Morteza Bonaydi

13PUBLICATIONS
19CO-AUTHORS
Gene mappingNeurology and neuromuscular diseasesEpigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)Neurogenetics
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Publications (13)

|Aug 18, 2026
Genetic Insights Into Retinitis Pigmentosa: A De Novo RPGR Mutation in an Iranian-Azeri Family.

|Aug 17, 2026
A de novo NR2F1 c.330 C > A variant in Bosch-Boonstra-Schaaf optic atrophy syndrome presenting with early-onset developmental and epileptic encephalopathy.

|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.

|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

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Frequent Collaborators

5 joint publications

Mohammad Barzegar

3 joint publications

Neda Jabbarpour

2 joint publications

Zakiyeh Ebadi

1 joint publications

Reza Abdolmohammadi