Philipp Korber

3.8k total citations
49 papers, 2.6k citations indexed

About

Philipp Korber is a scholar working on Molecular Biology, Plant Science and Materials Chemistry. According to data from OpenAlex, Philipp Korber has authored 49 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Molecular Biology, 17 papers in Plant Science and 3 papers in Materials Chemistry. Recurrent topics in Philipp Korber's work include Genomics and Chromatin Dynamics (36 papers), RNA and protein synthesis mechanisms (14 papers) and Chromosomal and Genetic Variations (12 papers). Philipp Korber is often cited by papers focused on Genomics and Chromatin Dynamics (36 papers), RNA and protein synthesis mechanisms (14 papers) and Chromosomal and Genetic Variations (12 papers). Philipp Korber collaborates with scholars based in Germany, United States and Croatia. Philipp Korber's co-authors include Wolfram Hörz, James C.A. Bardwell, Nils Krietenstein, B. Franklin Pugh, Corinna Lieleg, Slobodan Barbarić, Thomas Zander, Dorothea Blaschke, Annelie Strålfors and Karl Ekwall and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Philipp Korber

49 papers receiving 2.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Philipp Korber Germany 30 2.4k 526 193 183 110 49 2.6k
Randall H. Morse United States 31 2.8k 1.2× 518 1.0× 247 1.3× 185 1.0× 56 0.5× 71 3.2k
Matthew L. Bochman United States 21 2.8k 1.1× 427 0.8× 272 1.4× 149 0.8× 91 0.8× 44 3.1k
Michael F. Dion United States 8 2.2k 0.9× 422 0.8× 298 1.5× 184 1.0× 77 0.7× 10 2.4k
Namrita Dhillon United States 20 1.3k 0.5× 276 0.5× 214 1.1× 222 1.2× 85 0.8× 29 1.5k
Andrew K. Vershon United States 27 2.2k 0.9× 314 0.6× 385 2.0× 208 1.1× 77 0.7× 48 2.4k
Raffael Schaffrath Germany 31 2.3k 0.9× 534 1.0× 151 0.8× 115 0.6× 39 0.4× 91 2.6k
Howard M. Fried United States 21 2.3k 0.9× 304 0.6× 248 1.3× 123 0.7× 52 0.5× 31 2.6k
Nigel Roberts United Kingdom 16 1.6k 0.6× 376 0.7× 284 1.5× 98 0.5× 62 0.6× 25 1.8k
Katrin Paeschke Germany 21 3.9k 1.6× 350 0.7× 138 0.7× 65 0.4× 58 0.5× 47 4.1k
Marc R. Gartenberg United States 27 2.3k 0.9× 418 0.8× 429 2.2× 105 0.6× 39 0.4× 45 2.4k

