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Showing results 28 to 46 of 46 < previous

Issue Date	Title	Author(s)
2008	Linkage analysis in a familial case of idiopathic epilepsy and its implications in drug development	Cassar, Maria Louisa
2019	Low-prevalence of NOD2 polymorphisms in a Maltese IBD cohort	Schembri, J.; Pace, Nikolai Paul; Degenhardt, F.; Franke, A.; Ellul, P.
2014	METTL23, a transcriptional partner of GABPA, is essential for human cognition	Reiff, Rachel E.; Ali, Bassam R.; Baron, Byron; W. Yu, Timothy; Ben-Salem, Salma; E. Coulter, Michael; Schubert, Christian R.; Hill, R. Sean; Akawi, Nadia A.; Al-Younes, Banan; Kaya, Namik; Evrony, Gilad D.; Al-Saffar, Muna; Felie, Jillian M.; Partlow, Jennifer N.; Sunu, Christine M.; Schembri-Wismayer, Pierre; Alkuraya, Fowzan S.; Meyer, Brian F.; Walsh, Christopher A.; Al-Gazali, Lihadh; Mochida, Ganeshwaran H.
2017-03-23	Molecular cytogenetic characterisation of a novel de novo ring chromosome 6 involving a terminal 6p deletion and terminal 6q duplication in the different arms of the same chromosome	Pace, Nikolai Paul; Frideriki, Maggouta; Twigden, Melissa; Borg, Isabella
2014	The Negative Elongation Factor Complex – a poorly understood multi-faceted transcript-processing complex	Baron, Byron
2011	Novel interactions of the GABPα transcription factor complex	Baron, Byron
2010	Osteogenic bioactivity and oestrogen growth factor response induced by extracts from Ceratonia siliqua	Vella, Kevin
2016	Osteoporosis / Osteopoenia in Crohn's disease patients expressing the ATG16L1 gene variants	Azzopardi, Neville
2015	Pharmacogenetic implications in clopidogrel therapy : a pharmacist-Ied management approach	Wirth, Francesca
2012	Pharmacogenomic reactivation of foetal heamoglobin.	Grech, Laura
2019	Phenotypic and genetic markers of disease severity in a Maltese IBD cohort	Schembri, J.; Pace, Nikolai Paul; Piscopo, N.; Degenhardt, F.; Franke, A.; Ellul, P.
2000	A population study of FMR1 mutations in Malta	Said, Edith
2020	Rare variant burden analysis within enhancers identifies CAV1 as an ALS risk gene	Cooper-Knock, Johnathan; Zhang, Sai; Kenna, Kevin P.; Moll, Tobias; Franklin, John P.; Allen, Samantha; Ghahremani Nezhad, Helia; Iacoangeli, Alfredo; Yacovzada, Nancy Y.; Eitan, Chen; Hornstein, Eran; Elhaik, Eran; Celadova, Petra; Bose, Daniel; Farhan, Sali; Fishilevich, Simon; Lancet, Doron; Morrison, Karen E.; Shaw, Christopher E.; Al-Chalabi, Ammar; Veldink, Jan H.; Kirby, Janine; Snyder, Michael P.; Shaw, Pamela J.; Cauchi, Ruben J.; Project MinE ALS Sequencing Consortium
2023	Role of canonical WNT pathway genes in osteoporosis & fracture risk	Mallia, Sarah Ann (2023)
2018	The role of FLVCR1 isoforms on inter-erythrocytic distribution of human foetal haemoglobin	Grech, Laura; Scerri, Jeanesse; Mizzi, Clint; Galdies, Ruth; Scerri, Christian A.; Ijcken, Wilfred van; Özgür, Zeliha; Gillemans, Nynke; Borg, Joseph J.; Philipsen, Sjaak; Felice, Alex E.
2022	Role of the RUNX2 rs59983488 variant in bone mass determination and fracture risk in Malta	Sammut, Nigel (2022)
2008	Sequencing of genes in two Maltese families with severe osteoporosis	Cachia, Adela
2019	Two novel GJA1 variants in oculodentodigital dysplasia	Pace, Nikolai Paul; Benoit, Valerie; Agius, David; Grima, Maria Angela; Parascandalo, Raymond; Hilbert, Pascale; Borg, Isabella
2008	Xjenza madwarna 1 : programs 1-18	Bugeja, Christopher

Showing results 28 to 46 of 46 < previous