Recent research has significantly advanced our understanding of the genetic and molecular underpinnings of meningiomas, particularly focusing on specific genetic variants and their clinical implications. A study by Castilla-Vallmanya et al. explored the phenotypic spectrum and transcriptomic profiles associated with germline variants in TRAF7, revealing that these variants are linked to developmental syndromes characterized by various anomalies. The study provided a comprehensive analysis of the clinical and mutational spectrum associated with TRAF7, highlighting its role in meningioma pathogenesis (ref: Castilla-Vallmanya doi.org/10.1038/s41436-020-0792-7/). Additionally, Ahrendsen et al. identified multiple whole chromosomal gains that define angiomatous meningiomas, differentiating them from nonangiomatous variants through advanced chromosomal analysis techniques. This distinction is crucial for accurate diagnosis and treatment planning (ref: Ahrendsen doi.org/10.1093/jnen/). Furthermore, the study by Gauchotte et al. emphasized the prognostic value of histopathological features, particularly the loss of H3K27me3 immunolabeling in anaplastic meningiomas, indicating that patients with high mitotic indices have significantly shorter overall survival compared to those with atypical meningiomas (ref: Gauchotte doi.org/10.1093/jnen/). Collectively, these studies underscore the importance of genetic and molecular analyses in understanding meningioma biology and improving patient outcomes.