Roberta Russo

38PUBLICATIONS
80CO-AUTHORS
Adolescent healthEpigenetics (incl. genome methylation and epigenomics)Haematological tumoursMicroelectromechanical systems (MEMS)Gene expression (incl. microarray and other genome-wide approaches)
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Publications (38)

|Apr 22, 2026
Clinical variability of ATP11C-related hemolytic anemia: expanding the phenotypic and diagnostic spectrum.

|Apr 21, 2026
Refined classification and phenotype-driven analysis of PIEZO1 variants in hereditary red blood cell and iron disorders.

|Feb 09, 2026
Additive effect of multiple genetic variants in SEC23B and PIEZO1 on iron metabolism dyshomeostasis in hereditary anemias.

Antonella Nostroso, Roberta Marra, Barbara Eleni Rosato

|Jan 28, 2026
Targeted Therapy for a Rare PDGFRB-Rearranged Myeloproliferative Neoplasm: A Case Report.

Cosimo Barbato, Vito A Lasorsa, Francesco Grimaldi

|Apr 15, 2025
The evolving landscape of hereditary stomatocytosis.

Immacolata Andolfo, Achille Iolascon, Roberta Russo

|Jan 08, 2025
P2 Receptor Antagonists Rescue Defective Heme Content in an In Vitro SLC25A38-Associated Congenital Sideroblastic Anemia Cell Model.

Antonella Santoro, Silvia De Santis, Ferdinando Palmieri

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Frequent Collaborators

23 joint publications

Immacolata Andolfo

20 joint publications

Achille Iolascon

6 joint publications

Mario Capasso

4 joint publications

Gian Luca Forni