Sabina Barresi

Rome, Italy

Last Updated: 09/26/2026

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Found 100 publications

Monoallelic BRCA1/2 variants in pediatric, adolescent, and young adult patients with central nervous system tumors.

Monoallelic BRCA1/2 variants in pediatric, adolescent, and young adult patients with central nervous system tumors.

Journal: ESMO open

Published: February 27, 2026

Case Report: The revelation of a new pathogenic variant in the POT1 gene in a patient with a pediatric high-grade glioma and a renal cell carcinoma.

Case Report: The revelation of a new pathogenic variant in the POT1 gene in a patient with a pediatric high-grade glioma and a renal cell carcinoma.

Journal: Frontiers in oncology

Published: December 31, 2025

Pediatric high-grade gliomas and cancer predisposition syndromes: A retrospective study.

Pediatric high-grade gliomas and cancer predisposition syndromes: A retrospective study.

Journal: HGG advances

Published: December 18, 2025

First Report of a Child With a DeSanto-Shinawi Syndrome and a Polymorphous Low-Grade Neuroepithelial Tumor of the Young.

First Report of a Child With a DeSanto-Shinawi Syndrome and a Polymorphous Low-Grade Neuroepithelial Tumor of the Young.

Journal: American journal of medical genetics. Part A

Published: November 11, 2025

A 58-year-old woman experiencing occasional dizziness, impaired awareness, and deep feeling of fear.

A 58-year-old woman experiencing occasional dizziness, impaired awareness, and deep feeling of fear.

Journal: Brain pathology (Zurich, Switzerland)

Published: October 17, 2025

Novel HSPA8-NR4A2 rearrangement in extraskeletal myxoid chondrosarcoma: a sarcoma mimicker of neuroendocrine neoplasia.

Novel HSPA8-NR4A2 rearrangement in extraskeletal myxoid chondrosarcoma: a sarcoma mimicker of neuroendocrine neoplasia.

Journal: Virchows Archiv : an international journal of pathology

Published: October 15, 2025

Novel EWSR1::HOXB8 fusion identified in a rare spindle cell sarcoma of a young woman.

Novel EWSR1::HOXB8 fusion identified in a rare spindle cell sarcoma of a young woman.

Journal: Virchows Archiv : an international journal of pathology

Published: September 24, 2025

SOX11 is frequently expressed in ETV6::NTRK3-rearranged infantile fibrosarcoma and congenital mesoblastic nephroma.

SOX11 is frequently expressed in ETV6::NTRK3-rearranged infantile fibrosarcoma and congenital mesoblastic nephroma.

Journal: Virchows Archiv : an international journal of pathology

Published: August 18, 2025

USP8-Rearranged Mesenchymal Tumors With Myofibroblastic Phenotype: A Comprehensive Clinicopathologic, Genetic, and Epigenetic Characterization.

USP8-Rearranged Mesenchymal Tumors With Myofibroblastic Phenotype: A Comprehensive Clinicopathologic, Genetic, and Epigenetic Characterization.

Journal: Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc

Published: August 14, 2025

Epigenomic characterization and therapeutic challenges of melanoma arising in giant nevi in pediatric patients.

Epigenomic characterization and therapeutic challenges of melanoma arising in giant nevi in pediatric patients.

Journal: Discover oncology

Published: July 04, 2025

Melanomas and Mesenchymal Tumors Arising in Giant Congenital Melanocytic Nevi: Clinico-Pathological and Molecular Characterization of a Case Series.

Melanomas and Mesenchymal Tumors Arising in Giant Congenital Melanocytic Nevi: Clinico-Pathological and Molecular Characterization of a Case Series.

Journal: Pigment cell & melanoma research

Published: June 19, 2025

Germinal center trajectories and transcriptional signatures define CLL subtypes and their pathway regulators.

Germinal center trajectories and transcriptional signatures define CLL subtypes and their pathway regulators.

Journal: PloS one

Published: April 24, 2025

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Last Updated: 09/26/2026