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Neil V. Morgan
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Journal Articles

Somatic Mutational Landscape of Hereditary Hematopoietic Malignancies Associated with Germline Variants in RUNX1 , GATA2 and DDX41

Free
Anna L. Brown, Claire Homan, Michael W. Drazer, Kai Yu, David Lawrence, Jinghua Feng, Luis Arriola-Martinez, Matthew Pozsgai, Kelsey McNeely, Thuong Ha, Parvathy Venugopal, Peer Arts, Sarah King-Smith, Jesse JC Cheah, Mark Armstrong, Csaba Bödör, Paul Wang, Alan B. Cantor, Mario Cazzola, Erin Degelman, Courtney D. DiNardo, Nicolas Duployez, Remi Favier, Stefan Fröhling, Ana Rio-Machin, Jeffery M. Klco, Alwin Krämer, Mineo Kurokawa, Joanne Lee, Luca Malcovati, Neil V Morgan, Georges Natsoulis, Carolyn Owen, Keyur P. Patel, Claude Preudhomme, Hana Raslova, Hugh Young Rienhoff, Jr., Tim Ripperger, Rachael Schulte, Kiran Tawana, Elvira Deolinda Rodrigues Pereira Velloso, Benedict Yan, Raman Sood, Amy Hsu, Steven M. Holland, Kerry Phillips, Nicola Poplawski, Milena Babic, Erika M Kwon Kim, Andrew H. Wei, Cecily Forsyth, Helen Mar Fan, Ian D Lewis, Julian Cooney, Rachel Susman, Lucy C Fox, Piers Blombery, Deepak Singhal, Devendra Hiwase, Andreas W Schreiber, Christopher N Hahn, Hamish S Scott, Paul P. Liu, Lucy A. Godley
Journal: Blood
Blood (2022) 140 (Supplement 1): 4030–4033.
https://doi.org/10.1182/blood-2022-167600
Published: 2022
Journal Articles

Comprehensive Description of Monoallelic GP1BA Variants Associated with Thrombocytopenia

Free
Rachel C Peck, BSc,MRCP, Sarah Westbury, MBBChir, MRCP, Lucy Fitzgibbon, Neil V Morgan, Jose Rivera, PhD, Walter H. Kahr, MDPhDFRCPC, Nihr BioResource, Karyn Megy, Kate Downes, PhD, Daniel Greene, Ernest Turro, PhD, Andrew David Mumford
Journal: Blood
Blood (2020) 136 (Supplement 1): 34–35.
https://doi.org/10.1182/blood-2020-133987
Published: 2020
Journal Articles

Germline TET2 loss of function causes childhood immunodeficiency and lymphoma

Free
Jarmila Stremenova Spegarova, Dylan Lawless, Siti Mardhiana Binti Mohamad, Karin R. Engelhardt, Gina Doody, Jennifer Shrimpton, Anne Rensing-Ehl, Stephan Ehl, Frederic Rieux-Laucat, Catherine Cargo, Helen Griffin, Aneta Mikulasova, Meghan Acres, Neil V. Morgan, James A. Poulter, Eamonn G. Sheridan, Philip Chetcuti, Sean O'Riordan, Rashida Anwar, Clive R. Carter, Stefan Przyborski, Kevin Windebank, Andrew J. Cant, Majlinda Lako, Chris M. Bacon, Sinisa Savic, Sophie Hambleton
Journal: Blood
Blood (2020) 136 (9): 1055–1066.
https://doi.org/10.1182/blood.2020005844
Published: 2020
Includes: Supplemental data
Journal Articles

Mutation in GNE is associated with severe congenital thrombocytopenia

Free
Clinical Trials & Observations
Jane Futterer, Amanda Dalby, Gillian C. Lowe, Ben Johnson, Michael A. Simpson, Jayashree Motwani, Mike Williams, Steve P. Watson, Neil V. Morgan
Journal: Blood
Blood (2018) 132 (17): 1855–1858.
https://doi.org/10.1182/blood-2018-04-847798
Published: 2018
Includes: Supplemental data
Journal Articles

Characterization of multiple platelet activation pathways in patients with bleeding as a high-throughput screening option: use of 96-well Optimul assay

Free
e-blood
Marie Lordkipanidzé, Gillian C. Lowe, Nicholas S. Kirkby, Melissa V. Chan, Martina H. Lundberg, Neil V. Morgan, Danai Bem, Shaista P. Nisar, Vincenzo C. Leo, Matthew L. Jones, Stuart J. Mundell, Martina E. Daly, Andrew D. Mumford, Timothy D. Warner, Steve P. Watson
Journal: Blood
Blood (2014) 123 (8): e11–e22.
https://doi.org/10.1182/blood-2013-08-520387
Published: 2014
Includes: Supplemental data
Journal Articles

Enrichment of FLI1 and RUNX1 mutations in families with excessive bleeding and platelet dense granule secretion defects

Free
Brief Report
Jacqueline Stockley, Neil V. Morgan, Danai Bem, Gillian C. Lowe, Marie Lordkipanidzé, Ban Dawood, Michael A. Simpson, Kirsty Macfarlane, Kevin Horner, Vincenzo C. Leo, Katherine Talks, Jayashree Motwani, Jonathan T. Wilde, Peter W. Collins, Michael Makris, Steve P. Watson, Martina E. Daly
Journal: Blood
Blood (2013) 122 (25): 4090–4093.
https://doi.org/10.1182/blood-2013-06-506873
Published: 2013
Includes: Supplemental data
Journal Articles

Functional Variations In Genes Encoding Platelet G-Protein Coupled Receptors In Unselected and Platelet Function Disorder Populations

Free
Jane E Norman, Matthew L Jones, Neil V Morgan, Jacqui Stockley, Martina E Daly, Stuart J Mundell, Steve P Watson, Andrew D Mumford, UK GAPP study group
Journal: Blood
Blood (2013) 122 (21): 3511.
https://doi.org/10.1182/blood.V122.21.3511.3511
Published: 2013
Journal Articles

A common Fanconi anemia mutation in black populations of sub-Saharan Africa

Free
Clinical Trials & Observations Brief Report
Neil V. Morgan, Fahmida Essop, Ilja Demuth, Thomy de Ravel, Stander Jansen, Marc Tischkowitz, Cathryn M. Lewis, Linda Wainwright, Janet Poole, Hans Joenje, Martin Digweed, Amanda Krause, Christopher G. Mathew
Journal: Blood
Blood (2005) 105 (9): 3542–3544.
https://doi.org/10.1182/blood-2004-10-3968
Published: 2005
Journal Articles

Paraneoplastic erythrocytosis associated with an inactivating point mutation of the von Hippel-Lindau gene in a renal cell carcinoma

Free
Michael S. Wiesener, Melchior Seyfarth, Christina Warnecke, Jan Steffen Jürgensen, Christian Rosenberger, Neil V. Morgan, Eamonn R. Maher, Ulrich Frei, Kai-Uwe Eckardt
Journal: Blood
Blood (2002) 99 (10): 3562–3565.
https://doi.org/10.1182/blood.V99.10.3562
Published: 2002