Norbert Redemann

1000 total citations
20 papers, 833 citations indexed

About

Norbert Redemann is a scholar working on Molecular Biology, Surgery and Ophthalmology. According to data from OpenAlex, Norbert Redemann has authored 20 papers receiving a total of 833 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 3 papers in Surgery and 3 papers in Ophthalmology. Recurrent topics in Norbert Redemann's work include Genomics and Chromatin Dynamics (4 papers), Glycosylation and Glycoproteins Research (3 papers) and Retinal and Optic Conditions (3 papers). Norbert Redemann is often cited by papers focused on Genomics and Chromatin Dynamics (4 papers), Glycosylation and Glycoproteins Research (3 papers) and Retinal and Optic Conditions (3 papers). Norbert Redemann collaborates with scholars based in Germany, Austria and United States. Norbert Redemann's co-authors include P. Todd Stukenberg, Jan‐Michael Peters, Erich A. Nigg, Izabela Sumara, Ulrike Gaul, Herbert Jäckle, Bernhard Holzmann, Joseph Schlessinger, Erwin F. Wagner and T von Rüden and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Molecular Cell.

In The Last Decade

Norbert Redemann

20 papers receiving 817 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Norbert Redemann Germany 12 664 307 152 119 61 20 833
Peter Rellos Australia 7 614 0.9× 505 1.6× 71 0.5× 176 1.5× 47 0.8× 11 853
Chandra Childress United States 15 594 0.9× 220 0.7× 57 0.4× 133 1.1× 62 1.0× 18 843
Kostas D. Katsanakis United Kingdom 7 806 1.2× 143 0.5× 76 0.5× 158 1.3× 44 0.7× 7 1.0k
Kuntala Shome United States 14 850 1.3× 453 1.5× 57 0.4× 72 0.6× 33 0.5× 16 1.1k
Montserrat Jaumot Spain 17 687 1.0× 166 0.5× 105 0.7× 239 2.0× 44 0.7× 32 932
Willy Lemstra Netherlands 15 573 0.9× 262 0.9× 41 0.3× 131 1.1× 52 0.9× 28 749
Kaoru Sakabe United States 9 1.0k 1.5× 93 0.3× 50 0.3× 108 0.9× 32 0.5× 11 1.1k
Mark D. Roos United States 11 854 1.3× 86 0.3× 55 0.4× 89 0.7× 49 0.8× 12 1.0k
Iris Eisenmann-Tappe Germany 7 631 1.0× 106 0.3× 35 0.2× 171 1.4× 41 0.7× 8 832
Micah J. Maxwell United States 8 376 0.6× 162 0.5× 54 0.4× 84 0.7× 19 0.3× 13 599

