2005 - 2024年宏观经济研究热点与趋势可视化分析。

IF 3.5 2区 医学 Q2 GENETICS & HEREDITY
Yuan Liu, Zong-You Yang, Chao-Jian Pang, Xiao-Bo Fan, Chen-Yang Zhao, Zhi-Kun Wei
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引用次数: 0

摘要

目的:对2005 - 2024年宏观经济学研究进行可视化分析,全面概述宏观经济学的研究趋势、主要贡献者和新兴主题。方法:利用Web of Science Core Collection数据库,对2005 ~ 2024年与巨指相关的出版物进行可视化分析。分析了出版趋势、国家和机构贡献、作者合作网络和关键词共现情况。使用Microsoft Excel、R、VOSviewer和CiteSpace进行统计分析和可视化。结果:共纳入文献153篇。年度出版物趋势有波动,但随着时间的推移,人们的兴趣总体有所增长,2011年至2014年的增长显著,2014年达到了15种出版物的峰值。美国以128篇论文领先,其次是中国(60篇)、意大利(40篇)、日本(36篇)和土耳其(27篇),其中梅奥诊所和哈佛大学等知名机构发挥了关键作用。主要作者Marybeth Ezaki博士与德克萨斯苏格兰仪式儿童医院的团队合作,为建立诊断框架做出了重大贡献。最重要的是,关键词分析揭示了研究重点从临床和外科主题(早期以“足”、“手”和“截骨”等关键词为代表)向分子和遗传学研究(近年来以“PIK3CA”、“激活突变”和“过度生长”为特征)的根本性转变。引用爆发性最强的是“overgrowth”(2016-2020),其次是与遗传相关的术语,其中“激活突变”代表了最新的趋势(2020-2024),表明PIK3CA突变越来越受到重视,成为当前的研究热点。结论:本研究突出了宏观研究的演变,揭示了波动的出版趋势和主要国家、作者和机构的大量贡献。从临床和外科方法到分子和遗传研究的转变强调了该领域的进步。未来的研究应优先考虑将遗传学发现与临床应用结合起来,并推进诊断和治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A visual analysis of research hotspots and trends on macrodactyly between 2005 and 2024.

A visual analysis of research hotspots and trends on macrodactyly between 2005 and 2024.

A visual analysis of research hotspots and trends on macrodactyly between 2005 and 2024.

A visual analysis of research hotspots and trends on macrodactyly between 2005 and 2024.

Purpose: To conduct a visualization analysis of macrodactyly research from 2005 to 2024, providing a comprehensive overview of research trends, key contributors, and emerging topics.

Methods: A visual analysis of macrodactyly related publications from 2005 to 2024 was conducted using the Web of Science Core Collection database. Publication trends, country and institutional contributions, author collaboration networks, and keyword co-occurrences were analyzed. Statistical analysis and visualization were performed using Microsoft Excel, R, VOSviewer, and CiteSpace.

Results: One hundred and fifty-three publications were included. Annual publication trends showed fluctuations but an overall growth in interest over time, with notable growth from 2011 to 2014 peaking at 15 publications in 2014. The United States led with 128 publications, followed by China (60), Italy (40), Japan (36), and Turkey (27), with prominent institutions such as Mayo Clinic and Harvard University playing pivotal roles. Key authors like Dr. Marybeth Ezaki, working with the team at Texas Scottish Rite Hospital for Children, made substantial contributions to establishing diagnostic frameworks. Most importantly, keyword analysis revealed a fundamental shift in research focus from clinical and surgical themes (represented by keywords such as "foot," "hand," and "osteotomy" in early periods) to molecular and genetic investigations (characterized by "PIK3CA," "activating mutations," and "overgrowth" in recent years). The strongest citation burst was "overgrowth" (2016-2020), followed by genetic-related terms, with "activating mutations" representing the most recent trend (2020-2024), indicating increasing emphasis on PIK3CA mutations as the current research hotspot.

Conclusion: This study highlights the evolution of macrodactyly research and reveals fluctuating publication trends and substantial contributions from key countries, authors, and institutions. The transition from clinical and surgical approaches to molecular and genetic investigations underscores advancements in the field. Future research should prioritize integrating genetic findings with clinical applications and advancing diagnostics and treatment strategies.

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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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