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Journal of Thrombosis and Haemostasis : JTH|June 1, 2021
GATA1 pathogenic variants disrupt MYH10 silencing during megakaryopoiesisPaul Saultier, Sandrine Cabantous, Michel Puceat, et al.
European Journal of Medical Genetics|August 5, 2021
Novel partial loss-of-function variants in the tyrosyl-tRNA synthetase 1 (YARS1) gene involved in multisystem diseaseClothilde Estève, Céline Roman, Cécile DeLeusse, et al.
Cytometry. Part B, Clinical Cytometry|August 18, 2020
Multicentric MFI30 study: Standardization of flow cytometry analysis of CD30 expression in non-Hodgkin lymphomaAgathe Debliquis, Lucile Baseggio, Sabrina Bouyer, et al.
Blood|July 8, 2015
A mutation in the Gardos channel is associated with hereditary xerocytosisRaphael Rapetti-Mauss, Caroline Lacoste, Véronique Picard, et al.
Blood|April 30, 2011
Posttranscriptional deregulation of MYC via PTEN constitutes a major alternative pathway of MYC activation in T-cell acute lymphoblastic leukemiaMélanie Bonnet, Marie Loosveld, Bertrand Montpellier, et al.
Frontiers in Oncology|January 11, 2020
B-ALL With t(5;14)(q31;q32); IGH-IL3 Rearrangement and Eosinophilia: A Comprehensive Analysis of a Peculiar IGH-Rearranged B-ALLBenjamin Fournier, Estelle Balducci, Nicolas Duployez, et al.
American Journal of Hematology|July 4, 2026
High Proportion of PNH Type II Neutrophils Is Associated With Thrombosis in Patients Displaying a PNH Clone ≥ 1Orianne Wagner-Ballon, Anne-Catherine Lhoumeau, Anna Raimbault, et al.
Nature Communications|January 24, 2015
Site- and allele-specific polycomb dysregulation in T-cell leukaemiaJean-Marc Navarro, Aurore Touzart, Lydie C Pradel, et al.
Blood Advances|December 24, 2019
How should we diagnose and treat blastic plasmacytoid dendritic cell neoplasm patients?Francine Garnache-Ottou, Chrystelle Vidal, Sabeha Biichlé, et al.
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