Stefan Aretz

10.5k total citations
92 papers, 3.0k citations indexed

About

Stefan Aretz is a scholar working on Pathology and Forensic Medicine, Oncology and Cancer Research. According to data from OpenAlex, Stefan Aretz has authored 92 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 72 papers in Pathology and Forensic Medicine, 33 papers in Oncology and 33 papers in Cancer Research. Recurrent topics in Stefan Aretz's work include Genetic factors in colorectal cancer (71 papers), Cancer Genomics and Diagnostics (33 papers) and Colorectal Cancer Treatments and Studies (16 papers). Stefan Aretz is often cited by papers focused on Genetic factors in colorectal cancer (71 papers), Cancer Genomics and Diagnostics (33 papers) and Colorectal Cancer Treatments and Studies (16 papers). Stefan Aretz collaborates with scholars based in Germany, Netherlands and United Kingdom. Stefan Aretz's 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 and has published in prestigious journals such as Journal of Clinical Oncology, SHILAP Revista de lepidopterología and Gastroenterology.

In The Last Decade

Stefan Aretz

87 papers receiving 2.9k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Stefan Aretz Germany	31	2.1k	1.1k	876	827	624	92	3.0k
Ian M. Frayling United Kingdom	31	1.9k 0.9×	1.4k 1.3×	998 1.1×	789 1.0×	405 0.6×	72	3.3k
Frederik J. Hes Netherlands	38	1.8k 0.9×	1.3k 1.2×	1.2k 1.3×	1.7k 2.1×	1.2k 1.8×	136	4.1k
Gabriela Möslein Germany	31	2.9k 1.4×	2.0k 1.8×	815 0.9×	1.1k 1.4×	836 1.3×	100	4.1k
Ian Tomlinson United Kingdom	30	1.6k 0.8×	1.2k 1.0×	1.4k 1.6×	918 1.1×	372 0.6×	48	3.2k
J R Jass United Kingdom	17	1.6k 0.8×	1.6k 1.5×	589 0.7×	415 0.5×	625 1.0×	34	2.7k
Minna Nyström Finland	33	3.7k 1.8×	2.3k 2.1×	1.7k 2.0×	1.9k 2.4×	533 0.9×	70	5.1k
Rob B. van der Luijt Netherlands	28	804 0.4×	931 0.8×	802 0.9×	782 0.9×	445 0.7×	64	2.7k
Cristina Riva Italy	28	533 0.3×	821 0.7×	575 0.7×	606 0.7×	468 0.8×	69	2.3k
Claire Palles United Kingdom	17	604 0.3×	572 0.5×	634 0.7×	603 0.7×	185 0.3×	45	1.7k
Tsui-Lien Mao Taiwan	25	982 0.5×	574 0.5×	2.0k 2.3×	654 0.8×	256 0.4×	31	3.2k

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-authorship network of co-authors of Stefan Aretz

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

All Works

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20 of 20 papers shown

Klinkhammer, Hannah, Núria Bonifaci, Isabel Spier, et al.. (2023). Ability of a polygenic risk score to refine colorectal cancer risk in Lynch syndrome. Journal of Medical Genetics. 60(11). 1044–1051. 2 indexed citations

Beisvåg, Vidar, Elizabeth Holliday, Joan Brunet, et al.. (2023). MTHFR C677T and A1298C polymorphism’s effect on risk of colorectal cancer in Lynch syndrome. Scientific Reports. 13(1). 18783–18783. 3 indexed citations

Spier, Isabel, Hannah Klinkhammer, Friederike S. David, et al.. (2023). Clinically relevant combined effect of polygenic background, rare pathogenic germline variants, and family history on colorectal cancer incidence. BMC Medical Genomics. 16(1). 42–42. 12 indexed citations

Schreiner, Felix, Bettina Gohlke, C. James Kirkpatrick, et al.. (2017). Thyroid disease in children and adolescents with PTEN hamartoma tumor syndrome (PHTS). European Journal of Pediatrics. 177(3). 429–435. 23 indexed citations

Hüneburg, Robert, Tobias J. Weismüller, Jonel Trebicka, et al.. (2016). Chromoendoscopy in combination with random biopsies does not improve detection of gastric cancer foci in CDH1 mutation positive patients. SHILAP Revista de lepidopterología. 4(12). E1305–E1310. 24 indexed citations

