Showing results 27 to 46 of 53
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| Issue Date | Title | Author(s) |
| 1978 | Heredity : a fact that can be tampered with? | Balzan, Rena |
| 2010 | High resolution mapping of a DNA locus genetically linked to febrile seizures | Farrugia, Claudia-Ann |
| 2022 | An immune dysfunction score for stratification of patients with acute infection based on whole-blood gene expression | Cano-Gamez, Eddie; Burnham, Katie L.; Goh, Cyndi; Allcock, Alice; Malick, Zunaira H.; Overend, Lauren; Kwok, Andrew; Smith, David A.; Peters-Sengers, Hessel; Antcliffe, David; McKechnie, Stuart; Hall, Sally; Addison, Jenni; Roughton, Sian; Tennant, Heather; Guleri, Achyut; Waddington, Natalia; Arawwawala, Dilshan; Durcan, John; Short, Alasdair; Swan, Karen; Raymode, Parizade; Williams, Sarah; Smolen, Susan; Mitchell-Inwang, Christine; Gordon, Tony; Errington, Emily; Templeton, Maie; Venatesh, Pyda; Ward, Geraldine; McCauley, Marie; Baudouin, Simon; Thompson, Jonathan; Higham, Charley; Soar, Jasmeet; Grier, Sally; Hall, Elaine; Brett, Stephen; Kitson, David; Wilson, Robert; Mountford, Laura; Moreno, Juan; Hall, Peter; Bowrey, Sarah; Hewlett, Jackie; McKechnie, Stuart; Garrard, Christopher; Millo, Julian; Young, Duncan; Hutton, Paula; Parsons, Penny; Smiths, Alex; Faras-Arraya, Roser; Soar, Jasmeet; Kazembe, Sandra; Rich, Natalie; Andreou, Prem; Hales, Dawn; Roberts, Emma; Fletcher, Simon; Rosbergen, Melissa; Lowes, Sarah; Glister, Georgina; Moreno Cuesta, Jeronimo; Bion, Julian; Millar, Joanne; Perry, Elsa Jane; Willis, Heather; Mitchell, Natalie; Ruel, Sebastian; Carrera, Ronald; Wilde, Jude; Higham, Charley; Nilson, Annette; Lees, Sarah; Kapila, Atul; Jacques, Nicola; Atkinson, Jane; Brown, Abby; Prowse, Heather; Krige, Anton; Bland, Martin; Bullock, Lynne; Walsh, Helen; Harrison, Donna; Mills, Gary; Humphreys, John; Armitage, Kelsey; Laha, Shond; Baldwin, Jacqueline; Walsh, Angela; Doherty, Nicola; Drage, Stephen; Ortiz-Ruiz de Gordoa, Laura; Calder, Verity; Swan, Catherine; Payne, Heather; Higgins, David; Andrews, Sarah; Mappleback, Sarah; Hind, Charles; Scicluna, Brendon P.; Garrard, Chris; Watson, D.; McLees, Eleanor; Purdy, Alice; Stotz, Martin; Ochelli-Okpue, Adaeze; Bonner, Stephen; Whitehead, Iain; Hugil, Keith; Goodridge, Victoria; Poll, Tom van der; Cawthor, Louisa; Kuper, Martin; Pahary, Sheik; Bellingan, Geoffrey; Marshall, Richard; Montgomery, Hugh; Hyun Ryu, Jung; Bercades, Georgia; Boluda, Susan; Bentley, Andrew; Gordon, Anthony C.; Mccalman, Katie; Jefferies, Fiona; Knight, Julian; Davenport, Emma; Burnham, Katie L.; Maugeri, Narelle; Radhakrishnan, Jayachandran; Mi, Yuxin; Allcock, Alice; Goh, Cyndi; Hinds, Charles J.; Davenport, Emma E.; Knight, Julian C.; Webster, Nigel; Galley, Helen; Taylor, Jane; GAinS Investigators |
| 2015 | Impact on parents of HLA-DQ2/DQ8 genotyping in healthy children from coeliac families | Wessels, Margreet MS; Vriezinga, Sabine L.; Koletzko, Sybille; Werkstetter, Katharina; Castillejo-De Villasante, Gemma; Shamir, Raanan; Hartman, Corina; Putter, Hein; van der Pal, Sylvia M.; Wijmenga, Cisca; Bravi, Enzo; Mearin, M. Luisa; Scerri, Christian A.; PreventCD Study Group |
| 2014 | Improving coeliac disease risk prediction by testing non-HLA variants additional to HLA variants | Romanos, Jihane; Rosen, Anna; Kumar, Vinod; Trynka, Gosia; Franke, Lude; Szperl, Agata; Gutierrez-Achury, Javier; van Diemen, Cleo C.; Kanninga, Roan; Jankipersadsing, Soesma A.; Steck, Andrea; Eisenbarth, Georges; van Heel, David A.; Cukrowska, Bozena; Bruno, Valentina; Mazzilli, Maria Cristina; Nunez, Concepcion; Bilbao, Jose Ramon; Mearin, M. Luisa; Barisani, Donatella; Rewers, Marian; Norris, Jill M.; Ivarsson, Anneli; Boezen, H. Marieke; Liu, Edwin; Wijmenga, Cisca; Scerri, Christian A.; PreventCD Group |
| 2016 | Integrity and the dual use of research | Engerer, Vanessa |
| 2022 | Interpreting the spectrum of gamma-secretase complex missense variation in the context of hidradenitis suppurativa : an in-silico study | Mintoff, Dillon; Pace, Nikolai Paul; Borg, Isabella |
| 2013 | It's all in the family | Fiott, Alexandra |
| 2014-09 | Maltese olives and their genes | Mazzitelli, Oriana |
| 2002 | New insights in genetics of congenital heart defects | Digilio, Maria Cristina |
| 2021 | A novel c. 671_682del NCSTN variant in a family with Hidradenitis Suppurativa : a pilot study | Mintoff, Dillon; Pace, Nikolai Paul; Bauer, Peter; Borg, Isabella |
| 2019 | Nuclear paraspeckles function in mediating gene regulatory and apoptotic pathways | Pisani, Gabriel; Baron, Byron |
| 2016 | Pharmacogenetics : ethics and public policy | Abdilla, Bernice |
| 2011 | Phenotyping and genotyping of Maltese patients with acromegaly | Mercieca, Cecilia |
| 2014-06 | Preventing sudden death | Bezzina, Connie |
| 2015 | Preventive and predictive genetics : a perspective | Grech, Godfrey; Scerri, Christian A.; Scerri, Jeanesse; Cesuroglu, Tomris |
| 2011 | Quantitative trait loci for electrocardiographic parameters and arrhythmia in the mouse | Scicluna, Brendon P.; Tanck, Michael W.T.; Remme, Carol Ann; Beekman, Leander; Coronel, Ruben; Wilde, Arthur A. M.; Bezzina, Connie R. |
| 2011 | The re-creation of man genetic testing, genetic selection or a new form of eugenics | Grima, Christopher Paul (2011) |
| 2022 | Recalibration of minor alleles in the human reference sequence | Teuma, Helena (2022) |
| 2011 | Relation between biologic markers and genetic patterns as risk factors of Alzheimer's disease in a Mexican population | Treviño, Daniel Gerardo Gámez (2011) |
