Panagiotis Katsonis

5.0k total citations
44 papers, 1.2k citations indexed

About

Panagiotis Katsonis is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Panagiotis Katsonis has authored 44 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Molecular Biology, 17 papers in Genetics and 9 papers in Oncology. Recurrent topics in Panagiotis Katsonis's work include Genomics and Rare Diseases (9 papers), Evolution and Genetic Dynamics (8 papers) and Cancer Genomics and Diagnostics (7 papers). Panagiotis Katsonis is often cited by papers focused on Genomics and Rare Diseases (9 papers), Evolution and Genetic Dynamics (8 papers) and Cancer Genomics and Diagnostics (7 papers). Panagiotis Katsonis collaborates with scholars based in United States, Canada and Germany. Panagiotis Katsonis's co-authors include Olivier Lichtarge, Rhonald C. Lua, David C. Marciano, Amanda Koire, Oleg A. Shchelochkov, Marwan Shinawi, Christophe Herman, Anbu Karani Adikesavan, Angela D. Wilkins and Teng‐Kuei Hsu and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and Circulation.

In The Last Decade

Panagiotis Katsonis

44 papers receiving 1.2k citations

Peers

Panagiotis Katsonis

GENET

ONCOL

Kyunggon Kim South Korea

Chiara Romano Italy

Rick V. Hay United States

Kamini Singh United States

Kenji Kawai Japan

Susan Chung United States

Edith Magnenat Switzerland

Shinya Koyama Japan

Zailong Qin China

Onno B. Bleijerveld Netherlands

Kyunggon Kim South Korea

Panagiotis Katsonis

961 ×1.1

151 ×0.5

GENET

143 ×0.5

ONCOL

155 ×1.0

36 ×0.3

Citations per year, relative to Panagiotis Katsonis Panagiotis Katsonis (= 1×) peers Kyunggon Kim

Countries citing papers authored by Panagiotis Katsonis

Since Specialization

Citations

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

Fields of papers citing papers by Panagiotis Katsonis

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Panagiotis Katsonis

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

All Works

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20 of 20 papers shown

Chinnam, Naga Babu, Roopa Thapar, Altaf H. Sarker, et al.. (2024). ASCC1 structures and bioinformatics reveal a novel helix-clasp-helix RNA-binding motif linked to a two-histidine phosphodiesterase. Journal of Biological Chemistry. 300(6). 107368–107368. 4 indexed citations

Bourquard, Thomas, Kwanghyuk Lee, Ismael Al‐Ramahi, et al.. (2023). Functional variants identify sex-specific genes and pathways in Alzheimer’s Disease. Nature Communications. 14(1). 2765–2765. 11 indexed citations

Wang, Chen, et al.. (2023). ShinyBioHEAT: an interactive shiny app to identify phenotype driver genes in E.coli and B.subtilis. Bioinformatics. 39(8). 1 indexed citations

Marciano, David C., Chen Wang, Teng‐Kuei Hsu, et al.. (2022). Evolutionary action of mutations reveals antimicrobial resistance genes in Escherichia coli. Nature Communications. 13(1). 22 indexed citations

Hsu, Teng‐Kuei, Amanda Koire, Byung‐Kwon Choi, et al.. (2022). A general calculus of fitness landscapes finds genes under selection in cancers. Genome Research. 32(5). 916–929. 7 indexed citations

Wang, Chen, David C. Marciano, Amanda M. Williams, et al.. (2021). Identification of evolutionarily stable functional and immunogenic sites across the SARS-CoV-2 proteome and greater coronavirus family. Bioinformatics. 37(22). 4033–4040. 7 indexed citations

Sharma, Amit, Tikam Chand Dakal, Hongde Liu, et al.. (2021). PPAR-Responsive Elements Enriched with Alu Repeats May Contribute to Distinctive PPARγ–DNMT1 Interactions in the Genome. Cancers. 13(16). 3993–3993. 4 indexed citations

