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Alessandro Pecci

11PUBLICATIONS

49CO-AUTHORS

Gene expression (incl. microarray and other genome-wide approaches)Cardiology (incl. cardiovascular diseases)HaematologyAnthropological geneticsAutoimmunity

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Publications (11)

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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

|Mar 22, 2024

Bioprinting Soft 3D Models of Hematopoiesis using Natural Silk Fibroin-Based Bioink Efficiently Supports Platelet Differentiation.

Christian Andrea Di Buduo, Marco Lunghi, Volodymyr Kuzmenko

|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

|Oct 13, 2021

A Novel Mutation in <i>GP1BB</i> Reveals the Role of the Cytoplasmic Domain of GPIbβ in the Pathophysiology of Bernard-Soulier Syndrome and GPIb-IX Complex Assembly.

Serena Barozzi, Valeria Bozzi, Daniela De Rocco

|Jun 01, 2021

Miniaturized 3D bone marrow tissue model to assess response to Thrombopoietin-receptor agonists in patients.

Christian A Di Buduo, Pierre-Alexandre Laurent, Carlo Zaninetti

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Frequent Collaborators

4 joint publications

Serena Barozzi

3 joint publications

Valeria Bozzi

2 joint publications

Caterina Marconi

2 joint publications

Michela Faleschini

2 joint publications

Patrizia Noris

2 joint publications

Anna Savoia

2 joint publications

Alessandra Balduini

2 joint publications

Christian Andrea Di Buduo

1 joint publications

Kasturi Pal

1 joint publications

Remi Favier

Frequent Collaborators

4 joint publications

Serena Barozzi

3 joint publications

Valeria Bozzi

2 joint publications

Caterina Marconi

2 joint publications

Michela Faleschini

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