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Mahsa Mohammadi

CAR T cell therapy as a promising approach in cancer immunotherapy: challenges and opportunities
2021 · Maryam Akhoundi, Mahsa Mohammadi, et al. · Cellular Oncology · 65
The Therapeutic Potential of Regulatory T Cells: Challenges and Opportunities
2021 · Fatemeh Bayati, Mahsa Mohammadi, et al. · Frontiers in Immunology · 57
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Prediction and interpretation of rare missense variant in OTOG associated with hearing loss
2021 · Masomeh Askari, Zahra Moradi, et al. · Genomics · 8
Clinical and molecular assessment of a spastic ataxia 4 (SPAX4) patient with a novel variant in the MTPAP gene, and a systematic review
2025 · Moez Ravanbod, Mahsa Mohammadi, et al. · Gene · 3
Effects of Wii Fit on Functional Balance and Elbow Flexion in Children with Unilateral Spastic Cerebral Palsy: A Pilot Study
2026 · Mahshad Maleki, Mahsa Mohammadi, et al. · Neurorehabilitation
Expanding the genetic and clinical landscapes of hereditary spastic paraplegia (HSP): a cohort study of 103 families
2026 · Atefeh Davarzani, Moez Ravanbod, et al. · Orphanet Journal of Rare Diseases
Expanding the genetic and clinical landscapes of hereditary spastic paraplegia (HSP): a cohort study of 103 families
2026 · Atefeh Davarzani, Moez Ravanbod, et al. · Figshare
Additional file 3 of Expanding the genetic and clinical landscapes of hereditary spastic paraplegia (HSP): a cohort study of 103 families
2026 · Atefeh Davarzani, Moez Ravanbod, et al. · Figshare
Additional file 5 of Expanding the genetic and clinical landscapes of hereditary spastic paraplegia (HSP): a cohort study of 103 families
2026 · Atefeh Davarzani, Moez Ravanbod, et al. · Figshare
Additional file 1 of Expanding the genetic and clinical landscapes of hereditary spastic paraplegia (HSP): a cohort study of 103 families
2026 · Atefeh Davarzani, Moez Ravanbod, et al. · Figshare
Additional file 4 of Expanding the genetic and clinical landscapes of hereditary spastic paraplegia (HSP): a cohort study of 103 families
2026 · Atefeh Davarzani, Moez Ravanbod, et al. · Figshare
Additional file 2 of Expanding the genetic and clinical landscapes of hereditary spastic paraplegia (HSP): a cohort study of 103 families
2026 · Atefeh Davarzani, Moez Ravanbod, et al. · Figshare
Expanding the phenotypic spectrum of LAMA2-related disorders: Axonal neuropathy in the absence of muscular dystrophy
2026 · Mahsa Mohammadi, Mahdieh Rahimoghli, et al. · Journal of Human Genetics
Clinical and molecular spectrum of an Iranian Charcot-Marie-Tooth 2T cohort, and the diagnostic importance of whole exome sequencing in identifying co-occurrence inherited disorders
2025 · Zahra Salami, Mahsa Mohammadi, et al. · Neuromuscular Disorders
GDAP1 ‐Related Charcot–Marie–Tooth Disease: Axonal or Demyelinating Subtype? Autosomal Recessive or Autosomal Dominant Inheritance?
2025 · Moez Ravanbod, Mahsa Mohammadi, et al. · Journal of the Peripheral Nervous System
Genetic Homogeneity of a TDP1 Variant, c.1478A>G, as the Main Disease-Causing Variant of Spinocerebellar Ataxia With Axonal Neuropathy 1 (SCAN1) in the Middle East: A Systematic Review
2024 · Mahsa Mohammadi, Moez Ravanbod, et al. · Pediatric Neurology
Works count: 16
Citation count: 133
H-index: 3
I10-index: 2
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