Arnhild Grothey

623 total citations
18 papers, 465 citations indexed

About

Arnhild Grothey is a scholar working on Molecular Biology, Immunology and Epidemiology. According to data from OpenAlex, Arnhild Grothey has authored 18 papers receiving a total of 465 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 8 papers in Immunology and 7 papers in Epidemiology. Recurrent topics in Arnhild Grothey's work include PI3K/AKT/mTOR signaling in cancer (4 papers), Protein Kinase Regulation and GTPase Signaling (4 papers) and Herpesvirus Infections and Treatments (4 papers). Arnhild Grothey is often cited by papers focused on PI3K/AKT/mTOR signaling in cancer (4 papers), Protein Kinase Regulation and GTPase Signaling (4 papers) and Herpesvirus Infections and Treatments (4 papers). Arnhild Grothey collaborates with scholars based in United Kingdom, Germany and United States. Arnhild Grothey's co-authors include Georgios Giamas, Justin Stebbing, Ladislav Burýšek, Martin Pospíšek, Thomas Simmet, Uwe Knippschild, Heidrun Hirner, Doris Henne‐Bruns, Joachim Bischof and Lars Dölken and has published in prestigious journals such as Nature, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Arnhild Grothey

18 papers receiving 463 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Arnhild Grothey United Kingdom 13 308 113 104 75 62 18 465
Keli Song United States 10 336 1.1× 105 0.9× 120 1.2× 58 0.8× 37 0.6× 19 475
Victoria Izumi United States 13 432 1.4× 56 0.5× 137 1.3× 82 1.1× 50 0.8× 22 601
Hong‐Yong Cui China 14 434 1.4× 211 1.9× 106 1.0× 93 1.2× 32 0.5× 21 555
Claudia Tredup Germany 10 219 0.7× 93 0.8× 69 0.7× 80 1.1× 35 0.6× 15 415
Margie N. Sutton United States 13 309 1.0× 77 0.7× 84 0.8× 106 1.4× 154 2.5× 24 474
Kenna Shirasuna Japan 8 370 1.2× 84 0.7× 206 2.0× 61 0.8× 41 0.7× 12 515
Christian T. Hellwig Ireland 10 383 1.2× 100 0.9× 120 1.2× 60 0.8× 61 1.0× 11 517
Sumita Bandyopadhyay India 12 552 1.8× 80 0.7× 91 0.9× 94 1.3× 60 1.0× 19 651
Sarah J. Turner United Kingdom 7 304 1.0× 123 1.1× 144 1.4× 61 0.8× 19 0.3× 12 529
Sarah C. Nabinger United States 13 434 1.4× 196 1.7× 138 1.3× 116 1.5× 37 0.6× 23 637

Countries citing papers authored by Arnhild Grothey

Since Specialization
Citations

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

Fields of papers citing papers by Arnhild Grothey

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Arnhild Grothey

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

All Works

18 of 18 papers shown
1.
Kurzai, Oliver, Arnhild Grothey, Lars Dölken, et al.. (2025). Unveiling immune interference: how the dendritic cell response to co-infection with Aspergillus fumigatus is modulated by human cytomegalovirus and its virokine CMV IL-10. mBio. 16(11). e0154125–e0154125. 1 indexed citations
2.
Whisnant, Adam W., et al.. (2024). Herpes simplex virus 1 inhibits phosphorylation of RNA polymerase II CTD serine-7. Journal of Virology. 98(10). e0117824–e0117824. 1 indexed citations
3.
Jürges, Christopher, Vanda Juranić Lisnić, Anne L’Hernault, et al.. (2023). Decoding murine cytomegalovirus. PLoS Pathogens. 19(5). e1010992–e1010992. 4 indexed citations
4.
Hennig, Thomas, Katharina Reinisch, Andrea Milić, et al.. (2023). The HSV-1 ICP22 protein selectively impairs histone repositioning upon Pol II transcription downstream of genes. Nature Communications. 14(1). 4591–4591. 12 indexed citations
5.
Hennig, Thomas, Archana Bairavasundaram Prusty, Benedikt B. Kaufer, et al.. (2022). Selective inhibition of miRNA processing by a herpesvirus-encoded miRNA. Nature. 605(7910). 539–544. 44 indexed citations
6.
Schlösser, Andreas, Arnhild Grothey, Peter O’Hare, et al.. (2022). pUL36 Deubiquitinase Activity Augments Both the Initiation and the Progression of Lytic Herpes Simplex Virus Infection in IFN-Primed Cells. Journal of Virology. 96(22). e0096322–e0096322. 3 indexed citations
7.
Friedel, Caroline C., Adam W. Whisnant, Andrzej Rutkowski, et al.. (2020). Dissecting Herpes Simplex Virus 1-Induced Host Shutoff at the RNA Level. Journal of Virology. 95(3). 32 indexed citations
8.
Nunes, João, Hua Zhang, Nicos Angelopoulos, et al.. (2016). ATG9A loss confers resistance to trastuzumab via c-Cbl mediated Her2 degradation. Oncotarget. 7(19). 27599–27612. 23 indexed citations
10.
Zhang, Hua, Nicos Angelopoulos, Yichen Xu, et al.. (2015). Proteomic profile of KSR1-regulated signalling in response to genotoxic agents in breast cancer. Breast Cancer Research and Treatment. 151(3). 555–568. 9 indexed citations
11.
Stebbing, Justin, Yang Xu, Andrew R. Green, et al.. (2014). KSR1 regulates BRCA1 degradation and inhibits breast cancer growth. Oncogene. 34(16). 2103–2114. 14 indexed citations
12.
Xu, Yichen, Hua Zhang, Arnhild Grothey, et al.. (2014). The Kinase LMTK3 Promotes Invasion in Breast Cancer Through GRB2-Mediated Induction of Integrin β 1. Science Signaling. 7(330). ra58–ra58. 31 indexed citations
13.
Zhang, Hua, Α. Φωτίου, Arnhild Grothey, Justin Stebbing, & Georgios Giamas. (2012). The role of pseudokinases in cancer. Cellular Signalling. 24(6). 1173–1184. 28 indexed citations
14.
Hirner, Heidrun, Çagatay Güneş, Joachim Bischof, et al.. (2012). Impaired CK1 Delta Activity Attenuates SV40-Induced Cellular Transformation In Vitro and Mouse Mammary Carcinogenesis In Vivo. PLoS ONE. 7(1). e29709–e29709. 33 indexed citations
15.
Stebbing, Justin, Aleksandra Filipović, Kevin Blighe, et al.. (2012). LMTK3 is implicated in endocrine resistance via multiple signaling pathways. Oncogene. 32(28). 3371–3380. 39 indexed citations
16.
Bischof, Joachim, Johann Leban, Mirko Zaja, et al.. (2012). 2-Benzamido-N-(1H-benzo[d]imidazol-2-yl)thiazole-4-carboxamide derivatives as potent inhibitors of CK1δ/ε. Amino Acids. 43(4). 1577–1591. 43 indexed citations
17.
Giamas, Georgios, Heidrun Hirner, Arnhild Grothey, et al.. (2007). Phosphorylation of CK1δ: identification of Ser370 as the major phosphorylation site targeted by PKA in vitro and in vivo. Biochemical Journal. 406(3). 389–398. 49 indexed citations
18.
Pospíšek, Martin, et al.. (2004). Intracellular Interleukin-1α Functionally Interacts with Histone Acetyltransferase Complexes. Journal of Biological Chemistry. 279(6). 4017–4026. 87 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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