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Iscience|February 24, 2022
Identification of new ETV6 modulators through a high-throughput functional screeningBenjamin Neveu, Chantal Richer, Pauline Cassart, et al.
Oncotarget|September 8, 2016
Genomic characterization of pediatric T-cell acute lymphoblastic leukemia reveals novel recurrent driver mutationsJean-François Spinella, Pauline Cassart, Chantal Richer, et al.
British Journal of Cancer|December 4, 2023
Characterisation of FLT3 alterations in childhood acute lymphoblastic leukaemiaAngela Gutierrez-Camino, Chantal Richer, Manon Ouimet, et al.
BMC Cancer|May 16, 2019
Identification of genetic association between cardiorespiratory fitness and the trainability genes in childhood acute lymphoblastic leukemia survivorsMaxime Caru, Kateryna Petrykey, Simon Drouin, et al.
Plos One|March 28, 2017
Specific expression of novel long non-coding RNAs in high-hyperdiploid childhood acute lymphoblastic leukemiaMathieu Lajoie, Simon Drouin, Maxime Caron, et al.
Pharmacogenomics|May 7, 2020
HLA alleles associated with asparaginase hypersensitivity in childhood ALL: a report from the DFCI ConsortiumVincent Gagné, Pascal St-Onge, Patrick Beaulieu, et al.
Oncogene|December 22, 2018
Recurrent somatic BRAF insertion (p.V504_R506dup): a tumor marker and a potential therapeutic target in pilocytic astrocytomaFida Khater, Sylvie Langlois, Pauline Cassart, et al.
Epigenomics|November 27, 2020
Role of rs10406069 in miR-5196 in hyperdiploid childhood acute lymphoblastic leukemiaAngela Gutierrez-Camino, Chantal Richer, Pascal St-Onge, et al.
Genome Research|September 14, 2016
Genome-wide repression of eRNA and target gene loci by the ETV6-RUNX1 fusion in acute leukemiaSusanna Teppo, Saara Laukkanen, Thomas Liuksiala, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|December 5, 2023
Genetic Factors and Long-term Treatment-Related Neurocognitive Deficits, Anxiety, and Depression in Childhood Leukemia Survivors: An Exome-Wide Association StudyKateryna Petrykey, Sarah Lippé, Serge Sultan, et al.
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