Avigail Beryozkin

1.0k total citations
21 papers, 569 citations indexed

About

Avigail Beryozkin is a scholar working on Molecular Biology, Ophthalmology and Genetics. According to data from OpenAlex, Avigail Beryozkin has authored 21 papers receiving a total of 569 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 10 papers in Ophthalmology and 5 papers in Genetics. Recurrent topics in Avigail Beryozkin's work include Retinal Development and Disorders (18 papers), Retinal Diseases and Treatments (9 papers) and CRISPR and Genetic Engineering (5 papers). Avigail Beryozkin is often cited by papers focused on Retinal Development and Disorders (18 papers), Retinal Diseases and Treatments (9 papers) and CRISPR and Genetic Engineering (5 papers). Avigail Beryozkin collaborates with scholars based in Israel, United States and Germany. Avigail Beryozkin's co-authors include Dror Sharon, Eyal Banin, Lina Zelinger, Mor Hanany, Alexey Obolensky, Saul Merin, Prakadeeswari Gopalakrishnan, Dikla Bandah‐Rozenfeld, Tamar Ben‐Yosef and Erez Y. Levanon and has published in prestigious journals such as SHILAP Revista de lepidopterología, Scientific Reports and International Journal of Molecular Sciences.

In The Last Decade

Avigail Beryozkin

21 papers receiving 567 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Avigail Beryozkin Israel	13	512	224	158	90	64	21	569
Esther Pomares Spain	14	413 0.8×	176 0.8×	89 0.6×	70 0.8×	61 1.0×	30	489
Karin W. Littink Netherlands	12	669 1.3×	328 1.5×	142 0.9×	117 1.3×	146 2.3×	13	711
Suzanne Broadgate United Kingdom	10	351 0.7×	177 0.8×	87 0.6×	57 0.6×	49 0.8×	25	423
María González‐del Pozo Spain	13	408 0.8×	179 0.8×	123 0.8×	46 0.5×	41 0.6×	21	461
Frans P.M. Cremers Netherlands	9	375 0.7×	190 0.8×	78 0.5×	109 1.2×	31 0.5×	13	428
Michael W. Stuck United States	15	491 1.0×	111 0.5×	149 0.9×	192 2.1×	100 1.6×	22	547
Janneke J.C. van Lith-Verhoeven Netherlands	9	383 0.7×	289 1.3×	53 0.3×	86 1.0×	46 0.7×	12	483
Sajag Bhattarai United States	11	461 0.9×	77 0.3×	225 1.4×	100 1.1×	118 1.8×	24	547
Susan W. Gorman United States	7	596 1.2×	147 0.7×	232 1.5×	78 0.9×	120 1.9×	8	713
Fabrice Richard France	11	430 0.8×	87 0.4×	121 0.8×	236 2.6×	57 0.9×	17	550

Countries citing papers authored by Avigail Beryozkin

Since Specialization

Citations

This map shows the geographic impact of Avigail Beryozkin'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 Avigail Beryozkin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Avigail Beryozkin more than expected).

Fields of papers citing papers by Avigail Beryozkin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Avigail Beryozkin. 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 Avigail Beryozkin. The network helps show where Avigail Beryozkin may publish in the future.

Co-authorship network of co-authors of Avigail Beryozkin

This figure shows the co-authorship network connecting the top 25 collaborators of Avigail Beryozkin. A scholar is included among the top collaborators of Avigail Beryozkin 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 Avigail Beryozkin. Avigail Beryozkin is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Hanany, Mor, et al.. (2023). An In-Depth Single-Gene Worldwide Carrier Frequency and Genetic Prevalence Analysis of CYP4V2 as the Cause of Bietti Crystalline Dystrophy. Translational Vision Science & Technology. 12(2). 27–27. 5 indexed citations

Gopalakrishnan, Prakadeeswari, Avigail Beryozkin, Eyal Banin, & Dror Sharon. (2023). Morphological and Functional Comparison of Mice Models for Retinitis Pigmentosa. Advances in experimental medicine and biology. 1415. 365–370. 2 indexed citations

Beryozkin, Avigail, et al.. (2023). Factors Affecting Readthrough of Natural Versus Premature Termination Codons. Advances in experimental medicine and biology. 1415. 149–155. 4 indexed citations

Gopalakrishnan, Prakadeeswari, Ning Chang, Alexey Obolensky, et al.. (2023). Gene augmentation therapy attenuates retinal degeneration in a knockout mouse model of Fam161a retinitis pigmentosa. Molecular Therapy. 31(10). 2948–2961. 3 indexed citations

