Recent publications
Article
Bastida, JM, Malvestiti, S, Boeckelmann, D, Palma-Barqueros, V, Wolter, M, Lozano, ML, Glonnegger, H, Benito, R, Zaninetti, C, Sobotta, F, Schilling, FH, Morgan, NV, Freson, K, Rivera, J & Zieger, B 2022, 'A novel GATA1 variant in the C-terminal zinc finger compared with the platelet phenotype of patients with a likely pathogenic variant in the N-terminal zinc finger', Cells, vol. 11, no. 20, 3223. https://doi.org/10.3390/cells11203223
Markham-Lee, Z, Morgan, N & Emsley, J 2022, 'Inherited ADAMTS13 mutations associated with thrombotic thrombocytopenic purpura: a short review and update', Platelets. https://doi.org/10.1080/09537104.2022.2138306
Vyas, H, Alcheikh, A, Lowe, G, Stevenson, WS, Morgan, N & Rabbolini, DJ 2022, 'Prevalence and natural history of variants in the ANKRD26 gene: a short review and update of reported cases', Platelets, vol. 33, no. 8, pp. 1-6. https://doi.org/10.1080/09537104.2022.2071853
Lacey, J, Webster, SJ, Heath, P, Hill, CJ, Nicholson-Goult, L, Wagner, B, Khan, A, Morgan, N, Makris, M & Daly, ME 2022, 'Sorting Nexin 24 is required for α-granule biogenesis and cargo delivery in megakaryocytes', Haematologica, vol. 2022, no. 8, 279636, pp. 1902-1913. https://doi.org/10.3324/haematol.2021.279636
Almazni, IAF, Chudakou, P, Dawson-Meadows, A, Downes, K, Freson, K, Mason, J, Page, P, Reay, K, Myers, B & Morgan, N 2021, 'A novel RUNX1 exon 3 - 7 deletion causing a familial platelet disorder', Platelets. https://doi.org/10.1080/09537104.2021.1887470
Pike, J, Simms, V, Smith, C, Morgan, N, Khan, A, Poulter, N, Styles, I & Thomas, S 2021, 'An adaptable analysis workflow for characterization of platelet spreading and morphology', Platelets, vol. 32, no. 1, pp. 54-58. https://doi.org/10.1080/09537104.2020.1748588
Morgan, N, Yngvadottir, B, O'Driscoll, M, Clark, GR, Walsh, D, Martin, E, Tee, L, Reid, E, Titheradge, H & Maher, E 2021, 'Evidence that autosomal recessive spastic cerebral palsy-1 (CPSQ1) is caused by a missense variant in HPDL', Brain Communications, vol. 3, no. 1, fcab002. https://doi.org/10.1093/braincomms/fcab002
Megy, K, Downes, K, Morel‐kopp, M, Bastida, JM, Brooks, S, Bury, L, Leinoe, E, Gomez, K, Morgan, NV, Othman, M, Ouwehand, WH, Perez Botero, J, Rivera, J, Schulze, H, Trégouët, D & Freson, K 2021, 'GoldVariants, a resource for sharing rare genetic variants detected in bleeding, thrombotic and platelet disorders: communication from the ISTH SSC Subcommittee on Genomics in Thrombosis and Hemostasis', Journal of Thrombosis and Haemostasis, vol. 19, no. 10, pp. 2612-2617. https://doi.org/10.1111/jth.15459
Stapley, R, Smith, C, Haining, E, Bacon, A, Lax, S, Pisareva, V, Pisarev, A, Watson, S, Khan, A & Morgan, N 2021, 'Heterozygous mutation SLFN14 K208N in mice mediates species-specific differences in platelet and erythroid lineage commitment: SLFN14 mediates lineage commitment in mice', Blood Advances, vol. 5, no. 2, pp. 377–390. https://doi.org/10.1182/bloodadvances.2020002404
UK GAPP Study Group 2021, 'Novel gene variants in patients with platelet-based bleeding using combined exome sequencing and RNAseq murine expression data', Journal of Thrombosis and Haemostasis, vol. 19, no. 1, pp. 262-268. https://doi.org/10.1111/jth.15119
The UK GAPP Study Group, Stapley, R, Poulter, N, Khan, A, Smith, C, Bignell, P, Fratter, C, Lester, W, Lowe, G & Morgan, N 2021, 'Rare missense variants in Tropomyosin-4 (TPM4) are associated with platelet dysfunction, cytoskeletal defects and excessive bleeding', Journal of Thrombosis and Haemostasis. https://doi.org/10.1111/jth.15584
Almazni, IAF, Stapley, R, Khan, A & Morgan, N 2020, 'A comprehensive bioinformatic analysis of 126 patients with an inherited platelet disorder to identify both sequence and copy number genetic variants', Human Mutation, vol. 41, no. 11, pp. 1848-1865. https://doi.org/10.1002/humu.24114
Nagy, M, Perrella, G, Dalby, A, Becerra, F, Garcia Quintanilla, L, Pike, J, Morgan, N, Gardiner, EE, Heemskerk, JWM, Azocar, L, Miquel, JF, Mezzano, D & Watson, S 2020, 'Flow studies on human GPVI-deficient blood under coagulating and noncoagulating conditions', Blood Advances, vol. 4, no. 13, pp. 2953–2961. https://doi.org/10.1182/bloodadvances.2020001761
Stremenova Spegarova, J, Lawless, D, Mohamad, SMB, Engelhardt, KR, Doody, GM, Shrimpton, J, Rensing-Ehl, A, Ehl, S, Rieux-Laucat, F, Cargo, C, Griffin, H, Mikulasova, A, Acres, M, Morgan, N, Poulter, J, Sheridan, E, Chetcuti, P, O'Riordan, S, Anwar, R, Carter, C, Przyborski, S, Windebank, K, Cant, A, Lako, M, Bacon, C, Savic, S & Hambleton, S 2020, 'Germline TET2 loss of function causes childhood immunodeficiency and lymphoma', Blood, vol. 136, no. 9, pp. 1055-1066. <https://doi.org/10.1182/blood.2020005844>
Letter
RUNX1 international data-sharing consortium 2021, 'The RUNX1 Database (RUNX1db): establishment of an expert curated RUNX1 registry and genomics database as a public resource for familial platelet disorder with myeloid malignancy', Haematologica, vol. 106, no. 11, pp. 3004-3007. https://doi.org/10.3324/haematol.2021.278762
View all publications in research portal