Sian Drake

Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defects

S. Mundell, M. Simpson, S. Watson, 2016, Haematologica.

SLFN14 mutations underlie thrombocytopenia with excessive bleeding and platelet secretion defects.

M. Simpson, S. Watson, M. Lordkipanidzé, 2015, The Journal of clinical investigation.

Diversity and Impact of Rare Variants in Genes Encoding the Platelet G Protein-Coupled Receptors

S. Mundell, M. Simpson, S. Watson, 2015, Thrombosis and Haemostasis.

Use of next‐generation sequencing and candidate gene analysis to identify underlying defects in patients with inherited platelet function disorders

M. Simpson, M. Lordkipanidzé, P. Gissen, 2015, Journal of thrombosis and haemostasis : JTH.

Comparison of multiple electrode aggregometry with lumi‐aggregometry for the diagnosis of patients with mild bleeding disorders

N. Morgan, S. Watson, P. Harrison, 2017, Journal of thrombosis and haemostasis : JTH.