Jens Plaschke

6.4k total citations · 3 hit papers
46 papers, 5.2k citations indexed

About

Jens Plaschke is a scholar working on Pathology and Forensic Medicine, Oncology and Cancer Research. According to data from OpenAlex, Jens Plaschke has authored 46 papers receiving a total of 5.2k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Pathology and Forensic Medicine, 20 papers in Oncology and 16 papers in Cancer Research. Recurrent topics in Jens Plaschke's work include Genetic factors in colorectal cancer (31 papers), Cancer Genomics and Diagnostics (16 papers) and Colorectal Cancer Screening and Detection (13 papers). Jens Plaschke is often cited by papers focused on Genetic factors in colorectal cancer (31 papers), Cancer Genomics and Diagnostics (16 papers) and Colorectal Cancer Screening and Detection (13 papers). Jens Plaschke collaborates with scholars based in Germany, United Kingdom and United States. Jens Plaschke's co-authors include Martin W. Ganal, Marion S. Röder, Viktor Korzun, K. Wendehake, Philippe Leroy, Marie-Hélène Tixier, Andreas Börner, Hans K. Schackert, Steven D. Tanksley and Susanne König and has published in prestigious journals such as Advanced Materials, Journal of Clinical Oncology and Cancer Research.

In The Last Decade

Jens Plaschke

46 papers receiving 4.8k citations

Hit Papers

A Microsatellite Map of Wheat 1995 2026 2005 2015 1998 1995 1995 500 1000 1.5k 2.0k

Peers

Jens Plaschke
Jens Plaschke
Citations per year, relative to Jens Plaschke Jens Plaschke (= 1×) peers Toshiro Ito

