Igor Stevanovski

1.2k total citations
17 papers, 318 citations indexed

About

Igor Stevanovski is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Igor Stevanovski has authored 17 papers receiving a total of 318 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 6 papers in Cellular and Molecular Neuroscience and 5 papers in Genetics. Recurrent topics in Igor Stevanovski's work include Genetic Neurodegenerative Diseases (6 papers), Hereditary Neurological Disorders (3 papers) and Advanced biosensing and bioanalysis techniques (3 papers). Igor Stevanovski is often cited by papers focused on Genetic Neurodegenerative Diseases (6 papers), Hereditary Neurological Disorders (3 papers) and Advanced biosensing and bioanalysis techniques (3 papers). Igor Stevanovski collaborates with scholars based in Australia, United States and United Kingdom. Igor Stevanovski's co-authors include Ira W. Deveson, Jillian M. Hammond, Zin Naing, Thiruni Adikari, Rowena A. Bull, Malinna Yeang, William D. Rawlinson, Andrey Verich, Sacha Stelzer‐Braid and Ki Wook Kim and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Igor Stevanovski

16 papers receiving 315 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Igor Stevanovski Australia 9 150 128 60 58 57 17 318
Caroline Lacoux France 12 285 1.9× 107 0.8× 62 1.0× 30 0.5× 22 0.4× 15 439
Asako Shigeno Japan 6 161 1.1× 105 0.8× 16 0.3× 13 0.2× 72 1.3× 9 328
Alexandra B. Samal United States 12 215 1.4× 63 0.5× 12 0.2× 36 0.6× 41 0.7× 19 386
Jeremy Tuler United States 3 83 0.6× 228 1.8× 26 0.4× 22 0.4× 20 0.4× 4 413
Yaïr Glick Israel 12 207 1.4× 21 0.2× 86 1.4× 22 0.4× 36 0.6× 30 370
Michelle A. Loprieno United States 11 180 1.2× 166 1.3× 25 0.4× 12 0.2× 95 1.7× 15 426
Laine Goudy United States 5 478 3.2× 170 1.3× 42 0.7× 14 0.2× 36 0.6× 8 608
Patrícia Tiemi Fujimura Brazil 12 178 1.2× 24 0.2× 47 0.8× 44 0.8× 36 0.6× 21 328
Meleana M. Hinchman United States 10 192 1.3× 61 0.5× 35 0.6× 11 0.2× 52 0.9× 15 344
Adrian Coscia United States 6 125 0.8× 173 1.4× 19 0.3× 10 0.2× 38 0.7× 8 325

Countries citing papers authored by Igor Stevanovski

Since Specialization
Citations

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

Fields of papers citing papers by Igor Stevanovski

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Igor Stevanovski

This figure shows the co-authorship network connecting the top 25 collaborators of Igor Stevanovski. A scholar is included among the top collaborators of Igor Stevanovski 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 Igor Stevanovski. Igor Stevanovski is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

17 of 17 papers shown
1.
Stevanovski, Igor, Sanjog R. Chintalaphani, Pak Leng Cheong, et al.. (2025). Targeted Long‐Read Sequencing as a Single Assay Improves the Diagnosis of Spastic‐Ataxia Disorders. Annals of Clinical and Translational Neurology. 12(4). 832–841. 3 indexed citations
2.
Ziehr, David R., Martin S. Taylor, Max L. Valenstein, et al.. (2025). Polyglycine-mediated aggregation of FAM98B disrupts tRNA processing in GGC repeat disorders. Science. 389(6757). eado2403–eado2403.
3.
Fellner, Avi, Matthew Hobbs, Ira W. Deveson, et al.. (2024). An Inversion Affecting the GCH1 Gene as a Novel Finding in Dopa‐Responsive Dystonia. Movement Disorders Clinical Practice. 11(5). 582–585. 2 indexed citations
4.
Gunter, Helen M., Scott E. Youlten, Tim McCubbin, et al.. (2024). A universal molecular control for DNA, mRNA and protein expression. Nature Communications. 15(1). 2480–2480. 4 indexed citations
5.
Parmar, J., Melina Ellis, Samantha J. Bryen, et al.. (2024). A deep intronic variant in MME causes autosomal recessive Charcot–Marie–Tooth neuropathy through aberrant splicing. Journal of the Peripheral Nervous System. 29(2). 262–274. 1 indexed citations
6.
Ganesh, Vijay, Ben Weisburd, Catriona McLean, et al.. (2023). Transcriptome and Genome Analysis Uncovers a DMD Structural Variant. Neurology Genetics. 9(2). e200064–e200064. 2 indexed citations
7.
Hort, Yvonne, Patricia A. Sullivan, Lindsay Fowles, et al.. (2023). Atypical splicing variants in PKD1 explain most undiagnosed typical familial ADPKD. npj Genomic Medicine. 8(1). 16–16. 8 indexed citations
8.
Scriba, Carolin K., Igor Stevanovski, Sanjog R. Chintalaphani, et al.. (2023). RFC1 in an Australasian neurological disease cohort: extending the genetic heterogeneity and implications for diagnostics. Brain Communications. 5(4). fcad208–fcad208. 9 indexed citations
9.
Williams, Laura, Ira W. Deveson, Igor Stevanovski, et al.. (2023). NOTCH2NLC GGC Repeat Expansion Presenting as Adult‐Onset Cervical Dystonia. Movement Disorders Clinical Practice. 10(4). 704–706. 1 indexed citations
10.
Stevanovski, Igor, Sara Negri, Melina Ellis, et al.. (2022). Long read sequencing overcomes challenges in the diagnosis of SORD neuropathy. Journal of the Peripheral Nervous System. 27(2). 120–126. 9 indexed citations
11.
Hammond, Jillian M., Igor Stevanovski, Jonathon C. Arnold, et al.. (2022). Sex-specific transcriptomic and epitranscriptomic signatures of PTSD-like fear acquisition. iScience. 25(9). 104861–104861. 8 indexed citations
12.
Gunter, Helen M., Scott E. Youlten, Bindu Swapna Madala, et al.. (2022). Library adaptors with integrated reference controls improve the accuracy and reliability of nanopore sequencing. Nature Communications. 13(1). 6437–6437. 5 indexed citations
13.
Kim, Ki Wook, Ira W. Deveson, Chi Nam Ignatius Pang, et al.. (2021). Respiratory viral co-infections among SARS-CoV-2 cases confirmed by virome capture sequencing. Scientific Reports. 11(1). 3934–3934. 50 indexed citations
14.
Bull, Rowena A., Thiruni Adikari, James M. Ferguson, et al.. (2020). Analytical validity of nanopore sequencing for rapid SARS-CoV-2 genome analysis. Nature Communications. 11(1). 6272–6272. 170 indexed citations
15.
Samarakoon, Hiruna, Jillian M. Hammond, Igor Stevanovski, et al.. (2020). Genopo: a nanopore sequencing analysis toolkit for portable Android devices. Communications Biology. 3(1). 538–538. 15 indexed citations
16.
Stevanovski, Igor, Michelle van Geldermalsen, Jeff Holst, et al.. (2018). SAMHD1 enhances immunoglobulin hypermutation by promoting transversion mutation. Proceedings of the National Academy of Sciences. 115(19). 4921–4926. 21 indexed citations
17.
Sharbeen, George, et al.. (2016). Proximity to AGCT sequences dictates MMR-independent versus MMR-dependent mechanisms for AID-induced mutationviaUNG2. Nucleic Acids Research. 45(6). gkw1300–gkw1300. 10 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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