Alexandre Montpetit

3175 Côte Ste Catherine
Montreal, QC H3T1C5, Canada

Last Updated: 09/26/2026

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Found 33 publications

A multi-ancestry genetic reference for the Quebec population.

A multi-ancestry genetic reference for the Quebec population.

Journal: medRxiv : the preprint server for health sciences

Published: June 04, 2025

A multi-ancestry genetic reference for the Quebec population.

A multi-ancestry genetic reference for the Quebec population.

Journal: Nature communications

Published: May 25, 2025

Transcriptomic profiling of severe and critical COVID-19 patients reveals alterations in expression, splicing and polyadenylation.

Transcriptomic profiling of severe and critical COVID-19 patients reveals alterations in expression, splicing and polyadenylation.

Journal: Scientific reports

Published: September 10, 2024

Deciphering a novel complex inversion affecting F8 in a family with severe haemophilia A by optical genome mapping.

Deciphering a novel complex inversion affecting F8 in a family with severe haemophilia A by optical genome mapping.

Journal: Haemophilia : the official journal of the World Federation of Hemophilia

Published: January 02, 2023

A full molecular picture of F8 intron 1 inversion created with optical genome mapping.

A full molecular picture of F8 intron 1 inversion created with optical genome mapping.

Journal: Haemophilia : the official journal of the World Federation of Hemophilia

Published: January 12, 2021

The Biobanque québécoise de la COVID-19 (BQC19)-A cohort to prospectively study the clinical and biological determinants of COVID-19 clinical trajectories.

The Biobanque québécoise de la COVID-19 (BQC19)-A cohort to prospectively study the clinical and biological determinants of COVID-19 clinical trajectories.

Journal: PloS one

Published: December 23, 2020

Publisher Correction: Toxoplasma Modulates Signature Pathways of Human Epilepsy, Neurodegeneration & Cancer.

Publisher Correction: Toxoplasma Modulates Signature Pathways of Human Epilepsy, Neurodegeneration & Cancer.

Journal: Scientific reports

Published: May 28, 2019

Integrative genomic analysis of matched primary and metastatic pediatric osteosarcoma.

Integrative genomic analysis of matched primary and metastatic pediatric osteosarcoma.

Journal: The Journal of pathology

Published: December 31, 2018

H3K27M induces defective chromatin spread of PRC2-mediated repressive H3K27me2/me3 and is essential for glioma tumorigenesis.

H3K27M induces defective chromatin spread of PRC2-mediated repressive H3K27me2/me3 and is essential for glioma tumorigenesis.

Journal: Nature communications

Published: November 07, 2018

Publisher Correction: A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients.

Publisher Correction: A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients.

Journal: Nature communications

Published: February 04, 2018

APRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients.

APRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients.

Journal: Nature communications

Published: May 05, 2017

Toxoplasma Modulates Signature Pathways of Human Epilepsy, Neurodegeneration & Cancer.

Toxoplasma Modulates Signature Pathways of Human Epilepsy, Neurodegeneration & Cancer.

Journal: Scientific reports

Published: November 14, 2016

Showing 1-12 of 33

Last Updated: 09/26/2026