Ralph Bertram

2.3k total citations
56 papers, 1.8k citations indexed

About

Ralph Bertram is a scholar working on Molecular Biology, Genetics and Infectious Diseases. According to data from OpenAlex, Ralph Bertram has authored 56 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Molecular Biology, 32 papers in Genetics and 24 papers in Infectious Diseases. Recurrent topics in Ralph Bertram's work include Bacterial Genetics and Biotechnology (32 papers), Antimicrobial Resistance in Staphylococcus (18 papers) and Bacteriophages and microbial interactions (16 papers). Ralph Bertram is often cited by papers focused on Bacterial Genetics and Biotechnology (32 papers), Antimicrobial Resistance in Staphylococcus (18 papers) and Bacteriophages and microbial interactions (16 papers). Ralph Bertram collaborates with scholars based in Germany, United States and Austria. Ralph Bertram's co-authors include Christopher F. Schuster, Wolfgang Hillen, Marcel Prax, Friedrich Götz, Kim Lewis, Raja Biswas, Martin Schlag, Lalitha Biswas, Fritz Titgemeyer and Alexander Herbig and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and SHILAP Revista de lepidopterología.

In The Last Decade

Ralph Bertram

52 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ralph Bertram Germany 25 1.2k 697 575 345 289 56 1.8k
Edward Geisinger United States 16 1.3k 1.1× 467 0.7× 781 1.4× 301 0.9× 573 2.0× 23 2.0k
Christelle M. Roux United States 23 881 0.8× 301 0.4× 514 0.9× 250 0.7× 140 0.5× 28 1.7k
Hirofumi Nariya Japan 21 777 0.7× 488 0.7× 395 0.7× 413 1.2× 289 1.0× 55 1.4k
Orietta Massidda Italy 23 844 0.7× 531 0.8× 366 0.6× 207 0.6× 399 1.4× 54 1.7k
Yinduo Ji United States 23 1.3k 1.1× 425 0.6× 1.0k 1.8× 278 0.8× 187 0.6× 72 2.2k
Craig D. Ellermeier United States 23 917 0.8× 832 1.2× 516 0.9× 545 1.6× 220 0.8× 43 2.1k
Tobias Geiger Germany 18 1.1k 0.9× 528 0.8× 914 1.6× 148 0.4× 163 0.6× 32 1.5k
Peter J. McNamara United States 17 1.4k 1.2× 437 0.6× 1.3k 2.3× 189 0.5× 230 0.8× 20 2.3k
Bridget Gollan United Kingdom 11 800 0.7× 468 0.7× 290 0.5× 278 0.8× 413 1.4× 13 1.7k
Pavel Branny Czechia 22 869 0.7× 458 0.7× 227 0.4× 193 0.6× 153 0.5× 45 1.5k

Countries citing papers authored by Ralph Bertram

Since Specialization
Citations

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

Fields of papers citing papers by Ralph Bertram

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ralph Bertram

This figure shows the co-authorship network connecting the top 25 collaborators of Ralph Bertram. A scholar is included among the top collaborators of Ralph Bertram 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 Ralph Bertram. Ralph Bertram 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
3.
Bertram, Ralph, Walter Geißdörfer, Matthias Pauschinger, et al.. (2023). Microbiologic diagnostics and pathogen spectrum in infective endocarditis of surgically treated patients: a five-year, retrospective, monocentric study. Infection. 51(5). 1523–1530. 2 indexed citations
5.
Kirchhoff, Lisa, Diana Arweiler‐Harbeck, Judith Arnolds, et al.. (2020). Imaging studies of bacterial biofilms on cochlear implants—Bioactive glass (BAG) inhibits mature biofilm. PLoS ONE. 15(2). e0229198–e0229198. 21 indexed citations
6.
Tuchscherr, Lorena, Ralph Bertram, Janina Eisenbeis, et al.. (2019). ClpC affects the intracellular survival capacity of Staphylococcus aureus in non-professional phagocytic cells. Scientific Reports. 9(1). 16267–16267. 12 indexed citations
7.
Xu, Tao, Yang Wu, Zhiwei Lin, et al.. (2017). Identification of Genes Controlled by the Essential YycFG Two-Component System Reveals a Role for Biofilm Modulation in Staphylococcus epidermidis. Frontiers in Microbiology. 8. 724–724. 28 indexed citations
8.
Marx, Patrick, et al.. (2017). A tetracycline-inducible integrative expression system for Streptococcus pneumoniae. FEMS Microbiology Letters. 364(5). 6 indexed citations
9.
Prax, Marcel, et al.. (2016). Glucose Augments Killing Efficiency of Daptomycin Challenged Staphylococcus aureus Persisters. PLoS ONE. 11(3). e0150907–e0150907. 40 indexed citations
10.
Schuster, Christopher F., et al.. (2015). The MazEF Toxin-Antitoxin System Alters the β-Lactam Susceptibility of Staphylococcus aureus. PLoS ONE. 10(5). e0126118–e0126118. 40 indexed citations
11.
Bertram, Ralph. (2014). Complementation Plasmids, Inducible Gene-Expression Systems, and Reporters for Staphylococci. Methods in molecular biology. 1373. 25–32. 3 indexed citations
12.
Schuster, Christopher F. & Ralph Bertram. (2014). Fluorescence Based Primer Extension Technique to Determine Transcriptional Starting Points and Cleavage Sites of RNases <em>In Vivo</em>. Journal of Visualized Experiments. e52134–e52134. 11 indexed citations
13.
Willenborg, Jörg, et al.. (2014). Characterization of multi-drug tolerant persister cells in Streptococcus suis. BMC Microbiology. 14(1). 120–120. 37 indexed citations
14.
Lewis, Kim, et al.. (2012). Staphylococcus aureus Persisters Tolerant to Bactericidal Antibiotics. Microbial Physiology. 22(4). 235–244. 127 indexed citations
15.
Klumpp, Stefan, et al.. (2012). Interplay between Population Dynamics and Drug Tolerance of <b><i>Staphylococcus aureus</i></b> Persister Cells. Microbial Physiology. 22(6). 381–391. 16 indexed citations
16.
Mayer, Sonja, et al.. (2011). Intracellular monitoring of target protein production in Staphylococcus aureus by peptide tag‐induced reporter fluorescence. Microbial Biotechnology. 5(1). 129–134. 13 indexed citations
17.
Bertram, Ralph, Martina Kolb, & Wolfgang Hillen. (2009). In vivo Activation of Tetracycline Rep ressor by Cre/<i>lox</i>-Mediated Gene Assembly. Microbial Physiology. 17(3). 136–145. 4 indexed citations
18.
Roth, Heide M., et al.. (2009). Cloning, expression, purification, crystallization and preliminary X-ray diffraction analysis of YvoA fromBacillus subtilis. Acta Crystallographica Section F Structural Biology and Crystallization Communications. 65(4). 410–414. 5 indexed citations
19.
Bertram, Ralph, et al.. (2006). Regulated expression of HPrK/P does not affect carbon catabolite repression of thexynoperon and ofrocGinBacillus subtilis. FEMS Microbiology Letters. 259(1). 147–152. 3 indexed citations
20.
Scholz, Oliver, et al.. (2004). Activity reversal of Tet repressor caused by single amino acid exchanges. Molecular Microbiology. 53(3). 777–789. 65 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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