Nils Rahner

5.8k total citations
35 papers, 1.0k citations indexed

About

Nils Rahner is a scholar working on Pathology and Forensic Medicine, Molecular Biology and Oncology. According to data from OpenAlex, Nils Rahner has authored 35 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Pathology and Forensic Medicine, 15 papers in Molecular Biology and 14 papers in Oncology. Recurrent topics in Nils Rahner's work include Genetic factors in colorectal cancer (25 papers), Cancer Genomics and Diagnostics (13 papers) and Colorectal Cancer Screening and Detection (10 papers). Nils Rahner is often cited by papers focused on Genetic factors in colorectal cancer (25 papers), Cancer Genomics and Diagnostics (13 papers) and Colorectal Cancer Screening and Detection (10 papers). Nils Rahner collaborates with scholars based in Germany, France and Austria. Nils Rahner's co-authors include Verena Steinke, Peter Propping, Nicolaus Friedrichs, Stefan Aretz, Waltraut Friedl, Reinhard Buettner, Elisabeth Mangold, Reinhard Büttner, Frank Lammert and Constanze Walldorf and has published in prestigious journals such as Journal of Clinical Oncology, The Journal of Immunology and Brain Research.

In The Last Decade

Nils Rahner

33 papers receiving 1000 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Nils Rahner Germany	17	658	445	331	310	230	35	1.0k
Verena Steinke Germany	14	648 1.0×	413 0.9×	333 1.0×	214 0.7×	174 0.8×	22	869
Clyde Bailey United States	10	702 1.1×	645 1.4×	302 0.9×	425 1.4×	206 0.9×	35	1.3k
Stéphanie Baert‐Desurmont France	15	376 0.6×	419 0.9×	421 1.3×	596 1.9×	412 1.8×	38	1.2k
Barbro Werelius Sweden	15	514 0.8×	519 1.2×	299 0.9×	444 1.4×	257 1.1×	23	1.1k
Erin Salo‐Mullen United States	15	355 0.5×	886 2.0×	588 1.8×	331 1.1×	265 1.2×	44	1.3k
JT Wijnen Netherlands	16	877 1.3×	653 1.5×	291 0.9×	223 0.7×	279 1.2×	27	1.4k
Daniëlle Bodmer Netherlands	14	599 0.9×	437 1.0×	485 1.5×	522 1.7×	201 0.9×	21	1.2k
Michelle Landon United States	4	1.1k 1.7×	840 1.9×	542 1.6×	239 0.8×	238 1.0×	4	1.4k
Anna‐Maria Björkqvist Finland	6	377 0.6×	310 0.7×	272 0.8×	472 1.5×	286 1.2×	10	973
Constanze Pagenstecher Germany	22	1.4k 2.1×	908 2.0×	630 1.9×	469 1.5×	254 1.1×	27	1.7k

Countries citing papers authored by Nils Rahner

Since Specialization

Citations

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

Fields of papers citing papers by Nils Rahner

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nils Rahner

This figure shows the co-authorship network connecting the top 25 collaborators of Nils Rahner. A scholar is included among the top collaborators of Nils Rahner 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 Nils Rahner. Nils Rahner 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

Köhler, Wolfgang, Stephan Klebe, Saskia Biskup, et al.. (2024). Novel variants in CSF1R associated with adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP). Journal of Neurology. 271(9). 6025–6037.

Martinelli, Simone, Luca Pannone, Christina Lißewski, et al.. (2020). Pathogenic PTPN11 variants involving the poly‐glutamine Gln ²⁵⁵ ‐Gln ²⁵⁶ ‐Gln ²⁵⁷ stretch highlight the relevance of helix B in SHP2's functional regulation. Human Mutation. 41(6). 1171–1182. 1 indexed citations

Vangala, Deepak, Christian Pox, Christoph Engel, et al.. (2018). Clinical characteristics and EGD surveillance in Lynch-syndrome patients with small bowel/duodenal carcinomas.. Journal of Clinical Oncology. 36(15_suppl). 1555–1555. 2 indexed citations

Vangala, Deepak, Christian Pox, Christoph Engel, et al.. (2018). Value of EGD for gastric cancer surveillance in patients with hereditary non-polyposis colorectal cancer (HNPCC) or Lynch syndrome (LS).. Journal of Clinical Oncology. 36(15_suppl). 1522–1522. 3 indexed citations

Meyer, Robert, Lukas Soellner, Matthias Begemann, et al.. (2017). Targeted Next Generation Sequencing Approach in Patients Referred for Silver-Russell Syndrome Testing Increases the Mutation Detection Rate and Provides Decisive Information for Clinical Management. The Journal of Pediatrics. 187. 206–212.e1. 19 indexed citations

Basel‐Vanagaite, Lina, Rüstem Yilmaz, Sha Tang, et al.. (2014). Expanding the clinical and mutational spectrum of Kaufman oculocerebrofacial syndrome with biallelic UBE3B mutations. Human Genetics. 133(7). 939–949. 28 indexed citations

Rahner, Nils, et al.. (2014). Trichorhinophalangeal Syndrome Type I. Journal of Pediatric Orthopaedics. 35(1). e1–e5. 9 indexed citations

Rahner, Nils, Verena Steinke, Brigitte Schlegelberger, et al.. (2012). Clinical utility gene card for: Lynch syndrome (MLH1, MSH2, MSH6, PMS2, EPCAM) - update 2012. European Journal of Human Genetics. 21(1). 118–118. 13 indexed citations

Rahner, Nils, Felix F. Brockschmidt, Verena Steinke, et al.. (2011). Mutation and association analyses of the candidate genes ESR1, ESR2, MAX, PCNA, and KAT2A in patients with unexplained MSH2-deficient tumors. Familial Cancer. 11(1). 19–26. 1 indexed citations

10.

Gullotti, Lucia, Jutta Kirfel, Peter Propping, et al.. (2011). FHL2 expression in peritumoural fibroblasts correlates with lymphatic metastasis in sporadic but not in HNPCC-associated colon cancer. Laboratory Investigation. 91(12). 1695–1705. 25 indexed citations

11.

Rahner, Nils, Verena Steinke, Brigitte Schlegelberger, et al.. (2010). Clinical utility gene card for: Lynch syndrome (MLH1, MSH2, MSH6, PMS2). European Journal of Human Genetics. 18(9). 1071–1071. 12 indexed citations

12.

Ripperger, Tim, Carmela Beger, Nils Rahner, et al.. (2009). Constitutional mismatch repair deficiency and childhood leukemia/lymphoma - report on a novel biallelic MSH6 mutation. Haematologica. 95(5). 841–844. 38 indexed citations

13.

Engel, Christoph, Nils Rahner, Karsten Schulmann, et al.. (2009). Efficacy of Annual Colonoscopic Surveillance in Individuals With Hereditary Nonpolyposis Colorectal Cancer. Clinical Gastroenterology and Hepatology. 8(2). 174–182. 107 indexed citations

14.

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

15.

Morak, Monika, Hans Konrad Schackert, Nils Rahner, et al.. (2008). Further evidence for heritability of an epimutation in one of 12 cases with MLH1 promoter methylation in blood cells clinically displaying HNPCC. European Journal of Human Genetics. 16(7). 804–811. 79 indexed citations

16.

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

17.

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

18.

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

19.

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

20.

Rahner, Nils, Carsten Holzmann, Rejko Krüger, et al.. (2002). Neurofilament L gene is not a genetic factor of sporadic and familial Parkinson’s disease. Brain Research. 951(1). 82–86. 8 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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