Author

Aida Ghasemi

Observed name: Ghasemi, Aida

Institutions: University of Social Welfare and Rehabilitation Sciences, Tehran University of Medical Sciences

Observed institutions: University of Social Welfare and Rehabilitation Sciences, Tehran University of Medical Sciences

ORCID: 0000-0001-6386-7961

Observed ORCID: 0000-0001-6386-7961

OpenAlex ID: A5009484681

NMNAT1 and hereditary spastic paraplegia (HSP): expanding the phenotypic spectrum of NMNAT1 variants

2023 · Zahra Sadr, Aida Ghasemi, et al. · Neuromuscular Disorders · 12

Description of Phenotypic Heterogeneity in a GJC2-Related Family and Literature Review

2023 · Aida Ghasemi, Ali Reza Tavasoli, et al. · Molecular Syndromology · 11

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Copy Number Variations in Hereditary Spastic Paraplegia-Related Genes: Evaluation of an Iranian Hereditary Spastic Paraplegia Cohort and Literature Review

2023 · Aida Ghasemi, Zahra Sadr, et al. · Molecular Syndromology · 7

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Three Iranian patients with rare subtypes of hereditary spastic paraplegia (HSP): SPG76, SPG56, and SPG69

2024 · Zahra Sadr, Aida Ghasemi, et al. · Neurogenetics · 6

JAM2 variants can be more common in primary familial brain calcification (PFBC) cases than those appear; may be due to a founder mutation

2024 · Mana Khojasteh, Parsa Soleimani, et al. · Neurological Sciences · 6

COLQ-Congenital myasthenic syndrome in an Iranian cohort: the clinical and genetics spectrum

2024 · Omid Hesami, Mahtab Ramezani, et al. · Orphanet Journal of Rare Diseases · 5

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The first reports of FA2H-associated neurodegeneration from two unrelated Iranian families

2023 · Narges Hashemi, Reza Nejad Shahrokh Abadi, et al. · Neurological Sciences · 5

A Novel Homozygous Variant in the MCOLN1 Gene Associated With Severe Oromandibular Dystonia and Parkinsonism

2024 · Aida Ghasemi, Mahdieh Eslami Ardakani, et al. · Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques · 4

Clinical and genetic diversity in Iranian individuals with RAPSN-related congenital myasthenic syndrome

2024 · Aida Ghasemi, Seyed Jalaleddin Hadei, et al. · Neurogenetics · 3

2024 · Narges Karimi, Aida Ghasemi, et al. · Neuromuscular Disorders · 2

A Cohort of Iranian Patients With Congenital Myasthenic Syndrome due to Glycosylation Defects

2025 · Mahtab Ramezani, Ali Asghar Okhovat, et al. · Muscle & Nerve · 1

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Identifying novel AGRN variants in congenital myasthenic syndrome: insights from three Iranian families

2025 · Hadi Gharebaghian, Aida Ghasemi, et al. · Neuromuscular Disorders · 1

Beginning at the ends: telomere and telomere-based cancer therapeutics

2024 · Zahra Sadr, Masoumeh Ghasemi, et al. · Molecular Genetics and Genomics · 1

Phenotypic and genotyping spectrum of two Iranian cases with RBCK1 ‐associated polyglucosan body myopathy

2024 · Marzieh Babaee, Yalda Nilipour, et al. · Neuropathology · 1

Focal Demyelinating Electrophysiological Features in MTRFR-Related Spastic Paraplegia Type 55 (SPG55): A Case Report

2026 · Aida Ghasemi, Fatemeh Barshooi, et al. · Current Genetic Medicine Reports

Variable phenotypic manifestations of two splice-site variants in DNAJB2: insights from two families and a systematic review

2026 · Fatemeh Ghermezcheshmeh, Nazila Malekian, et al. · Journal of Human Genetics

Disease course, survival, and genetic heterogeneity in chorea-acanthocytosis: a case series of 34 patients

2026 · Aida Ghasemi, Elahe Amini, et al. · Journal of Movement Disorders

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Charcot-Marie-Tooth type 4 C misdiagnosed as CIDP: electrodiagnostic pitfalls and genetic confirmation

2026 · Ali Asghar Okhovat, Hamed Shahriyari, et al. · Neurogenetics

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