Global research dynamics in urea cycle disorders: a bibliometric study highlighting key players and future directions.

IF 3.5 2区 医学 Q2 GENETICS & HEREDITY Orphanet Journal of Rare Diseases Pub Date : 2025-03-04 DOI:10.1186/s13023-025-03625-3
Yan Wang, Xueer Wang, Huiqin Zhang, Binhui Zhu
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Abstract

Background: This study aims to explore the research hotspots and trends of urea cycle disorders through bibliometric analysis.

Methods: Using the Web of Science Core Collection as the database, we retrieved literature published from 2007 to 2024. We utilized CiteSpace, VOSviewer, and Bibliometrix R package to conduct a bibliometric visualization analysis, including the number of publications, citation frequency, publishing countries, institutions, journals, authors, references, and keywords.

Results: A total of 926 publications on UCDs were published in 318 journals by 4807 authors at 1494 institutions from 49 countries/regions. The USA had the highest number of publications and citation frequency. The Children's National Health System in the USA published the most literature. The most frequent collaboration was between the USA and Germany. The journal with the most publications was Molecular Genetics and Metabolism. The author with the most publications was Johannes Häberle. The most frequently cited reference was the 2019 publication of the revised guidelines for the diagnosis and management of UCDs. The identified future research hotspots are expected to focus on "gene therapy", "mutations" and "efficacy".

Conclusion: This study is the first bibliometric analysis of publications in the field of UCDs. These findings suggest that European and American countries dominate UCD research, it is necessary to further strengthen global cooperation in the field of UCDs. Early detection of the disease and emerging therapies, including gene therapy, are likely to be future research hotspots.

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尿素循环紊乱的全球研究动态:一项文献计量学研究,突出了关键参与者和未来方向。
背景:本研究旨在通过文献计量学分析,探讨尿素循环障碍的研究热点和趋势。方法:以Web of Science Core Collection为数据库,检索2007 - 2024年发表的文献。利用CiteSpace、VOSviewer和Bibliometrix R软件包进行文献计量可视化分析,包括发表论文数量、被引频次、出版国家、机构、期刊、作者、参考文献、关键词等。结果:49个国家/地区的1494个机构的4807位作者在318种期刊上发表了926篇关于ucd的论文。美国的论文发表数量和引用频率最高。美国儿童国家健康系统发表的文献最多。最频繁的合作发生在美国和德国之间。发表论文最多的杂志是《分子遗传学与代谢》。发表论文最多的作者是Johannes Häberle。最常被引用的参考文献是2019年出版的修订后的ucd诊断和管理指南。确定的未来研究热点有望集中在“基因治疗”、“突变”和“疗效”三个方面。结论:本研究首次对ucd领域的出版物进行文献计量分析。这些研究结果表明,欧美国家在UCD研究中占据主导地位,有必要进一步加强UCD领域的全球合作。早期发现疾病和新兴疗法,包括基因疗法,可能是未来的研究热点。
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来源期刊
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases 医学-医学:研究与实验
CiteScore
6.30
自引率
8.10%
发文量
418
审稿时长
4-8 weeks
期刊介绍: Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.
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