Uwe Claussen

4.2k total citations
105 papers, 2.9k citations indexed

About

Uwe Claussen is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Uwe Claussen has authored 105 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Genetics, 49 papers in Molecular Biology and 30 papers in Plant Science. Recurrent topics in Uwe Claussen's work include Genomic variations and chromosomal abnormalities (41 papers), Chromosomal and Genetic Variations (28 papers) and Prenatal Screening and Diagnostics (17 papers). Uwe Claussen is often cited by papers focused on Genomic variations and chromosomal abnormalities (41 papers), Chromosomal and Genetic Variations (28 papers) and Prenatal Screening and Diagnostics (17 papers). Uwe Claussen collaborates with scholars based in Germany, Russia and France. Uwe Claussen's co-authors include Thomas Liehr, Gabriele Senger, Bernhard Horsthemke, Ferdinand von Eggeling, Heike Starke, Anita Heller, Hermann‐Josef Lüdecke, Anja Weise, Günther Ernst and Kristin Mrasek and has published in prestigious journals such as Nature, Gastroenterology and Cancer.

In The Last Decade

Uwe Claussen

104 papers receiving 2.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Uwe Claussen Germany 30 1.5k 1.4k 808 527 313 105 2.9k
Hidenori Kato Japan 33 1.8k 1.2× 366 0.3× 587 0.7× 245 0.5× 272 0.9× 167 4.4k
Taiki Tamaoki Canada 34 2.6k 1.7× 1.1k 0.8× 84 0.1× 146 0.3× 347 1.1× 124 3.8k
Joost H.A. Martens Netherlands 33 4.2k 2.7× 792 0.6× 533 0.7× 117 0.2× 530 1.7× 84 5.5k
Heinz W. Kunz United States 30 1.2k 0.8× 451 0.3× 75 0.1× 183 0.3× 221 0.7× 198 3.2k
Christelle Borel Switzerland 27 1.6k 1.0× 858 0.6× 137 0.2× 133 0.3× 604 1.9× 50 2.8k
Wei‐Hua Wang China 35 1.3k 0.9× 568 0.4× 128 0.2× 652 1.2× 89 0.3× 113 3.7k
Paul Oeth United States 27 950 0.6× 559 0.4× 46 0.1× 1.2k 2.2× 449 1.4× 39 2.7k
Richard L. Davidson United States 37 2.7k 1.8× 868 0.6× 359 0.4× 58 0.1× 431 1.4× 111 3.8k
J.S. Sussenbach Netherlands 39 3.1k 2.1× 2.1k 1.6× 100 0.1× 166 0.3× 409 1.3× 123 4.6k
Natarajan V. Bhanu United States 33 2.0k 1.3× 206 0.2× 140 0.2× 111 0.2× 250 0.8× 72 3.7k

Countries citing papers authored by Uwe Claussen

Since Specialization
Citations

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

Fields of papers citing papers by Uwe Claussen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Uwe Claussen

