| Rapid and simultaneous typing of hemoglobin S, hemoglobin C, and seven Mediterranean beta-thalassemia mutations by covalent reverse dot-blot analysis: application to prenatal … A Maggio, A Giambona, SP Cai, J Wall, YW Kan, FF Chehab | 204 | 1993 |
| The significance of the hemoglobin A2 value in screening for hemoglobinopathies A Giambona, C Passarello, D Renda, A Maggio Clinical biochemistry 42 (18), 1786-1796, 2009 | 133 | 2009 |
| Significance of borderline hemoglobin A2 values in an Italian population with a high prevalence of β-thalassemia A Giambona, C Passarello, M Vinciguerra, RL Muli, P Teresi, M Anzà, ... Haematologica 93 (9), 1380-1384, 2008 | 81 | 2008 |
| 2p15-p16.1 microdeletions encompassing and proximal to BCL11A are associated with elevated HbF in addition to neurologic impairment APW Funnell, P Prontera, V Ottaviani, M Piccione, A Giambona, A Maggio, ... Blood, The Journal of the American Society of Hematology 126 (1), 89-93, 2015 | 77 | 2015 |
| Attitude of potential users in Sicily towards preimplantation genetic diagnosis for beta-thalassaemia and aneuploidies. S Chamayou, A Guglielmino, A Giambona, S Siciliano, G Di Stefano, ... Human Reproduction (Oxford, England) 13 (7), 1936-1944, 1998 | 75 | 1998 |
| β-thalassemia microelectronic chip: a fast and accurate method for mutation detection B Foglieni, L Cremonesi, M Travi, A Ravani, A Giambona, MC Rosatelli, ... Clinical Chemistry 50 (1), 73-79, 2004 | 55 | 2004 |
| The great heterogeneity of thalassemia molecular defects in Sicily AGPL Gioco, M Marino, I Abate, RDMM Renda, F Di Trapani, F Messana, ... Hum Genet 95, 526-530, 1995 | 50 | 1995 |
| New analytical tools and epidemiological data for the identification of HbA2 borderline subjects in the screening for beta-thalassemia A Mosca, R Paleari, R Galanello, C Sollaino, L Perseu, FR Demartis, ... Bioelectrochemistry 73 (2), 137-140, 2008 | 48 | 2008 |
| Iron deficiency does not compromise the diagnosis of high HbA2 β thalassemia trait C Passarello, A Giambona, M Cannata, M Vinciguerra, D Renda, ... Haematologica 97 (3), 472, 2012 | 46 | 2012 |
| Analysis of delta-globin gene alleles in the Sicilian population: identification of five new mutations A Giambona, C Passarello, G Ruggeri, D Renda, P Teresi, M Anza, ... Haematologica 91 (12), 1681-1684, 2006 | 44 | 2006 |
| Successful application of preimplantation genetic diagnosis for β-thalassaemia and sickle cell anaemia in Italy S Chamayou, C Alecci, C Ragolia, A Giambona, S Siciliano, A Maggio, ... Human Reproduction 17 (5), 1158-1165, 2002 | 42 | 2002 |
| Rapid detection of six common Mediterranean and three non‐Mediterranean α‐thalassemia point mutations by reverse dot blot analysis E Foglietta, I Bianco, A Maggio, A Giambona American journal of hematology 74 (3), 191-195, 2003 | 32 | 2003 |
| Human coelomic fluid investigation: A MS-based analytical approach to prenatal screening D Aiello, A Giambona, F Leto, C Passarello, G Damiani, A Maggio, ... Scientific Reports 8 (1), 10973, 2018 | 30 | 2018 |
| The genetic heterogeneity of β-globin gene defects in Sicily reflects the historic population migrations of the island A Giambona, M Vinciguerra, M Cannata, F Cassarà, G Fiorentino, F Leto, ... Blood Cells, Molecules, and Diseases 46 (4), 282-287, 2011 | 30 | 2011 |
| External quality assessment of hemoglobin A2 measurement: data from an Italian pilot study with fresh whole blood samples and commercial HPLC systems R Paleari, A Giambona, M Cannata, F Leto, A Maggio, A Mosca, ... Walter de Gruyter 45 (1), 88-92, 2007 | 30 | 2007 |
| Evidence of induced non-tolerance in HLA-identical twins with hemoglobinopathy after in utero fetal transplantation. F Orlandi, A Giambona, F Messana, M Marino, I Abate, R Calzolari, ... Bone marrow transplantation 18 (3), 637-639, 1996 | 30 | 1996 |
| Genetic disorder prenatal diagnosis and pregnancy termination practices among high consanguinity population, Saudi Arabia S AbdulAzeez, NH Al Qahtani, NB Almandil, AM Al-Amodi, SA Aldakeel, ... Scientific reports 9 (1), 17248, 2019 | 29 | 2019 |
| Lentiviral globin gene therapy with reduced-intensity conditioning in adults with β-thalassemia: a phase 1 trial F Boulad, A Maggio, X Wang, P Moi, S Acuto, F Kogel, C Takpradit, ... Nature medicine 28 (1), 63-70, 2022 | 28 | 2022 |
| Incidence of haemoglobinopathies in Sicily: the impact of screening and prenatal diagnosis A Giambona, G Damiani, M Vinciguerra, C Jakil, M Cannata, F Cassara, ... International journal of clinical practice 69 (10), 1129-1138, 2015 | 24 | 2015 |
| βA and βthal DNA haplotypes in Sicily A Maggio, S Acuto, P Lo Gioco, R Di Marzo, A Giambona, P Sammarco, ... Human genetics 72, 229-230, 1986 | 22 | 1986 |
