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Journal Articles (4)
Meeting Abstract (3)

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Investigative Ophthalmology & Visual Science (7)

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ARVO Annual Meeting Abstract (3)
Genetics (3)
Biochemistry and Molecular Biology (1)

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Genetics (4)
Eye Anatomy and Disorders (2)
Retina (2)
Biochemistry and Molecular Biology (1)

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mutation (4)
autosomal recessive inheritance (3)
genes (2)
homozygote (2)
retinal degeneration (2)
retinitis pigmentosa (2)
alleles (1)
family (1)
mutation, nonsense (1)
recurrence (1)

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Genetics November 2015

A Nonsense Mutation in FAM161A Is a Recurrent Founder Allele in Dutch and Belgian Individuals With Autosomal Recessive Retinitis Pigmentosa

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Kristof Van Schil; B. Jeroen Klevering; Bart P. Leroy; Jan Willem R. Pott; Dikla Bandah-Rozenfeld; Marijke N. Zonneveld-Vrieling; Dror Sharon; Anneke I. den Hollander; Frans P. M. Cremers; Elfride De Baere; Rob W. J. Collin; L. Ingeborgh van den Born
TAGS: alleles, autosomal recessive inheritance, mutation, mutation, nonsense, recurrence, retinitis pigmentosa
Invest. Ophthalmol. Vis. Sci.. 2015; 56(12):7418-7426. doi: https://doi.org/10.1167/iovs.15-17920

Includes: Supplemental Content

Genetics February 2014

Identification of Mutations Causing Inherited Retinal Degenerations in the Israeli and Palestinian Populations Using Homozygosity Mapping

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Avigail Beryozkin; Lina Zelinger; Dikla Bandah-Rozenfeld; Elia Shevach; Anat Harel; Tim Storm; Michal Sagi; Dalia Eli; Saul Merin; Eyal Banin; Dror Sharon
TAGS: family, genes, homozygote, mutation, retinal degeneration
Invest. Ophthalmol. Vis. Sci.. 2014; 55(2):1149-1160. doi: https://doi.org/10.1167/iovs.13-13625

Includes: Supplemental Content

Genetics March 2013

Mutations in CRB1 are a Relatively Common Cause of Autosomal Recessive Early-Onset Retinal Degeneration in the Israeli and Palestinian Populations

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Avigail Beryozkin; Lina Zelinger; Dikla Bandah-Rozenfeld; Anat Harel; Tim A. Strom; Saul Merin; Itay Chowers; Eyal Banin; Dror Sharon
TAGS: autosomal recessive inheritance, mutation, retinal degeneration, homozygote
Invest. Ophthalmol. Vis. Sci.. 2013; 54(3):2068-2075. doi: https://doi.org/10.1167/iovs.12-11419

Includes: Supplemental Content

ARVO Annual Meeting Abstract March 2012

FAM161A Produces Two Protein Isoforms with a Differential Retinal Expression Pattern

Dror Sharon; Alexey Obolensky; Elia Shevach; Eyal Banin; Shahar Frenkel; Adi Inbal; Dikla Bandah-Rozenfeld

Invest. Ophthalmol. Vis. Sci.. 2012; 53(14):1618. doi:

ARVO Annual Meeting Abstract April 2011

Mutation Survey of FAM161A in Patients with Retinitis Pigmentosa and Analysis of Protein Localization in the Human Retina

Dror Sharon; Dikla Bandah-Rozenfeld; Alexey Obolensky; Liliana Mizrahi-Meissonnier; Tamar Ben-Yosef; Sharon B. Schwartz; Artur V. Cideciyan; Samuel G. Jacobson; Eyal Banin

Invest. Ophthalmol. Vis. Sci.. 2011; 52(14):5388. doi:

ARVO Annual Meeting Abstract April 2011

Characterization of Phenotype and Genotype in Israeli Patients with Hereditary Retinal Disease

Eyal Banin; Dikla Bandah-Rozenfeld; Lina Zelinger; Liliana Mizrahi-Meissonnier; Alexey Obolensky; Dalia Eli; Anat Blumenfeld; Itay Chowers; Saul Merin; Dror Sharon

Invest. Ophthalmol. Vis. Sci.. 2011; 52(14):6607. doi:

Biochemistry and Molecular Biology September 2010

Novel Null Mutations in the EYS Gene Are a Frequent Cause of Autosomal Recessive Retinitis Pigmentosa in the Israeli Population

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Dikla Bandah-Rozenfeld; Karin W. Littink; Tamar Ben-Yosef; Tim M. Strom; Itay Chowers; Rob W. J. Collin; Anneke I. den Hollander; L. Ingeborgh van den Born; Marijke N. Zonneveld; Saul Merin; Eyal Banin; Frans P. M. Cremers; Dror Sharon
TAGS: autosomal recessive inheritance, genes, mutation, retinitis pigmentosa
Invest. Ophthalmol. Vis. Sci.. 2010; 51(9):4387-4394. doi: https://doi.org/10.1167/iovs.09-4732

Includes: Supplemental Content

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Online ISSN: 1552-5783

Investigative Ophthalmology & Visual Science
Journal of Vision
Translational Vision Science & Technology

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