Valeria Spina
Bellinzona, TI, Switzerland
Last Updated: 09/26/2026
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Found 43 publications
A comprehensive genetic study of classic Hodgkin lymphoma using circulating tumor DNA.
Journal: Blood
Published: October 23, 2024
Antigen selection reflected in the subclonal architecture of the B-cell receptor immunoglobulin gene repertoire in splenic marginal zone lymphoma.
Journal: HemaSphere
Published: August 31, 2024
Detection of clinically relevant variants in the TP53 gene below 10% allelic frequency: A multicenter study by ERIC, the European Research Initiative on CLL.
Journal: HemaSphere
Published: July 11, 2024
How much should we sequence? An analysis of the Swiss SARS-CoV-2 surveillance effort.
Journal: Microbiology spectrum
Published: March 18, 2024
XPO1 mutations identify early-stage CLL characterized by shorter time to first treatment and enhanced BCR signalling.
Journal: British journal of haematology
Published: May 23, 2023
Distinct Hodgkin lymphoma subtypes defined by noninvasive genomic profiling.
Journal: Nature
Published: December 19, 2022
Anatomical heterogeneity of residual disease in chronic lymphocytic leukemia treated with ibrutinib.
Anatomical heterogeneity of residual disease in chronic lymphocytic leukemia treated with ibrutinib.
Journal: Hematological oncology
Published: June 03, 2022
Ibrutinib dose intensity in high-risk chronic lymphocytic leukemia.
Journal: Hematological oncology
Published: May 25, 2022
Genetic and phenotypic attributes of splenic marginal zone lymphoma.
Journal: Blood
Published: May 10, 2021
Frequency and clinical relevance of coding and noncoding NOTCH1 mutations in early stage Binet A chronic lymphocytic leukemia patients.
Journal: Hematological oncology
Published: December 13, 2019
Last Updated: 09/26/2026