Serena Barozzi

ResearcherID Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 9

Top Venues

Annals of hematology

British journal of haematology

Blood

Fondazione IRCCS Policlinico San Matteo

Università degli Studi di Pavia (BSC)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Fondazione IRCCS Policlinico San Matteo Jan 01 2015

Italy

Research Fellow :: Internal Medicine

Fondazione IRCCS Policlinico San Matteo

Italy

Scholarship :: Internal Medicine

Università degli Studi di Pavia

Italy

Scholarship :: Human Physiology

Education History

Università degli Studi di Pavia

Italy

BSC

Publications

Antonio Marzollo, Stefania Zampieri, Serena Barozzi, Muhammad Abrar Yousaf, Jade Quartararo, Daniela De Rocco, Michela Faleschini, Caterina Marconi, Camilla Ceccatelli Berti, Valeria Bozzi, Giovanna Russo, Paola Giordano, Paola Goffrini, Silvia Bresolin, Annalisa Pastore, Anna Savoia, Alessandro Pecci
Thrombocytopenia 4 (THC4): Six novel families with mutations of the cytochrome c gene. British journal of haematology 205 (1) (2024)
Antonio Marzollo, Stefania Zampieri, Serena Barozzi, Muhammad Abrar Yousaf, Jade Quartararo, Daniela De Rocco, Michela Faleschini, Caterina Marconi, Camilla Ceccatelli Berti, Valeria Bozzi, Giovanna Russo, Paola Giordano, Paola Goffrini, Silvia Bresolin, Annalisa Pastore, Anna Savoia, Alessandro Pecci
Thrombocytopenia 4 (THC4): Six novel families with mutations of the cytochrome c gene. British journal of haematology (2024)
Antonio Marzollo, Stefania Zampieri, Serena Barozzi, Muhammad Abrar Yousaf, Jade Quartararo, Daniela De Rocco, Michela Faleschini, Caterina Marconi, Camilla Ceccatelli Berti, Valeria Bozzi, Giovanna Russo, Paola Giordano, Paola Goffrini, Silvia Bresolin, Annalisa Pastore, Anna Savoia, Alessandro Pecci
Thrombocytopenia 4 (THC4): Six novel families with mutations of the cytochrome c gene. British journal of haematology (2024)
Serena Barozzi, Alessandro Pecci, Maddalena Marinoni, Giorgia Fontana, Melania Eva Zanchetta, Patrizia Noris, Anna Savoia, Michela Faleschini
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. Annals of hematology (2022)
Serena Barozzi, Alessandro Pecci, Maddalena Marinoni, Giorgia Fontana, Melania Eva Zanchetta, Patrizia Noris, Anna Savoia, Michela Faleschini
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. Annals of hematology 102 (3) (2022)
Serena Barozzi, Alessandro Pecci, Maddalena Marinoni, Giorgia Fontana, Melania Eva Zanchetta, Patrizia Noris, Anna Savoia, Michela Faleschini
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. Annals of hematology 102 (3) (2022)
Serena Barozzi, Alessandro Pecci, Maddalena Marinoni, Giorgia Fontana, Melania Eva Zanchetta, Patrizia Noris, Anna Savoia, Michela Faleschini
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. Annals of hematology 102 (3) (2022)
Serena Barozzi, Alessandro Pecci, Maddalena Marinoni, Giorgia Fontana, Melania Eva Zanchetta, Patrizia Noris, Anna Savoia, Michela Faleschini
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. Annals of hematology 102 (3) (2022)
Caterina Marconi, Christian A Di Buduo, Kellie LeVine, Serena Barozzi, Michela Faleschini, Valeria Bozzi, Flavia Palombo, Spencer U McKinstry, Giuseppe Lassandro, Paola Giordano, Patrizia Noris, Carlo L Balduini, Anna Savoia, Alessandra Balduini, Tommaso Pippucci, Marco Seri, Nicholas Katsanis, Alessandro Pecci
Loss-of-function mutations in PTPRJ cause a new form of inherited thrombocytopenia. Blood 133 (12) (2018)

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Publication Activity (10 Years)

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Serena Barozzi