C. Richer

D. Labuda, M. Krajinovic, D. Sinnett, 2000, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

Replication analysis confirms the association of ARID5B with childhood B-cell acute lymphoblastic leukemia

D. Sinnett, C. Richer, E. Kritikou, 2010, Haematologica.

Isolation of stable bacterial artificial chromosome DNA using a modified alkaline lysis method.

D. Sinnett, C. Richer, A. Baccichet, 1998, BioTechniques.

ALG: Automated Genotype Calling of Luminex Assays

D. Sinnett, C. Richer, M. Bourgey, 2011, PloS one.

Susceptibility to Childhood Acute Lymphoblastic Leukemia : Influence of CYP 1 A 1 , CYP 2 D 6 , GSTM 1 , and GSTT 1 Genetic Polymorphisms

D. Labuda, M. Krajinovic, D. Sinnett, 1999 .

Heart failure drug proscillaridin A targets MYC overexpressing leukemia through global loss of lysine acetylation

N. Krogan, A. Haman, T. Hoang, 2019, Journal of Experimental & Clinical Cancer Research.

Genomic loci susceptible to replication errors in cancer cells.

D. Labuda, M. Krajinovic, D. Sinnett, 1998, British Journal of Cancer.

Chromosomal assignment of loci susceptible to replication errors by radiation hybrid mapping.

D. Labuda, M. Krajinovic, D. Sinnett, 1998, Mutation research.

Detection of Fetomaternal Genotype Associations in Early-Onset Disorders: Evaluation of Different Methods and Their Application to Childhood Leukemia

D. Sinnett, C. Richer, M. Roy-Gagnon, 2010, Journal of biomedicine & biotechnology.

CLIC5: a novel ETV6 target gene in childhood acute lymphoblastic leukemia

D. Sinnett, C. Richer, S. Drouin, 2016, Haematologica.

Role of NQO1, MPO and CYP2E1 genetic polymorphisms in the susceptibility to childhood acute lymphoblastic leukemia

D. Labuda, M. Krajinovic, D. Sinnett, 2002, International journal of cancer.

Integration of high-resolution methylome and transcriptome analyses to dissect epigenomic changes in childhood acute lymphoblastic leukemia.

T. Pastinen, D. Sinnett, B. Ge, 2013, Cancer research.

Alu RNA transcripts in human embryonal carcinoma cells. Model of post-transcriptional selection of master sequences.

D. Labuda, D. Sinnett, C. Richer, 1992, Journal of molecular biology.

Alu RNA secondary structure consists of two independent 7 SL RNA-like folding units.

D. Labuda, D. Sinnett, C. Richer, 1991, The Journal of biological chemistry.

Role of rs10406069 in miR-5196 in hyperdiploid childhood acute lymphoblastic leukemia.

D. Sinnett, C. Richer, E. Lopez-Lopez, 2020, Epigenomics.

Mutational dynamics of early and late relapsed childhood ALL: rapid clonal expansion and long-term dormancy.

D. Sinnett, C. Richer, Jean-François Spinella, 2018, Blood advances.

Susceptibility to childhood acute lymphoblastic leukemia: influence of CYP1A1, CYP2D6, GSTM1, and GSTT1 genetic polymorphisms.

D. Labuda, M. Krajinovic, D. Sinnett, 1999, Blood.

A young Alu subfamily amplified independently in human and African great apes lineages.

J. Jurka, D. Labuda, W. Makałowski, 1994, Nucleic acids research.

Evolution of mouse B1 repeats: 7SL RNA folding pattern conserved

D. Labuda, G. Striker, D. Sinnett, 1991, Journal of Molecular Evolution.

Phylogenetic affinities of tarsier in the context of primate Alu repeats.

D. Labuda, E. Ziętkiewicz, C. Richer, 1999, Molecular phylogenetics and evolution.

Molecular and Cellular Pathobiology Integration of High-Resolution Methylome and Transcriptome Analyses to Dissect Epigenomic Changes in Childhood Acute Lymphoblastic Leukemia

T. Pastinen, D. Sinnett, B. Ge, 2013 .

miR-431-5p Knockdown Protects Against Angiotensin II–Induced Hypertension and Vascular Injury

E. Schiffrin, D. Sinnett, C. Richer, 2019, Hypertension.

To the editor: KMT2E-ASNS: a novel relapse-specific fusion gene in early T-cell precursor acute lymphoblastic leukemia

M. Minden, M. Krajinovic, D. Sinnett, 2017 .

Identification of new ETV6 modulators through a high-throughput functional screening

