Masoumeh Falah

5PUBLICATIONS
14CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Neurology and neuromuscular diseasesMicro- and nanosystemsPredictive and prognostic markersNeural engineering
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Publications (5)

|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

|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

|Nov 11, 2023
Expanding phenotype heterogeneity of NARS2 by presenting subdural hematoma and parenchymal hemorrhage.

Mehrnoosh Khodaeian, Fatemeh Bitarafan, Fatemeh Garrousi

|Nov 27, 2021
Association between TBXT rs2305089 polymorphism and chordoma in Iranian patients identified by a developed T-ARMS-PCR assay.

Maryam Jalessi, Mohammad Saeed Gholami, Ehsan Razmara

|May 14, 2021
How Transmembrane Inner Ear (TMIE) plays role in the auditory system: A mystery to us.

Mohammad Farhadi, Ehsan Razmara, Maryam Balali

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