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 and email address may be missing. Find their university profile.
Research
Latest papers
Exploring and visualizing stratified GWAS results with PheWeb2
Nature Genetics · 2026
A multi-ancestry genetic reference for the Quebec population.
Nature communications · 2026
Phenome-Wide Mendelian Randomization Identifying Circulating Proteins for Cardiovascular Traits in Populations of African Ancestry.
Circulation. Genomic and precision medicine · 2026
Latest funding
- $70,000
Expanding CLSA PheWeb: Interactive visualization of ordinal categorical genetic variant-phenotype associations and time-to-event associations
CIHR · 2024 · Principal investigator
- $70,000
Interactive visualization of genetic variant-trait associations in the CLSA dataset
CIHR · 2023 · Principal investigator
8 publications.
Exploring and visualizing stratified GWAS results with PheWeb2
Bellavance J, Xiao H, Chang L, Kazemi M, Wickramasinghe S, Mayhew AJ, Raina P, VandeHaar P, Taliun D, Gagliano Taliun SA
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
Phenome-Wide Mendelian Randomization Identifying Circulating Proteins for Cardiovascular Traits in Populations of African Ancestry.
Selber-Hnatiw S, Trajanoska K, Pelletier J, Su CY, McClelland P, Taliun D, Yoshiji S, Mooser V, Bhérer C, Zhou S
CRISPR-BEasy: a free web-based service for designing sgRNA tiling libraries for CRISPR-dependent base editing screens.
Chapdelaine-Trépanier V, Shenoy S, Masud W, Minju-Op A, Bérubé MA, Schönherr S, Forer L, Fradet-Turcotte A, Taliun D, Cuella-Martin R
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
A multi-ancestry genetic reference for the Quebec population.
McClelland P, Femerling G, Laflamme R, Mejia-Garcia A, Dehkordi MS, Xiao H, Diaz-Papkovich A, Pelletier J, Grenier JC, Lo KS, Anderson-Trocmé L, Bellavance J, Chapdelaine V, Gagnon G, 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
Imputation Server PGS: an automated approach to calculate polygenic risk scores on imputation servers.
Forer L, Taliun D, LeFaive J, Smith AV, Boughton AP, Coassin S, Lamina C, Kronenberg F, Fuchsberger C, Schönherr S
From target discovery to clinical drug development with human genetics.
Trajanoska K, Bhérer C, Taliun D, Zhou S, Richards JB, Mooser V
Expanding CLSA PheWeb: Interactive visualization of ordinal categorical genetic variant-phenotype associations and time-to-event associations
Principal investigators: Gagliano Taliun, Sarah A; Taliun, Daniel
Keywords: Genome-Wide Association; Longitudinal Data; Ordinal Categorical Data
Interactive visualization of genetic variant-trait associations in the CLSA dataset
Principal investigators: Gagliano Taliun, Sarah A; Taliun, Daniel
Keywords: Genome-Wide Association; Phenome-Wide Association; Traits Of Aging
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
- Vincent Mooser and Sirui Zhou: 10 shared papers
- Sirui Zhou and Satoshi Yoshiji: 9 shared papers
- Daniel Taliun and Daniel Taliun: 8 shared papers
- Vincent Mooser and Daniel Taliun: 4 shared papers
- Sirui Zhou and Daniel Taliun: 4 shared papers
- Guillaume Lettre and Simon Gravel: 3 shared papers
- Guillaume Lettre and Daniel Taliun: 3 shared papers
- Guillaume Lettre and Daniel Taliun: 3 shared papers
- Simon Gravel and Daniel Taliun: 3 shared papers
- Simon Gravel and Daniel Taliun: 3 shared papers
- Vincent Mooser and Satoshi Yoshiji: 3 shared papers
- Daniel Taliun and Satoshi Yoshiji: 3 shared papers
- Guillaume Lettre and Anne-Marie Laberge: 2 shared papers
- Anne-Marie Laberge and Simon Gravel: 2 shared papers
- Anne-Marie Laberge and Daniel Taliun: 2 shared papers
- Vincent Mooser and Daniel Taliun: 2 shared papers
- Sirui Zhou and Daniel Taliun: 2 shared papers
- Parminder Raina and Sirui Zhou: 1 shared paper
- Parminder Raina and Daniel Taliun: 1 shared paper
- Parminder Raina and Daniel Taliun: 1 shared paper
- Raquel Cuella Martin and Daniel Taliun: 1 shared paper
- Raquel Cuella Martin and Daniel Taliun: 1 shared paper
- Daniel Taliun and Satoshi Yoshiji: 1 shared paper
- Human Genetics
- Pediatrics
- Health Research Methods, Evidence, and Impact
- 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.
Daniel Taliun
Human Genetics
8 shared papers, latest 2026
Simon Gravel
Human Genetics
3 shared papers, latest 2026
Guillaume Lettre
Faculty
3 shared papers, latest 2026
Anne-Marie Laberge
Pediatrics
2 shared papers, latest 2026
Vincent Mooser
Faculty
2 shared papers, latest 2026
Sirui Zhou
Faculty
2 shared papers, latest 2026
Satoshi Yoshiji
Human Genetics
1 shared papers, latest 2026
Parminder Raina
Health Research Methods, Evidence, and Impact
1 shared papers, latest 2026
Raquel Cuella Martin
Human Genetics
1 shared papers, latest 2025
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.