Peter Seranski
Impact in
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- Genomic variations and chromosomal abnormalities
- Glioma Diagnosis and Treatment
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- Genomics and Chromatin Dynamics
- Hedgehog Signaling Pathway Studies
- RNA Research and Splicing
- Chromatin Remodeling and Cancer
Papers in
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- RNA Research and Splicing 3
- Genomics and Chromatin Dynamics 2
- Ion channel regulation and function 1
- Genetics 3
- Genomic variations and chromosomal abnormalities 3
- Co-authors
- Annemarie Poustka (7 shared papers)Klaus K. Wilgenbus (3 shared papers)Richard Reinhardt (3 shared papers)Steffen Hennig (3 shared papers)Uwe Radelof (3 shared papers)Wolfram Scheurlen (2 shared papers)Nina S. Heiss (2 shared papers)Céline Hoff (2 shared papers)
- Journals
- Genomics (3 papers)Genes Chromosomes and Cancer (2 papers)Gene (1 paper)Nucleic Acids Research (1 paper)Naunyn-Schmiedeberg s Archives of Pharmacology (1 paper)
- Partner nations
- GermanyUnited StatesUnited Kingdom
In The Last Decade
Peter Seranski
8 papers receiving 204 citations
Peers
Comparison fields: 5 of 45
- Genetics 50
- Genetics 85
- Molecular Biology 149
- Cancer Research 23
- Aging 2
Countries citing papers authored by Peter Seranski
This map shows the geographic impact of Peter Seranski'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 Peter Seranski with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Peter Seranski more than expected).
Fields of papers citing papers by Peter Seranski
This network shows the impact of papers produced by Peter Seranski. 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 Peter Seranski. The network helps show where Peter Seranski may publish in the future.
Co-authors
The 25 scholars most cited alongside Peter Seranski, 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 | 1997 | 47 | |
| 2 | 1999 | 35 | |
| 3 | 2001 | 29 | |
| 4 | 1998 | 29 | |
| 5 | 1997 | 25 | |
| 6 | 1999 | 24 | |
| 7 | 2000 | 15 | |
| 8 | 2002 | 4 |
About Peter Seranski
Peter Seranski is a scholar working on Molecular Biology, Genetics, Genetics, Pathology and Forensic Medicine and Pulmonary and Respiratory Medicine, having authored 8 papers that have together received 208 indexed citations. Recurring topics across this work include RNA Research and Splicing (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Genomics and Chromatin Dynamics (2 papers), Sarcoma Diagnosis and Treatment (2 papers), Cardiac electrophysiology and arrhythmias (1 paper), Ion channel regulation and function (1 paper), Cancer Genomics and Diagnostics (1 paper) and Lymphoma Diagnosis and Treatment (1 paper). The work is most often cited by research in Genetics (50 citations), Genetics (85 citations), Molecular Biology (149 citations), Cancer Research (23 citations) and Aging (2 citations). Peter Seranski has collaborated with scholars based in Germany, United States and United Kingdom. Frequent co-authors include Annemarie Poustka, Klaus K. Wilgenbus, Richard Reinhardt, Steffen Hennig, Uwe Radelof, Wolfram Scheurlen, Nina S. Heiss, Céline Hoff, Joachim Kühl and Jürgen Krauß. Their work appears in journals such as Genomics, Genes Chromosomes and Cancer, Gene, Nucleic Acids Research and Naunyn-Schmiedeberg s Archives of Pharmacology.
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.