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Author Details
Full Name
Pascal St-Onge
Affiliation
CHU Sainte-Justine Research Center
ORCID
Career Start Year
2007
Papers
36
H Index
13
Expertise
CM4AI Collaborator
Nevan J Krogan (CM4AI)
PMID
Paper Title
Journal Title
Published Year
38049555
Characterisation of FLT3 alterations in childhood acute lymphoblastic leukaemia.
Br J Cancer
2024
38051303
Genetic Factors and Long-term Treatment-Related Neurocognitive Deficits, Anxiety, and Depression in Childhood Leukemia Survivors: An Exome-Wide Association Study.
Cancer Epidemiol Biomarkers Prev
2024
37777587
Repurposing disulfiram, an alcohol-abuse drug, in neuroblastoma causes KAT2A downregulation and in vivo activity with a water/oil emulsion.
Sci Rep
2023
34446917
Genetic factors contributing to late adverse musculoskeletal effects in childhood acute lymphoblastic leukemia survivors.
Pharmacogenomics J
2022
34933343
Whole-transcriptome analysis in acute lymphoblastic leukemia: a report from the DFCI ALL Consortium Protocol 16-001.
Blood Adv
2022
35198911
Identification of new ETV6 modulators through a high-throughput functional screening.
iScience
2022
34331108
Repurposing proscillaridin A in combination with decitabine against embryonal rhabdomyosarcoma RD cells.
Cancer Chemother Pharmacol
2021
33654212
Publisher Correction: Single-cell analysis of childhood leukemia reveals a link between developmental states and ribosomal protein expression as a source of intra-individual heterogeneity.
Sci Rep
2021
34505544
Genetic factors in treatment-related cardiovascular complications in survivors of childhood acute lymphoblastic leukemia.
Pharmacogenomics
2021
34215854
Genetic susceptibility to acute graft versus host disease in pediatric patients undergoing HSCT.
Bone Marrow Transplant
2021
32372697
HLA alleles associated with asparaginase hypersensitivity in childhood ALL: a report from the DFCI Consortium.
Pharmacogenomics
2020
31790828
Genetic Susceptibility to Hepatic Sinusoidal Obstruction Syndrome in Pediatric Patients Undergoing Hematopoietic Stem Cell Transplantation.
Biol Blood Marrow Transplant
2020
33245684
Role of rs10406069 in miR-5196 in hyperdiploid childhood acute lymphoblastic leukemia.
Epigenomics
2020
32476062
An optimized workflow to improve reliability of detection of KIAA1549:BRAF fusions from RNA sequencing data.
Acta Neuropathol
2020
32415257
Single-cell analysis of childhood leukemia reveals a link between developmental states and ribosomal protein expression as a source of intra-individual heterogeneity.
Sci Rep
2020
30575814
Recurrent somatic BRAF insertion (p.V504_R506dup): a tumor marker and a potential therapeutic target in pilocytic astrocytoma.
Oncogene
2019
31686588
Genes identified through genome-wide association studies of osteonecrosis in childhood acute lymphoblastic leukemia patients.
Pharmacogenomics
2019
31181069
Influence of genetic factors on long-term treatment related neurocognitive complications, and on anxiety and depression in survivors of childhood acute lymphoblastic leukemia: The Petale study.
PLoS One
2019
31196146
Heart failure drug proscillaridin A targets MYC overexpressing leukemia through global loss of lysine acetylation.
J Exp Clin Cancer Res
2019
30983502
Identification of a single-nucleotide polymorphism within <i>CDH2</i> gene associated with bone morbidity in childhood acute lymphoblastic leukemia survivors.
Pharmacogenomics
2019
31088516
Identification of genetic association between cardiorespiratory fitness and the trainability genes in childhood acute lymphoblastic leukemia survivors.
BMC Cancer
2019
31114288
Identification of genetic variants associated with skeletal muscle function deficit in childhood acute lymphoblastic leukemia survivors.
Pharmgenomics Pers Med
2019
31026031
Molecular Profiling of Hard-to-Treat Childhood and Adolescent Cancers.
JAMA Netw Open
2019
30440012
Very long intergenic non-coding RNA transcripts and expression profiles are associated to specific childhood acute lymphoblastic leukemia subtypes.
PLoS One
2018
30385747
TRPV4 and KRAS and FGFR1 gain-of-function mutations drive giant cell lesions of the jaw.
Nat Commun
2018
28069604
KMT2E-ASNS: a novel relapse-specific fusion gene in early T-cell precursor acute lymphoblastic leukemia.
Blood
2017
28346506
Specific expression of novel long non-coding RNAs in high-hyperdiploid childhood acute lymphoblastic leukemia.
PLoS One
2017
29126409
Genomic determinants of long-term cardiometabolic complications in childhood acute lymphoblastic leukemia survivors.
BMC Cancer
2017
29113332
LncRNAs downregulated in childhood acute lymphoblastic leukemia modulate apoptosis, cell migration, and DNA damage response.
Oncotarget
2017
28877255
Characterization of the microDNA through the response to chemotherapeutics in lymphoblastoid cell lines.
PLoS One
2017
27980230
A childhood acute lymphoblastic leukemia-specific lncRNA implicated in prednisolone resistance, cell proliferation, and migration.
Oncotarget
2017
27620872
Genome-wide repression of eRNA and target gene loci by the ETV6-RUNX1 fusion in acute leukemia.
Genome Res
2016
27602765
Genomic characterization of pediatric T-cell acute lymphoblastic leukemia reveals novel recurrent driver mutations.
Oncotarget
2016
21234765
Genomic and genealogical investigation of the French Canadian founder population structure.
Hum Genet
2011
21769930
Genome-wide detection and characterization of mating asymmetry in human populations.
Genet Epidemiol
2011
18021709
[Childhood leukemia: a genetic disease!].
Med Sci (Paris)
2007
1 - 36 of 36
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