Showing results 11 to 24 of 24
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| Issue Date | Title | Author(s) |
| 2010 | Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin | Borg, Joseph J.; Papadopoulos, Petros; Georgitsi, Marianthi; Gutierrez, Laura; Grech, Godfrey; Fanis, Pavlos; Phylactides, Marios; Verkerk, Annemieke J.M.H.; van der Spek, Peter J.; Scerri, Christian A.; Cassar, Wilhelmina; Galdies, Ruth; van IJcken, Wilfred; Ozgur, Zeliha; Gillemans, Nynke; Hou, Jun; Bugeja, Marisa; Grosveld, Frank G.; von Lindern, Marieke; Felice, Alex; Patrinos, George P.; Philipsen, Sjaak |
| 2015 | Identification of cancer predisposition variants in apparently healthy individuals using a next-generation sequencing-based family genomics approach | Karageorgos, Ioannis; Mizzi, Clint; Giannopoulou, Efstathia; Pavlidis, Cristiana; Peters, Brock A.; Zagoriti, Zoi; Stenson, Peter D.; Mitropoulos, Konstantinos; Borg, Joseph J.; Kalofonos, Haralabos P.; Drmanac, Radoje; Stubbs, Andrew; Spek, Peter van der; Cooper, David N.; Katsila, Theodora; Patrinos, George P. |
| 2015 | Implementation of pre-emptive pharmacogenomics in the Maltese population | Grech, Godfrey; Fenech, Anthony G.; Mizzi, Clint; Borg, Joseph; Patrinos, George P. |
| 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. |
| 2014 | Key challenges for next‐generation pharmacogenomics | Kampourakis, Kostas; Vayena, Effy; Mitropoulou, Christina; Schaik, Ron H.; Cooper, David N.; Borg, Joseph J.; Patrinos, George P. |
| 2012 | KLF10 gene expression is associated with high fetal hemoglobin levels and with response to hydroxyurea treatment in β-hemoglobinopathy patients | Borg, Joseph J.; Phylactides, Marios; Bartsakoulia, Marina; Tafrali, Christina; Lederer, Carsten W.; Felice, Alex; Papachatzopoulou, Adamantia; Kourakli, Alexandra; Stavrou, Eleana F.; Christou, Soteroula; Hou, Jun; Karkabouna, Sophia; Lappa-Manakou, Christina; Ozgur, Zeliha; Ijcken, Wilfred van; Lindern, Marieke von; Grosveld, Frank G.; Georgitsi, Marianthi; Kleanthous, Marina; Philipsen, Sjaak; Patrinos, George P. |
| 2016 | Krüppeling erythropoiesis : an unexpected broad spectrum of human red blood cell disorders due to KLF1 variants | Perkins, Andrew; Xu, Xiangmin; Higgs, Douglas R.; Patrinos, George P.; Arnaud, Lionel; Bieker, James J.; Philipsen, Sjaak; Borg, Joseph J.; Klf1 Consensus and Workgroup |
| 2016 | Novel genetic risk variants for pediatric celiac disease | Balasopoulou, Angeliki; Stanković, Biljana; Panagiotara, Angeliki; Nikčevic, Gordana; Peters, Brock A.; John, Anne; Mendrinou, Effrosyni; Stratopoulos, Apostolos; Legaki, Aigli Ioanna; Stathakopoulou, Vasiliki; Tsolia, Aristoniki; Govaris, Nikolaos; Govari, Sofia; Zagoriti, Zoi; Poulas, Konstantinos; Kanariou, Maria; Constantinidou, Nikki; Krini, Maro; Spanou, Kleopatra; Radlovic, Nedeljko; Ali, Bassam R.; Borg, Joseph J.; Drmanac, Radoje; Chrousos, George; Pavlovic, Sonja; Roma, Eleftheria; Zukic, Branka; Patrinos, George P.; Katsila, Theodora |
| 2014 | Personalized pharmacogenomics profiling using whole-genome sequencing | Mizzi, Clint; Peters, Brock; Mitropoulou, Christina; Mitropoulos, Konstantinos; Katsila, Theodora; Agarwal, Misha R.; Schaik, Ron H. N. van; Drmanac, Radoje; Borg, Joseph J.; Patrinos, George P. |
| 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. |
| 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. |
| 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. |
| 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. |
