Cyrielle I. Kint

Leuven, VLG, Belgium

Last Updated: 09/26/2026

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Found 18 publications

Multigene panel analysis of connective tissue and vascular genes in patients with a bleeding disorder of unknown cause or a cerebrovascular event.

Multigene panel analysis of connective tissue and vascular genes in patients with a bleeding disorder of unknown cause or a cerebrovascular event.

Journal: Research and practice in thrombosis and haemostasis

Published: June 11, 2026

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

Clinical utility of panel-based genetic sequencing for von Willebrand disease.

Clinical utility of panel-based genetic sequencing for von Willebrand disease.

Journal: Research and practice in thrombosis and haemostasis

Published: November 27, 2024

Genotype vs laboratory phenotype correlation of defects in natural anticoagulants in patients with venous thromboembolism.

Genotype vs laboratory phenotype correlation of defects in natural anticoagulants in patients with venous thromboembolism.

Journal: Journal of thrombosis and haemostasis : JTH

Published: October 16, 2024

Multigene panel for thrombophilia testing in venous thromboembolism.

Multigene panel for thrombophilia testing in venous thromboembolism.

Journal: Journal of thrombosis and haemostasis : JTH

Published: September 26, 2024

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

A novel heterozygous likely pathogenic SLC5A2 variant in a diabetic patient with glucosuria and aminoaciduria.

A novel heterozygous likely pathogenic SLC5A2 variant in a diabetic patient with glucosuria and aminoaciduria.

Journal: Endocrinology, diabetes & metabolism case reports

Published: May 11, 2024

Partially automated whole-genome sequencing reanalysis of previously undiagnosed pediatric patients can efficiently yield new diagnoses.

Partially automated whole-genome sequencing reanalysis of previously undiagnosed pediatric patients can efficiently yield new diagnoses.

Journal: NPJ genomic medicine

Published: February 13, 2020

Biochemical determinants of ObgE-mediated persistence.

Biochemical determinants of ObgE-mediated persistence.

Journal: Molecular microbiology

Published: September 01, 2019

A Randomized, Controlled Trial of the Analytic and Diagnostic Performance of Singleton and Trio, Rapid Genome and Exome Sequencing in Ill Infants.

A Randomized, Controlled Trial of the Analytic and Diagnostic Performance of Singleton and Trio, Rapid Genome and Exome Sequencing in Ill Infants.

Journal: American journal of human genetics

Published: July 03, 2019

Diagnosis of genetic diseases in seriously ill children by rapid whole-genome sequencing and automated phenotyping and interpretation.

Diagnosis of genetic diseases in seriously ill children by rapid whole-genome sequencing and automated phenotyping and interpretation.

Journal: Science translational medicine

Published: March 17, 2018

A Single-Amino-Acid Substitution in Obg Activates a New Programmed Cell Death Pathway in Escherichia coli.

A Single-Amino-Acid Substitution in Obg Activates a New Programmed Cell Death Pathway in Escherichia coli.

Journal: mBio

Published: December 24, 2015

Showing 1-12 of 18

Last Updated: 09/26/2026