Paschalis Kratsios

2.5k total citations
38 papers, 1.6k citations indexed

About

Paschalis Kratsios is a scholar working on Molecular Biology, Aging and Endocrine and Autonomic Systems. According to data from OpenAlex, Paschalis Kratsios has authored 38 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 22 papers in Aging and 14 papers in Endocrine and Autonomic Systems. Recurrent topics in Paschalis Kratsios's work include Genetics, Aging, and Longevity in Model Organisms (22 papers), Circadian rhythm and melatonin (14 papers) and Neurobiology and Insect Physiology Research (6 papers). Paschalis Kratsios is often cited by papers focused on Genetics, Aging, and Longevity in Model Organisms (22 papers), Circadian rhythm and melatonin (14 papers) and Neurobiology and Insect Physiology Research (6 papers). Paschalis Kratsios collaborates with scholars based in United States, Italy and United Kingdom. Paschalis Kratsios's co-authors include Oliver Hobert, Nadia Rosenthal, Foteini Mourkioti, Catarina Catela, Baris Tursun, Tulsi Patel, Michael Levine, Alberto Stolfi, Patrice Delafontaine and Valeria Parente and has published in prestigious journals such as Science, Journal of Clinical Investigation and Nature Communications.

In The Last Decade

Paschalis Kratsios

37 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Paschalis Kratsios United States 18 1.0k 630 334 272 210 38 1.6k
Fabio Demontis United States 25 1.5k 1.5× 653 1.0× 134 0.4× 532 2.0× 727 3.5× 48 2.5k
Joy Alcedo United States 19 974 0.9× 694 1.1× 405 1.2× 237 0.9× 250 1.2× 26 1.8k
Danielle Carmignac United Kingdom 27 743 0.7× 285 0.5× 489 1.5× 148 0.5× 566 2.7× 46 2.5k
Gad D. Vatine Israel 19 711 0.7× 84 0.1× 421 1.3× 456 1.7× 237 1.1× 37 2.1k
Koyomi Miyazaki Japan 24 415 0.4× 165 0.3× 823 2.5× 194 0.7× 380 1.8× 49 1.6k
J. Edward van Veen United States 11 488 0.5× 121 0.2× 114 0.3× 424 1.6× 484 2.3× 16 1.6k
Eun-Kyung Bae South Korea 22 817 0.8× 94 0.1× 271 0.8× 610 2.2× 93 0.4× 75 1.9k
Marijke Sage United States 10 823 0.8× 327 0.5× 1.2k 3.7× 350 1.3× 841 4.0× 11 2.3k
Birgitte Georg Denmark 21 700 0.7× 73 0.1× 954 2.9× 768 2.8× 261 1.2× 58 1.9k

