Profile


Emeritus Prof Willem OUWEHAND
Principal Investigator
Willem H Ouwehand received his PhD and medical degree from the University of Amsterdam in 1984. After a 5 years stint at the Sanquin laboratory in Amsterdam, he accepted an academic position at the University of Cambridge. He is now emeritus Professor of Experimental Haematology and holds Honorary Consultant Haematology positions at Cambridge University Hospitals, University College London Hospitals and NHS Blood and Transplant. He is a Fellow of the Academy of Medical Sciences and emeritus NIHR Senior Investigator.
His research on rare diseases focused on inherited haemostasis disorders.(1-5) As one of the founders of the NIHR BioResource, Willem did lead the NIHR BioResource whole genome sequencing pilot study for Rare Diseases for the 100 000 Genomes Project. With Professor Nicole Soranzo, he unravelled the genetic architecture of blood cell formation by genome wide association studies for complete blood count (CBC) parameters in large-scale population studies, including the blood donor health cohorts INTERVAL, COMPARE and STRIDES.
With Asst Prof Nicholas Gleadall, he founded the Blood transfusion Genomics Consortium, with participating institutes in 14 countries, which has developed and validated an affordable array DNA test for high throughput blood cell antigen typing with the aim to improve the matching between donor and recipient. He also supports him and Professor Michael Roberts for the BloodCounts! consortium project, which develops foundational models for blood using the CBC and blood smear images from millions of patients in The Gambia, Ghana, The Netherlands, Singapore and the UK. All together, foundation models of blood will enhance the operational efficiency of the CBC test and amplify its diagnostic, predictive, and inferential power, without disrupting clinical pathways, and at minimal cost.
who1000@cam.ac.uk
Cambridge
Principal Investigators
BloodCounts!
Research Interest
Key Publications
Google Scholar Link
Verdier, H. et al. A signature of platelet reactivity in CBC scattergrams reveals genetic predictors of thrombotic disease risk. Blood, 2023
Akbari, P., et al. (Ouwehand - shared last author) A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Nature Communications, 2023.
Turro et al. (Ouwehand - last and corresponding author). Whole-genome sequencing of rare disease patients in a national health system. Nature, 2020
Thaventhiran et al. (Ouwehand - shared last author). Whole Genome Sequencing of Primary Immunodeficiency reveals a role for common and rare variants in coding and non-coding sequences. Nature, 2020
Astle et al. (Ouwehand - shared last author). The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. Cell. 2016
Internal Comments Only
Achievements
- Sol Sherry Memorial Lecture, International Society for Thrombosis and Haemostasis, 2017
- Oliver Memorial Award, Royal College of Pathologists, London, 2017
- Investigator Recognition Award, International Society for Thrombosis and Haemostasis, 2015
- Kenneth Goldsmith Award, British Blood Transfusion Society, 2003