Stefanie Bug
Impact in
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- Chronic Lymphocytic Leukemia Research
- Genomic variations and chromosomal abnormalities
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- Lymphoma Diagnosis and Treatment
Papers in ⓘ
- Genetics 4
- Chronic Lymphocytic Leukemia Research 3
- Genomic variations and chromosomal abnormalities 2
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- Lymphoma Diagnosis and Treatment 4
- Co-authors
- Reiner Siebert (7 shared papers)José I. Martı́n-Subero (4 shared papers)Jan Dürig (3 shared papers)Ulrich Dührsen (3 shared papers)Lana Harder (2 shared papers)Ludger Klein‐Hitpaß (2 shared papers)Michael Baudis (2 shared papers)Ralf Küppers (3 shared papers)
- Journals
- British Journal of Haematology (2 papers)Leukemia (2 papers)Journal of Biological Chemistry (1 paper)Molecular Cytogenetics (1 paper)Apmis (1 paper)
- Partner nations
- GermanySwitzerlandSweden
In The Last Decade
Stefanie Bug
10 papers receiving 241 citations
Peers
Comparison fields: 5 of 45
- Genetics 76
- Pathology and Forensic Medicine 105
- Immunology 46
- Cancer Research 30
- Neurology 29
Countries citing papers authored by Stefanie Bug
This map shows the geographic impact of Stefanie Bug'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 Stefanie Bug with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stefanie Bug more than expected).
Fields of papers citing papers by Stefanie Bug
This network shows the impact of papers produced by Stefanie Bug. 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 Stefanie Bug. The network helps show where Stefanie Bug may publish in the future.
Co-authors
The 25 scholars most cited alongside Stefanie Bug, 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 | 2007 | 64 | |
| 2 | 2008 | 41 | |
| 3 | 2014 | 29 | |
| 4 | 2007 | 25 | |
| 5 | 2008 | 25 | |
| 6 | 2009 | 24 | |
| 7 | 2009 | 14 | |
| 8 | 2007 | 13 | |
| 9 | 2005 | 11 | |
| 10 | 2013 | 1 |
About Stefanie Bug
Stefanie Bug is a scholar working on Genetics, Pathology and Forensic Medicine, Genetics, Pediatrics, Perinatology and Child Health and Immunology, having authored 10 papers that have together received 247 indexed citations. Recurring topics across this work include Lymphoma Diagnosis and Treatment (4 papers), Chronic Lymphocytic Leukemia Research (3 papers), Prenatal Screening and Diagnostics (2 papers), Genomics and Chromatin Dynamics (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Gestational Trophoblastic Disease Studies (1 paper), Cytomegalovirus and herpesvirus research (1 paper) and Cancer Genomics and Diagnostics (1 paper). The work is most often cited by research in Genetics (76 citations), Pathology and Forensic Medicine (105 citations), Immunology (46 citations), Cancer Research (30 citations) and Neurology (29 citations). Stefanie Bug has collaborated with scholars based in Germany, Switzerland and Sweden. Frequent co-authors include Reiner Siebert, José I. Martı́n-Subero, Jan Dürig, Ulrich Dührsen, Lana Harder, Ludger Klein‐Hitpaß, Michael Baudis, Ralf Küppers, Thomas Jöns and Tanja Boes. Their work appears in journals such as British Journal of Haematology, Leukemia, Journal of Biological Chemistry, Molecular Cytogenetics and Apmis.
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.