Fatemeh Suri
机构: Assistant Professor, Shahid Beheshti University of Medical Sciences
每年引用次数
引用次数
引用: 772
H-指数: 14
I10-指数 : 18
出版物: 49
Myocilin mutations are not a major cause of primary congenital glaucoma in Iranian patients.
Mehrnaz Narooie-Nejhad , Elahe Elahi , Fatemeh Suri , Shahin yazdani
Journal of ophthalmic and vision research 5 ( 2) 101 -104
2
2010
Screening of common CYP1B1 mutations in Iranian POAG patients using a microarray-based PrASE protocol
Mehrnaz Narooie-Nejhad , Navid Nilforooshan , Elahe Elahi , Fatemeh Suri
Molecular Vision 14 2349 -2356
26
2008
Contributions of MYOC and CYP1B1 mutations to JOAG.
Mehrnaz Narooie-Nejhad , Fereshteh Chitsazian , Elahe Elahi , Mohammad H Sanati
Molecular Vision 14 508 -517
38
2008
Oxidative stress effects in glaucoma may be mediated by the TGF-β signaling pathway
Hamid Ahmadieh , Elahe Elahi , Fatemeh Suri , Fatemeh Suri
Investigative Ophthalmology & Visual Science 57 ( 12) 6015 -6015
2016
NOGO-A Gene Expression in Amniotic Fluid Treated Human RPE Cells
Hamid Ahmadieh , Mozhgan Rezaeikanavi , Iman Salahshourifar , Fatemeh Suri
Investigative Ophthalmology & Visual Science 58 ( 8) 608 -608
2017
Enhanced Expression of NOGO-A Gene and its Receptors in Amniotic Fluid Treated Human RPE Cells
Hamid Ahmadieh , Mozhgan Rezaeikanavi , Fatemeh Suri , Zahra-Soheila Soheili
Investigative Ophthalmology & Visual Science 59 ( 9) 3087 -3087
2018
Intravitreal Connective Tissue Growth Factor Neutralizing Antibody Reduces Subretinal Fibrosis Associated with Experimental Choroidal Neovascular Membrane
Ali Hafezi-Moghadam , Hamid Ahmadieh , Narsis Daftarian , Fatemeh Suri
Investigative Ophthalmology & Visual Science 60 ( 9) 2978 -2978
2019
Autosomal Recessive Bestrophinopathy: Clinical and Genetic Characteristics of Twenty-Four Cases.
Hamid Riazi-Esfahani , Hamid Ahmadieh , Narges Hassanpoor , Masoud Reza Manaviat
Journal of Ophthalmology 2021 6674290
2021
Intravitreal connective tissue growth factor neutralizing antibody or bevacizumab alone or in combination for prevention of proliferative vitreoretinopathy in an experimental model.
Hamid Ahmadieh , Sahar Balagholi , Ramin Nourinia , Narsis Daftarian
Experimental Eye Research 208 108622
2021
Identification of three novel homozygous variants in COL9A3 causing autosomal-recessive Stickler Syndrome
Barbara Vona , Mohammad Doosti , Narsis Daftarian , Fatemeh Suri
1
2021
PRPH2 mutation as the cause of various clinical manifestations in a family affected with inherited retinal dystrophy.
Narsis Daftarian , Mehraban Mirrahimi , Hamideh Sabbaghi , Afrooz Moghadasi
Ophthalmic Genetics 40 ( 5) 436 -442
2
2019
A novel PAX6 mutation causes congenital aniridia with or without retinal detachment
Mehraban Mirrahimi , Hamideh Sabbaghi , Hamid Ahmadieh , Mehdi Jahanmard
Ophthalmic Genetics 40 ( 2) 146 -149
1
2019
Incomplete penetrance of CRX gene for autosomal dominant form of cone-rod dystrophy.
Marjan Chapi , Hamideh Sabbaghi , Fatemeh Suri , Elham Alehabib
Ophthalmic Genetics 40 ( 3) 259 -266
6
2019
Association of Saitohin gene rs62063857 polymorphism with dry type age-related macular degeneration.
Mortaza Bonyadi , Hamid Ahmadieh , Mohammad Hossein Jabbarpoor Bonyadi , Koorosh Shahpasand
Ophthalmic Genetics 41 ( 5) 505 -506
2020
The p.Gly61Glu Mutation in CYP1B1 Affects the Extracellular Matrix in Glaucoma Patients
Iman Safari , Fatemeh Suri , Ramona Haji-Seyed-Javadi , Shahin Yazdani
Ophthalmic Research 56 ( 2) 98 -103
7
2016
COL18A1 is a candidate eye iridocorneal angle-closure gene in humans
Fatemeh Suri , Shahin Yazdani , Marjan Chapi , Iman Safari
Human Molecular Genetics 27 ( 21) 3772 -3786
17
2018
Variable Expressivity and High Penetrance of CYP1B1 Mutations Associated with Primary Congenital Glaucoma
Seyed Hassan Paylakhi , Sirous Zeinali , Mohammad Pakravan , Elahe Elahi
Ophthalmology 116 ( 11) 2101 -2109
36
2009
Diagnosis of cystathionine beta-synthase deficiency by genetic analysis
Fatemeh Suri , Mehrnaz Narooie-Nejad , Iman Safari , Hamidreza Moazzeni
Journal of the Neurological Sciences 347 ( 1) 305 -309
2014
LTBP2 knockdown and oxidative stress affect glaucoma features including TGFβ pathways, ECM genes expression and apoptosis in trabecular meshwork cells
Fatemeh Suri , Shahin Yazdani , Elahe Elahi
Gene 673 70 -81
10
2018
Choroidal Thickness in Different Types of Inherited Retinal Dystrophies.
Hamideh Sabbaghi , Hamid Ahmadieh , Jalil Jalili , Nazanin Behnaz
Journal of ophthalmic and vision research 15 ( 3) 351 -361
2020