Bernhard Korn

7.9k total citations
54 papers, 3.6k citations indexed

About

Bernhard Korn is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Bernhard Korn has authored 54 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Molecular Biology, 15 papers in Genetics and 5 papers in Cell Biology. Recurrent topics in Bernhard Korn's work include Genomics and Chromatin Dynamics (7 papers), Epigenetics and DNA Methylation (7 papers) and RNA Research and Splicing (7 papers). Bernhard Korn is often cited by papers focused on Genomics and Chromatin Dynamics (7 papers), Epigenetics and DNA Methylation (7 papers) and RNA Research and Splicing (7 papers). Bernhard Korn collaborates with scholars based in Germany, United Kingdom and United States. Bernhard Korn's co-authors include Annemarie Poustka, Hermann Brenner, Rongxi Yang, Lutz Philipp Breitling, Barbara Burwinkel, Stefan Wiemann, Andreas von Deimling, Jan Mollenhauer, Klaus K. Wilgenbus and Wolfgang Wagner and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and Nature Genetics.

In The Last Decade

Bernhard Korn

54 papers receiving 3.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Bernhard Korn Germany 30 2.5k 1.0k 354 297 297 54 3.6k
Michael Bonin Germany 34 2.3k 0.9× 869 0.9× 488 1.4× 247 0.8× 377 1.3× 110 4.2k
Luisa Bonafé Switzerland 36 1.8k 0.7× 1.4k 1.4× 312 0.9× 204 0.7× 203 0.7× 97 3.5k
Koh-ichiro Yoshiura Japan 31 1.8k 0.7× 1.2k 1.2× 469 1.3× 192 0.6× 306 1.0× 159 3.4k
Dean Nižetić United Kingdom 35 1.8k 0.7× 977 1.0× 227 0.6× 168 0.6× 334 1.1× 92 3.5k
Eric Rappaport United States 37 2.6k 1.0× 673 0.7× 343 1.0× 424 1.4× 269 0.9× 108 4.3k
Hülya Kayserili Türkiye 35 2.8k 1.1× 1.7k 1.7× 229 0.6× 285 1.0× 177 0.6× 152 4.4k
Jorge Laborda Spain 39 2.9k 1.1× 925 0.9× 509 1.4× 251 0.8× 542 1.8× 86 4.4k
Michele D’Urso Italy 35 2.8k 1.1× 1.4k 1.4× 221 0.6× 145 0.5× 186 0.6× 100 4.2k
Laura P. O’Neill United Kingdom 33 3.4k 1.3× 1.1k 1.1× 408 1.2× 148 0.5× 284 1.0× 53 4.2k
Robert M. Greene United States 33 1.9k 0.7× 1.1k 1.1× 363 1.0× 160 0.5× 138 0.5× 155 3.4k

