Faculty profile
James Ellis
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Research
Latest papers
Pathological disruption of CELF2 shuttling causes neuronal hyperactivity, learning deficits, and seizures.
The Journal of clinical investigation · 2026
An X-linked long non-coding RNA, PTCHD1-AS, and the core features of autism.
Nature · 2026
Advanced physiological maturation of human iPSC-derived cardiomyocytes using an algorithm-directed optimization of defined media components.
Nature communications · 2026
Latest funding
- $1,400,000
Canada Research Chair - Tier 1
CIHR · 2021 · Nominated PI
- $940,950
A role for novel regulatory variants in childhood cardiomyopathy
CIHR · 2020 · Principal investigator
- $914,175
Post-transcriptional regulation of functionally significant gene sets during neurodevelopment of Rett syndrome
CIHR · 2019 · Nominated PI
75 publications.
Pathological disruption of CELF2 shuttling causes neuronal hyperactivity, learning deficits, and seizures.
Hua M, Aghanoori MR, MacPherson MJ, Ren Y, Siripala SV, Yang Y, Or YYY, Nguyen M, Duba-Kiss R, Feng D, Williams L, Gafuik CJ, Wang G, Quelin C, Keren B, Schuhmann S, Vasileiou G, Bourgois A, Vitobello A, Philippe C, Stark Z, Leventer RJ, McGillivray G, Tran Mau-Them F, Tessarech M, Prouteau C, Lakeman P, Motazacker MM, Latner DR, Caylor RC, van Ierland Y, Prijoles E, Lichty A, Theodorou E, Sweetser DA, Steel E, Cobben J, Dasouki MJ, Calame DG, Isidor B, Cogné B, Kesler M, Rackel B, Clark I, Kurrasch DM, Teskey GC, Ellis J, He G, Ryan SD, Mahoney DJ, Innes AM, Epp JR, Yang G
An X-linked long non-coding RNA, PTCHD1-AS, and the core features of autism.
Bradley CA, Ko SY, Tian M, Ralph LT, D'Abate L, Lee J, Liu T, Wang J, Tidball P, Mendes M, Fan X, Howe JL, Alexandrova R, Pellecchia G, Casallo G, Paton T, Wybenga-Groot LE, Engchuan W, Thiruvahindrapuram B, Trost B, de Rijke J, Kadia A, Jin F, Salazar NB, Diaz-Mejia JJ, MacDonald JR, Deneault E, Ross PJ, Ellis J, Shum C, Georgiou J, Rennie O, Reuter MS, Hoang N, Sarikaya E, Selvanayagam T, Amini AE, Rutherford A, Rivera-Alfaro N, Marshall CR, Scala M, Runke CK, Kearney HM, Christodoulou J, Francis DI, Chung BHY, Pluciniczak J, Iaboni A, Wigby KM, Nordahl CW, Amaral DG, Hudson ML, Sjaarda CP, Guerin A, Elsabbagh M, Landa R, Mital S, Lesurf R, Jain A, Wilson MD, Ellegood J, Lerch JP, Lee LJ, Frey BJ, Salter MW, Vorstman JAS, Anagnostou E, Frankland PW, Collingridge GL, Scherer SW
Advanced physiological maturation of human iPSC-derived cardiomyocytes using an algorithm-directed optimization of defined media components.
Callaghan NI, Durland LJ, Chen W, Kuzmanov U, Miranda MZ, Ding Y, Mirzaei Z, Ireland RG, Reitz C, Gorman RA, Wang EY, Wagner K, Kim MM, Audet J, Santerre JP, Gramolini AO, Billia F, Radisic M, Mital S, Ellis J, Backx PH, Simmons CA
Abnormal Lipid Signaling Characterizes Diastolic Dysfunction in Pediatric Cardiomyopathy.
