Elisabeth Härtig

2.0k total citations
28 papers, 849 citations indexed

About

Elisabeth Härtig is a scholar working on Molecular Biology, Genetics and Ecology. According to data from OpenAlex, Elisabeth Härtig has authored 28 papers receiving a total of 849 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 13 papers in Genetics and 11 papers in Ecology. Recurrent topics in Elisabeth Härtig's work include Microbial Fuel Cells and Bioremediation (11 papers), Bacterial Genetics and Biotechnology (11 papers) and Microbial Community Ecology and Physiology (8 papers). Elisabeth Härtig is often cited by papers focused on Microbial Fuel Cells and Bioremediation (11 papers), Bacterial Genetics and Biotechnology (11 papers) and Microbial Community Ecology and Physiology (8 papers). Elisabeth Härtig collaborates with scholars based in Germany, United Kingdom and Italy. Elisabeth Härtig's co-authors include Walter G. Zumft, Dieter Jahn, Kai‐Uwe Vollack, Richard Münch, Heinz Körner, Anja Hartmann, Thorben Dammeyer, Lars H. Böttger, Alfred X. Trautwein and Max Schobert and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and PLoS ONE.

In The Last Decade

Elisabeth Härtig

28 papers receiving 840 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Elisabeth Härtig Germany 19 504 268 221 149 123 28 849
Jeong‐Il Oh South Korea 18 656 1.3× 187 0.7× 160 0.7× 64 0.4× 144 1.2× 48 1.0k
James M. Dubbs Thailand 16 680 1.3× 190 0.7× 106 0.5× 91 0.6× 95 0.8× 29 952
Terry H. Bird United States 12 665 1.3× 344 1.3× 330 1.5× 67 0.4× 123 1.0× 19 892
Ulrike Gerischer Germany 20 646 1.3× 115 0.4× 306 1.4× 178 1.2× 75 0.6× 26 920
Aresa Toukdarian United States 18 539 1.1× 222 0.8× 420 1.9× 116 0.8× 64 0.5× 28 883
Yongliang Yan China 21 564 1.1× 226 0.8× 149 0.7× 237 1.6× 133 1.1× 63 1.1k
Yuejin Hua China 19 564 1.1× 125 0.5× 186 0.8× 185 1.2× 29 0.2× 47 1.1k
Jean Huang United States 12 727 1.4× 157 0.6× 218 1.0× 59 0.4× 83 0.7× 21 1.0k
Cécile Jourlin‐Castelli France 20 742 1.5× 258 1.0× 462 2.1× 58 0.4× 137 1.1× 34 1.1k
Gerhard Burchhardt Germany 17 599 1.2× 160 0.6× 170 0.8× 315 2.1× 85 0.7× 30 1.1k

