Identification of new <i>F8</i> deep intronic variations in patients with haemophilia AAmy Dericquebourg, Christine Vinciguerra, Catherine Ternisien et al.|Haemophilia|2020Cited by 14
Whole F9 gene sequencing identified deep intronic variations in genetically unresolved hemophilia B patientsAmy Dericquebourg, Yohann Jourdy, Hérvè Chambost et al.|Journal of Thrombosis and Haemostasis|2023Cited by 8
Comprehensive analysis of F8 large deletions: Characterization of full breakpoint junctions and description of a possible DNA breakage hotspot in intron 6Yohann Jourdy, Christine Vinciguerra, Mathilde Frétigny et al.|Journal of Thrombosis and Haemostasis|2022Cited by 6
Whole F8 gene sequencing combined with splicing functional analyses led to a substantial increase of the molecular diagnosis yield for non‐severe haemophilia AAmy Dericquebourg, Yohann Jourdy, Sabine‐Marie Castet et al.|Haemophilia|2023Cited by 6
Utilising Thrombin Generation Assay to Guide Co‐Administration of Factor Therapies With FitusiranYesim Dargaud, Anne Lienhart, Amy Dericquebourg et al.|Haemophilia|2025Cited by 3