| Pubmed ID | Year | Title | Citations |
|---|
| 39910685 | 2025 | Current molecular understanding of central nervous system schwannomas. | 207 |
| 31161239 | 2020 | An update on the CNS manifestations of neurofibromatosis type 2. | 122 |
| 35628268 | 2022 | A Critical Overview of Targeted Therapies for Vestibular Schwannoma. | 78 |
| 33773637 | 2021 | Genetic basis of lacunar stroke: a pooled analysis of individual patient data and genome-wide association studies. | 76 |
| 33025139 | 2021 | Epigenomic, genomic, and transcriptomic landscape of schwannomatosis. | 45 |
| 37075810 | 2023 | LOGGIC Core BioClinical Data Bank: Added clinical value of RNA-Seq in an international molecular diagnostic registry for pediatric low-grade glioma patients. | 32 |
| 34213706 | 2021 | The SH3PXD2A-HTRA1 fusion transcript is extremely rare in Norwegian sporadic vestibular schwannoma patients. | 13 |
| 38219951 | 2024 | Systematic Characterization of the Clinical and Pathological Features of Schwannomas Harboring SH3PXD2A::HTRA1 Fusion. | 0 |
| 27723760 | 2016 | The genomic landscape of schwannoma. | 0 |
| 35169096 | 2022 | [Schwannoma:Update on Molecular Profiling and Therapeutic Advances]. | 0 |
| 39717921 | 2024 | Clinical and Pathological Features of a Schwannoma Harboring a SH3PXD2A::HTRA1 Gene Fusion in a Pre-pubescent Patient. | 0 |
| 37743328 | 2023 | [Classification and Molecular Diagnosis of Benign Brain Tumors]. | 0 |
