Channa Maayan

2.7k total citations
61 papers, 2.0k citations indexed

About

Channa Maayan is a scholar working on Cellular and Molecular Neuroscience, Cell Biology and Neurology. According to data from OpenAlex, Channa Maayan has authored 61 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Cellular and Molecular Neuroscience, 18 papers in Cell Biology and 17 papers in Neurology. Recurrent topics in Channa Maayan's work include Hereditary Neurological Disorders (43 papers), Neurological diseases and metabolism (17 papers) and Genetic Neurodegenerative Diseases (11 papers). Channa Maayan is often cited by papers focused on Hereditary Neurological Disorders (43 papers), Neurological diseases and metabolism (17 papers) and Genetic Neurodegenerative Diseases (11 papers). Channa Maayan collaborates with scholars based in Israel, United States and Germany. Channa Maayan's co-authors include Felicia B. Axelrod, James F. Gusella, Susan A. Slaugenhaupt, Chaim Springer, Anat Blumenfeld, S. Godfrey, James Mull, Maire Leyne, Sandra Gill and Math P. Cuajungco and has published in prestigious journals such as Journal of Clinical Investigation, Nature Genetics and PLoS ONE.

In The Last Decade

Channa Maayan

60 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Channa Maayan Israel 24 877 695 453 365 246 61 2.0k
Marcello Villanova Italy 27 385 0.4× 1.3k 1.8× 208 0.5× 217 0.6× 136 0.6× 86 2.3k
Jacques Lamarche Canada 22 567 0.6× 684 1.0× 134 0.3× 153 0.4× 116 0.5× 46 1.7k
Tine V. Karlsen Norway 17 772 0.9× 349 0.5× 194 0.4× 104 0.3× 419 1.7× 35 2.1k
Toru Kawanami Japan 30 578 0.7× 688 1.0× 215 0.5× 152 0.4× 343 1.4× 92 2.4k
M. N. Ghabriel Australia 22 443 0.5× 340 0.5× 97 0.2× 119 0.3× 364 1.5× 65 1.5k
J. R. Muddle United Kingdom 25 521 0.6× 408 0.6× 74 0.2× 190 0.5× 191 0.8× 41 1.6k
Yoshihiro Wakayama Japan 22 207 0.2× 1.4k 2.0× 142 0.3× 238 0.7× 103 0.4× 114 1.7k
Adnan Y. Manzur United Kingdom 26 351 0.4× 1.5k 2.2× 94 0.2× 215 0.6× 88 0.4× 63 2.1k
Carlo Fusco Italy 21 276 0.3× 565 0.8× 160 0.4× 135 0.4× 142 0.6× 118 1.8k
A Lagueny France 25 776 0.9× 370 0.5× 137 0.3× 105 0.3× 144 0.6× 106 2.1k

Countries citing papers authored by Channa Maayan

Since Specialization
Citations

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

Fields of papers citing papers by Channa Maayan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Channa Maayan

