Type 1 versus Type 2 calreticulin mutations in essential thrombocythemia: A collaborative study of 1027 patients
Tefferi, Ayalew, Wassie, Emnet A., Guglielmelli, Paola, Gangat, Naseema, Belachew, Alem A., Lasho, Terra L., Finke, Christy, Ketterling, Rhett P., Hanson, Curtis A., Pardanani, Animesh, Wolanskyj, Alexandra P., Maffioli, Margherita, Casalone, Rosario, Pacilli, Annalisa, Vannucchi, Alessandro M., Passamonti, Francesco
Published in American journal of hematology (01.08.2014)
Published in American journal of hematology (01.08.2014)
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Platelet count predicts driver mutations' co-occurrence in low JAK2 mutated essential thrombocythemia and myelofibrosis
Mora, Barbara, Siracusa, Claudia, Rumi, Elisa, Maffioli, Margherita, Casetti, Ilaria Carola, Barraco, Daniela, Merli, Michele, Rossi, Marianna, Ubezio, Marta, Accetta, Raffaella, Libera, Laura, Pietra, Daniela, Trotti, Chiara, Uccella, Silvia, Pallotti, Francesco, Casalone, Rosario, Bertù, Lorenza, Arcaini, Luca, Della Porta, Matteo Giovanni, Passamonti, Francesco
Published in Leukemia (01.05.2021)
Published in Leukemia (01.05.2021)
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Whole Exome Sequencing in 16p13.11 Microdeletion Patients Reveals New Variants Through Deductive and Systems Medicine Approaches
Granata, Paola, Cocciadiferro, Dario, Zito, Alessandra, Pessina, Chiara, Bassani, Alessandro, Zambonin, Fabio, Novelli, Antonio, Fasano, Mauro, Casalone, Rosario
Published in Frontiers in genetics (15.03.2022)
Published in Frontiers in genetics (15.03.2022)
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Value of cytogenetic abnormalities in post-polycythemia vera and post-essential thrombocythemia myelofibrosis: a study of the MYSEC project
Mora, Barbara, Giorgino, Toni, Guglielmelli, Paola, Rumi, Elisa, Maffioli, Margherita, Rambaldi, Alessandro, Caramella, Marianna, Komrokji, Rami, Gotlib, Jason, Kiladjian, Jean Jacques, Cervantes, Francisco, Devos, Timothy, Palandri, Francesca, De Stefano, Valerio, Ruggeri, Marco, Silver, Richard T, Benevolo, Giulia, Albano, Francesco, Cavalloni, Chiara, Barraco, Daniela, Merli, Michele, Pietra, Daniela, Casalone, Rosario, Barbui, Tiziano, Rotunno, Giada, Cazzola, Mario, Vannucchi, Alessandro Maria, Passamonti, Francesco
Published in Haematologica (Roma) (01.09.2018)
Published in Haematologica (Roma) (01.09.2018)
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WWP1 germline variants are associated with normocephalic autism spectrum disorder
Novelli, Giuseppe, Novelli, Antonio, Borgiani, Paola, Cocciadiferro, Dario, Biancolella, Michela, Agolini, Emanuele, Pietrosanto, Marco, Casalone, Rosario, Helmer-Citterich, Manuela, Giardina, Emiliano, Jain, Suresh K, Wei, Wenyi, Eng, Charis, Pandolfi, Pier Paolo
Published in Cell death & disease (23.07.2020)
Published in Cell death & disease (23.07.2020)
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Koolen-de Vries Syndrome: Preliminary Observations of Topiramate Efficacy
Paolo, Piccinelli, Matteo, Ferri, Rossella, Lipari, Anna, Mercuri, Rosario, Casalone, Paola, Granata, Cristiano, Termine, Giorgio, Rossi
Published in Child neurology open (01.01.2021)
Published in Child neurology open (01.01.2021)
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Isolation and Characterization of Multipotent Cells from Human Fetal Dermis
Chinnici, Cinzia Maria, Amico, Giandomenico, Monti, Marcello, Motta, Stefania, Casalone, Rosario, Petri, Sergio Li, Spada, Marco, Gridelli, Bruno, Conaldi, Pier Giulio
