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Author Details

Alexandre Montpetit
McGill University and Genome Quebec Innovation Centre
1998
96
49
PMIDPaper TitleJournal TitlePublished Year
36897533Deciphering a novel complex inversion affecting F8 in a family with severe haemophilia A by optical genome mapping.Haemophilia2023
36897533Deciphering a novel complex inversion affecting F8 in a family with severe haemophilia A by optical genome mapping.Haemophilia2023
34232555A full molecular picture of F8 intron 1 inversion created with optical genome mapping.Haemophilia2021
34232555A full molecular picture of F8 intron 1 inversion created with optical genome mapping.Haemophilia2021
34010280The Biobanque québécoise de la COVID-19 (BQC19)-A cohort to prospectively study the clinical and biological determinants of COVID-19 clinical trajectories.PLoS One2021
34010280The Biobanque québécoise de la COVID-19 (BQC19)-A cohort to prospectively study the clinical and biological determinants of COVID-19 clinical trajectories.PLoS One2021
30890717H3K27M induces defective chromatin spread of PRC2-mediated repressive H3K27me2/me3 and is essential for glioma tumorigenesis.Nat Commun2019
31236944Integrative genomic analysis of matched primary and metastatic pediatric osteosarcoma.J Pathol2019
30890717H3K27M induces defective chromatin spread of PRC2-mediated repressive H3K27me2/me3 and is essential for glioma tumorigenesis.Nat Commun2019
31236944Integrative genomic analysis of matched primary and metastatic pediatric osteosarcoma.J Pathol2019
29302025APRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients.Nat Commun2018
29396438Publisher Correction: A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients.Nat Commun2018
29302025APRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients.Nat Commun2018
29396438Publisher Correction: A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients.Nat Commun2018
28904337Toxoplasma Modulates Signature Pathways of Human Epilepsy, Neurodegeneration & Cancer.Sci Rep2017
28904337Toxoplasma Modulates Signature Pathways of Human Epilepsy, Neurodegeneration & Cancer.Sci Rep2017
27624058Immunoseq: the identification of functionally relevant variants through targeted capture and sequencing of active regulatory regions in human immune cells.BMC Med Genomics2016
26242991Screening of dementia genes by whole-exome sequencing in early-onset Alzheimer disease: input and lessons.Eur J Hum Genet2016
27624058Immunoseq: the identification of functionally relevant variants through targeted capture and sequencing of active regulatory regions in human immune cells.BMC Med Genomics2016
27960086Integrated (epi)-Genomic Analyses Identify Subgroup-Specific Therapeutic Targets in CNS Rhabdoid Tumors.Cancer Cell2016
27581031RNA-Seq as a Tool to Study the Tumor Microenvironment.Methods Mol Biol2016
26242991Screening of dementia genes by whole-exome sequencing in early-onset Alzheimer disease: input and lessons.Eur J Hum Genet2016
27581031RNA-Seq as a Tool to Study the Tumor Microenvironment.Methods Mol Biol2016
27960086Integrated (epi)-Genomic Analyses Identify Subgroup-Specific Therapeutic Targets in CNS Rhabdoid Tumors.Cancer Cell2016
25882982Molecular subgroups of atypical teratoid rhabdoid tumours in children: an integrated genomic and clinicopathological analysis.Lancet Oncol2015
25882982Molecular subgroups of atypical teratoid rhabdoid tumours in children: an integrated genomic and clinicopathological analysis.Lancet Oncol2015
26378811Non-random aneuploidy specifies subgroups of pilocytic astrocytoma and correlates with older age.Oncotarget2015
26378811Non-random aneuploidy specifies subgroups of pilocytic astrocytoma and correlates with older age.Oncotarget2015
24121462Control of spasticity in a multiple sclerosis model using central nervous system-excluded CB1 cannabinoid receptor agonists.FASEB J2014
24362726Variation at the DPP4 locus influences apolipoprotein B levels in South Asians and exhibits heterogeneity in Europeans related to BMI.Diabetologia2014
24316981Fusion of TTYH1 with the C19MC microRNA cluster drives expression of a brain-specific DNMT3B isoform in the embryonal brain tumor ETMR.Nat Genet2014