Countries citing papers authored by Elisabeth Härtig

Since Specialization
Citations

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

Fields of papers citing papers by Elisabeth Härtig

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elisabeth Härtig

This figure shows the co-authorship network connecting the top 25 collaborators of Elisabeth Härtig. A scholar is included among the top collaborators of Elisabeth Härtig 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 Elisabeth Härtig. Elisabeth Härtig 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
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Wang, Hui, Matthias Ebert, Elisabeth Härtig, et al.. (2022). The Influence of Genes on the “Killer Plasmid” of Dinoroseobacter shibae on Its Symbiosis With the Dinoflagellate Prorocentrum minimum. Frontiers in Microbiology. 12. 804767–804767. 7 indexed citations
3.
Kucklick, Martin, et al.. (2021). Adaptation of Dinoroseobacter shibae to oxidative stress and the specific role of RirA. PLoS ONE. 16(3). e0248865–e0248865. 2 indexed citations
4.
Baabe, Dirk, et al.. (2020). RirA of Dinoroseobacter shibae senses iron via a [3Fe–4S]1+ cluster co-ordinated by three cysteine residues. Biochemical Journal. 477(1). 191–212. 9 indexed citations
5.
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Ebert, Matthias, et al.. (2017). Heme and nitric oxide binding by the transcriptional regulator DnrF from the marine bacterium Dinoroseobacter shibae increases napD promoter affinity. Journal of Biological Chemistry. 292(37). 15468–15480. 10 indexed citations
7.
Ebert, Matthias, Andrea Thürmer, Denitsa Eckweiler, et al.. (2017). FnrL and Three Dnr Regulators Are Used for the Metabolic Adaptation to Low Oxygen Tension in Dinoroseobacter shibae. Frontiers in Microbiology. 8. 642–642. 18 indexed citations
8.
Krausze, J., et al.. (2013). Purification, crystallization and preliminary X-ray analysis of the effector domain of AlsR, an LysR-type transcriptional regulator fromBacillus subtilis. Acta Crystallographica Section F Structural Biology and Crystallization Communications. 69(5). 581–584. 3 indexed citations
9.
Härtig, Elisabeth & Dieter Jahn. (2012). Regulation of the Anaerobic Metabolism in Bacillus subtilis. Advances in microbial physiology. 61. 195–216. 55 indexed citations
10.
Hartmann, Anja, et al.. (2011). The Transcription Factor AlsR Binds and Regulates the Promoter of the alsSD Operon Responsible for Acetoin Formation in Bacillus subtilis. Journal of Bacteriology. 194(5). 1100–1112. 49 indexed citations
11.
Böttger, Lars H., et al.. (2010). Aspartate 141 Is the Fourth Ligand of the Oxygen-sensing [4Fe-4S]2+ Cluster of Bacillus subtilis Transcriptional Regulator Fnr. Journal of Biological Chemistry. 286(3). 2017–2021. 33 indexed citations
12.
Buettner, Falk F. R., Janine T. Bossé, Jochen Meens, et al.. (2009). Analysis of the Actinobacillus pleuropneumoniae HlyX (FNR) regulon and identification of iron‐regulated protein B as an essential virulence factor. PROTEOMICS. 9(9). 2383–2398. 32 indexed citations
13.
Marinoni, Ilaria, Simona Nonnis, Carmine G. Monteferrante, et al.. (2008). Characterization of l‐aspartate oxidase and quinolinate synthase from Bacillus subtilis. FEBS Journal. 275(20). 5090–5107. 36 indexed citations
14.
Münch, Richard, et al.. (2006). The Fnr Regulon of Bacillus subtilis. Journal of Bacteriology. 188(3). 1103–1112. 76 indexed citations
15.
Scheer, Maurice, Frank Klawonn, Richard Münch, et al.. (2006). JProGO: a novel tool for the functional interpretation of prokaryotic microarray data using Gene Ontology information. Nucleic Acids Research. 34(Web Server). W510–W515. 26 indexed citations
16.
Böttger, Lars H., Gunhild Layer, Peter Heathcote, et al.. (2006). Bacillus subtilis Fnr senses oxygen via a [4Fe‐4S] cluster coordinated by three cysteine residues without change in the oligomeric state. Molecular Microbiology. 60(6). 1432–1445. 47 indexed citations
17.
Härtig, Elisabeth, et al.. (2006). The Bacillus subtilis nrdEF Genes, Encoding a Class Ib Ribonucleotide Reductase, Are Essential for Aerobic and Anaerobic Growth. Applied and Environmental Microbiology. 72(8). 5260–5265. 30 indexed citations
18.
Vollack, Kai‐Uwe, Elisabeth Härtig, Heinz Körner, & Walter G. Zumft. (1999). Multiple transcription factors of the FNR family in denitrifying Pseudomonas stutzeri : characterization of four fnr‐like genes, regulatory responses and cognate metabolic processes. Molecular Microbiology. 31(6). 1681–1694. 75 indexed citations
19.
20.
Härtig, Elisabeth & Andrew C.B. Cato. (1994). In vivo binding of proteins to stably integrated MMTV DNA in murine cell lines: occupancy of NFI and OTF1 binding sites in the absence and presence of glucocorticoids.. PubMed. 40(7-8). 643–52. 1 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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