This profile is built from public research funding records (CIHR, NSERC and SSHRC) and PubMed. We have not imported them from a Université de Montréal directory, so their courses may be missing. Find their university profile.
Research
Latest papers
Comparing bulk and single-cell methodologies and models to profile gene expression, chromatin accessibility and regulatory links in endothelial cells treated with TNFα.
bioRxiv : the preprint server for biology · 2026 · senior author
Comparing bulk and single-cell methodologies and models to profile gene expression, chromatin accessibility and regulatory links in endothelial cells treated with TNFα.
Biochemistry and biophysics reports · 2026 · senior author
Plasma proteome signatures are predictive of mortality in sickle cell disease.
Blood advances · 2026 · senior author
Latest funding
- $27,000
Identification de biomarqueurs génétiques et protéomiques associés à la réponse aux entraînements physiques et cognitifs
CIHR · 2026 · Supervisor
- $140,000
Projet Omics intégrés en maladie falciforme (Projet FALC-OMICS)
CIHR · 2026 · Supervisor
- $140,000
Enabling sensitive genome-wide associations of structural variants with disease traits using a Quebec pangenome
CIHR · 2024 · Supervisor
128 publications.
Comparing bulk and single-cell methodologies and models to profile gene expression, chromatin accessibility and regulatory links in endothelial cells treated with TNFα.
Zevounou J, Lo KS, McGinnis CS, Satpathy AT, Lettre G
Comparing bulk and single-cell methodologies and models to profile gene expression, chromatin accessibility and regulatory links in endothelial cells treated with TNFα.
Zevounou J, Lo KS, McGinnis CS, Satpathy AT, Lettre G
Plasma proteome signatures are predictive of mortality in sickle cell disease.
Chignon A, Zaouali Y, Galactéros F, Bartolucci P, Lettre G
Genetic Contribution to Asthma Informs Acute Chest Syndrome Pathophysiology and Risk Stratification.
El Aouhel S, Bellegarde V, Da Silva Faria S, St-Laurent T, Lecluze E, Pham Hung d'Alexandry d'Orengiani AL, Galactéros F, Bartolucci P, Legault MA, Lettre G, Pincez T
Whole Blood Transcriptomic Analysis of Sickle Cell Trait.
Johnson M, Cai Y, Vasconcelos AG, Orchard P, Auer PL, Lettre G, Wen J, Franceschini N, Kooperberg C, Sun W, Hsu L, Raffield LM, Reiner AP
A multi-ancestry genetic reference for the Quebec population.
McClelland P, Femerling G, Laflamme R, Mejia-Garcia A, Sayahian Dehkordi M, Xiao H, Diaz-Papkovich A, Pelletier J, Grenier JC, Lo KS, Anderson-Trocmé L, Bellavance J, Chapdelaine V, Gagnon G, De Mori A, Martinez G, Mohler K, de Malliard T, Labbé C, Labrecque M, Montpetit A, Spiegelman D, Rouleau GA, Théroux JF, Zhou H, Girard SL, Hussin JG, Laberge AM, Bhérer C, Tetreault M, Gagliano Taliun SA, Taliun D, Gravel S, Lettre G
Long-read Sequences Mapped to a Complete Reference Genome Uncover Uncaptured Structural Variants across the Beta-globin Cluster in Africans with Sickle Cell Disease.
Lurie P, Mahmoud M, Haldipur A, Han Y, Li Q, Wonkam-Tingang E, Asmus N, Banfield E, Hall NJ, Tayo B, Cooper R, Akingbola T, Ayodo G, Obaro S, Lettre G, Meng Q, Jhangiani S, Harris RA, Worley KC, Kim J, Rhie A, Phillippy AM, Sedlazeck F, Wonkam A, Hanchard NA
Albuminuria Predicts a Rapid Decline in Kidney Function in 2 International, Longitudinal Cohorts of Adults With Sickle Cell Anemia.
Bartolucci P, Audureau É, Audard V, Galactéros F, Lettre G, Anthony C, Egbujo O, Han J, Ruiz MA, Lash JP, Gordeuk VR, Zhang X, Saraf SL
Using the ancestral recombination graph to study the history of rare variants in founder populations.
