Andreas Claas

739 total citations
16 papers, 611 citations indexed

About

Andreas Claas is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Andreas Claas has authored 16 papers receiving a total of 611 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 6 papers in Genetics and 5 papers in Cancer Research. Recurrent topics in Andreas Claas's work include Genomic variations and chromosomal abnormalities (5 papers), DNA Repair Mechanisms (4 papers) and BRCA gene mutations in cancer (4 papers). Andreas Claas is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), DNA Repair Mechanisms (4 papers) and BRCA gene mutations in cancer (4 papers). Andreas Claas collaborates with scholars based in Germany, United Kingdom and Spain. Andreas Claas's co-authors include Larissa Savelyeva, Manfred Schwab, Purificacı́on Muñoz, Marı́a A. Blasco, Stephen C. West, Madalena Tarsounas, Douglas L. Pittman, Simone Seiter, Margot Zöller and Christoph Claas and has published in prestigious journals such as Cell, The Journal of Cell Biology and International Journal of Cancer.

In The Last Decade

Andreas Claas

16 papers receiving 599 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Andreas Claas Germany	11	463	146	117	112	101	16	611
Carla Danussi Italy	11	412 0.9×	98 0.7×	63 0.5×	200 1.8×	50 0.5×	15	709
Ettore Meccia Italy	12	616 1.3×	133 0.9×	69 0.6×	152 1.4×	39 0.4×	18	837
Brad J. Zerlanko United States	10	535 1.2×	168 1.2×	131 1.1×	96 0.9×	55 0.5×	10	670
Ludger Klewes Canada	15	437 0.9×	56 0.4×	107 0.9×	80 0.7×	35 0.3×	18	634
A J Klein-Szanto United States	9	291 0.6×	94 0.6×	155 1.3×	208 1.9×	98 1.0×	10	571
François Morlé France	18	631 1.4×	58 0.4×	223 1.9×	48 0.4×	91 0.9×	49	1.1k
Carl Hilliker Belgium	13	222 0.5×	65 0.4×	40 0.3×	62 0.6×	37 0.4×	23	416
Sonja E. Gustin Australia	10	406 0.9×	112 0.8×	37 0.3×	169 1.5×	34 0.3×	13	676
Anita Olofsson Sweden	10	382 0.8×	107 0.7×	62 0.5×	61 0.5×	184 1.8×	10	615
M Fukumoto Japan	6	709 1.5×	83 0.6×	56 0.5×	195 1.7×	66 0.7×	7	910

Countries citing papers authored by Andreas Claas

Since Specialization

Citations

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

Fields of papers citing papers by Andreas Claas

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andreas Claas

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

All Works

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16 of 16 papers shown

Gossage, Lucy, Muhammed Murtaza, Conrad Lichtenstein, et al.. (2013). Clinical and pathological impact of VHL, PBRM1, BAP1, SETD2, KDM6A, and JARID1c in clear cell renal cell carcinoma. Genes Chromosomes and Cancer. 53(1). 38–51. 106 indexed citations

Schulte, Tobias L., et al.. (2009). An extremely rare abnormality of a double tracheoesophageal fistula without atresia of the esophagus; a case report and review of the literature. Journal of Pediatric Surgery. 44(10). e9–e12. 8 indexed citations

Praml, Christian, Wolfgang A. Schulz, Andreas Claas, et al.. (2008). Genetic variation of Aflatoxin B1 aldehyde reductase genes (AFAR) in human tumour cells. Cancer Letters. 272(1). 160–166. 8 indexed citations

Henrich, Kai-Oliver, Andreas Claas, Christian Praml, et al.. (2007). Allelic variants of CAMTA1 and FLJ10737 within a commonly deleted region at 1p36 in neuroblastoma. European Journal of Cancer. 43(3). 607–616. 10 indexed citations

Sagulenko, Evgeny, Larissa Savelyeva, Volker Ehemann, et al.. (2007). Suppression of polyploidy by the BRCA2 protein. Cancer Letters. 257(1). 65–72. 10 indexed citations

Nazarenko, Irina, et al.. (2007). CEBPβ, JunD and c‐Jun contribute to the transcriptional activation of the metastasis‐associated C4.4A gene. International Journal of Cancer. 120(10). 2135–2147. 12 indexed citations

Tarsounas, Madalena, Purificacı́on Muñoz, Andreas Claas, et al.. (2004). Telomere Maintenance Requires the RAD51D Recombination/Repair Protein. Cell. 117(3). 337–347. 178 indexed citations

Schwab, Manfred, Andreas Claas, & Larissa Savelyeva. (2002). BRCA2: a genetic risk factor for breast cancer. Cancer Letters. 175(1). 1–8. 19 indexed citations

Bauer, Anja, Larissa Savelyeva, Andreas Claas, et al.. (2001). Smallest region of overlapping deletion in 1p36 in human neuroblastoma: A 1 Mbp cosmid and PAC contig. Genes Chromosomes and Cancer. 31(3). 228–239. 47 indexed citations

10.

Würfel, Jens, Simone Seiter, Marike Stassar, et al.. (2001). Cloning of the human homologue of the metastasis-associated rat C4.4A. Gene. 262(1-2). 35–41. 36 indexed citations

11.

Claas, Andreas, et al.. (2001). Chromosomal mapping of human genes by radioactive hybridization of cDNAs to CEPH-YAC high density gridded filter sets. Cancer Letters. 162(1). 125–131. 2 indexed citations

12.

Savelyeva, Larissa, Andreas Claas, P. Schlag, et al.. (2001). Constitutional genomic instability with inversions, duplications, and amplifications in 9p23-24 in BRCA2 mutation carriers.. PubMed. 61(13). 5179–85. 33 indexed citations

13.

Savelyeva, Larissa, Andreas Claas, Han‐Xiang An, et al.. (1999). Retention of polysomy at 9p23-24 during karyotypic evolution in human breast cancer cell line COLO 824. Genes Chromosomes and Cancer. 24(1). 87–93. 13 indexed citations

14.

An, Han‐Xiang, Andreas Claas, Larissa Savelyeva, et al.. (1999). Two regions of deletion in 9p23-24 in sporadic breast cancer.. PubMed. 59(16). 3941–3. 29 indexed citations

15.

Claas, Christoph, Simone Seiter, Andreas Claas, et al.. (1998). Association Between the Rat Homologue of CO-029, a Metastasis-associated Tetraspanin Molecule and Consumption Coagulopathy. The Journal of Cell Biology. 141(1). 267–280. 81 indexed citations

16.

Savelyeva, Larissa, Andreas Claas, P. Schlag, et al.. (1998). An interstitial tandem duplication of 9p23-24 coexists with a mutation in the BRCA2 gene in the germ line of three brothers with breast cancer.. PubMed. 58(5). 863–6. 19 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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