Claudia Saitta

Monza, Italy

Last Updated: 09/26/2026

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Found 15 publications

Measurable Residual Disease-Dependent Unfavorable Outcomes in Pediatric PAX5-Rearranged B-Acute Lymphoblastic Leukemia.

Measurable Residual Disease-Dependent Unfavorable Outcomes in Pediatric PAX5-Rearranged B-Acute Lymphoblastic Leukemia.

Journal: Blood

Published: February 13, 2026

Cohesins: Crossroad Between Cornelia de Lange Spectrum and Cancer Predisposition.

Cohesins: Crossroad Between Cornelia de Lange Spectrum and Cancer Predisposition.

Journal: American journal of medical genetics. Part A

Published: October 09, 2024

Diverse mechanisms of leukemogenesis associated with PAX5 germline mutation.

Diverse mechanisms of leukemogenesis associated with PAX5 germline mutation.

Journal: Leukemia

Published: June 27, 2024

The recombinome of IKZF1 deletions in B-cell precursor ALL.

The recombinome of IKZF1 deletions in B-cell precursor ALL.

Journal: Leukemia

Published: March 15, 2023

Definition and Prognostic Value of Ph-like and IKZF1plus Status in Children With Down Syndrome and B-cell Precursor Acute Lymphoblastic Leukemia.

Definition and Prognostic Value of Ph-like and IKZF1plus Status in Children With Down Syndrome and B-cell Precursor Acute Lymphoblastic Leukemia.

Journal: HemaSphere

Published: October 04, 2022

Recurrent Germline Variant in RAD21 Predisposes Children to Lymphoblastic Leukemia or Lymphoma.

Recurrent Germline Variant in RAD21 Predisposes Children to Lymphoblastic Leukemia or Lymphoma.

Journal: International journal of molecular sciences

Published: April 12, 2022

PAX5 fusion genes are frequent in poor risk childhood acute lymphoblastic leukaemia and can be targeted with BIBF1120.

PAX5 fusion genes are frequent in poor risk childhood acute lymphoblastic leukaemia and can be targeted with BIBF1120.

Journal: EBioMedicine

Published: February 28, 2022

Potential role of STAG1 mutations in genetic predisposition to childhood hematological malignancies.

Potential role of STAG1 mutations in genetic predisposition to childhood hematological malignancies.

Journal: Blood cancer journal

Published: January 28, 2022

The Genetics of Myelodysplastic Syndromes: Clinical Relevance.

The Genetics of Myelodysplastic Syndromes: Clinical Relevance.

Journal: Genes

Published: May 20, 2021

Clinical relevance of clonal hematopoiesis in persons aged ≥80 years.

Clinical relevance of clonal hematopoiesis in persons aged ≥80 years.

Journal: Blood

Published: February 16, 2021

Classification and Personalized Prognostic Assessment on the Basis of Clinical and Genomic Features in Myelodysplastic Syndromes.

Classification and Personalized Prognostic Assessment on the Basis of Clinical and Genomic Features in Myelodysplastic Syndromes.

Journal: Journal of clinical oncology : official journal of the American Society of Clinical Oncology

Published: February 04, 2021

Dysregulation of NIPBL leads to impaired RUNX1 expression and haematopoietic defects.

Dysregulation of NIPBL leads to impaired RUNX1 expression and haematopoietic defects.

Journal: Journal of cellular and molecular medicine

Published: December 04, 2019

Showing 1-12 of 15

Last Updated: 09/26/2026