• 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

尼日利亚的医学遗传学与基因组医学

Medical genetics and genomic medicine in Nigeria.

作者信息

Adeyemo Adebowale A, Amodu Olukemi K, Ekure Ekanem E, Omotade Olayemi O

机构信息

National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland.

Institute of Child Health, College of Medicine, University of Ibadan, Ibadan, Nigeria.

出版信息

Mol Genet Genomic Med. 2018 May;6(3):314-321. doi: 10.1002/mgg3.419. Epub 2018 Jun 5.

DOI:10.1002/mgg3.419
PMID:29871027
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6014475/
Abstract

Medical genetics and genomic medicine in Nigeria. [Image: see text]

摘要

尼日利亚的医学遗传学与基因组医学。[图片：见正文]

相似文献

1
Medical genetics and genomic medicine in Nigeria.尼日利亚的医学遗传学与基因组医学
Mol Genet Genomic Med. 2018 May;6(3):314-321. doi: 10.1002/mgg3.419. Epub 2018 Jun 5.
2
Genetics and genomic medicine.遗传学与基因组医学。
Radiol Technol. 2009 Mar-Apr;80(4):318-35; quiz 336-9.
3
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.
4
Charting a course for genomic medicine from base pairs to bedside.为基因组医学绘制从碱基对到床边的路线图。
Nature. 2011 Feb 10;470(7333):204-13. doi: 10.1038/nature09764.
5
Perspectives in Genetics and Sickle Cell Disease Prevention in Africa: Beyond the Preliminary Data from Cameroon.非洲遗传学与镰状细胞病预防的前景：超越喀麦隆的初步数据
Public Health Genomics. 2015;18(4):237-41. doi: 10.1159/000431020. Epub 2015 Jun 4.
6
Genetics & genomics: what every oncology nurse needs to know.遗传学与基因组学：每位肿瘤护理人员都应了解的知识。
ONS Connect. 2011 Feb;26(2):8-12.
7
You say genomics, I say genetics..你说基因组学，我说遗传学。
Nature. 2005 Oct 20;437(7062):1202-3. doi: 10.1038/nj7062-1202a.
8
Medical genetics and genomic medicine in the United States. Part 2: Reproductive genetics, newborn screening, genetic counseling, training, and registries.美国的医学遗传学与基因组医学。第2部分：生殖遗传学、新生儿筛查、遗传咨询、培训及登记处。
Mol Genet Genomic Med. 2017 Nov;5(6):621-630. doi: 10.1002/mgg3.343.
9
The importance of genetics education for undergraduate and graduate nursing programs.遗传学教育对本科和研究生护理专业课程的重要性。
J Nurs Educ. 2009 Oct;48(10):535-6. doi: 10.3928/01484834-20090918-01.
10
What do you know about genetics?你对遗传学了解多少？
Nurse Pract. 2006 May;31(5):5. doi: 10.1097/00006205-200605000-00001.

引用本文的文献

1
Knowledge and perceptions of genetic testing for patients with breast cancer in Nigeria: a survey of healthcare providers.尼日利亚乳腺癌患者对基因检测的认知与看法：医疗服务提供者调查
Hered Cancer Clin Pract. 2025 May 19;23(1):16. doi: 10.1186/s13053-025-00315-w.
2
Premarital Genotype Screening for Sickle Cell Disease: Knowledge Gaps, Perception and Determinants of Uptake among Final Year Undergraduates of a Tertiary Institution in South-West Nigeria.尼日利亚西南部一所高等院校本科最后一年学生对镰状细胞病婚前基因型筛查的认知差距、看法及接受程度的决定因素
Niger Med J. 2022 Sep 10;63(1):50-58. doi: 10.60787/NMJ-63-1-94. eCollection 2022 Jan-Feb.
3

