Simon Edvardson

5.9k total citations
84 papers, 3.6k citations indexed

About

Simon Edvardson is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Simon Edvardson has authored 84 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 56 papers in Molecular Biology, 17 papers in Genetics and 16 papers in Cell Biology. Recurrent topics in Simon Edvardson's work include Mitochondrial Function and Pathology (19 papers), Metabolism and Genetic Disorders (15 papers) and RNA modifications and cancer (12 papers). Simon Edvardson is often cited by papers focused on Mitochondrial Function and Pathology (19 papers), Metabolism and Genetic Disorders (15 papers) and RNA modifications and cancer (12 papers). Simon Edvardson collaborates with scholars based in Israel, United States and Germany. Simon Edvardson's co-authors include Orly Elpeleg, Avraham Shaag, Ann Saada, Chaim Jalas, Shamir Zenvirt, John M. Gomori, Yuval Cinnamon, Itai Berger, Ivan Tarassov and Asaf Ta‐Shma and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and PLoS ONE.

In The Last Decade

Simon Edvardson

83 papers receiving 3.5k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Simon Edvardson 2.3k 708 615 576 546 84 3.6k
Tobias B. Haack 2.7k 1.2× 1.1k 1.5× 523 0.9× 274 0.5× 576 1.1× 165 3.7k
Rosalba Carrozzo 4.0k 1.8× 1.5k 2.1× 627 1.0× 484 0.8× 845 1.5× 143 5.3k
Albena Jordanova 1.9k 0.8× 247 0.3× 1.7k 2.7× 570 1.0× 479 0.9× 87 3.6k
Henna Tyynismaa 3.0k 1.3× 1.1k 1.5× 407 0.7× 232 0.4× 406 0.7× 82 3.8k
Mary B. Davis 2.3k 1.0× 292 0.4× 1.8k 2.9× 463 0.8× 461 0.8× 111 4.3k
Bart Dermaut 1.9k 0.8× 575 0.8× 540 0.9× 232 0.4× 373 0.7× 64 3.3k
Graziella Uziel 4.8k 2.1× 2.8k 3.9× 652 1.1× 353 0.6× 415 0.8× 121 6.1k
Cinzia Gellera 3.7k 1.6× 1.2k 1.7× 2.3k 3.7× 260 0.5× 479 0.9× 155 5.5k
Daniele Ghezzi 2.6k 1.1× 1.1k 1.5× 408 0.7× 131 0.2× 225 0.4× 91 3.2k
Paul J. Lockhart 2.3k 1.0× 117 0.2× 1.2k 2.0× 477 0.8× 820 1.5× 126 5.2k

Countries citing papers authored by Simon Edvardson

Since Specialization
Citations

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

Fields of papers citing papers by Simon Edvardson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Simon Edvardson

