Neil Morgan

Accepting PhD Students

PhD projects

Neil Morgan’s current research focuses on the molecular genetics of patients with platelet bleeding disorders and low platelet counts (thrombocytopaenia). The identification of novel gene defects would provide clues to genes and proteins involved in normal platelet physiology, and the ultimate aim is to extrapolate these findings to devising new treatments and treatment strategies to minimise risk of bleeding in selected cohorts of patients. Dr Morgan’s past research has primarily involved identification of novel genes for autosomal recessive inherited diseases and he has made many significant contributions in this field.

Research activity per year

86 Article
5 Review article
3 Letter
2 Abstract
More
- 1 Book
- 1 Chapter
- 1 Poster
- 1 Editorial
- 1 Preprint

1 - 50 out of 101 results

2025
Structural and functional insights into α-actinin isoforms and their implications in cardiovascular disease
Noureddine, M., Mikolajek, H., Morgan, N., Denning, C., Loughna, S., Gehmlich, K. & Mohammed, F., 7 Feb 2025, In: Journal of General Physiology. 157, 2, e202413684.
Research output: Contribution to journal › Article › peer-review

Open Access
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21 Downloads (Pure)
Venous Thrombosis Unchained: Pandora's Box of Non-Inflammatory Mechanisms
Smith, S. R. M., Morgan, N. & Brill, A., 13 Mar 2025, In: Blood Advances.
Research output: Contribution to journal › Article › peer-review
2024
Comprehensive functional characterisation of a novel ANO6 variant in a new patient with Scott Syndrome
Montague, S., Price, J., Pennycott, K., Pavey, N., Slater, E., Thirlwell, I., Kemble, S., Monteiro, C., Redmond-Motteram, L., Lawson, N., Reynolds, K., Fratter, C., Bignell, P., Groenheide, A., Huskens, D., Laat, B. D., Pike, J., Poulter, N., Thomas, S. & Lowe, G. & 3 others, Lancashire, J., Harrison, P. & Morgan, N., 15 Mar 2024, (E-pub ahead of print) In: Journal of Thrombosis and Haemostasis.
Research output: Contribution to journal › Article › peer-review

Open Access
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PITX2 deficiency leads to atrial mitochondrial dysfunction
Reyat, J., Sommerfeld, L., O'Reilly, M., Roth Cardoso, V., Thiemann, E., Khan, A., O'Shea, C., Harder, S., Müller, C., Barlow, J., Stapley, R., Chua, W. W. L., Kabir, N., Grech, O., Hummel, O., Hübner, N., Kaab, S., Mont, L., Hatem, S. N. & Winters, J. & 14 others, Zeemering, S., Morgan, N., Rayes, J., Gehmlich, K., Stoll, M., Brand, T., Schweizer , M., Piasecki, A., Schotten, U., Gkoutos, G., Lorenz, K., Cuello, F., Kirchhof, P. & Fabritz, L., 12 Aug 2024, (E-pub ahead of print) In: Cardiovascular Research. cvae169.
Research output: Contribution to journal › Article › peer-review

Open Access
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24 Downloads (Pure)
2023

Editorial: Case reports in cardiovascular genetics and systems medicine: 2022
Morgan, N. V., 11 Sept 2023, In: Frontiers in cardiovascular medicine. 10, 2 p., 1282147.
Research output: Contribution to journal › Editorial › peer-review

Open Access
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62 Downloads (Pure)
Efficient megakaryopoiesis and platelet production require phospholipid remodeling and PUFA uptake through CD36
Barrachina, M. N., Pernes, G., Becker, I. C., Allaeys, I., Hirsch, T. I., Groeneveld, D. J., Khan, A. O., Freire, D., Guo, K., Carminita, E., Morgan, P. K., Collins, T. J. C., Mellett, N. A., Wei, Z., Almazni, I., Italiano, J. E., Luyendyk, J., Meikle, P. J., Puder, M. & Morgan, N. V. & 3 others, Boilard, E., Murphy, A. J. & Machlus, K. R., 17 Jul 2023, In: Nature Cardiovascular Research. 2, 8, p. 746-763 18 p.
Research output: Contribution to journal › Article › peer-review

