This profile is built from public research funding records (CIHR, NSERC and SSHRC) and PubMed. We have not imported them from a McGill University directory, so their courses may be missing. Find their university profile.
Research
Latest papers
H3K27me3 spreading organizes canonical PRC1 chromatin architecture to regulate developmental programs.
Nature genetics · 2026
Report of two patients with variants in FOXL2 and KASH5 and review of gestational trophoblastic neoplasia after recurrent moles.
Journal of assisted reproduction and genetics · 2026
Lessons learned from the exome sequencing of nine cases of infertility and the way forward.
Reproductive biomedicine online · 2026
Latest funding
- $120,000
Mechanisms and Role of DNA Methylation in X-chromosome Inactivation
NSERC · 2022 · Principal investigator
- $187,500
HIT-GLIO – Targeting tumour-host interactions in paediatric malignant gliomas to reinvigorate immunity and improve radio- and immunotherapy efficacy
SSHRC · 2022 · Principal investigator
- $845,326
Investigating interdependencies between epigenetic modifications: towards combinatorial epigenetic cancer therapeutics
CIHR · 2022 · Nominated PI
From the 150 most recent of 217 publications.
H3K27me3 spreading organizes canonical PRC1 chromatin architecture to regulate developmental programs.
Krug B, Hu B, Chen H, Negrón-Lomas C, Chen X, El Mouatani A, Gretarsson KH, Ptack A, Deshmukh S, Kabir N, Jawhar W, Andrade AF, Jabbour E, Harutyunyan AS, Wang X, Taylor R, Lee JJY, Hulswit M, Faury D, Russo C, Xu X, Yang J, Baguette A, Dahl NA, Weil AG, Ellezam B, Dali R, Blanchette M, Wilson K, Garcia BA, Soni RK, Gallo M, Taylor MD, Kleinman CL, Majewski J, Jabado N, Lu C
Report of two patients with variants in FOXL2 and KASH5 and review of gestational trophoblastic neoplasia after recurrent moles.
Saharan A, Hemida R, Lefebvre M, Bareke E, Carile V, Abdalla E, Majewski J, Slim R
Lessons learned from the exome sequencing of nine cases of infertility and the way forward.
Broojeni JV, Elmahdy M, Mitchell S, Rezaei M, Saharan A, Elhady G, Safwat S, Bareke E, Abdelrazek I, Xu C, Li L, Buckett W, Ao A, Miron P, Majewski J, Abdalla E, Slim R
NSD2 inhibitors rewire chromatin to treat lung and pancreatic cancers.
Jeong J, Hausmann S, Dong H, Szczepski K, Flores NM, Garcia Gonzalez A, Shi L, Lu X, Lempiäinen J, Jakab M, Zeng L, Chasan T, Bareke E, Dong R, Carlson E, Padilla R, Husmann D, Thompson J, Shipman GA, Zahn E, Barnes CA, Khan LF, Albertorio-Sáez LM, Brill E, Kumary VUS, Marunde MR, Maryanski DN, Szany CC, Venters BJ, Windham CL, Nowakowski ME, Czaban I, Jaremko M, Keogh MC, Le K, Soth MJ, Garcia BA, Jaremko Ł, Majewski J, Mazur PK, Gozani O
Cellular reprogramming of H3K27M pediatric high-grade glioma to neuron-like state.
Uthamacumaran A, Horth C, Bareke E, Gravel M, Majewski J
H3K36 Methylation as a Guardian of Epigenome Integrity.
Padilla R, Shipman GA, Horth C, Gravel M, Bareke E, Majewski J
The mitotic STAG3-cohesin complex shapes male germline nucleome.
Nagano M, Hu B, Ogata K, Umemura F, Ishikura Y, Suzuki S, Katsifis CC, Yoshinaga M, Litos G, Nagasaka K, Tang W, Nosaka Y, Sasada H, Wang H, Kondo D, Katou Y, Mizuta K, Yabuta Y, Ohta H, de Luna Vitorino FN, Arima H, Ichikawa T, Gabriele M, Majewski J, Garcia BA, Takeuchi O, Yoshida S, Hansen AS, Peters JM, Ishihama Y, Saitou M
Two Novel Protein-Truncating Variants in NLRP2 and Their Functional Impacts on the Subcortical Maternal Complex.
Yalcin Z, Gao Z, Abdelrazek IM, Bareke E, Majewski J, Abdalla E, Tan SL, Li L, Slim R
Using multiple modalities to confirm diagnosis in patients with suspected peroxisome biogenesis disorders.
Cheung ACT, Di Pietro E, Argyriou C, Bareke E, D'Souza Y, Puri RD, Muhammed Shabeer P, Ganetzky R, Goldstein A, Vanderver A, Mohan S, Majewski J, Yergeau C, Braverman N
ChIPbinner: an R package for analyzing broad histone marks binned in uniform windows from ChIP-Seq or CUT&RUN/TAG data.
