Serena Barozzi
4PUBLICATIONS
27CO-AUTHORS
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Publications (4)
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|Oct 08, 2024
Two novel families with RUNX1 variants indicate glycine 168 as a new mutational hotspot: Implications for FPD/AML diagnosis.Laureano J Kamiya, Serena Barozzi, Federica Isidori
|May 30, 2024
Thrombocytopenia 4 (THC4): Six novel families with mutations of the cytochrome c gene.Antonio Marzollo, Stefania Zampieri, Serena Barozzi
|Dec 20, 2022
GP1BB c.179C > T is the most frequent cause of monoallelic Bernard-Soulier syndrome in the Italian population after the Bolzano variant: a report of two new families.Serena Barozzi, Alessandro Pecci, Maddalena Marinoni
|Dec 29, 2018
Loss-of-function mutations in PTPRJ cause a new form of inherited thrombocytopenia.Caterina Marconi, Christian A Di Buduo, Kellie LeVine
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Frequent Collaborators
4 joint publications
Alessandro Pecci
2 joint publications
Caterina Marconi
2 joint publications
Anna Savoia
2 joint publications
Michela Faleschini
2 joint publications
Valeria Bozzi
1 joint publications
Spencer McKinstry
1 joint publications
Giorgia Fontana
1 joint publications
Patrizia Noris
1 joint publications
Antonio Marzollo
1 joint publications
Stefania Zampieri