Open Access
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38 Downloads (Pure)
Evaluating the clinical validity of genes related to hemostasis and thrombosis using the ClinGen gene curation framework
Ross, J. E., Mohan, S., Zhang, J., Sullivan, M. J., Bury, L., Lee, K., Futchi, I., Frantz, A., McDougal, D., Perez Botero, J., Cattaneo, M., Cooper, N., Downes, K., Gresele, P., Keenan, C., Lee, A., Megy, K., Morange, P., Morgan, N. & Schulze, H. & 3 others, Zimowski, K., Freson, K. & P.Lambert, M., 26 Nov 2023, (E-pub ahead of print) In: Thrombosis and Haemostasis.
Research output: Contribution to journal › Article › peer-review

Open Access
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23 Downloads (Pure)
Somatic mutational landscape of hereditary hematopoietic malignancies caused by germline variants in RUNX1, GATA2, and DDX41
Homan, C. C., Drazer, M. W., Yu, K., Lawrence, D. M., Feng, J., Arriola-Martinez, L., Pozsgai, M. J., McNeely, K. E., Ha, T., Venugopal, P., Arts, P., King-Smith, S. L., Cheah, J., Armstrong, M., Wang, P., Bödör, C., Cantor, A. B., Cazzola, M., Degelman, E. & DiNardo, C. D. & 45 others, Duployez, N., Favier, R., Fröhling, S., Rio-Machin, A., Klco, J. M., Krämer, A., Kurokawa, M., Lee, J., Malcovati, L., Morgan, N. V., Natsoulis, G., Owen, C., Patel, K. P., Preudhomme, C., Raslova, H., Rienhoff, H., Ripperger, T., Schulte, R., Tawana, K., Velloso, E., Yan, B., Kim, E., Sood, R., Hsu, A. P., Holland, S. M., Phillips, K., Poplawski, N. K., Babic, M., Wei, A. H., Forsyth, C., Mar Fan, H., Lewis, I. D., Cooney, J., Susman, R., Fox, L. C., Blombery, P., Singhal, D., Hiwase, D., Phipson, B., Schreiber, A. W., Hahn, C. N., Scott, H. S., Liu, P., Godley, L. A. & Brown, A. L., 24 Oct 2023, In: Blood Advances. 7, 20, p. 6092-6107 16 p.
Research output: Contribution to journal › Article › peer-review

Open Access
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99 Downloads (Pure)
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
Bastida, J. M., Malvestiti, S., Boeckelmann, D., Palma-Barqueros, V., Wolter, M., Lozano, M. L., Glonnegger, H., Benito, R., Zaninetti, C., Sobotta, F., Schilling, F. H., Morgan, N. V., Freson, K., Rivera, J. & Zieger, B., 14 Oct 2022, In: Cells. 11, 20, 18 p., 3223.
Research output: Contribution to journal › Article › peer-review

Open Access
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97 Downloads (Pure)
Inherited ADAMTS13 mutations associated with thrombotic thrombocytopenic purpura: a short review and update
Markham-Lee, Z., Morgan, N. & Emsley, J., 25 Oct 2022, (E-pub ahead of print) In: Platelets.
Research output: Contribution to journal › Article › peer-review

Open Access
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94 Downloads (Pure)
Prevalence and natural history of variants in the ANKRD26 gene: a short review and update of reported cases
Vyas, H., Alcheikh, A., Lowe, G., Stevenson, W. S., Morgan, N. & Rabbolini, D. J., 17 Nov 2022, In: Platelets. 33, 8, p. 1107-1112 6 p.
Research output: Contribution to journal › Review article › peer-review

Open Access
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200 Downloads (Pure)
Sorting Nexin 24 is required for α-granule biogenesis and cargo delivery in megakaryocytes
Lacey, J., Webster, S. J., Heath, P., Hill, C. J., Nicholson-Goult, L., Wagner, B., Khan, A., Morgan, N., Makris, M. & Daly, M. E., 13 Jan 2022, In: Haematologica. 2022, 8, p. 1902-1913 279636.
Research output: Contribution to journal › Article › peer-review

Open Access
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61 Downloads (Pure)
2021
An adaptable analysis workflow for characterization of platelet spreading and morphology
Pike, J., Simms, V., Smith, C., Morgan, N., Khan, A., Poulter, N., Styles, I. & Thomas, S., 2 Jan 2021, In: Platelets. 32, 1, p. 54-58 5 p.
Research output: Contribution to journal › Article › peer-review

Open Access
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3 Citations (Scopus)

