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绘制过去26年努南综合征研究的现状与展望:文献计量与可视化分析

Mapping the current status and outlook of research on noonan syndrome over the last 26 years: a bibliometric and visual analysis.

作者信息

Cui Zhengjiu, Wang Yuanyuan, Luo Fei, Diao Juanjuan, Yuan Bin

机构信息

Department of Pediatrics, Affiliated Hospital of Nanjing University of Chinese Medicine, Nanjing, China.

Department of Pediatrics, Suqian Affiliated Hospital of Nanjing University of Chinese Medicine, Suqian, China.

出版信息

Front Genet. 2024 Dec 12;15:1488425. doi: 10.3389/fgene.2024.1488425. eCollection 2024.

Abstract

BACKGROUND

Noonan syndrome (NS) is a rare group of autosomal genetic disorders. In recent years, with the exploration and development of molecular diagnostic techniques, more and more researchers have begun to pay attention to NS. However, there is still a lack of reports on the bibliometric analysis of NS worldwide. This study aims to assess the current research status and development trend of NS, to explore the research hotspots and emerging topics, and to point out the direction for future scientific research.

METHODS

Web of Science Core Collection was selected as the search database for bibliometric analysis of NS-related publications from 1998 to 2023. Statistical and visual analysis of the number of publications, countries, institutions, authors, journals, keywords, and references were analyzed using Citespace, VOSviewer, Scimago Graphica, and BibliometrixR.

RESULTS

A total of 2041 articles were included in this study. The United States had the highest number of publications, and Istituto Superiore di Sanità, Italy, was the institution with the highest number of publications. TARTAGLIA M was the scientist with the highest number of publications and citations. Among the journals, AMERICAN JOURNAL OF MEDICAL GENETICS PART A has the highest output, and Nature Genetics is the most frequently cited. The reference with the highest outburst intensity is Roberts AE, LANCET, 2013. the cluster diagram divides all the keywords into seven categories, with the most vigorous outburst being "of function mutations."

CONCLUSION

Research hotspots in the field of NS focus on the correspondence between NS genotype and phenotype and the precise diagnosis of NS. Future research efforts will explore more deeply from the perspective of long-term intervention strategies for NS. There is an urgent need to rely on significant research countries, institutions, journals, and authors to lead the construction of a more robust global collaborative network that will enhance research efficacy.

摘要

背景

努南综合征(NS)是一组罕见的常染色体遗传性疾病。近年来,随着分子诊断技术的探索与发展,越来越多的研究者开始关注NS。然而,全球范围内关于NS的文献计量学分析仍缺乏报道。本研究旨在评估NS的当前研究现状和发展趋势,探索研究热点和新兴主题,并指出未来科学研究的方向。

方法

选择Web of Science核心合集作为搜索数据库,对1998年至2023年与NS相关的出版物进行文献计量学分析。使用Citespace、VOSviewer、Scimago Graphica和BibliometrixR对出版物数量、国家、机构、作者、期刊、关键词和参考文献进行统计和可视化分析。

结果

本研究共纳入2041篇文章。美国的出版物数量最多,意大利的高等卫生研究院是出版物数量最多的机构。TARTAGLIA M是发表文章和被引次数最多的科学家。在期刊方面,《美国医学遗传学杂志A辑》的产出最高,《自然遗传学》被引用频率最高。爆发强度最高的参考文献是Roberts AE,《柳叶刀》,2013年。聚类图将所有关键词分为七类,爆发最为活跃的是“功能突变”。

结论

NS领域的研究热点集中在NS基因型与表型的对应关系以及NS的精准诊断上。未来的研究将从NS的长期干预策略角度进行更深入的探索。迫切需要依靠重要的研究国家、机构、期刊和作者来引领构建更强大的全球合作网络,以提高研究效率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1d4/11669677/2ce8f9e13d02/fgene-15-1488425-g001.jpg

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