Recent studies have significantly advanced our understanding of the molecular and genetic landscape of meningiomas, revealing distinct biological drivers and therapeutic vulnerabilities. One pivotal study identified gene transcript fusions in meningiomas, utilizing paired-end RNA sequencing from 302 samples to characterize these fusions and their association with clinical outcomes. The Oncofuse bioinformatic pipeline was employed to discern oncogenic fusions from passenger fusions, suggesting that certain fusions correlate with specific molecular groups and clinical outcomes (ref: Zakimi doi.org/10.1007/s00401-024-02708-y/). Another study highlighted racial and ethnic disparities in meningioma genomic profiles, finding that Black patients exhibited higher rates of aggressive tumor characteristics and poorer clinical outcomes compared to other groups, which underscores the need for tailored therapeutic strategies (ref: Tabor doi.org/10.3171/2024.1.JNS231633/). Additionally, the prevalence of NF2 mutations was linked to worse outcomes in psammomatous meningiomas, emphasizing the importance of genetic profiling in predicting prognosis (ref: Ren doi.org/10.3171/2024.1.JNS232450/). These findings collectively suggest that genetic alterations play a crucial role in meningioma behavior and patient outcomes, paving the way for potential targeted therapies.