Carsten Schwäenen

4.1k total citations
25 papers, 1.4k citations indexed

About

Carsten Schwäenen is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Carsten Schwäenen has authored 25 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 12 papers in Genetics and 11 papers in Pathology and Forensic Medicine. Recurrent topics in Carsten Schwäenen's work include Genomic variations and chromosomal abnormalities (12 papers), Lymphoma Diagnosis and Treatment (10 papers) and Chronic Lymphocytic Leukemia Research (6 papers). Carsten Schwäenen is often cited by papers focused on Genomic variations and chromosomal abnormalities (12 papers), Lymphoma Diagnosis and Treatment (10 papers) and Chronic Lymphocytic Leukemia Research (6 papers). Carsten Schwäenen collaborates with scholars based in Germany, United States and United Kingdom. Carsten Schwäenen's co-authors include Peter Lichter, Swen Weßendorf, Bernhard Radlwimmer, Martin Bentz, Hartmut Döhner, Gunnar Wrobel, Michelle Neßling, Hans A. Kestler, Stefan Joos and Holger Kohlhammer and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Oncology and Blood.

In The Last Decade

Carsten Schwäenen

25 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Carsten Schwäenen Germany 19 663 420 377 362 347 25 1.4k
Swen Weßendorf Germany 19 521 0.8× 665 1.6× 624 1.7× 299 0.8× 325 0.9× 31 1.6k
Yan Aalto Finland 17 560 0.8× 242 0.6× 368 1.0× 256 0.7× 174 0.5× 25 1.2k
Sigitas Verselis United States 16 918 1.4× 402 1.0× 693 1.8× 308 0.9× 315 0.9× 31 1.7k
Dirk Kienle Germany 24 630 1.0× 807 1.9× 358 0.9× 273 0.8× 149 0.4× 37 1.7k
Samuli Hemmer Finland 10 694 1.0× 312 0.7× 410 1.1× 340 0.9× 473 1.4× 12 1.4k
EJ Dreef Netherlands 13 320 0.5× 261 0.6× 290 0.8× 147 0.4× 135 0.4× 19 992
Jonathan C. Strefford United Kingdom 30 960 1.4× 589 1.4× 344 0.9× 293 0.8× 357 1.0× 89 2.5k
José María Sayagués Spain 23 367 0.6× 249 0.6× 292 0.8× 216 0.6× 68 0.2× 66 1.3k
Anna D. Panani Greece 18 375 0.6× 220 0.5× 217 0.6× 221 0.6× 221 0.6× 66 1.1k
Ella R. Thompson Australia 25 1.5k 2.2× 588 1.4× 585 1.6× 1.0k 2.9× 684 2.0× 67 2.7k

Countries citing papers authored by Carsten Schwäenen

Since Specialization
Citations

This map shows the geographic impact of Carsten Schwäenen'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 Carsten Schwäenen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Carsten Schwäenen more than expected).

Fields of papers citing papers by Carsten Schwäenen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Carsten Schwäenen. 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 Carsten Schwäenen. The network helps show where Carsten Schwäenen may publish in the future.

