Faculty profile

Myriam Srour

ResearcherPediatricsMcGill University

This profile is built from public research funding records (CIHR, NSERC and SSHRC) and PubMed. We have not imported them from a McGill University directory, so their courses may be missing. Find their university profile.

Myriam Srour

Researcher

Pediatrics

Health Sciences

McGill University

Montreal, Quebec, Canada

Supervision signals

Has led research grants, which requires an independent research appointment. Ask their department whether they supervise graduate students.
42 publications in the last five years, latest in 2026.
Senior (last) author on 10 recent papers, a sign of leading a research group.
Principal investigator on 3 research grants (3 CIHR), most recently in 2022.
Supervised 1 trainee who won CIHR awards, most recently in 2023.

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

105

Citations

h-index

Collaborators

Grants

Publications by year

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

Profiles and links

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Signals and details

Research

Dcc Exome Sequencing Gait Human Genetics Lateralization Of Motor Control Mirror Movements Netrin Neurodevelopment

Latest papers

Cerebellar Abnormalities in the Neuroimaging Spectrum of CLTC-Related Disorder.
American journal of medical genetics. Part A · 2026 · senior author
The microtubule-binding protein EML3 is required for mammalian embryonic growth and cerebral cortical development, and Eml3 null mice are a model of cobblestone brain malformation.
eLife · 2026
Initial negative imaging in GATOR1-associated genetic epilepsy does not preclude the existence of a focal, resectable epileptogenic zone: illustrative cases.
Journal of neurosurgery. Case lessons · 2026

All 99 publications

Latest funding

Unveiling New Genetic Players in Axon Guidance and neuronal migration Defects
CIHR · 2023 · Supervisor
$105,000
Precision neuroimaging of atypical brain network hierarchy in autism
CIHR · 2023 · Co-investigator
$883,575
Understanding the genetic architecture and pathophysiology of focal cortical dysplasias using single nucleus RNA sequencing
CIHR · 2022 · Nominated PI
$925,650

All 7 grants and awards

99 publications.

Cerebellar Abnormalities in the Neuroimaging Spectrum of CLTC-Related Disorder.

Charouf D, Accogli A, Hamdan FF, Nardecchia F, Itai T, Myers KA, Martin CS, Srour M

American journal of medical genetics. Part A2026Senior author

DOI: 10.1002/ajmg.a.70245 PMID: 42425907

The microtubule-binding protein EML3 is required for mammalian embryonic growth and cerebral cortical development, and Eml3 null mice are a model of cobblestone brain malformation.

Carrier I, Diez E, Piscopo VE, Bechstedt S, van Bokhoven H, Srour M, Berghuis AM, Stifani S, Yamanaka Y, McInnes R

eLife2026

DOI: 10.7554/elife.107102 PMID: 42423433

Initial negative imaging in GATOR1-associated genetic epilepsy does not preclude the existence of a focal, resectable epileptogenic zone: illustrative cases.

Ruan Y, Hill E, Bahmanpour Z, Badner B, Caldairou B, Bernasconi A, Bernasconi N, Baillet S, Srour M, Dufresne D, Dudley RWR

Journal of neurosurgery. Case lessons2026

DOI: 10.3171/case26127 PMID: 42330554

Posterior Fossa Malformations in a Cohort of 116 Fetuses: A Retrospective Analysis of Imaging Characteristics, Postnatal Imaging Concordance, Pregnancy Outcomes and Yield of Genetic Testing.

Malta M, Fortin O, Badner B, Charouf D, Addour-Boudrahem N, Beaudet-Leclair O, Rampakakis E, Rosenblatt DS, Nedelchev AA, Shear R, Carpineta L, Srour M

Cerebellum (London, England)2026Senior author

DOI: 10.1007/s12311-026-02009-y PMID: 42126681

Short telomeres in mitochondrial DNA depletion disorders.

Dille Y, Rampakakis E, Aubert G, Dassi C, Mannherz W, Berrahmoune S, Srour M, Buhas D, Agarwal S, Myers KA

Mitochondrion2026

DOI: 10.1016/j.mito.2026.102131 PMID: 41679577

Gait Alterations Due to DCC Gene Variants in Individuals with Congenital Mirror Movements.

Law NY, Desrosiers S, Sivanesan S, Tonkov H, Charron F, Bretzner F, Srour M, Barthélemy D

Movement disorders clinical practice2026

DOI: 10.1002/mdc3.70601 PMID: 41958228

Progressive Multifocal Systemic Arteriopathy with Recurrent Hypoperfusion Strokes in a Child with Smith-Magenis Syndrome.

