Samer Khateb

1.2k citations
45 papers · 687 · h-index 17

Impact in

Papers in

  • Molecular Biology 28
    • Retinal Development and Disorders 24
    • CRISPR and Genetic Engineering 4
  • Ophthalmology 11
    • Retinal Diseases and Treatments 8
    • Glaucoma and retinal disorders 2
Co-authors
Eyal Banin (26 shared papers)Dror Sharon (26 shared papers)Pnina Weisman-Shomer (2 shared papers)Michael Fry (2 shared papers)Menachem Gross (5 shared papers)Tamar Ben‐Yosef (13 shared papers)A. L. Ludwig (1 shared paper)Lina Zelinger (3 shared papers)
Journals
Genes (4 papers)Retina (3 papers)European Journal of Ophthalmology (3 papers)Scientific Reports (3 papers)Genetics in Medicine (2 papers)
Partner nations
IsraelUnited StatesNetherlands

In The Last Decade

Samer Khateb

41 papers receiving 678 citations

Peers

Samer Khateb
Comparison fields: 5 of 58
  • Ophthalmology 116
  • Sensory Systems 63
  • Molecular Biology 480
  • Cell Biology 82
  • Genetics 126
Replace Imad Ghazi with:
Imad Ghazi France
Krysta Voesenek Netherlands
Karmen M Trzupek United States
Eva Lenassi United Kingdom
F. P. M. Cremers Netherlands
Antje Bernd Germany
Blanca García‐Sandoval Spain
F.P.M. Cremers Netherlands
Zubin Saihan United Kingdom
Emma Bedoukian United States
Samer Khateb relative to Imad Ghazi France Imad Ghazi's profile →
Citations per field
00.5×2×4×6×8×9.7×
Imad Ghazi · 1×
Citations per year

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-authors

The 25 scholars most cited alongside Samer Khateb, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Samer Khateb Line = papers co-authored together Samer Khateb links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 45 papers — load more, or switch the sort, to bring in the rest.