Coscolín, Cristina, Panagiotis Katsonis, Rafael Bargiela, et al.. (2021). Structure and evolutionary trace-assisted screening of a residue swapping the substrate ambiguity and chiral specificity in an esterase. Computational and Structural Biotechnology Journal. 19. 2307–2317. 5 indexed citations

Tsutakawa, Susan E., Albino Bacolla, Panagiotis Katsonis, et al.. (2021). Decoding Cancer Variants of Unknown Significance for Helicase–Nuclease–RPA Complexes Orchestrating DNA Repair During Transcription and Replication. Frontiers in Molecular Biosciences. 8. 791792–791792. 8 indexed citations

10.

Sharma, Amit, Arijit Biswas, Hongde Liu, et al.. (2019). Mutational Landscape of the BAP1 Locus Reveals an Intrinsic Control to Regulate the miRNA Network and the Binding of Protein Complexes in Uveal Melanoma. Cancers. 11(10). 1600–1600. 31 indexed citations

11.

Clarke, Callisia N., Panagiotis Katsonis, Amanda Koire, et al.. (2018). Comprehensive Genomic Characterization of Parathyroid Cancer Identifies Novel Candidate Driver Mutations and Core Pathways. Journal of the Endocrine Society. 3(3). 544–559. 47 indexed citations

12.

Koire, Amanda, Young Won Kim, Jarey H. Wang, et al.. (2017). Codon-level co-occurrences of germline variants and somatic mutations in cancer are rare but often lead to incorrect variant annotation and underestimated impact prediction. PLoS ONE. 12(3). e0174766–e0174766. 2 indexed citations

13.

Osman, Abdullah A., Marcus M. Monroe, Marcus V. Ortega Alves, et al.. (2014). Wee-1 Kinase Inhibition Overcomes Cisplatin Resistance Associated with High-Risk TP53 Mutations in Head and Neck Cancer through Mitotic Arrest Followed by Senescence. Molecular Cancer Therapeutics. 14(2). 608–619. 88 indexed citations

14.

Katsonis, Panagiotis & Olivier Lichtarge. (2014). A formal perturbation equation between genotype and phenotype determines the Evolutionary Action of protein-coding variations on fitness. Genome Research. 24(12). 2050–2058. 86 indexed citations

15.

Marciano, David C., et al.. (2014). Negative Feedback in Genetic Circuits Confers Evolutionary Resilience and Capacitance. Cell Reports. 7(6). 1789–1795. 21 indexed citations

16.

Lua, Rhonald C., David C. Marciano, Panagiotis Katsonis, et al.. (2014). Prediction and redesign of protein–protein interactions. Progress in Biophysics and Molecular Biology. 116(2-3). 194–202. 22 indexed citations

17.

Rababa’h, Abeer, Fatin Atrooz, Sonal Singh, et al.. (2013). Protein Kinase A and Phosphodiesterase-4D3 Binding to Coding Polymorphisms of Cardiac Muscle Anchoring Protein (mAKAP). Journal of Molecular Biology. 425(18). 3277–3288. 16 indexed citations

18.

Adikesavan, Anbu Karani, Panagiotis Katsonis, David C. Marciano, et al.. (2011). Separation of Recombination and SOS Response in Escherichia coli RecA Suggests LexA Interaction Sites. PLoS Genetics. 7(9). e1002244–e1002244. 71 indexed citations

19.

Häberle, Johannes, Oleg A. Shchelochkov, Jing Wang, et al.. (2010). Molecular defects in human carbamoy phosphate synthetase I: mutational spectrum, diagnostic and protein structure considerations. Human Mutation. 32(6). 579–589. 53 indexed citations

20.

Shaibani, Aziz, Oleg A. Shchelochkov, Shulin Zhang, et al.. (2009). Mitochondrial Neurogastrointestinal Encephalopathy Due to Mutations in RRM2B. Archives of Neurology. 66(8). 1028–32. 89 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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