Knowledge mapping of alström syndrome research: a bibliometric and visualization analysis based on WoS data from 2000 to 2025

Alström syndrome (ALMS) is an ultra-rare autosomal recessive disorder caused by mutations in the ALMS1 gene, leading to a complex spectrum of multi-organ failure, including early-onset sensory loss, obesity, and cardiomyopathy. Despite its clinical significance, a systematic overview of the global r...

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Auteurs principaux:	Heng Zhang, Hang Fu, Xiaohui Sui, Shangan Si, Yuan Zhang, Kaifeng Li, Mengran Wang, Zhe Song, Yuxin Yang, Ziqi Liu, Guiju Zhang
Format:	Artigo
Langue:	Inglês
Publié:	Frontiers Media S.A. 2026-06-01
Collection:	Frontiers in Genetics
Sujets:	ALMS1 alstrom syndrome bibliometric analysis ciliopathy web of science (WOS)
Accès en ligne:	https://www.frontiersin.org/articles/10.3389/fgene.2026.1812729/full
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