Mejia-Garcia A, Diaz-Papkovich A, Sillon G, D'Agostino D, Chong AL, Chong G, Lo KS, Baret L, Hamel N, Chapdelaine V, Foulkes WD, Taliun D, Shapiro AJ, Lettre G, Gravel S
Visceral adipose tissue and hepatic fat as determinants of carotid atherosclerosis.
de Souza RJ, Pigeyre ME, Schulze KM, Lamri A, Al-Khazraji BK, Awadalla P, Beyene J, Desai D, Despres JP, Dummer TJB, Friedrich MG, Hicks J, Ho V, LaRose É, Lear SA, Lee DS, Leipsic JA, Lettre G, Moody AR, Noseworthy MD, Pare G, Parraga G, Poirier P, Tardif JC, Yusuf S, Vena J, Anand SS
Identification de biomarqueurs génétiques et protéomiques associés à la réponse aux entraînements physiques et cognitifs
Principal investigators: van der Schaaf, Arianne
Keywords: Apprentissage Machine; Biobanques; Biomarqueurs; Entraînement Physique Et Cognitif; Génétique Humaine; Médecine De Précision; Protéomique; Réponse À L'Exercice; Santé Cardiovasculaire Et Cérébrale; Études De Population
Projet Omics intégrés en maladie falciforme (Projet FALC-OMICS)
Principal investigators: Hachemi, Hamid
Keywords: Bioinformatique; Génétique; Intelligence Artificielle; Maladie Falciforme; Médecine De Précision; Métabolomique; Protéomique; Prédiction; Sciences Omics
Enabling sensitive genome-wide associations of structural variants with disease traits using a Quebec pangenome
Principal investigators: Groza, Cristian
Keywords: Biostatistics; Genetics
Discovery of new biomarkers and drug targets in sickle cell disease
Principal investigators: Lettre, Guillaume
Keywords: Biomarkers; Drug Targets; Human Genetics; Polygenic Scores; Proteomics; Sickle Cell Disease; Single-Cell Transcriptomics
Canada Research Chair Tier 1
Principal investigators: Lettre, Guillaume
Keywords: Crc
Endothelial cell genetics and blood pressure regulation
Principal investigators: Lettre, Guillaume
Keywords: Blood Pressure; Coding/Non-Coding Rare Variants; Crispr/Cas9; Functional Genomics; Genome-Wide Association Studies (Gwas); Human Genetics; Hypertension; Vascular Endothelial Cells; Whole-Genome Sequencing
Complex genetics of hypertrophic cardiomyopathy: Towards an integration of polygenic risk in clinical care
Principal investigators: Tadros, Rafik; Lettre, Guillaume
Keywords: Cardiac Arrhythmia; Cardiac Magnetic Resonance; Cardiac Ultrasound; Genetics; Genome-Wide Association Study; Hypertrophic Cardiomyopathy; Polygenic Risk Score
The genetics of erythrocyte volume homeostasis
Principal investigators: Lettre, Guillaume
Keywords: Anemia; Genome Editing/Crispr-Cas9; Genome-Wide Association Study; Malaria; Next-Generation Dna Sequencing; Red Blood Cell/Erythrocyte Volume; Sickle Cell Disease
Developing cellular models to study hematopoiesis
Principal investigators: Lettre, Guillaume
Identification of cardiovascular risk factors using whole-genome sequencing
Principal investigators: Gauthier, Louis
Keywords: Ics Studentship
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
- Medicine
- Psychiatry
- Human Genetics
- Nutrition
- Chemical Engineering
- Surgery
- Pediatrics
- Other
Co-authors at Université de Montréal, colored by department. Thicker lines mean more shared papers; select anyone to open their profile and their own map.
Jean-Claude Tardif
Chemical Engineering
26 shared papers, latest 2025
Jean-Claude Tardif
Medicine
26 shared papers, latest 2025
Simon De Denus
Faculty
7 shared papers, latest 2025
Rudolf Uher
Psychiatry
5 shared papers, latest 2019
Rafik Tadros
Faculty
5 shared papers, latest 2025
Eric Thorin
Faculty
4 shared papers, latest 2025
Eric Thorin
Surgery
4 shared papers, latest 2025
Julia Cadrin-Tourigny
Faculty
4 shared papers, latest 2025
Stanley Nattel
Medicine
4 shared papers, latest 2025
Simon Gravel
Human Genetics
3 shared papers, latest 2026
Daniel Taliun
Faculty
3 shared papers, latest 2026
Daniel Taliun
Human Genetics
3 shared papers, latest 2026
Marie-Claude Vohl
Nutrition
3 shared papers, latest 2025
Matthieu Ruiz
Nutrition
2 shared papers, latest 2023
Louis Pérusse
Kinesiologie
2 shared papers, latest 2025
Manuel Mattheisen
Psychiatry
2 shared papers, latest 2025
Anne-Marie Laberge
Pediatrics
2 shared papers, latest 2026
Jason Roberts
Medicine
2 shared papers, latest 2022
Mark Walker
Faculty
1 shared papers, latest 2012
Alain Bitton
Faculty
1 shared papers, latest 2013
Christine Des Rosiers
Faculty
1 shared papers, latest 2023
Guillaume Pare
Pathology & Molecular Medicine
1 shared papers, latest 2012
Jeff Healey
Medicine
1 shared papers, latest 2022
A short, specific email works best. This draft uses one of their recent papers; replace the parts in brackets with your own details before sending.