Gopalakrishnan, Prakadeeswari, et al.. (2022). Retinal Structure and Function in a Knock-in Mouse Model for the FAM161A-p.Arg523∗ Human Nonsense Pathogenic Variant. SHILAP Revista de lepidopterología. 3(1). 100229–100229. 6 indexed citations

Beryozkin, Avigail, A. Samanta, Prakadeeswari Gopalakrishnan, et al.. (2022). Translational Read-Through Drugs (TRIDs) Are Able to Restore Protein Expression and Ciliogenesis in Fibroblasts of Patients with Retinitis Pigmentosa Caused by a Premature Termination Codon in FAM161A. International Journal of Molecular Sciences. 23(7). 3541–3541. 8 indexed citations

Beryozkin, Avigail, Alexey Obolensky, Corinne Kostic, et al.. (2021). A new mouse model for retinal degeneration due to Fam161a deficiency. Scientific Reports. 11(1). 2030–2030. 18 indexed citations

Gopalakrishnan, Prakadeeswari, Avigail Beryozkin, Mor Hanany, et al.. (2021). Inherited retinal diseases: Linking genes, disease-causing variants, and relevant therapeutic modalities. Progress in Retinal and Eye Research. 89. 101029–101029. 102 indexed citations

Beryozkin, Avigail, Frans P.M. Cremers, Muhammad Imran Khan, et al.. (2021). 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. 9. 746781–746781. 13 indexed citations

10.

Mbefo, Martial, Adeline Berger, Xavier Gérard, et al.. (2021). Enhancer of Zeste Homolog 2 (EZH2) Contributes to Rod Photoreceptor Death Process in Several Forms of Retinal Degeneration and Its Activity Can Serve as a Biomarker for Therapy Efficacy. International Journal of Molecular Sciences. 22(17). 9331–9331. 6 indexed citations

11.

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

12.

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

13.

Beryozkin, Avigail, Gal Levy, Anat Blumenfeld, et al.. (2016). Genetic Analysis of the Rhodopsin Gene Identifies a Mosaic Dominant Retinitis Pigmentosa Mutation in a Healthy Individual. Investigative Ophthalmology & Visual Science. 57(3). 940–940. 12 indexed citations

14.

Lazar, Csilla H., Prasanthi Namburi, Mousumi Mutsuddi, et al.. (2015). Nonsyndromic Early-Onset Cone-Rod Dystrophy and Limb-Girdle Muscular Dystrophy in a Consanguineous Israeli Family are Caused by Two Independent yet Linked Mutations inALMS1andDYSF. Human Mutation. 36(9). 836–841. 14 indexed citations

15.

Beryozkin, Avigail, Lina Zelinger, Dikla Bandah‐Rozenfeld, et al.. (2014). Identification of Mutations Causing Inherited Retinal Degenerations in the Israeli and Palestinian Populations Using Homozygosity Mapping. Investigative Ophthalmology & Visual Science. 55(2). 1149–1149. 44 indexed citations

16.

Roosing, Susanne, Klaus Rohrschneider, Avigail Beryozkin, et al.. (2013). Mutations in RAB28, Encoding a Farnesylated Small GTPase, Are Associated with Autosomal-Recessive Cone-Rod Dystrophy. The American Journal of Human Genetics. 93(1). 110–117. 67 indexed citations

17.

Roosing, Susanne, Klaus Rohrschneider, Avigail Beryozkin, et al.. (2013). The farnesylated small GTPase RAB28 is mutated in autosomal recessive cone-rod dystrophy. 54(15). 1228–1228. 1 indexed citations

18.

Beryozkin, Avigail, Lina Zelinger, Dikla Bandah‐Rozenfeld, et al.. (2013). Mutations inCRB1are a Relatively Common Cause of Autosomal Recessive Early-Onset Retinal Degeneration in the Israeli and Palestinian Populations. Investigative Ophthalmology & Visual Science. 54(3). 2068–2068. 26 indexed citations

19.

Zelinger, Lina, Eyal Banin, Alexey Obolensky, et al.. (2011). A Missense Mutation in DHDDS, Encoding Dehydrodolichyl Diphosphate Synthase, Is Associated with Autosomal-Recessive Retinitis Pigmentosa in Ashkenazi Jews. The American Journal of Human Genetics. 88(2). 207–215. 93 indexed citations

20.

Özgül, Rıza Köksal, Anna M. Siemiatkowska, Connie A. Myers, et al.. (2011). Exome Sequencing and cis-Regulatory Mapping Identify Mutations in MAK, a Gene Encoding a Regulator of Ciliary Length, as a Cause of Retinitis Pigmentosa. The American Journal of Human Genetics. 89(2). 253–264. 80 indexed citations

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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