Ettore Rizzo

Pavia, Italy

Last Updated: 09/26/2026

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Found 29 publications

Direct-Acting Antiviral Agents in Hepatitis C-Associated Indolent Lymphomas.

Direct-Acting Antiviral Agents in Hepatitis C-Associated Indolent Lymphomas.

Journal: The New England journal of medicine

Published: December 30, 2025

CHEK2 Germline Variants in Early-Onset and Familial Myeloproliferative Neoplasms.

CHEK2 Germline Variants in Early-Onset and Familial Myeloproliferative Neoplasms.

Journal: American journal of hematology

Published: July 07, 2025

Digenic variant interpretation with hypothesis-driven explainable AI.

Digenic variant interpretation with hypothesis-driven explainable AI.

Journal: NAR genomics and bioinformatics

Published: October 28, 2024

Large clones of clonal hematopoiesis affect outcome in mantle cell lymphoma: results from the FIL MCL0208 clinical trial.

Large clones of clonal hematopoiesis affect outcome in mantle cell lymphoma: results from the FIL MCL0208 clinical trial.

Journal: Blood advances

Published: September 30, 2024

Molecular characterization of diffuse large B-cell lymphomas associated with hepatitis C virus infection.

Molecular characterization of diffuse large B-cell lymphomas associated with hepatitis C virus infection.

Journal: British journal of haematology

Published: November 24, 2023

VarChat: the generative AI assistant for the interpretation of human genomic variations.

VarChat: the generative AI assistant for the interpretation of human genomic variations.

Journal: Bioinformatics (Oxford, England)

Published: November 16, 2023

Critical assessment of variant prioritization methods for rare disease diagnosis within the Rare Genomes Project.

Critical assessment of variant prioritization methods for rare disease diagnosis within the Rare Genomes Project.

Journal: medRxiv : the preprint server for health sciences

Published: August 14, 2023

Critical assessment of variant prioritization methods for rare disease diagnosis within the rare genomes project.

Critical assessment of variant prioritization methods for rare disease diagnosis within the rare genomes project.

Journal: Human genomics

Published: August 11, 2023

An AI-based approach driven by genotypes and phenotypes to uplift the diagnostic yield of genetic diseases.

An AI-based approach driven by genotypes and phenotypes to uplift the diagnostic yield of genetic diseases.

Journal: Human genetics

Published: July 28, 2023

Prevalence and clinical expression of germ line predisposition to myeloid neoplasms in adults with marrow hypocellularity.

Prevalence and clinical expression of germ line predisposition to myeloid neoplasms in adults with marrow hypocellularity.

Journal: Blood

Published: December 05, 2022

Sequential next generation sequencing analysis in homogeneously treated low risk NPM1-mutated acute myeloid leukemia with an adverse clinical outcome.

Sequential next generation sequencing analysis in homogeneously treated low risk NPM1-mutated acute myeloid leukemia with an adverse clinical outcome.

Journal: American journal of hematology

Published: October 08, 2021

Enrichment of Double RUNX1 Mutations in Acute Leukemias of Ambiguous Lineage.

Enrichment of Double RUNX1 Mutations in Acute Leukemias of Ambiguous Lineage.

Journal: Frontiers in oncology

Published: June 17, 2021

Showing 1-12 of 29

Last Updated: 09/26/2026