| A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants LG Fritsche, W Igl, JNC Bailey, F Grassmann, S Sengupta, ... Nature genetics 48 (2), 134-143, 2016 | 1404 | 2016 |
| Seven new loci associated with age-related macular degeneration Nature genetics 45 (4), 433-439, 2013 | 855 | 2013 |
| Impaired cholesterol efflux in senescent macrophages promotes age-related macular degeneration A Sene, AA Khan, D Cox, REI Nakamura, A Santeford, BM Kim, R Sidhu, ... Cell metabolism 17 (4), 549-561, 2013 | 243 | 2013 |
| Lack of BRAF mutation in primary uveal melanoma Y Cohen, N Goldenberg-Cohen, P Parrella, I Chowers, SL Merbs, J Pe’er, ... Investigative ophthalmology & visual science 44 (7), 2876-2878, 2003 | 158 | 2003 |
| Proliferative activity and p53 expression in primary and recurrent pterygia I Chowers, J Pe’er, E Zamir, N Livni, M Ilsar, J Frucht-Pery Ophthalmology 108 (5), 985-988, 2001 | 122 | 2001 |
| Adult-onset foveomacular vitelliform dystrophy: a fresh perspective I Chowers, L Tiosano, I Audo, M Grunin, CJF Boon Progress in retinal and eye research 47, 64-85, 2015 | 120 | 2015 |
| Homozygosity mapping reveals null mutations in FAM161A as a cause of autosomal-recessive retinitis pigmentosa D Bandah-Rozenfeld, L Mizrahi-Meissonnier, C Farhy, A Obolensky, ... The American Journal of Human Genetics 87 (3), 382-391, 2010 | 117 | 2010 |
| Identification of gene expression changes associated with the progression of retinal degeneration in the rd1 mouse AS Hackam, R Strom, D Liu, J Qian, C Wang, D Otteson, T Gunatilaka, ... Investigative ophthalmology & visual science 45 (9), 2929-2942, 2004 | 117 | 2004 |
| The iron carrier transferrin is upregulated in retinas from patients with age-related macular degeneration I Chowers, R Wong, T Dentchev, RH Farkas, J Iacovelli, TL Gunatilaka, ... Investigative ophthalmology & visual science 47 (5), 2135-2140, 2006 | 111 | 2006 |
| Increased expression of iron-regulating genes in monkey and human glaucoma RH Farkas, I Chowers, AS Hackam, M Kageyama, RW Nickells, ... Investigative ophthalmology & visual science 45 (5), 1410-1417, 2004 | 103 | 2004 |
| Ophthalmology practice during the COVID-19 pandemic K Safadi, JM Kruger, I Chowers, A Solomon, R Amer, H Aweidah, ... BMJ open ophthalmology 5 (1), e000487, 2020 | 101 | 2020 |
| Long-term assessment of combined vitamin A and E treatment for the prevention of retinal degeneration in abetalipoproteinaemia and hypobetalipo-proteinaemia patients I Chowers, E Banin, S Merin, M Cooper, E Granot Eye 15 (4), 525-530, 2001 | 94 | 2001 |
| Sequence variants in HTRA1 and LOC387715/ARMS2 and phenotype and response to photodynamic therapy in neovascular age-related macular degeneration in populations from Israel I Chowers, T Meir, M Lederman, N Goldenberg-Cohen, Y Cohen, E Banin, ... Molecular vision 14, 2263, 2008 | 85 | 2008 |
| T1799A BRAF mutations in conjunctival melanocytic lesions N Goldenberg-Cohen, Y Cohen, E Rosenbaum, Z Herscovici, I Chowers, ... Investigative ophthalmology & visual science 46 (9), 3027-3030, 2005 | 80 | 2005 |
| Identification of regulatory targets of tissue-specific transcription factors: application to retina-specific gene regulation J Qian, N Esumi, Y Chen, Q Wang, I Chowers, DJ Zack Nucleic acids research 33 (11), 3479-3491, 2005 | 76 | 2005 |
| Identification of novel genes preferentially expressed in the retina using a custom human retina cDNA microarray I Chowers, TL Gunatilaka, RH Farkas, J Qian, AS Hackam, E Duh, ... Investigative ophthalmology & visual science 44 (9), 3732-3741, 2003 | 75 | 2003 |
| Whole exome sequencing reveals mutations in known retinal disease genes in 33 out of 68 Israeli families with inherited retinopathies A Beryozkin, E Shevah, A Kimchi, L Mizrahi-Meissonnier, S Khateb, ... Scientific reports 5 (1), 13187, 2015 | 72 | 2015 |
| Fellow eye effect of unilateral intravitreal bevacizumab injection in eyes with diabetic macular edema J Hanhart, L Tiosano, E Averbukh, E Banin, I Hemo, I Chowers Eye 28 (6), 646-653, 2014 | 69 | 2014 |
| Gene expression variation in the adult human retina I Chowers, D Liu, RH Farkas, TL Gunatilaka, AS Hackam, SL Bernstein, ... Human molecular genetics 12 (22), 2881-2893, 2003 | 68 | 2003 |
| Novel null mutations in the EYS gene are a frequent cause of autosomal recessive retinitis pigmentosa in the Israeli population D Bandah-Rozenfeld, KW Littink, T Ben-Yosef, TM Strom, I Chowers, ... Investigative ophthalmology & visual science 51 (9), 4387-4394, 2010 | 67 | 2010 |