Countries citing papers authored by Jens Plaschke

Since Specialization
Citations

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

Fields of papers citing papers by Jens Plaschke

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jens Plaschke

This figure shows the co-authorship network connecting the top 25 collaborators of Jens Plaschke. A scholar is included among the top collaborators of Jens Plaschke 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 Jens Plaschke. Jens Plaschke 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.
Bürk, Katrin, Frank J. Kaiser, Stephanie Tennstedt, et al.. (2014). A novel missense mutation in CACNA1A evaluated by in silico protein modeling is associated with non-episodic spinocerebellar ataxia with slow progression. European Journal of Medical Genetics. 57(5). 207–211. 17 indexed citations
2.
Plaschke, Jens, et al.. (2012). Aberrant protein expression and frequent allelic loss of MSH3 in colorectal cancer with low-level microsatellite instability. International Journal of Colorectal Disease. 27(7). 911–919. 19 indexed citations
3.
Taioli, Emanuela, Mary A. Garza, D. Timothy Bishop, et al.. (2009). Meta- and Pooled Analyses of the Methylenetetrahydrofolate Reductase (MTHFR) C677T Polymorphism and Colorectal Cancer: A HuGE-GSEC Review. American Journal of Epidemiology. 170(10). 1207–1221. 83 indexed citations
4.
Plaschke, Jens, Harald Luksch, Katrin Friedrich, et al.. (2008). Microsatellite instability and loss of heterozygosity in squamous cell carcinoma of the head and neck. Head & Neck. 30(8). 1105–1113. 18 indexed citations
5.
Pistorius, Steffen, Heike Görgens, Jens Plaschke, et al.. (2006). Genomic rearrangements in MSH2, MLH1 or MSH6 are rare in HNPCC patients carrying point mutations. Cancer Letters. 248(1). 89–95. 18 indexed citations
6.
Engel, Christoph, Elke Holinski‐Feder, Constanze Pagenstecher, et al.. (2005). Novel strategy for optimal sequential application of clinical criteria, immunohistochemistry and microsatellite analysis in the diagnosis of hereditary nonpolyposis colorectal cancer. International Journal of Cancer. 118(1). 115–122. 71 indexed citations
7.
Krüger, Stefan, Christoph Engel, Andrea Bier, et al.. (2005). Absence of association between cyclin D1 (CCND1) G870A polymorphism and age of onset in hereditary nonpolyposis colorectal cancer. Cancer Letters. 236(2). 191–197. 27 indexed citations
8.
Krüger, Stefan, August Bier, Christoph Engel, et al.. (2005). The p53 codon 72 variation is associated with the age of onset of hereditary non-polyposis colorectal cancer (HNPCC). Journal of Medical Genetics. 42(10). 769–773. 30 indexed citations
9.
Martínez, Ramón, et al.. (2004). Molecular Mechanisms Associated with Chromosomal and Microsatellite Instability in Sporadic Glioblastoma multiforme. Oncology. 66(5). 395–403. 29 indexed citations
10.
Martínez, Ramón, et al.. (2004). Low-level microsatellite instability phenotype in sporadic glioblastoma multiforme. Journal of Cancer Research and Clinical Oncology. 131(2). 87–93. 31 indexed citations
11.
Plaschke, Jens, Uta Schwanebeck, Steffen Pistorius, H. D. Saeger, & Hans K. Schackert. (2003). Methylenetetrahydrofolate reductase polymorphisms and risk of sporadic and hereditary colorectal cancer with or without microsatellite instability. Cancer Letters. 191(2). 179–185. 43 indexed citations
12.
Krüger, Stefan, Jens Plaschke, Heike Görgens, et al.. (2003). Identification of six novelMSH2andMLH1germline mutations in HNPCC. Human Mutation. 21(4). 445–446. 12 indexed citations
13.
Holinski‐Feder, Elke, Waltraut Friedl, Gabriela Möslein, et al.. (2001). DHPLC mutation analysis of the hereditary nonpolyposis colon cancer (HNPCC) genes hMLH1 and hMSH2. Journal of Biochemical and Biophysical Methods. 47(1-2). 21–32. 82 indexed citations
14.
Plaschke, Jens, Stefan Krüger, Steffen Pistorius, et al.. (2001). Involvement of hMSH6 in the development of hereditary and sporadic colorectal cancer revealed by immunostaining is based on germline mutations, but rarely on somatic inactivation. International Journal of Cancer. 97(5). 643–648. 65 indexed citations
15.
Krüger, Stefan, Jens Plaschke, Steffen Pistorius, et al.. (2001). Seven novel MLH1 and MSH2 germline mutations in hereditary nonpolyposis colorectal cancer. Human Mutation. 19(1). 82–82. 10 indexed citations
16.
Pistorius, Steffen, Michael Nagel, Stefan Krüger, et al.. (2001). Combined molecular and clinical approach for decision making for surgery in HNPCC patients: a report on three cases in two families. International Journal of Colorectal Disease. 16(6). 402–407. 13 indexed citations
17.
Plaschke, Jens, T. Bocker, Steffen Pistorius, et al.. (2000). Sequence analysis of the mismatch repair gene hMSH6 in the germline of patients with familial and sporadic colorectal cancer. International Journal of Cancer. 85(5). 606–613. 52 indexed citations
18.
Frank, Stephan, J. Müller, Jens Plaschke, et al.. (1997). The putative tumor suppressor gene FHIT at 3p14.2 is rarely affected by loss of heterozygosity in primary human brain tumors.. PubMed. 57(13). 2638–41. 12 indexed citations
19.
Goessl, Carsten, Jens Plaschke, Steffen Pistorius, et al.. (1997). An intronic germline transition in the HNPCC gene hMSH2 is associated with sporadic colorectal cancer. European Journal of Cancer. 33(11). 1869–1874. 33 indexed citations
20.
Plaschke, Jens, Andreas Börner, Dong Xie, et al.. (1993). RFLP mapping of genes affecting plant height and growth habit in rye. Theoretical and Applied Genetics. 85(8). 1049–1054. 86 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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