| Issue Date | Title | Author(s) |
| 2019 | Diagnosis of beta thalassaemia trait | Borg, Joseph J.; Grech, Laura |
| 2020 | Genetic heterogeneity of KLF1, a master regulator of erythropoiesis, revealed an autosomal recessive Ψβ-thalassemia and a very strong promoter in vivo | Grech, Laura; Borg, Joseph J.; Galdies, Ruth; Attard, Carmen; Scerri, Christian A.; Philipsen, Sjaak; Felice, Alexander E. |
| 2009 | Genetic recombination as a major cause of mutagenesis in the human globin gene clusters | Borg, Joseph J.; Georgitsi, Marianthi; Aleporou-Marinou, Vassiliki; Kollia, Panagoula; Patrinos, George P. |
| 2015 | A genetic score for the prediction of beta-thalassemia severity | Danjou, Fabrice; Francavilla, Marcella; Anni, Franco; Satta, Stefania; Demartis, Franca-Rosa; Perseu, Lucia; Manca, Matteo; Sollaino, Maria Carla; Manunza, Laura; Mereu, Elisabetta; Marceddu, Giuseppe; Pissard, Serge; Joly, Philippe; Thuret, Isabelle; Origa, Raffaella; Borg, Joseph J.; Forni, Gian Luca; Piga, Antonio; Lai, Maria Eliana; Badens, Catherine; Moi, Paolo; Galanello, Renzo |
| 2006 | Hb F Malta I in association with Hb F Sardinia (AyT) and Hb Valletta in heterozygotes : quantification of the six globins suggests developmental control of the XMN-I site and interplay with the (AT)xTy sequence in connection with globin gene switching | Felice, Alex E.; Borg, Joseph J.; Cassar, Wilma; Galdies, Ruth; Pizzuto, Monica; Caruana, Maryrose; Scerri, Christian A. |
| 1872 | Il Barth : gazzetta di medicina e scienze naturali : Vol. 2, No. 10 | Gulia, Gavino |
| 2014 | Individualizing fetal hemoglobin augmenting therapy for β-type hemoglobinopathies patients | Gravia, Aikaterini; Chondrou, Vasiliki; Sgourou, Argyro; Papantoni, Ioanna; Borg, Joseph J.; Katsila, Theodora; Papachatzopoulou, Adamantia; Patrinos, George P. |
| 2022 | Novel therapies in β-thalassaemia | Grech, Laura; Borg, Karen; Borg, Joseph J. |
| 2008-05 | Thalassaemia : a review | Scerri, Christian A. |
| 2014 | Transfusion-independent β 0 -thalassemia after bone marrow transplantation failure : proposed involvement of high parental HbF and an epigenetic mechanism | Paciaroni, Katia; Lucarelli, Guido; Martelli, Fabrizio; Migliaccio, Anna Rita; Lindern, Marieke von; Borg, Joseph J.; Gillemans, Nynke; Dijk, Thamar B. van; Philipsen, Sjaak |
| 2019 | A twenty-five year prospective clinical review and family studies revealed new globin gene regulators for Hb F induction | Felice, Alex E.; Borg, Joseph J.; Grech, Laura; Scerri, Christian A.; Galdies, Ruth; Philipsen, Sjaak |
| 2014 | Updates of the HbVar database of human hemoglobin variants and thalassemia mutations | Giardine, Belinda; Borg, Joseph J.; Viennas, Emmanouil; Pavlidis, Cristiana; Moradkhani, Kamran; Joly, Philippe; Bartsakoulia, Marina; Riemer, Cathy; Miller, Webb; Tzimas, Gianni; Wajcman, Henri; Hardison, Ross C.; Patrinos, George P. |
| n.d. | X’ għandek tkun taf fuq it-thalassemia | - |
