Hanneke Okkenhaug

1.8k total citations
30 papers, 1.1k citations indexed

About

Hanneke Okkenhaug is a scholar working on Molecular Biology, Immunology and Cell Biology. According to data from OpenAlex, Hanneke Okkenhaug has authored 30 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 7 papers in Immunology and 6 papers in Cell Biology. Recurrent topics in Hanneke Okkenhaug's work include Epigenetics and DNA Methylation (4 papers), Cellular transport and secretion (4 papers) and Signaling Pathways in Disease (4 papers). Hanneke Okkenhaug is often cited by papers focused on Epigenetics and DNA Methylation (4 papers), Cellular transport and secretion (4 papers) and Signaling Pathways in Disease (4 papers). Hanneke Okkenhaug collaborates with scholars based in United Kingdom, Germany and Japan. Hanneke Okkenhaug's co-authors include Nicholas T. Ktistakis, Simon Walker, Maria Manifava, Eleftherios Karanasios, Eric Hummel, Hans Zimmermann, Marie‐Charlotte Domart, Lucy Collinson, Plamen Georgiev and Simon J. Cook and has published in prestigious journals such as Journal of Clinical Investigation, Nature Communications and Neuron.

In The Last Decade

Hanneke Okkenhaug

28 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hanneke Okkenhaug United Kingdom 18 698 268 255 124 105 30 1.1k
Mateus T. Guerra United States 20 809 1.2× 219 0.8× 238 0.9× 70 0.6× 116 1.1× 32 1.4k
Steve Jean Canada 15 655 0.9× 254 0.9× 462 1.8× 108 0.9× 161 1.5× 32 1.1k
Jason E. Lee United States 14 884 1.3× 187 0.7× 391 1.5× 103 0.8× 140 1.3× 20 1.3k
Shotaro Saita Japan 13 936 1.3× 297 1.1× 229 0.9× 48 0.4× 133 1.3× 14 1.2k
Hervé Barrière Canada 16 799 1.1× 123 0.5× 352 1.4× 155 1.3× 117 1.1× 17 1.3k
Holger Lorenz Germany 17 1.0k 1.5× 295 1.1× 411 1.6× 67 0.5× 122 1.2× 27 1.4k
Christine Powers United States 20 768 1.1× 345 1.3× 331 1.3× 77 0.6× 117 1.1× 23 1.3k
Hong-Wen Tang United States 18 702 1.0× 345 1.3× 171 0.7× 131 1.1× 81 0.8× 26 1.1k
Carol A. Bertrand United States 19 805 1.2× 101 0.4× 202 0.8× 76 0.6× 144 1.4× 37 1.4k
Emélie Braschi Canada 6 1.5k 2.1× 604 2.3× 211 0.8× 105 0.8× 248 2.4× 7 1.8k