Aretz, Stefan, Rossella Tricarico, Laura Papi, et al.. (2013). MUTYH-associated polyposis (MAP): evidence for the origin of the common European mutations p.Tyr179Cys and p.Gly396Asp by founder events. European Journal of Human Genetics. 22(7). 923–929. 36 indexed citations

Pin, Elisa, Chiara Pastrello, Rossella Tricarico, et al.. (2012). MUTYH c.933+3A>C, associated with a severely impaired gene expression, is the first Italian founder mutation in MUTYH‐Associated Polyposis. International Journal of Cancer. 132(5). 1060–1069. 11 indexed citations

Aretz, Stefan, Maurizio Genuardi, & Frederik J. Hes. (2012). Clinical utility gene card for: MUTYH-associated polyposis (MAP), Autosomal recessive colorectal adenomatous polyposis, Multiple colorectal adenomas, Multiple adenomatous polyps (MAP) - update 2012. European Journal of Human Genetics. 21(1). 118–118. 33 indexed citations

Aretz, Stefan, Hans F. A. Vasen, & Sylviane Olschwang. (2011). Clinical utility gene card for: Familial adenomatous polyposis (FAP) and attenuated FAP (AFAP). European Journal of Human Genetics. 19(7). 832–832. 11 indexed citations

10.

Nielsen, Maartje, Liza N. van Steenbergen, Nicola Jones, et al.. (2010). Survival of MUTYH-Associated Polyposis Patients With Colorectal Cancer and Matched Control Colorectal Cancer Patients. JNCI Journal of the National Cancer Institute. 102(22). 1724–1730. 27 indexed citations

11.

Aretz, Stefan. (2010). The Differential Diagnosis and Early Detection of Hereditary Gastrointestinal Polyposis Syndromes. Deutsches Ärzteblatt international. 107(10). 163–73. 69 indexed citations

12.

Rahner, Nils, Gerald Höefler, Christoph Högenauer, et al.. (2008). Compound heterozygosity for two MSH6 mutations in a patient with early onset colorectal cancer, vitiligo and systemic lupus erythematosus. American Journal of Medical Genetics Part A. 146A(10). 1314–1319. 34 indexed citations

13.

Aretz, Stefan, Dietlinde Stienen, Siegfried Uhlhaas, et al.. (2007). High proportion of large genomic deletions and a genotype–phenotype update in 80 unrelated families with juvenile polyposis syndrome. Journal of Medical Genetics. 44(11). 702–709. 151 indexed citations

14.

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

15.

Aretz, Stefan, Dietlinde Stienen, Nicolaus Friedrichs, et al.. (2007). SomaticAPCmosaicism: a frequent cause of familial adenomatous polyposis (FAP). Human Mutation. 28(10). 985–992. 101 indexed citations

16.

Romero‐Giménez, Jordi, Higinio Dopeso, Ignacio Blanco, et al.. (2007). Germline hypermethylation of the APC promoter is not a frequent cause of familial adenomatous polyposis in APC/MUTYH mutation negative families. International Journal of Cancer. 122(6). 1422–1425. 13 indexed citations

17.

Rahner, Nils, Nicolaus Friedrichs, Verena Steinke, et al.. (2007). Coexisting somatic promoter hypermethylation and pathogenic MLH1 germline mutation in Lynch syndrome. The Journal of Pathology. 214(1). 10–16. 54 indexed citations

18.

Mangold, Elisabeth, Nils Rahner, Nicolaus Friedrichs, et al.. (2006). MSH6 mutation in Muir?Torre syndrome: could this be a rare finding?. British Journal of Dermatology. 156(1). 158–162. 26 indexed citations

19.

Friedl, Waltraut & Stefan Aretz. (2005). Familial Adenomatous Polyposis: Experience from a Study of 1164 Unrelated German Polyposis Patients. Hereditary Cancer in Clinical Practice. 3(3). 95–114. 82 indexed citations

20.

Aretz, Stefan, et al.. (1999). Right sternoclavicular dislocation after traumatic delivery: A case report. Journal of Pediatric Surgery. 34(12). 1872–1873. 4 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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