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Issue Date | Title | Author(s) |
1972 | Abnormal hemoglobins in Malta : the significance of two fetal and an adult variant | Bannister, William H.; Grech, J.L.; Huisman, Titus Hendrik Jan; Schroeder, W.A. |
2006 | The aetiology of ectopic maxillary canine teeth | McDonald, Fraser; Scerri, Christian A.; Camilleri, Simon |
2009 | Allele scoring of genetic risk in previous gestational diabetes mellitus (pGDM) | Abou Hussein, Samir |
2015 | Analysis of the molecular diversity of Olea Europaea in the Mediterranean Island of Malta | Mazzitelli, Oriana; Calleja, Alan; Sardella, Davide; Farrugia, Claude; Zammit-Mangion, Marion |
1995 | Clinical pathology and molecular biology of the b IVS-I,6C thalassaemia in homozygous Maltese children | Felice, A. E.; Scerri, C. A.; Buhagiar, S.; Grech, J. L.; Pizzuto, M.; Galdies, R.; Gauci, M. R.; Parascandolo, R.; Xuereb, A.; Muscat Baron, I. |
2011 | Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease | Trynka, Gosia; Hunt, Karen A.; Bockett, Nicholas A.; Romanos, Jihane; Mistry, Vanisha; Szperl, Agata; Bakker, Sjoerd F.; Bardella, Maria Teresa; Bhaw-Rosun, Leena; Castillejo, Gemma; de la Concha, Emilio G.; Coutinho de Almeida, Rodrigo; Dias, Kerith-Rae M.; van Diemen, Cleo C.; Dubois, Patrick C. A.; Duerr, Richard H.; Edkins, Sarah; Franke, Lude; Fransen, Karin; Gutierrez, Javier; Heap, Graham A. R.; Hrdlickova, Barbara; Hunt, Sarah; Izurieta, Leticia Plaza; Izzo, Valentina; Joosten, Leo A. B.; Cordelia, Langford; Mazzilli, Maria Cristina; Mein, Charles A.; Midah, Vandana; Mitrovic, Mitja; Mora, Barbara; Morelli, Marinita; Nutland, Sarah; Nunez, Concepcion; Onengut-Gumuscu, Suna; Pearce, Kerra; Platteel, Mathieu; Polanco, Isabel; Potter, Simon; Ribes-Koninckx, Carmen; Ricano-Ponce, Isis; Rich, Stephen S.; Rybak, Anna; Santiago, Jose Luis; Senapati, Sabyasachi; Soot, Ajit; Szajewska, Hania; Troncone, Riccardo; Varade, Jezabel; Wallace, Chris; Wolters, Victorien M.; Zhernakova, Alexandra; Scerri, Christian A.; Spanish Consortium on the Genetics of Coeliac Disease (CEGEC); PreventCD Study Group; Wellcome Trust Case Control Consortium (WTCCC); Thelma, B. K.; Cukrowska, Bozena; Urcelay, Elena; Bilbao, Jose Ramon; Mearin, M. Luisa; Barisani, Donatella; Barrett, Jeffrey C.; Plagnol, Vincent; Deloukas, Panos; Wijmenga, Cisca; van Heel, David A. |
2015 | Dental anomalies in first-degree relatives of transposed canine probands | Bartolo, Adriana; Calleja, Neville; McDonald, Fraser; Camilleri, Simon |
2018 | Determining the frequency of RH blood group system in the Maltese population | Giordmaina, Antonella; Borg, Joseph J.; Debono, Jesmond; Debattista, Neville |
2017 | Determining the genotype of the Rh blood group system in the Maltese population | Giordmaina, Antonella |
2018 | Determining the genotype of the RH blood group system in the Maltese population | Giordmaina, Antonella; Borg, Joseph J.; Debono, Jesmond; Debattista, Neville |
2013-09 | Diabetes : from genes to blood | Duca, Edward |
2022 | Epigenomic analysis of KLF1 haploinsufficiency in primary human erythroblasts | Heshusius, Steven; Grech, Laura; Gillemans, Nynke; Brouwer, Rutger W. W.; Dekker, Xander T. den; IJcken, Wilfred F. J. van; Nota, Benjamin; Felice, Alex E.; Dijk, Thamar B. van; Lindern, Marieke von; Borg, Joseph J.; Akker, Emile van den; Philipsen, Sjaak |
2021 | Flagellin induces innate immune genes in bronchial epithelial cells in vivo : role of TET2 | Qin, Wanhai; Brands, Xanthe; Veer, Cornelis Van't; Vos, Alex F. de; Scicluna, Brendon P.; Poll, Tom van der |
2014 | Flying in the face of neurodegeneration | Cauchi, Ruben J. |
1995 | Framework-dependent in vivo expression of two missense mutations (pro¹²³-->thr and ala²⁴⁴-->val) in the coagulation factor vii gene from a Maltese kindred | Al Shinawi, C.; Scerri, C.; Galdies, R.; Aquilina, A.; Felice, A. E. |
2020 | Functional characterisation and pharmacogenetic relevance of a novel gene associated with poor lung function | Farrugia Bajada, Edwina (2020) |
2012 | The further development of DNA pooling for gene discovery and public health genomics | Bugeja, Marisa |
2017-12 | Genetic determinants of low birth weight | Mallia, Theresa; Grech, Alexia; Hili, Abigail; Calleja-Agius, Jean; Pace, Nikolai Paul |
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. |
2023 | Genetic subtypes of Hereditary Spastic Paraplegia | Bonello, David |