Reccurrent F8 Intronic Deletion Found in Mild Hemophilia A Causes Alu ExonizationYohann Jourdy, Christine Vinciguerra, Alexandre Janin et al.|The American Journal of Human Genetics|2018Cited by 29
Splicing analysis of 26 <i>F8</i> nucleotide variations using a minigene assayYohann Jourdy, Christine Vinciguerra, Mathilde Frétigny et al.|Haemophilia|2019Cited by 17
Severe hemophilia A caused by an unbalanced chromosomal rearrangement identified using nanopore sequencingNicolas Chatron, Yohann Jourdy, Caroline Schluth‐Bolard et al.|Journal of Thrombosis and Haemostasis|2019Cited by 15
Study of six patients with complete F9 deletion characterized by cytogenetic microarray: role of the SOX3 gene in intellectual disabilityYohann Jourdy, Christine Vinciguerra, Nicolas Chatron et al.|Journal of Thrombosis and Haemostasis|2016Cited by 14
Identification of new <i>F8</i> deep intronic variations in patients with haemophilia AAmy Dericquebourg, Christine Vinciguerra, Anne Lienhart et al.|Haemophilia|2020Cited by 14