Neil V Morgan

ResearcherID Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2017-2023
Publications (10 Years): 20

Top Topics

Dna Methylation

High Throughput Sequencing

Top Venues

Journal of thrombosis and haemostasis : JTH

Scientific reports

This page only lists publications with an associated author ORCID identifier.

Publications

Claire C Homan, Michael W Drazer, Kai Yu, David Michael Lawrence, Jinghua Feng, Luis Alberto Arriola-Martinez, Matthew J Pozsgai, Kelsey E McNeely, Thuong Thi Ha, Parvathy Venugopal, Peer Arts, Sarah King-Smith, Jesse Jc Cheah, Mark Armstrong, Paul Wang, Csaba Bödör, Alan B Cantor, Mario Cazzola, Erin S Degelman, Courtney D D DiNardo, Nicolas Duployez, Rémi Favier, Stefan Fröhling, Ana Rio-Machin, Jeffery M Klco, Alwin Krämer, Mineo Kurokawa, Joanne Lee, Luca Malcovati, Neil V Morgan, Natsoulis Georges, Carolyn Owen, Keyur Pravinchandra Patel, Claude Preudhomme, Hana Raslova, Hugh Young Rienhoff, Tim Ripperger, Rachael R Schulte, Kiran Tawana, Elvira Velloso, Yan Benedict, Erika Mijin Kwon Kim, Raman Sood, Amy P Hsu, Steven M Holland, Kerry Phillips, Nicola Poplawski, Milena Babic, Andrew H Wei, Cecily Jane Forsyth, Helen Mar Fan, Ian Lewis, Julian P Cooney, Rachel Susman, Lucy C Fox, Piers Blombery, Deepak Singhal, Devendra K Hiwase, Belinda Phipson, Andreas W Schreiber, Christopher N Hahn, Hamish S Scott, Paul P Liu, Lucy A Godley, Anna L Brown
Somatic mutational landscape of hereditary hematopoietic malignancies caused by germ line RUNX1, GATA2, and DDX41 variants. Blood advances (2023)
Amanda Dalby, Diego Mezzano, José Rivera, Stephen P Watson, Neil V Morgan
Introduction of an ancient founder glycoprotein VI mutation into the Chilean population. Blood advances 6 (22) (2022)
Zoe Markham-Lee, Neil V Morgan, Jonas Emsley
Inherited ADAMTS13 mutations associated with Thrombotic Thrombocytopenic Purpura: a short review and update. Platelets 34 (1) (2022)
Hrushikesh Vyas, Ahmad Alcheikh, Gillian Lowe, William S Stevenson, Neil V Morgan, David J Rabbolini
Prevalence and natural history of variants in the ANKRD26 gene: a short review and update of reported cases. Platelets 33 (8) (2022)
José Maria Bastida, Stefano Malvestiti, Doris Boeckelmann, Verónica Palma-Barqueros, Mira Wolter, María Luisa Lozano, Hannah Glonnegger, Rocío Benito, Carlo Zaninetti, Felix Sobotta, Freimut H Schilling, Neil V Morgan, Kathleen Freson, José Rivera, Barbara Zieger
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 11 (20) (2022)
Karyn Megy, Kate Downes, Marie-Christine Morel-Kopp, José Maria Bastida, Shannon Brooks, Loredana Bury, Eva Leinoe, Keith Gomez, Neil V Morgan, Maha Othman, Willem H Ouwehand, Juliana Perez Botero, José Rivera, Harald Schulze, David-Alexandre Trégouët, Kathleen Freson
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 : JTH 19 (10) (2021)
Ibrahim Almazni, Pavel Chudakou, Alison Dawson-Meadows, Kate Downes, Kathleen Freson, Joanne Mason, Paula Page, Kim Reay, Bethan Myers, Neil V Morgan
A novel RUNX1 exon 3 - 7 deletion causing a familial platelet disorder. Platelets (2021)
Rachel J Stapley, Natalie S Poulter, Abdullah Obaid Khan, Christopher W Smith, Patricia Bignell, Carl Fratter, Will Lester, Gillian Lowe, Neil V Morgan, null null
