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Issue DateTitleAuthor(s)
2011Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approachGiardine, Belinda; Borg, Joseph; 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 E.; 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, 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.
2007A 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 trialsFelice, Alex E.; Borg, Joseph; Pizzuto, Monica; Cassar, Wilhelmina; Galdies, Ruth; Bezzina Wettinger, Stephanie; Pulis, Svetlana; Hunter, Gary J.; Caruana, Mary R.; Farrugia, Mario; Scerri, Christian A.
2011Recommendations for genetic variation data capture in developing countries to ensure a comprehensive worldwide data collectionPatrinos, George P.; Al-Aama, Jumana Yousuf; Al-Mulla, Fahd; Borg, Joseph; Devereux, Andrew; Felice, Alex E.; Macrae, Finlay A.; Marafie, Makia J.; Peterson, Michael B.; Qi, Ming; Ramesar, Rajkumar S.; Zlotogora, Joel; Cotton, Richard G. H.; Al Aqeel, Aida
2011Does quantitative heterogeneity of human fetal hemoglobin (Hb F) reveal friends or foes of KLF1 in globin gene switching?Felice, Alex E.; Galdies, Ruth; Borg, Joseph; Grech, Godfrey; Cassar, Wilhelmina; Scerri, Christian A.; Patrinos, George P.; Philipsen, Sjaak
2013Genomic variation in the MAP3K5 gene is associated with β-thalassemia disease severity and hydroxyurea treatment efficacyTafrali, Christina; Paizi, Arsinoi; Borg, Joseph; Radmilovic, Milena; Bartsakoulia, Marina; Giannopoulou, Emily; Giannakopoulou, Olga; Stojiljkovic-Petrovic, Maja; Zukic, Branka; Poulas, Konstantinos; Stavrou, Eleana F.; Lambropoulou, Polyxeni; Kourakli, Alexandra; Felice, Alex E.; Papachatzopoulou, Adamantia; Philipsen, Sjaak; Pavlovic, Sonja; Georgitsi, Marianthi; Patrinos, George P.
2011Erythroid phenotypes associated with KLF1 mutationsBorg, Joseph; Patrinos, George P.; Felice, Alex E.; Philipsen, Sjaak
2012KLF10 gene expression is associated with high fetal hemoglobin levels and with response to hydroxyurea treatment in β-hemoglobinopathy patientsBorg, Joseph; Phylactides, Marios; Bartsakoulia, Marina; Tafrali, Christina; Lederer, Carsten W.; Felice, Alex E.; 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.