D. Sinnett, C. Richer, M. Caron, 2022, iScience.

Genome wide mapping of ETV6 binding sites in pre-B leukemic cells

D. Sinnett, C. Richer, M. Caron, 2018, Scientific Reports.

A novel somatic mutation in ACD induces telomere lengthening and apoptosis resistance in leukemia cells

D. Sinnett, C. Richer, C. Autexier, 2015, BMC Cancer.

Impact of promoter polymorphisms in key regulators of the intrinsic apoptosis pathway on the outcome of childhood acute lymphoblastic leukemia

D. Neuberg, J. Kutok, S. Sallan, 2014, Haematologica.

Recurrent somatic BRAF insertion (p.V504_R506dup): a tumor marker and a potential therapeutic target in pilocytic astrocytoma

D. Sinnett, S. Langlois, C. Richer, 2018, Oncogene.

A childhood acute lymphoblastic leukemia-specific lncRNA implicated in prednisolone resistance, cell proliferation, and migration

Pascal St-Onge, Daniel Sinnett, Maxime Caron, 2016, Oncotarget.

Genetic susceptibility to breast cancer in French‐Canadians: Role of carcinogen‐metabolizing enzymes and gene–environment interactions

A. LaCroix, D. Labuda, M. Krajinovic, 2001, International journal of cancer.

Detection of a mutator phenotype in cancer cells by inter-Alu polymerase chain reaction.

D. Labuda, M. Krajinovic, D. Sinnett, 1996, Cancer research.

Whole-exome sequencing of a rare case of familial childhood acute lymphoblastic leukemia reveals putative predisposing mutations in Fanconi anemia genes

D. Sinnett, C. Richer, Jean-François Spinella, 2015, BMC Cancer.

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

G. Bourque, D. Sinnett, C. Richer, 2020, Scientific Reports.

Targeting MYC Overexpressing Leukemia with Cardiac Glycoside Proscillaridin Through Downregulation of Histone Acetyltransferases

N. Krogan, A. Haman, T. Hoang, 2018, bioRxiv.

Rapid detection of CYP1A1, CYP2D6, and NAT variants by multiplex polymerase chain reaction and allele-specific oligonucleotide assay.

D. Labuda, M. Krajinovic, D. Sinnett, 1999, Analytical biochemistry.

Genomic characterization of pediatric T-cell acute lymphoblastic leukemia reveals novel recurrent driver mutations

M. Minden, D. Sinnett, S. Langlois, 2016, Oncotarget.

Analyses of bulky DNA adduct levels in human breast tissue and genetic polymorphisms of cytochromes P450 (CYPs), myeloperoxidase (MPO), quinone oxidoreductase (NQO1), and glutathione S-transferases (GSTs).

D. Labuda, M. Krajinovic, D. Sinnett, 2002, Mutation research.

Leadership for Social Justice Throughout Fifteen Years of Intervention in a Disadvantaged and Multicultural Canadian Urban Area: The Supporting Montréal Schools Program

C. Richer, Jean-Marie Archambault, 2014 .

Repurposing proscillaridin A in combination with decitabine against embryonal rhabdomyosarcoma RD cells

R. Najmanovich, D. Sinnett, C. Richer, 2021, Cancer Chemotherapy and Pharmacology.

Single-strand conformational polymorphisms (SSCP): detection of useful polymorphisms at the dystrophin locus

D. Labuda, D. Sinnett, C. Richer, 1992, Human Genetics.

LncRNAs downregulated in childhood acute lymphoblastic leukemia modulate apoptosis, cell migration, and DNA damage response

D. Sinnett, C. Richer, M. Caron, 2017, Oncotarget.

Circulating let-7g-5p and miR-191-5p are independent predictors of chronic kidney disease in hypertensive patients.

E. Schiffrin, D. Sinnett, M. Briet, 2020, American journal of hypertension.

Chromosome 2 Fragment Substitutions in Dahl Salt-Sensitive Rats and RNA Sequencing Identified Enpep and Hs2st1 as Vascular Inflammatory Modulators

E. Schiffrin, A. Kwitek, D. Sinnett, 2020, Hypertension.

Repurposing disulfiram, an alcohol-abuse drug, in neuroblastoma causes KAT2A downregulation and in vivo activity with a water/oil emulsion

C. Richer, X. Banquy, P. St-Onge, 2023, Scientific reports.

CircRNAome of Childhood Acute Lymphoblastic Leukemia: Deciphering Subtype-Specific Expression Profiles and Involvement in TCF3::PBX1 ALL

C. Richer, P. St-Onge, I. Martín-Guerrero, 2024, International journal of molecular sciences.