Browsing by Subject Genes

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 36 to 45 of 45 < previous 
Issue DateTitleAuthor(s)
2015Pharmacogenetic implications in clopidogrel therapy : a pharmacist-Ied management approachWirth, Francesca
2012Pharmacogenomic reactivation of foetal heamoglobin.Grech, Laura
2019Phenotypic and genetic markers of disease severity in a Maltese IBD cohortSchembri, J.; Pace, Nikolai Paul; Piscopo, N.; Degenhardt, F.; Franke, A.; Ellul, P.
2000A population study of FMR1 mutations in MaltaSaid, Edith
2020Rare variant burden analysis within enhancers identifies CAV1 as an ALS risk geneCooper-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
2018The role of FLVCR1 isoforms on inter-erythrocytic distribution of human foetal haemoglobinGrech, 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.
2022Role of the RUNX2 rs59983488 variant in bone mass determination and fracture risk in MaltaSammut, Nigel (2022)
2008Sequencing of genes in two Maltese families with severe osteoporosisCachia, Adela
2019Two novel GJA1 variants in oculodentodigital dysplasiaPace, Nikolai Paul; Benoit, Valerie; Agius, David; Grima, Maria Angela; Parascandalo, Raymond; Hilbert, Pascale; Borg, Isabella
2008Xjenza madwarna 1 : programs 1-18Bugeja, Christopher