Stefanie Bug

552 total citations
10 papers, 247 citations indexed

About

Stefanie Bug is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Stefanie Bug has authored 10 papers receiving a total of 247 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 4 papers in Genetics and 4 papers in Pathology and Forensic Medicine. Recurrent topics in Stefanie Bug's work include Lymphoma Diagnosis and Treatment (4 papers), Chronic Lymphocytic Leukemia Research (3 papers) and Prenatal Screening and Diagnostics (2 papers). Stefanie Bug is often cited by papers focused on Lymphoma Diagnosis and Treatment (4 papers), Chronic Lymphocytic Leukemia Research (3 papers) and Prenatal Screening and Diagnostics (2 papers). Stefanie Bug collaborates with scholars based in Germany, Switzerland and Sweden. Stefanie Bug's co-authors include Reiner Siebert, José I. Martı́n-Subero, Ulrich Dührsen, Jan Dürig, Ludger Klein‐Hitpaß, Michael Baudis, Lana Harder, Ralf Küppers, Thomas Jöns and Tanja Boes and has published in prestigious journals such as Journal of Biological Chemistry, British Journal of Haematology and Journal of Neuropathology & Experimental Neurology.

In The Last Decade

Stefanie Bug

10 papers receiving 241 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Stefanie Bug Germany 9 105 92 76 46 46 10 247
Dominique Penther France 7 73 0.7× 52 0.6× 46 0.6× 67 1.5× 33 0.7× 13 219
D Falzetti Italy 10 75 0.7× 113 1.2× 87 1.1× 46 1.0× 29 0.6× 21 297
Teresa Vela Mexico 5 89 0.8× 122 1.3× 52 0.7× 119 2.6× 19 0.4× 6 276
Bettina R. Bonn Germany 7 145 1.4× 73 0.8× 46 0.6× 95 2.1× 30 0.7× 9 224
Laurence Baranger France 12 63 0.6× 110 1.2× 104 1.4× 35 0.8× 43 0.9× 19 362
Eva Lumbreras Spain 10 42 0.4× 146 1.6× 62 0.8× 59 1.3× 26 0.6× 23 306
Marianne Brodtkorb Eide Norway 5 109 1.0× 89 1.0× 41 0.5× 98 2.1× 18 0.4× 5 247
Triantafyllia Brozou Germany 9 52 0.5× 69 0.8× 17 0.2× 31 0.7× 15 0.3× 24 237
P. Yussanne United Kingdom 6 158 1.5× 119 1.3× 25 0.3× 101 2.2× 22 0.5× 7 307

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-authorship network of co-authors of Stefanie Bug

This figure shows the co-authorship network connecting the top 25 collaborators of Stefanie Bug. A scholar is included among the top collaborators of Stefanie Bug based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Stefanie Bug. Stefanie Bug is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

10 of 10 papers shown
1.
2.
Bug, Stefanie, et al.. (2013). The Correct Genetic Diagnosis Has Already Been Determined More Often Than We Think, Let’s Report It to the Parents!. Clinical Pediatrics. 53(1). 8–10. 1 indexed citations
3.
Bug, Stefanie, Jan Dürig, Florian Oyen, et al.. (2009). Recurrent loss, but lack of mutations, of the SMARCB1 tumor suppressor gene in T-cell prolymphocytic leukemia with TCL1A–TCRAD juxtaposition. Cancer Genetics and Cytogenetics. 192(1). 44–47. 14 indexed citations
4.
Hartmann, Sylvia, Stefan Gesk, René Scholtysik, et al.. (2009). High resolution SNP array genomic profiling of peripheral T cell lymphomas, not otherwise specified, identifies a subgroup with chromosomal aberrations affecting the REL locus. British Journal of Haematology. 148(3). 402–412. 24 indexed citations
5.
Courts, Cornelius, Manuel Montesinos‐Rongen, Anna Brunn, et al.. (2008). Recurrent Inactivation of the PRDM1 Gene in Primary Central Nervous System Lymphoma. Journal of Neuropathology & Experimental Neurology. 67(7). 720–727. 41 indexed citations
6.
Giefing, Maciej, Joachim Arnemann, José I. Martı́n-Subero, et al.. (2008). Identification of candidate tumour suppressor gene loci for Hodgkin and Reed‐Sternberg cells by characterisation of homozygous deletions in classical Hodgkin lymphoma cell lines. British Journal of Haematology. 142(6). 916–924. 25 indexed citations
7.
Röth, Alexander, Jan Dürig, Stefanie Bug, et al.. (2007). Short telomeres and high telomerase activity in T-cell prolymphocytic leukemia. Leukemia. 21(12). 2456–2462. 25 indexed citations
8.
9.
Bug, Stefanie, et al.. (2007). Combining array‐based approaches for the identification of candidate tumor suppressor loci in mature lymphoid neoplasms. Apmis. 115(10). 1107–1134. 13 indexed citations
10.
Bug, Stefanie, et al.. (2005). Nucleotide-dependent Formation of Catalytically Competent Dimers from Engineered Monomeric Ribonucleotide Reductase Protein R1. Journal of Biological Chemistry. 280(15). 14997–15003. 11 indexed citations

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.

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