Faculty profile

Jean Michaud

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Full ProfessorPathology and Laboratory MedicineUniversity of Ottawa

Jean Michaud

Full Professor

Pathology and Laboratory Medicine

Faculty of Medicine

University of Ottawa

Ottawa, Ontario, Canada

Supervision signals

Professors usually supervise graduate students in their department's programs.
4 publications in the last five years, latest in 2024.
Senior (last) author on 1 recent paper, a sign of leading a research group.

These signals come from public records, including CIHR, NSERC and SSHRC funding decisions. Ask the professor or the graduate program whether they are taking new students.

Academic metrics

Publications

532

Citations

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Collaborators

Publications by year

Counts cover the works listed on the university profile; citation counts come from Dimensions.

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Signals and details

Research

Read how they describe their research on their University of Ottawa profile.

Latest papers

Towards a histological diagnosis of childhood small vessel CNS vasculitis.
Pediatric rheumatology online journal · 2024
IRF2BPL-Related Disorder, Causing Neurodevelopmental Disorder with Regression, Abnormal Movements, Loss of Speech and Seizures (NEDAMSS) Is Characterized by Pathology Consistent with DRPLA.
Movement disorders : official journal of the Movement Disorder Society · 2024
SCA34 caused by ELOVL4 L168F mutation is a lysosomal lipid storage disease sharing pathology features with neuronal ceroid lipofuscinosis and peroxisomal disorders.
Acta neuropathologica · 2023 · senior author

All 45 publications

45 publications.

Towards a histological diagnosis of childhood small vessel CNS vasculitis.

Nouri MN, Dropol A, Tyrrell PN, Sheikh S, Twilt M, Michaud J, Ellezam B, Sarnat HB, Dunham C, Schutz PW, Keith J, Munoz DG, Vinters HV, Hawkins C, Benseler SM

Pediatric rheumatology online journal2024

DOI: 10.1186/s12969-024-01053-4 PMID: 39732702

IRF2BPL-Related Disorder, Causing Neurodevelopmental Disorder with Regression, Abnormal Movements, Loss of Speech and Seizures (NEDAMSS) Is Characterized by Pathology Consistent with DRPLA.

Venkateswaran S, Michaud J, Ito Y, Geraghty M, Lewis EC, Ellezam B, Boycott KM, Dyment DA, Kernohan KD, Care4Rare Canada Consortium

Movement disorders : official journal of the Movement Disorder Society2024

DOI: 10.1002/mds.29938 PMID: 39224955

SCA34 caused by ELOVL4 L168F mutation is a lysosomal lipid storage disease sharing pathology features with neuronal ceroid lipofuscinosis and peroxisomal disorders.

Ellezam B, Kaseka ML, Nguyen DK, Michaud J

Acta neuropathologica2023Senior author

DOI: 10.1007/s00401-023-02582-0 PMID: 37184663

Ballooned neurons in semi-recent severe traumatic brain injury.

Michaud J, Plu I, Parai J, Bourgault A, Tanguay C, Seilhean D, Woulfe J

Acta neuropathologica communications2023First author

DOI: 10.1186/s40478-023-01516-x PMID: 36899399

SMN Depleted Mice Offer a Robust and Rapid Onset Model of Nonalcoholic Fatty Liver Disease.

Deguise MO, Pileggi C, De Repentigny Y, Beauvais A, Tierney A, Chehade L, Michaud J, Llavero-Hurtado M, Lamont D, Atrih A, Wishart TM, Gillingwater TH, Schneider BL, Harper ME, Parson SH, Kothary R

Cellular and molecular gastroenterology and hepatology2021

DOI: 10.1016/j.jcmgh.2021.01.019 PMID: 33545428

A recurrent de novo ATP5F1A substitution associated with neonatal complex V deficiency.

Lines MA, Cuillerier A, Chakraborty P, Naas T, Duque Lasio ML, Michaud J, Pileggi C, Harper ME, Burelle Y, Toler TL, Sondheimer N, Crawford HP, Millan F, Geraghty MT

European journal of human genetics : EJHG2021

DOI: 10.1038/s41431-021-00956-0 PMID: 34483339

Histologic Correlates of Molecular Group 4 Pediatric Medulloblastoma: A Retrospective Canadian Review.

Triscott J, Yip S, Johnston D, Michaud J, Rassekh SR, Hukin J, Dunn S, Dunham C

Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society2021

DOI: 10.1177/10935266211001986 PMID: 33749384

Whole genome sequencing reveals biallelic PLA2G6 mutations in siblings with cerebellar atrophy and cap myopathy.

McMillan HJ, Marshall AE, Venkateswaran S, Hartley T, Warman-Chardon J, Ramani AK, Marshall CR, Michaud J, Boycott KM, Dyment DA, Kernohan KD

Clinical genetics2021

DOI: 10.1111/cge.13935 PMID: 33576074

Motor transmission defects with sex differences in a new mouse model of mild spinal muscular atrophy.

Deguise MO, De Repentigny Y, Tierney A, Beauvais A, Michaud J, Chehade L, Thabet M, Paul B, Reilly A, Gagnon S, Renaud JM, Kothary R

EBioMedicine2020

DOI: 10.1016/j.ebiom.2020.102750 PMID: 32339936

Spinal muscular atrophy type III complicated by spinal superficial siderosis: a case report with molecular and neuropathological findings.

Pringle CE, Nelson R, Miller W, Kothary R, Michaud J

Acta neuropathologica communications2020Senior author

DOI: 10.1186/s40478-020-01063-9 PMID: 33168084

Profile data last refreshed on September 25, 2026 from the university directory, publication records and CIHR, NSERC and SSHRC funding.

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Jean Michaud

Research

Latest papers

Towards a histological diagnosis of childhood small vessel CNS vasculitis.

IRF2BPL-Related Disorder, Causing Neurodevelopmental Disorder with Regression, Abnormal Movements, Loss of Speech and Seizures (NEDAMSS) Is Characterized by Pathology Consistent with DRPLA.

SCA34 caused by ELOVL4 L168F mutation is a lysosomal lipid storage disease sharing pathology features with neuronal ceroid lipofuscinosis and peroxisomal disorders.

Ballooned neurons in semi-recent severe traumatic brain injury.

SMN Depleted Mice Offer a Robust and Rapid Onset Model of Nonalcoholic Fatty Liver Disease.

A recurrent de novo ATP5F1A substitution associated with neonatal complex V deficiency.

Histologic Correlates of Molecular Group 4 Pediatric Medulloblastoma: A Retrospective Canadian Review.

Whole genome sequencing reveals biallelic PLA2G6 mutations in siblings with cerebellar atrophy and cap myopathy.

Motor transmission defects with sex differences in a new mouse model of mild spinal muscular atrophy.

Spinal muscular atrophy type III complicated by spinal superficial siderosis: a case report with molecular and neuropathological findings.

Frequent collaborators

Jacek Majewski

Eric Bouffet

Mary-Ellen Harper

Pranesh Chakraborty

Rashmi Kothary

Annie Huang

Martin Holcik

Uri Tabori

Cynthia Hawkins

Donna Johnston

Ute Bartels

Nada Jabado

Michael Brudno

Peter Humphreys

Robert Hammond

Sandra Dunn

Vijay Ramaswamy

David Grynspan

Jodi Warman Chardon

Dalia Barsyte-Lovejoy

Adam Fleming

Jennifer Chan

Dina El Demellawy

Karine Khatchadourian

Michael Geraghty

Santanu Chakraborty