Gregor Rot

4.3k total citations · 2 hit papers
24 papers, 3.1k citations indexed

About

Gregor Rot is a scholar working on Molecular Biology, Cancer Research and Neurology. According to data from OpenAlex, Gregor Rot has authored 24 papers receiving a total of 3.1k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 3 papers in Cancer Research and 2 papers in Neurology. Recurrent topics in Gregor Rot's work include RNA Research and Splicing (15 papers), RNA modifications and cancer (10 papers) and RNA and protein synthesis mechanisms (8 papers). Gregor Rot is often cited by papers focused on RNA Research and Splicing (15 papers), RNA modifications and cancer (10 papers) and RNA and protein synthesis mechanisms (8 papers). Gregor Rot collaborates with scholars based in Slovenia, United Kingdom and United States. Gregor Rot's co-authors include Tomaž Curk, Blaž Zupan, Jernej Ule, Melis Kayikci, Kathi Zarnack, Nicholas M. Luscombe, Julian König, Daniel J. Turner, Michael Briese and Boris Rogelj and has published in prestigious journals such as Nucleic Acids Research, Nature Neuroscience and Molecular Cell.

In The Last Decade

Gregor Rot

23 papers receiving 3.1k citations

Hit Papers

iCLIP reveals the function of hnRNP particles in splicing... 2010 2026 2015 2020 2010 2011 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Gregor Rot Slovenia 15 2.7k 726 527 516 176 24 3.1k
Tiffany Y Liang United States 12 2.4k 0.9× 729 1.0× 551 1.0× 515 1.0× 66 0.4× 18 3.0k
Andrea D’Ambrogio Italy 10 1.8k 0.7× 1.4k 1.9× 313 0.6× 841 1.6× 71 0.4× 10 2.5k
Mark W. Kankel United States 16 1.8k 0.7× 281 0.4× 144 0.3× 310 0.6× 273 1.6× 18 2.4k
C.‐K. James Shen United States 30 2.0k 0.8× 1.3k 1.8× 101 0.2× 897 1.7× 114 0.6× 55 2.9k
Sergey Paushkin United States 24 4.3k 1.6× 107 0.1× 580 1.1× 1.1k 2.1× 137 0.8× 31 4.7k
Liqun Liu‐Yesucevitz United States 6 1.3k 0.5× 512 0.7× 56 0.1× 307 0.6× 201 1.1× 7 1.6k
Soonmoon Yoo United States 28 1.7k 0.6× 126 0.2× 347 0.7× 149 0.3× 305 1.7× 37 2.3k
Leeanne McGurk United States 16 1.1k 0.4× 476 0.7× 53 0.1× 236 0.5× 172 1.0× 19 1.5k
Anindya Sen United States 18 1.4k 0.5× 168 0.2× 104 0.2× 304 0.6× 295 1.7× 22 1.9k
Ranhui Duan China 21 2.2k 0.8× 167 0.2× 845 1.6× 107 0.2× 114 0.6× 63 2.6k

