Bernhard Köster
Impact in
- Nephrology top 5%
- Parathyroid Disorders and Treatments
- Rheumatology top 5%
- Heterotopic Ossification and Related Conditions
- Bone Tumor Diagnosis and Treatments
Papers in
- Genetics 2
- Genomics and Rare Diseases 1
- Genetic Syndromes and Imprinting 1
- Genetics and Neurodevelopmental Disorders 1
- Genomic variations and chromosomal abnormalities 1
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- Infectious Encephalopathies and Encephalitis 1
- Co-authors
- Gabriele Gillessen‐Kaesbach (2 shared papers)J. M. Connor (1 shared paper)Stefan Mundlos (1 shared paper)Rolf Morhart (1 shared paper)Michael Zasloff (1 shared paper)Eileen M. Shore (1 shared paper)Stephen J. Forman (1 shared paper)Frederick S. Kaplan (1 shared paper)
- Journals
- Human Mutation (1 paper)Der Radiologe (1 paper)American Journal of Medical Genetics (1 paper)
- Partner nations
- GermanyIrelandUnited Kingdom
In The Last Decade
Bernhard Köster
3 papers receiving 328 citations
Peers
Comparison fields: 5 of 36
- Nephrology 137
- Rheumatology 279
- Pulmonary and Respiratory Medicine 214
- Genetics 94
- Genetics 21
Countries citing papers authored by Bernhard Köster
This map shows the geographic impact of Bernhard Köster'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 Köster with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Bernhard Köster more than expected).
Fields of papers citing papers by Bernhard Köster
This network shows the impact of papers produced by Bernhard Köster. 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 Köster. The network helps show where Bernhard Köster may publish in the future.
Co-authors
The 24 scholars most cited alongside Bernhard Köster, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2008 | 322 | |
| 2 | 2002 | 10 | |
| 3 | 2011 | 6 |
About Bernhard Köster
Bernhard Köster is a scholar working on Genetics, Infectious Diseases, Surgery, Pulmonary and Respiratory Medicine and Rheumatology, having authored 3 papers that have together received 338 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (1 paper), Medical Imaging and Pathology Studies (1 paper), Bacterial Infections and Vaccines (1 paper), Infectious Encephalopathies and Encephalitis (1 paper), Heterotopic Ossification and Related Conditions (1 paper), Genetic Syndromes and Imprinting (1 paper), Genetics and Neurodevelopmental Disorders (1 paper) and Genomic variations and chromosomal abnormalities (1 paper). The work is most often cited by research in Nephrology (137 citations), Rheumatology (279 citations), Pulmonary and Respiratory Medicine (214 citations), Genetics (94 citations) and Genetics (21 citations). Bernhard Köster has collaborated with scholars based in Germany, Ireland and United Kingdom. Frequent co-authors include Gabriele Gillessen‐Kaesbach, J. M. Connor, Stefan Mundlos, Rolf Morhart, Michael Zasloff, Eileen M. Shore, Stephen J. Forman, Frederick S. Kaplan, Liam Carroll and Patricia Delai. Their work appears in journals such as Human Mutation, Der Radiologe and American Journal of Medical Genetics.
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.