Sahly AN, Lambert G, Srour M, Saint-Martin C, Moussaddy A, Klostranec JM, Shevell MI

The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques2026

DOI: 10.1017/cjn.2026.10583 PMID: 42003744

Enhanced myelination potential of human mature oligodendrocytes by TNF and IFNG combination.

Mohammadnia A, Cui QL, Yaqubi M, Blaszczyk GJ, Weng C, Hall JA, Dudley R, Stratton JA, Zandee S, Kennedy TE, Srour M, Antel JP

Journal of neuroinflammation2026

DOI: 10.1186/s12974-026-03753-y PMID: 41808190

Age and Maturation Stage Linked Consequences of Fibrinogen on Human Oligodendroglia.

Blaszczyk GJ, Weng C, Mohammadnia A, Cui QL, Giurleo A, Groh AMR, Plouffe C, Sirois J, Piscopo VEC, Yaqubi M, Taqvi A, Cassidy E, Martin LC, Hall JA, Dudley RWR, Srour M, Zandee SEJ, Klement W, Larouche S, Prat A, Durcan TM, Stratton JA, Antel JP, Moore GRW

Journal of neuroscience research2026

DOI: 10.1002/jnr.70120 PMID: 41866764

Antenatal Corticosteroids and Risk of Cerebral Palsy: A Regression Discontinuity Study.

Socha PM, Hutcheon JA, Strumpf EC, Liauw J, Srour M, Ting JY, Skoll MA, Harper S

The Journal of pediatrics2026

DOI: 10.1016/j.jpeds.2025.114960 PMID: 41448265

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Myriam Srour

Research

Latest papers

Latest funding

Cerebellar Abnormalities in the Neuroimaging Spectrum of CLTC-Related Disorder.

The microtubule-binding protein EML3 is required for mammalian embryonic growth and cerebral cortical development, and Eml3 null mice are a model of cobblestone brain malformation.

Initial negative imaging in GATOR1-associated genetic epilepsy does not preclude the existence of a focal, resectable epileptogenic zone: illustrative cases.

Posterior Fossa Malformations in a Cohort of 116 Fetuses: A Retrospective Analysis of Imaging Characteristics, Postnatal Imaging Concordance, Pregnancy Outcomes and Yield of Genetic Testing.

Short telomeres in mitochondrial DNA depletion disorders.

Gait Alterations Due to DCC Gene Variants in Individuals with Congenital Mirror Movements.

Progressive Multifocal Systemic Arteriopathy with Recurrent Hypoperfusion Strokes in a Child with Smith-Magenis Syndrome.

Enhanced myelination potential of human mature oligodendrocytes by TNF and IFNG combination.

Age and Maturation Stage Linked Consequences of Fibrinogen on Human Oligodendroglia.

Antenatal Corticosteroids and Risk of Cerebral Palsy: A Regression Discontinuity Study.

Unveiling New Genetic Players in Axon Guidance and neuronal migration Defects

Precision neuroimaging of atypical brain network hierarchy in autism

Understanding the genetic architecture and pathophysiology of focal cortical dysplasias using single nucleus RNA sequencing

Development of intraoperative label-free Raman Spectroscopy techniques to delineate Focal Cortical Dysplasia borders in Epilepsy surgery and detect cells carrying somatic variants

The physiological, molecular and genetic mechanisms underlying lateralization of motor control

The physiological, molecular and genetic mechanisms underlying lateralization of motor control

Mapping Neural Function in Individuals with DCC Haplotype

Frequent collaborators

Myriam Srour

Roy Dudley

Kevin Petrecca

Alexandre Prat

Catherine Larochelle

Kevin Petrecca

Jessica Liauw

Daniela Pohl

Jacek Majewski

Guy Rouleau

Philippe Major

Elana Pinchefsky

Annette Majnemer

Elsa Rossignol

Nancy Braverman

Zoha Kibar

Maryam Oskoui

Frederic Charron

Bernard Brais

Birgit Ertl-Wagner

Marco Leyton

Jean Ouellet

Natalia Jaworska

Cecilia Flores

John Mitchell

Birgit Ertl-Wagner

Roberta La Piana

Jason Karamchandani

Jason Karamchandani

Alexander Weil

Yojiro Yamanaka

Alfonso Fasano

Jack Antel

Rikard Blunck

Nathalie Arbour

Alain Dagher

Kevin Petrecca

Samuel Kadoury