#Work
1
A homozygous nonsense CEP250 mutation combined with a heterozygous nonsense C2orf71 mutation is associated with atypical Usher syndrome
Journal of Medical Genetics ·Samer Khateb, Lina Zelinger, Liliana Mizrahi‐Meissonnier, Carmen Ayuso, Robert K. Koenekoop, Uri Laxer, Menachem Gross, Eyal Banin, Dror Sharon
201466
2
The tetraplex (CGG)n destabilizing proteins hnRNP A2 and CBF-A enhance the in vivo translation of fragile X premutation mRNA
Nucleic Acids Research ·Samer Khateb, Pnina Weisman-Shomer, I. Hershco-Shani, A. L. Ludwig, Michael Fry
200765
3
Destabilization of tetraplex structures of the fragile X repeat sequence (CGG)n is mediated by homolog-conserved domains in three members of the hnRNP family
Nucleic Acids Research ·Samer Khateb
200459
4
A homozygous founder missense variant in arylsulfatase G abolishes its enzymatic activity causing atypical Usher syndrome in humans
Genetics in Medicine ·Samer Khateb, Björn Kowalewski, Nicola Bedoni, (unknown), Netta Pollack, Ann Saada, Alexey Obolensky, Tamar Ben‐Yosef, Menachem Gross, Thomas Dierks, Eyal Banin, Carlo Rivolta, Dror Sharon
201845
5
Homodimeric MyoD Preferentially Binds Tetraplex Structures of Regulatory Sequences of Muscle-specific Genes
Journal of Biological Chemistry ·Shulamit Etzioni, Anat Yafe, Samer Khateb, Pnina Weisman-Shomer, Eyal Bengal, Michael Fry
200536
6
Docking interactions of the JNK scaffold protein WDR62
Biochemical Journal ·Ksenya Cohen‐Katsenelson, Tanya Wasserman, Samer Khateb, Alan J. Whitmarsh, Ami Aronheim
201132
7
Nonsyndromic Retinitis Pigmentosa in the Ashkenazi Jewish Population
Ophthalmology ·Adva Kimchi, Samer Khateb, Rong Wen, Ziqiang Guan, Alexey Obolensky, Avigail Beryozkin, Shoshi Kurtzman, Anat Blumenfeld, Eran Pras, Samuel G. Jacobson, Tamar Ben‐Yosef, Hadas Newman, Dror Sharon, Eyal Banin
201729
8
Analysis of the Aqueous Humor Proteome in Patients With Age-Related Macular Degeneration
Investigative Ophthalmology & Visual Science ·Batya Rinsky, Gala Beykin, Michelle Grunin, Radgonde Amer, Samer Khateb, Liran Tiosano, Diego Almeida, Shira Hagbi-Levi, Sarah Elbaz-Hayoun, Itay Chowers
202129
9
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 ·Samer Khateb, Lina Zelinger, Tamar Ben‐Yosef, Saul Merin, Ornit Crystal‐Shalit, Menachem Gross, Eyal Banin, Dror Sharon
201227
10
Longitudinal Clinical Follow-up and Genetic Spectrum of Patients With Rod-Cone Dystrophy Associated With Mutations inPDE6AandPDE6B
JAMA Ophthalmology ·Samer Khateb, Marco Nassisi, Kinga M. Bujakowska, Cécile Méjécase, Christel Condroyer, Aline Antonio, Marine Foussard, Vanessa Démontant, Saddek Mohand‐Saïd, José‐Alain Sahel, Christina Zeitz, Isabelle Audo
201926
11
Bi-allelic Truncating Mutations in CEP78 , Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing Loss
The American Journal of Human Genetics ·Prasanthi Namburi, Rinki Ratnapriya, Samer Khateb, Csilla H. Lazar, Yael Kinarty, Alexey Obolensky, Inbar Erdinest, Devorah Marks-Ohana, Eran Pras, Tamar Ben‐Yosef, Hadas Newman, Menachem Gross, Anand Swaroop, Eyal Banin, Dror Sharon
201624
12
Whole-exome sequencing reveals POC5 as a novel gene associated with autosomal recessive retinitis pigmentosa
Human Molecular Genetics ·Monika Weisz Hubshman, Sanne Broekman, Erwin van Wijk, Frans P.M. Cremers, Alaa Abu-Diab, Samer Khateb, Shay Tzur, Irina Lagovsky, Pola Smirin‐Yosef, Dror Sharon, Lonneke Haer‐Wigman, Eyal Banin, Lina Basel‐Vanagaite, Erik de Vrieze
201722
13
Identification of genomic deletions causing inherited retinal degenerations by coverage analysis of whole exome sequencing data
Journal of Medical Genetics ·Samer Khateb, Mor Hanany, Ayat Khalaileh, Avigail Beryozkin, Segev Meyer, Alaa Abu-Diab, Fathieh Abu Turky, Liliana Mizrahi‐Meissonnier, Sari Lieberman, Tamar Ben‐Yosef, Eyal Banin, Dror Sharon
201621
14
Elschnig's Spots in the Acute and Remission Stages in Preeclampsia: Spectral-Domain Optical Coherence Tomographic Features
European Journal of Ophthalmology ·Alaa AlTalbishi, Samer Khateb, Radgonde Amer
201518
15
TRPM1 Mutations are the Most Common Cause of Autosomal Recessive Congenital Stationary Night Blindness (CSNB) in the Palestinian and Israeli Populations
Scientific Reports ·Alaa AlTalbishi, Lina Zelinger, Christina Zeitz, Karen Hendler, Prasanthi Namburi, Isabelle Audo, Ruth Sheffer, Claudia Yahalom, Samer Khateb, Eyal Banin, Dror Sharon
201918
16
Retinal Degeneration Associated With RPGRIP1: A Review of Natural History, Mutation Spectrum, and Genotype–Phenotype Correlation in 228 Patients
Frontiers in Cell and Developmental Biology ·Avigail Beryozkin, Hamzah Aweidah, Roque Daniel Carrero Valenzuela, Myriam Berman, Oscar Iguzquiza, Frans P.M. Cremers, Muhammad Imran Khan, Anand Swaroop, Radgonde Amer, Samer Khateb, Tamar Ben‐Yosef, Dror Sharon, Eyal Banin
202116
17
Unique combination of clinical features in a large cohort of 100 patients with retinitis pigmentosa caused by FAM161A mutations
Scientific Reports ·Avigail Beryozkin, Samer Khateb, Carlos Alberto Idrobo-Robalino, Muhammad Imran Khan, Frans P.M. Cremers, Alexey Obolensky, Mor Hanany, Eedy Mezer, Itay Chowers, Hadas Newman, Tamar Ben‐Yosef, Dror Sharon, Eyal Banin
202016
18
Mild aniridia phenotype: an under-recognized diagnosis of a severe inherited ocular disease
Graefe s Archive for Clinical and Experimental Ophthalmology ·Claudia Yahalom, Anat Blumenfeld, Karen Hendler, Orly Wussuki-Lior, Michal Macarov, Mordechai Shohat, Samer Khateb
201815
19
The combination of whole‐exome sequencing and clinical analysis allows better diagnosis of rare syndromic retinal dystrophies
Acta Ophthalmologica ·Alaa Abu Diab, Alaa AlTalbishi, Boris Rosin, Moien Kanaan, Lara Kamal, Anand Swaroop, Itay Chowers, Eyal Banin, Dror Sharon, Samer Khateb
201914
20
PHENOTYPIC CHARACTERISTICS OF ROD–CONE DYSTROPHY ASSOCIATED WITH MYO7A MUTATIONS IN A LARGE FRENCH COHORT
Retina ·Samer Khateb, Saddek Mohand‐Saïd, Marco Nassisi, Crystel Bonnet, Anne‐Françoise Roux, Camille Andrieu, Aline Antonio, Christel Condroyer, Christina Zeitz, Céline Devisme, Natalie Loundon, Sandrine Marlin, Christine Petit, Bahram Bodaghi, José‐Alain Sahel, Isabelle Audo
201913

About Samer Khateb

Samer Khateb is a scholar working on Molecular Biology, Ophthalmology, Genetics, Radiology, Nuclear Medicine and Imaging and Cell Biology, having authored 45 papers that have together received 687 indexed citations. Recurring topics across this work include Retinal Development and Disorders (24 papers), Retinal Diseases and Treatments (8 papers), Retinal and Macular Surgery (4 papers), CRISPR and Genetic Engineering (4 papers), Hearing, Cochlea, Tinnitus, Genetics (3 papers), Genetics and Neurodevelopmental Disorders (2 papers), Cellular transport and secretion (2 papers) and Glaucoma and retinal disorders (2 papers). The work is most often cited by research in Ophthalmology (116 citations), Sensory Systems (63 citations), Molecular Biology (480 citations), Cell Biology (82 citations) and Genetics (126 citations). Samer Khateb has collaborated with scholars based in Israel, United States and Netherlands. Frequent co-authors include Eyal Banin, Dror Sharon, Pnina Weisman-Shomer, Michael Fry, Menachem Gross, Tamar Ben‐Yosef, A. L. Ludwig, Lina Zelinger, Radgonde Amer and Liliana Mizrahi‐Meissonnier. Their work appears in journals such as Genes, Retina, European Journal of Ophthalmology, Scientific Reports and Genetics in Medicine.

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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