This figure shows the co-authorship network connecting the top 25 collaborators of Uwe Claussen. A scholar is included among the top collaborators of Uwe Claussen 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 Uwe Claussen. Uwe Claussen 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.
Kosyakova, Nadezda, et al.. (2009). The hierarchically organized splitting of chromosomal bands for all human chromosomes. Molecular Cytogenetics. 2(1). 4–4. 10 indexed citations
2.
Bucsky, Peter, Uwe Claussen, Jochen Decker, et al.. (2006). Characteristic genomic imbalances in pediatric pheochromocytoma. Genes Chromosomes and Cancer. 45(6). 602–607. 11 indexed citations
3.
Kinne, Raimund W., Elke Kunisch, Volkmar Beensen, et al.. (2003). Synovial fibroblasts and synovial macrophages from patients with rheumatoid arthritis and other inflammatory joint diseases show chromosomal aberrations. Genes Chromosomes and Cancer. 38(1). 53–67. 17 indexed citations
4.
Kuechler, Alma, Susann Neubauer, Gerhard G. Grabenbauer, et al.. (2002). Is 24-Color FISH Detection of In-Vitro Radiation-Induced Chromosomal Aberrations Suited to Determine Individual Intrinsic Radiosensitivity?. Strahlentherapie und Onkologie. 178(4). 209–215. 23 indexed citations
5.
Liehr, Thomas, Matthias Schmidt, Heike Starke, et al.. (2002). First Case of Trisomy 13 plus Mosaic Trisomy 1q. Fetal Diagnosis and Therapy. 17(3). 133–136. 5 indexed citations
6.
Liehr, Thomas, Anita Heller, Heike Starke, & Uwe Claussen. (2002). FISH banding methods: applications in research and diagnostics. Expert Review of Molecular Diagnostics. 2(3). 217–225. 29 indexed citations
7.
Starke, Heike, Martin Kristian Raida, Vladimir A. Trifonov, et al.. (2001). Molecular cytogenetic characterization of an acquired minute supernumerary marker chromosome as the sole abnormality in a case clinically diagnosed as atypical Philadelphia‐negative chronic myelogenous leukaemia. British Journal of Haematology. 113(2). 435–438. 18 indexed citations
8.
Kinne, Raimund W., Thomas Liehr, Volkmar Beensen, et al.. (2001). Mosaic chromosomal aberrations in synovial fibroblasts of patients with rheumatoid arthritis, osteoarthritis, and other inflammatory joint diseases. Arthritis Research & Therapy. 3(5). 319–30. 37 indexed citations
9.
Lemke, Johannes R., Ilse Chudoba, Gabriele Senger, et al.. (2001). Improved definition of chromosomal breakpoints using high-resolution multicolour banding. Human Genetics. 108(6). 478–483. 17 indexed citations
10.
Eggeling, Ferdinand von, et al.. (2001). Fluorescent dual colour 2D-protein gel electrophoresis for rapid detection of differences in protein pattern with standard image analysis software. International Journal of Molecular Medicine. 8(4). 373–7. 41 indexed citations
11.
Claussen, Uwe, Günther Ernst, Ivan Lončarević, et al.. (2001). A long distance-PCR derived FISH probe detects a deletion between p15 and p16 in CML and T-ALL patients. International Journal of Molecular Medicine. 7(6). 591–5. 3 indexed citations
12.
Junker, Kerstin, et al.. (1999). Determination of telomerase activity for differential analysis of multifocal renal cell carcinomas. Kidney International. 56(4). 1286–1288. 7 indexed citations
13.
Claussen, Uwe, Eric D. Green, Bernhard Horsthemke, et al.. (1997). Isolation of DNA from the centromere of human chromosome 7 by microdissection. Chromosome Research. 5(4). 215–220. 5 indexed citations
14.
Eggeling, Ferdinand von, et al.. (1997). Determination of the origin of single nucleated cells in maternal circulation by means of random PCR and a set of length polymorphisms. Human Genetics. 99(2). 266–270. 27 indexed citations
15.
Eggeling, Ferdinand von, et al.. (1993). Rapid detection of trisomy 21 by quantitative PCR. Human Genetics. 91(6). 567–570. 42 indexed citations
16.
Carey, Alisoun H., Uwe Claussen, Bernhard Horsthemke, et al.. (1992). Interstitial deletions in DiGeorge syndrome detected with microclones from 22q11. Mammalian Genome. 3(2). 101–105. 12 indexed citations
17.
Davis, Lisa M., Bernhard Zabel, Gabriele Senger, et al.. (1991). A tumor chromosome rearrangement further defines the 11p13 Wilms tumor locus. Genomics. 10(3). 588–592. 17 indexed citations
18.
19.
Senger, Gabriele, et al.. (1990). Microdissection of banded human chromosomes. Human Genetics. 84(6). 507–11. 81 indexed citations
20.
Lüdecke, Hermann‐Josef, Gabriele Senger, Uwe Claussen, & Bernhard Horsthemke. (1989). Cloning defined regions of the human genome by microdissection of banded chromosomes and enzymatic amplification. Nature. 338(6213). 348–350. 261 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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