从过去到现在的遗传代谢疾病:一个圣经测量分析 (1968-2023)
Banu Kadıoğlu Yılmaz1, Ayşe Hümeyra Akgül2
1Department of Pediatric Nutrition and Metabolism, Faculty of Medicine, Selçuk University, Konya 42250, Turkey.
Children (Basel, Switzerland)
|July 29, 2023
概括
这项文献计量研究分析了2702篇关于遗传代谢疾病 (IMD) 的出版物. 它揭示了关键的研究趋势,并确定了IMDs遗传和分子诊断的未来方向.
科学领域:
- 医学遗传学和基因组学
- 代谢障碍 代谢障碍 代谢障碍
- 圣经计量学和科学计量学
背景情况:
- 科学文献中缺乏遗传代谢性疾病 (IMD) 的文献分析分析.
- 了解出版环境对于识别IMD的研究缺口和未来方向至关重要.
研究的目的:
- 对IMD研究进行全面的文献分析.
- 为了确定IMD出版物中的当前状态,趋势主题和研究缺口.
- 为未来的IMD研究和临床实践提供见解.
主要方法:
- 在SCOPUS数据库上从1968年到2023年使用关键字"遗传代谢疾病"进行文献搜索.
- 包括2702篇英语医学研究文章.
- 使用VOSviewer,SciMAT,Rstudio,R包"bibliometrix"和BibExcel.com进行的图书识别分析
主要成果:
- 美国,英国和中国是IMD研究的领先国家.
- 最受欢迎的关键词包括新生儿查,突变,,儿童,遗传学和糖尿病.
- 新兴趋势包括骨质疏松症,下一代测序和家族性高胆固醇血症,表明向分子和遗传方法的转变.
结论:
- 分子和遗传研究对于IMD的诊断和治疗越来越重要.
- 这种图书统计分析为IMD研究的演变和未来轨迹提供了新的视角.
- 这些发现凸显了遗传洞察力在管理遗传代谢疾病方面的日益重要.
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