Publications by authors named "Eyal Banin"

100Publications

Correlation of Response between Both Eyes to First- and Second-Line Anti-VEGF Therapy in Diabetic Macular Edema.

Curr Eye Res 2020 Aug 30:1-7. Epub 2020 Aug 30.

Department of Ophthalmology, Hadassah-Hebrew University Medical Center , Jerusalem, Israel.

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http://dx.doi.org/10.1080/02713683.2020.1812085DOI Listing
August 2020

A unique -associated variant in a Georgian Jewish family with probable North Carolina macular dystrophy and the possible contribution of a unique variant.

Mol Vis 2020 16;26:299-310. Epub 2020 Apr 16.

Department of Ophthalmology, Hadassah Medical Center, Faculty of Medicine, The Hebrew University Jerusalem, Jerusalem, Israel.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7245606PMC
April 2020

Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomics.

Genet Med 2020 Jul 20;22(7):1235-1246. Epub 2020 Apr 20.

Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.

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http://dx.doi.org/10.1038/s41436-020-0787-4DOI Listing
July 2020

The combination of whole-exome sequencing and clinical analysis allows better diagnosis of rare syndromic retinal dystrophies.

Acta Ophthalmol 2019 Sep 29;97(6):e877-e886. Epub 2019 Mar 29.

Department of Ophthalmology, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.

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http://dx.doi.org/10.1111/aos.14095DOI Listing
September 2019

Consecutive unilateral recording of the two eyes affects dark-adapted ERG responses, when compared to simultaneous bilateral recording.

Doc Ophthalmol 2018 12 9;137(3):183-192. Epub 2018 Nov 9.

Koret School of Veterinary Medicine, The Hebrew University of Jerusalem, Rehovot, Israel.

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http://link.springer.com/10.1007/s10633-018-9661-y
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http://dx.doi.org/10.1007/s10633-018-9661-yDOI Listing
December 2018

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?

Exp Eye Res 2018 11 29;176:227-234. Epub 2018 Aug 29.

Koret School of Veterinary Medicine, Hebrew University of Jerusalem, Rehovot, Israel. Electronic address:

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http://dx.doi.org/10.1016/j.exer.2018.08.021DOI Listing
November 2018

Immunological Properties of Human Embryonic Stem Cell-Derived Retinal Pigment Epithelial Cells.

Stem Cell Reports 2018 09 16;11(3):681-695. Epub 2018 Aug 16.

The Hadassah Human Embryonic Stem Cell Research Center, The Goldyne Savad Institute of Gene Therapy, Hadassah Medical Center, Jerusalem 91120, Israel; Department of Obstetrics & Gynecology, Hadassah Medical Center, Jerusalem 91120, Israel. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S22136711183031
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http://dx.doi.org/10.1016/j.stemcr.2018.07.009DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6135721PMC
September 2018

Contrary to popular belief, chinchillas do not have a pure rod retina.

Vet Ophthalmol 2019 Jan 10;22(1):93-97. Epub 2018 Jun 10.

Koret School of Veterinary Medicine, Hebrew University of Jerusalem, Rehovot, Israel.

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http://dx.doi.org/10.1111/vop.12581DOI Listing
January 2019

The Genetics of Usher Syndrome in the Israeli and Palestinian Populations.

Invest Ophthalmol Vis Sci 2018 02;59(2):1095-1104

Department of Ophthalmology, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.

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http://dx.doi.org/10.1167/iovs.17-22817DOI Listing
February 2018

Nonsyndromic Retinitis Pigmentosa in the Ashkenazi Jewish Population: Genetic and Clinical Aspects.

Ophthalmology 2018 05 22;125(5):725-734. Epub 2017 Dec 22.

Department of Ophthalmology, Hadassah-Hebrew University Medical Center, Jerusalem, Israel. Electronic address:

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http://dx.doi.org/10.1016/j.ophtha.2017.11.014DOI Listing
May 2018

Course of Sodium Iodate-Induced Retinal Degeneration in Albino and Pigmented Mice.

