Chantal Thys

Leuven, VLG, Belgium

Last Updated: 09/26/2026

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Found 31 publications

Prothrombotic PROC variant rebalancing hemostasis in severe hemophilia A with attenuated bleeding risk.

Prothrombotic PROC variant rebalancing hemostasis in severe hemophilia A with attenuated bleeding risk.

Journal: Journal of thrombosis and haemostasis : JTH

Published: November 09, 2025

Reduced platelet formation associated with serine metabolic dysregulation in integrin αIIbβ3-deficient megakaryocytes.

Reduced platelet formation associated with serine metabolic dysregulation in integrin αIIbβ3-deficient megakaryocytes.

Journal: Blood

Published: October 01, 2025

Transcriptome profiling of megakaryocytes and platelets: Application to GP9- and IKZF5-related thrombocytopenia.

Transcriptome profiling of megakaryocytes and platelets: Application to GP9- and IKZF5-related thrombocytopenia.

Journal: HemaSphere

Published: April 02, 2025

Functional assessment of genetic variants in thrombomodulin detected in patients with bleeding and thrombosis.

Functional assessment of genetic variants in thrombomodulin detected in patients with bleeding and thrombosis.

Journal: Blood

Published: August 06, 2024

Mutations in the U4 snRNA gene RNU4-2 cause one of the most prevalent monogenic neurodevelopmental disorders.

Mutations in the U4 snRNA gene RNU4-2 cause one of the most prevalent monogenic neurodevelopmental disorders.

Journal: Nature medicine

Published: April 11, 2024

Genetic association analysis of 77,539 genomes reveals rare disease etiologies.

Genetic association analysis of 77,539 genomes reveals rare disease etiologies.

Journal: Nature medicine

Published: October 21, 2022

Clinical application of multigene panel testing for bleeding, thrombotic, and platelet disorders: a 3-year Belgian experience.

Clinical application of multigene panel testing for bleeding, thrombotic, and platelet disorders: a 3-year Belgian experience.

Journal: Journal of thrombosis and haemostasis : JTH

Published: September 23, 2022

Ribosome dysfunction underlies SLFN14-related thrombocytopenia.

Ribosome dysfunction underlies SLFN14-related thrombocytopenia.

Journal: Blood

Published: July 08, 2022

Methylome analysis for haemophilia A intron 22 inversion patients with and without inhibitors: A pilot study.

Methylome analysis for haemophilia A intron 22 inversion patients with and without inhibitors: A pilot study.

Journal: Haemophilia : the official journal of the World Federation of Hemophilia

Published: June 14, 2022

F11 Gene Duplication Causes Elevated FXI Plasma Levels and Is a Risk for Venous Thrombosis.

F11 Gene Duplication Causes Elevated FXI Plasma Levels and Is a Risk for Venous Thrombosis.

Journal: Thrombosis and haemostasis

Published: November 15, 2021

Combined transcriptome and proteome profiling of SRC kinase activity in healthy and E527K defective megakaryocytes.

Combined transcriptome and proteome profiling of SRC kinase activity in healthy and E527K defective megakaryocytes.

Journal: Haematologica

Published: May 17, 2021

The brain-derived neurotrophic factor prompts platelet aggregation and secretion.

The brain-derived neurotrophic factor prompts platelet aggregation and secretion.

Journal: Blood advances

Published: December 22, 2020

Showing 1-12 of 31

Last Updated: 09/26/2026