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Author Details

Maxime Caron
Centre Hospitalier Universitaire Sainte-Justine
2010
40
22
Nevan J Krogan (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
37419244Outlier Expression of Isoforms by Targeted or Total RNA Sequencing Identifies Clinically Significant Genomic Variants in Hematolymphoid Tumors.J Mol Diagn2023
35198911Identification of new ETV6 modulators through a high-throughput functional screening.iScience2022
34933343Whole-transcriptome analysis in acute lymphoblastic leukemia: a report from the DFCI ALL Consortium Protocol 16-001.Blood Adv2022
33433612Invasive growth associated with cold-inducible RNA-binding protein expression drives recurrence of surgically resected brain metastases.Neuro Oncol2021
33654212Publisher 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 Rep2021
34425890Pre-implantation alcohol exposure induces lasting sex-specific DNA methylation programming errors in the developing forebrain.Clin Epigenetics2021
34335193Single Cell Transcriptomics of Ependymal Cells Across Age, Region and Species Reveals Cilia-Related and Metal Ion Regulatory Roles as Major Conserved Ependymal Cell Functions.Front Cell Neurosci2021
34331108Repurposing proscillaridin A in combination with decitabine against embryonal rhabdomyosarcoma RD cells.Cancer Chemother Pharmacol2021
32415257Single-cell analysis of childhood leukemia reveals a link between developmental states and ribosomal protein expression as a source of intra-individual heterogeneity.Sci Rep2020
30819122Development and validation of five behavioral indices of flood adaptation.BMC Public Health2019
31185495GenPipes: an open-source framework for distributed and scalable genomic analyses.Gigascience2019
31196146Heart failure drug proscillaridin A targets MYC overexpressing leukemia through global loss of lysine acetylation.J Exp Clin Cancer Res2019
30440012Very long intergenic non-coding RNA transcripts and expression profiles are associated to specific childhood acute lymphoblastic leukemia subtypes.PLoS One2018
30341373Genome wide mapping of ETV6 binding sites in pre-B leukemic cells.Sci Rep2018
27980230A childhood acute lymphoblastic leukemia-specific lncRNA implicated in prednisolone resistance, cell proliferation, and migration.Oncotarget2017
28245871Conserved expression of transposon-derived non-coding transcripts in primate stem cells.BMC Genomics2017
28346506Specific expression of novel long non-coding RNAs in high-hyperdiploid childhood acute lymphoblastic leukemia.PLoS One2017
29054174Long-term nutritional impact of sleeve gastrectomy.Surg Obes Relat Dis2017
29113332LncRNAs downregulated in childhood acute lymphoblastic leukemia modulate apoptosis, cell migration, and DNA damage response.Oncotarget2017
28754017Development and Validation of a Behavioural Index for Adaptation to High Summer Temperatures among Urban Dwellers.Int J Environ Res Public Health2017
28724614Nuclear mTOR acts as a transcriptional integrator of the androgen signaling pathway in prostate cancer.Genes Dev2017
26804918The PGC-1α/ERRα Axis Represses One-Carbon Metabolism and Promotes Sensitivity to Anti-folate Therapy in Breast Cancer.Cell Rep2016
27791185Control of embryonic stem cell self-renewal and differentiation via coordinated alternative splicing and translation of YY2.Proc Natl Acad Sci U S A2016
27863956The International Human Epigenome Consortium Data Portal.Cell Syst2016
27863251Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells.Cell2016
27624058Immunoseq: the identification of functionally relevant variants through targeted capture and sequencing of active regulatory regions in human immune cells.BMC Med Genomics2016
27402251ERRα mediates metabolic adaptations driving lapatinib resistance in breast cancer.Nat Commun2016
25578964Transient DNMT1 suppression reveals hidden heritable marks in the genome.Nucleic Acids Res2015
