Manon Ouimet

发表

SNooPer: a machine learning-based method for somatic variant identification from low-pass next-generation sequencing

Daniel Sinnett, Virginie Saillour, Jean-François Spinella, 2016, BMC Genomics.

Functional Analysis of Promoter Variants in Genes Involved in Sex Steroid Action, DNA Repair and Cell Cycle Control

M. Dumont, J. Simard, D. Sinnett, 2019, Genes.

Specific expression of novel long non-coding RNAs in high-hyperdiploid childhood acute lymphoblastic leukemia

D. Sinnett, C. Richer, M. Caron, 2017, PloS one.

Allele-specific chromatin remodeling in the ZPBP2/GSDMB/ORMDL3 locus associated with the risk of asthma and autoimmune disease.

K. Dewar, M. Świątek, J. Celedón, 2009, American journal of human genetics.

Population genomics in a disease targeted primary cell model.

Daniel Sinnett, Fernando Rivadeneira, Claes Ohlsson, 2009, Genome research.

Interaction between genetic and epigenetic variation defines gene expression patterns at the asthma-associated locus 17q12-q21 in lymphoblastoid cell lines

T. Pastinen, D. Sinnett, D. Verlaan, 2012, Human Genetics.

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.

Interaction between genetic and epigenetic variation defines gene expression patterns at the asthma-associated locus 17q12-q21 in lymphoblastoid cell lines

T. Pastinen, D. Sinnett, D. Verlaan, 2012, Human Genetics.

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

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

Identification of functional DNA variants in the constitutive promoter region of MDM2

D. Sinnett, E. Kritikou, M. Lalonde, 2012, Human Genomics.

Functional analysis of promoter variants in KU70 and their role in cancer susceptibility

J. Simard, D. Sinnett, E. Kritikou, 2012, Genes, chromosomes & cancer.

Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers.

F. Couch, T. Rebbeck, J. Benítez, 2011, Human molecular genetics.

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

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

Promoter polymorphisms in CHI3L1 are associated with asthma.

T. Pastinen, D. Sinnett, D. Sirois-Gagnon, 2012, The Journal of allergy and clinical immunology.

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.

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

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

A CHO stable pool production platform for rapid clinical development of trimeric SARS‐CoV‐2 spike subunit vaccine antigens

J. Schrag, J. Baardsnes, J. Kelly, 2023, Biotechnology and bioengineering.

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

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