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Issue Date	Title	Author(s)
2020	Towards an understanding of the genetic aspects of hypoplastic left heart syndrome (HLHS)	Al-Qahtani, Ahlam
2020	Molecular genetic studies of inherited cystic kidney disease in Oman	Al Alawi, Intisar Hamed
2020	Optimisation of protocols for ex vivo expansion of limbal stem cells and their enrichment	Bojic, Sanja
2019	The role of endoglin in endothelial and mesenchymal cells during development, maintenance and repair of the heart	Singh, Esha
2019	The role of MYO9A at the neuromuscular junction	O'Connor, Emily Ann
2019	The role of WT1 in nephron endowment and glomeruloscerosis (GS) / Chronic Kidney Disease (CKD) /	Bin Ahmad, Ahzah Hadi
2019	Investigating inherited renal disorders and identification of a novel cause of Joubert syndrome	Alkanderi, Sumaya
2019	Congenital myasthenic syndromes and the therapeutic modulation of the neuromuscular junction	McMacken, Grace Maria
2019	Quantitative magnetic resonance imaging in muscular dystrophies	Murphy, Alexander Peter
2019	Clinical significance and regulation of cohesin depletion in mammalian oocytes	Cooney, Dan
2019	Biomarkers of mismatch repair deficiency in colorectal cancer and cancer predisposition syndromes	Gallon, Richard John
2018	Characterisation of MYB and TRKB as candidate targets in CYLD cutaneous syndrome	Sinclair, Naomi Kathryn
2018	a Circulating cell free mitochondrial DNA copy number variation in neurodegenerative disease	Lowes, Hannah
2019	Characterisation of a zebrafish model of Wolfram Syndrome	Cairns, George Edward
2019	Studying arrythmogenic right ventricular cardiomyopathy : dysplasia using induced pluripotent stem cells	Lee, David Charles
2018	Genetic heterogeneity in collagen VI-related myopathy	Torabi Farsani, Golara
2018	Investigating the role of the extracellular matrix (ECM) on pluripotent stem cell differentiation towards retinal lineages	Felemban, Majed Abdulsamad A
2018	Can short sprints during moderate intensity exercise reduce the incidence of exercise mediated hypoglycaemia in individuals with type 1 diabetes?	Chetty, Tarini
2018	The disease mechanisms of skeletal dysplasia caused by two aggrecan mutations	Gibson, Beth Grace
2018	A systematic comparison of integrated genomic platforms and bioinformatics pipelines for next generation sequencing in patients with rare neuromuscular disease	Alrohaif, Hadil E. D. M.