Showing results 73 to 90 of 90
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| Issue Date | Title | Author(s) |
| 2015-03 | Rare disease research and the Malta biobank | Vella, Joanna; Borg, Joseph J.; Grech, Laura; Galdies, Ruth; Scerri, Jeanesse; Cassar, Wilhelmina; Scerri, Christian A.; Grech, Godfrey; Soler, Doriette; Said, Edith; Borg, Isabella; Vella, Norbert; Camilleri-Podesta, Marie Therese; Ellul, Bridget; Abela, Mark; Grima, David; Zammit, Esther; Pace, Nikolai Paul; Felice, Alex; Said Conti, Valerie |
| 2011 | Recommendations for genetic variation data capture in developing countries to ensure a comprehensive worldwide data collection | Patrinos, George P.; Al-Aama, Jumana Yousuf; Al-Mulla, Fahd; Borg, Joseph J.; Devereux, Andrew; Felice, Alex; Macrae, Finlay A.; Marafie, Makia J.; Peterson, Michael B.; Qi, Ming; Ramesar, Rajkumar S.; Zlotogora, Joel; Cotton, Richard G. H.; Al Aqeel, Aida |
| 2012 | Relevance of pharmacogenomics for developing countries in Europe : implementation in the Maltese population | Mitropoulou, Christina; Grech, Godfrey; Fenech, Anthony G.; Borg, Joseph J.; Mitropoulos, Konstantinos; Vozikis, Athanassios; Patrinos, George P. |
| 2007 | A review of cis-trans interplay between DNA sequences 5′ to the Gγ-and β-globin genes among Hb F-Malta-I heterozygotes/homozygotes and β-thalassemia homozygotes/compound heterozygotes, and the effects of hydroxyurea on the Hb F/F-erythrocyte; the need for large multicenter trials | Felice, Alex; Borg, Joseph J.; Pizzuto, Monica; Cassar, Wilhelmina; Galdies, Ruth; Bezzina Wettinger, Stephanie; Pulis, Svetlana; Hunter, Gary J.; Caruana, Mary Rose; Farrugia, Mario; Scerri, Christian A. |
| 2018 | The role of FLVCR1 isoforms on inter-erythrocytic distribution of human foetal haemoglobin | Grech, Laura; Scerri, Jeanesse; Mizzi, Clint; Galdies, Ruth; Scerri, Christian A.; Ijcken, Wilfred van; Özgür, Zeliha; Gillemans, Nynke; Borg, Joseph J.; Philipsen, Sjaak; Felice, Alex E. |
| 2022 | Routine omics collection is a golden opportunity for European human research in space and analog environments | Cope, Henry; Willis, Craig R. G.; MacKay, Matthew J.; Rutter, Lindsay A.; Toh, Li Shean; Williams, Philip M.; Herranz, Raul; Borg, Joseph J.; Bezdan, Daniela; Giacomello, Stefania; Muratani, Masafumi; Mason, Christopher E.; Etheridge, Timothy; Szewczyk, Nathaniel J. |
| 2018 | Science Odyssey | Borg, Joseph J. |
| 2020 | Sickle cell disease | Grech, Laura; Borg, Joseph J. |
| 2009-11 | The significance of quantitative HB epidemiology in public health genomics and genetic models of complex disease | Felice, Alex; Galdies, Ruth; Cassar, Wilhelmina; Pizzuto, Monica; Borg, Joseph J.; Bugeja, Marisa; Caruana, Mary Rose; Farrugia, Mario; Scerri, Christian A. |
| 2022 | Space omics research in Europe : contributions, geographical distribution and ESA member state funding schemes | Deane, Colleen S.; Silveira, Willian A. da; Herranz, Raul; Borg, Joseph J.; Space Omics Topical Team |
| 2011 | Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach | Giardine, Belinda; Borg, Joseph J.; Higgs, Douglas R.; Peterson, Kenneth R.; Philipsen, Sjaak; Maglott, Donna; Singleton, Belinda K.; Anstee, David J.; Basak, Ayse Nazli; Clark, Barnaby; Costa, Flavia C.; Faustino, Paula; Fedosyuk, Halyna; Felice, Alex; Francina, Alain; Galanello, Renzo; Gallivan, Monica V. E.; Georgitsi, Marianthi; Gibbons, Richard J.; Giordano, Piero C.; Harteveld, Cornelis L.; Hoyer, James D.; Jarvis, Martin; Joly, Philippe; Kanavakis, Emmanuel; Kollia, Panagoula; Menzel, Stephan; Miller, Webb; Moradkhani, Kamran; Old, John; Papachatzopoulou, Adamantia; Papadakis, Manoussos N.; Papadopoulos, Petros; Pavlovic, Sonja; Perseu, Lucia; Radmilovic, Milena; Riemer, Cathy; Satta, Stefania; Schrijver, Iris; Stojiljkovic-Petrovic, Maja; Thein, Swee Lay; Traeger-Synodinos, Jan; Tully, Ray; Wada, Takahito; Waye, John S.; Wiemann, Claudia; Zukic, Branka; Chui, David H. K.; Wajcman, Henri; Hardison, Ross C.; Patrinos, George P. |
| 2018 | Tracing Maltese genetic origins | Vella, Joanna; Bodner, Martin; Huber, Nicole; Geppert, M.; Zimmermann, Bettina; Borg, Joseph J.; Felice, Alex E.; Roewer, L.; Parson, W. |
| 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. |
| 2015-12 | Validation of a Polymerase Chain Reaction technique for Kidd blood group genotyping | Xuereb, Karl; Debono, Jesmond; Borg, Joseph J. |
| 2009 | Variants within protectin (CD59) and CD44 genes linked to an inherited haplotype in a family with coeliac disease | Vidal, Christopher; Borg, Joseph J.; Xuereb-Anastasi, Angela; Scerri, Christian A. |
| 2010 | Whole genome pharmacogenomic analysis of bipolar disease patients under lithium treatment | Squassina, Alessio; Borg, Joseph J.; Manchia, Mirko; Chillotti, Caterina; Ardau, Raffaella; Severino, Giovanni; Georgitsi, Marianthi; Mitropoulos, Konstantinos; Zompo, Maria del; Patrinos, George P. |