Invest Ophthalmol Vis Sci 2017 04;58(4):2239-2249

Center for Retinal and Macular Degenerations, Department of Ophthalmology, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.

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http://dx.doi.org/10.1167/iovs.16-21255DOI Listing
April 2017

Novel GUCY2D mutation causes phenotypic variability of Leber congenital amaurosis in a large kindred.

BMC Med Genet 2016 07 30;17(1):52. Epub 2016 Jul 30.

The Morris Kahn Laboratory of Human Genetics, National Institute for Biotechnology in the Negev and Faculty of Health Sciences, Ben Gurion University of the Negev, Beer-Sheva, 84105, Israel.

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http://dx.doi.org/10.1186/s12881-016-0314-2DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4967317PMC
July 2016

Characterising the phenotype and progression of sporadic adult-onset foveomacular vitelliform dystrophy.

Br J Ophthalmol 2016 Nov 22;100(11):1476-1481. Epub 2016 Jan 22.

Department of Ophthalmology, Hadassah-Hebrew University Medical Center and the Hebrew University School of Medicine, Jerusalem, Israel.

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http://bjo.bmj.com/lookup/doi/10.1136/bjophthalmol-2015-3076
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http://dx.doi.org/10.1136/bjophthalmol-2015-307658DOI Listing
November 2016

Retinal Phenotype following Combined Deletion of the Chemokine Receptor CCR2 and the Chemokine CX3CL1 in Mice.

Ophthalmic Res 2016 16;55(3):126-34. Epub 2015 Dec 16.

Department of Ophthalmology, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.

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http://dx.doi.org/10.1159/000441794DOI Listing
September 2016

Nonsyndromic retinitis pigmentosa is highly prevalent in the Jerusalem region with a high frequency of founder mutations.

Mol Vis 2015 17;21:783-92. Epub 2015 Jul 17.

Department of Ophthalmology, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4506056PMC
May 2016

Bevacizumab treatment for neovascular age-related macular degeneration in the setting of a clinic: "real life" long-term outcome.

BMC Ophthalmol 2015 Apr 11;15:39. Epub 2015 Apr 11.

Department of Ophthalmology, Hadassah - Hebrew University Medical Center, PO Box 12000, Jerusalem, 91120, Israel.

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http://bmcophthalmol.biomedcentral.com/articles/10.1186/s128
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http://dx.doi.org/10.1186/s12886-015-0019-xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4404564PMC
April 2015

Biology and therapy of inherited retinal degenerative disease: insights from mouse models.

Dis Model Mech 2015 Feb;8(2):109-29

Neurobiology-Neurodegeneration and Repair Laboratory, National Eye Institute, National Institutes of Health, Bethesda, MD 20892, USA.

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http://dmm.biologists.org/content/dmm/8/2/109.full.pdf
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http://dmm.biologists.org/lookup/doi/10.1242/dmm.017913
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http://dx.doi.org/10.1242/dmm.017913DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4314777PMC
February 2015

Whole exome sequencing reveals GUCY2D as a major gene associated with cone and cone-rod dystrophy in Israel.

Invest Ophthalmol Vis Sci 2014 Dec 16;56(1):420-30. Epub 2014 Dec 16.

Neurobiology-Neurodegeneration & Repair Laboratory, National Eye Institute, National Institutes of Health, Bethesda, Maryland, United States Department of Ophthalmology, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.

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http://dx.doi.org/10.1167/iovs.14-15647DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4296770PMC
December 2014

Flicker cone function in normal and day blind sheep: a large animal model for human achromatopsia caused by CNGA3 mutation.

Doc Ophthalmol 2014 Dec 10;129(3):141-50. Epub 2014 Sep 10.

Koret School of Veterinary Medicine, Hebrew University of Jerusalem, PO Box 12, 7610001, Rehovot, Israel.

