical center in the United States.COVID-19 大流行与生殖遗传咨询：美国一家学术医疗中心在咨询途径和服务提供方面的变化。
J Genet Couns. 2021 Aug;30(4):958-968. doi: 10.1002/jgc4.1462. Epub 2021 Jul 5.

引用本文的文献

1
Randomized control trial comparing genetic counseling service delivery models in an underserved population.在服务不足人群中比较遗传咨询服务提供模式的随机对照试验。
J Genet Couns. 2025 Apr;34(2):e1975. doi: 10.1002/jgc4.1975. Epub 2024 Oct 7.
2
Current status of hereditary breast and ovarian cancer practice among gynecologic oncologists in Japan: a nationwide survey by the Japan Society of Gynecologic Oncology (JSGO).日本妇科肿瘤学家中遗传性乳腺癌和卵巢癌实践的现状：日本妇科肿瘤学会（JSGO）的全国性调查。
J Gynecol Oncol. 2022 Sep;33(5):e61. doi: 10.3802/jgo.2022.33.e61. Epub 2022 Jul 18.

本文引用的文献

1
Development and early implementation of an Accessible, Relational, Inclusive and Actionable approach to genetic counseling: The ARIA model.开发并早期实施一种便于获取、注重关系、具包容性和能付诸行动的遗传咨询方法：ARIA 模型。
Patient Educ Couns. 2021 May;104(5):969-978. doi: 10.1016/j.pec.2020.12.017. Epub 2020 Dec 23.
2
Telemedicine and healthcare disparities: a cohort study in a large healthcare system in New York City during COVID-19.远程医疗与医疗保健差距：在 COVID-19 期间纽约市大型医疗系统中的一项队列研究。
J Am Med Inform Assoc. 2021 Jan 15;28(1):33-41. doi: 10.1093/jamia/ocaa217.
3
Lack of Telemedicine Training in Academic Medicine: Are We Preparing the Next Generation?学术医学中远程医疗培训的缺失：我们是否在为下一代做好准备？
Telemed J E Health. 2021 Jan;27(1):62-67. doi: 10.1089/tmj.2019.0287. Epub 2020 Apr 15.
4
Racial/Ethnic Disparities in BRCA Counseling and Testing: a Narrative Review.BRCA 咨询和检测中的种族/民族差异：叙述性评论。
J Racial Ethn Health Disparities. 2019 Jun;6(3):570-583. doi: 10.1007/s40615-018-00556-7. Epub 2019 Apr 8.
5
Effective communication in the era of precision medicine: A pilot intervention with low health literacy patients to improve genetic counseling communication.精准医学时代的有效沟通：针对健康素养低的患者进行的一项改善遗传咨询沟通的试点干预措施。
Eur J Med Genet. 2019 May;62(5):357-367. doi: 10.1016/j.ejmg.2018.12.004. Epub 2018 Dec 13.
6
Genetic Counselor and Healthcare Interpreter Perspectives on the Role of Interpreters in Cancer Genetic Counseling.遗传咨询师和医疗保健口译员对翻译员在癌症遗传咨询中角色的看法。
Health Commun. 2019 Nov;34(13):1608-1618. doi: 10.1080/10410236.2018.1514684. Epub 2018 Sep 19.
7
The Clinical Sequencing Evidence-Generating Research Consortium: Integrating Genomic Sequencing in Diverse and Medically Underserved Populations.临床测序证据生成研究联盟：在不同和医疗资源不足的人群中整合基因组测序。
Am J Hum Genet. 2018 Sep 6;103(3):319-327. doi: 10.1016/j.ajhg.2018.08.007.
8
Differences in US healthcare coverage policies in BRCA testing and potential implications.美国BRCA检测中医疗保健覆盖政策的差异及潜在影响。
Per Med. 2012 Jan;9(1):5-8. doi: 10.2217/pme.11.85.
9
Information Mismatch: Cancer Risk Counseling with Diverse Underserved Patients.信息不对称：为不同的医疗服务不足患者提供癌症风险咨询
J Genet Couns. 2017 Oct;26(5):1090-1104. doi: 10.1007/s10897-017-0089-4. Epub 2017 Mar 13.
10
Validation of an Efficient Screening Tool to Identify Low-Income Women at High Risk for Hereditary Breast Cancer.一种用于识别遗传性乳腺癌高危低收入女性的高效筛查工具的验证
Public Health Genomics. 2016;19(6):342-351. doi: 10.1159/000452095. Epub 2016 Oct 28.