Browsing by Subject Genetics

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Issue DateTitleAuthor(s)
1972Abnormal hemoglobins in Malta : the significance of two fetal and an adult variantBannister, William H.; Grech, J.L.; Huisman, Titus Hendrik Jan; Schroeder, W.A.
2006The aetiology of ectopic maxillary canine teethMcDonald, Fraser; Scerri, Christian A.; Camilleri, Simon
2009Allele scoring of genetic risk in previous gestational diabetes mellitus (pGDM)Abou Hussein, Samir
2015Analysis of the molecular diversity of Olea Europaea in the Mediterranean Island of MaltaMazzitelli, Oriana; Calleja, Alan; Sardella, Davide; Farrugia, Claude; Zammit-Mangion, Marion
1995Clinical pathology and molecular biology of the b IVS-I,6C thalassaemia in homozygous Maltese childrenFelice, A. E.; Scerri, C. A.; Buhagiar, S.; Grech, J. L.; Pizzuto, M.; Galdies, R.; Gauci, M. R.; Parascandolo, R.; Xuereb, A.; Muscat Baron, I.
2011Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac diseaseTrynka, 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.
2015Dental anomalies in first-degree relatives of transposed canine probandsBartolo, Adriana; Calleja, Neville; McDonald, Fraser; Camilleri, Simon
2018Determining the frequency of RH blood group system in the Maltese populationGiordmaina, Antonella; Borg, Joseph J.; Debono, Jesmond; Debattista, Neville
2017Determining the genotype of the Rh blood group system in the Maltese populationGiordmaina, Antonella
2018Determining the genotype of the RH blood group system in the Maltese populationGiordmaina, Antonella; Borg, Joseph J.; Debono, Jesmond; Debattista, Neville
2013-09Diabetes : from genes to bloodDuca, Edward
2022Epigenomic analysis of KLF1 haploinsufficiency in primary human erythroblastsHeshusius, 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
2021Flagellin induces innate immune genes in bronchial epithelial cells in vivo : role of TET2Qin, Wanhai; Brands, Xanthe; Veer, Cornelis Van't; Vos, Alex F. de; Scicluna, Brendon P.; Poll, Tom van der
2014Flying in the face of neurodegenerationCauchi, Ruben J.
1995Framework-dependent in vivo expression of two missense mutations (pro¹²³-->thr and ala²⁴⁴-->val) in the coagulation factor vii gene from a Maltese kindredAl Shinawi, C.; Scerri, C.; Galdies, R.; Aquilina, A.; Felice, A. E.
2020Functional characterisation and pharmacogenetic relevance of a novel gene associated with poor lung functionFarrugia Bajada, Edwina (2020)
2012The further development of DNA pooling for gene discovery and public health genomicsBugeja, Marisa
2017-12Genetic determinants of low birth weightMallia, Theresa; Grech, Alexia; Hili, Abigail; Calleja-Agius, Jean; Pace, Nikolai Paul
2020Genetic heterogeneity of KLF1, a master regulator of erythropoiesis, revealed an autosomal recessive Ψβ-thalassemia and a very strong promoter in vivoGrech, Laura; Borg, Joseph J.; Galdies, Ruth; Attard, Carmen; Scerri, Christian A.; Philipsen, Sjaak; Felice, Alexander E.
2023Genetic subtypes of Hereditary Spastic ParaplegiaBonello, David