Frida Abel
Goeteborg, O, Sweden
Last Updated: 09/26/2026
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Found 18 publications
Drug resistant epilepsy driven by RHEB gene variants - Current evidence and a novel report of a paedatric case.
Journal: Epilepsy & behavior reports
Published: November 21, 2025
Comprehensive characterization and targeted treatment of a pediatric epithelioid glioblastoma with a rare TRIM24-NTRK2 fusion.
Journal: NPJ precision oncology
Published: June 18, 2025
Gain of chromosome 17 is an early genetic abnormality in neuroblastoma with PPM1D emerging as a strong candidate oncogene driving tumor progression.
Journal: Cancer letters
Published: February 25, 2025
A pilocytic astrocytoma with novel ATG16L1::NTRK2 fusion responsive to larotrectinib: a case report with genomic and functional analysis.
Journal: The oncologist
Published: June 13, 2024
Diagnostic yield and clinical impact of germline sequencing in children with CNS and extracranial solid tumors-a nationwide, prospective Swedish study.
Journal: The Lancet regional health. Europe
Published: November 20, 2023
Diagnostic Yield From a Nationwide Implementation of Precision Medicine for all Children With Cancer.
Journal: JCO precision oncology
Published: June 29, 2023
Cytoplasmic HIF-2α as tissue biomarker to identify metastatic sympathetic paraganglioma.
Journal: Scientific reports
Published: March 20, 2023
Novel TPR::ROS1 Fusion Gene Activates MAPK, PI3K and JAK/STAT Signaling in an Infant-type Pediatric Glioma.
Journal: Cancer genomics & proteomics
Published: June 27, 2022
Discovery of a rare GKAP1-NTRK2 fusion in a pediatric low-grade glioma, leading to targeted treatment with TRK-inhibitor larotrectinib.
Journal: Cancer biology & therapy
Published: April 06, 2021
MYO5B mutations in pheochromocytoma/paraganglioma promote cancer progression.
Journal: PLoS genetics
Published: August 10, 2019
Correction: A new GTF2I-BRAF fusion mediating MAPK pathway activation in pilocytic astrocytoma.
Journal: PloS one
Published: September 08, 2017
Last Updated: 09/26/2026