Countries citing papers authored by Gregor Rot

Since Specialization
Citations

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

Fields of papers citing papers by Gregor Rot

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gregor Rot

This figure shows the co-authorship network connecting the top 25 collaborators of Gregor Rot. A scholar is included among the top collaborators of Gregor Rot 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 Gregor Rot. Gregor Rot 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.
Weber, Joachim, S L Streicher, Thomas Schmutzer, et al.. (2024). The Arabidopsis U1 snRNP regulates mRNA 3′-end processing. Nature Plants. 10(10). 1514–1531. 3 indexed citations
2.
Rot, Gregor, et al.. (2023). Analysis of RNA Polyadenylation in Healthy and Osteoarthritic Human Articular Cartilage. International Journal of Molecular Sciences. 24(7). 6611–6611. 4 indexed citations
3.
Spruce, Thomas, Mireya Plass, André Gohr, et al.. (2022). The X-linked splicing regulator MBNL3 has been co-opted to restrict placental growth in eutherians. PLoS Biology. 20(4). e3001615–e3001615. 7 indexed citations
5.
Bai, Yu, Emmanuel Caussinus, Stefano Léo, et al.. (2021). A cis-regulatory element promoting increased transcription at low temperature in cultured ectothermic Drosophila cells. BMC Genomics. 22(1). 771–771. 3 indexed citations
6.
Modic, Miha, Markus Grosch, Gregor Rot, et al.. (2019). Cross-Regulation between TDP-43 and Paraspeckles Promotes Pluripotency-Differentiation Transition. Molecular Cell. 74(5). 951–965.e13. 92 indexed citations
7.
Modic, Miha, Gregor Rot, Markus Grosch, et al.. (2018). Cross-Regulation Between TDP-43 and Paraspeckles Promotes Pluripotency-Differentiation Transition. SSRN Electronic Journal. 2 indexed citations
8.
Rot, Gregor, Zhen Wang, Ina Huppertz, et al.. (2017). High-Resolution RNA Maps Suggest Common Principles of Splicing and Polyadenylation Regulation by TDP-43. Cell Reports. 19(5). 1056–1067. 67 indexed citations
9.
Miranda, Edward Roshan, Gregor Rot, Marko Toplak, et al.. (2013). Transcriptional Profiling of Dictyostelium with RNA Sequencing. Methods in molecular biology. 983. 139–171. 10 indexed citations
10.
Nasser, Waleed, Balaji Santhanam, Edward Roshan Miranda, et al.. (2013). Bacterial Discrimination by Dictyostelid Amoebae Reveals the Complexity of Ancient Interspecies Interactions. Current Biology. 23(10). 862–872. 51 indexed citations
11.
Wagnon, Jacy L., Michael Briese, Wenzhi Sun, et al.. (2012). CELF4 Regulates Translation and Local Abundance of a Vast Set of mRNAs, Including Genes Associated with Regulation of Synaptic Function. PLoS Genetics. 8(11). e1003067–e1003067. 84 indexed citations
12.
Rogelj, Boris, Laura E. Easton, Gireesh K. Bogu, et al.. (2012). Widespread binding of FUS along nascent RNA regulates alternative splicing in the brain. Scientific Reports. 2(1). 603–603. 206 indexed citations
13.
Curk, Tomaž, Gregor Rot, & Blaž Zupan. (2011). SNPsyn: detection and exploration of SNP–SNP interactions. Nucleic Acids Research. 39(suppl_2). W444–W449. 30 indexed citations
14.
Tollervey, James, Zhen Wang, Tibor Hortobágyi, et al.. (2011). Analysis of alternative splicing associated with aging and neurodegeneration in the human brain. Genome Research. 21(10). 1572–1582. 186 indexed citations
15.
König, Julian, Kathi Zarnack, Gregor Rot, et al.. (2011). iCLIP - Transcriptome-wide Mapping of Protein-RNA Interactions with Individual Nucleotide Resolution. Journal of Visualized Experiments. 160 indexed citations
16.
Tollervey, James, Tomaž Curk, Boris Rogelj, et al.. (2011). Characterizing the RNA targets and position-dependent splicing regulation by TDP-43. Nature Neuroscience. 14(4). 452–458. 859 indexed citations breakdown →
17.
Parikh, Anup, Edward Roshan Miranda, Mariko Katoh‐Kurasawa, et al.. (2010). Conserved developmental transcriptomes in evolutionarily divergent species. Genome biology. 11(3). R35–R35. 139 indexed citations
18.
König, Julian, Kathi Zarnack, Gregor Rot, et al.. (2010). iCLIP reveals the function of hnRNP particles in splicing at individual nucleotide resolution. Nature Structural & Molecular Biology. 17(7). 909–915. 879 indexed citations breakdown →
19.
Wang, Zhen, Melis Kayikci, Michael Briese, et al.. (2010). iCLIP Predicts the Dual Splicing Effects of TIA-RNA Interactions. PLoS Biology. 8(10). e1000530–e1000530. 187 indexed citations
20.
Rot, Gregor, Anup Parikh, Tomaž Curk, et al.. (2009). dictyExpress: a Dictyostelium discoideum gene expression database with an explorative data analysis web-based interface. BMC Bioinformatics. 10(1). 265–265. 61 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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