Author

Nicholas Gleadall

Observed names: Gleadall, Nicholas, Gleadall, Nicholas S, Gleadall, Nicholas S., Gleadall, Nick, N. Gleadall, Nicholas S Gleadall, Nicholas S. Gleadall, Nick Gleadall

Institutions: National Health Service, NHS Blood and Transplant, University of Cambridge

Observed institutions: National Health Service, NHS Blood and Transplant, Queen Mary University of London, University of Basel, Barts Health NHS Trust, University of Cambridge, Rosie Hospital, St George’s University Hospitals NHS Foundation Trust, Royal London Hospital, Cambridge University Hospitals NHS Foundation Trust, University Hospital of Basel, Public Health England, National Institute for Health and Care Research, ETH Zurich, Addenbrooke's Hospital, NIHR BioResource, University College London, Newcastle University

ORCID: 0000-0002-1132-1059

Observed ORCID: 0000-0002-1132-1059

OpenAlex ID: A5028954792

SARS-CoV-2 B.1.617.2 Delta variant replication and immune evasion

2021 · Petra Mlcochova, Steven A. Kemp, et al. · Nature · 1,331

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Altered TMPRSS2 usage by SARS-CoV-2 Omicron impacts infectivity and fusogenicity

2022 · Bo Meng, Adam Abdullahi, et al. · Nature · 1,142

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SARS-CoV-2 evolution during treatment of chronic infection

2021 · Steven A. Kemp, Dami A. Collier, et al. · Nature · 1,093

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2021 · Dami A. Collier, Isabella A. T. M. Ferreira, et al. · Nature · 746

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Whole-genome sequencing of patients with rare diseases in a national health system

2020 · Ernest Turro, William J. Astle, et al. · Nature · 567

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Whole-genome sequencing of a sporadic primary immunodeficiency cohort

2020 · James E. D. Thaventhiran, Hana Lango Allen, et al. · Nature · 240

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Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders

2019 · Kate Downes, Karyn Megy, et al. · Blood · 222

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Complex structural variants in Mendelian disorders: identification and breakpoint resolution using short- and long-read genome sequencing

2018 · Alba Sanchis-Juan, Jonathan Stephens, et al. · Genome Medicine · 173

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Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations

2020 · Tiziana Lorenzini, Manfred Fliegauf, et al. · Journal of Allergy and Clinical Immunology · 140

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Nuclear-mitochondrial DNA segments resemble paternally inherited mitochondrial DNA in humans

2020 · Wei Wei, Alistair T. Pagnamenta, et al. · Nature Communications · 123

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Recent methodological advances in federated learning for healthcare

2024 · Fan Zhang, Daniel Kreuter, et al. · Patterns · 122

Automated typing of red blood cell and platelet antigens: a whole-genome sequencing study

2018 · William J Lane, Connie M Westhoff, et al. · The Lancet Haematology · 92

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Brain injury in COVID-19 is associated with dysregulated innate and adaptive immune responses

2022 · Edward J Needham, Alexander L Ren, et al. · Brain · 90

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Iron dysregulation and inflammatory stress erythropoiesis associates with long-term outcome of COVID-19

2024 · Aimee L. Hanson, Matthew P. Mulè, et al. · Nature Immunology · 82

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Identification of LukPQ, a novel, equid-adapted leukocidin of Staphylococcus aureus

2017 · Gerrit Koop, Manouk Vrieling, et al. · Scientific Reports · 70

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Genomic identification of cryptic susceptibility to penicillins and β-lactamase inhibitors in methicillin-resistant Staphylococcus aureus

2019 · Ewan M. Harrison, Xiaoliang Ba, et al. · Nature Microbiology · 69

Development and validation of a universal blood donor genotyping platform: a multinational prospective study

2020 · Nicholas S. Gleadall, Barbera Veldhuisen, et al. · Blood Advances · 64

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SARS-CoV-2 spike N-terminal domain modulates TMPRSS2-dependent viral entry and fusogenicity

2022 · Bo Meng, Rawlings Datir, et al. · Cell Reports · 56

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Bayesian Inference Associates Rare KDR Variants With Specific Phenotypes in Pulmonary Arterial Hypertension

2020 · Emilia M. Swietlik, Daniel Greene, et al. · Circulation Genomic and Precision Medicine · 49

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Old Drugs To Treat Resistant Bugs: Methicillin-Resistant Staphylococcus aureus Isolates with mecC Are Susceptible to a Combination of Penicillin and Clavulanic Acid

2015 · Xiaoliang Ba, Ewan M. Harrison, et al. · Antimicrobial Agents and Chemotherapy · 42

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Next‐generation sequencing for the diagnosis ofMYH9‐RD: Predicting pathogenic variants

2019 · Loredana Bury, Karyn Megy, et al. · Human Mutation · 41

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Germline mutations in the transcription factor IKZF5 cause thrombocytopenia

2019 · Claire Lentaigne, Daniel Greene, et al. · Blood · 39

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International Society of Blood Transfusion Working Party on Red Cell Immunogenetics and Blood Group Terminology Report of Basel and three virtual business meetings: Update on blood group systems

2022 · Christoph Gassner, Lilian Castilho, et al. · Vox Sanguinis · 34

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G protein–coupled receptor kinase 5 regulates thrombin signaling in platelets via PAR-1

2021 · Kate Downes, Xuefei Zhao, et al. · Blood Advances · 26

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Long-Read Sequencing Identifies the First Retrotransposon Insertion and Resolves Structural Variants Causing Antithrombin Deficiency

2022 · Belén de la Morena-Barrio, Jonathan Stephens, et al. · Thrombosis and Haemostasis · 25

Works count: 84

Citation count: 7,310

H-index: 26

I10-index: 37