Countries citing papers authored by Norbert Redemann

Since Specialization
Citations

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

Fields of papers citing papers by Norbert Redemann

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Norbert Redemann

This figure shows the co-authorship network connecting the top 25 collaborators of Norbert Redemann. A scholar is included among the top collaborators of Norbert Redemann 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 Norbert Redemann. Norbert Redemann 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.
Becker, Kolja, Carina Marianne Weigelt, Holger Fuchs, et al.. (2022). Transcriptome analysis of AAV-induced retinopathy models expressing human VEGF, TNF-α, and IL-6 in murine eyes. Scientific Reports. 12(1). 19395–19395. 3 indexed citations
2.
Weigelt, Carina Marianne, Nina Zippel, Holger Fuchs, et al.. (2022). Characterization and Validation of In Vitro and In Vivo Models to Investigate TNF-α-Induced Inflammation in Retinal Diseases. Translational Vision Science & Technology. 11(5). 18–18. 8 indexed citations
3.
Weigelt, Carina Marianne, Holger Fuchs, Tanja Schönberger, et al.. (2021). AAV-Mediated Expression of Human VEGF, TNF-α, and IL-6 Induces Retinal Pathology in Mice. Translational Vision Science & Technology. 10(11). 15–15. 12 indexed citations
4.
Winter, Martin, Tom Bretschneider, Robert Ries, et al.. (2018). Establishing MALDI-TOF as Versatile Drug Discovery Readout to Dissect the PTP1B Enzymatic Reaction. SLAS DISCOVERY. 23(6). 561–573. 31 indexed citations
5.
Perdikari, Aliki, et al.. (2017). A high-throughput, image-based screen to identify kinases involved in brown adipocyte development. Science Signaling. 10(466). 18 indexed citations
6.
Schiele, Felix, John Park, Norbert Redemann, Gerd Luippold, & Herbert Nar. (2013). An Antibody against the C-Terminal Domain of PCSK9 Lowers LDL Cholesterol Levels In Vivo. Journal of Molecular Biology. 426(4). 843–852. 28 indexed citations
7.
Mack, Jürgen, et al.. (2011). Discovery of BI 99179, a potent and selective inhibitor of type I fatty acid synthase with central exposure. Bioorganic & Medicinal Chemistry Letters. 21(19). 5924–5927. 20 indexed citations
8.
Sharff, Andrew, Anne Cleasby, Mark C. Williams, et al.. (2007). Structure of a CBS-domain pair from the regulatory γ1 subunit of human AMPK in complex with AMP and ZMP. Acta Crystallographica Section D Biological Crystallography. 63(5). 587–596. 75 indexed citations
9.
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11.
Sumara, Izabela, et al.. (2002). The Dissociation of Cohesin from Chromosomes in Prophase Is Regulated by Polo-like Kinase. Molecular Cell. 9(3). 515–525. 371 indexed citations
12.
Hofmann, Johannes, et al.. (2001). G1-Cdk activity is required for both proliferation and viability of cytokine-dependent myeloid and erythroid cells. Oncogene. 20(31). 4198–4208. 3 indexed citations
13.
Redemann, Norbert, et al.. (1996). Hypotensive effects of the angiotensin II antagonist telmisartan in conscious chronically-instrumented transgenic rats.. PubMed. 46(8). 755–9. 9 indexed citations
14.
Meel, J. C. A. van, et al.. (1995). Low concentrations of UD-CG 212 enhance myocyte contractility by an increase in calcium responsiveness in the presence of inorganic phosphate. Naunyn-Schmiedeberg s Archives of Pharmacology. 351(6). 644–650. 3 indexed citations
15.
Meel, J. C. A. van, Michael Entzeroth, Norbert Redemann, & R. Haigh. (1995). Effects of pimobendan and its metabolite on myofibrillar calcium responsiveness and ATPase activity in the presence of inorganic phosphate.. PubMed. 45(2). 136–41. 9 indexed citations
16.
Redemann, Norbert, Bernhard Holzmann, T von Rüden, et al.. (1992). Anti-oncogenic activity of signalling-defective epidermal growth factor receptor mutants.. Molecular and Cellular Biology. 12(2). 491–498. 110 indexed citations
17.
Redemann, Norbert, Bernhard Holzmann, T von Rüden, et al.. (1992). Anti-Oncogenic Activity of Signalling-Defective Epidermal Growth Factor Receptor Mutants. Molecular and Cellular Biology. 12(2). 491–498. 9 indexed citations
18.
Gaul, Ulrike, Norbert Redemann, & Herbert Jäckle. (1989). Single amino acid exchanges in the finger domain impair the function of the Drosophila gene Krüppel (Kr).. Proceedings of the National Academy of Sciences. 86(12). 4599–4603. 13 indexed citations
19.
Redemann, Norbert, Ulrike Gaul, & Herbert Jäckle. (1988). Disruption of a putative Cys–zinc interaction eliminates the biological activity of the Krüppel finger protein. Nature. 332(6159). 90–92. 70 indexed citations
20.
Jäckle, Herbert, Ulrike Gaul, & Norbert Redemann. (1988). Regulation and putative function of the Drosophila gap gene Krüppel. Development. 104(Supplement). 29–34. 4 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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