Stefan Aretz

10.7k citations

97 papers · 3.2k · h-index 31

Impact in

Pathology and Forensic Medicine top 0.2%
- Genetic factors in colorectal cancer
Cancer Research top 2%
- Cancer Genomics and Diagnostics

Papers in

Pathology and Forensic Medicine 68
- Genetic factors in colorectal cancer 67
Molecular Biology 23
- PI3K/AKT/mTOR signaling in cancer 5

Co-authors: Waltraut Friedl (18 shared papers)Peter Propping (19 shared papers)Siegfried Uhlhaas (11 shared papers)Elisabeth Mangold (13 shared papers)Constanze Pagenstecher (9 shared papers)Frederik J. Hes (11 shared papers)Stefanie Vogt (12 shared papers)Hans F. A. Vasen (11 shared papers)
Journals: European Journal of Human Genetics (10 papers)International Journal of Cancer (4 papers)Gastroenterology (4 papers)Human Mutation (4 papers)Journal of Medical Genetics (3 papers)
Partner nations: Germany Netherlands United Kingdom

In The Last Decade

Stefan Aretz

89 papers receiving 3.1k citations

Peers

Countries citing papers authored by Stefan Aretz

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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.

Border = papers with Stefan Aretz Line = papers co-authored together Stefan Aretz links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 97 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Expanded Extracolonic Tumor Spectrum in MUTYH-Associated Polyposis Gastroenterology ·Stefanie Vogt, Natalie Jones, Daria Christian, Christoph Engel, Maartje Nielsen, Astrid Kaufmann, Verena Steinke, Hans F. A. Vasen, Peter Propping, Julian R. Sampson, Frederik J. Hes, Stefan Aretz	2009	246
2	High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome Human Mutation ·Stefan Aretz, Dietlinde Stienen, Siegfried Uhlhaas, Steffan Loff, Walter Back, Constanze Pagenstecher, D. Ross McLeod, Gail E. Graham, Elisabeth Mangold, René Santer, Peter Propping, Waltraut Friedl	2005	193
3	High proportion of large genomic deletions and a genotype–phenotype update in 80 unrelated families with juvenile polyposis syndrome Journal of Medical Genetics ·Stefan Aretz, Dietlinde Stienen, Siegfried Uhlhaas, M. Stolte, Mark M. Entius, Steffan Loff, Walter Back, Astrid Kaufmann, KM Keller, Stefan Blaas, Reiner Siebert, Stefanie Vogt, S Spranger, Elke Holinski‐Feder, Lone Sunde, Peter Propping, W Friedl	2007	167
4	MUTYH‐associated polyposis: 70 of 71 patients with biallelic mutations present with an attenuated or atypical phenotype International Journal of Cancer ·Stefan Aretz, Siegfried Uhlhaas, Heike Goergens, Kirsten Siberg, Matthias Vogel, Constanze Pagenstecher, Elisabeth Mangold, Reiner Caspari, Peter Propping, Waltraut Friedl	2006	155
5	Analysis of MUTYH Genotypes and Colorectal Phenotypes in Patients With MUTYH-Associated Polyposis Gastroenterology ·Maartje Nielsen, Mirjam C. Joerink - van de Beld, Natalie Jones, Stefanie Vogt, Carli M.J. Tops, Hans F. A. Vasen, Julian R. Sampson, Stefan Aretz, Frederik J. Hes	2008	125
6	Frequency and parental origin of de novo APC mutations in familial adenomatous polyposis European Journal of Human Genetics ·Stefan Aretz, Siegfried Uhlhaas, Reiner Caspari, Elisabeth Mangold, Constanze Pagenstecher, Peter Propping, Waltraut Friedl	2003	110
7	SomaticAPCmosaicism: a frequent cause of familial adenomatous polyposis (FAP) Human Mutation ·Stefan Aretz, Dietlinde Stienen, Nicolaus Friedrichs, Susanne Stemmler, Siegfried Uhlhaas, Nils Rahner, Peter Propping, Waltraut Friedl	2007	108
8	Frequency and phenotypic spectrum of germline mutations in POLE and seven other polymerase genes in 266 patients with colorectal adenomas and carcinomas International Journal of Cancer ·Isabel Spier, Stefanie Holzapfel, Janine Altmüller, Bixiao Zhao, Sukanya Horpaopan, Stefanie Vogt, Sophia Chen, Monika Morak, Susanne Raeder, Katrin Kayser, Dietlinde Stienen, R. Adam, Peter Nürnberg, Guido Plotz, Elke Holinski‐Feder, Richard P. Lifton, Hölger Thiele, Per Hoffmann, Verena Steinke, Stefan Aretz	2014	108
9	Increased Colorectal Cancer Incidence in Obligate Carriers of Heterozygous Mutations in MUTYH Gastroenterology ·Natalie Jones, Stefanie Vogt, Maartje Nielsen, Daria Christian, Petra A. Wark, Diana Eccles, Emma Edwards, D. Gareth Evans, Eamonn R. Maher, Hans F. A. Vasen, Frederik J. Hes, Stefan Aretz, Julian R. Sampson	2009	103
