Alessandro Pecci

Scopus Author ID ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 19

Top Topics

Acute Myeloid Leukemia

Top Venues

Annals of hematology

Advanced science (Weinheim, Baden-Wurttemberg, Germany)

British journal of haematology

American journal of hematology

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

Publications

Christian Andrea Di Buduo, Marco Lunghi, Volodymyr Kuzmenko, Pierre-Alexandre Laurent, Giulia Della Rosa, Claudia Del Fante, Damian Edward Dalle Nogare, Florian Jug, Cesare Perotti, Koji Eto, Alessandro Pecci, Itedale Namro Redwan, Alessandra Balduini
Bioprinting Soft 3D Models of Hematopoiesis using Natural Silk Fibroin-Based Bioink Efficiently Supports Platelet Differentiation. Advanced science (Weinheim, Baden-Wurttemberg, Germany) 11 (18) (2024)
Christian Andrea Di Buduo, Marco Lunghi, Volodymyr Kuzmenko, Pierre-Alexandre Laurent, Giulia Della Rosa, Claudia Del Fante, Damian Edward Dalle Nogare, Florian Jug, Cesare Perotti, Koji Eto, Alessandro Pecci, Itedale Namro Redwan, Alessandra Balduini
Bioprinting Soft 3D Models of Hematopoiesis using Natural Silk Fibroin-Based Bioink Efficiently Supports Platelet Differentiation. Advanced science (Weinheim, Baden-Wurttemberg, Germany) 11 (18) (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 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)
Christian Andrea Di Buduo, Marco Lunghi, Volodymyr Kuzmenko, Pierre-Alexandre Laurent, Giulia Della Rosa, Claudia Del Fante, Damian Edward Dalle Nogare, Florian Jug, Cesare Perotti, Koji Eto, Alessandro Pecci, Itedale Namro Redwan, Alessandra Balduini
Bioprinting Soft 3D Models of Hematopoiesis using Natural Silk Fibroin-Based Bioink Efficiently Supports Platelet Differentiation. Advanced science (Weinheim, Baden-Wurttemberg, Germany) (2024)
Christian Andrea Di Buduo, Marco Lunghi, Volodymyr Kuzmenko, Pierre-Alexandre Laurent, Giulia Della Rosa, Claudia Del Fante, Damian Edward Dalle Nogare, Florian Jug, Cesare Perotti, Koji Eto, Alessandro Pecci, Itedale Namro Redwan, Alessandra Balduini
Bioprinting Soft 3D Models of Hematopoiesis using Natural Silk Fibroin-Based Bioink Efficiently Supports Platelet Differentiation. Advanced science (Weinheim, Baden-Wurttemberg, Germany) 11 (18) (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)
Serena Barozzi, Valeria Bozzi, Daniela De Rocco, Tania Giangregorio, Patrizia Noris, Anna Savoia, Alessandro Pecci
A Novel Mutation in GP1BB Reveals the Role of the Cytoplasmic Domain of GPIbβ in the Pathophysiology of Bernard-Soulier Syndrome and GPIb-IX Complex Assembly. International journal of molecular sciences 22 (19) (2021)
Christian Andrea Di Buduo, Pierre-Alexandre Laurent, Carlo Zaninetti, Larissa Lordier, Paolo M Soprano, Aikaterini Ntai, Serena Barozzi, Alberto La Spada, Ida Biunno, Hana Raslova, James B Bussel, David Lee Kaplan, Carlo L Balduini, Alessandro Pecci, Alessandra Balduini
Miniaturized 3D bone marrow tissue model to assess response to Thrombopoietin-receptor agonists in patients. eLife 10 (2021)
Paolo Gresele, Sara Orsini, Patrizia Noris, Emanuela Falcinelli, Marie-Christine Alessi, Loredana Bury, Munira Borhany, Cristina Santoro, Ana C Glembotsky, Ana Rosa Cid, Alberto Tosetto, Erica De Candia, Andreas Greinacher, Giuseppe Guglielmini, Alessandro Pecci, null null
Validation of the ISTH/SSC bleeding assessment tool for inherited platelet disorders: A communication from the Platelet Physiology SSC. Journal of thrombosis and haemostasis : JTH 18 (3) (2019)
Alyson S Smith, Kasturi Pal, Roberta B Nowak, Anastasiya Demenko, Carlo Zaninetti, Lydie Da Costa, Rémi Favier, Alessandro Pecci, Velia M Fowler
MYH9-related disease mutations cause abnormal red blood cell morphology through increased myosin-actin binding at the membrane. American journal of hematology 94 (6) (2019)
Carlo Zaninetti, Serena Barozzi, Valeria Bozzi, Paolo Gresele, Carlo L Balduini, Alessandro Pecci
Eltrombopag in preparation for surgery in patients with severe MYH9-related thrombocytopenia. American journal of hematology 94 (8) (2019)
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)
Caterina Marconi, Ilaria Canobbio, Valeria Bozzi, Tommaso Pippucci, Giorgia Simonetti, Federica Melazzini, Silvia Angori, Giovanni Martinelli, Giuseppe Saglio, Mauro Torti, Ira Pastan, Marco Seri, Alessandro Pecci
5'UTR point substitutions and N-terminal truncating mutations of ANKRD26 in acute myeloid leukemia. Journal of hematology & oncology 10 (1) (2017)