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Itay Chowers
Itay Chowers
Chairman Department of Ophthalmoloy Hadassah Medical Center
在 hadassah.org.il 的电子邮件经过验证
标题
引用次数
引用次数
年份
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
14562016
Seven new loci associated with age-related macular degeneration
Nature genetics 45 (4), 433-439, 2013
8622013
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
2482013
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
1602003
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
1222015
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
1212001
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
1182004
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
1172010
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
1152006
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
1062004
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
1032020
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
962001
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
852008
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
802005
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
762005
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
752015
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
752003
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
692014
Zinc–desferrioxamine attenuates retinal degeneration in the rd10 mouse model of retinitis pigmentosa
A Obolensky, E Berenshtein, M Lederman, B Bulvik, R Alper-Pinus, ...
Free Radical Biology and Medicine 51 (8), 1482-1491, 2011
692011
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
692010
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