Showing results 2 to 18 of 18
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Issue Date | Title | Author(s) |
2021 | Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology | Rheenen, 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 |
2019 | Construction and benchmarking of a multi-ethnic reference panel for the imputation of HLA class I and II alleles | Degenhardt, 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 |
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. |
2012 | Extracting protein sequence class descriptors using eMotifs | Agius, Ian (2012) |
2017-12 | Genetic determinants of low birth weight | Mallia, Theresa; Grech, Alexia; Hili, Abigail; Calleja-Agius, Jean; Pace, Nikolai Paul |
2021 | Genome sequences of 10 SARS-CoV-2 viral strains obtained by nanopore sequencing of nasopharyngeal swabs in Malta | Biazzo, Manuele; Madeddu, Silvia; Elnifro, Elfath; Sultana, Tessabella; Muscat, Josie; Scerri, Christian A.; Santoro, Francesco; Pinzauti, David |
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 |
2013 | HERVs, transposons and human diseases : part 3 | Grech, Alfred; Baldacchino, Sandra |
2012 | HERVs, transposons and human diseases : part I | Grech, Alfred; Baldacchino, Sandra |
2013 | HERVs, transposons and human diseases : part II | Grech, Alfred; Baldacchino, Sandra |
2022 | Identifying genetic determinants of osteoporosis in Malta | Schembri, Marichela (2022) |
2008 | IFNGRI and TNFAIP3 in a Maltese family with a highly penetrant form of osteoporosis | Gatt, Claire |
2007 | Modular decomposition of metabolic systems via null space analysis | Poolman, Mark G.; Sebu, Cristiana; Pidcock, Michael K.; Fell, David A. |
2020-08 | A preliminary assessment of the effects of EM radiation on eubacterial genomes | Aquilina, Maria; Bellia, Andrea Francesca; Meekers, Leah; Borg, Joseph J.; Borg, Josef; Zarb Adami, Kristian; Lanfranco, Sandro |
2023 | Rare gene variant discovery in Maltese ALS patients and functional characterisation of a gene linked to juvenile-onset ALS | Farrugia Wismayer, Maria (2023) |
2008 | Sequencing of genes in two Maltese families with severe osteoporosis | Cachia, Adela |
2022 | The use of high throughput sequencing for the identification of variants contributing to Hirschsprung disease in the Maltese | Gatt, Veronique (2022) |