Samer Khateb

1.2k total citations
43 papers, 662 citations indexed

About

Samer Khateb is a scholar working on Molecular Biology, Ophthalmology and Genetics. According to data from OpenAlex, Samer Khateb has authored 43 papers receiving a total of 662 indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Molecular Biology, 19 papers in Ophthalmology and 9 papers in Genetics. Recurrent topics in Samer Khateb's work include Retinal Development and Disorders (30 papers), Retinal Diseases and Treatments (15 papers) and CRISPR and Genetic Engineering (6 papers). Samer Khateb is often cited by papers focused on Retinal Development and Disorders (30 papers), Retinal Diseases and Treatments (15 papers) and CRISPR and Genetic Engineering (6 papers). Samer Khateb collaborates with scholars based in Israel, United States and Netherlands. Samer Khateb's co-authors include Eyal Banin, Dror Sharon, Pnina Weisman-Shomer, Michael Fry, Tamar Ben‐Yosef, Menachem Gross, A. L. Ludwig, Lina Zelinger, Radgonde Amer and Alexey Obolensky and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and PLoS ONE.

In The Last Decade

Samer Khateb

36 papers receiving 653 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Samer Khateb Israel 16 525 178 147 94 67 43 662
Tobias Eisenberger Germany 11 437 0.8× 175 1.0× 165 1.1× 66 0.7× 75 1.1× 14 531
Karmen M Trzupek United States 12 420 0.8× 278 1.6× 76 0.5× 51 0.5× 122 1.8× 16 617
Sakae Ikeda United States 15 421 0.8× 99 0.6× 58 0.4× 139 1.5× 56 0.8× 29 611
Wendy M. Aartsen Netherlands 13 574 1.1× 149 0.8× 100 0.7× 153 1.6× 62 0.9× 16 815
Krysta Voesenek Netherlands 9 863 1.6× 228 1.3× 524 3.6× 154 1.6× 44 0.7× 11 1.0k
Eva Lenassi United Kingdom 17 595 1.1× 436 2.4× 141 1.0× 54 0.6× 77 1.1× 29 859
Margaret R. Starostik United States 7 340 0.6× 148 0.8× 102 0.7× 32 0.3× 17 0.3× 10 502
Elisabeth M. Bleeker‐Wagemakers Netherlands 10 664 1.3× 265 1.5× 105 0.7× 195 2.1× 42 0.6× 13 781
Imad Ghazi France 10 618 1.2× 366 2.1× 120 0.8× 86 0.9× 87 1.3× 15 688
N. L. Hawes United States 10 650 1.2× 196 1.1× 79 0.5× 103 1.1× 33 0.5× 19 763

Countries citing papers authored by Samer Khateb

Since Specialization
Citations

This map shows the geographic impact of Samer Khateb's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Samer Khateb with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Samer Khateb more than expected).

Fields of papers citing papers by Samer Khateb

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Samer Khateb. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Samer Khateb. The network helps show where Samer Khateb may publish in the future.