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http://dx.doi.org/10.1007/s10633-014-9458-6DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4452202PMC
December 2014

Bevacizumab treatment for choroidal neovascularization associated with adult-onset foveomacular vitelliform dystrophy.

Eur J Ophthalmol 2014 Nov-Dec;24(6):890-6. Epub 2014 May 20.

Department of Ophthalmology, Hadassah-Hebrew University Medical Center, Jerusalem - Israel.

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http://dx.doi.org/10.5301/ejo.5000486DOI Listing
December 2014

Degeneration modulates retinal response to transient exogenous oxidative injury.

PLoS One 2014 21;9(2):e87751. Epub 2014 Feb 21.

Department of Ophthalmology, Hadassah-Hebrew University Medical Center, and the Hebrew University-Hadassah School of Medicine, Jerusalem, Israel.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0087751PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3931611PMC
January 2015

Identification of mutations causing inherited retinal degenerations in the israeli and palestinian populations using homozygosity mapping.

Invest Ophthalmol Vis Sci 2014 Feb 24;55(2):1149-60. Epub 2014 Feb 24.

Department of Ophthalmology, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.

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http://dx.doi.org/10.1167/iovs.13-13625DOI Listing
February 2014

Ocular phenotype analysis of a family with biallelic mutations in the BEST1 gene.

Am J Ophthalmol 2014 Mar 15;157(3):697-709.e1-2. Epub 2013 Dec 15.

Department of Ophthalmology, Glostrup Hospital, Glostrup, Denmark; National Eye Clinic, Kennedy Center, Glostrup, Denmark; Department of Ophthalmology, Clinical Sciences, Scane County University Hospital, University of Lund, Sweden. Electronic address:

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http://dx.doi.org/10.1016/j.ajo.2013.12.010DOI Listing
March 2014

Genetic heterogeneity and consanguinity lead to a "double hit": homozygous mutations of MYO7A and PDE6B in a patient with retinitis pigmentosa.

Mol Vis 2013 20;19:1565-71. Epub 2013 Jul 20.

The Krieger Eye Research Laboratory, Felsenstein Medical Research Center, Schneider Children's Medical Center, Beilinson Campus, Petah Tikva, Israel.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3718492PMC
September 2013

Clinical characteristics of rod and cone photoreceptor dystrophies in patients with mutations in the C8orf37 gene.

Invest Ophthalmol Vis Sci 2013 Jul 12;54(7):4683-90. Epub 2013 Jul 12.

Department of Ophthalmology, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.

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http://dx.doi.org/10.1167/iovs.12-11439DOI Listing
July 2013

Cone dystrophy with supernormal rod response: novel KCNV2 mutations in an underdiagnosed phenotype.

Ophthalmology 2013 Nov 29;120(11):2338-43. Epub 2013 May 29.

Department of Ophthalmology, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.

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http://linkinghub.elsevier.com/retrieve/pii/S016164201300316
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http://dx.doi.org/10.1016/j.ophtha.2013.03.031DOI Listing
November 2013

Mutations in CRB1 are a relatively common cause of autosomal recessive early-onset retinal degeneration in the Israeli and Palestinian populations.

Invest Ophthalmol Vis Sci 2013 Mar 1;54(3):2068-75. Epub 2013 Mar 1.

Department of Ophthalmology, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.

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http://dx.doi.org/10.1167/iovs.12-11419DOI Listing
March 2013

Association of pattern dystrophy with an HTRA1 single-nucleotide polymorphism.

Arch Ophthalmol 2012 Aug;130(8):987-91

Department of Ophthalmology, Hadassah–Hebrew University Medical Center, POB 12000, Jerusalem, Israel 91120.

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http://dx.doi.org/10.1001/archophthalmol.2012.1483DOI Listing
August 2012

Fundus albipunctatus: novel mutations and phenotypic description of Israeli patients.

Mol Vis 2012 23;18:1712-8. Epub 2012 Jun 23.

