Stefan Aretz
Impact in
- Pathology and Forensic Medicine top 0.1%
- Genetic factors in colorectal cancer
- Cancer Research top 1%
- Cancer Genomics and Diagnostics
Papers in
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- Genetic factors in colorectal cancer 113
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- Cancer Genomics and Diagnostics 34
- Co-authors
- Waltraut Friedl (18 shared papers)Peter Propping (19 shared papers)Siegfried Uhlhaas (11 shared papers)Elisabeth Mangold (13 shared papers)Frederik Jan Hes (11 shared papers)Stefanie Vogt (12 shared papers)Constanze Pagenstecher (9 shared papers)Hans F. A. Vasen (11 shared papers)
- Journals
- European Journal of Human Genetics (13 papers)International Journal of Cancer (10 papers)Genetics in Medicine (8 papers)Human Mutation (7 papers)Gastroenterology (6 papers)
- Partner nations
- GermanyNetherlandsUnited Kingdom
In The Last Decade
Stefan Aretz
154 papers receiving 7.8k citations
Stefan Aretz's Hit Papers
Peers
Comparison fields: 5 of 119
- Pathology and Forensic Medicine 5.2k
- Cancer Research 1.6k
- Oncology 2.5k
- Genetics 1.3k
- Gastroenterology 201
Countries citing papers authored by Stefan Aretz
This map shows the geographic impact of Stefan Aretz'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 Stefan Aretz with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stefan Aretz more than expected).
Fields of papers citing papers by Stefan Aretz
This network shows the impact of papers produced by Stefan Aretz. 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 Stefan Aretz. The network helps show where Stefan Aretz may publish in the future.
Co-authors
The 25 scholars most cited alongside Stefan Aretz, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 167 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts Hit paper breakdown → | 2013 | 580 |
| 2 | Peutz–Jeghers syndrome: a systematic review and recommendations for management Hit paper breakdown → | 2010 | 536 |
| 3 | Guidelines for the clinical management of familial adenomatous polyposis (FAP) Hit paper breakdown → | 2008 | 526 |
| 4 | Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database Hit paper breakdown → | 2019 | 481 |
| 5 | 2009 | 264 | |
| 6 | 2005 | 202 | |
| 7 | 2016 | 180 | |
| 8 | 2007 | 177 | |
| 9 | 2006 | 165 | |
| 10 | 2018 | 162 | |
| 11 | 2008 | 141 | |
| 12 | 2018 | 121 | |
| 13 | 2007 | 120 | |
| 14 | 2014 | 118 | |
| 15 | 2003 | 117 | |
| 16 | 2013 | 116 | |
| 17 | 2009 | 112 | |
| 18 | 2013 | 105 | |
| 19 | 2009 | 103 | |
| 20 | 2005 | 103 |
About Stefan Aretz
Stefan Aretz is a scholar working on Pathology and Forensic Medicine, Cancer Research, Oncology, Genetics and Surgery, having authored 167 papers that have together received 8.0k indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (113 papers), Cancer Genomics and Diagnostics (34 papers), Colorectal Cancer Treatments and Studies (19 papers), Colorectal Cancer Screening and Detection (18 papers), PI3K/AKT/mTOR signaling in cancer (10 papers), Multiple and Secondary Primary Cancers (8 papers), Genomics and Rare Diseases (7 papers) and RNA modifications and cancer (7 papers). The work is most often cited by research in Pathology and Forensic Medicine (5.2k citations), Cancer Research (1.6k citations), Oncology (2.5k citations), Genetics (1.3k citations) and Gastroenterology (201 citations). Stefan Aretz has collaborated with scholars based in Germany, Netherlands and United Kingdom. Frequent co-authors include Waltraut Friedl, Peter Propping, Siegfried Uhlhaas, Elisabeth Mangold, Frederik Jan Hes, Stefanie Vogt, Constanze Pagenstecher, Hans F. A. Vasen, Dietlinde Stienen and Maartje Nielsen. Their work appears in journals such as European Journal of Human Genetics, International Journal of Cancer, Genetics in Medicine, Human Mutation and Gastroenterology.
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.