Bernhard Korn
Impact in
- Molecular Biology top 2%
- Epigenetics and DNA Methylation
- RNA modifications and cancer
- Ubiquitin and proteasome pathways
- RNA Research and Splicing
- Cancer-related gene regulation
- Genetics top 2%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
Papers in
-
- RNA Research and Splicing 7
- Genomics and Chromatin Dynamics 7
- Epigenetics and DNA Methylation 7
- Molecular Biology Techniques and Applications 6
- RNA and protein synthesis mechanisms 6
- RNA modifications and cancer 5
- Genetics 15
- Genomic variations and chromosomal abnormalities 5
- Animal Genetics and Reproduction 5
- Co-authors
- Annemarie Poustka (19 shared papers)Barbara Burwinkel (1 shared paper)Hermann Brenner (1 shared paper)Lutz Philipp Breitling (1 shared paper)Rongxi Yang (1 shared paper)Stefan Wiemann (6 shared papers)Andreas von Deimling (2 shared papers)Jan Mollenhauer (3 shared papers)
- Journals
- Genomics (8 papers)Human Molecular Genetics (5 papers)Genome Research (4 papers)Nature Genetics (3 papers)Circulation Research (2 papers)
- Partner nations
- GermanyUnited KingdomUnited States
In The Last Decade
Bernhard Korn
54 papers receiving 3.5k citations
Peers
Comparison fields: 5 of 125
- Molecular Biology 2.5k
- Genetics 1.0k
- Genetics 297
- Cancer Research 354
- Aging 38
Countries citing papers authored by Bernhard Korn
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
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-authors
The 25 scholars most cited alongside Bernhard Korn, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 54 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2011 | 487 | |
| 2 | 1997 | 376 | |
| 3 | 2009 | 333 | |
| 4 | 2010 | 189 | |
| 5 | 1992 | 167 | |
| 6 | 2001 | 157 | |
| 7 | A microdeletion of less than 250 kb, including the proximal part of the FMR-I gene and the fragile-X site, in a male with the clinical phenotype of fragile-X syndrome. | 1992 | 140 |
| 8 | 2011 | 117 | |
| 9 | 1994 | 110 | |
| 10 | 1995 | 105 | |
| 11 | 1992 | 99 | |
| 12 | 2007 | 86 | |
| 13 | 2001 | 86 | |
| 14 | 2004 | 70 | |
| 15 | 2008 | 68 | |
| 16 | Candidate genes for cross-resistance against DNA-damaging drugs. | 2002 | 57 |
| 17 | 1995 | 56 | |
| 18 | 2012 | 47 | |
| 19 | 1997 | 46 | |
| 20 | 1993 | 45 |
About Bernhard Korn
Bernhard Korn is a scholar working on Molecular Biology, Genetics, Cell Biology, Cardiology and Cardiovascular Medicine and Oncology, having authored 54 papers that have together received 3.6k indexed citations. Recurring topics across this work include RNA Research and Splicing (7 papers), Genomics and Chromatin Dynamics (7 papers), Epigenetics and DNA Methylation (7 papers), Molecular Biology Techniques and Applications (6 papers), RNA and protein synthesis mechanisms (6 papers), RNA modifications and cancer (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Animal Genetics and Reproduction (5 papers). The work is most often cited by research in Molecular Biology (2.5k citations), Genetics (1.0k citations), Genetics (297 citations), Cancer Research (354 citations) and Aging (38 citations). Bernhard Korn has collaborated with scholars based in Germany, United Kingdom and United States. Frequent co-authors include Annemarie Poustka, Barbara Burwinkel, Hermann Brenner, Lutz Philipp Breitling, Rongxi Yang, Stefan Wiemann, Andreas von Deimling, Jan Mollenhauer, Klaus K. Wilgenbus and Patrick Horn. Their work appears in journals such as Genomics, Human Molecular Genetics, Genome Research, Nature Genetics and Circulation Research.
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.