Stefanie Bug
Impact in
- Pathology and Forensic Medicine top 10%
- Lymphoma Diagnosis and Treatment
-
- Chronic Lymphocytic Leukemia Research
- Genomic variations and chromosomal abnormalities
Papers in
-
- Lymphoma Diagnosis and Treatment 6
- Genetics 5
- Genomic variations and chromosomal abnormalities 4
- Chronic Lymphocytic Leukemia Research 2
- Co-authors
- Reiner Siebert (8 shared papers)José Ignacio Martín-Subero (5 shared papers)Ulrich Dührsen (3 shared papers)Jan Dürig (3 shared papers)Lana Harder (3 shared papers)Ludger Klein‐Hitpaß (2 shared papers)Michael Baudis (2 shared papers)Thomas Jöns (1 shared paper)
- Journals
- Leukemia (3 papers)British Journal of Haematology (2 papers)Molecular Cytogenetics (1 paper)PLoS ONE (1 paper)Apmis (1 paper)
- Partner nations
- GermanySwitzerlandSweden
In The Last Decade
Stefanie Bug
12 papers receiving 422 citations
Peers
Comparison fields: 5 of 33
- Pathology and Forensic Medicine 128
- Genetics 53
- Cancer Research 45
- Immunology 58
- Neurology 37
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 | 2009 | 105 | |
| 2 | 2007 | 76 | |
| 3 | 2008 | 51 | |
| 4 | 2009 | 43 | |
| 5 | 2009 | 31 | |
| 6 | 2014 | 30 | |
| 7 | 2007 | 29 | |
| 8 | 2008 | 28 | |
| 9 | 2009 | 19 | |
| 10 | 2007 | 13 | |
| 11 | 2005 | 10 | |
| 12 | 2013 | 1 |
About Stefanie Bug
Stefanie Bug is a scholar working on Pathology and Forensic Medicine, Genetics, Genetics, Pediatrics, Perinatology and Child Health and Neurology, having authored 12 papers that have together received 436 indexed citations. Recurring topics across this work include Lymphoma Diagnosis and Treatment (6 papers), Genomic variations and chromosomal abnormalities (4 papers), Chronic Lymphocytic Leukemia Research (2 papers), Prenatal Screening and Diagnostics (1 paper), Telomeres, Telomerase, and Senescence (1 paper), Gene expression and cancer classification (1 paper), Epigenetics and DNA Methylation (1 paper) and Enzyme Structure and Function (1 paper). The work is most often cited by research in Pathology and Forensic Medicine (128 citations), Genetics (53 citations), Cancer Research (45 citations), Immunology (58 citations) and Neurology (37 citations). Stefanie Bug has collaborated with scholars based in Germany, Switzerland and Sweden. Frequent co-authors include Reiner Siebert, José Ignacio Martín-Subero, Ulrich Dührsen, Jan Dürig, Lana Harder, Ludger Klein‐Hitpaß, Michael Baudis, Thomas Jöns, Tanja Boes and Ralf Küppers. Their work appears in journals such as Leukemia, British Journal of Haematology, Molecular Cytogenetics, PLoS ONE 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.