• 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
Genomic testing in Low- and Middle-Income Countries (LMIC).低收入和中等收入国家（LMIC）的基因组检测。
Eur J Hum Genet. 2024 Oct;32(10):1193-1194. doi: 10.1038/s41431-024-01622-x. Epub 2024 Oct 23.
2
Building functional and sustainable pharmacovigilance systems: an analysis of pharmacovigilance development across high-, middle- and low-income countries.建立功能完善且可持续的药物警戒系统：对高、中、低收入国家药物警戒发展情况的分析
Ther Adv Drug Saf. 2025 Jun 10;16:20420986251342941. doi: 10.1177/20420986251342941. eCollection 2025.
3
Gaps in Guidelines for the Management of Diabetes in Low- and Middle-Income Versus High-Income Countries-A Systematic Review.中低收入国家与高收入国家在糖尿病管理指南方面的差距：一项系统评价。
Diabetes Care. 2018 May;41(5):1097-1105. doi: 10.2337/dc17-1795.
4
Cognitive performance in depression in low- and middle-income countries: A systematic review with meta-analytic components.中低收入国家抑郁症患者的认知表现：系统评价与荟萃分析。
J Affect Disord. 2023 Dec 1;342:16-32. doi: 10.1016/j.jad.2023.09.007. Epub 2023 Sep 9.
5
Promoting physical activity for children and adolescents in low- and middle-income countries: An umbrella systematic review: A review on promoting physical activity in LMIC.在低收入和中等收入国家促进儿童和青少年的身体活动：一项综合性系统评价：关于在低收入和中等收入国家促进身体活动的综述
Prev Med. 2016 Jul;88:115-26. doi: 10.1016/j.ypmed.2016.03.025. Epub 2016 Apr 9.
6
Pharmacovigilance processes in low- and middle-income countries: moving from data collection to data analysis and interpretation.低收入和中等收入国家的药物警戒流程：从数据收集转向数据分析与解读
Ther Adv Drug Saf. 2025 Jun 11;16:20420986241300006. doi: 10.1177/20420986241300006. eCollection 2025.
7
Unit costs for delivery of antiretroviral treatment and prevention of mother-to-child transmission of HIV: a systematic review for low- and middle-income countries.抗逆转录病毒治疗和预防艾滋病毒母婴传播的单位成本： 中低收入国家的系统评价。
Pharmacoeconomics. 2011 Jul;29(7):579-99. doi: 10.2165/11586120-000000000-00000.
8
Systematic Review of Physical Activity, Sedentary Behaviour and Sleep Among Adults Living with Chronic Respiratory Disease in Low- and Middle-Income Countries.在中低收入国家，慢性呼吸系统疾病患者的体力活动、久坐行为和睡眠的系统评价。
Int J Chron Obstruct Pulmon Dis. 2022 Apr 18;17:821-854. doi: 10.2147/COPD.S345034. eCollection 2022.
9
Implementation of local/hospital-based health technology assessment initiatives in low- and middle-income countries.在中低收入国家实施基于当地/医院的卫生技术评估计划。
Int J Technol Assess Health Care. 2012 Oct;28(4):445-51. doi: 10.1017/S026646231200058X. Epub 2012 Sep 21.
10
A Comparative Analysis of Otolaryngology Journal Characteristics and Metrics Across World Bank Income Groups.世界银行收入组间耳鼻喉科期刊特征与指标的比较分析
Indian J Otolaryngol Head Neck Surg. 2024 Oct;76(5):4001-4005. doi: 10.1007/s12070-024-04762-0. Epub 2024 May 31.

引用本文的文献

1
Genomic sequencing technologies for rare disease in mainstream healthcare: the current state of implementation.主流医疗保健中用于罕见病的基因组测序技术：实施现状
Eur J Hum Genet. 2025 Aug 22. doi: 10.1038/s41431-025-01925-7.
2
Addressing Anemia in High-Altitude Populations: Global Impact, Prevalence, Challenges, and Potential Solutions.解决高海拔人群的贫血问题：全球影响、患病率、挑战及潜在解决方案
Am J Hematol. 2025 Sep;100(9):1590-1602. doi: 10.1002/ajh.27761. Epub 2025 Jul 2.

