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Samer Khateb

Showing results (41-50 of 70) with videos related to

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Clinical Ophthalmology (Auckland, N.Z.)|March 19, 2019
Chromatic pupilloperimetry for objective diagnosis of Best vitelliform macular dystrophyDaniel Ben Ner, Ifat Sher, Amit Hamburg, et al.
Retina (Philadelphia, Pa.)|January 29, 2021
SENIOR-LØKEN SYNDROME: A Case Series and Review of the Renoretinal Phenotype and Advances of Molecular DiagnosisClaudia Yahalom, Oded Volovelsky, Michal Macarov, et al.
Ophthalmology|December 26, 2017
Nonsyndromic Retinitis Pigmentosa in the Ashkenazi Jewish Population: Genetic and Clinical AspectsAdva Kimchi, Samer Khateb, Rong Wen, et al.
Scientific Reports|September 17, 2020
Unique combination of clinical features in a large cohort of 100 patients with retinitis pigmentosa caused by FAM161A mutationsAvigail Beryozkin, Samer Khateb, Carlos Alberto Idrobo-Robalino, et al.
Frontiers in Cell and Developmental Biology|November 1, 2021
Retinal Degeneration Associated With RPGRIP1: A Review of Natural History, Mutation Spectrum, and Genotype-Phenotype Correlation in 228 PatientsAvigail Beryozkin, Hamzah Aweidah, Roque Daniel Carrero Valenzuela, et al.
JAMA Ophthalmology|July 17, 2025
Founder Homozygous Nonsense CREB3 Variant and Variable-Onset Retinal DegenerationManar Salameh, Ghadeer Abu Tair, Samira Mousa, et al.
Retina (Philadelphia, Pa.)|May 13, 2025
Bilateral Idiopathic Multifocal Pigment Epithelial Detachments: A Case Series and Review of LiteratureSamer Khateb, Sean Ghiam, Jordan Safran, et al.
NPJ Genomic Medicine|April 10, 2026
Variants in the ciliopathy gene SCLT1 are associated with non-syndromic and syndromic retinal degeneration of variable severityRiccardo Sangermano, Kaoru Fujinami, Suk Ho Byeon, et al.
Medrxiv : the Preprint Server for Health Sciences|September 21, 2023
Genome-wide association study and genomic risk prediction of age-related macular degeneration in IsraelMichelle Grunin, Daria Triffon, Gala Beykin, et al.
American Journal of Human Genetics|September 3, 2016
Bi-allelic Truncating Mutations in CEP78, Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing LossPrasanthi Namburi, Rinki Ratnapriya, Samer Khateb, et al.
Pageof 7

Showing results (41-50 of 70) with videos related to

Sort By:
Pageof 7
Clinical Ophthalmology (Auckland, N.Z.)|March 19, 2019
Chromatic pupilloperimetry for objective diagnosis of Best vitelliform macular dystrophyDaniel Ben Ner, Ifat Sher, Amit Hamburg, et al.
Retina (Philadelphia, Pa.)|January 29, 2021
SENIOR-LØKEN SYNDROME: A Case Series and Review of the Renoretinal Phenotype and Advances of Molecular DiagnosisClaudia Yahalom, Oded Volovelsky, Michal Macarov, et al.
Ophthalmology|December 26, 2017
Nonsyndromic Retinitis Pigmentosa in the Ashkenazi Jewish Population: Genetic and Clinical AspectsAdva Kimchi, Samer Khateb, Rong Wen, et al.
Scientific Reports|September 17, 2020
Unique combination of clinical features in a large cohort of 100 patients with retinitis pigmentosa caused by FAM161A mutationsAvigail Beryozkin, Samer Khateb, Carlos Alberto Idrobo-Robalino, et al.
Frontiers in Cell and Developmental Biology|November 1, 2021
Retinal Degeneration Associated With RPGRIP1: A Review of Natural History, Mutation Spectrum, and Genotype-Phenotype Correlation in 228 PatientsAvigail Beryozkin, Hamzah Aweidah, Roque Daniel Carrero Valenzuela, et al.
JAMA Ophthalmology|July 17, 2025
Founder Homozygous Nonsense CREB3 Variant and Variable-Onset Retinal DegenerationManar Salameh, Ghadeer Abu Tair, Samira Mousa, et al.
Retina (Philadelphia, Pa.)|May 13, 2025
Bilateral Idiopathic Multifocal Pigment Epithelial Detachments: A Case Series and Review of LiteratureSamer Khateb, Sean Ghiam, Jordan Safran, et al.
NPJ Genomic Medicine|April 10, 2026
Variants in the ciliopathy gene SCLT1 are associated with non-syndromic and syndromic retinal degeneration of variable severityRiccardo Sangermano, Kaoru Fujinami, Suk Ho Byeon, et al.
Medrxiv : the Preprint Server for Health Sciences|September 21, 2023
Genome-wide association study and genomic risk prediction of age-related macular degeneration in IsraelMichelle Grunin, Daria Triffon, Gala Beykin, et al.
American Journal of Human Genetics|September 3, 2016
Bi-allelic Truncating Mutations in CEP78, Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing LossPrasanthi Namburi, Rinki Ratnapriya, Samer Khateb, et al.
Pageof 7