1. A homozygous nonsense CEP250 mutation combined with a heterozygous nonsense C2orf71 mutation is associated with atypical Usher syndrome. Issue 7 (29th April 2014) Authors: Khateb, Samer; Zelinger, Lina; Mizrahi-Meissonnier, Liliana; Ayuso, Carmen; Koenekoop, Robert K; Laxer, Uri; Gross, Menachem; Banin, Eyal; Sharon, Dror Journal: Journal of medical genetics Issue: Volume 51:Issue 7(2014) Page Start: 460 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A nationwide genetic analysis of inherited retinal diseases in Israel as assessed by the Israeli inherited retinal disease consortium (IIRDC). Issue 1 (15th September 2019) Authors: Sharon, Dror; Ben‐Yosef, Tamar; Goldenberg‐Cohen, Nitza; Pras, Eran; Gradstein, Libe; Soudry, Shiri; Mezer, Eedy; Zur, Dinah; Abbasi, Anan H.; Zeitz, Christina; Cremers, Frans P. M.; Khan, Muhammad I.; Levy, Jaime; Rotenstreich, Ygal; Birk, Ohad S.; Ehrenberg, Miriam; Leibu, Rina; Newman, Hadas; ... Journal: Human mutation Issue: Volume 41:Issue 1(2020) Page Start: 140 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Bevacizumab Treatment for Choroidal Neovascularization Associated with Adult-Onset Foveomacular Vitelliform Dystrophy. Issue 6 (November 2014) Authors: Tiosano, Liran; Jaouni, Tareq; Averbukh, Edward; Grunin, Michelle; Banin, Eyal; Chowers, Itay Journal: European journal of ophthalmology Issue: Volume 24:Issue 6(2014) Page Start: 890 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Can an in vivo imaging system be used to determine localization and biodistribution of AAV5-mediated gene expression following subretinal and intravitreal delivery in mice?. (November 2018) Authors: Ezra-Elia, Raaya; Obolensky, Alexey; Ejzenberg, Ayala; Ross, Maya; Mintz, Dvir; Banin, Eyal; Ofri, Ron Journal: Experimental eye research Issue: Volume 176(2018) Page Start: 227 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Characterising the phenotype and progression of sporadic adult-onset foveomacular vitelliform dystrophy. Issue 11 (22nd January 2016) Authors: Tiosano, Liran; Grunin, Michelle; Hagbi-Levi, Shira; Banin, Eyal; Averbukh, Edward; Chowers, Itay Journal: British journal of ophthalmology Issue: Volume 100:Issue 11(2016) Page Start: 1476 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Contrary to popular belief, chinchillas do not have a pure rod retina. (10th June 2018) Authors: Sandalon, Shai; Boykova, Anna; Ross, Maya; Obolensky, Alexey; Banin, Eyal; Ofri, Ron Journal: Veterinary ophthalmology Issue: Volume 22:Number 1(2019) Page Start: 93 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Correlation of Response between Both Eyes to First- and Second-Line Anti-VEGF Therapy in Diabetic Macular Edema. (3rd April 2021) Authors: Tiosano, Liran; Ayalon, Anfisa; Banin, Eyal; Averbukh, Edward; Jaouni, Tareq; Chowers, Itay Journal: Current eye research Issue: Volume 46:Number 4(2021) Page Start: 539 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Enhanced S-Cone Syndrome Masquerading as TORCH in an Infant and a Toddler. (7th February 2023) Authors: Navarrete, Ana; Matanis-Suidan, Milka; Hemo, Itzhak; Mechoulam, Hadas; Banin, Eyal; Amer, Radgonde Journal: Ocular immunology and inflammation Issue: Volume 31:Number 2(2023) Page Start: 455 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Gene transfer by viral vectors into blood vessels in a rat model of retinopathy of prematurity. Issue 8 (1st August 2001) Authors: Chowers, Itay; Banin, Eyal; Hemo, Yitzchak; Porat, Rinat; Falk, Haya; Keshet, Eli; Pe'er, Jacob; Panet, Amos Journal: British journal of ophthalmology Issue: Volume 85:Issue 8(2001) Page Start: 991 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Identification of genomic deletions causing inherited retinal degenerations by coverage analysis of whole exome sequencing data. Issue 9 (22nd April 2016) Authors: Khateb, Samer; Hanany, Mor; Khalaileh, Ayat; Beryozkin, Avigail; Meyer, Segev; Abu-Diab, Alaa; Abu Turky, Fathieh; Mizrahi-Meissonnier, Liliana; Lieberman, Sari; Ben-Yosef, Tamar; Banin, Eyal; Sharon, Dror Journal: Journal of medical genetics Issue: Volume 53:Issue 9(2016) Page Start: 600 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