Stefanie Bug

555 citations
10 papers · 265 · h-index 9

Impact in

Papers in

    • Genomics and Chromatin Dynamics 2
    • RNA and protein synthesis mechanisms 1
    • Glycosylation and Glycoproteins Research 1
    • Chronic Lymphocytic Leukemia Research 3
    • Genomic variations and chromosomal abnormalities 2
    • Genomics and Rare Diseases 1

Stefanie Bug

10 papers receiving 254 citations

Peers

Stefanie Bug
Comparison fields: 5 of 43
  • Genetics 76
  • Pathology and Forensic Medicine 108
  • Neurology 32
  • Immunology 46
  • Oncology 47
Replace Bettina R. Bonn with:
Bettina R. Bonn Germany
Teresa Vela Mexico
Marianne Brodtkorb Eide Norway
Jasmin Lisfeld Germany
D Falzetti Italy
Dominique Penther France
Triantafyllia Brozou Germany
F Davi France
Eva Lumbreras Spain
Stefanie Bug relative to Bettina R. Bonn Germany Bettina R. Bonn's profile →
Citations per field
00.5×1.7×
Bettina R. Bonn · 1×
Citations per year

Countries citing papers authored by Stefanie Bug

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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.

Border = papers with Stefanie Bug Line = papers co-authored together Stefanie Bug links everyone, so they are left out of the graph.

All Works

10 of 10 papers shown
#Work
1 200768
2 200846
3 201429
4 200928
5 200827
6 200727
7 200915
8 200713
9 200511
10 20131

About Stefanie Bug

Stefanie Bug is a scholar working on Molecular Biology, Genetics, Pathology and Forensic Medicine, Genetics and Immunology, having authored 10 papers that have together received 265 indexed citations. Recurring topics across this work include Lymphoma Diagnosis and Treatment (4 papers), Chronic Lymphocytic Leukemia Research (3 papers), Genomics and Chromatin Dynamics (2 papers), Genomic variations and chromosomal abnormalities (2 papers), RNA and protein synthesis mechanisms (1 paper), Genomics and Rare Diseases (1 paper), Glycosylation and Glycoproteins 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 (108 citations), Neurology (32 citations), Immunology (46 citations) and Oncology (47 citations). Stefanie Bug has collaborated with scholars based in Germany, Switzerland and Poland. Frequent co-authors include Reiner Siebert, José I. Martín‐Subero, Ulrich Dührsen, Jan Dürig, Michael Baudis, Lana Harder, Ludger Klein‐Hitpaß, Tanja Boes, Ralf Küppers and Thomas Jöns. Their work appears in journals such as British Journal of Haematology, Leukemia, Apmis, Journal of Neuropathology & Experimental Neurology and Journal of Biological Chemistry.

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.

Explore authors with similar magnitude of impact