Turinsky AL, Hanafi N, Said A, Kinnear C, Lesurf R, López-Guillén JL, Akilen R, Patel S, Meng G, Wei W, Robillard Frayne I, Daneault C, Mertens L, Ellis J, Ruiz M, Mital S
Navigating Human Astrocyte Differentiation: Direct and Rapid One-Step Differentiation of Induced Pluripotent Stem Cells to Functional Astrocytes Supporting Neuronal Network Development.
Schuurmans IME, Mordelt A, Guevara-Ferrer M, Linda K, Duineveld D, Puvogel S, Hommersom MP, Scheefhals N, Rahm L, Dyke E, Scholten GJ, Knorz C, Jimenez CG, van Egmond N, Oudakker A, Bijnagte-Schoenmaker C, van Bokhoven H, Wei W, Hofmann S, Jung-Klawitter S, Mojica-Perez S, Parent J, Carotenuto L, Weckhuysen S, Maas N, Elgersma Y, van de Ven E, Lefeber D, Lygeroudi A, de Vries HE, Jordi L, Polymenidou M, Mitchell-Garcia T, Dragan I, Dolga A, de Witte LD, van Karnebeek CDM, Ellis J, Garanto A, Nadif Kasri N
Hypersynchronous iPSC-derived SHANK2 neuronal networks are rescued by mGluR5 agonism.
McCready FP, Pradeepan KS, Khaki M, Wei W, Guevara-Ferrer M, Matusiak N, Feng B, Piekna A, Martinez-Trujillo J, Ellis J
Diversifying the reference iPSC line concept.
Ellis J, Woltjen K, Mital S, Saito MK, Hotta A, Loring JF
iPSC-derived healthy human astrocytes selectively load miRNAs targeting neuronal genes into extracellular vesicles.
Gordillo-Sampedro S, Antounians L, Wei W, Mufteev M, Lendemeijer B, Kushner SA, de Vrij FMS, Zani A, Ellis J
Myosin inhibitor reverses hypertrophic cardiomyopathy in genotypically diverse pediatric iPSC-cardiomyocytes to mirror variant correction.
Kinnear C, Said A, Meng G, Zhao Y, Wang EY, Rafatian N, Parmar N, Wei W, Billia F, Simmons CA, Radisic M, Ellis J, Mital S
Generation and characterization of a human iPSC line and gene-corrected isogenic line derived from a patient with a CELF2 gene mutation.
Hua M, Williams L, Burns K, Liu S, Ellis J, Innes AM, McPherson M, Yang G
Canada Research Chair - Tier 1
Principal investigators: Ellis, James R
Keywords: Crc
A role for novel regulatory variants in childhood cardiomyopathy
Principal investigators: Mital, Seema; Ellis, James R
Keywords: Cardiomyopathy; Drug Testing; Gene Expression; Genomics; Myocyte Function; Regulatory Variants; Stem Cells
Post-transcriptional regulation of functionally significant gene sets during neurodevelopment of Rett syndrome
Principal investigators: Ellis, James R
Keywords: Micro And Long Concoding Rna; Neurodevelopment; Neuron Function; Pluripotent Stem Cells; Proteomics; Rett Syndrome; Ribosome Engagement; Rna Binding Proteins; Rna Stability; Ubiquitin
Identification of converging Molecular Pathways Across Chromatinopathies as Targets for Therapy: IMPACT
Principal investigators: Ellis, James R
Keywords: Cortical Neurons; Ipsc; Neurodevelopmental Disorders; Translatome
Regulation of mRNA stability and translation during human neurodevelopment
Principal investigators: Ellis, James R
Keywords: 3' Utr; Differentiation; Mecp2; Neurodevelopment; Neurons; Pluripotent Stem Cells; Rna Binding Proteins; Rna Stability; Rnaseq; Translational Efficiency
Genomes to Outcomes in Autism Spectrum Disorders
Principal investigators: Scherer, Stephen W
Keywords: Autism Spectrum Disorders; Diagnostics; Individualized Treatment; Variants; Whole Genome Sequencing
MECP2 function and rescue in neurons derived from Rett syndrome patient iPS cells
Principal investigators: Ellis, James R