Countries citing papers authored by Hanneke Okkenhaug

Since Specialization
Citations

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

Fields of papers citing papers by Hanneke Okkenhaug

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hanneke Okkenhaug

This figure shows the co-authorship network connecting the top 25 collaborators of Hanneke Okkenhaug. A scholar is included among the top collaborators of Hanneke Okkenhaug 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 Hanneke Okkenhaug. Hanneke Okkenhaug 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.
Bertran, M. Teresa, Robert Walmsley, Iker Valle Aramburu, et al.. (2024). A cyclic peptide toolkit reveals mechanistic principles of peptidylarginine deiminase IV regulation. Nature Communications. 15(1). 9746–9746. 5 indexed citations
2.
Stuart, Kate, et al.. (2024). Reporter cell lines to screen for inhibitors or regulators of the KRAS-RAF-MEK1/2-ERK1/2 pathway. Biochemical Journal. 481(6). 405–422.
3.
Okkenhaug, Hanneke, et al.. (2023). The GPCR adaptor protein Norbin regulates S1PR1 trafficking and the morphology, cell cycle and survival of PC12 cells. Scientific Reports. 13(1). 18237–18237. 2 indexed citations
4.
Johnsson, Anna‐Karin, Hanneke Okkenhaug, Anne Segonds-Pichon, et al.. (2023). Dock2 generates characteristic spatiotemporal patterns of Rac activity to regulate neutrophil polarisation, migration and phagocytosis. Frontiers in Immunology. 14. 1180886–1180886. 4 indexed citations
5.
Baker, Martin J., Anna‐Karin Johnsson, Melanie Stammers, et al.. (2023). The Rac-GEF Tiam1 controls integrin-dependent neutrophil responses. Frontiers in Immunology. 14. 1223653–1223653. 6 indexed citations
6.
Robinson, Emma, Faye Drawnel, Saher Mehdi, et al.. (2022). MSK-Mediated Phosphorylation of Histone H3 Ser28 Couples MAPK Signalling with Early Gene Induction and Cardiac Hypertrophy. Cells. 11(4). 604–604. 17 indexed citations
7.
Novo, Clara Lopes, Colin Hockings, Chetan Poudel, et al.. (2022). Satellite repeat transcripts modulate heterochromatin condensates and safeguard chromosome stability in mouse embryonic stem cells. Nature Communications. 13(1). 3525–3525. 30 indexed citations
8.
Gill, Diljeet, Aled Parry, Fátima Santos, et al.. (2022). Multi-omic rejuvenation of human cells by maturation phase transient reprogramming. eLife. 11. 90 indexed citations
9.
Balmanno, Kathryn, et al.. (2022). IKKα plays a major role in canonical NF-κB signalling in colorectal cells. Biochemical Journal. 479(3). 305–325. 20 indexed citations
10.
Murdoch, Sharlene, Andrea F. Lopez‐Clavijo, Hanneke Okkenhaug, et al.. (2021). Neuronal HSF-1 coordinates the propagation of fat desaturation across tissues to enable adaptation to high temperatures in C. elegans. PLoS Biology. 19(11). e3001431–e3001431. 17 indexed citations
11.
Kazakevych, Juri, Jérémy Denizot, Anke Liebert, et al.. (2020). Smarcad1 mediates microbiota-induced inflammation in mouse and coordinates gene expression in the intestinal epithelium. Genome biology. 21(1). 64–64. 17 indexed citations
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Lehmann, Laura C., Graeme Hewitt, Klaus Brackmann, et al.. (2020). Mechanistic Insights into Regulation of the ALC1 Remodeler by the Nucleosome Acidic Patch. Cell Reports. 33(12). 108529–108529. 28 indexed citations
15.
Lozano, Teresa, Christopher Bot, Sarah K. Whiteside, et al.. (2020). A cell-based bioluminescence assay reveals dose-dependent and contextual repression of AP-1-driven gene expression by BACH2. Scientific Reports. 10(1). 18902–18902. 4 indexed citations
16.
Chrysanthou, Stephanie, Claire E. Senner, Laura Woods, et al.. (2018). A Critical Role of TET1/2 Proteins in Cell-Cycle Progression of Trophoblast Stem Cells. Stem Cell Reports. 10(4). 1355–1368. 40 indexed citations
17.
Thienpont, Bernard, Jan Magnus Aronsen, Emma Robinson, et al.. (2016). The H3K9 dimethyltransferases EHMT1/2 protect against pathological cardiac hypertrophy. Journal of Clinical Investigation. 127(1). 335–348. 90 indexed citations
18.
Georgiev, Plamen, Hanneke Okkenhaug, Anna Drews, et al.. (2010). TRPM Channels Mediate Zinc Homeostasis and Cellular Growth during Drosophila Larval Development. Cell Metabolism. 12(4). 386–397. 37 indexed citations
19.
Okkenhaug, Hanneke, Karsten H. Weylandt, David Carmena, et al.. (2006). The human ClC‐4 protein, a member of the CLC chloride channel/transporter family, is localized to the endoplasmic reticulum by its N‐terminus. The FASEB Journal. 20(13). 2390–2392. 29 indexed citations
20.
García-Murillas, Isaac, Trevor R. Pettitt, Hanneke Okkenhaug, et al.. (2006). lazaro Encodes a Lipid Phosphate Phosphohydrolase that Regulates Phosphatidylinositol Turnover during Drosophila Phototransduction. Neuron. 49(4). 533–546. 56 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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