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Samer Khateb

Showing results (51-60 of 70) with videos related to

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Scientific Reports|June 6, 2024
Genome wide association study and genomic risk prediction of age related macular degeneration in IsraelMichelle Grunin, Daria Triffon, Gala Beykin, et al.
Retina (Philadelphia, Pa.)|September 4, 2019
PHENOTYPIC CHARACTERISTICS OF ROD-CONE DYSTROPHY ASSOCIATED WITH MYO7A MUTATIONS IN A LARGE FRENCH COHORTSamer Khateb, Saddek Mohand-Saïd, Marco Nassisi, et al.
Human Molecular Genetics|December 23, 2017
Whole-exome sequencing reveals POC5 as a novel gene associated with autosomal recessive retinitis pigmentosaMonika Weisz Hubshman, Sanne Broekman, Erwin van Wijk, et al.
Genes|June 27, 2024
Genetic and Clinical Analyses of the <i>KIZ</i>-c.226C>T Variant Resulting in a Dual Mutational MechanismYogapriya Sundaresan, Antonio Rivera, Alexey Obolensky, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|February 17, 2026
Choroidal imaging biomarkers as predictors of recurrent central serous chorioretinopathy: A multicenter retrospective study - MICRoN report number fiveArman Zarnegar, Nasiq Hasan, Sumit Randhir Singh, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|October 11, 2025
Predictors of persistent central serous chorioretinopathy: a multicenter retrospective study - MICRoN report number fourPriyanka Gandhi, Nasiq Hasan, Korrina Gidwani, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 7, 2025
Non-coding single-nucleotide and structural variants affecting the EYS putative promoter cause autosomal recessive retinitis pigmentosaTamar Hayman, Shai Ovadia, Jaya Krishnan, et al.
Investigative Ophthalmology & Visual Science|February 27, 2024
Best Disease: Global Mutations Review, Genotype-Phenotype Correlation, and Prevalence Analysis in the Israeli PopulationAvigail Beryozkin, Ifat Sher, Miriam Ehrenberg, et al.
JAMA Ophthalmology|May 16, 2024
Nationwide Prevalence of Inherited Retinal Diseases in the Israeli PopulationSapir Shalom, Tamar Ben-Yosef, Ifat Sher, et al.
Scientific Reports|August 27, 2015
Whole Exome Sequencing Reveals Mutations in Known Retinal Disease Genes in 33 out of 68 Israeli Families with Inherited RetinopathiesAvigail Beryozkin, Elia Shevah, Adva Kimchi, et al.
Pageof 7

Showing results (51-60 of 70) with videos related to

Sort By:
Pageof 7
Scientific Reports|June 6, 2024
Genome wide association study and genomic risk prediction of age related macular degeneration in IsraelMichelle Grunin, Daria Triffon, Gala Beykin, et al.
Retina (Philadelphia, Pa.)|September 4, 2019
PHENOTYPIC CHARACTERISTICS OF ROD-CONE DYSTROPHY ASSOCIATED WITH MYO7A MUTATIONS IN A LARGE FRENCH COHORTSamer Khateb, Saddek Mohand-Saïd, Marco Nassisi, et al.
Human Molecular Genetics|December 23, 2017
Whole-exome sequencing reveals POC5 as a novel gene associated with autosomal recessive retinitis pigmentosaMonika Weisz Hubshman, Sanne Broekman, Erwin van Wijk, et al.
Genes|June 27, 2024
Genetic and Clinical Analyses of the <i>KIZ</i>-c.226C>T Variant Resulting in a Dual Mutational MechanismYogapriya Sundaresan, Antonio Rivera, Alexey Obolensky, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|February 17, 2026
Choroidal imaging biomarkers as predictors of recurrent central serous chorioretinopathy: A multicenter retrospective study - MICRoN report number fiveArman Zarnegar, Nasiq Hasan, Sumit Randhir Singh, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|October 11, 2025
Predictors of persistent central serous chorioretinopathy: a multicenter retrospective study - MICRoN report number fourPriyanka Gandhi, Nasiq Hasan, Korrina Gidwani, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 7, 2025
Non-coding single-nucleotide and structural variants affecting the EYS putative promoter cause autosomal recessive retinitis pigmentosaTamar Hayman, Shai Ovadia, Jaya Krishnan, et al.
Investigative Ophthalmology & Visual Science|February 27, 2024
Best Disease: Global Mutations Review, Genotype-Phenotype Correlation, and Prevalence Analysis in the Israeli PopulationAvigail Beryozkin, Ifat Sher, Miriam Ehrenberg, et al.
JAMA Ophthalmology|May 16, 2024
Nationwide Prevalence of Inherited Retinal Diseases in the Israeli PopulationSapir Shalom, Tamar Ben-Yosef, Ifat Sher, et al.
Scientific Reports|August 27, 2015
Whole Exome Sequencing Reveals Mutations in Known Retinal Disease Genes in 33 out of 68 Israeli Families with Inherited RetinopathiesAvigail Beryozkin, Elia Shevah, Adva Kimchi, et al.
Pageof 7