Recent studies have provided significant insights into the genetic and molecular characteristics of meningiomas, particularly focusing on sex-specific differences and prognostic implications. One study highlighted that meningiomas in females often exhibit a loss of one X chromosome, which was found in 57% of malignant cases. This chromosomal alteration is associated with poorer progression-free survival, suggesting that genomic instability, particularly the loss of the X chromosome, is a critical factor in the malignancy of these tumors (ref: Berghaus doi.org/10.1093/neuonc/). Another study validated a DNA methylation-based recurrence predictor, demonstrating that this model outperforms the 2021 WHO grading system in predicting early postoperative recurrence, emphasizing the importance of molecular markers in clinical outcomes (ref: Landry doi.org/10.1093/neuonc/). Additionally, the differential expression of proteins at the tumor-brain interface has been investigated, revealing that higher levels of DTX1, RASGFR1, and Ki-67 are associated with brain invasion, indicating their potential roles in the invasive behavior of meningiomas (ref: Senglek doi.org/10.1002/gcc.70007/). MicroRNA analysis has also emerged as a promising tool for understanding the molecular underpinnings of meningioma stiffness, which is crucial for surgical planning (ref: Duba doi.org/10.1227/neu.0000000000003222/). Overall, these studies underscore the multifaceted genetic landscape of meningiomas and the potential for molecular markers to guide clinical management.