Countries citing papers authored by Paschalis Kratsios

Since Specialization
Citations

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

Fields of papers citing papers by Paschalis Kratsios

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Paschalis Kratsios

This figure shows the co-authorship network connecting the top 25 collaborators of Paschalis Kratsios. A scholar is included among the top collaborators of Paschalis Kratsios 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 Paschalis Kratsios. Paschalis Kratsios 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.
Li, Jingxian, Shouqiang Cheng, Minglei Zhao, et al.. (2025). Structural basis and functional roles for Toll-like receptor binding to Latrophilin in C. elegans development. Nature Structural & Molecular Biology. 32(9). 1683–1696.
2.
Kratsios, Paschalis & Oliver Hobert. (2024). Almost 40 years of studying homeobox genes in C. elegans. Development. 151(21). 1 indexed citations
3.
Taylor, Seth R., Jacob A. Blum, Weidong Feng, et al.. (2024). A molecular atlas of adult C. elegans motor neurons reveals ancient diversity delineated by conserved transcription factor codes. Cell Reports. 43(3). 113857–113857. 16 indexed citations
4.
Cizeron, Mélissa, et al.. (2024). UNC-30/PITX coordinates neurotransmitter identity with postsynaptic GABA receptor clustering. Development. 151(16). 3 indexed citations
5.
Li, Yinan, et al.. (2023). Cell context-dependent CFI-1/ARID3 functions control neuronal terminal differentiation. Cell Reports. 42(3). 112220–112220. 5 indexed citations
6.
Mitra, Koushambi, Palapuravan Anees, Aneesh Tazhe Veetil, et al.. (2023). A DNA nanodevice for mapping sodium at single-organelle resolution. Nature Biotechnology. 42(7). 1075–1083. 27 indexed citations
7.
Sonobe, Yoshifumi, Soojin Lee, Gopinath Krishnan, et al.. (2023). Translation of dipeptide repeat proteins in C9ORF72 ALS/FTD through unique and redundant AUG initiation codons. eLife. 12. 6 indexed citations
8.
Reilly, Molly B., Cyril Cros, Itai Antoine Toker, et al.. (2022). Widespread employment of conserved C. elegans homeobox genes in neuronal identity specification. PLoS Genetics. 18(9). e1010372–e1010372. 22 indexed citations
9.
Kratsios, Paschalis, et al.. (2022). Hox gene functions in the C. elegans nervous system: From early patterning to maintenance of neuronal identity. Seminars in Cell and Developmental Biology. 152-153. 58–69. 11 indexed citations
10.
Medwig-Kinney, Taylor N., Michael A. Q. Martinez, Nicholas J. Palmisano, et al.. (2022). The SWI/SNF chromatin remodeling assemblies BAF and PBAF differentially regulate cell cycle exit and cellular invasion in vivo. PLoS Genetics. 18(1). e1009981–e1009981. 19 indexed citations
11.
Sonobe, Yoshifumi, Gopinath Krishnan, Ghanashyam D. Ghadge, et al.. (2021). A C. elegans model of C9orf72-associated ALS/FTD uncovers a conserved role for eIF2D in RAN translation. Nature Communications. 12(1). 6025–6025. 36 indexed citations
12.
Chakraborty, Kasturi, Palapuravan Anees, Sunaina Surana, et al.. (2021). Tissue-specific targeting of DNA nanodevices in a multicellular living organism. eLife. 10. 11 indexed citations
13.
14.
Catela, Catarina, et al.. (2019). An ancient role for collier/Olf/Ebf (COE)-type transcription factors in axial motor neuron development. Neural Development. 14(1). 2–2. 17 indexed citations
15.
Kratsios, Paschalis & Oliver Hobert. (2018). Nervous System Development: Flies and Worms Converging on Neuron Identity Control. Current Biology. 28(19). R1154–R1157. 6 indexed citations
16.
Kerk, Sze Yen, et al.. (2017). Diversification of C. elegans Motor Neuron Identity via Selective Effector Gene Repression. Neuron. 93(1). 80–98. 54 indexed citations
17.
Kratsios, Paschalis, Bérangère Pinan‐Lucarré, Sze Yen Kerk, et al.. (2015). Transcriptional Coordination of Synaptogenesis and Neurotransmitter Signaling. Current Biology. 25(10). 1282–1295. 50 indexed citations
18.
Kratsios, Paschalis, Alberto Stolfi, Michael Levine, & Oliver Hobert. (2011). Coordinated regulation of cholinergic motor neuron traits through a conserved terminal selector gene. Nature Neuroscience. 15(2). 205–214. 133 indexed citations
19.
Tursun, Baris, Tulsi Patel, Paschalis Kratsios, & Oliver Hobert. (2010). Direct Conversion of C. elegans Germ Cells into Specific Neuron Types. Science. 331(6015). 304–308. 168 indexed citations
20.
Catela, Catarina, et al.. (2010). Serum and glucocorticoid‐inducible kinase 1 (SGK1) is necessary for vascular remodeling during angiogenesis. Developmental Dynamics. 239(8). 2149–2160. 36 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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