Liao Ruyu, Geng Rongrong, Yang Yue, Xue Yufan, Chen Lili, Chen Lan
Department of Orthopedics, The Third People's Hospital of Chengdu, Chengdu, China.
Front Genet. 2024 Apr 12;15:1377743. doi: 10.3389/fgene.2024.1377743. eCollection 2024.
Bibliometrics can trace general research trends in a particular field. Mucopolysaccharidoses (MPS), as a group of rare genetic diseases, seriously affect the quality of life of patients and their families. Scholars have devoted themselves to studying MPS's pathogenesis and treatment modalities and have published many papers. Therefore, we conducted a bibliometric and visual study of the top 100 most highly cited articles to provide researchers with an indication of the current state of research and potential directions in the field. The Web of Science Core Collection was searched for articles on MPS from 1 January 1900, to 8 November 2023, and the top 100 most cited articles were screened. The title, year of publication, institution, country, and first author of the articles were extracted and statistically analyzed using Microsoft Excel 2007. Keyword co-occurrence and collaborative networks were analyzed using VOSviewer 1.6.16. A total of 9,273 articles were retrieved, and the top 100 most cited articles were filtered out. The articles were cited 18,790 times, with an annual average of 188 citations (122-507). Forty-two journals published these articles, with Molecular Genetics and Metabolism and Proceedings of the National Academy of Sciences of the United States being the most published journal (N = 8), followed by Pediatrics (N = 7), Blood (N = 6). The United States (N = 68), the UK (N = 25), and Germany (N = 20) were the top contributing countries. The Royal Manchester Children's Hospital (N = 20) and the University of North Carolina (N = 18) were the most contributing institutions. Muenzer J was the most prolific author (N = 14). We conducted a bibliometric and visual analysis of the top 100 cited articles in MPS. This study identifies the most influential articles currently available in the field of MPS, which provides a good basis for a better understanding of the disease and informs future research directions.
文献计量学可以追踪特定领域的总体研究趋势。黏多糖贮积症(MPS)作为一组罕见的遗传疾病,严重影响患者及其家庭的生活质量。学者们致力于研究MPS的发病机制和治疗方式,并发表了许多论文。因此,我们对被引频次最高的100篇文章进行了文献计量学和可视化研究,为研究人员提供该领域的研究现状和潜在方向的指示。在科学网核心合集中检索了1900年1月1日至2023年11月8日关于MPS的文章,并筛选出被引频次最高的100篇文章。提取文章的标题、发表年份、机构、国家和第一作者,并使用Microsoft Excel 2007进行统计分析。使用VOSviewer 1.6.16分析关键词共现和合作网络。共检索到9273篇文章,并筛选出被引频次最高的100篇文章。这些文章被引用了18790次,年均被引188次(122 - 507次)。发表这些文章的期刊有42种,其中《分子遗传学与代谢》和《美国国家科学院院刊》是发表文章最多的期刊(N = 8),其次是《儿科学》(N = 7)、《血液》(N = 6)。贡献最大的国家是美国(N = 68)、英国(N = 25)和德国(N = 20)。贡献最大的机构是皇家曼彻斯特儿童医院(N = 20)和北卡罗来纳大学(N = 18)。Muenzer J是发表文章最多的作者(N = 14)。我们对MPS领域被引频次最高的100篇文章进行了文献计量学和可视化分析。本研究确定了MPS领域目前最具影响力的文章,为更好地了解该疾病提供了良好的基础,并为未来的研究方向提供了参考。