Willem H. Ouwehand

University College Hospital — United Kingdom

Medicine · Health Sciences

129h-index106.7kcitations556works9.32yr avg
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Research Topics

Platelet Disorders and Treatments(181), Blood groups and transfusion(114), Genetic Associations and Epidemiology(93), Cell Adhesion Molecules Research(51), Immunodeficiency and Autoimmune Disorders(51)

Publications501 total

Deep generative classification of blood cell morphology
Nature Machine Intelligence·2025· 3 citedOpen Access
Artificial Intelligence for Pre-Anaemic Iron Deficiency Detection Using Rich Complete Blood Count Data
2025· 1 citedOpen Access
Array genotyping of transfusion-relevant blood cell antigens in 6946 ancestrally diverse study participants
Blood·2025· 7 citedOpen Access
Array Genotyping of Transfusion Relevant Blood Cell Antigens in 6946 Ancestrally Diverse Subjects
2025Open Access
Expected outcomes of stratified post‐donation testing in whole blood donation in <scp>England</scp>: A discrete event simulation modeling study
Transfusion·2025Open Access
Novel loci and biomedical consequences of iron homoeostasis variation
Communications Biology·2024· 8 citedOpen Access
A National Programme of a High Throughput Axiom Array Genotyping Platform for HEA and HLA Testing for All Patients with Sickle Cell, Thalassaemia and Transfusion Dependent Rare Inherited Anaemias in the United Kingdom
Blood·2024
The common VTE-protective G haplotype of <i>F5</i> increases factor V-short, TFPI function, and risk of bleeding
Blood Advances·2024· 1 citedOpen Access
Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders
UNC Libraries·2024Open Access
Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction
Nature Genetics·2024· 41 citedOpen Access
Recent methodological advances in federated learning for healthcare
Patterns·2024· 61 citedOpen Access
Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder
UNC Libraries·2024Open Access
The Pattern of Red Cell Antibodies in a Large Population of People with Sickle Cell Disease and Thalassemia
Blood·2023
Detection and annotation of transposable element insertions and deletions on the human genome using nanopore sequencing
iScience·2023· 8 citedOpen Access
Platelet Receptor Glycoprotein VI-Dimer Is Overexpressed in Patients with Atrial Fibrillation at High Risk of Ischemic Stroke
TH Open·2023· 2 citedOpen Access
PB0355 Knock-in of Homozygous NBEAL2 Variants to Model Gray Platelet Syndrome in Megakaryocytes Derived from CRISPR-Cas9-edited Pluripotent Stem Cells
Research and Practice in Thrombosis and Haemostasis·2023Open Access
A signature of platelet reactivity in CBC scattergrams reveals genetic predictors of thrombotic disease risk
Blood·2023· 9 citedOpen Access
The effects of pathogenic and likely pathogenic variants for inherited hemostasis disorders in 140 214 UK Biobank participants
Blood·2023· 16 citedOpen Access
A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology
Nature Communications·2023· 33 citedOpen Access
A signature of platelet reactivity in CBC scattergrams reveals genetic predictors of thrombotic disease risk
2023Open Access
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Frequent Co-authors

Nilesh J. Samani(15), Panos Deloukas(14), Alistair S. Hall(14), David J. Roberts(11), John Danesh(10), Emanuele Di Angelantonio(10), Mark I. McCarthy(9), Nicole Soranzo(9), Jeanette Erdmann(9), Carmel Moore(9), Peter S. Braund(8), Massimo Mangino(8), Paul R. Burton(7), Jeffrey C. Barrett(7), Martin D. Tobin(7), Antony Attwood(7), François Cambien(7), Jennifer Sambrook(7), Stephen G. Ball(6), Anthony J. Balmforth(6)