Clonally unrelated Richter syndrome are truly de novo diffuse large B‐cell lymphomas with a mutational profile reminiscent of clonally related Richter syndromeChiara Favini, Riccardo Moia, Samir Mouhssine et al.|British Journal of Haematology|2022Cited by 24
Stiffer Spleen Predicts Higher Bone Marrow Fibrosis and Higher JAK2 Allele Burden in Patients With Myeloproliferative NeoplasmsRiccardo Moia, Cristina Rigamonti, Micol Giulia Cittone et al.|Frontiers in Oncology|2021Cited by 10
<i>XPO1</i> mutations identify early‐stage <scp>CLL</scp> characterized by shorter time to first treatment and enhanced <scp>BCR</scp> signallingRiccardo Moia, Gianluca Gaïdano, Lodovico Terzi di Bergamo et al.|British Journal of Haematology|2023Cited by 7
Immunoglobulin light chain mutational status refines IGHV prognostic value in identifying chronic lymphocytic leukemia patients with early treatment requirementJana Nabki, Riccardo Moia, Bashar Al Deeban et al.|Leukemia|2024Cited by 4
P597: XPO1 MUTATIONS IDENTIFY EARLY STAGE CLL CHARACTERIZED BY SHORTER TIME TO FIRST TREATMENT AND ENHANCED BCR SIGNALINGDonatella Talotta, Gianluca Gaïdano, Riccardo Moia et al.|HemaSphere|2023Cited by 0