281 Downloads (Pure)
A novel RUNX1 exon 3 - 7 deletion causing a familial platelet disorder
Almazni, I. A. F., Chudakou, P., Dawson-Meadows, A., Downes, K., Freson, K., Mason, J., Page, P., Reay, K., Myers, B. & Morgan, N., 22 Feb 2021, (E-pub ahead of print) In: Platelets.
Research output: Contribution to journal › Article › peer-review

Open Access
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36 Downloads (Pure)
Evidence that autosomal recessive spastic cerebral palsy-1 (CPSQ1) is caused by a missense variant in HPDL
Morgan, N., Yngvadottir, B., O'Driscoll, M., Clark, G. R., Walsh, D., Martin, E., Tee, L., Reid, E., Titheradge, H. & Maher, E., 16 Jan 2021, In: Brain Communications. 3, 1, 10 p., fcab002.
Research output: Contribution to journal › Article › peer-review

Open Access
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158 Downloads (Pure)
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
Megy, K., Downes, K., Morel‐kopp, M., Bastida, J. M., Brooks, S., Bury, L., Leinoe, E., Gomez, K., Morgan, N. V., Othman, M., Ouwehand, W. H., Perez Botero, J., Rivera, J., Schulze, H., Trégouët, D. & Freson, K., 13 Jul 2021, In: Journal of Thrombosis and Haemostasis. 19, 10, p. 2612-2617
Research output: Contribution to journal › Article › peer-review

Open Access
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49 Downloads (Pure)
Heterozygous mutation SLFN14 K208N in mice mediates species-specific differences in platelet and erythroid lineage commitment: SLFN14 mediates lineage commitment in mice
Stapley, R., Smith, C., Haining, E., Bacon, A., Lax, S., Pisareva, V., Pisarev, A., Watson, S., Khan, A. & Morgan, N., 26 Jan 2021, In: Blood Advances. 5, 2, p. 377–390 14 p.
Research output: Contribution to journal › Article › peer-review

Open Access
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195 Downloads (Pure)
Novel gene variants in patients with platelet-based bleeding using combined exome sequencing and RNAseq murine expression data
UK GAPP Study Group, Jan 2021, In: Journal of Thrombosis and Haemostasis. 19, 1, p. 262-268 7 p.
Research output: Contribution to journal › Article › peer-review

Open Access
File
2 Citations (Scopus)

210 Downloads (Pure)
Rare missense variants in Tropomyosin-4 (TPM4) are associated with platelet dysfunction, cytoskeletal defects and excessive bleeding
The UK GAPP Study Group, Stapley, R., Poulter, N., Khan, A., Smith, C., Bignell, P., Fratter, C., Lester, W., Lowe, G. & Morgan, N., 10 Nov 2021, In: Journal of Thrombosis and Haemostasis. 8 p.
Research output: Contribution to journal › Article › peer-review

Open Access
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131 Downloads (Pure)
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
RUNX1 international data-sharing consortium, 8 Jul 2021, In: Haematologica. 106, 11, p. 3004-3007
Research output: Contribution to journal › Letter › peer-review

Open Access
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69 Downloads (Pure)
2020
A comprehensive bioinformatic analysis of 126 patients with an inherited platelet disorder to identify both sequence and copy number genetic variants
Almazni, I. A. F., Stapley, R., Khan, A. & Morgan, N., 28 Oct 2020, In: Human Mutation. 41, 11, p. 1848-1865
Research output: Contribution to journal › Article › peer-review

Open Access
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4 Citations (Scopus)

271 Downloads (Pure)
Flow studies on human GPVI-deficient blood under coagulating and noncoagulating conditions
Nagy, M., Perrella, G., Dalby, A., Becerra, F., Garcia Quintanilla, L., Pike, J., Morgan, N., Gardiner, E. E., Heemskerk, J. W. M., Azocar, L., Miquel, J. F., Mezzano, D. & Watson, S., 14 Jul 2020, In: Blood Advances. 4, 13, p. 2953–2961 9 p.
Research output: Contribution to journal › Article › peer-review

Open Access
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9 Citations (Scopus)

155 Downloads (Pure)
Germline TET2 loss of function causes childhood immunodeficiency and lymphoma
Stremenova Spegarova, J., Lawless, D., Mohamad, S. M. B., Engelhardt, K. R., Doody, G. M., 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. & 7 others, Przyborski, S., Windebank, K., Cant, A., Lako, M., Bacon, C., Savic, S. & Hambleton, S., 27 Aug 2020, In: Blood. 136, 9, p. 1055-1066 12 p.
Research output: Contribution to journal › Article › peer-review

