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Author Details

Willem H Ouwehand
University of Cambridge
1984
334
99
PMIDPaper TitleJournal TitlePublished Year
36737374Corrigendum to 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 [J Thromb Haemost. 2021 Oct;19(10):2612-2617].J Thromb Haemost2023
37596262A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology.Nat Commun2023
37647652A signature of platelet reactivity in CBC scattergrams reveals genetic predictors of thrombotic disease risk.Blood2023
37647632The effects of pathogenic and likely pathogenic variants for inherited hemostasis disorders in 140â¿¿214 UK Biobank participants.Blood2023
37964899Platelet Receptor Glycoprotein VI-Dimer Is Overexpressed in Patients with Atrial Fibrillation at High Risk of Ischemic Stroke.TH Open2023
37953943Detection and annotation of transposable element insertions and deletions on the human genome using nanopore sequencing.iScience2023
36737374Corrigendum to 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 [J Thromb Haemost. 2021 Oct;19(10):2612-2617].J Thromb Haemost2023
37964899Platelet Receptor Glycoprotein VI-Dimer Is Overexpressed in Patients with Atrial Fibrillation at High Risk of Ischemic Stroke.TH Open2023
37596262A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology.Nat Commun2023
37953943Detection and annotation of transposable element insertions and deletions on the human genome using nanopore sequencing.iScience2023
37647652A signature of platelet reactivity in CBC scattergrams reveals genetic predictors of thrombotic disease risk.Blood2023
37647632The effects of pathogenic and likely pathogenic variants for inherited hemostasis disorders in 140â¿¿214 UK Biobank participants.Blood2023
34581777G protein-coupled receptor kinase 5 regulates thrombin signaling in platelets via PAR-1.Blood Adv2022
35396579Rare coding variants in ten genes confer substantial risk for schizophrenia.Nature2022
35764313Long-Read Sequencing Identifies the First Retrotransposon Insertion and Resolves Structural Variants Causing Antithrombin Deficiency.Thromb Haemost2022
35568032Whole-exome sequencing identifies rare genetic variants associated with human plasma metabolites.Am J Hum Genet2022
36253349Systematic Mendelian randomization using the human plasma proteome to discover potential therapeutic targets for stroke.Nat Commun2022
34581777G protein-coupled receptor kinase 5 regulates thrombin signaling in platelets via PAR-1.Blood Adv2022
35041713Platelet surface receptor glycoprotein VI-dimer is overexpressed in stroke: The Glycoprotein VI in Stroke (GYPSIE) study results.PLoS One2022
34732567Circular RNAs exhibit limited evidence for translation, or translation regulation of the mRNA counterpart in terminal hematopoiesis.RNA2022
35218943Molecular Dissection of Structural Variations Involved in Antithrombin Deficiency.J Mol Diagn2022
35072137Machine learning optimized polygenic scores for blood cell traits identify sex-specific trajectories and genetic correlations with disease.Cell Genom2022
35224470Coagulation factor V is a T-cell inhibitor expressed by leukocytes in COVID-19.iScience2022
35764313Long-Read Sequencing Identifies the First Retrotransposon Insertion and Resolves Structural Variants Causing Antithrombin Deficiency.Thromb Haemost2022
35396579Rare coding variants in ten genes confer substantial risk for schizophrenia.Nature2022
35568032Whole-exome sequencing identifies rare genetic variants associated with human plasma metabolites.Am J Hum Genet2022
36253349Systematic Mendelian randomization using the human plasma proteome to discover potential therapeutic targets for stroke.Nat Commun2022
35224470Coagulation factor V is a T-cell inhibitor expressed by leukocytes in COVID-19.iScience2022
35072137Machine learning optimized polygenic scores for blood cell traits identify sex-specific trajectories and genetic correlations with disease.Cell Genom2022
35041713Platelet surface receptor glycoprotein VI-dimer is overexpressed in stroke: The Glycoprotein VI in Stroke (GYPSIE) study results.PLoS One2022
35218943Molecular Dissection of Structural Variations Involved in Antithrombin Deficiency.J Mol Diagn2022
34732567Circular RNAs exhibit limited evidence for translation, or translation regulation of the mRNA counterpart in terminal hematopoiesis.RNA2022
32703790Cell type-specific novel long non-coding RNA and circular RNA in the BLUEPRINT hematopoietic transcriptomes atlas.Haematologica2021
33587817Transcriptional characterization of human megakaryocyte polyploidization and lineage commitment.J Thromb Haemost2021
34226637Effects of adiposity on the human plasma proteome: observational and Mendelian randomisation estimates.Int J Obes (Lond)2021
33674754Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder.Mol Psychiatry2021
34135082Plasma Proteomics of Renal Function: A Transethnic Meta-Analysis and Mendelian Randomization Study.J Am Soc Nephrol2021
34355501GoldVariants, 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.J Thromb Haemost2021
33496751Neutrophil specific granule and NETosis defects in gray platelet syndrome.Blood Adv2021
33496735Elevated levels of tissue factor pathway inhibitor in patients with mild to moderate bleeding tendency.Blood Adv2021
32703790Cell type-specific novel long non-coding RNA and circular RNA in the BLUEPRINT hematopoietic transcriptomes atlas.Haematologica2021
33341984Comparison of four methods to measure haemoglobin concentrations in whole blood donors (COMPARE): A diagnostic accuracy study.Transfus Med2021
34611362Polygenic basis and biomedical consequences of telomere length variation.Nat Genet2021
34426706Mitochondrial DNA variants modulate N-formylmethionine, proteostasis and risk of late-onset human diseases.Nat Med2021
34758253100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report.N Engl J Med2021
34475573Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression.Nat Genet2021
34750571Integrative analysis of the plasma proteome and polygenic risk of cardiometabolic diseases.Nat Metab2021
33674754Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder.Mol Psychiatry2021
33587817Transcriptional characterization of human megakaryocyte polyploidization and lineage commitment.J Thromb Haemost2021
33496751Neutrophil specific granule and NETosis defects in gray platelet syndrome.Blood Adv2021
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King's College London
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University of Cambridge
Co-authored papers 17
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