Georg Stoecklin

11.4k total citations · 3 hit papers
74 papers, 8.6k citations indexed

About

Georg Stoecklin is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Georg Stoecklin has authored 74 papers receiving a total of 8.6k indexed citations (citations by other indexed papers that have themselves been cited), including 70 papers in Molecular Biology, 7 papers in Cardiology and Cardiovascular Medicine and 4 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Georg Stoecklin's work include RNA Research and Splicing (56 papers), RNA modifications and cancer (37 papers) and RNA and protein synthesis mechanisms (37 papers). Georg Stoecklin is often cited by papers focused on RNA Research and Splicing (56 papers), RNA modifications and cancer (37 papers) and RNA and protein synthesis mechanisms (37 papers). Georg Stoecklin collaborates with scholars based in Germany, United States and Switzerland. Georg Stoecklin's co-authors include Nancy Kedersha, Paul Anderson, Christoph Moroni, Jens Lykke‐Andersen, Sevim Ozgur, Sarah Hofmann, Patrick W. Yacono, Paul Anderson, Marvin J. Fritzler and Randal J. Kaufman and has published in prestigious journals such as Nature, Cell and Nucleic Acids Research.

In The Last Decade

Georg Stoecklin

73 papers receiving 8.5k citations

Hit Papers

Stress granules and processing bodies are dynamically lin... 2001 2026 2009 2017 2005 2004 2001 250 500 750 1000

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Georg Stoecklin Germany 41 7.5k 1.5k 1.0k 524 515 74 8.6k
Javier F. Cáceres United Kingdom 52 11.0k 1.5× 2.4k 1.6× 618 0.6× 663 1.3× 691 1.3× 89 12.2k
Juan Valcárcel Spain 53 10.0k 1.3× 1.4k 0.9× 622 0.6× 221 0.4× 374 0.7× 117 11.1k
Gary Brewer United States 54 7.4k 1.0× 1.4k 0.9× 1.1k 1.0× 272 0.5× 817 1.6× 114 9.0k
Jens Lykke‐Andersen United States 40 7.1k 0.9× 974 0.7× 414 0.4× 313 0.6× 264 0.5× 61 7.8k
Ann‐Bin Shyu United States 36 6.5k 0.9× 1.4k 0.9× 756 0.7× 196 0.4× 566 1.1× 53 7.5k
Bo Porse Denmark 46 5.8k 0.8× 1.1k 0.7× 1.2k 1.2× 310 0.6× 754 1.5× 112 7.8k
Katherine L. B. Borden Canada 53 6.6k 0.9× 750 0.5× 1.2k 1.2× 419 0.8× 930 1.8× 118 8.2k
Mamie Z. Li United States 28 5.8k 0.8× 1.8k 1.2× 908 0.9× 617 1.2× 839 1.6× 37 7.8k
Stéphane Pyronnet France 36 3.5k 0.5× 576 0.4× 467 0.4× 475 0.9× 967 1.9× 84 4.9k
Marc R. Fabian Canada 31 5.8k 0.8× 3.3k 2.2× 550 0.5× 265 0.5× 239 0.5× 58 7.4k

Countries citing papers authored by Georg Stoecklin

Since Specialization
Citations

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

Fields of papers citing papers by Georg Stoecklin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Georg Stoecklin