Rare missense variants in Tropomyosin-4 (TPM4) are associated with platelet dysfunction, cytoskeletal defects, and excessive bleeding. Journal of thrombosis and haemostasis : JTH (2021)
Ibrahim Almazni, Rachel J Stapley, Abdullah O Khan, Neil V Morgan
A comprehensive bioinformatic analysis of 126 patients with an inherited platelet disorder to identify both sequence and copy number genetic variants. Human mutation 41 (11) (2020)
Abdullah Obaid Khan, Rachel J Stapley, Jeremy A Pike, Susanne N Wijesinghe, Jasmeet S Reyat, Ibrahim Almazni, Kellie R Machlus, Neil V Morgan, null null
Novel gene variants in patients with platelet-based bleeding using combined exome sequencing and RNAseq murine expression data. Journal of thrombosis and haemostasis : JTH 19 (1) (2020)
Emily Colley, Adam J Devall, Helen Marie Williams, Susan Hamilton, Paul Smith, Neil V Morgan, Siobhan Quenby, Arri Coomarasamy, Stephanie Allen
Cell-Free DNA in the Investigation of Miscarriage. Journal of clinical medicine 9 (11) (2020)
Jack Yule, Neil V Morgan, Natalie S Poulter
New insights into glycoprotein Ibα desialylation-mediated platelet clearance. Platelets 31 (5) (2020)
Jeremy M Pike, Victoria A Simms, Christopher W Smith, Neil V Morgan, Abdullah Obaid Khan, Natalie S Poulter, Iain B Styles, Steven G Thomas
An adaptable analysis workflow for characterization of platelet spreading and morphology. Platelets 32 (1) (2020)
Rachel J Stapley, Vera P Pisareva, Andrey V Pisarev, Neil V Morgan
SLFN14 gene mutations associated with bleeding. Platelets 31 (3) (2019)
Abdullah Obaid Khan, Carl W White, Jeremy A Pike, Jack Yule, Alexandre Slater, Stephen J Hill, Natalie S Poulter, Steven G Thomas, Neil V Morgan
Optimised insert design for improved single-molecule imaging and quantification through CRISPR-Cas9 mediated knock-in. Scientific reports 9 (1) (2019)
Jane Futterer, Amanda Dalby, Gillian C Lowe, Ben Johnson, Michael A Simpson, Jayashree Motwani, Mike Williams, Steve P Watson, Neil V Morgan, null null
Mutation in GNE is associated with severe congenital thrombocytopenia. Blood 132 (17) (2018)
Gillian C Lowe, Roksana Fickowska, Rashid Al Ghaithi, Annabel Maclachlan, Paul Harrison, Will Lester, Stephen P Watson, Bethan Myers, Justin Clark, Neil V Morgan
Investigation of the contribution of an underlying platelet defect in women with unexplained heavy menstrual bleeding. Platelets 30 (1) (2018)
Rashid Al Ghaithi, Jun Mori, Zoltan Nagy, Annabel Maclachlan, Lewis Hardy, Helen Philippou, Emma Hethershaw, Neil V Morgan, Yotis A Senis, Paul Harrison
Evaluation of the Total Thrombus-Formation System (T-TAS): application to human and mouse blood analysis. Platelets 30 (7) (2018)
Ben Johnson, Rachel Doak, David Allsup, Emma Astwood, Gillian Evans, Charlotte Grimley, Beki James, Bethan Myers, Simone Stokley, Jecko Thachil, Jonathan Wilde, Mike Williams, Mike Makris, Gillian C Lowe, Yvonne Wallis, Martina E Daly, Neil V Morgan, null null
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) (2018)
Abdullah O Khan, Victoria A Simms, Jeremy A Pike, Steven G Thomas, Neil V Morgan
CRISPR-Cas9 Mediated Labelling Allows for Single Molecule Imaging and Resolution. Scientific reports 7 (1) (2017)