Matthias Jungck

846 total citations
16 papers, 647 citations indexed

About

Matthias Jungck is a scholar working on Pathology and Forensic Medicine, Molecular Biology and Oncology. According to data from OpenAlex, Matthias Jungck has authored 16 papers receiving a total of 647 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Pathology and Forensic Medicine, 8 papers in Molecular Biology and 7 papers in Oncology. Recurrent topics in Matthias Jungck's work include Genetic factors in colorectal cancer (15 papers), Cancer Genomics and Diagnostics (5 papers) and DNA Repair Mechanisms (4 papers). Matthias Jungck is often cited by papers focused on Genetic factors in colorectal cancer (15 papers), Cancer Genomics and Diagnostics (5 papers) and DNA Repair Mechanisms (4 papers). Matthias Jungck collaborates with scholars based in Germany, China and Poland. Matthias Jungck's co-authors include Waltraut Friedl, Peter Propping, Micaela Mathiak, Roland Kruse, Yaping Wang, Christof Lamberti, Elisabeth Mangold, Tilman Sauerbruch, Arno Rütten and Thomas Ruzicka and has published in prestigious journals such as Gut, The American Journal of Human Genetics and International Journal of Cancer.

In The Last Decade

Matthias Jungck

14 papers receiving 628 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Matthias Jungck Germany 11 495 322 255 229 111 16 647
Isis Dove‐Edwin United Kingdom 8 502 1.0× 423 1.3× 138 0.5× 88 0.4× 119 1.1× 8 636
A. Mitri Canada 7 535 1.1× 326 1.0× 229 0.9× 327 1.4× 103 0.9× 9 741
Marie-Luise Bisgaard United Kingdom 3 650 1.3× 412 1.3× 248 1.0× 271 1.2× 125 1.1× 4 771
Iordanis Arzimanoglou United States 9 185 0.4× 167 0.5× 149 0.6× 193 0.8× 50 0.5× 14 444
Steven A. Narod Canada 5 273 0.6× 309 1.0× 202 0.8× 100 0.4× 99 0.9× 6 447
E. Pietrzak United States 6 261 0.5× 193 0.6× 85 0.3× 119 0.5× 126 1.1× 8 466
J S Terhaar Sive Droste Netherlands 7 144 0.3× 212 0.7× 281 1.1× 277 1.2× 54 0.5× 9 588
Lucy J. Curtis United Kingdom 10 451 0.9× 330 1.0× 246 1.0× 215 0.9× 109 1.0× 12 599
Elisenda Pons Spain 8 552 1.1× 493 1.5× 200 0.8× 96 0.4× 58 0.5× 8 631
Qingyi Wei United States 11 90 0.2× 141 0.4× 176 0.7× 419 1.8× 71 0.6× 26 542

Countries citing papers authored by Matthias Jungck

Since Specialization
Citations

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

Fields of papers citing papers by Matthias Jungck

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Matthias Jungck

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

All Works

16 of 16 papers shown
1.
Caspari, Reiner, Matthias Jungck, C. Lamberti, et al.. (2008). Diagnostik hereditärer kolorektaler Karzinome*. DMW - Deutsche Medizinische Wochenschrift. 125(6). 153–158.
2.
Grünhage, F, Matthias Jungck, Hildegard Keppeler, et al.. (2008). Effects of common haplotypes of the ileal sodium dependent bile acid transporter gene on the development of sporadic and familial colorectal cancer: A case control study. BMC Medical Genetics. 9(1). 70–70. 9 indexed citations
3.
Grünhage, F, Matthias Jungck, Christof Lamberti, et al.. (2008). Contribution of common monoallelic MUTYH gene variants in German patients with familial colorectal cancer. Cancer Biomarkers. 4(2). 55–61. 9 indexed citations
4.
Grünhage, F, Matthias Jungck, Christine D. Berg, et al.. (2007). Association of familial colorectal cancer with variants in the E-cadherin (CDH1) and cyclin D1 (CCND1) genes. International Journal of Colorectal Disease. 23(2). 147–154. 53 indexed citations
5.
Lamberti, C., Elisabeth Mangold, Constanze Pagenstecher, et al.. (2006). Frequency of Hereditary Non-Polyposis Colorectal Cancer among Unselected Patients with Colorectal Cancer in Germany. Digestion. 74(1). 58–67. 23 indexed citations
6.
Jungck, Matthias, Ulrich Spengler, Micaela Mathiak, et al.. (2004). E-cadherin expression is homogeneously reduced in adenoma from patients with familial adenomatous polyposis: an immunohistochemical study of E-cadherin, ?-catenin and cyclooxygenase-2 expression. International Journal of Colorectal Disease. 19(5). 438–45. 12 indexed citations
7.
Wang, Yaping, Waltraut Friedl, Christof Lamberti, et al.. (2002). Hereditary nonpolyposis colorectal cancer: Frequent occurrence of large genomic deletions in MSH2 and MLH1 genes. International Journal of Cancer. 103(5). 636–641. 87 indexed citations
8.
Wang, Yaping, Waltraut Friedl, Matthias Jungck, et al.. (2002). A modified multiplex PCR assay for detection of large deletions inMSH2 andMLH1. Human Mutation. 19(3). 279–286. 31 indexed citations
9.
Lamberti, Christof, Matthias Jungck, Michael Knapp, et al.. (2002). Arylamine N-acetyltransferase type 2 and glutathione S-transferases M1 and T1 polymorphisms in familial adenomatous polyposis. Pharmacogenetics. 12(1). 49–54. 10 indexed citations
10.
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
11.
Jungck, Matthias, W. Friedl, & Peter Propping. (1999). Erblich bedingte gastrointestinale Tumorerkrankungen. Der Internist. 40(5). 502–512. 1 indexed citations
12.
Friedl, Waltraut, Roland Kruse, Siegfried Uhlhaas, et al.. (1999). Frequent 4‐bp deletion in exon 9 of the SMAD4MADH4 gene in familial juvenile polyposis patients. Genes Chromosomes and Cancer. 25(4). 403–406. 5 indexed citations
13.
Friedl, Waltraut, Roland Kruse, Siegfried Uhlhaas, et al.. (1999). Frequent 4-bp deletion in exon 9 of theSMAD4/MADH4 gene in familial juvenile polyposis patients. Genes Chromosomes and Cancer. 25(4). 403–406. 63 indexed citations
14.
Kruse, Roland, Siegfried Uhlhaas, Klaus Keller, et al.. (1999). Peutz-Jeghers syndrome: Four novel inactivating germline mutations in theSTK11 gene. Human Mutation. 13(3). 257–258. 18 indexed citations
15.
16.
Kruse, Roland, Arno Rütten, Christof Lamberti, et al.. (1998). Muir-Torre Phenotype Has a Frequency of DNA Mismatch-Repair-Gene Mutations Similar to That in Hereditary Nonpolyposis Colorectal Cancer Families Defined by the Amsterdam Criteria. The American Journal of Human Genetics. 63(1). 63–70. 168 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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