Immacolata Andolfo

27PUBLICATIONS
68CO-AUTHORS
Tissue engineeringAdolescent healthEpigenetics (incl. genome methylation and epigenomics)Microelectromechanical systems (MEMS)Medical devices
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Publications (27)

|Jul 06, 2026
EIF2AK1 As a Key Genetic Determinant of Luspatercept Resistance in Transfusion-Dependent Thalassemia.

|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

|Nov 18, 2024
RAS signaling pathway is essential in regulating PIEZO1-mediated hepatic iron overload in dehydrated hereditary stomatocytosis.

Barbara Eleni Rosato, Vanessa D'Onofrio, Roberta Marra

|Nov 07, 2024
Relevance of the E756del common variant in the PIEZO1 gene for haemolytic anaemia and hepatic iron overload.

Federica Maria Esposito, Vanessa D'Onofrio, Barbara Eleni Rosato

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Frequent Collaborators

23 joint publications

Roberta Russo

14 joint publications

Achille Iolascon

5 joint publications

Mario Capasso

4 joint publications

Gian Luca Forni