Published in Cell transplantation (01.01.2014)
Published in Cell transplantation (01.01.2014)
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Testing single/combined clinical categories on 5110 Italian patients with developmental phenotypes to improve array‐based detection rate
Catusi, Ilaria, Recalcati, Maria Paola, Bestetti, Ilaria, Garzo, Maria, Valtorta, Chiara, Alfonsi, Melissa, Alghisi, Alberta, Cappellani, Stefania, Casalone, Rosario, Caselli, Rossella, Ceccarini, Caterina, Ceglia, Carlo, Ciaschini, Anna Maria, Coviello, Domenico, Crosti, Francesca, D'Aprile, Annamaria, Fabretto, Antonella, Genesio, Rita, Giagnacovo, Marzia, Granata, Paola, Longo, Ilaria, Malacarne, Michela, Marseglia, Giuseppina, Montaldi, Annamaria, Nardone, Anna Maria, Palka, Chiara, Pecile, Vanna, Pessina, Chiara, Postorivo, Diana, Redaelli, Serena, Renieri, Alessandra, Rigon, Chiara, Tiberi, Fabiola, Tonelli, Mariella, Villa, Nicoletta, Zilio, Anna, Zuccarello, Daniela, Novelli, Antonio, Larizza, Lidia, Giardino, Daniela
Published in Molecular genetics & genomic medicine (01.01.2020)
Published in Molecular genetics & genomic medicine (01.01.2020)
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Culture of skeletal myoblasts from human donors aged over 40 years: dynamics of cell growth and expression of differentiation markers
Baj, Andreina, Bettaccini, Alessia A, Casalone, Rosario, Sala, Andrea, Cherubino, Paolo, Toniolo, Antonio Q
Published in Journal of translational medicine (12.05.2005)
Published in Journal of translational medicine (12.05.2005)
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A particular case of AML patient with the polymorphism G105G (rs11554137) and the missense mutation R132C in IDH1 gene
Accetta, Raffaella, Campiotti, Leonardo, Elli, Lorenzo, Casalone, Rosario, Pallotti, Francesco
Published in Clinical chemistry and laboratory medicine (01.02.2019)
Published in Clinical chemistry and laboratory medicine (01.02.2019)
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The p.Gly130Val mutation in the GJB2 gene: A familiar case of autosomal dominant non-syndromic hearing loss
Bussini, Adelaide, Righi, Rossana, Pessina, Chiara, Genoni, Angelo, Cristofari, Eliana, Meli, Annalisa, Granata, Paola, Meroni, Emanuela, Broccolo, Francesco, Casalone, Rosario
Published in International journal of pediatric otorhinolaryngology (01.12.2019)
Published in International journal of pediatric otorhinolaryngology (01.12.2019)
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Analysis of three screening methods for the detection of calreticulin gene mutations
Accetta, Raffaella, Elli, Lorenzo, Libera, Laura, Siracusa, Claudia, Cassavia, Francesca, Orsini, Francesco, Orlandi, Linda, Passamonti, Francesco, Casalone, Rosario, Pallotti, Francesco
Published in International journal of laboratory hematology (01.04.2020)
Published in International journal of laboratory hematology (01.04.2020)
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Technical Issues Behind Molecular Monitoring in Chronic Myeloid Leukemia
Mattarucchi, Elia, Pallotti, Francesco, Casalone, Rosario
Published in Molecular diagnosis & therapy (01.06.2015)
Published in Molecular diagnosis & therapy (01.06.2015)
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Targeted re-sequencing in malformations of cortical development: genotype-phenotype correlations
