Mohammad Barzegar

8PUBLICATIONS
11CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)Neural engineeringNeurogeneticsNeonatology
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Publications (8)

|Jun 17, 2026
Novel Variants in PLPBP, SCN1A, and SLC6A1: Genetics, Bioinformatics, and clinical Elucidation of Three Distinct Cases of Developmental and Epileptic Encephalopathy.

|May 04, 2026
Clinical, genetics and in silico analysis of a novel BSCL2 variant in a patient with CGL2 from Iranian Azeri Turkish ethnic group: expanding the genotypic spectrum through a comparative review.

|Jan 05, 2026
Guanidinoacetate methyltransferase deficiency presenting as epileptic encephalopathy: A clinical vignette.

Baharak Maddahi, Sina Raeisi, Shadi Shiva

|Sep 05, 2025
Identification of a Novel TRIT1 Mutation in a Consanguineous Iranian-Azeri-Turkish Family With Global Developmental Delay.

Fatemeh Beyad, Mortaza Bonyadi, Mohammad Barzegar

|Nov 27, 2024
Giant axonal neuropathy: a rare inherited neuropathy with a novel mutation.

Bita Poorshiri, Neda Jabbarpour, Mohammad Barzegar

|Jan 27, 2022
A Toddler With Acute Encephalitis Associated With COVID-19: A Case Report.

Bita Poorshiri, Sina Raeisi, Mohammad Barzegar

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Frequent Collaborators

4 joint publications

Morteza Bonaydi

2 joint publications

Neda Jabbarpour

1 joint publications

Sina Raeisi

1 joint publications

Bita Poorshiri