Fatemeh Suri
5PUBLICATIONS
20CO-AUTHORS
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Publications (5)
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|Mar 07, 2025
Uncovering the genetic architecture of inherited retinal disease in a consanguineous Iranian cohort.Lieselot Vincke, Kristof Van Schil, Hamid Ahmadieh
|Mar 06, 2024
Bilateral helicoid peri-papillary sub-retinal fibrosis due to a biallelic NR2E3 mutation: Describing variable expressivity of a mutation.Narges Hassanpoor, Nazanin Ebrahimiadib, Hamid Riazi-Esfahani
|Nov 29, 2021
Variable Expressivity of Wolfram Syndrome in a Family with Multiple Affected Subjects.Mehraban Mirrahimi, Sare Safi, Maryam Mohammadzadeh
|Nov 03, 2021
Prenatal diagnosis of primary congenital glaucoma and histopathological features in a fetal globe with cytochrome p4501B1 mutations.Mozhgan Rezaei Kanavi, Shahin Yazdani, Elahe Elahi
|May 20, 2021
Autosomal Recessive Bestrophinopathy: Clinical and Genetic Characteristics of Twenty-Four Cases.Hassan Khojasteh, Mohsen Azarmina, Nazanin Ebrahimiadib
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Frequent Collaborators
2 joint publications
Hamid Riazi-Esfahani
1 joint publications
Hassan Khojasteh
1 joint publications
Nazanin Ebrahimiadib
1 joint publications
Narsis Daftarian
1 joint publications
Houra Naraghi
1 joint publications
Hamideh Sabbaghi
1 joint publications
Alireza Khodabande
1 joint publications
Hooshang Faghihi
1 joint publications
Fatemeh Bazvand
1 joint publications
Hamid Ahmadieh