26307085High-dose folic acid supplementation alters the human sperm methylome and is influenced by the MTHFR C677T polymorphism.Hum Mol Genet2015
26699896Population whole-genome bisulfite sequencing across two tissues highlights the environment as the principal source of human methylome variation.Genome Biol2015
26185018Epigenome data release: a participant-centered approach to privacy protection.Genome Biol2015
26219997Erratum: Characterization of functional methylomes by next-generation capture sequencing identifies novel disease-associated variants.Nat Commun2015
26021296Characterization of functional methylomes by next-generation capture sequencing identifies novel disease-associated variants.Nat Commun2015
25529140Identification of intrinsic and reflexive contributions to low-back stiffness: medium-term reliability and construct validity.J Biomech2015
24316981Fusion of TTYH1 with the C19MC microRNA cluster drives expression of a brain-specific DNMT3B isoform in the embryonal brain tumor ETMR.Nat Genet2014
25234136The effect of different lumbar belt designs on the lumbopelvic rhythm in healthy subjects.BMC Musculoskelet Disord2014
25326100Allelic expression mapping across cellular lineages to establish impact of non-coding SNPs.Mol Syst Biol2014
24520174Tissue factor expression provokes escape from tumor dormancy and leads to genomic alterations.Proc Natl Acad Sci U S A2014
24183450Global analysis of DNA methylation variation in adipose tissue from twins reveals links to disease-associated variants in distal regulatory elements.Am J Hum Genet2013
20453028Designing small multiple-target artificial RNAs.Nucleic Acids Res2010
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Collaborators

Guillaume Bourque
Institute for the Advanced Study of Human Biology (ASHBi), Kyoto University
Co-authored papers 19
Tomi Pastinen
Co-authored papers 13
Daniel Sinnett
Sainte-Justine University Hospital Research Center
Co-authored papers 13
Chantal Richer
CHU Sainte-Justine Research Center
Co-authored papers 10
Pascal St-Onge
CHU Sainte-Justine Research Center
Co-authored papers 10
Tony Kwan
Co-authored papers 8
Panos Deloukas
William Harvey Research Institute, Queen Mary University of London
Co-authored papers 5
Mark Lathrop
Victor Philip Dahdaleh Institute of Genomic Medicine at McGill University
Co-authored papers 5
Lars Rönnblom
Co-authored papers 5
Tim D Spector
King's College London
Co-authored papers 4
Mark I McCarthy
Co-authored papers 4
Serge McGraw
Centre Hospitalier Universitaire Sainte-Justine Research Center
Co-authored papers 4
Simon Drouin
Centre Hospitalier Universitaire Sainte-Justine
Co-authored papers 4
Elin Grundberg
Co-authored papers 4
Jacquetta M Trasler
McGill University and Research Institute of the McGill University Health Centre
Co-authored papers 3
ÿsa K Hedman
Co-authored papers 3
Hendrik G Stunnenberg
Co-authored papers 3
David Bujold
McGill University
Co-authored papers 3
Emmanouil T Dermitzakis
University of Geneva
Co-authored papers 2
Sylvie Langlois
Research Center, Centre Hospitalier Universitaire Sainte-Justine
Co-authored papers 2
Willem H Ouwehand
University of Cambridge
Co-authored papers 2
Stephan Beck
UCL Cancer Institute, University College London
Co-authored papers 2
Paul Flicek
European Bioinformatics Institute
Co-authored papers 2
Todd A Richmond
Co-authored papers 2
Nada Jabado
McGill University Health Centre (MUHC), Montreal Children's Hospital (MCH)
Co-authored papers 2
Jordana T Bell
King's College London
Co-authored papers 2
Marie-Claude Vohl
Co-authored papers 2
No??l J-M Raynal
Sainte-Justine University Hospital Research Center
Co-authored papers 2
Thai Hoa Tran
Universite de Montreal
Co-authored papers 2
Alexandre Montpetit
McGill University and Genome Quebec Innovation Centre
Co-authored papers 2
Release 1.2