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Author Details

Mathieu Bourgey
McGill University
2004
36
17
PMIDPaper TitleJournal TitlePublished Year
35943854Epigenetic and integrative cross-omics analyses of cerebral white matter hyperintensities on MRI.Brain2023
36515678Human CARMIL2 deficiency underlies a broader immunological and clinical phenotype than CD28 deficiency.J Exp Med2023
36327219Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative.PLoS Genet2022
35648852A systems biology approach identifies candidate drugs to reduce mortality in severely ill patients with COVID-19.Sci Adv2022
35720974PrecisionFDA Truth Challenge V2: Calling variants from short and long reads in difficult-to-map regions.Cell Genom2022
33976190A coordinated progression of progenitor cell states initiates urinary tract development.Nat Commun2021
33521749Cell-free DNA tissues of origin by methylation profiling reveals significant cell, tissue, and organ-specific injury related to COVID-19 severity.Med2021
34706766A small number of early introductions seeded widespread transmission of SARS-CoV-2 in Québec, Canada.Genome Med2021
34623332Inherited human c-Rel deficiency disrupts myeloid and lymphoid immunity to multiple infectious agents.J Clin Invest2021
34043590Rare loss-of-function variants in type I IFN immunity genes are not associated with severe COVID-19.J Clin Invest2021
34183838Inherited PD-1 deficiency underlies tuberculosis and autoimmunity in a child.Nat Med2021
34214472Humans with inherited T cell CD28 deficiency are susceptible to skin papillomaviruses but are otherwise healthy.Cell2021
31504792Legacy Data Confound Genomics Studies.Mol Biol Evol2020
31953485Latency and interval therapy affect the evolution in metastatic colorectal cancer.Sci Rep2020
33335541A Distributed Whole Genome Sequencing Benchmark Study.Front Genet2020
33398295Failure to replicate the association of rare loss-of-function variants in type I IFN immunity genes with severe COVID-19.medRxiv2020
32766608Cell-Free DNA in Blood Reveals Significant Cell, Tissue and Organ Specific injury and Predicts COVID-19 Severity.medRxiv2020
30582441Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot.Circ Res2019
31185495GenPipes: an open-source framework for distributed and scalable genomic analyses.Gigascience2019
27960086Integrated (epi)-Genomic Analyses Identify Subgroup-Specific Therapeutic Targets in CNS Rhabdoid Tumors.Cancer Cell2016
26588606Changes in the expression profiles of claudins during gonocyte differentiation and in seminomas.Andrology2016
27581031RNA-Seq as a Tool to Study the Tumor Microenvironment.Methods Mol Biol2016
24705254Genomic analysis of diffuse intrinsic pontine gliomas identifies three molecular subgroups and recurrent activating ACVR1 mutations.Nat Genet2014
25351205Variation in genomic landscape of clear cell renal cell carcinoma across Europe.Nat Commun2014
21572464Use of immunoglobulins in the prevention of GvHD in a xenogeneic NOD/SCID/γc- mouse model.Bone Marrow Transplant2012
22661320K27M mutation in histone H3.3 defines clinically and biologically distinct subgroups of pediatric diffuse intrinsic pontine gliomas.Acta Neuropathol2012
21573116ALG: automated genotype calling of Luminex assays.PLoS One2011
21769930Genome-wide detection and characterization of mating asymmetry in human populations.Genet Epidemiol2011
20617153Detection of fetomaternal genotype associations in early-onset disorders: evaluation of different methods and their application to childhood leukemia.J Biomed Biotechnol2010
20460642Replication analysis confirms the association of ARID5B with childhood B-cell acute lymphoblastic leukemia.Haematologica2010
17344279HLA related genetic risk for coeliac disease.Gut2007
18466566Power of the 2-locus TDT for testing the interaction of two susceptibility genes.BMC Proc2007
18466535Modeling the effect of PTPN22 in rheumatoid arthritis.BMC Proc2007
18046758Using linkage and association to identify and model genetic effects: summary of GAW15 Group 4.Genet Epidemiol2007
16451702Modeling the effect of a genetic factor for a complex trait in a simulated population.BMC Genet2005
15140032HLA-DQ relative risks for coeliac disease in European populations: a study of the European Genetics Cluster on Coeliac Disease.Tissue Antigens2004
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Collaborators

Guillaume Bourque
Institute for the Advanced Study of Human Biology (ASHBi), Kyoto University
Co-authored papers 16
David Langlais
McGill University
Co-authored papers 6
Louis Letourneau
Victor Philip Dahdaleh Institute of Genomic Medicine at McGill University
Co-authored papers 6
Robert Eveleigh
Victor Philip Dahdaleh Institute of Genomic Medicine at McGill University
Co-authored papers 6
Françoise Clerget-Darpoux
Co-authored papers 6
Pierre Lepage
Co-authored papers 5
Mark Lathrop
Victor Philip Dahdaleh Institute of Genomic Medicine at McGill University
Co-authored papers 5
Jiannis Ragoussis
McGill University
Co-authored papers 5
Alexandre Montpetit
McGill University and Genome Quebec Innovation Centre
Co-authored papers 4
Daniel Sinnett
Sainte-Justine University Hospital Research Center
Co-authored papers 4
Cynthia Hawkins
The Hospital for Sick Children
Co-authored papers 3
Ning Shang
Columbia University Irving Medical Center
Co-authored papers 3
Chadi Saad
Qatar Foundation Research, Qatar Foundation
Co-authored papers 3
Saleh A Alqahtani
King Faisal Specialist Hospital & Research Centre
Co-authored papers 3
Malak Abedalthagafi
Emory School of Medicine
Co-authored papers 3
Nada Jabado
McGill University Health Centre (MUHC), Montreal Children's Hospital (MCH)
Co-authored papers 3
Stephen W Scherer
The Hospital for Sick Children
Co-authored papers 3
Guillaume Butler-Laporte
McGill University
Co-authored papers 3
Said I Ismail
Qatar Foundation
Co-authored papers 3
Eric Bouffet
The Hospital for Sick Children
Co-authored papers 3
Krzysztof Kiryluk
Columbia University
Co-authored papers 3
Hamdi Mbarek
Vrije Universiteit
Co-authored papers 3
John Brent Richards
Lady Davis Institute for Medical Research, Jewish General Hospital
Co-authored papers 3
Yaseen M Arabi
King Saud bin Abdulaziz Medical City for Science and Technology
Co-authored papers 3
Manal Alaamery
National Centre for Genomic Technologies
Co-authored papers 3
Salam Massadeh
National Centre for Genomic Technologies
Co-authored papers 3
Vincent Mooser
McGill University
Co-authored papers 3
David B Goldstein
Institute for Genomic Medicine, Columbia University Irving Medical Center
Co-authored papers 3
Gundula Povysil
Institute for Genomic Medicine, Columbia University Medical Center
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Chantal Richer
CHU Sainte-Justine Research Center
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