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Morteza Heidari is an expert in Neurology at Children's Medical Center (Iran) (Iran). Morteza Heidari has authored 176 publications, the most recent in 2026, and is an investigator in 1 clinical trial. SLR score: 482 (community average: 125). How the SLR is computed.

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Morteza Heidari Children's Medical Center (Iran) Iran
482 ScienceLeadR Reputation 482

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Neurology

Subspecialties: Genetics - Pediatrics - Biochemistry

Full career – Last 3 years

Main Topics

Publications and Clinical Studies

Publications – Clinical Studies

Profile data updated on

Organizations

Career arc: 2014 - 2026
Source: PubMed

Tehran University of Medical Sciences

Publications Synthesis

Sources: PubMed, OpenAlex

Number : 176

Citations

Citations: 1 811 1st author: 17 Last author: 34 Unique author: 1

Main journals

Iran J Pediatr 9
Iran J Child Neurol 8
Medical Imaging 2018: Computer-Aided Diagnosis 8
J Mol Neurosci 7
Health Spirituality and Medical Ethics 6

Best Journals

Nat Rev Neurol 1

Breakdown by type

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Latest Publications

5 most recent indexed articles

Source: Pubmed

Title Journal Year Citations
Pediatric Leukodystrophy Classification from 3D MRI: A Comparative Study of Radiomics-Based Machine Learning, Deep Transfer Learning, and Hybrid Models.
PMID 42946206 — classification, machine learning, deep learning, learning		J Neuroradiol20260
Genetic heterogeneity, movement disorders, and white matter abnormalities in pediatric developmental and epileptic encephalopathies: A retrospective cohort study from a National Neurodegenerative and Leukodystrophy Registry.
PMID 42407302 — registries, white matter, genes, epilepsy, genetic heterogeneity, cohort studies, movement disorders, seizures, movement		Epilepsy Res20260
Neuroradiological patterns and prognostic implications in type I Alexander disease.
PMID 42314609 — alexander disease, metabolic diseases, molecular biology, corpus callosum		Mol Genet Metab20260
Exploratory Analysis of Neuroimaging and Molecular Findings in a Cohort of Neuronal Ceroid Lipofuscinosis: a Descriptive study.
PMID 42283952 — neuroimaging, neuronal ceroid-lipofuscinoses, ceroid, neurosciences, diagnosis		J Mol Neurosci20260
A novel homozygous variant in the POLR1A gene: a complicated hereditary spastic paraplegia (c-HSP) or a hypomyelinating leukodystrophy type-27 (HLD27) phenotype?
PMID 42271096 — genes, phenotype, enzymes, neurosciences, genes, vif, paraplegia, spastic paraplegia, hereditary		Neurol Sci20260

Clinical Studies 1

Sources: ClinicalTrials, EU CTIS

Synthesis

By phase:

Phase 2 1

By status:

Unknown 1

By type:

Interventional 1

By Monocentric/Multicentric:

monocentric 0
multicentric2to4 1
multicentric5to9 0
multicentricup10 0

Main Topics

LeadR Networks

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Sources: PubMed, OpenAlex, ClinicalTrials, EU CTIS