Department of Ophthalmology, Assaf Harofeh Medical Center, Zerifin, Israel.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3399783PMC
November 2012

Subsurface femtosecond tissue alteration: selectively photobleaching macular degeneration pigments in near retinal contact.

J Phys Chem B 2012 Jun 29;116(23):6945-51. Epub 2012 May 29.

Division of Applied Physics, Selim and Rachel Benin, School of Engineering, The Hebrew University, Givat Ram, Jerusalem 91904, Israel.

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http://dx.doi.org/10.1021/jp300355mDOI Listing
June 2012

Retinal function and structure in the hypotransferrinemic mouse.

Invest Ophthalmol Vis Sci 2012 Feb 2;53(2):605-12. Epub 2012 Feb 2.

Department of Ophthalmology, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.

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http://dx.doi.org/10.1167/iovs.11-7436DOI Listing
February 2012

Zinc-desferrioxamine attenuates retinal degeneration in the rd10 mouse model of retinitis pigmentosa.

Free Radic Biol Med 2011 Oct 23;51(8):1482-91. Epub 2011 Jul 23.

Department of Ophthalmology, Hadassah-Hebrew University Medical Center, Jerusalem 91120, Israel.

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http://dx.doi.org/10.1016/j.freeradbiomed.2011.07.014DOI Listing
October 2011

A homozygous frameshift mutation in BEST1 causes the classical form of Best disease in an autosomal recessive mode.

Invest Ophthalmol Vis Sci 2011 Jul 18;52(8):5332-8. Epub 2011 Jul 18.

Department of Ophthalmology, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.

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http://dx.doi.org/10.1167/iovs.11-7174DOI Listing
July 2011

Human retinal disease from AIPL1 gene mutations: foveal cone loss with minimal macular photoreceptors and rod function remaining.

Invest Ophthalmol Vis Sci 2011 Jan 5;52(1):70-9. Epub 2011 Jan 5.

Department of Ophthalmology, University of Pennsylvania, Philadelphia, PA, USA.

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http://dx.doi.org/10.1167/iovs.10-6127DOI Listing
January 2011

An ancient autosomal haplotype bearing a rare achromatopsia-causing founder mutation is shared among Arab Muslims and Oriental Jews.

Hum Genet 2010 Sep 13;128(3):261-7. Epub 2010 Jun 13.

Department of Ophthalmology, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.

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http://dx.doi.org/10.1007/s00439-010-0846-zDOI Listing
September 2010

Variable retinal phenotypes caused by mutations in the X-linked photopigment gene array.

Invest Ophthalmol Vis Sci 2010 Aug 10;51(8):3884-92. Epub 2010 Mar 10.

Department of Ophthalmology, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.

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https://sites.oxy.edu/clint/physio/article/VariableRetinalPh
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http://iovs.arvojournals.org/article.aspx?doi=10.1167/iovs.0
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http://dx.doi.org/10.1167/iovs.09-4592DOI Listing
August 2010

Effect of para-aminobenzoic acid on the course of retinal degeneration in the rd10 mouse.

J Ocul Pharmacol Ther 2009 Dec;25(6):475-82

Department of Ophthalmology, The Hebrew University-Hadassah Schools of Medicine and Dental Medicine, Jerusalem, Israel.

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http://dx.doi.org/10.1089/jop.2009.0020DOI Listing
December 2009

Directed differentiation of human embryonic stem cells into functional retinal pigment epithelium cells.

Cell Stem Cell 2009 Oct;5(4):396-408

The Hadassah Human Embryonic Stem Cell Research Center, The Goldyne Savad Institute of Gene Therapy & Department of Gynecology, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.

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http://dx.doi.org/10.1016/j.stem.2009.07.002DOI Listing
October 2009

A novel day blindness in sheep: epidemiological, behavioural, electrophysiological and histopathological studies.

Vet J 2010 Aug 9;185(2):130-7. Epub 2009 Jul 9.

Koret School of Veterinary Medicine, The Hebrew University of Jerusalem, Rehovot 76100, Israel.