24123875Somatic point mutations occurring early in development: a monozygotic twin study.J Med Genet2014
24121462Control of spasticity in a multiple sclerosis model using central nervous system-excluded CB1 cannabinoid receptor agonists.FASEB J2014
24705254Genomic analysis of diffuse intrinsic pontine gliomas identifies three molecular subgroups and recurrent activating ACVR1 mutations.Nat Genet2014
24885784Disruption of Mycobacterium avium subsp. paratuberculosis-specific genes impairs in vivo fitness.BMC Genomics2014
24686056ALOX12 in human toxoplasmosis.Infect Immun2014
24885784Disruption of Mycobacterium avium subsp. paratuberculosis-specific genes impairs in vivo fitness.BMC Genomics2014
24686056ALOX12 in human toxoplasmosis.Infect Immun2014
24705254Genomic analysis of diffuse intrinsic pontine gliomas identifies three molecular subgroups and recurrent activating ACVR1 mutations.Nat Genet2014
24316981Fusion of TTYH1 with the C19MC microRNA cluster drives expression of a brain-specific DNMT3B isoform in the embryonal brain tumor ETMR.Nat Genet2014
24362726Variation at the DPP4 locus influences apolipoprotein B levels in South Asians and exhibits heterogeneity in Europeans related to BMI.Diabetologia2014
24123875Somatic point mutations occurring early in development: a monozygotic twin study.J Med Genet2014
22935230Harnessing genomics to identify environmental determinants of heritable disease.Mutat Res2013
22935230Harnessing genomics to identify environmental determinants of heritable disease.Mutat Res2013
23603917Genetic information and the prediction of incident type 2 diabetes in a high-risk multiethnic population: the EpiDREAM genetic study.Diabetes Care2013
23423674MEDNIK syndrome: a novel defect of copper metabolism treatable by zinc acetate therapy.Brain2013
23417712Mutations in SETD2 and genes affecting histone H3K36 methylation target hemispheric high-grade gliomas.Acta Neuropathol2013
23538714Buccals are likely to be a more informative surrogate tissue than blood for epigenome-wide association studies.Epigenetics2013
23250129Diversity of ARSACS mutations in French-Canadians.Can J Neurol Sci2013
23603917Genetic information and the prediction of incident type 2 diabetes in a high-risk multiethnic population: the EpiDREAM genetic study.Diabetes Care2013
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Collaborators

Thomas J Hudson
Ontario Institute for Cancer Research
Co-authored papers 29
James C Engert
Co-authored papers 12
Nada Jabado
McGill University Health Centre (MUHC), Montreal Children's Hospital (MCH)
Co-authored papers 11
Pierre Lepage
Co-authored papers 9
Tomi Pastinen
Co-authored papers 8
Sonia S Anand
Co-authored papers 8
L??szl?? Bogn??r
BRC-Biological Research Centre
Co-authored papers 8
Daniel Sinnett
Sainte-Justine University Hospital Research Center
Co-authored papers 8
Swneke D Bailey
Research Institute of the McGill University Health Centre
Co-authored papers 7
Guillaume Paré
Co-authored papers 7
Cynthia Hawkins
The Hospital for Sick Children
Co-authored papers 6
Almos Klekner
University of Debrecen
Co-authored papers 6
Vincent Ferretti
Ontario Institute for Cancer Research
Co-authored papers 6
Robert Sladek
Co-authored papers 6
Guillaume Bourque
Institute for the Advanced Study of Human Biology (ASHBi), Kyoto University
Co-authored papers 6
Salim Yusuf
Co-authored papers 6
Uri Tabori
Co-authored papers 5
Louis Letourneau
Victor Philip Dahdaleh Institute of Genomic Medicine at McGill University
Co-authored papers 5
Brent W Zanke
University of Toronto
Co-authored papers 5
Andrei Verner
Co-authored papers 5
Steven Gallinger
Lunenfeld Tanenbaum Research Institute, Mount Sinai Hospital, University of Toronto
Co-authored papers 5
Celia M T Greenwood
Co-authored papers 5
Mathieu Lemire
The Hospital for Sick Children
Co-authored papers 5
Eric Bouffet
The Hospital for Sick Children
Co-authored papers 5
Daniel Gaudet
Co-authored papers 5
Mathieu Bourgey
McGill University
Co-authored papers 4
David Meyre
Co-authored papers 4
Marcel Kool
Hopp Children's Cancer Center (KiTZ)
Co-authored papers 4
Andrey Korshunov
Institute of Pathology, University Hospital Heidelberg
Co-authored papers 4
Philippe Froguel
Co-authored papers 4
Release 1.2