Countries citing papers authored by Bernhard Korn

Since Specialization
Citations

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

Fields of papers citing papers by Bernhard Korn

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bernhard Korn

This figure shows the co-authorship network connecting the top 25 collaborators of Bernhard Korn. A scholar is included among the top collaborators of Bernhard Korn 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 Bernhard Korn. Bernhard Korn 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.
Ammerpohl, Ole, Susanne Bens, Mahesh Appari, et al.. (2013). Androgen Receptor Function Links Human Sexual Dimorphism to DNA Methylation. PLoS ONE. 8(9). e73288–e73288. 25 indexed citations
2.
Spaich, Sebastian, Rainer Will, Steffen Just, et al.. (2012). F-Box and Leucine-Rich Repeat Protein 22 Is a Cardiac-Enriched F-Box Protein That Regulates Sarcomeric Protein Turnover and Is Essential for Maintenance of Contractile Function In Vivo. Circulation Research. 111(12). 1504–1516. 47 indexed citations
3.
Meder, Benjamin, Jan Haas, Andreas Keller, et al.. (2011). Targeted Next-Generation Sequencing for the Molecular Genetic Diagnostics of Cardiomyopathies. Circulation Cardiovascular Genetics. 4(2). 110–122. 117 indexed citations
4.
Breitling, Lutz Philipp, Rongxi Yang, Bernhard Korn, Barbara Burwinkel, & Hermann Brenner. (2011). Tobacco-Smoking-Related Differential DNA Methylation: 27K Discovery and Replication. The American Journal of Human Genetics. 88(4). 450–457. 487 indexed citations
5.
Siegelin, Markus D., et al.. (2009). Epigenetic Silencing of Death Receptor 4 Mediates Tumor Necrosis Factor–Related Apoptosis-Inducing Ligand Resistance in Gliomas. Clinical Cancer Research. 15(17). 5457–5465. 41 indexed citations
6.
Rolfs, Andreas, Yanhui Hu, Lars Ebert, et al.. (2008). A Biomedically Enriched Collection of 7000 Human ORF Clones. PLoS ONE. 3(1). e1528–e1528. 20 indexed citations
7.
Koehnke, Jesko, et al.. (2007). Ubc9 fusion–directed SUMOylation (UFDS): a method to analyze function of protein SUMOylation. Nature Methods. 4(3). 245–250. 86 indexed citations
8.
Zink, Dorothea, Jürgen Schmitz, Timofey S. Rozhdestvensky, et al.. (2006). An anthropoid-specific segmental duplication on human chromosome 1q22. Genomics. 88(2). 143–151. 21 indexed citations
9.
Mendrzyk, Frank, Andrey Korshunov, Grischa Toedt, et al.. (2006). Isochromosome breakpoints on 17p in medulloblastoma are flanked by different classes of DNA sequence repeats. Genes Chromosomes and Cancer. 45(4). 401–410. 31 indexed citations
10.
Murphy, Derek, Angelika Lueking, Andrea Koenig, et al.. (2005). Mouse protein arrays from a TH1 cell cDNA library for antibody screening and serum profiling. Genomics. 85(3). 285–296. 17 indexed citations
11.
Yuille, Martin, Bernhard Korn, Troy Moore, et al.. (2004). The Responsibility to Share: Sharing the Responsibility. Genome Research. 14(10b). 2015–2019. 2 indexed citations
12.
Brockmann, Christoph, Anne Diehl, Kristina Rehbein, et al.. (2004). The Oxidized Subunit B8 from Human Complex I Adopts a Thioredoxin Fold. Structure. 12(9). 1645–1654. 25 indexed citations
13.
Gupta, Shobhit, Dorothea Zink, Bernhard Korn, Martin Vingron, & Stefan A. Haas. (2004). Strengths and weaknesses of EST-based prediction of tissue-specific alternative splicing. BMC Genomics. 5(1). 72–72. 37 indexed citations
14.
Boer, Judith M., Wolfgang Huber, Holger Sültmann, et al.. (2001). Identification and Classification of Differentially Expressed Genes in Renal Cell Carcinoma by Expression Profiling on a Global Human 31,500-Element cDNA Array. Genome Research. 11(11). 1861–1870. 157 indexed citations
15.
Heiss, Nina S., Ute C. Rogner, Petra Kioschis, Bernhard Korn, & Annemarie Poustka. (1996). Transcription mapping in a 700-kb region around the DXS52 locus in Xq28: isolation of six novel transcripts and a novel ATPase isoform (hPMCA5).. Genome Research. 6(6). 478–491. 19 indexed citations
16.
Kioschis, Petra, Ute C. Rogner, Sabine M. Klauck, et al.. (1996). A 900-kb Cosmid Contig and 10 New Transcripts within the Candidate Region for Myotubular Myopathy (MTM1). Genomics. 33(3). 365–373. 22 indexed citations
17.
Yaspo, Marie‐Laure, Richard Mott, Bernhard Korn, et al.. (1995). Model for a transcript map of human chromosome 21: isolation of new coding sequences from exon and enriched cDNA libraries. Human Molecular Genetics. 4(8). 1291–1304. 56 indexed citations
18.
Wilgenbus, Klaus K., Antoaneta Mincheva, Bernhard Korn, Peter Lichter, & Annemarie Poustka. (1994). IRS-long range (LR) PCR: A simple method for efficient amplification of human genomic DNA from complex sources. 5(4). 214–221. 14 indexed citations
19.
Gedeon, Ági K., Emma K. Baker, Harriet L. Robinson, et al.. (1992). Fragile X syndrome without CCG amplification has an FMR1 deletion. Nature Genetics. 1(5). 341–344. 167 indexed citations
20.
Dietrich, Alexander, Bernhard Korn, & Poustka Annemarie. (1992). Completion of the physical map of Xq28: the location of the gene for L1CAM on the human X Chromosome. Mammalian Genome. 3(3). 168–172. 11 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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