Mortaza Bonyadi

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 10

Top Venues

Journal of neurogenetics

Human genome variation

Journal of cellular biochemistry

BMC ophthalmology

University of Tabriz (PHD)

This page only lists publications with an associated author ORCID identifier.

Education History

University of Tabriz

Iran

PHD :: Center of Excellence for Biodiversity

Publications

Hasan Azizi, Mortaza Bonyadi, Abbas Rafat
A novel splice site variant of the BBS2 gene in a patient with Bardet-Biedl syndrome. Human genome variation 11 (1) (2024)
Asal Asghari Sarfaraz, Neda Jabbarpour, Mortaza Bonyadi, Mohammad Khalaj-Kondori
Identification and bioinformatics analysis of a novel variant in the HERC2 gene in a patient with intellectual developmental disorder. Journal of neurogenetics 38 (1) (2024)
Asal Asghari Sarfaraz, Neda Jabbarpour, Mortaza Bonyadi, Mohammad Khalaj-Kondori
Identification and bioinformatics analysis of a novel variant in the HERC2 gene in a patient with intellectual developmental disorder. Journal of neurogenetics 38 (1) (2024)
Asal Asghari Sarfaraz, Neda Jabbarpour, Mortaza Bonyadi, Mohammad Khalaj-Kondori
Identification and bioinformatics analysis of a novel variant in the HERC2 gene in a patient with intellectual developmental disorder. Journal of neurogenetics (2024)
Hasan Azizi, Mortaza Bonyadi, Abbas Rafat
A novel splice site variant of the BBS2 gene in a patient with Bardet-Biedl syndrome. Human genome variation 11 (1) (2024)
Neda Jabbarpour, Mortaza Bonyadi, Leila Sadeghi
A novel loss of function mutation in the PHD domain of the RAG2 gene, affecting zinc-binding affinity. Molecular biology reports (2023)
Nasrin Roshanipour, Maryam Ghaffari Laleh, Mortaza Bonyadi, Mohammad Hossein Jabbarpoor Bonyadi, Masoud Soheilian, Alireza Javadzadeh, Mehdi Yaseri
Role of complement factor B rs4151667 (L9H) polymorphisms and its interactional role with CFH Y402H and C3 rs2230199 (R102G) risk variants in age-related macular degeneration: a case control study. BMC ophthalmology 20 (1) (2020)
Samaneh Mesgari, Saba A Nazm, Mortaza Bonyadi, Mohammad Hossein Jabbarpoor Bonyadi, Masoud Soheilian
Paroxonase (PON1-L55M) gene polymorphism and its association with Behçet's disease among Iranian population. Ophthalmic genetics 41 (3) (2020)
Shahin Ramazi, Hafez Heydari-Zarnagh, Maryam Goudarzian, Mohammad Khalaj-Kondori, Mortaza Bonyadi
Thromboxane A synthase 1 gene expression and promotor haplotypes are associated with risk of large artery-atherosclerosis stroke in Iranian population. Journal of cellular biochemistry 120 (9) (2019)
Reza Abdolmohammadi, Mortaza Bonyadi
Polymorphisms of Promoter Region of TNF-α Gene in Iranian Azeri Turkish Patients with Behçet's Disease. Journal of Korean medical science 32 (1) (2017)

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Publication Activity (10 Years)

Top Topics

Top Venues

Mortaza Bonyadi