Open Access
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11 Citations (Scopus)

330 Downloads (Pure)
High-throughput platelet spreading analysis: a tool for the diagnosis of platelet-based bleeding disorders
Khan, A., Maclachlan, A., Lowe, G., Nicolson, P., Al Ghaithi, R. H. R., Thomas, S., Watson, S., Pike, J. & Morgan, N., Mar 2020, In: Haematologica. 105, 3, p. e124-e128
Research output: Contribution to journal › Article › peer-review

Open Access
File

9 Citations (Scopus)

246 Downloads (Pure)
New insights into Glycoprotein Ibα desialylation-mediated platelet clearance
Yule, J., Morgan, N. & Poulter, N., 3 Jul 2020, In: Platelets. 31, 5, p. 621-623 3 p.
Research output: Contribution to journal › Article › peer-review

Open Access
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206 Downloads (Pure)
Post-translational polymodification of β1-tubulin regulates motor protein localisation in platelet production and function
Khan, A., Slater, A., Maclachlan, A., Nicolson, P., Pike, J., Reyat, J., Yule, J., Stapley, R., Rayes, J., Thomas, S. & Morgan, N., 17 Dec 2020, (E-pub ahead of print) In: Haematologica. 2020, 00, p. 1-43
Research output: Contribution to journal › Article › peer-review

Open Access
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1 Citation (Scopus)

309 Downloads (Pure)
2019
Inherited thrombocytopenia: update on genes and genetic variants which may be associated with bleeding
Almazni, I. A. F., Stapley, R. & Morgan, N., 19 Jun 2019, In: Frontiers in cardiovascular medicine. 6, 9 p., 80.
Research output: Contribution to journal › Review article › peer-review

Open Access
File
12 Citations (Scopus)

224 Downloads (Pure)
Optimised insert design for improved single-molecule imaging and quantification through CRISPR-Cas9 mediated knock-in
Khan, A., White, C. W., Pike, J., Yule, J., Slater, A., Hill, S. J., Poulter, N., Thomas, S. & Morgan, N., 2 Oct 2019, In: Scientific Reports. 9, 1, 14219.
Research output: Contribution to journal › Article › peer-review

Open Access
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10 Citations (Scopus)

191 Downloads (Pure)
Potential genetic causes of miscarriage in euploid pregnancies: a systematic review
Morgan, N., Colley, E., Smith, P., Allen, S., Hamilton, S. & Coomarasamy, A., Jul 2019, In: Human Reproduction Update. 25, 4, p. 452-472 dmz015.
Research output: Contribution to journal › Article › peer-review

Open Access
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18 Citations (Scopus)

613 Downloads (Pure)
SLFN14 gene mutations associated with bleeding
Stapley, R., Pisareva, V., Pisarev, A. & Morgan, N., 4 Aug 2019, (E-pub ahead of print) In: Platelets. p. 1-4 4 p.
Research output: Contribution to journal › Article › peer-review

Open Access
File

2 Citations (Scopus)

224 Downloads (Pure)
2018
A comprehensive targeted next-generation sequencing panel for genetic diagnosis of patients with suspected inherited thrombocytopenia
Morgan, N., Johnson, B., Doke, R., Allsup, D., Astwood, E., Evans, G., Grimley, C., James, B., Myers, B., Stokley, S., Thachil, J., Wilde, J., Williams, M., Makris, M., Lowe, G., Wallis, Y. & Daly, M., 10 Oct 2018, In: Research and Practice in Thrombosis and Haemostasis. 2, 4, p. 640–652 13 p.
Research output: Contribution to journal › Article › peer-review

Open Access
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300 Downloads (Pure)
Evaluation of the Total Thrombus-Formation System (T-TAS): application to human and mouse blood analysis: evaluation of T-TAS in assessing clot formation
Al Ghaithi, R. H. R., Mori, J., Nagy, Z., Maclachlan, A., Hardy, L., Philippou, H., Hethershaw, E., Morgan, N., Senis, Y. & Harrison, P., 26 Oct 2018, (E-pub ahead of print) In: Platelets. 22 p.
Research output: Contribution to journal › Article › peer-review

Open Access
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6 Citations (Scopus)