Co-authorship network of co-authors of Carsten Schwäenen

This figure shows the co-authorship network connecting the top 25 collaborators of Carsten Schwäenen. A scholar is included among the top collaborators of Carsten Schwäenen 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 Carsten Schwäenen. Carsten Schwäenen is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Salaverría, Itziar, Idoia Martín‐Guerrero, Birgit Burkhardt, et al.. (2012). High resolution copy number analysis of IRF4 translocation‐positive diffuse large B‐cell and follicular lymphomas. Genes Chromosomes and Cancer. 52(2). 150–155. 21 indexed citations
2.
Sanjmyatav, Jimsgene, Kerstin Junker, Markus Kreuz, et al.. (2011). Identification of Genomic Alterations Associated With Metastasis and Cancer Specific Survival in Clear Cell Renal Cell Carcinoma. The Journal of Urology. 186(5). 2078–2083. 27 indexed citations
3.
Scholtysik, René, Inga Nagel, Markus Kreuz, et al.. (2011). Recurrent deletions of the TNFSF7 and TNFSF9 genes in 19p13.3 in diffuse large B‐cell and Burkitt lymphomas. International Journal of Cancer. 131(5). E830–5. 25 indexed citations
4.
Kreuz, Markus, Wolfram Klapper, A.C. Feller, et al.. (2010). Detection of genomic aberrations in molecularly defined Burkitt's lymphoma by array-based, high resolution, single nucleotide polymorphism analysis. Haematologica. 95(12). 2047–2055. 41 indexed citations
5.
Bentink, Stefan, Swen Weßendorf, Carsten Schwäenen, et al.. (2008). Conserved oncogenic module activation patterns (COMAPS) identify biologically homogeneous groups of diffuse large B-cell lymphomas and clearly define Burkitt lymphoma. Annals of Oncology. 19. 83–83. 2 indexed citations
6.
7.
Berger, Hilmar, et al.. (2007). Development and Implementation of an Analysis Tool for Array-based Comparative Genomic Hybridization. Methods of Information in Medicine. 46(5). 608–613. 8 indexed citations
8.
Weßendorf, Swen, Thomas F.E. Barth, Andreas Viardot, et al.. (2007). Further delineation of chromosomal consensus regions in primary mediastinal B-cell lymphomas: an analysis of 37 tumor samples using high-resolution genomic profiling (array-CGH). Leukemia. 21(12). 2463–2469. 50 indexed citations
9.
Fensterer, H, Bernhard Radlwimmer, Jörn Sträter, et al.. (2007). Matrix-comparative genomic hybridization from multicenter formalin-fixed paraffin-embedded colorectal cancer tissue blocks. BMC Cancer. 7(1). 58–58. 13 indexed citations
10.
Rücker, Frank G., Lars Bullinger, Carsten Schwäenen, et al.. (2006). Disclosure of Candidate Genes in Acute Myeloid Leukemia With Complex Karyotypes Using Microarray-Based Molecular Characterization. Journal of Clinical Oncology. 24(24). 3887–3894. 107 indexed citations
11.
Freier, Kolja, Carsten Schwäenen, Carsten Sticht, et al.. (2006). Recurrent FGFR1 amplification and high FGFR1 protein expression in oral squamous cell carcinoma (OSCC). Oral Oncology. 43(1). 60–66. 132 indexed citations
12.
Pscherer, Armin, Kathrin Wildenberger, Antoaneta Mincheva, et al.. (2006). Antagonizing inactivated tumor suppressor genes and activated oncogenes by a versatile transgenesis system: application in mantle cell lymphoma. The FASEB Journal. 20(8). 1188–1190. 20 indexed citations
13.
Neßling, Michelle, Karsten Richter, Carsten Schwäenen, et al.. (2005). Candidate Genes in Breast Cancer Revealed by Microarray-Based Comparative Genomic Hybridization of Archived Tissue. Cancer Research. 65(2). 439–447. 101 indexed citations
14.
Roerig, Peter, Michelle Neßling, Bernhard Radlwimmer, et al.. (2005). Molecular classification of human gliomas using matrix-based comparative genomic hybridization. International Journal of Cancer. 117(1). 95–103. 30 indexed citations
15.
Radlwimmer, Bernhard, Swen Weßendorf, Carsten Schwäenen, et al.. (2005). Automated Screening for Genomic Imbalances in Multiple Myeloma Using Microarray-Based Comparative Genomic Hybridization (mCGH).. Blood. 106(11). 499–499. 1 indexed citations
16.
Kohlhammer, Holger, Carsten Schwäenen, Swen Weßendorf, et al.. (2004). Genomic DNA-chip hybridization in t(11;14)-positive mantle cell lymphomas shows a high frequency of aberrations and allows a refined characterization of consensus regions. Blood. 104(3). 795–801. 96 indexed citations
17.
Steins, Martin, Teresa Padró, Carsten Schwäenen, et al.. (2004). Overexpression of urokinase receptor and cell surface urokinase-type plasminogen activator in the human vessel wall with different types of atherosclerotic lesions. Blood Coagulation & Fibrinolysis. 15(5). 383–391. 49 indexed citations
18.
Weßendorf, Swen, Carsten Schwäenen, Holger Kohlhammer, et al.. (2003). Hidden gene amplifications in aggressive B-cell non-Hodgkin lymphomas detected by microarray-based comparative genomic hybridization. Oncogene. 22(9). 1425–1429. 79 indexed citations
19.
Schwäenen, Carsten, et al.. (2003). DNA microarray analysis in malignant lymphomas. Annals of Hematology. 82(6). 323–332. 12 indexed citations
20.
Weßendorf, Swen, Björn Fritz, Gunnar Wrobel, et al.. (2002). Automated Screening for Genomic Imbalances using Matrix-Based Comparative Genomic Hybridization. Laboratory Investigation. 82(1). 47–60. 76 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Swen Weßendorf Breakdown of academic impact, for papers by Yan Aalto Breakdown of academic impact, for papers by Sigitas Verselis Breakdown of academic impact, for papers by Dirk Kienle Breakdown of academic impact, for papers by Samuli Hemmer Breakdown of academic impact, for papers by EJ Dreef Breakdown of academic impact, for papers by Jonathan C. Strefford Breakdown of academic impact, for papers by José María Sayagués Breakdown of academic impact, for papers by Anna D. Panani Breakdown of academic impact, for papers by Ella R. Thompson
Rankless by CCL
2026