Browsing by Subject Genetics

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
or enter first few letters:  
Showing results 18 to 37 of 53 < previous   next >
Issue DateTitleAuthor(s)
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
2019Genetic variability assessment in different Mediterranean canine breeds using microsatellite markersLasagna, 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
2009Genetically determined differences in sodium current characteristics modulate conduction disease severity in mice with cardiac sodium channelopathyRemme, 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.
2008Genome-wide expression analysis of a spinal muscular atrophy model : towards discovery of new drug targetsLee, Sheena; Sayin, Arzu; Cauchi, Ruben J.; Grice, Stuart; Burdett, Howard; Baban, Dilair; van den Heuvel, Marcel
2022Genome-wide identification of the genetic basis of amyotrophic lateral sclerosisZhang, 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
2022The genomic architecture of hidradenitis suppurativa - a systematic reviewPace, Nikolai Paul; Mintoff, Dillon; Borg, Isabella
2010Glossarju dwar il-ġenetikaDegiorgio, Reuben (2010)
1978Heredity : a fact that can be tampered with?Balzan, Rena
2010High resolution mapping of a DNA locus genetically linked to febrile seizuresFarrugia, Claudia-Ann
2022An immune dysfunction score for stratification of patients with acute infection based on whole-blood gene expressionCano-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
2015Impact on parents of HLA-DQ2/DQ8 genotyping in healthy children from coeliac familiesWessels, 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
2014Improving coeliac disease risk prediction by testing non-HLA variants additional to HLA variantsRomanos, 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
2016Integrity and the dual use of researchEngerer, Vanessa
2022Interpreting the spectrum of gamma-secretase complex missense variation in the context of hidradenitis suppurativa : an in-silico studyMintoff, Dillon; Pace, Nikolai Paul; Borg, Isabella
2013It's all in the familyFiott, Alexandra
2014-09Maltese olives and their genesMazzitelli, Oriana
2002New insights in genetics of congenital heart defectsDigilio, Maria Cristina
2021A novel c. 671_682del NCSTN variant in a family with Hidradenitis Suppurativa : a pilot studyMintoff, Dillon; Pace, Nikolai Paul; Bauer, Peter; Borg, Isabella