150 Downloads (Pure)
Introducing high-throughput sequencing into mainstream genetic diagnosis practice in inherited platelet disorders
Bastida, J. M., Lozano, M. L., Benito, R., Janusz, K., Palma-Barqueros, V., Del Rey, M., Hernández-Sánchez, J. M., Riesco, S., Bermejo, N., González-García, H., Rodriguez-Alén, A., Aguilar, C., Sevivas, T., López-Fernández, M. F., Marneth, A. E., van der Reijden, B. A., Morgan, N. V., Watson, S. P., Vicente, V. & Hernández-Rivas, J. M. & 2 others, Rivera, J. & González-Porras, J. R., Jan 2018, In: Haematologica. 103, 1, p. 148-162 15 p.
Research output: Contribution to journal › Article › peer-review

Open Access
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53 Citations (Scopus)

215 Downloads (Pure)
Investigation of the contribution of an underlying platelet defect in women with unexplained heavy menstrual bleeding
Lowe, G., Fickowska, R., Al Ghaithi, R. H. R., Maclachlan, A., Harrison, P., Lester, W., Watson, S., Myers, B., Clark, T. J. & Morgan, N., 6 Dec 2018, (E-pub ahead of print) In: Platelets.
Research output: Contribution to journal › Article › peer-review

Open Access
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3 Citations (Scopus)

246 Downloads (Pure)
Mutation in GNE is associated with a Severe Form of Congenital Thrombocytopenia
Futterer, J., Dalby, A., Lowe, G., Johnson, B., Simpson, M., Motwani, J., Williams, M., Watson, S. & Morgan, N., 25 Jun 2018, (E-pub ahead of print) In: Blood.
Research output: Contribution to journal › Letter › peer-review

Open Access
File

18 Citations (Scopus)

189 Downloads (Pure)
Optimised CRISPR-Cas9 mediated single molecule imaging for accurate quantification through endogenous expression
Khan, A. O., White, C. W., Pike, J. A., Yule, J., Slater, A., Hill, S. J., Poulter, N. S., Thomas, S. G. & Morgan, N. V., 30 Nov 2018.
Research output: Working paper/Preprint › Preprint
Role of the novel endoribonuclease SLFN14 and its disease causing mutations in ribosomal degradation
Morgan, N., Fletcher, S., Khan, A., Pisarev, A., Pisareva, V. & Tcherepanov, A., Jul 2018, In: RNA. 24, 7, p. 939-949
Research output: Contribution to journal › Article › peer-review

Open Access
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5 Citations (Scopus)

192 Downloads (Pure)
2017
A novel ESR2 frameshift mutation predisposes to medullary thyroid carcinoma and causes inappropriate RET expression
Read, M., Smith, J., Hoffman, J., Smith, V., Morgan, N., Campbell, C., Wake, N., Watkinson, J., Wallis, Y., Maher, E., McCabe, C. & Woodward, E., 13 Feb 2017, In: Thyroid Research. 10(Suppl 1), 2, p. 5 1 p., P4.
Research output: Contribution to journal › Abstract › peer-review

Open Access
File
264 Downloads (Pure)
Comparison of multiple electrode aggregometry with lumi-aggregometry for the diagnosis of patients with mild bleeding disorders: Comparison of MEA and LTA
Al Ghaithi, R. H. R., Drake, S., Watson, S., Morgan, N. & Harrison, P., Oct 2017, In: Journal of thrombosis and haemostasis : JTH. 15, 10, p. 2045-2052 8 p.
Research output: Contribution to journal › Article › peer-review

Open Access
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19 Citations (Scopus)

248 Downloads (Pure)
CRISPR-Cas9 mediated labelling allows for single molecule imaging and resolution
Thomas, S., Morgan, N., Pike, J., Simms, V. & Khan, A., 16 Aug 2017, (E-pub ahead of print) In: Scientific Reports. 7, 8450.
Research output: Contribution to journal › Article › peer-review

Open Access
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22 Citations (Scopus)

274 Downloads (Pure)
Gene of the issue – RUNX1 mutations and inherited bleeding
Morgan, N. & Daly, M. E., 2017, In: Platelets. 28, 2, p. 208-210
Research output: Contribution to journal › Review article › peer-review

Open Access
File

7 Citations (Scopus)

223 Downloads (Pure)
Schlafen 14 (SLFN14) is a novel antiviral factor involved in the control of viral replication
Seong, R.-K., Seo, S.-W., Kim, J.-A., Fletcher, S., Morgan, N., Kumar, M., Choi, Y.-K. & Shin, O. S., 11 Jul 2017, (E-pub ahead of print) In: Immunobiology.
Research output: Contribution to journal › Article › peer-review

