A bibliometric analysis of GWAS on Rheumatoid Arthritis from 2002 to 2024.

IF 1.1 4区 生物学 Q4 GENETICS & HEREDITY
Human Heredity Pub Date : 2025-04-03 DOI:10.1159/000543947
Wen-Hui Wang, Ming-Hui Xia, Xin-Ru Liu, Shu-Feng Lei, Pei He
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引用次数: 0

Abstract

Introduction Rheumatoid arthritis (RA) has become a serious threat to human health and quality of life worldwide. Previous studies have demonstrated that genetic factors play a crucial role in the onset and progression of RA. Due to the rapid development of Genome-wide association study (GWAS) technology and large-scale genetic analysis, research on GWAS and RA has received widespread attention in recent years. Therefore, we conducted a comprehensive visualization and bibliometric analysis of publications to identify hotspots and future trends in research on RA and GWAS. Methods Literature on RA and GWAS published between 2002 and 2024 was extracted from the Web of Science Core Collection (WoSCC) database by strategic screening. Collected data were further analyzed by using VOSviewer, CiteSpace and Excel. The collaborations networks of countries, authors, institutions and the co-citation networks of publications were visualized. Moreover, research hotspots and fronts were examined. Results A total of 713 publications with 45,773 citations were identified. The number of publications and citations has a significant surge since 2007. The United States (U.S.) contributed the most publications globally. Okada, Yukinori was the most influential author. The highest productive institutions in this field was the University of Manchester. The analysis of keywords revealed that "mendelian randomization analysis", "association", "innate", "instruments", "bias", "pathogenesis", and "genome-wide association study" are likely to be the frontiers of research in this field. Conclusion This study can be used to predict future research advances in the fields of GWAS in RA and helps to promote academic collaboration among scholars.

2002 年至 2024 年类风湿性关节炎基因组研究文献计量分析。
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来源期刊
Human Heredity
Human Heredity 生物-遗传学
CiteScore
2.50
自引率
0.00%
发文量
12
审稿时长
>12 weeks
期刊介绍: Gathering original research reports and short communications from all over the world, ''Human Heredity'' is devoted to methodological and applied research on the genetics of human populations, association and linkage analysis, genetic mechanisms of disease, and new methods for statistical genetics, for example, analysis of rare variants and results from next generation sequencing. The value of this information to many branches of medicine is shown by the number of citations the journal receives in fields ranging from immunology and hematology to epidemiology and public health planning, and the fact that at least 50% of all ''Human Heredity'' papers are still cited more than 8 years after publication (according to ISI Journal Citation Reports). Special issues on methodological topics (such as ‘Consanguinity and Genomics’ in 2014; ‘Analyzing Rare Variants in Complex Diseases’ in 2012) or reviews of advances in particular fields (‘Genetic Diversity in European Populations: Evolutionary Evidence and Medical Implications’ in 2014; ‘Genes and the Environment in Obesity’ in 2013) are published every year. Renowned experts in the field are invited to contribute to these special issues.
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