This profile is built from public research funding records (CIHR, NSERC and SSHRC) and PubMed. We have not imported them from a University of Toronto directory, so their courses and email address may be missing. Find their university profile.
Research
Latest papers
Biallelic Pathogenic Variants in PYGM Impair Retinal Glycogenolysis Causing a Range of Phenotypes.
Investigative Ophthalmology and Visual Science · 2026
Co-assembly of oligo-urethane nanoparticles with defined lipid additives to tailor RNA delivery into cells.
Acta biomaterialia · 2025
Autosomal-dominant macular dystrophy linked to a chromosome 17 tandem duplication.
JCI insight · 2024
Latest funding
- $120,000
Targeted treatment of brain development disorders caused by mutations in TUBB
CIHR · 2025 · Supervisor
- $990,675
Next-Generation Gene Editing for DMD: Efficacy and Safety of AAV-Compatible Adenine Base and Prime Editing in a Humanized Mouse Model
CIHR · 2024 · Principal investigator
- $910,350
Accurate classification of NPC1 variants with saturational genome editing
CIHR · 2021 · Nominated PI
7 publications.
Biallelic Pathogenic Variants in PYGM Impair Retinal Glycogenolysis Causing a Range of Phenotypes.
Hussein R, Tayyib A, Lin S, Parameswarappa D, Mehta M, Mohla A, Ahmed K, Tumber A, Tavares E, Schiff ER
Co-assembly of oligo-urethane nanoparticles with defined lipid additives to tailor RNA delivery into cells.
Shrestha S, Yan E, Yang B, Blundell A, Teng ACT, Marks RM, Cohn R, Ivakine E, Gramolini AO, Santerre JP
Autosomal-dominant macular dystrophy linked to a chromosome 17 tandem duplication.
Adele R, Hussein R, Tavares E, Ahmed K, Di Scipio M, Charish J, Liang M, Monis S, Tumber A, Chen X, Paton TA, Roslin NM, Eileen C, Ivakine E, Sunny NE, Wilson MD, Campos E, Rajala RV, Maynes JT, Monnier PP, Paterson AD, Héon E, Vincent A
An efficient and cost-effective purification protocol for Staphylococcus aureus Cas9 nuclease.
Teng ACT, Tavassoli M, Shrestha S, Marks RM, McFadden MJ, Evagelou SL, Lindsay K, Vandenbelt A, Li W, Ivakine E, Cohn R, Santerre JP, Gramolini AO
Kainate receptor auxiliary subunit NETO2 is required for normal fear expression and extinction.
Mennesson M, Rydgren E, Lipina T, Sokolowska E, Kulesskaya N, Morello F, Ivakine E, Voikar V, Risbrough V, Partanen J, Hovatta I
Neto2 interacts with the scaffolding protein GRIP and regulates synaptic abundance of kainate receptors.
Tang M, Ivakine E, Mahadevan V, Salter MW, McInnes RR
Neto1 is an auxiliary subunit of native synaptic kainate receptors.
Tang M, Pelkey KA, Ng D, Ivakine E, McBain CJ, Salter MW, McInnes RR
Targeted treatment of brain development disorders caused by mutations in TUBB
Principal investigators: Steiman, Sydney
Keywords: Antisense Oligonucleotides; Ciliopathies; Disease Modeling; Drug Screening; Microtubules; Pathogenic Variants; Primary Cilia; Tubulinopathies
Next-Generation Gene Editing for DMD: Efficacy and Safety of AAV-Compatible Adenine Base and Prime Editing in a Humanized Mouse Model
Principal investigators: Cohn, Ronald D; Ivakine, Evgueni
Keywords: Base Editing; Crispr; Duchenne Muscular Dystrophy; Humanized Mouse Models; Prime Editing
Accurate classification of NPC1 variants with saturational genome editing
Principal investigators: Ivakine, Evgueni
Keywords: Crispr; Lysosomal Storage Disorders; Niemann Pick Disease Type C; Screen; Variants Of Unknown Significance
Transcriptional control of disease modifiers for the treatment of Duchenne Muscular Dystrophy
Principal investigators: Cohn, Ronald D
Keywords: Control Of Gene Expression; Crispr; Disease Modifiers; Duchenne Muscular Dystrophy; Genome Engineering; Osteopontin; Utrophin
Interrogation of genome editing applications for the treatment of Duchenne Muscular Dystrophy
Principal investigators: Cohn, Ronald D
Keywords: Crispr; Deletions; Dmd; Duchenne Muscular Dystrophy; Dystrophin; Gene Correction; Gene Editing; Open Reading Frame
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
- Pediatrics
- Genetics and Genome Biology
- Other
Co-authors at University of Toronto, colored by department. Thicker lines mean more shared papers; select anyone to open their profile and their own map.
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.