Showing results 5 to 24 of 53
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| Issue Date | Title | Author(s) |
| 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 |
| 2019 | Genetic variability assessment in different Mediterranean canine breeds using microsatellite markers | Lasagna, Emiliano; Ceccobelli, Simone; Martinez Martinez, Amparo; Lancioni, Hovirag; Landi, Vincenzo; Cosenza, Mario; Gruppetta, Anthony; Sarti, Francesca Maria; Chiofalo, Vincenzo; San Jose, Carlos; Monteagudo Ibanez, Luis; Liotta, Luigi; Attard, George |
| 2009 | Genetically determined differences in sodium current characteristics modulate conduction disease severity in mice with cardiac sodium channelopathy | Remme, Carol Ann; Scicluna, Brendon P.; Verkerk, Arie O.; Amin, Ahmad S.; Brunschot, Sandra van; Beekman, Leander; Deneer, Vera H. M.; Chevalier, Catherine; Oyama, Fumitaka; Miyazaki, Haruko; Nukina, Nobuyuki; Wilders, Ronald; Escande, Denis; Houlgatte, Rémi; Wilde, Arthur A. M.; Tan, Hanno L.; Veldkamp, Marieke W.; Bakker, Jacques M. T. de; Bezzina, Connie R. |
| 2008 | Genome-wide expression analysis of a spinal muscular atrophy model : towards discovery of new drug targets | Lee, Sheena; Sayin, Arzu; Cauchi, Ruben J.; Grice, Stuart; Burdett, Howard; Baban, Dilair; van den Heuvel, Marcel |
| 2022 | Genome-wide identification of the genetic basis of amyotrophic lateral sclerosis | Zhang, Sai; Cooper-Knock, Johnathan; Weimer, Annika K.; Shi, Minyi; Moll, Tobias; Marshall, Jack N.G.; Harvey, Calum; Ghahremani Nezhad, Helia; Franklin, John; Santos Souza, Cleide dos; Ning, Ke; Wang, Cheng; Li, Jingjing; Dilliott, Allison A.; Farhan, Sali; Elhaik, Eran; Pasniceanu, Iris; Livesey, Matthew R.; Eitan, Chen; Hornstein, Eran; Kenna, Kevin P.; Veldink, Jan H.; Ferraiuolo, Laura; Shaw, Pamela J.; Snyder, Michael P.; Cauchi, Ruben J.; Project MinE ALS Sequencing Consortium |