This figure shows the co-authorship network connecting the top 25 collaborators of Simon Edvardson. A scholar is included among the top collaborators of Simon Edvardson 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 Simon Edvardson. Simon Edvardson 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.
Ben-Moshe, Zohar, Joel Reiter, Talya Dor, et al.. (2024). A deleterious variant of INTS1 leads to disrupted sleep–wake cycles. Disease Models & Mechanisms. 17(8).
2.
Abela, Lucia, Erica Tagliatti, Kimberley M. Reid, et al.. (2024). Neurodevelopmental and synaptic defects in DNAJC6 parkinsonism, amenable to gene therapy. Brain. 147(6). 2023–2037. 7 indexed citations
3.
Nasca, Alessia, Ivano Di Meo, Yakov Fellig, et al.. (2021). A novel homozygous MSTO1 mutation in Ashkenazi Jewish siblings with ataxia and myopathy. Journal of Human Genetics. 66(8). 835–840. 3 indexed citations
4.
Edvardson, Simon, Claudia M. Nicolae, Grace Noh, et al.. (2018). Heterozygous RNF13 Gain-of-Function Variants Are Associated with Congenital Microcephaly, Epileptic Encephalopathy, Blindness, and Failure to Thrive. The American Journal of Human Genetics. 104(1). 179–185. 18 indexed citations
5.
Milev, Miroslav P., Megan E. Grout, Djenann Saint‐Dic, et al.. (2017). Mutations in TRAPPC12 Manifest in Progressive Childhood Encephalopathy and Golgi Dysfunction. The American Journal of Human Genetics. 101(2). 291–299. 32 indexed citations
6.
Shahrour, Maher, et al.. (2017). Hypomyelinating leukodystrophy associated with a deleterious mutation in the ATRN gene. Neurogenetics. 18(3). 135–139. 9 indexed citations
7.
Edvardson, Simon, Laurence Prunetti, Jennifer Hu, et al.. (2017). tRNA N6-adenosine threonylcarbamoyltransferase defect due to KAE1/TCS3 (OSGEP) mutation manifest by neurodegeneration and renal tubulopathy. European Journal of Human Genetics. 25(5). 545–551. 67 indexed citations
8.
Mevorach, Dror, Yackov Berkun, Asaf Ta‐Shma, et al.. (2016). Therapy with eculizumab for patients with CD59 p.Cys89Tyr mutation. Annals of Neurology. 80(5). 708–717. 38 indexed citations
9.
Danson, Chris M., Bassam Abu‐Libdeh, Matthew Gallon, et al.. (2015). A defect in the retromer accessory protein, SNX27, manifests by infantile myoclonic epilepsy and neurodegeneration. Neurogenetics. 16(3). 215–221. 38 indexed citations
10.
Edvardson, Simon, Shimrit Oz, Avraham Shaag, et al.. (2013). Early infantile epileptic encephalopathy associated with a high voltage gated calcium channelopathy. Journal of Medical Genetics. 50(2). 118–123. 55 indexed citations
11.
Spiegel, Ronen, Ophry Pines, Asaf Ta‐Shma, et al.. (2012). Infantile Cerebellar-Retinal Degeneration Associated with a Mutation in Mitochondrial Aconitase, ACO2. The American Journal of Human Genetics. 90(3). 518–523. 76 indexed citations
12.
Erlich, Yaniv, Simon Edvardson, Emily Hodges, et al.. (2011). Exome sequencing and disease-network analysis of a single family implicate a mutation in KIF1A in hereditary spastic paraparesis. Genome Research. 21(5). 658–664. 134 indexed citations
13.
Shen, Xin‐Ming, Thomas O. Crawford, Joan M. Brengman, et al.. (2011). Functional consequences and structural interpretation of mutations of human choline acetyltransferase. Human Mutation. 32(11). 1259–1267. 30 indexed citations
14.
Straussberg, Rachel, Hanna Mandel, Aviva Fattal‐Valevski, et al.. (2010). Infantile Cerebral and Cerebellar Atrophy Is Associated with a Mutation in the MED17 Subunit of the Transcription Preinitiation Mediator Complex. The American Journal of Human Genetics. 87(5). 667–670. 58 indexed citations
15.
Edvardson, Simon, Avraham Shaag, Shamir Zenvirt, et al.. (2010). Joubert Syndrome 2 (JBTS2) in Ashkenazi Jews Is Associated with a TMEM216 Mutation. The American Journal of Human Genetics. 86(2). 294–294. 4 indexed citations
16.
Edvardson, Simon, Stanley H. Korman, A. Livne, et al.. (2010). l-arginine:glycine amidinotransferase (AGAT) deficiency: Clinical presentation and response to treatment in two patients with a novel mutation. Molecular Genetics and Metabolism. 101(2-3). 228–232. 32 indexed citations
17.
Saada, Ann, Simon Edvardson, Avraham Shaag, et al.. (2008). C6ORF66 Is an Assembly Factor of Mitochondrial Complex I. The American Journal of Human Genetics. 82(1). 32–38. 134 indexed citations
18.
Edvardson, Simon, Hiroko Hama, Avraham Shaag, et al.. (2008). Mutations in the Fatty Acid 2-Hydroxylase Gene Are Associated with Leukodystrophy with Spastic Paraparesis and Dystonia. The American Journal of Human Genetics. 83(5). 643–648. 154 indexed citations
19.
Edvardson, Simon, Avraham Shaag, Olga A. Kolesnikova, et al.. (2007). Deleterious Mutation in the Mitochondrial Arginyl–Transfer RNA Synthetase Gene Is Associated with Pontocerebellar Hypoplasia. The American Journal of Human Genetics. 81(4). 857–862. 258 indexed citations
20.
Edvardson, Simon, et al.. (2005). A case of Tourette syndrome presenting with oral self‐injurious behaviour. International Journal of Paediatric Dentistry. 15(5). 370–374. 17 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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