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Mohammad Farid Mohammadi
Institutions:
Kharazmi University,
Children's Medical Center,
Tehran University of Medical Sciences
Observed institutions:
Kharazmi University,
Children's Medical Center,
Tehran University of Medical Sciences
ORCID:
0000-0002-9626-8110
Observed ORCIDs:
0000-0002-9626-8110,
0000-0003-4966-6658
OpenAlex ID:
A5071668137
Whole‐exome sequencing identified first homozygous frameshift variant in the COLEC10 gene in an Iranian patient causing 3MC syndrome type 3
2021
·
Pouria Mohammadi
, Elham Salehi Siavashani
, et al.
·
Molecular Genetics & Genomic Medicine
·
16
Unraveling neuroimaging insights in developmental epileptic encephalopathy type 25: a comprehensive review of reported cases and a novel SLC13A5 variant
2024
·
Mohammad Farid Mohammadi
, Sahand Tehrani Fateh
, et al.
·
Acta Neurologica Belgica
·
3
Genetic Analysis of Forty MLPA-Negative Duchenne Muscular Dystrophy Patients by Whole-Exome Sequencing
2022
·
Gholam Reza Zamani
, Mohammad Farid Mohammadi
, et al.
·
Journal of Molecular Neuroscience
·
3
Expanding the neuroimaging findings of guanidinoacetate methyltransferase deficiency in an Iranian girl with a homozygous frameshift variant in the GAMT
2023
·
Seyedeh Atiyeh Afjei
, Mohammad Farid Mohammadi
, et al.
·
Neurogenetics
·
2
Phenotypic variability and preserved cognition in a family with KCNA2-related developmental epileptic encephalopathy
2025
·
Arastoo Kaki
, Maedeh Ganji
, et al.
·
Neurogenetics
·
1
Persistent basal ganglia involvement in aminoacylase-1 deficiency: expanding imaging findings and review of literature
2023
·
Mohammad Farid Mohammadi
, Ali Dehghani
, et al.
·
Irish Journal of Medical Science (1971 -)
·
1
EEF1D ‐Associated Neurodevelopmental Disorders: Evidence From Iranian Siblings With a Biallelic Splice Junction Loss Variant
2026
·
Maedeh Ganji
, Arastoo Kaki
, et al.
·
Molecular Genetics & Genomic Medicine
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
2026
·
Pouria Mohammadi
, Sahand Fateh Tehrani
, et al.
·
Epilepsy Research
Subtype-specific expression of lncRNAs SNHG12 and HAGLR as non-invasive biomarkers for diagnosis and prognosis in breast cancer
2025
·
Mohammad Farid Mohammadi
, Arezoo Farhadi
, et al.
·
Irish Journal of Medical Science (1971 -)
Expression assay of the COLQ in a family with congenital myasthenic syndrome and symptomatic carriers
2023
·
Mohammad Farid Mohammadi
, Sahand Tehrani Fateh
, et al.
·
Clinical Case Reports
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Works count:
10
Citation count:
26
H-index:
3
I10-index:
1
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