Carla Roca
Barcelona, CT, Spain
Last Updated: 09/26/2026
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Found 9 publications
Rare solid tumours as indicators of hereditary cancer syndromes.
Journal: European journal of human genetics : EJHG
Published: November 02, 2025
A comprehensive genomic framework for identifying genes predisposing to homologous recombination repair-deficient breast or ovarian cancer.
Journal: BJC reports
Published: October 18, 2025
Tracing the molecular route to progression in miRNA-biogenesis-defective thyroid lesions.
Journal: JCI insight
Published: July 23, 2025
Concurrence of FGFR1 mutations modulates oncogenesis in glioneuronal tumors.
Journal: The EMBO journal
Published: January 17, 2025
Detection of germline CNVs from gene panel data: benchmarking the state of the art.
Journal: Briefings in bioinformatics
Published: June 11, 2024
vaRHC: an R package for semi-automation of variant classification in hereditary cancer genes according to ACMG/AMP and gene-specific ClinGen guidelines.
Journal: Bioinformatics (Oxford, England)
Published: November 07, 2022
A decade of RAD51C and RAD51D germline variants in cancer.
Journal: Human mutation
Published: August 25, 2021
DGCR8 and the six hit, three-step model of schwannomatosis.
Journal: Acta neuropathologica
Published: August 11, 2021
Showing 1-9 of 9
Last Updated: 09/26/2026