Items where authors include "Daly, M.E."

Article

Lacey, J., Webster, S.J., Heath, P.R. et al. (7 more authors) (2022) Sorting Nexin 24 is required for α-granule biogenesis and cargo delivery in megakaryocytes. Haematologica, 107 (8). pp. 1902-1913. ISSN 0390-6078

Johnson, B., Doak, R., Allsup, D. et al. (15 more authors) (2018) A comprehensive targeted next-generation sequencing panel for genetic diagnosis of patients with suspected inherited thrombocytopenia. Research and Practice in Thrombosis and Haemostasis, 2 (4). pp. 640-652. ISSN 2475-0379

Morgan, N.V. and Daly, M.E. orcid.org/0000-0002-4597-8921 (2017) Gene of the issue: RUNX1 mutations and inherited bleeding. Platelets, 28 (2). pp. 208-210. ISSN 0953-7104

Daly, M.E. orcid.org/0000-0002-4597-8921, Cooper, P.C., Hickey, K.P. et al. (2 more authors) (2017) Transient inherited antithrombin deficiency: a real phenomenon? Thrombosis and Haemostasis, 117 (03). pp. 642-643. ISSN 0340-6245

Daly, M.E. orcid.org/0000-0002-4597-8921 (2016) Transcription factor defects causing platelet disorders. Blood Reviews. ISSN 0268-960X

Ali, S., Shetty, S., Ghosh, K. et al. (5 more authors) (2016) Congenital macrothrombocytopenia is a heterogeneous disorder in India. Haemophilia, 22 (4). pp. 570-582. ISSN 1351-8216

Johnson, B., Lowe, G.C., Futterer, J. et al. (31 more authors) (2016) Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defects. Haematologica. ISSN 0390-6078

Jones, M.L., Norman, J.E., Morgan, N.V. et al. (9 more authors) (2016) Diversity and impact of rare variants in genes encoding the platelet G protein-coupled receptors. THROMBOSIS AND HAEMOSTASIS, 113 (4). pp. 826-837. ISSN 0340-6245

Stockley, J., Nisar, S.P., Leo, V.C. et al. (9 more authors) (2015) Identification and Characterization of Novel Variations in Platelet G-Protein Coupled Receptor (GPCR) Genes in Patients Historically Diagnosed with Type 1 von Willebrand Disease. PLoS ONE, 10 (12). e0143913. ISSN 1932-6203

Fletcher, S.J., Johnson, B., Lowe, G.C. et al. (12 more authors) (2015) SLFN14 mutations underlie thrombocytopenia with excessive bleeding and platelet secretion defects. Journal of Clinical Investigation, 125 (9). 3600 - 3605. ISSN 0021-9738

Leo, V.C., Morgan, N.V., Bem, D. et al. (9 more authors) (2015) Use of next-generation sequencing and candidate gene analysis to identify underlying defects in patients with inherited platelet function disorders. Journal of Thrombosis and Haemostasis, 13 (4). pp. 643-650. ISSN 1538-7933