本文引用的文献

1
Optimizing genetic testing strategies for congenital anomalies in Iran.优化伊朗先天性异常的基因检测策略。
Eur J Hum Genet. 2024 Oct;32(10):1204-1205. doi: 10.1038/s41431-024-01578-y. Epub 2024 Mar 7.
2
Perceptions and preferences for genetic testing for sickle cell disease or trait: a qualitative study in Cameroon, Ghana and Tanzania.针对镰状细胞病或特征的基因检测的认知和偏好：在喀麦隆、加纳和坦桑尼亚开展的定性研究。
Eur J Hum Genet. 2024 Oct;32(10):1307-1313. doi: 10.1038/s41431-024-01553-7. Epub 2024 Feb 19.
3
Overcoming barriers to equitable genomic healthcare.克服公平基因组医疗的障碍。
Eur J Hum Genet. 2024 Oct;32(10):1202-1203. doi: 10.1038/s41431-024-01557-3. Epub 2024 Feb 13.
4
Bi-allelic PRRT2 variants may predispose to Self-limited Familial Infantile Epilepsy.双等位基因 PRRT2 变异可能导致自限性家族性婴儿癫痫。
Eur J Hum Genet. 2024 Oct;32(10):1338-1342. doi: 10.1038/s41431-024-01541-x. Epub 2024 Feb 5.
5
Towards solving the genetic diagnosis odyssey in Iranian patients with congenital anomalies.致力于解决伊朗先天性畸形患者的基因诊断难题。
Eur J Hum Genet. 2024 Oct;32(10):1238-1249. doi: 10.1038/s41431-024-01533-x. Epub 2024 Jan 26.
6
Diagnostic outcome of pro bono neurogenetic diagnostic service in Sri Lanka: A wealth creation.斯里兰卡公益神经遗传学诊断服务的诊断结果：创造财富。
Eur J Hum Genet. 2024 Oct;32(10):1299-1306. doi: 10.1038/s41431-023-01525-3. Epub 2024 Jan 23.
7
Decoding complex inherited phenotypes in rare disorders: the DECIPHERD initiative for rare undiagnosed diseases in Chile.解码罕见疾病中的复杂遗传表型：智利罕见未确诊疾病的 DECIPHERD 计划。
Eur J Hum Genet. 2024 Oct;32(10):1227-1237. doi: 10.1038/s41431-023-01523-5. Epub 2024 Jan 4.
8
De novo variants underlying monogenic syndromes with intellectual disability in a neurodevelopmental cohort from India.印度神经发育队列中单基因综合征伴智力障碍的新生变异。
Eur J Hum Genet. 2024 Oct;32(10):1291-1298. doi: 10.1038/s41431-023-01513-7. Epub 2023 Dec 20.
9
Genetic basis of osteogenesis imperfecta from a single tertiary centre in South Africa.南非单一三级医疗中心的成骨不全的遗传学基础。
Eur J Hum Genet. 2024 Oct;32(10):1285-1290. doi: 10.1038/s41431-023-01509-3. Epub 2023 Dec 15.
10
Ethical considerations for genetic research in low-income countries: perceptions of informed consent, data sharing, and expectations in Nicaragua.低收入国家遗传研究的伦理考量：尼加拉瓜对知情同意、数据共享和期望的看法。
Eur J Hum Genet. 2024 Oct;32(10):1278-1284. doi: 10.1038/s41431-023-01505-7. Epub 2023 Dec 5.

Genomic testing in Low- and Middle-Income Countries (LMIC).

作者信息

Girisha Katta M, Moosa Shahida

机构信息

Department of Medical Genetics, Kasturba Medical College, Manipal, Manipal Academy of Higher Education, Manipal, India.

Department of Genetics, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, Oman.

出版信息

Eur J Hum Genet. 2024 Oct;32(10):1193-1194. doi: 10.1038/s41431-024-01622-x. Epub 2024 Oct 23.

DOI:10.1038/s41431-024-01622-x
PMID:39443810
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11500087/
Abstract
摘要