Molecular features in gangliogliomas: a systematic review
BRAF<sup>V600E</sup> mutation was the most common alteration observed in gangliogliomas, whereas mutations in other genes, such as FGFR1, H3K27M, KRAS, IDH1, and RAF1, were rare.
Authors
- Yuri Reis Casal (ORCID: https://orcid.org/0000-0002-0488-5307)
- Benedito Jamilson Araújo Pereira (ORCID: https://orcid.org/0000-0001-5871-6405)
- Antônio Nogueira de Almeida (ORCID: https://orcid.org/0000-0002-0796-7025)
- Sueli Mieko Oba‐Shinjo (ORCID: https://orcid.org/0000-0002-1650-5973)
- Suely Kazue Nagahashi Marie (ORCID: https://orcid.org/0000-0003-4419-7928)
- Wen Hung Tzu
- Paiva WS
- Isabel C. Azevedo
Institutions
- Universidade de São Paulo (BR)
- Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo (BR)
Publication Details
- Journal
- Child s Nervous System
- Published
- 2026-02-21
- DOI
- https://doi.org/10.1007/s00381-026-07170-7
- Primary Topic
- Glioma Diagnosis and Treatment
- Type
- article
- Field-Weighted Citation Impact
- 0.00