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Showing results 42 to 48 of 48 < previous

Issue Date	Title	Author(s)
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 42 to 48 of 48 < previous