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http://dx.doi.org/10.1016/j.tvjl.2009.05.029DOI Listing
August 2010

The spectrum of retinal diseases caused by NR2E3 mutations in Israeli and Palestinian patients.

Arch Ophthalmol 2009 Mar;127(3):297-302

Department of Ophthalmology, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.

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http://dx.doi.org/10.1001/archophthalmol.2008.615DOI Listing
March 2009

Antioxidant or neurotrophic factor treatment preserves function in a mouse model of neovascularization-associated oxidative stress.

J Clin Invest 2009 Mar 2;119(3):611-23. Epub 2009 Feb 2.

Department of Cell Biology, Scripps Center for Mass Spectrometry, The Scripps Research Institute, La Jolla, California 92037, USA.

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http://dx.doi.org/10.1172/JCI35977DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2648679PMC
March 2009

The potential of desferrioxamine-gallium as an anti-Pseudomonas therapeutic agent.

Proc Natl Acad Sci U S A 2008 Oct 17;105(43):16761-6. Epub 2008 Oct 17.

Department of Microbiology, School of Medicine, University of Washington, Seattle, WA 98195, USA.

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http://dx.doi.org/10.1073/pnas.0808608105DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2575493PMC
October 2008

Four USH2A founder mutations underlie the majority of Usher syndrome type 2 cases among non-Ashkenazi Jews.

Genet Test 2008 Jun;12(2):289-94

Department of Genetics and The Rappaport Family Institute for Research in the Medical Sciences, Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, Israel.

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http://www.liebertpub.com/doi/10.1089/gte.2007.0107
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http://dx.doi.org/10.1089/gte.2007.0107DOI Listing
June 2008

P35S mutation in the NOG gene associated with Teunissen-Cremers syndrome and features of multiple NOG joint-fusion syndromes.

Eur J Med Genet 2008 Jul-Aug;51(4):351-7. Epub 2008 Mar 20.

Department of Otolaryngology/Head and Neck Surgery, Hadassah Hebrew University Medical Center, 91120 Jerusalem, Israel.

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http://dx.doi.org/10.1016/j.ejmg.2008.02.008DOI Listing
October 2008

A novel de novo PAX6 mutation in an Ashkenazi-Jewish family with aniridia.

Mol Vis 2008 Jan 28;14:142-5. Epub 2008 Jan 28.

Department of Ophthalmology, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2255027PMC
January 2008

Hypomorphic mutations in syndromic encephalocele genes are associated with Bardet-Biedl syndrome.

Nat Genet 2008 Apr 9;40(4):443-8. Epub 2008 Mar 9.

McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, 733. N Broadway, Baltimore, Maryland 21205, USA.

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http://dx.doi.org/10.1038/ng.97DOI Listing
April 2008

Retinal disease in Usher syndrome III caused by mutations in the clarin-1 gene.

Invest Ophthalmol Vis Sci 2008 Jun 15;49(6):2651-60. Epub 2008 Feb 15.

Scheie Eye Institute, Department of Ophthalmology, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA.

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http://dx.doi.org/10.1167/iovs.07-1505DOI Listing
June 2008

Ischemic preconditioning of the rat retina: protective role of ferritin.

Free Radic Biol Med 2008 Apr 21;44(7):1286-94. Epub 2007 Nov 21.

Department of Ophthalmology, The Hebrew University-Hadassah Schools of Medicine and Dental Medicine, Jerusalem 91120, Israel.

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http://dx.doi.org/10.1016/j.freeradbiomed.2007.10.060DOI Listing
April 2008

A common founder mutation of CERKL underlies autosomal recessive retinal degeneration with early macular involvement among Yemenite Jews.

Invest Ophthalmol Vis Sci 2007 Dec;48(12):5431-8

Department of Genetics, The Rappaport Family Institute for Research in the Medical Sciences, Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, Israel.

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http://dx.doi.org/10.1167/iovs.07-0736DOI Listing
December 2007