This profile is built from public research funding records (CIHR, NSERC and SSHRC) and PubMed. We have not imported them from a Université Laval directory, so their courses may be missing. Find their university profile.
Research
Latest papers
CRISPR-Cas9-driven antigen conversion of clinically relevant blood group systems.
Human molecular genetics · 2025
In vivo dissection of the mouse tyrosine catabolic pathway with CRISPR-Cas9 identifies modifier genes affecting hereditary tyrosinemia type 1.
Genetics · 2024 · senior author
Dairy phages escape CRISPR defence of Streptococcus thermophilus via the anti-CRISPR AcrIIA3.
International journal of food microbiology · 2023
Latest funding
- $1,120,725
In vivo genome editing for inborn errors of metabolism.
CIHR · 2024 · Nominated PI
- $937,126
Orthologous CRISPR-Cas9 systems for genome editing: discovery, characterization and development for novel biotechnological applications.
CIHR · 2019 · Nominated PI
- $105,000
CRISPR-mediated engineering of autophagy-deficient human T lymphocytes for CAR-T cell immunotherapy
CIHR · 2018 · Supervisor
20 publications.
CRISPR-Cas9-driven antigen conversion of clinically relevant blood group systems.
Boccacci Y, Dumont N, Doyon Y, Laganière J
In vivo dissection of the mouse tyrosine catabolic pathway with CRISPR-Cas9 identifies modifier genes affecting hereditary tyrosinemia type 1.
Rivest JF, Carter S, Goupil C, Antérieux P, Cyr D, Ung RV, Dal Soglio D, Mac-Way F, Waters PJ, Paganelli M, Doyon Y
Dairy phages escape CRISPR defence of Streptococcus thermophilus via the anti-CRISPR AcrIIA3.
Pastuszka A, Rousseau GM, Somerville V, Levesque S, Fiset JP, Goulet A, Doyon Y, Moineau S
Accessory-cell-free differentiation of hematopoietic stem and progenitor cells into mature red blood cells.
Boccacci Y, Dumont N, Doyon Y, Laganière J
Marker-free co-selection for successive rounds of prime editing in human cells.
Levesque S, Mayorga D, Fiset JP, Goupil C, Duringer A, Loiselle A, Bouchard E, Agudelo D, Doyon Y
Recurrent chromosomal translocations in sarcomas create a megacomplex that mislocalizes NuA4/TIP60 to Polycomb target loci.
Sudarshan D, Avvakumov N, Lalonde ME, Alerasool N, Joly-Beauparlant C, Jacquet K, Mameri A, Lambert JP, Rousseau J, Lachance C, Paquet E, Herrmann L, Thonta Setty S, Loehr J, Bernardini MQ, Rouzbahman M, Gingras AC, Coulombe B, Droit A, Taipale M, Doyon Y, Côté J
Rewired Cas9s with Minimal Sequence Constraints.
Levesque S, Agudelo D, Doyon Y
Versatile and robust genome editing with Streptococcus thermophilus CRISPR1-Cas9.
Agudelo D, Carter S, Velimirovic M, Duringer A, Rivest JF, Levesque S, Loehr J, Mouchiroud M, Cyr D, Waters PJ, Laplante M, Moineau S, Goulet A, Doyon Y
Cas9 Allosteric Inhibition by the Anti-CRISPR Protein AcrIIA6.
Fuchsbauer O, Swuec P, Zimberger C, Amigues B, Levesque S, Agudelo D, Duringer A, Chaves-Sanjuan A, Spinelli S, Rousseau GM, Velimirovic M, Bolognesi M, Roussel A, Cambillau C, Moineau S, Doyon Y, Goulet A
Widespread anti-CRISPR proteins in virulent bacteriophages inhibit a range of Cas9 proteins
Hynes AP, Rousseau GM, Agudelo D, Goulet A, Amigues B, Loehr J, Romero DA, Fremaux C, Horvath P, Doyon Y
In vivo genome editing for inborn errors of metabolism.
Principal investigators: Doyon, Yannick
Keywords: Adeno Associated Virus (Aav); Crispr-Cas9; Genome Editing; In Vivo Genetic Correction; Inherited Metabolic Disorders; Lipid Nanoparticle Technology; Liver; Metabolic Rewiring; Rare Diseases
Orthologous CRISPR-Cas9 systems for genome editing: discovery, characterization and development for novel biotechnological applications.
Principal investigators: Doyon, Yannick
Keywords: Adeno Associated Virus (Aav); Crispr-Cas9; Genetic Disorders; Genome Editing; In Vivo Genetic Correction; Liver; Metabolic Rewiring; Rare Diseases
CRISPR-mediated engineering of autophagy-deficient human T lymphocytes for CAR-T cell immunotherapy
Principal investigators: Levesque, Sébastien
Keywords: Autophagy; Cancer Metabolism; Car-T Cells; Crispr-Cas9; Genetic Engineering; Immunotherapy; Solid Tumours
Deciphering DNA repair pathways using engineered nucleases
Principal investigators: Doyon, Yannick
In vivo genome editing as a novel class of human therapeutics to treat pediatric metabolic disorders
Principal investigators: Doyon, Yannick
Keywords: Adeno-Associated Virus (Aav); Dna Repair; Gene Therapy; Genome Editing; Liver; Lysosomal Storage Diseases; Protein Engineering; Rare Genetic Diseases; Zinc-Finger Nucleases
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
- Molecular Medicine
- Department of Molecular Genetics
- Microbiologie et immunologie
- Lunenfeld-Tanenbaum Research Institute
- Pathology
- Donnelly Centre
- Other
Co-authors at Université Laval, colored by department. Thicker lines mean more shared papers; select anyone to open their profile and their own map.
Sylvain Moineau
Faculty
4 shared papers, latest 2023
Anne-Claude Gingras
Department of Molecular Genetics
2 shared papers, latest 2022
Fabrice Mac-Way
Medicine
1 shared papers, latest 2024
Mikko Taipale
Donnelly Centre
1 shared papers, latest 2022
Graham Dellaire
Pathology
1 shared papers, latest 2017
Mathieu Dalvai
Faculty
1 shared papers, latest 2015
Jean-Philippe Lambert
Molecular Medicine
1 shared papers, latest 2022
Amine Nourani
Faculty
1 shared papers, latest 2008
Alexander Hynes
Medicine
1 shared papers, latest 2018
Mathieu Laplante
Medicine
1 shared papers, latest 2020
Daniel Durocher
Lunenfeld-Tanenbaum Research Institute
1 shared papers, latest 2016
Steve Lacroix
Médecine moléculaire
1 shared papers, latest 2015
Arnaud Droit
Microbiologie et immunologie
1 shared papers, latest 2022
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