Concepedia

Author

Fatemeh Suri

Shahid Beheshti University of Medical SciencesORCID

Also Known As

Fatemeh Suri, Mohammad Hossein Jabbarpoor Bonyadi, Mozhgan Rezaei Kanavi, Suri, Fatemeh

40

Publications

236

Citations

10

H-Index

11

Concepts

All Affiliations

Shahid Beheshti University of Medical SciencesTehran University of Medical SciencesUniversity of TübingenNational Institute of Genetic Engineering and BiotechnologyUniversity of Würzburg
FS

About

Fatemeh Suri is an author at Shahid Beheshti University of Medical Sciences specializing in medicine, ophthalmology, and pathology.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

2

2

56

2

Pathology

2

2

56

3

Immunology

1

1

16

4

Molecular Genetics

1

1

40

5

Cholangiopathies

1

1

16

Fatemeh Suri

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10

Publications

178

Citations

10

H-Index

YearCitations

COL18A1 is a candidate eye iridocorneal angle-closure gene in humans

Fatemeh Suri, Shahin Yazdani, Marjan Chapi,

Human Molecular Genetics

2018

40

Incomplete penetrance of <i>CRX</i> gene for autosomal dominant form of cone-rod dystrophy

Marjan Chapi, Hamideh Sabbaghi, Fatemeh Suri,

Ophthalmic Genetics

2019

18

<i>PRPH2</i> mutation as the cause of various clinical manifestations in a family affected with inherited retinal dystrophy

Narsis Daftarian, Mehraban Mirrahimi, Hamideh Sabbaghi,

Ophthalmic Genetics

2019

18

The First Inherited Retinal Disease Registry in Iran: Research Protocol and Results of a Pilot Study

Hamideh Sabbaghi, Narsis Daftarian, Fatemeh Suri,

Archives of Iranian Medicine

2020

17

Effects of intravitreal connective tissue growth factor neutralizing antibody on choroidal neovascular membrane-associated subretinal fibrosis

Narsis Daftarian, Shirin Rohani, Mozhgan Rezaei Kanavi,

Experimental Eye Research

2019

16

Autosomal Recessive Bestrophinopathy: Clinical and Genetic Characteristics of Twenty-Four Cases

Hassan Khojasteh, Mohsen Azarmina, Nazanin Ebrahimiadib,

Journal of Ophthalmology

2021

16

Unraveling the genetic complexities of combined retinal dystrophy and hearing impairment

Paulina Bahena, Narsis Daftarian, Reza Maroofian,

Human Genetics

2021

15

Sex Bias in Primary Congenital Glaucoma Patients with and without CYP1B1 Mutations

Fatemeh Suri, Fereshteh Chitsazian, Betsabeh Khoramian-Tusi

2016

15

Choroidal structure investigated by choroidal vascularity index in patients with inherited retinal diseases

Kia Bayat, Kiana Hassanpour, Hamideh Sabbaghi,

International Journal of Retina and Vitreous

2023

13

The p.Gly61Glu Mutation in &lt;b&gt;&lt;i&gt;CYP1B1&lt;/i&gt;&lt;/b&gt; Affects the Extracellular Matrix in Glaucoma Patients

Iman Safari, Fatemeh Suri, Ramona Haji‐Seyed‐Javadi,

Ophthalmic Research

2016

10

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