This figure shows the co-authorship network connecting the top 25 collaborators of Georg Stoecklin. A scholar is included among the top collaborators of Georg Stoecklin 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 Georg Stoecklin. Georg Stoecklin 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.
Schott, Johanna, Doris Lindner, Joris Messens, et al.. (2023). Stress-induced nuclear speckle reorganization is linked to activation of immediate early gene splicing. The Journal of Cell Biology. 222(12). 12 indexed citations
2.
Legrand, Carine, Johanna Schott, Daniel Pérez-Hernández, et al.. (2023). Queuosine‐tRNA promotes sex‐dependent learning and memory formation by maintaining codon‐biased translation elongation speed. The EMBO Journal. 42(19). e112507–e112507. 24 indexed citations
3.
Stoecklin, Georg, et al.. (2022). Mitochondrial Inhibition by Sodium Azide Induces Assembly of eIF2α Phosphorylation-Independent Stress Granules in Mammalian Cells. International Journal of Molecular Sciences. 23(10). 5600–5600. 5 indexed citations
4.
Haneke, Katharina, Johanna Schott, Doris Lindner, et al.. (2020). CDK1 couples proliferation with protein synthesis. The Journal of Cell Biology. 219(3). 66 indexed citations
5.
Lafarga, Vanesa, Katharina Haneke, Anne‐Laure Pauleau, et al.. (2018). TIAR marks nuclear G2/M transition granules and restricts CDK 1 activity under replication stress. EMBO Reports. 20(1). 15 indexed citations
6.
Poetz, Fabian, et al.. (2016). Acetylation-Dependent Control of Global Poly(A) RNA Degradation by CBP/p300 and HDAC1/2. Molecular Cell. 63(6). 927–938. 35 indexed citations
7.
Leppek, Kathrin, et al.. (2015). A Distinct, Sequence-Induced Conformation Is Required for Recognition of the Constitutive Decay Element RNA by Roquin. Structure. 23(8). 1437–1447. 9 indexed citations
8.
Leppek, Kathrin & Georg Stoecklin. (2013). An optimized streptavidin-binding RNA aptamer for purification of ribonucleoprotein complexes identifies novel ARE-binding proteins. Nucleic Acids Research. 42(2). e13–e13. 113 indexed citations
9.
Leppek, Kathrin, Johanna Schott, Sonja Reitter, et al.. (2013). Roquin Promotes Constitutive mRNA Decay via a Conserved Class of Stem-Loop Recognition Motifs. Cell. 153(4). 869–881. 249 indexed citations
10.
Hofmann, Sarah, Silke Druffel‐Augustin, Axel Mogk, et al.. (2013). Coordination of Translational Control and Protein Homeostasis during Severe Heat Stress. Current Biology. 23(24). 2452–2462. 186 indexed citations
11.
Hofmann, Sarah, et al.. (2012). Translation suppression promotes stress granule formation and cell survival in response to cold shock. Molecular Biology of the Cell. 23(19). 3786–3800. 137 indexed citations
12.
Ruggieri, Alessia, Eva Dazert, Philippe Metz, et al.. (2012). Dynamic Oscillation of Translation and Stress Granule Formation Mark the Cellular Response to Virus Infection. Cell Host & Microbe. 12(1). 71–85. 148 indexed citations
13.
Timmers, H. T. Marc, et al.. (2011). Not1 mediates recruitment of the deadenylase Caf1 to mRNAs targeted for degradation by tristetraprolin. Nucleic Acids Research. 39(10). 4373–4386. 188 indexed citations
14.
Stoecklin, Georg, Scott A. Tenenbaum, Sridar V. Chittur, et al.. (2008). Genome-wide Analysis Identifies Interleukin-10 mRNA as Target of Tristetraprolin. Journal of Biological Chemistry. 283(17). 11689–11699. 207 indexed citations
15.
Benjamin, Don, et al.. (2006). A GFP-based assay for monitoring post-transcriptional regulation of ARE-mRNA turnover. Molecular BioSystems. 2(11). 561–567. 8 indexed citations
16.
Stoecklin, Georg, et al.. (2005). ARE‐mRNA degradation requires the 5′–3′ decay pathway. EMBO Reports. 7(1). 72–77. 199 indexed citations
17.
Stoecklin, Georg, Nancy Kedersha, Stephen Wax, et al.. (2004). MK2‐induced tristetraprolin:14‐3‐3 complexes prevent stress granule association and ARE‐mRNA decay. The EMBO Journal. 23(6). 1313–1324. 434 indexed citations
18.
Stoecklin, Georg. (2002). Functional cloning of BRF1, a regulator of ARE-dependent mRNA turnover. The EMBO Journal. 21(17). 4709–4718. 186 indexed citations
19.
Chen, Ching‐Yi, Roberto Gherzi, Shao‐En Ong, et al.. (2001). AU Binding Proteins Recruit the Exosome to Degrade ARE-Containing mRNAs. Cell. 107(4). 451–464. 720 indexed citations breakdown →
20.
Hankes, L. V., H.H. Coenen, Eugenia Rota, et al.. (1991). Effect of Huntington’s and Alzheimer’s Diseases on the Transport of Nicotinic Acid or Nicotinamide Across the Human Blood-Brain Barrier. Advances in experimental medicine and biology. 294. 675–678. 19 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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