Accogli, Andrea, Severino, Mariasavina, Riva, Antonella, Madia, Francesca, Balagura, Ganna, Iacomino, Michele, Carlini, Barbara, Baldassari, Simona, Giacomini, Thea, Croci, Carolina, Pisciotta, Livia, Messana, Tullio, Boni, Antonella, Russo, Angelo, Bilo, Leonilda, Tonziello, Rosa, Coppola, Antonietta, Filla, Alessandro, Mecarelli, Oriano, Casalone, Rosario, Pisani, Francesco, Falsaperla, Raffaele, Marino, Silvia, Parisi, Pasquale, Ferretti, Alessandro, Elia, Maurizio, Luchetti, Anna, Milani, Donatella, Vanadia, Francesca, Silvestri, Laura, Rebessi, Erika, Parente, Eliana, Vatti, Giampaolo, Mancardi, Maria Margherita, Nobili, Lino, Capra, Valeria, Salpietro, Vincenzo, Striano, Pasquale, Zara, Federico
Published in Seizure (London, England) (01.08.2020)
Published in Seizure (London, England) (01.08.2020)
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Positive predictive values and outcomes for uninformative cell‐free DNA tests: An Italian multicentric Cytogenetic and cytogenomic Audit of diagnOstic testing (ICARO study)
Grati, Francesca Romana, Bestetti, Ilaria, De Siero, Daria, Malvestiti, Francesca, Villa, Nicoletta, Sala, Elena, Crosti, Francesca, Parisi, Valentina, Nardone, Anna Maria, Di Giacomo, Gianluca, Pettinari, Antonella, Tortora, Giada, Montaldi, Annamaria, Calò, Annapaola, Saccilotto, Donatella, Zanchetti, Sara, Celli, Paola, Guerneri, Silvana, Silipigni, Rosamaria, Cardarelli, Laura, Lippi, Elisabetta, Cavani, Simona, Malacarne, Michela, Genesio, Rita, Beltrami, Nicola, Pittalis, Maria Carla, Desiderio, Laura, Gentile, Mattia, Ficarella, Romina, Recalcati, Maria Paola, Catusi, Ilaria, Garzo, Maria, Miele, Lorena, Corti, Cecilia, Ghezzo, Sara, Bertini, Veronica, Cambi, Francesca, Valetto, Angelo, Facchinetti, Barbara, Bernardini, Laura, Capalbo, Anna, Balducci, Federica, Pelo, Elisabetta, Minuti, Barbara, Pescucci, Chiara, Giuliani, Costanza, Renieri, Alessandra, Longo, Ilaria, Tita, Rossella, Castello, Giuseppe, Casalone, Rosario, Righi, Rossana, Raso, Barbara, Civolani, Alessandro, Muzi, Maria Cristina, Natale, Manuela, Varriale, Luigia, Gasperini, Daniela, Nuzzi, Maria Cristina, Cellamare, Angelo, Casieri, Paola, Busuito, Rosa, Ceccarini, Caterina, Cesarano, Carla, Privitera, Orsola, Melani, Daniela, Menozzi, Cristina, Falcinelli, Cristina, Calabrese, Olga, Battaglia, Paola, Tanzariello, Antonella, Stampalija, Tamara, Ardisia, Carmela, Gasparini, Paolo, Benn, Peter, Novelli, Antonio
Published in Prenatal diagnosis (01.12.2022)
Published in Prenatal diagnosis (01.12.2022)
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A new acute myeloid leukemia case with STAT5B-RARA gene fusion due to 17q21.2 interstitial deletion
Pessina, Chiara, Basilico, Claudia, Genoni, Angelo, Meroni, Emanuela, Elli, Lorenzo, Granata, Paola, Righi, Rossana, Pallotti, Francesco, Mora, Barbara, Ferrario, Andrea, Passamonti, Francesco, Casalone, Rosario
Published in Leukemia & lymphoma (03.08.2017)
Published in Leukemia & lymphoma (03.08.2017)
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Mutations and thrombosis in essential thrombocythemia: prognostic interaction with age and thrombosis history
Gangat, Naseema, Wassie, Emnet A., Lasho, Terra L., Finke, Christy, Ketterling, Rhett P., Hanson, Curtis A., Pardanani, Animesh, Wolanskyj, Alexandra P., Maffioli, Margherita, Casalone, Rosario, Passamonti, Francesco, Tefferi, Ayalew
Published in European journal of haematology (01.01.2015)
Published in European journal of haematology (01.01.2015)
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