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Showing results 1 to 18 of 18
Issue DateTitleAuthor(s)
2018Analysing the building blocks : gene sequencing for disease treatmentFarrugia, Rosienne
2021Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biologyRheenen, Wouter van; Spek, Rick A.A. van der; Bakker, Mark K.; Vugt, Joke J.F.A. van; Hop, Paul J.; Zwamborn, Ramona A. J.; Klein, Niek de; Westra, Harm-Jan; Bakker, Olivier B.; Deelen, Patrick; Shireby, Gemma; Hannon, Eilis; Moisse, Matthieu; Baird, Denis; Restuadi, Restuadi; Dolzhenko, Egor; Dekker, Annelot M.; Gawor, Klara; Westeneng, Henk-Jan; Tazelaar, Gijs H.P.; Eijk, Kristel R. van; Kooyman, Maarten; Byrne, Ross P.; Doherty, Mark; Heverin, Mark; Khleifat, Ahmad Al; Iacoangeli, Alfredo; Shatunov, Aleksey; Ticozzi, Nicola; Cooper-Knock, Johnathan; Smith, Bradley N.; Gromicho, Marta; Chandran, Siddharthan; Pal, Suvankar; Morrison, Karen E.; Shaw, Pamela J.; Hardy, John; Orrell, Richard W.; Sendtner, Michael; Meyer, Thomas; Başak, Nazli; Kooi, Anneke J. van der; Ratti, Antonia; Fogh, Isabella; Gellera, Cinzia; Lauria, Giuseppe; Corti, Stefania; Cereda, Cristina; Sproviero, Daisy; D’Alfonso, Sandra; Sorarù, Gianni; Siciliano, Gabriele; Filosto, Massimiliano; Padovani, Alessandro; Chiò, Adriano; Calvo, Andrea; Moglia, Cristina; Brunetti, Maura; Canosa, Antonio; Grassano, Maurizio; Beghi, Ettore; Pupillo, Elisabetta; Logroscino, Giancarlo; Nefussy, Beatrice; Osmanovic, Alma; Nordin, Angelica; Lerner, Yossef; Zabari, Michal; Gotkine, Marc; Baloh, Robert H.; Bell, Shaughn; Vourc’h, Patrick; Corcia, Philippe; Couratier, Philippe; Millecamps, Stéphanie; Meininger, Vincent; Salachas, François; Mora Pardina, Jesus S.; Assialioui, Abdelilah; Rojas-García, Ricardo; Dion, Patrick A.; Ross, Jay P.; Ludolph, Albert C.; Weishaupt, Jochen H.; Brenner, David; Freischmidt, Axel; Bensimon, Gilbert; Brice, Alexis; Durr, Alexandra; Payan, Christine A.M.; Saker-Delye, Safa; Wood, Nicholas W.; Topp, Simon; Rademakers, Rosa; Tittmann, Lukas; Lieb, Wolfgang; Franke, Andre; Ripke, Stephan; Braun, Alice; Kraft, Julia; Whiteman, David C.; Olsen, Catherine M.; Uitterlinden, Andre G.; Hofman, Albert; Rietschel, Marcella; Cichon, Sven; Nöthen, Markus M.; Amouyel, Philippe; Traynor, Bryan J.; Singleton, Andrew B.; Mitne Neto, Miguel; Cauchi, Ruben J.; Ophoff, Roel A.; Wiedau-Pazos, Martina; Lomen-Hoerth, Catherine; Deerlin, Vivianna M. van; Grosskreutz, Julian; Roediger, Annekathrin; Gaur, Nayana; Jörk, Alexander; Barthel, Tabea; Theele, Erik; Ilse, Benjamin; Stubendorff, Beatrice; Witte, Otto W.; Steinbach, Robert; Hübner, Christian A.; Graff, Caroline; Brylev, Lev; Fominykh, Vera; Demeshonok, Vera; Ataulina, Anastasia; Rogelj, Boris; Koritnik, Blaž; Zidar, Janez; Ravnik-Glavač, Metka; Glavač, Damjan; Stević, Zorica; Drory, Vivian; Povedano, Monica; Blair, Ian P.; Kiernan, Matthew C.; Benyamin, Beben; Henderson, Robert D.; Furlong, Sarah; Mathers, Susan; McCombe, Pamela A.; Needham, Merrilee; Ngo, Shyuan T.; Nicholson, Garth A.; Pamphlett, Roger; Rowe, Dominic B.; Steyn, Frederik J.; Williams, Kelly L.; Mather, Karen