L. Pécheux

Functional characterization of a novel non-coding mutation “Ghent +49A > G” in the iron-responsive element of L-ferritin causing hereditary hyperferritinaemia-cataract syndrome

E. De Baere, J. Couso, Mayka Sánchez, 2017, Scientific Reports.

Modeling human MLL-AF9 translocated acute myeloid leukemia from single donors reveals RET as a potential therapeutic target

B. Wilhelm, J. Pelloux, M. Celton, 2017, Leukemia.

Outcomes of Coronavirus Disease 2019 Infection in Children and Adolescents With Cancer in Canada: Population-based Study and Systematic Review

S. Alexander, S. Oberoi, L. Pécheux, 2023, Journal of pediatric hematology/oncology.