Ortal Barel

2.3k total citations
63 papers, 868 citations indexed

About

Ortal Barel is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Ortal Barel has authored 63 papers receiving a total of 868 indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 25 papers in Genetics and 22 papers in Immunology. Recurrent topics in Ortal Barel's work include Immunodeficiency and Autoimmune Disorders (17 papers), Genomics and Rare Diseases (8 papers) and RNA modifications and cancer (8 papers). Ortal Barel is often cited by papers focused on Immunodeficiency and Autoimmune Disorders (17 papers), Genomics and Rare Diseases (8 papers) and RNA modifications and cancer (8 papers). Ortal Barel collaborates with scholars based in Israel, United States and Italy. Ortal Barel's co-authors include Zamir Shorer, Gal Finer, Rivka Ofir, Ohad S. Birk, Raz Somech, Eran Eyal, Gideon Rechavi, Atar Lev, Anthony Simon and Ben Pode‐Shakked and has published in prestigious journals such as The Journal of Immunology, International Journal of Molecular Sciences and The American Journal of Human Genetics.

In The Last Decade

Ortal Barel

59 papers receiving 865 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ortal Barel Israel 15 450 247 189 104 79 63 868
Anas M. Alazami Saudi Arabia 22 857 1.9× 584 2.4× 147 0.8× 95 0.9× 52 0.7× 55 1.5k
Asaf Ta‐Shma Israel 16 450 1.0× 224 0.9× 126 0.7× 102 1.0× 47 0.6× 19 988
Boris Keren France 21 649 1.4× 515 2.1× 115 0.6× 44 0.4× 49 0.6× 70 1.1k
Zeynep Coban‐Akdemir United States 18 544 1.2× 396 1.6× 131 0.7× 66 0.6× 23 0.3× 50 965
Reeval Segel Israel 18 649 1.4× 249 1.0× 50 0.3× 87 0.8× 174 2.2× 40 1.1k
Thomas Koed Doktor Denmark 15 862 1.9× 78 0.3× 182 1.0× 42 0.4× 53 0.7× 33 1.1k
Hanan E. Shamseldin Saudi Arabia 24 981 2.2× 590 2.4× 127 0.7× 61 0.6× 159 2.0× 55 1.5k
Chyuan-Sheng Lin United States 9 386 0.9× 125 0.5× 171 0.9× 42 0.4× 49 0.6× 11 639
Haike Reznik‐Wolf Israel 15 554 1.2× 171 0.7× 128 0.7× 50 0.5× 40 0.5× 39 888
Shun-Ai Li Japan 14 643 1.4× 238 1.0× 77 0.4× 59 0.6× 99 1.3× 17 1.0k

Countries citing papers authored by Ortal Barel

Since Specialization
Citations

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

Fields of papers citing papers by Ortal Barel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ortal Barel

