Institut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement · FR
Area of research
Hematology · Cancer Research
Research interest
Research interests include Blood Coagulation and Thrombosis Mechanisms, Platelet Disorders and Treatments, Protease and Inhibitor Mechanisms, and Antiplatelet Therapy and Cardiovascular Diseases.
Selection and optimization strategy for Rap1-targeting single-domain antibodies as platelet activation markers.
Effects of Spectral Interfering Substances on Light Transmission Platelet Aggregation Using Infrared Based Aggregometer.
Efficacy and safety of recombinant activated factor VII in Glanzmann thrombasthenia: A systematic literature review.
A gain of function variant in RGS18 candidate for a familial mild bleeding syndrome.
FLI1 and GATA1 govern <i>TLN1</i> transcription: new insights into FLI1-related platelet disorders.
How Clot Composition Influences Fibrinolysis in the Acute Phase of Stroke: A Proteomic Study of Cerebral Thrombi.
Prospective, international, multisite comparison of platelet isolation techniques for genome-wide transcriptomics: communication from the SSC of the ISTH.
Early Metabolic Disruption and Predictive Biomarkers of Delayed-Cerebral Ischemia in Aneurysmal Subarachnoid Hemorrhage.
Association of laboratory test results with the bleeding history in patients with inherited platelet function disorders (the Bleeding Assesment Tool - LABoratory tests substudy): communication from the Platelet Physiology ISTH-SSC.
APOLD1 loss causes endothelial dysfunction involving cell junctions, cytoskeletal architecture, and Weibel-Palade bodies, while disrupting hemostasis.
Multicenter evaluation of light transmission platelet aggregation reagents: communication from the ISTH SSC Subcommittee on Platelet Physiology
Emergency management of patients with Glanzmann thrombasthenia: consensus recommendations from the French reference center for inherited platelet disorders.
Multicenter evaluation of light transmission platelet aggregation reagents: communication from the ISTH SSC Subcommittee on Platelet Physiology.
Single-cell analysis of megakaryopoiesis in peripheral CD34<sup>+</sup> cells: insights into ETV6-related thrombocytopenia.
Early metabolic disruption and predictive biomarkers of delayed-cerebral ischemia in aneurysmal subarachnoid haemorrhage
APOLD1 loss causes endothelial dysfunction involving cell junctions, cytoskeletal architecture, and Weibel-Palade bodies, while disrupting hemostasis
Granulocyte microvesicles with a high plasmin generation capacity promote clot lysis and improve outcome in septic shock.
Platelets Purification Is a Crucial Step for Transcriptomic Analysis.
Screening platelet function in blood donors.
Atypical late diagnosis of Noonan syndrome revealed by bleedings due to platelet dysfunction.
Single-cell analysis of megakaryopoiesis in peripheral CD34
<sup>+</sup>
cells: insights into ETV6-related thrombocytopenia
The ISTH bleeding assessment tool as predictor of bleeding events in inherited platelet disorders: Communication from the ISTH SSC Subcommittee on Platelet Physiology
Impaired adhesion of neutrophils expressing Slc44a2/HNA-3b to VWF protects against NETosis under venous shear rates.
The ISTH bleeding assessment tool as predictor of bleeding events in inherited platelet disorders: Communication from the ISTH SSC Subcommittee on Platelet Physiology.
Severe thrombophilia in a factor V-deficient patient homozygous for the Ala2086Asp mutation (FV Besançon).
Platelets: a potential role in chronic respiratory diseases?
A rare coding mutation in the MAST2 gene causes venous thrombosis in a French family with unexplained thrombophilia: The Breizh MAST2 Arg89Gln variant.
On-Ticagrelor Platelet Reactivity and Clinical Outcome in Patients Undergoing Percutaneous Coronary Intervention for Acute Coronary Syndrome.
GATA1 pathogenic variants disrupt MYH10 silencing during megakaryopoiesis.
Validation of the ISTH/SSC bleeding assessment tool for inherited platelet disorders: A communication from the Platelet Physiology SSC.