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Martina E. Daly

University of Sheffield
Royal Hallamshire Hospital

82

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Gene of the issue: RUNX1 mutations and inherited bleeding

2017 Platelets
- Neil V. Morgan
- Martina E. Daly
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Citations (11)
Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defects

2016 Haematologica
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ISTH Advanced Training Course on platelet bleeding disorders: How should they be investigated?

2016 Platelets
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Transient inherited antithrombin deficiency: a real phenomenon?

2016 Thrombosis and Haemostasis
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Congenital macrothrombocytopenia is a heterogeneous disorder in India

2016 Haemophilia
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Identification and Characterization of Novel Variations in Platelet G-Protein Coupled Receptor (GPCR) Genes in Patients Historically Diagnosed with Type 1 von

2015
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GPCR gene variations identified in type 1 VWD patients and their predicted effects.

2015 PLOS ONE
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Use of next‐generation sequencing and candidate gene analysis to identify underlying defects in patients with inherited platelet function disorders

2015 Journal of Thrombosis and Haemostasis
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Diversity and impact of rare variants in genes encoding the platelet G protein-coupled receptors.

2015 Thrombosis and Haemostasis
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A novel mutation in the P2Y12 receptor and a function‐reducing polymorphism in protease‐activated receptor 1 in a patient with chronic bleeding

2014 Journal of Thrombosis and Haemostasis
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Citations (38)