Artificial intelligence empowering rare diseases: a bibliometric perspective over the last two decades

Over two decades, research on the AI applications in RDs has made remarkable progress and shown promising results in the development. Advancing international transboundary cooperation is essential moving forward. Utilizing AI will play a more crucial role across the spectrum of RDs management, encompassing rapid diagnosis, personalized treatment, drug development, data integration and sharing, and continuous monitoring and care.

Authors

Institutions

Publication Details

Journal
Orphanet Journal of Rare Diseases
Published
2024-09-13
DOI
https://doi.org/10.1186/s13023-024-03352-1
Citations
7
Primary Topic
Genomics and Rare Diseases
Type
article
Field-Weighted Citation Impact
3.85

Funders

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article

Artificial intelligence empowering rare diseases: a bibliometric perspective over the last two decades

Chen Liu, Ru Wen, Jian Wang, Linfeng Shi et al.
7 citations
Orphanet Journal of Rare Diseases
Genomics and Rare Diseases
3.85
article

Artificial intelligence empowering rare diseases: a bibliometric perspective over the last two decades

Chen Liu, Ru Wen, Jian Wang, Linfeng Shi, Peiling Ou
article en
7 citations

Abstract

Over two decades, research on the AI applications in RDs has made remarkable progress and shown promising results in the development. Advancing international transboundary cooperation is essential moving forward. Utilizing AI will play a more crucial role across the spectrum of RDs management, encompassing rapid diagnosis, personalized treatment, drug development, data integration and sharing, and continuous monitoring and care.

Orphanet Journal of Rare DiseasesVol. 19(1)
Army Medical University (CN), Southwest Hospital (CN)
National Natural Science Foundation of China, Army Medical University
Partnerships for the goals
Openalex Percentile: Top 6%
Genomics and Rare Diseases
3.85
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Artificial intelligence empowering rare diseases: a bibliometric perspective over the last two decades — Chen Liu, Ru Wen, et al. · Orphanet Journal of Rare Diseases (2024) | TGRS Research Map | TGRS