A.; Sachdev, Perminder S.; Henders, Anjali K.; Wallace, Leanne; Carvalho, Mamede de; Pinto, Susana; Petri, Susanne; Weber, Markus; Rouleau, Guy A.; Silani, Vincenzo; Curtis, Charles J.; Breen, Gerome; Glass, Jonathan D.; Brown Jr., Robert H.; Landers, John E.; Shaw, Christopher E.; Andersen, Peter M.; Groen, Ewout J.N.; Es, Michael A. van; Jeroen Pasterkamp, R.; Fan, Dongsheng; Garton, Fleur C.; McRae, Allan F.; Davey Smith, George; Gaunt, Tom R.; Eberle, Michael A.; Mill, Jonathan; McLaughlin, Russell L.; Hardiman, Orla; Kenna, Kevin P.; Wray, Naomi R.; Tsai, Ellen; Runz, Heiko; Franke, Lude; Al-Chalabi, Ammar; Damme, Philip Van; Berg, Leonard H. van den; Veldink, Jan H.; SLALOM Consortium; PARALS Consortium; SLAGEN Consortium; SLAP Consortium
2019Construction and benchmarking of a multi-ethnic reference panel for the imputation of HLA class I and II allelesDegenhardt, Frauke; Wendorff, Mareike; Wittig, Michael; Ellinghaus, Eva; Datta, Lisa W.; Schembri, John; Ng, Siew C.; Rosati, Elisa; Hübenthal, Matthias; Ellinghaus, David; Jung, Eun Suk; Lieb, Wolfgang; Abedian, Shifteh; Malekzadeh, Reza; Cheon, Jae Hee; Ellul, Pierre; Sood, Ajit; Midha, Vandana; Thelma, B.K.; Wong, Sunny H.; Schreiber, Stefan; Yamazaki, Keiko; Kubo, Michiaki; Boucher, Gabrielle; Rioux, John D.; Lenz, Tobias L.; Brant, Steven R.; Franke, Andre
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.
2012Extracting protein sequence class descriptors using eMotifsAgius, Ian (2012)
2017-12Genetic determinants of low birth weightMallia, Theresa; Grech, Alexia; Hili, Abigail; Calleja-Agius, Jean; Pace, Nikolai Paul
2021Genome sequences of 10 SARS-CoV-2 viral strains obtained by nanopore sequencing of nasopharyngeal swabs in MaltaBiazzo, Manuele; Madeddu, Silvia; Elnifro, Elfath; Sultana, Tessabella; Muscat, Josie; Scerri, Christian A.; Santoro, Francesco; Pinzauti, David
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
2013HERVs, transposons and human diseases : part 3Grech, Alfred; Baldacchino, Sandra
2012HERVs, transposons and human diseases : part IGrech, Alfred; Baldacchino, Sandra
2013HERVs, transposons and human diseases : part IIGrech, Alfred; Baldacchino, Sandra
2022Identifying genetic determinants of osteoporosis in MaltaSchembri, Marichela (2022)
2008IFNGRI and TNFAIP3 in a Maltese family with a highly penetrant form of osteoporosisGatt, Claire
2007Modular decomposition of metabolic systems via null space analysisPoolman, Mark G.; Sebu, Cristiana; Pidcock, Michael K.; Fell, David A.
2020-08A preliminary assessment of the effects of EM radiation on eubacterial genomesAquilina, Maria; Bellia, Andrea Francesca; Meekers, Leah; Borg, Joseph J.; Borg, Josef; Zarb Adami, Kristian; Lanfranco, Sandro
2023Rare gene variant discovery in Maltese ALS patients and functional characterisation of a gene linked to juvenile-onset ALSFarrugia Wismayer, Maria (2023)
2008Sequencing of genes in two Maltese families with severe osteoporosisCachia, Adela
2022The use of high throughput sequencing for the identification of variants contributing to Hirschsprung disease in the MalteseGatt, Veronique (2022)