| Loss of function mutations in the gene encoding latent transforming growth factor beta binding protein 2, LTBP2, cause primary congenital glaucoma M Narooie-Nejad, SH Paylakhi, S Shojaee, Z Fazlali, M Rezaei Kanavi, ... Human molecular genetics 18 (20), 3969-3977, 2009 | 173 | 2009 |
| Contributions of MYOC and CYP1B1 mutations to JOAG B Bayat, S Yazdani, A Alavi, M Chiani, F Chitsazian, BK Tusi, F Suri, ... Molecular vision 14, 508, 2008 | 75 | 2008 |
| Variable expressivity and high penetrance of CYP1B1 mutations associated with primary congenital glaucoma F Suri, S Yazdani, M Narooie-Nejhad, SJ Zargar, SH Paylakhi, S Zeinali, ... Ophthalmology 116 (11), 2101-2109, 2009 | 59 | 2009 |
| Contribution of the latent transforming growth factor-beta binding protein 2 gene to etiology of primary open angle glaucoma and pseudoexfoliation syndrome S Jelodari-Mamaghani, R Haji-Seyed-Javadi, F Suri, N Nilforushan, ... Molecular vision 19, 333, 2013 | 56 | 2013 |
| FOXC1 in human trabecular meshwork cells is involved in regulatory pathway that includes miR-204, MEIS2, and ITGβ1 SH Paylakhi, H Moazzeni, S Yazdani, P Rassouli, E Arefian, E Jaberi, ... Experimental Eye Research 111, 112-121, 2013 | 54 | 2013 |
| Screening of common CYP1B1 mutations in Iranian POAG patients using a microarray-based PrASE protocol F Suri, R Kalhor, SJ Zargar, N Nilforooshan, S Yazdani, H Nezari, ... Molecular vision 14, 2349, 2008 | 47 | 2008 |
| COL18A1 is a candidate eye iridocorneal angle-closure gene in humans F Suri, S Yazdani, M Chapi, I Safari, P Rasooli, N Daftarian, ... Human molecular genetics 27 (21), 3772-3786, 2018 | 34 | 2018 |
| LTBP2 knockdown and oxidative stress affect glaucoma features including TGFβ pathways, ECM genes expression and apoptosis in trabecular meshwork cells F Suri, S Yazdani, E Elahi Gene 673, 70-81, 2018 | 31 | 2018 |
| SVEP1 as a genetic modifier of TEK-related primary congenital glaucoma TL Young, KN Whisenhunt, J Jin, SM LaMartina, SM Martin, T Souma, ... Investigative ophthalmology & visual science 61 (12), 6-6, 2020 | 29 | 2020 |
| Glaucoma in Iran and contributions of studies in Iran to the understanding of the etiology of glaucoma F Suri, S Yazdani, E Elahi Journal of ophthalmic & vision research 10 (1), 68, 2015 | 21 | 2015 |
| Sex bias in primary congenital glaucoma patients with and without CYP1B1 mutations F Suri, F Chitsazian, B Khoramian-Tusi, H Amini, S Yazdani, ... Journal of Ophthalmic & Vision Research 4 (2), 75, 2009 | 19 | 2009 |
| PRPH2 mutation as the cause of various clinical manifestations in a family affected with inherited retinal dystrophy N Daftarian, M Mirrahimi, H Sabbaghi, A Moghadasi, N Zal, ... Ophthalmic Genetics 40 (5), 436-442, 2019 | 17 | 2019 |
| Effects of intravitreal connective tissue growth factor neutralizing antibody on choroidal neovascular membrane-associated subretinal fibrosis N Daftarian, S Rohani, MR Kanavi, F Suri, M Mirrahimi, ... Experimental Eye Research 184, 286-295, 2019 | 15 | 2019 |
| Incomplete penetrance of CRX gene for autosomal dominant form of cone-rod dystrophy M Chapi, H Sabbaghi, F Suri, E Alehabib, S Rahimi-Aliabadi, F Jamali, ... Ophthalmic Genetics 40 (3), 259-266, 2019 | 14 | 2019 |
| The first inherited retinal disease registry in Iran: research protocol and results of a pilot study H Sabbaghi, N Daftarian, F Suri, M Mirrahimi, S Madani, A Sheikhtaheri, ... | 12 | 2020 |
| The p. Gly61Glu mutation in CYP1B1 affects the extracellular matrix in glaucoma patients I Safari, F Suri, R Haji-Seyed-Javadi, S Yazdani, E Elahi Ophthalmic Research 56 (2), 98-103, 2016 | 12 | 2016 |
| Autosomal recessive bestrophinopathy: Clinical and genetic characteristics of twenty-four cases H Khojasteh, M Azarmina, N Ebrahimiadib, N Daftarian, H Riazi-Esfahani, ... Journal of Ophthalmology 2021, 2021 | 11 | 2021 |
| Unraveling the genetic complexities of combined retinal dystrophy and hearing impairment P Bahena, N Daftarian, R Maroofian, P Linares, D Villalobos, M Mirrahimi, ... Human Genetics 141 (3), 785-803, 2022 | 10 | 2022 |
| P. Gly61Glu and P. Arg368His mutations in CYP1B1 that cause congenital glaucoma may be relatively frequent in certain regions of Gilan province, Iran M Qashqai, F Suri, M Yaseri, E Elahi Journal of Ophthalmic & Vision Research 13 (4), 403, 2018 | 9 | 2018 |
| Choroidal thickness in different types of inherited retinal dystrophies H Sabbaghi, H Ahmadieh, J Jalili, N Behnaz, M Fakhri, F Suri, B Kheiri, ... Journal of ophthalmic & vision research 15 (3), 351, 2020 | 8 | 2020 |