Keywords: Activity Dependent Expression; Drug Screen; Electrophysiology; Epigenetic Reprogramming; Mecp2; Neuronal Differentiation; Neuronal Maturation; Patient Ips Cells; Rett Syndrome
NADPH oxidase function in the pathogenesis of pediatric IBD and JIA
Principal investigators: Brumell, John H
Keywords: Chronic Disease; Environmental Impacts On Disease; Inflammation; Inflammatory Bowel Diseases; Innate Immunity; Juvenile Idiopathic Arthritis; Microbiota; Nadph Oxidase; Reactive Oxygen Species; Treatment Modalities
NADPH oxidase function in the pathogenesis of paediatric IBD and JIA
Principal investigators: Brumell, John H
Keywords: Environmental Factors In Disease; Immune Deficiency; Inflammatory Bowel Disease; Juvenile Idiopathic Arthritis; Microbiota; Nadph Oxidase; Treatment Outcomes
iPS cells to model vascular disease in patients with Williams Beuren syndrome
Principal investigators: Ellis, James R; Mital, Seema
Keywords: Cell Engineering; Directed Differentiation; Drug Screens; Elastin; Induced Pluripotent Stem Cells; Progenitor Cells; Smooth Muscle Cells; Vascular Disease; Williams Beuren Syndrome
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
- Developmental and Stem Cell Biology
- Physiology and Pharmacology
- Lunenfeld-Tanenbaum Research Institute
- Medical Genetics
- Institute of Biomaterials and Biomedical Engineering
- Psychology
- 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.
Seema Mital
Pediatrics
13 shared papers, latest 2026
Julio Martinez-Trujillo
Physiology and Pharmacology
4 shared papers, latest 2025
Andras Nagy
Lunenfeld-Tanenbaum Research Institute
3 shared papers, latest 2020
Guang Yang
Medical Genetics
3 shared papers, latest 2026
Janet Rossant
Faculty
3 shared papers, latest 2012
Milica Radisic
Institute of Biomaterials and Biomedical Engineering
3 shared papers, latest 2026
Evdokia Anagnostou
Psychology
2 shared papers, latest 2026
Filio Billia
Physiology
2 shared papers, latest 2026
Brett Trost
Faculty
2 shared papers, latest 2026
Phedias Diamandis
Laboratory Medicine and Pathology
2 shared papers, latest 2020
Luc Mertens
Pediatrics
2 shared papers, latest 2026
Quaid Morris
Donnelly Centre
2 shared papers, latest 2020
Gordon Keller
Medical Biophysics
2 shared papers, latest 2011
Matthieu Ruiz
Nutrition
1 shared papers, latest 2026
Lyle Muller
Mathematics
1 shared papers, latest 2022
David Hodgson
Faculty
1 shared papers, latest 2020
Dalia Barsyte-Lovejoy
Pharmacology and Toxicology
1 shared papers, latest 2011
Michael Hart
Division of Social and Behavioural Health Sciences
1 shared papers, latest 2012
Marie-A. Chaix
Faculty
1 shared papers, latest 2020
Rosanna Weksberg
Genetics and Genome Biology
1 shared papers, latest 2011
Michael Brudno
Computer Science
1 shared papers, latest 2019
Arturas Petronis
Neurosciences
1 shared papers, latest 2011
Stacey Marjerrison
Pediatrics
1 shared papers, latest 2020
Daria Grafodatskaya
Pathology & Molecular Medicine
1 shared papers, latest 2011
Mick Bhatia
Biochemistry & Biomedical Sciences
1 shared papers, latest 2009
Rejane Dillenburg
Pediatrics
1 shared papers, latest 2020
Mayada Elsabbagh
Faculty
1 shared papers, latest 2026
Hong Han
Biochemistry & Biomedical Sciences
1 shared papers, latest 2013
Tapas Mondal
Pediatrics
1 shared papers, latest 2022
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