10	Cancer risk and genotype–phenotype correlations in PTEN hamartoma tumor syndrome Familial Cancer ·Marry H. Nieuwenhuis, C. Marleen Kets, Maureen Murphy‐Ryan, Helger G. Yntema, D. Gareth Evans, Chrystelle Colas, Pål Møller, Frederik J. Hes, Shirley V. Hodgson, Maran J.W. Olderode-Berends, Stefan Aretz, Karl Heinimann, E. Gómez, Fiona Douglas, Allan D. Spigelman, Susanne Timshel, Noralane M. Lindor, Hans F. A. Vasen	2013	97
11	Should children at risk for familial adenomatous polyposis be screened for hepatoblastoma and children with apparently sporadic hepatoblastoma be screened for APC germline mutations? Pediatric Blood & Cancer ·Stefan Aretz, Arend Koch, Siegfried Uhlhaas, Waltraut Friedl, Peter Propping, Dietrich von Schweinitz, Torsten Pietsch	2005	93
12	Familial adenomatous polyposis: Aberrant splicing due to missense or silent mutations in theAPCgene Human Mutation ·Stefan Aretz, Siegfried Uhlhaas, Yuli Sun, Constanze Pagenstecher, Elisabeth Mangold, Reiner Caspari, Gabriela Möslein, Karsten Schulmann, Peter Propping, Waltraut Friedl	2004	90
13	Familial Adenomatous Polyposis: Experience from a Study of 1164 Unrelated German Polyposis Patients Hereditary Cancer in Clinical Practice ·Waltraut Friedl, Stefan Aretz	2005	86
14	Tumours from MSH2 mutation carriers show loss of MSH2 expression but many tumours from MLH1 mutation carriers exhibit weak positive MLH1 staining The Journal of Pathology ·Elisabeth Mangold, Constanze Pagenstecher, Waltraut Friedl, Hans‐Peter Fischer, Sabine Merkelbach‐Bruse, Maike Ohlendorf, Nicolaus Friedrichs, Stefan Aretz, Reinhard Buettner, Peter Propping, Micaela Mathiak	2005	82
15	The Management of Peutz–Jeghers Syndrome: European Hereditary Tumour Group (EHTG) Guideline Journal of Clinical Medicine ·Anja Wagner, Stefan Aretz, Annika Auranen, Marco J. Bruno, Giulia Martina Cavestro, Emma J. Crosbie, Anne Goverde, Anne Marie Jelsig, Andrew Latchford, Monique E. van Leerdam, Anna Lepistö, Marta Puzzono, Ingrid Winship, Veronica Zuber, Gabriela Möslein	2021	75
16	Aberrant splicing in MLH1 and MSH2 due to exonic and intronic variants Human Genetics ·Constanze Pagenstecher, Maria Wehner, Waltraut Friedl, Nils Rahner, Stefan Aretz, Nicolaus Friedrichs, Marlies Sengteller, Wolfram Henn, Reinhard Buettner, Peter Propping, Elisabeth Mangold	2005	73
17	The Differential Diagnosis and Early Detection of Hereditary Gastrointestinal Polyposis Syndromes Deutsches Ärzteblatt international ·Stefan Aretz	2010	70
18	Autoimmunity, Intestinal Lymphoid Hyperplasia, and Defects in Mucosal B-Cell Homeostasis in Patients With PTEN Hamartoma Tumor Syndrome Gastroenterology ·Mario Heindl, Norman Händel, Joanne Ngeow, Janina Kionke, Christian Wittekind, Manja Kamprad, Anne Rensing‐Ehl, Stephan Ehl, J. Reifenberger, Christoph Loddenkemper, Jochen Maul, Albrecht Hoffmeister, Stefan Aretz, Wieland Kieß, Charis Eng, Holm H. Uhlig	2012	61
19	Coexisting somatic promoter hypermethylation and pathogenic MLH1 germline mutation in Lynch syndrome The Journal of Pathology ·Nils Rahner, Nicolaus Friedrichs, Verena Steinke, Stefan Aretz, Waltraut Friedl, Reinhard Buettner, Elisabeth Mangold, Peter Propping, Constanze Walldorf	2007	56
20	Deep intronicAPCmutations explain a substantial proportion of patients with familial or early-onset adenomatous polyposis Human Mutation ·Isabel Spier, Sukanya Horpaopan, Stefanie Vogt, Siegfried Uhlhaas, Monika Morak, Dietlinde Stienen, Markus Draaken, Michael Ludwig, Elke Holinski‐Feder, Markus M. Nöthen, Per Hoffmann, Stefan Aretz	2012	56

About Stefan Aretz

Stefan Aretz is a scholar working on Pathology and Forensic Medicine, Molecular Biology, Oncology, Cancer Research and Surgery, having authored 97 papers that have together received 3.2k indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (67 papers), Cancer Genomics and Diagnostics (22 papers), Colorectal Cancer Treatments and Studies (13 papers), Colorectal Cancer Screening and Detection (7 papers), Cholangiocarcinoma and Gallbladder Cancer Studies (6 papers), Digestive system and related health (5 papers), PI3K/AKT/mTOR signaling in cancer (5 papers) and Gastric Cancer Management and Outcomes (5 papers). The work is most often cited by research in Pathology and Forensic Medicine (2.1k citations), Cancer Research (677 citations), Oncology (964 citations), Genetics (576 citations) and Gastroenterology (83 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, Constanze Pagenstecher, Frederik J. Hes, Stefanie Vogt, 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, Gastroenterology, Human Mutation and Journal of Medical Genetics.

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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