Masoud Garshasbi

26PUBLICATIONS
38CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Developmental genetics (incl. sex determination)Neurology and neuromuscular diseasesCancer geneticsAutonomic nervous system
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Publications (26)

|Nov 13, 2025
Genetic and clinical aspects of TMC1-related hearing loss in Iranian families: identification of two novel variants.

Mohammad Amin Ghalavand, Alimohamad Asghari, Mina Mohammadi Sarband

|Aug 16, 2025
Genetic Heterogeneity of Autism Spectrum Disorder: Identification of Five Novel Mutations (RIMS2, FOXG1, AUTS2, ZCCHC17, and SPTBN5) in Iranian Families via Whole-Exome and Whole-Genome Sequencing.

Maryam Mirahmadi, Seyyed Mohammad Kahani, Ali Sharifi-Zarchi

|Apr 18, 2025
High de novo mutation rate in Iranian NF2-related schwannomatosis patients with a report of a novel NF2 mutation.

Mohammad Amin Ghalavand, Alimohamad Asghari, Amin Jahanbakhshi

|Oct 26, 2023
Expression assay of the COLQ in a family with congenital myasthenic syndrome and symptomatic carriers.

Mohammad Farid Mohammadi, Sahand Tehrani Fateh, Hadi Aghajani

|Jul 31, 2023
Persistent basal ganglia involvement in aminoacylase-1 deficiency: expanding imaging findings and review of literature.

Mohammad Farid Mohammadi, Ali Dehghani, Kiana Zarabadi

|Jul 13, 2022
Symptomatic care of late-onset Alexander disease presenting with area postrema-like syndrome with prednisolone; a case report.

Safoura Zardadi, Ehsan Razmara, Maryam Rasoulinezhad

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Frequent Collaborators

9 joint publications

Ehsan Razmara

5 joint publications

Pouria Mohammadi

4 joint publications

Fatemeh Bitarafan

3 joint publications

Ali Reza Tavasoli