Nili Avidan

5.8k total citations
40 papers, 2.9k citations indexed

About

Nili Avidan is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Nili Avidan has authored 40 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 11 papers in Genetics and 10 papers in Immunology. Recurrent topics in Nili Avidan's work include T-cell and Retrovirus Studies (3 papers), Genetic Associations and Epidemiology (3 papers) and Computational Drug Discovery Methods (3 papers). Nili Avidan is often cited by papers focused on T-cell and Retrovirus Studies (3 papers), Genetic Associations and Epidemiology (3 papers) and Computational Drug Discovery Methods (3 papers). Nili Avidan collaborates with scholars based in Israel, United States and France. Nili Avidan's co-authors include Edna Ben‐Asher, Doron Lancet, Ariel Miller, J. Beckmann, Gustavo Glusman, Hadas Lahat, Elon Pras, Orna Man, Etgar Levy‐Nissenbaum and Michael Eldar and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Blood.

In The Last Decade

Nili Avidan

40 papers receiving 2.8k citations

Peers

Nili Avidan
Edna Ben‐Asher Israel
Yoji Hakamata Japan
Takashi Murayama Japan
Bernard Himpens Belgium
T. Voyno-Yasenetskaya United States
Susan Treves Switzerland
Serge Arnaudeau Switzerland
Susanne Feil Germany
Daniel C. Devor United States
Patricia E. Martin United Kingdom
Edna Ben‐Asher Israel
Nili Avidan
Citations per year, relative to Nili Avidan Nili Avidan (= 1×) peers Edna Ben‐Asher

Countries citing papers authored by Nili Avidan

Since Specialization
Citations

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

Fields of papers citing papers by Nili Avidan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nili Avidan

This figure shows the co-authorship network connecting the top 25 collaborators of Nili Avidan. A scholar is included among the top collaborators of Nili Avidan 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 Nili Avidan. Nili Avidan 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.
Avidan, Nili, Frédérique Truffault, Elsebeth Staun-Ram, et al.. (2017). Methylome and transcriptome profiling in Myasthenia Gravis monozygotic twins. Journal of Autoimmunity. 82. 62–73. 21 indexed citations
2.
3.
Avidan, Nili, Rozen Le Panse, Sonia Berrih‐Aknin, & Ariel Miller. (2013). Genetic basis of myasthenia gravis – A comprehensive review. Journal of Autoimmunity. 52. 146–153. 85 indexed citations
4.
Benedek, Gil, Tamar Paperna, Nili Avidan, et al.. (2010). Opposing effects of the HLA-DRB1*0301-DQB1*0201 haplotype on the risk for multiple sclerosis in diverse Arab populations in Israel. Genes and Immunity. 11(5). 423–431. 19 indexed citations
5.
Nousbeck, Janna, Ofer Sarig, Nili Avidan, et al.. (2009). Insulin-Like Growth Factor-Binding Protein 7 Regulates Keratinocyte Proliferation, Differentiation and Apoptosis. Journal of Investigative Dermatology. 130(2). 378–387. 34 indexed citations
6.
Miller, Ariel, Nili Avidan, Lea Glass‐Marmor, et al.. (2008). Translation towards personalized medicine in Multiple Sclerosis. Journal of the Neurological Sciences. 274(1-2). 68–75. 22 indexed citations
7.
Pannu, Hariyadarshi, Nili Avidan, Van Tran‐Fadulu, & Dianna M. Milewicz. (2006). Genetic Basis of Thoracic Aortic Aneurysms and Dissections. Annals of the New York Academy of Sciences. 1085(1). 242–255. 30 indexed citations
8.
Feldmesser, Ester, Dani Bercovich, Nili Avidan, et al.. (2006). Mutations in Olfactory Signal Transduction Genes Are Not a Major Cause of Human Congenital General Anosmia. Chemical Senses. 32(1). 21–30. 28 indexed citations
9.
Nakabayashi, Kazuhiko, Yan Ren, Ulpu Saarialho‐Kere, et al.. (2005). Identification of C7orf11 (TTDN1) Gene Mutations and Genetic Heterogeneity in Nonphotosensitive Trichothiodystrophy. The American Journal of Human Genetics. 76(3). 510–516. 55 indexed citations
10.
Grossman, Iris, et al.. (2005). Trick or treat: The effect of placebo on the power of pharmacogenetic association studies. Human Genomics. 2(1). 28–28. 7 indexed citations
11.
Kohn, Yoav, Kyra Kanyas, Chi‐Un Pae, et al.. (2005). Fine mapping of a schizophrenia susceptibility locus at chromosome 6q23: increased evidence for linkage and reduced linkage interval. European Journal of Human Genetics. 13(6). 763–771. 33 indexed citations
12.
Hasin-Brumshtein, Yehudit, Nili Avidan, Dani Bercovich, et al.. (2004). A paradigm for single nucleotide polymorphism analysis: The case of the acetylcholinesterase gene. Human Mutation. 24(5). 408–416. 17 indexed citations
13.
Grossman, I., Nili Avidan, Tamar Paperna, et al.. (2004). Genomic profiling of interpopulation diversity guides prioritization of candidate-genes for autoimmunity. Genes and Immunity. 5(6). 493–504. 10 indexed citations
14.
Adato, Avital, Sarah Vreugde, Tarja Joensuu, et al.. (2002). USH3A transcripts encode clarin-1, a four-transmembrane-domain protein with a possible role in sensory synapses. European Journal of Human Genetics. 10(6). 339–350. 130 indexed citations
15.
Conticello, Silvestro G., Yoav Gilad, Nili Avidan, et al.. (2001). Mechanisms for Evolving Hypervariability: The Case of Conopeptides. Molecular Biology and Evolution. 18(2). 120–131. 183 indexed citations
16.
Lahat, Hadas, Elon Pras, Nili Avidan, et al.. (2001). A Missense Mutation in a Highly Conserved Region of CASQ2 Is Associated with Autosomal Recessive Catecholamine-Induced Polymorphic Ventricular Tachycardia in Bedouin Families from Israel. The American Journal of Human Genetics. 69(6). 1378–1384. 461 indexed citations
17.
Bargal, Ruth, Nili Avidan, Marcia Zeigler, et al.. (2001). Mucolipidosis type IV: NovelMCOLN1 mutations in Jewish and non-Jewish patients and the frequency of the disease in the Ashkenazi Jewish population. Human Mutation. 17(5). 397–402. 64 indexed citations
18.
Levanon, Ditsa, Gustavo Glusman, Thorsten Bangsow, et al.. (2001). Architecture and anatomy of the genomic locus encoding the human leukemia-associated transcription factor RUNX1/AML1. Gene. 262(1-2). 23–33. 123 indexed citations
19.
Eisenberg, Iris, Nili Avidan, Tamara Potikha, et al.. (2001). The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy. Nature Genetics. 29(1). 83–87. 393 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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