Co-authorship network of co-authors of Samer Khateb

This figure shows the co-authorship network connecting the top 25 collaborators of Samer Khateb. A scholar is included among the top collaborators of Samer Khateb based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Samer Khateb. Samer Khateb is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Obolensky, Alexey, Anand Swaroop, Susanne Roosing, et al.. (2025). Founder Homozygous Nonsense CREB3 Variant and Variable-Onset Retinal Degeneration. JAMA Ophthalmology. 143(8). 692–692.
2.
Krishnan, Jaya, Milton A. English, Frans P.M. Cremers, et al.. (2025). Non-coding single-nucleotide and structural variants affecting the EYS putative promoter cause autosomal recessive retinitis pigmentosa. Genetics in Medicine. 27(7). 101427–101427.
3.
Michaeli, Tomer, Samer Khateb, & Jaime Levy. (2024). The Effect of Glucagon-like-Peptide-1 Receptor Agonists on Diabetic Retinopathy Progression, Central Subfield Thickness, and Response to Intravitreal Injections. Journal of Clinical Medicine. 13(20). 6269–6269. 2 indexed citations
4.
Obolensky, Alexey, Prakadeeswari Gopalakrishnan, Samer Khateb, et al.. (2024). Genetic and Clinical Analyses of the KIZ-c.226C>T Variant Resulting in a Dual Mutational Mechanism. Genes. 15(6). 804–804.
5.
6.
7.
Levy, Jaime, et al.. (2024). Intravitreal Injections for Macular Edema in Silicone Oil Filled Eyes. Clinical ophthalmology. Volume 18. 3405–3416.
8.
Gopalakrishnan, Prakadeeswari, Alexey Obolensky, Menachem Gross, et al.. (2023). Homozygous Knockout of Cep250 Leads to a Relatively Late-Onset Retinal Degeneration and Sensorineural Hearing Loss in Mice. Translational Vision Science & Technology. 12(3). 3–3. 4 indexed citations
9.
Yahalom, Claudia, Oded Volovelsky, Mor Hanany, et al.. (2021). SENIOR–LØKEN SYNDROME. Retina. 41(10). 2179–2187. 11 indexed citations
10.
Grunin, Michelle, Radgonde Amer, Samer Khateb, et al.. (2021). Analysis of the Aqueous Humor Proteome in Patients With Age-Related Macular Degeneration. Investigative Ophthalmology & Visual Science. 62(10). 18–18. 28 indexed citations
11.
Khateb, Samer, et al.. (2021). Postoperative Macular Proliferative Vitreoretinopathy: A Case Series and Literature Review. Case Reports in Ophthalmology. 12(2). 464–472. 1 indexed citations
12.
Beryozkin, Avigail, Samer Khateb, Muhammad Imran Khan, et al.. (2020). Unique combination of clinical features in a large cohort of 100 patients with retinitis pigmentosa caused by FAM161A mutations. Scientific Reports. 10(1). 15156–15156. 15 indexed citations
13.
Sher, Ifat, Estela Derazne, Eran Pras, et al.. (2019). <p>Chromatic pupilloperimetry for objective diagnosis of Best vitelliform macular dystrophy</p>. Clinical ophthalmology. Volume 13. 465–475. 8 indexed citations
14.
Khateb, Samer, Nicola Bedoni, Markus Daμμe, et al.. (2018). A homozygous founder missense variant in arylsulfatase G abolishes its enzymatic activity causing atypical Usher syndrome in humans. Genetics in Medicine. 20(9). 1004–1012. 45 indexed citations
15.
Khateb, Samer, Rong Wen, Ziqiang Guan, et al.. (2017). Nonsyndromic Retinitis Pigmentosa in the Ashkenazi Jewish Population. Ophthalmology. 125(5). 725–734. 29 indexed citations
16.
Namburi, Prasanthi, Rinki Ratnapriya, Samer Khateb, et al.. (2016). Bi-allelic Truncating Mutations in CEP78 , Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing Loss. The American Journal of Human Genetics. 99(3). 777–784. 23 indexed citations
17.
Khateb, Samer, Lina Zelinger, Tamar Ben‐Yosef, et al.. (2012). Exome Sequencing Identifies a Founder Frameshift Mutation in an Alternative Exon of USH1C as the Cause of Autosomal Recessive Retinitis Pigmentosa with Late-Onset Hearing Loss. PLoS ONE. 7(12). e51566–e51566. 27 indexed citations
18.
Khateb, Samer, et al.. (2007). The tetraplex (CGG)n destabilizing proteins hnRNP A2 and CBF-A enhance the in vivo translation of fragile X premutation mRNA. Nucleic Acids Research. 35(17). 5775–5788. 64 indexed citations
19.
Khateb, Samer, et al.. (2005). Homodimeric MyoD Preferentially Binds Tetraplex Structures of Regulatory Sequences of Muscle-specific Genes. Journal of Biological Chemistry. 280(29). 26805–26812. 36 indexed citations
20.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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