This figure shows the co-authorship network connecting the top 25 collaborators of Ortal Barel. A scholar is included among the top collaborators of Ortal Barel 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 Ortal Barel. Ortal Barel 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.
Giladi, Moshe, Silvia Piccirillo, Ortal Barel, et al.. (2025). A Gain-of -Function SLC4A3 Mutation Causes Short-QT Syndrome. JACC. Clinical electrophysiology. 11(7). 1583–1594. 1 indexed citations
2.
Frizinsky, Shirly, Atar Lev, Anthony Simon, et al.. (2024). Investigating concomitant RAG-2 and LRBA mutations in SCID and autoimmunity. Clinical & Experimental Immunology. 220(1). 1 indexed citations
3.
Lev, Atar, et al.. (2024). A novel mutation in FNIP1 associated with a syndromic immunodeficiency and cardiomyopathy. Immunogenetics. 77(1). 2–2. 1 indexed citations
4.
Lesman‐Segev, Orit H., Nofar Mor, Ortal Barel, et al.. (2023). Adult-onset Alexander disease among patients of Jewish Syrian descent. Neurogenetics. 24(4). 303–310. 3 indexed citations
5.
Kurolap, Alina, Isaiah D. Wexler, Adi Mory, et al.. (2023). A common benign intronic deletion masking a pathogenic deep intronic PCCB variant - genome sequencing and RNA studies to the rescue. Molecular Genetics and Metabolism. 140(3). 107702–107702. 1 indexed citations
6.
Baker, Elizabeth, Ben Pode‐Shakked, Laura Cross, et al.. (2022). PPP2R1A neurodevelopmental disorder is associated with congenital heart defects. American Journal of Medical Genetics Part A. 188(11). 3262–3277. 7 indexed citations
7.
Shamriz, Oded, Anthony Simon, Atar Lev, et al.. (2022). GATA2 Deficiency in Adult Life Is Characterized by Phenotypic Diversity and Delayed Diagnosis. Frontiers in Immunology. 13. 886117–886117. 2 indexed citations
8.
Shamriz, Oded, Limor Rubin, Anthony Simon, et al.. (2022). Dominant-negative signal transducer and activator of transcription (STAT)3 variants in adult patients: A single center experience. Frontiers in Immunology. 13. 1044933–1044933. 4 indexed citations
9.
Eliyahu, Aviva, Ortal Barel, Lior Greenbaum, et al.. (2022). Refining the Phenotypic Spectrum of KMT5B-Associated Developmental Delay. Frontiers in Pediatrics. 10. 844845–844845. 10 indexed citations
10.
Hirsch, Yoel, Hanna Mandel, Tova Hershkovitz, et al.. (2022). Vici syndrome in Israel: Clinical and molecular insights. Frontiers in Genetics. 13. 991721–991721.
11.
Chermesh, Irit, Lael Werner, Ortal Barel, et al.. (2020). Monogenic Inflammatory Bowel Disease: It's Never Too Late to Make a Diagnosis. Frontiers in Immunology. 11. 1775–1775. 6 indexed citations
12.
Simon, Anthony, Atar Lev, Tali Stauber, et al.. (2020). Whole exome sequencing (WES) approach for diagnosing primary immunodeficiencies (PIDs) in a highly consanguineous community. Clinical Immunology. 214. 108376–108376. 23 indexed citations
13.
Pode‐Shakked, Ben, Asaf Vivante, Ortal Barel, et al.. (2019). Progressive Pseudorheumatoid Dysplasia resolved by whole exome sequencing: a novel mutation in WISP3 and review of the literature. BMC Medical Genetics. 20(1). 53–53. 13 indexed citations
14.
Frizinsky, Shirly, Erez Rechavi, Ortal Barel, et al.. (2019). Novel MALT1 Mutation Linked to Immunodeficiency, Immune Dysregulation, and an Abnormal T Cell Receptor Repertoire. Journal of Clinical Immunology. 39(4). 401–413. 27 indexed citations
15.
Barel, Ortal, Eran Eyal, Itai M. Pessach, et al.. (2018). Somatic NRAS mutation in patient with generalized lymphatic anomaly. Angiogenesis. 21(2). 287–298. 57 indexed citations
16.
Barel, Ortal, Michael Schvimer, Michael Field, et al.. (2018). Genetic and Structural Analysis of a SKIV2L Mutation Causing Tricho-hepato-enteric Syndrome. Digestive Diseases and Sciences. 63(5). 1192–1199. 8 indexed citations
17.
Rechavi, Erez, Atar Lev, Eran Eyal, et al.. (2016). A Novel Mutation in a Critical Region for the Methyl Donor Binding in DNMT3B Causes Immunodeficiency, Centromeric Instability, and Facial Anomalies Syndrome (ICF). Journal of Clinical Immunology. 36(8). 801–809. 12 indexed citations
18.
Stephen, Joshi, Thierry Vilboux, Yael Haberman, et al.. (2016). Congenital protein losing enteropathy: an inborn error of lipid metabolism due to DGAT1 mutations. European Journal of Human Genetics. 24(9). 1268–1273. 34 indexed citations
19.
Barel, Ortal, Stavit A. Shalev, Rivka Ofir, et al.. (2008). Maternally Inherited Birk Barel Mental Retardation Dysmorphism Syndrome Caused by a Mutation in the Genomically Imprinted Potassium Channel KCNK9. The American Journal of Human Genetics. 83(2). 193–199. 137 indexed citations
20.
Barel, Ortal, Zamir Shorer, Hagit Flusser, et al.. (2008). Mitochondrial Complex III Deficiency Associated with a Homozygous Mutation in UQCRQ. The American Journal of Human Genetics. 82(5). 1211–1216. 92 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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