This figure shows the co-authorship network connecting the top 25 collaborators of Channa Maayan. A scholar is included among the top collaborators of Channa Maayan 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 Channa Maayan. Channa Maayan 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.
Cheishvili, David, Channa Maayan, Jeanna Tsenter, et al.. (2016). Tocotrienol Treatment in Familial Dysautonomia: Open-Label Pilot Study. Journal of Molecular Neuroscience. 59(3). 382–391. 7 indexed citations
2.
Cohen, Malkiel A., David Cheishvili, Tikva Turetsky, et al.. (2015). Familial Dysautonomia (FD) Human Embryonic Stem Cell Derived PNS Neurons Reveal that Synaptic Vesicular and Neuronal Transport Genes Are Directly or Indirectly Affected by IKBKAP Downregulation. PLoS ONE. 10(10). e0138807–e0138807. 20 indexed citations
3.
Cheishvili, David, Paula Dietrich, Channa Maayan, et al.. (2014). IKAP Deficiency in an FD Mouse Model and in Oligodendrocyte Precursor Cells Results in Downregulation of Genes Involved in Oligodendrocyte Differentiation and Myelin Formation. PLoS ONE. 9(4). e94612–e94612. 11 indexed citations
4.
Cheishvili, David, et al.. (2011). IKAP/Elp1 involvement in cytoskeleton regulation and implication for familial dysautonomia. Human Molecular Genetics. 20(8). 1585–1594. 49 indexed citations
5.
Simson, Gabrielle Gold‐von, et al.. (2009). Neoplasia in Familial Dysautonomia: A 20-Year Review in a Young Patient Population. The Journal of Pediatrics. 155(6). 934–936. 3 indexed citations
6.
7.
Cuajungco, Math P., Maire Leyne, James Mull, et al.. (2003). Tissue-Specific Reduction in Splicing Efficiency of IKBKAP Due to the Major Mutation Associated with Familial Dysautonomia. The American Journal of Human Genetics. 72(3). 749–758. 108 indexed citations
8.
Shoseyov, David, et al.. (2002). Short-term Course and Outcome of Treatments of Pleural Empyema in Pediatric Patients. CHEST Journal. 121(3). 836–840. 54 indexed citations
9.
Maayan, Channa, Elhanan Bar‐On, A. Joseph Foldes, Benjamin Gesundheit, & Rivka Dresner Pollak. (2002). Bone Mineral Density and Metabolism in Familial Dysautonomia. Osteoporosis International. 13(5). 429–433. 32 indexed citations
10.
Axelrod, Felicia B., Judith D. Goldberg, Xiang Y. Ye, & Channa Maayan. (2002). Survival in familial dysautonomia: Impact of early intervention. The Journal of Pediatrics. 141(4). 518–523. 59 indexed citations
11.
Slaugenhaupt, Susan A., Anat Blumenfeld, Sandra Gill, et al.. (2001). Tissue-Specific Expression of a Splicing Mutation in the Gene Causes Familial Dysautonomia. The American Journal of Human Genetics. 68(3). 598–605. 448 indexed citations
12.
Chadwick, Brian P., Maire Leyne, Sandra Gill, et al.. (2000). Cloning, mapping, and expression of a novel brain-specific transcript in the Familial Dysautonomia candidate region on Chromosome 9q31. Mammalian Genome. 11(1). 81–83. 5 indexed citations
13.
Blumenfeld, Anat, Susan A. Slaugenhaupt, Christopher B. Liebert, et al.. (1999). Precise Genetic Mapping and Haplotype Analysis of the Familial Dysautonomia Gene on Human Chromosome 9q31. The American Journal of Human Genetics. 64(4). 1110–1118. 53 indexed citations
14.
Chadwick, Brian P., James Mull, Sandra Gill, et al.. (1999). Cloning, Mapping, and Expression of Two Novel Actin Genes, Actin-like-7A (ACTL7A) and Actin-like-7B (ACTL7B), from the Familial Dysautonomia Candidate Region on 9q31. Genomics. 58(3). 302–309. 32 indexed citations
15.
Slaugenhaupt, Susan A., Anat Blumenfeld, Christopher B. Liebert, et al.. (1995). The human gene for neurotrophic tyrosine kinase receptor type 2 (NTRK2) is located on chromosome 9 but is not the familial dysautonomia gene. Genomics. 25(3). 730–732. 8 indexed citations
16.
Avital, A., S. Godfrey, Channa Maayan, Yoram Z. Diamant, & Chaim Springer. (1994). Chloroquine treatment of interstitial lung disease in children. Pediatric Pulmonology. 18(6). 356–360. 28 indexed citations
17.
Krausz, Yodphat, et al.. (1994). Scintigraphic evaluation of esophageal transit and gastric emptying in familial dysautonomia. European Journal of Radiology. 18(1). 52–56. 21 indexed citations
18.
Blumenfeld, Anat, Susan Slaugenhaupt, Diane Lucente, et al.. (1993). The gene for familial dysautonomia is linked to chromosome 9 and shows strong linkage disequilibrium with D9S58. The Society for Neuroscience Abstracts. 19. 1463. 7 indexed citations
19.
Maayan, Channa, et al.. (1993). Complications following oat head aspiration. Pediatric Pulmonology. 15(1). 52–54. 19 indexed citations
20.
Blumenfeld, Anat, Susan A. Slaugenhaupt, Felicia B. Axelrod, et al.. (1993). Localization of the gene for familial dysautonomia on chromosome 9 and definition of DNA markers for genetic diagnosis. Nature Genetics. 4(2). 160–164. 104 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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