Ribosome levels selectively regulate translation and lineage commitment in human hematopoiesis RK Khajuria, M Munschauer, JC Ulirsch, C Fiorini, LS Ludwig, ... Cell 173 (1), 90-103. e19, 2018 | 356 | 2018 |
The genetic landscape of Diamond-Blackfan anemia JC Ulirsch, JM Verboon, S Kazerounian, MH Guo, D Yuan, LS Ludwig, ... The American Journal of Human Genetics 103 (6), 930-947, 2018 | 234 | 2018 |
Mutational Analysis of Human BAFF Receptor TNFRSF13C (BAFF-R) in Patients with Common Variable Immunodeficiency CG Losi, A Silini, C Fiorini, A Soresina, A Meini, S Ferrari, LD Notarangelo, ... Journal of clinical immunology 25, 496-502, 2005 | 122 | 2005 |
Targeted application of human genetic variation can improve red blood cell production from stem cells FC Giani, C Fiorini, A Wakabayashi, LS Ludwig, RM Salem, CD Jobaliya, ... Cell stem cell 18 (1), 73-78, 2016 | 88 | 2016 |
T cell–dependent survival of CD20+ and CD20− plasma cells in human secondary lymphoid tissue DR Withers, C Fiorini, RT Fischer, R Ettinger, PE Lipsky, AC Grammer Blood, The Journal of the American Society of Hematology 109 (11), 4856-4864, 2007 | 74 | 2007 |
Functional defects of dendritic cells in patients with CD40 deficiency S Fontana, D Moratto, S Mangal, M De Francesco, W Vermi, S Ferrari, ... Blood 102 (12), 4099-4106, 2003 | 67 | 2003 |
Insight into GATA1 transcriptional activity through interrogation of cis elements disrupted in human erythroid disorders A Wakabayashi, JC Ulirsch, LS Ludwig, C Fiorini, M Yasuda, A Choudhuri, ... Proceedings of the National Academy of Sciences 113 (16), 4434-4439, 2016 | 65 | 2016 |
Next generation sequencing reveals skewing of the T and B cell receptor repertoires in patients with Wiskott–Aldrich syndrome AE O’Connell, S Volpi, K Dobbs, C Fiorini, E Tsitsikov, H de Boer, ... Frontiers in immunology 5, 340, 2014 | 51 | 2014 |
Impaired human hematopoiesis due to a cryptic intronic GATA1 splicing mutation NJ Abdulhay, C Fiorini, JM Verboon, LS Ludwig, JC Ulirsch, B Zieger, ... Journal of Experimental Medicine 216 (5), 1050-1060, 2019 | 34 | 2019 |
Hypomorphic Janus kinase 3 mutations result in a spectrum of immune defects, including partial maternal T-cell engraftment F Cattaneo, M Recher, S Masneri, SN Baxi, C Fiorini, F Antonelli, ... Journal of allergy and clinical immunology 131 (4), 1136-1145, 2013 | 29 | 2013 |
Developmentally‐faithful and effective human erythropoiesis in immunodeficient and Kit mutant mice C Fiorini, NJ Abdulhay, SK McFarland, M Munschauer, JC Ulirsch, ... American journal of hematology 92 (9), E513-E519, 2017 | 23 | 2017 |
A novel activation-induced cytidine deaminase gene mutation in a Tunisian family with hyper IgM syndrome C Fiorini, S Jilani, CG Losi, A Silini, S Giliani, S Ferrari, LD Notarangelo, ... European journal of pediatrics 163, 704-708, 2004 | 13 | 2004 |
Normal hematologic parameters and fetal hemoglobin silencing with heterozygous IKZF1 mutations N Abdulhay, C Fiorini, A Kumánovics, AA Sun, J Hansen-Rejali, ... Blood, The Journal of the American Society of Hematology 128 (16), 2100-2103, 2016 | 8 | 2016 |
Schü tz S, Lian J, Gripp KW, Weinberg OK, Pinkus GS, Gehrke L, et al. 2018. Ribosome levels selectively regulate translation and lineage commitment in human hematopoiesis RK Khajuria, M Munschauer, JC Ulirsch, C Fiorini, LS Ludwig, ... Cell 173, 90-103, 0 | 8 | |
Macrothrombocytopenia associated with a rare GFI1B missense variant confounding the presentation of immune thrombocytopenia AN Cheng, EL Bao, C Fiorini, VG Sankaran Pediatric blood & cancer 66 (9), e27874, 2019 | 5 | 2019 |
High Throughput Sequencing of the T Cell and B Cell Receptor Repertoires in Patients with Wiskott Aldrich Syndrome AE OConnell, S Volpi, K Dobbs, C Fiorini, GW Hopkins, J Chu, YN Lee, ... JOURNAL OF CLINICAL IMMUNOLOGY 34 (3), 349-350, 2014 | | 2014 |
CD154 engagement on tonsillar B cells induces proximal signaling events and differentiation to plasma cells C Fiorini, V Lougaris, P Lugar, R Slota, B van der Zouwen, M Melchers, ... JOURNAL OF IMMUNOLOGY 176, S210-S210, 2006 | | 2006 |
Sclerosing cholangitis in a patient with hyper IgM syndrome caused by CD40 deficiency A Soresina, M Meini, V Villanacci, D Falchetti, M Gulletta, V Lougaris, ... THE ITALIAN JOURNAL OF PEDIATRICS 30, 401-404, 2004 | | 2004 |
B cell receptor repertoires in patients with Wiskott–Aldrich syndrome AE O’Connell, S Volpi, K Dobbs, C Fiorini, E Tsitsikov, H de Boer, ... | | |