本文引用的文献

1
Novel GREM1 Variations in Sub-Saharan African Patients With Cleft Lip and/or Cleft Palate.撒哈拉以南非洲唇裂和/或腭裂患者中的新型GREM1变异
Cleft Palate Craniofac J. 2018 May;55(5):736-742. doi: 10.1177/1055665618754948. Epub 2018 Feb 28.
2
Pattern of Congenital Anomalies in Newborn: A 4-Year Surveillance of Newborns Delivered in a Tertiary Healthcare Facility in the South-East Nigeria.新生儿先天性异常模式：对尼日利亚东南部一家三级医疗机构分娩的新生儿进行的4年监测
J Trop Pediatr. 2018 Aug 1;64(4):304-311. doi: 10.1093/tropej/fmx067.
3
Loss-of-Function GRHL3 Variants Detected in African Patients with Isolated Cleft Palate.
Perceptions of Nigerian medical students regarding their preparedness for precision medicine: a cross-sectional survey in Lagos, Nigeria.
尼日利亚医学生对精准医学准备情况的认知：尼日利亚拉各斯的横断面调查。
BMC Med Educ. 2023 Nov 17;23(1):879. doi: 10.1186/s12909-023-04841-w.
4
The Challenges and Opportunities for Mental Health Twin Research in Nigeria.尼日利亚精神健康双胞胎研究的挑战与机遇。
Behav Genet. 2024 Jan;54(1):42-50. doi: 10.1007/s10519-023-10153-y. Epub 2023 Sep 21.
5
Knowledge, attitudes, and decision making towards prenatal testing among antenatal clinic attendees in Lagos University Teaching Hospital: an institution-based cross-sectional study.拉各斯大学教学医院产前检查就诊者对产前检查的知识、态度和决策：一项基于机构的横断面研究。
Pan Afr Med J. 2021 Jun 4;39:106. doi: 10.11604/pamj.2021.39.106.23667. eCollection 2021.
6
Frequency of beta S globin gene haplotypes among sickle cell patients in Nigeria.尼日利亚镰状细胞病患者中βS珠蛋白基因单倍型的频率
J Int Med Res. 2021 Jun;49(6):3000605211019918. doi: 10.1177/03000605211019918.
7
Health insurance and the financial implications of sickle cell disease among parents of affected children attending a tertiary facility in Lagos, south-west Nigeria.尼日利亚拉各斯一家三级医疗机构中，镰状细胞病患儿父母的健康保险和经济影响。
Pan Afr Med J. 2020 Jul 29;36:227. doi: 10.11604/pamj.2020.36.227.24636. eCollection 2020.
8
The Nigerian Bioinformatics and Genomics Network (NBGN): a collaborative platform to advance bioinformatics and genomics in Nigeria.尼日利亚生物信息学和基因组学网络（NBGN）：一个推进尼日利亚生物信息学和基因组学发展的协作平台。
Glob Health Epidemiol Genom. 2020 Jul 15;5:e3. doi: 10.1017/gheg.2020.3. eCollection 2020.
9
Prospects of genetic testing for steroid-resistant nephrotic syndrome in Nigerian children: a narrative review of challenges and opportunities.尼日利亚儿童类固醇抵抗性肾病综合征基因检测的前景：挑战与机遇的叙述性综述
Int J Nephrol Renovasc Dis. 2019 May 8;12:119-136. doi: 10.2147/IJNRD.S193874. eCollection 2019.
在患有孤立性腭裂的非洲患者中检测到功能丧失型GRHL3变体。
J Dent Res. 2018 Jan;97(1):41-48. doi: 10.1177/0022034517729819. Epub 2017 Sep 8.
4
Noonan syndrome in diverse populations.不同人群中的努南综合征。
Am J Med Genet A. 2017 Sep;173(9):2323-2334. doi: 10.1002/ajmg.a.38362. Epub 2017 Jul 27.
5
22q11.2 deletion syndrome in diverse populations.不同人群中的22q11.2缺失综合征
Am J Med Genet A. 2017 Apr;173(4):879-888. doi: 10.1002/ajmg.a.38199.
6
Genome-wide analysis identifies an african-specific variant in SEMA4D associated with body mass index.全基因组分析确定了与体重指数相关的SEMA4D基因中的一个非洲特异性变异。
Obesity (Silver Spring). 2017 Apr;25(4):794-800. doi: 10.1002/oby.21804. Epub 2017 Mar 13.
7
Rare coding variants associated with blood pressure variation in 15 914 individuals of African ancestry.与15914名非洲裔个体血压变异相关的罕见编码变异
J Hypertens. 2017 Jul;35(7):1381-1389. doi: 10.1097/HJH.0000000000001319.
8
Characterisation of the opposing effects of G6PD deficiency on cerebral malaria and severe malarial anaemia.葡萄糖 - 6 - 磷酸脱氢酶缺乏症对脑型疟疾和严重疟疾贫血的相反作用的特征描述
Elife. 2017 Jan 9;6:e15085. doi: 10.7554/eLife.15085.
9
Down syndrome in diverse populations.不同人群中的唐氏综合征。
Am J Med Genet A. 2017 Jan;173(1):42-53. doi: 10.1002/ajmg.a.38043.
10
Nigeria's National Health Act: An assessment of health professionals' knowledge and perception.尼日利亚《国家卫生法案》：对卫生专业人员知识与认知的评估
Niger Med J. 2016 Sep-Oct;57(5):260-265. doi: 10.4103/0300-1652.190594.