Alix Rousseau

Biallelic inactivation of REV7 is associated with Fanconi anemia.

J. Soulier, A. Baruchel, D. Bluteau, 2016, The Journal of clinical investigation.

A role for Ral GTPase‐activating protein subunit β in mitotic regulation

A. Gautreau, P. Cossart, H. Bierne, 2014, The FEBS journal.

TGF-β Inhibition Rescues Hematopoietic Stem Cell Defects and Bone Marrow Failure in Fanconi Anemia.

J. Soulier, A. D’Andrea, D. Kozono, 2016, Cell stem cell.

Clonal hematopoiesis driven by chromosome 1q/MDM4 trisomy defines a canonical route toward leukemia in Fanconi anemia.

E. Gilson, F. Sigaux, J. Soulier, 2023, Cell stem cell.

Amendment history : Corrigendum ( March 2017 ) Biallelic inactivation of REV 7 is associated with Fanconi anemia

J. Soulier, A. Baruchel, D. Bluteau, 2019 .

Studies in an Early Development Window Unveils a Severe HSC Defect in both Murine and Human Fanconi Anemia

J. Soulier, M. Pla, P. de la Grange, 2018, Stem cell reports.