Open Access
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10 Citations (Scopus)

229 Downloads (Pure)
Whole exome sequencing identifies a mutation in thrombomodulin as the genetic cause of a suspected platelet disorder in a family with normal platelet function
Maclachlan, A., Watson, S., Morgan, N., Dolan, G. & Grimley, C., 2017, In: Platelets. 28, 6, p. 611-613
Research output: Contribution to journal › Article › peer-review

Open Access
File
7 Citations (Scopus)

168 Downloads (Pure)
2016
A novel ESR2 frameshift mutation predisposes to medullary thyroid carcinoma and causes inappropriate RET expression
Read, M., Smith, J., Smith, V., Morgan, N., Wake, N., Watkinson, J., Wallis, Y., Maher, E., McCabe, C. & Woodward, E., 1 Jul 2016, In: European Journal of Cancer. 61, Suppl 1, p. S20 1 p., 141.
Research output: Contribution to journal › Abstract › peer-review
11 Citations (Scopus)
A novel ESR2 frameshift mutation predisposes to medullary thyroid carcinoma and causes inappropriate RET expression
Read, M., Smith, J., Hoffman, J., Smith, V., Morgan, N., Campbell, C., Wake, N., Watkinson, J., Wallis, Y., Maher, E., McCabe, C. & Woodward, E., 13 May 2016.
Research output: Contribution to conference (unpublished) › Poster › peer-review
Defective Leukocyte Adhesion and Chemotaxis Contributes to Combined Immunodeficiency in Humans with Autosomal Recessive MST1 Deficiency
Dang, T. S., Willet, J. D., Griffin, H. R., Morgan, N. V., O'Boyle, G., Arkwright, P. D., Hughes, S. M., Abinun, M., Tee, L. J., Barge, D., Engelhardt, K. R., Jackson, M., Cant, A. J., Maher, E. R., Koref, M. S., Reynard, L. N., Ali, S. & Hambleton, S., Feb 2016, In: Journal of Clinical Immunology. 36, 2, p. 117-122
Research output: Contribution to journal › Article › peer-review

Open Access
36 Citations (Scopus)
Germline ESR2mutation predisposes to medullary thyroid carcinoma and causes up-regulation of RET expression
Smith, J., Read, M., Hoffman, J., Brown, R., Bradshaw, B., Campbell, C., Cole, T., Dieguez Navas, J., Eatock, F., Gundara, J., Lian, E., McMullan, D., MacDonald, F., Morgan, N., Mulligan, L., Morrison, P. J., Robledo, M., Simpson, M., Smith, V. & Stewart, S. & 10 others, Trembath, R., Sidhu, S., Togneri, F., Vialard, L., Wake, N., Wallis, Y., Watkinson, J., Maher, E., McCabe, C. & Woodward, E., 1 May 2016, In: Human Molecular Genetics. 25, 9, p. 1836-1845
Research output: Contribution to journal › Article › peer-review

Open Access
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18 Citations (Scopus)

213 Downloads (Pure)
Inherited Platelet Disorders - Insight from Platelet Genomics using Next Generation Sequencing
Maclachlan, A., Watson, S. & Morgan, N., 27 Jun 2016, (E-pub ahead of print) In: Platelets.
Research output: Contribution to journal › Review article › peer-review

Open Access
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19 Citations (Scopus)

254 Downloads (Pure)
Inherited thrombocytopenia: Novel insights into megakaryocyte maturation, proplatelet formation and platelet lifespan
Johnson, B., Fletcher, S. & Morgan, N., 2016, In: Platelets. 27, 6, p. 519-525
Research output: Contribution to journal › Review article › peer-review

Open Access
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23 Citations (Scopus)

202 Downloads (Pure)
ISTH Advanced Training Course on platelet bleeding disorders: How should they be investigated?St. Anne's College, Oxford, 6-9(th) September 2016
Watson, S. P., Daly, M. E., Harrison, P., Lowe, G. C., Paterson, A., Rivera, J., Warner, T. D. & Morgan, N. V., 2016, In: Platelets. 27, 8, p. 719-721 3 p.
Research output: Contribution to journal › Article › peer-review

Neil Morgan

Research output

Search results