Countries citing papers authored by Philipp Korber

Since Specialization
Citations

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

Fields of papers citing papers by Philipp Korber

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Philipp Korber

This figure shows the co-authorship network connecting the top 25 collaborators of Philipp Korber. A scholar is included among the top collaborators of Philipp Korber 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 Philipp Korber. Philipp Korber 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.
Lieleg, Corinna, et al.. (2023). Nucleosome Remodeling at the Yeast PHO8 and PHO84 Promoters without the Putatively Essential SWI/SNF Remodeler. International Journal of Molecular Sciences. 24(5). 4949–4949. 2 indexed citations
2.
Eustermann, Sebastian, Avinash B. Patel, Karl‐Peter Hopfner, Yuan He, & Philipp Korber. (2023). Energy-driven genome regulation by ATP-dependent chromatin remodellers. Nature Reviews Molecular Cell Biology. 25(4). 309–332. 47 indexed citations
3.
Ragoczy, Tobias, David Hörl, Eric Haugen, et al.. (2022). Differences in nanoscale organization of regulatory active and inactive human chromatin. Biophysical Journal. 121(6). 977–990. 8 indexed citations
4.
Schmid, Andrea, et al.. (2021). Effective dynamics of nucleosome configurations at the yeast PHO5 promoter. eLife. 10. 5 indexed citations
5.
Mrozek-Górska, Paulina, Alexander Buschle, Takanobu Tagawa, et al.. (2019). BZLF1 interacts with chromatin remodelers promoting escape from latent infections with EBV. Life Science Alliance. 2(2). e201800108–e201800108. 35 indexed citations
6.
Oberbeckmann, Elisa, Nils Krietenstein, B. Mark Heron, et al.. (2019). Absolute nucleosome occupancy map for the Saccharomyces cerevisiae genome. Genome Research. 29(12). 1996–2009. 59 indexed citations
7.
Richardson, Mary O.G., et al.. (2018). Large-Scale Analysis of the Evolution of Functions Mediated by Intrinsically Disordered Regions. Biophysical Journal. 114(3). 79a–79a. 1 indexed citations
8.
Eustermann, Sebastian, Elisa Oberbeckmann, Gabriele Stoehr, et al.. (2018). The nuclear actin-containing Arp8 module is a linker DNA sensor driving INO80 chromatin remodeling. Nature Structural & Molecular Biology. 25(9). 823–832. 56 indexed citations
9.
Atkinson, Sophie, Samuel Marguerat, Danny A. Bitton, et al.. (2018). Long noncoding RNA repertoire and targeting by nuclear exosome, cytoplasmic exonuclease, and RNAi in fission yeast. RNA. 24(9). 1195–1213. 44 indexed citations
10.
Ansari, Suraiya Anjum, Sebastian-Patrick Sommer, Corinna Lieleg, et al.. (2014). Mediator, TATA-binding Protein, and RNA Polymerase II Contribute to Low Histone Occupancy at Active Gene Promoters in Yeast. Journal of Biological Chemistry. 289(21). 14981–14995. 24 indexed citations
11.
Nuebler, Johannes, et al.. (2014). Replication-guided nucleosome packing and nucleosome breathing expedite the formation of dense arrays. Nucleic Acids Research. 42(22). 13633–13645. 10 indexed citations
12.
Korber, Philipp & Slobodan Barbarić. (2014). The yeast PHO5 promoter: from single locus to systems biology of a paradigm for gene regulation through chromatin. Nucleic Acids Research. 42(17). 10888–10902. 40 indexed citations
13.
Lieleg, Corinna, et al.. (2014). Nucleosome positioning in yeasts: methods, maps, and mechanisms. Chromosoma. 124(2). 131–151. 41 indexed citations
14.
Krietenstein, Nils, et al.. (2012). Genome-Wide In Vitro Reconstitution of Yeast Chromatin with In Vivo-Like Nucleosome Positioning. Methods in enzymology on CD-ROM/Methods in enzymology. 513. 205–232. 21 indexed citations
15.
Jiang, Lin‐Hua, Christiane Schaffitzel, Nenad Ban, et al.. (2008). Recycling of Aborted Ribosomal 50S Subunit-Nascent Chain-tRNA Complexes by the Heat Shock Protein Hsp15. Journal of Molecular Biology. 386(5). 1357–1367. 30 indexed citations
16.
Korber, Philipp, et al.. (2006). The Histone Chaperone Asf1 Increases the Rate of Histone Eviction at the Yeast PHO5 and PHO8 Promoters. Journal of Biological Chemistry. 281(9). 5539–5545. 88 indexed citations
17.
Korber, Philipp, et al.. (2004). Evidence for Histone Eviction in trans upon Induction of the Yeast PHO5 Promoter. Molecular and Cellular Biology. 24(24). 10965–10974. 80 indexed citations
18.
Korber, Philipp & Wolfram Hörz. (2004). SWRred Not Shaken. Cell. 117(1). 5–7. 52 indexed citations
19.
Staker, Bart L., Philipp Korber, James C.A. Bardwell, & Mark A. Saper. (2000). Structure of Hsp15 reveals a novel RNA-binding motif. The EMBO Journal. 19(4). 749–757. 46 indexed citations
20.
Grauschopf, Ulla, et al.. (1995). Why is DsbA such an oxidizing disulfide catalyst?. Cell. 83(6). 947–955. 259 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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