Padilla R, Bareke E, Hu B, Majewski J
Mechanisms and Role of DNA Methylation in X-chromosome Inactivation
Principal investigators: Majewski, Jacek
HIT-GLIO – Targeting tumour-host interactions in paediatric malignant gliomas to reinvigorate immunity and improve radio- and immunotherapy efficacy
Principal investigators: Majewski, Jacek
Keywords: Paeditric Glioma; Tumor microenvironment; Immune therapy; Genomics; Bioinformatics; Epigenetics
Investigating interdependencies between epigenetic modifications: towards combinatorial epigenetic cancer therapeutics
Principal investigators: Majewski, Jacek A
Keywords: Cancer; Dna Methylation; Epigenetics; Genomics; Histone Modifications
The role of spliceosome proteins in disease and development
Principal investigators: Jerome-Majewska, Loydie A
Keywords: Congenital Malformations; Craniofacial Development; Mfdm; Mouse Models; Nager; Splicing
Resolving the cis-regulatory role of the histone post-translational modification H3K36me2 in driving tumorigenesis
Principal investigators: Hu, Bo
Keywords: Chromatin Conformation Capture; Cis-Regulation; Dna Methylation; Enhancer; Epigenetics; H3k36me2; Histone Modifications; Nuclear Architecture; Oncohistones; Tumorigenesis
Tackling Childhood Brain Cancer at the root to improve survival and quality of life
Principal investigators: Jabado, Nada
Keywords: Epigenetically Deregulated Cancers
Splicing Defects in Human Hereditary Disease
Principal investigators: Majewski, Jacek A
Keywords: Animal Models; Genetic Disease; Genome Editing; Genomics; Rna Sequencing
Inherited susceptibility to cancer: from gene discovery to mechanisms to clinical applications
Principal investigators: Foulkes, William D
Keywords: Dicer1; Founder Mutations; Genetic Predisposition; Hereditary Cancer; Multiple Primary Tumors; Rare Tumours
ICS IG 2014 Computational Biology Undergraduate Summer Student Health Research award - Analysis of RNA-sequencing data.
Principal investigators: Osmond, Matthew
Keywords: Graphic Interface
Identifying the genetic causes of ataxias using Next-generation sequencing (NGS) methods.
Principal investigators: Tetreault, Martine
Keywords: Ataxia; Gene Identification; Human Genetics; Mri Anomalies; Neurodegenerative Disorder; Next-Generation Sequencing; Whole-Exome Sequencing
From CIHR, NSERC and SSHRC funding decisions: CIHR since 2008, NSERC since 1991 and SSHRC since 1998, including their latest published competition results.
Frequent collaborators
- Human Genetics
- Pediatrics
- Neurology and Neurosurgery
- Pathology and Laboratory Medicine
- Social Studies of Medicine
- Nutritional Sciences
- Biochemistry
- Other
Co-authors at McGill University, colored by department. Thicker lines mean more shared papers; select anyone to open their profile and their own map.
Nada Jabado
Pediatrics
35 shared papers, latest 2026
Rima Slim
Human Genetics
12 shared papers, latest 2026
Taila Hartley
Faculty
11 shared papers, latest 2020
Tomi Pastinen
Human Genetics
10 shared papers, latest 2022
Bernard Brais
Neurology and Neurosurgery
9 shared papers, latest 2020
Frank Rauch
Faculty
7 shared papers, latest 2015
Mark Lathrop
Faculty
7 shared papers, latest 2020
Jason Karamchandani
Neurology and Neurosurgery
6 shared papers, latest 2022
Jason Karamchandani
Faculty
6 shared papers, latest 2022
Mathieu Blanchette
Faculty
6 shared papers, latest 2026
Jean Michaud
Pathology and Laboratory Medicine
5 shared papers, latest 2016
Mark Basik
Social Studies of Medicine
5 shared papers, latest 2023
Adam Fleming
Pediatrics
5 shared papers, latest 2016
David Grynspan
Nutritional Sciences
4 shared papers, latest 2017
Roberta La Piana
Neurology and Neurosurgery
4 shared papers, latest 2017
Guillaume Bourque
Human Genetics
4 shared papers, latest 2024
Nancy Braverman
Human Genetics
4 shared papers, latest 2025
Philippe Gros
Biochemistry
4 shared papers, latest 2020
Pierre Moffatt
Human Genetics
4 shared papers, latest 2015
Myriam Srour
Pediatrics
3 shared papers, latest 2015
Myriam Srour
Faculty
3 shared papers, latest 2015
Pranesh Chakraborty
Pediatrics
3 shared papers, latest 2016
Marco Gallo
Biochemistry and Molecular Biology
3 shared papers, latest 2026
David Langlais
Rheumatology
3 shared papers, latest 2020
Mark Tarnopolsky
Pediatrics
3 shared papers, latest 2020
Catalin Mihalcioiu
Medicine
3 shared papers, latest 2023
Annie Huang
Pediatrics
3 shared papers, latest 2017
Yasser Riazalhosseini
Human Genetics
3 shared papers, latest 2020
François Rousseau
Faculty
3 shared papers, latest 2017
Peter Siegel
Experimental Medicine
3 shared papers, latest 2012
Peter Humphreys
Pediatrics
2 shared papers, latest 2015
Gelareh Zadeh
Faculty
2 shared papers, latest 2013
Eva Tomiak
Department of Medicine
2 shared papers, latest 2017
Jana Feberova
Faculty
2 shared papers, latest 2015
Daniel Schramek
Lunenfeld-Tanenbaum Research Institute
2 shared papers, latest 2019
Karine Khatchadourian
Faculty
2 shared papers, latest 2015
Simon Gravel
Human Genetics
2 shared papers, latest 2019
Malgorzata Nowaczyk
Pathology & Molecular Medicine
2 shared papers, latest 2017
Peter Roughley
Faculty
2 shared papers, latest 2013
Frank Sicheri
Lunenfeld-Tanenbaum Research Institute
2 shared papers, latest 2019
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