Anthony Simon

5.1k total citations
111 papers, 3.3k citations indexed

About

Anthony Simon is a scholar working on Immunology, Molecular Biology and Genetics. According to data from OpenAlex, Anthony Simon has authored 111 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 52 papers in Immunology, 46 papers in Molecular Biology and 33 papers in Genetics. Recurrent topics in Anthony Simon's work include Immunodeficiency and Autoimmune Disorders (44 papers), Blood disorders and treatments (18 papers) and Immune Cell Function and Interaction (17 papers). Anthony Simon is often cited by papers focused on Immunodeficiency and Autoimmune Disorders (44 papers), Blood disorders and treatments (18 papers) and Immune Cell Function and Interaction (17 papers). Anthony Simon collaborates with scholars based in Israel, United States and Germany. Anthony Simon's co-authors include Gideon Rechavi, Ninette Amariglio, Raz Somech, Atar Lev, Sigal Shaklai, Chaim M. Roifman, Harjit Dadi, Einav Nili Gal‐Yam, Shai Izraeli and F. Brok‐Simoni and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and The Journal of Experimental Medicine.

In The Last Decade

Anthony Simon

109 papers receiving 3.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anthony Simon Israel 34 1.8k 970 588 371 340 111 3.3k
Eric Campeau United States 17 2.2k 1.2× 705 0.7× 214 0.4× 558 1.5× 275 0.8× 32 3.6k
Valérie Vouret‐Craviari France 29 1.4k 0.8× 797 0.8× 280 0.5× 240 0.6× 409 1.2× 46 2.9k
Irma Dianzani Italy 35 3.4k 1.9× 655 0.7× 622 1.1× 521 1.4× 267 0.8× 142 5.0k
Andrew Wilber United States 28 1.7k 0.9× 387 0.4× 556 0.9× 895 2.4× 170 0.5× 62 2.8k
Victoria L. Heath United Kingdom 27 1.2k 0.7× 901 0.9× 272 0.5× 414 1.1× 231 0.7× 44 3.2k
Jiusong Sun United States 27 900 0.5× 1.4k 1.5× 379 0.6× 597 1.6× 672 2.0× 37 3.8k
Sean Bong Lee United States 36 2.8k 1.6× 540 0.6× 475 0.8× 564 1.5× 294 0.9× 83 4.1k
Gaetano Romano United States 27 2.1k 1.2× 413 0.4× 704 1.2× 723 1.9× 239 0.7× 80 3.3k
Chaker N. Adra United States 32 1.6k 0.9× 649 0.7× 636 1.1× 363 1.0× 106 0.3× 57 3.5k
Hitoshi Kohsaka Japan 36 1.2k 0.7× 1.5k 1.6× 244 0.4× 586 1.6× 828 2.4× 158 4.0k

Countries citing papers authored by Anthony Simon

Since Specialization
Citations

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

Fields of papers citing papers by Anthony Simon

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anthony Simon

This figure shows the co-authorship network connecting the top 25 collaborators of Anthony Simon. A scholar is included among the top collaborators of Anthony Simon 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 Anthony Simon. Anthony Simon 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.
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
2.
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
3.
Keller, Baerbel, Shlomit Kfir‐Erenfeld, Frederike A. Hartl, et al.. (2023). Combined Immunodeficiency Caused by a Novel Nonsense Mutation in LCK. Journal of Clinical Immunology. 44(1). 4–4. 4 indexed citations
4.
Jonas, Michael, Anthony Simon, Boris Gilburd, & Jacob Schneiderman. (2023). Intrarenal Anti-Leptin Treatment Attenuates Ischemia and Reperfusion Injury. American Journal of Nephrology. 54(7-8). 337–348. 3 indexed citations
5.
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
6.
Ling, Eduard, Arnon Broides, George Shubinsky, et al.. (2021). A novel zeta-associated protein 70 homozygous mutation causing combined immunodeficiency presenting as neonatal autoimmune hemolytic anemia. Immunologic Research. 69(1). 100–106.
7.
Lee, Yu Nee, Anthony Simon, Atar Lev, et al.. (2019). A Large Cohort of RAG1/2-Deficient SCID Patients—Clinical, Immunological, and Prognostic Analysis. Journal of Clinical Immunology. 40(1). 211–222. 13 indexed citations
8.
Lev, Atar, Anthony Simon, Daphna Hutt, et al.. (2019). Immune reconstitution after HSCT in SCID—a cohort of conditioned and unconditioned patients. Immunologic Research. 67(2-3). 166–175. 6 indexed citations
9.
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
10.
Gothelf, Doron, Amos Frisch, Abraham Weizman, et al.. (2015). Thymic and bone marrow output in individuals with 22q11.2 deletion syndrome. Pediatric Research. 77(4). 579–585. 20 indexed citations
11.
Basel‐Vanagaite, Lina, Noam Zevit, Liang Guo, et al.. (2012). Transient Infantile Hypertriglyceridemia, Fatty Liver, and Hepatic Fibrosis Caused by Mutated GPD1, Encoding Glycerol-3-Phosphate Dehydrogenase 1. The American Journal of Human Genetics. 90(1). 49–60. 73 indexed citations
12.
Simon, Anthony, Yael Nevo‐Caspi, David Mishali, et al.. (2011). Increased RNA editing in children with cyanotic congenital heart disease. Intensive Care Medicine. 37(10). 1664–1671. 33 indexed citations
13.
Simon, Anthony, Atar Lev, Baruch Wolach, et al.. (2010). The Effect of Gentamicin-Induced Readthrough on a Novel Premature Termination Codon of CD18 Leukocyte Adhesion Deficiency Patients. PLoS ONE. 5(11). e13659–e13659. 13 indexed citations
14.
Somech, Raz, Anthony Simon, Atar Lev, et al.. (2009). Reduced central tolerance in Omenn syndrome leads to immature self-reactive oligoclonal T cells. Journal of Allergy and Clinical Immunology. 124(4). 793–800. 39 indexed citations
15.
Olins, Ada L., Monika Zwerger, Harald Herrmann, et al.. (2008). The human granulocyte nucleus: Unusual nuclear envelope and heterochromatin composition. European Journal of Cell Biology. 87(5). 279–290. 78 indexed citations
16.
Pasvolsky, Ronit, Sara W. Feigelson, Sara Şebnem Kılıç, et al.. (2007). A LAD-III syndrome is associated with defective expression of the Rap-1 activator CalDAG-GEFI in lymphocytes, neutrophils, and platelets. The Journal of Experimental Medicine. 204(7). 1571–1582. 118 indexed citations
17.
Somech, Raz, Einav Nili Gal‐Yam, Sigal Shaklai, et al.. (2007). Enhanced expression of the nuclear envelope LAP2 transcriptional repressors in normal and malignant activated lymphocytes. Annals of Hematology. 86(6). 393–401. 20 indexed citations
18.
Simon, Anthony. (2007). Nuclear lamina organization and new functions. FEBS Journal. 274(6). 1353–1353. 2 indexed citations
19.
Peles, Einat, Zvi Lidar, Anthony Simon, et al.. (2004). Angiogenic Factors in the Cerebrospinal Fluid of Patients with Astrocytic Brain Tumors. Neurosurgery. 55(3). 562–568. 52 indexed citations
20.
Toren, Amos, Ninette Amariglio, Galit Rozenfeld-Granot, et al.. (1999). Genetic Linkage of Autosomal-Dominant Alport Syndrome with Leukocyte Inclusions and Macrothrombocytopenia (Fechtner Syndrome) to Chromosome 22q11-13. The American Journal of Human Genetics. 65(6). 1711–1717. 23 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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