Verena Steinke

2.5k total citations
22 papers, 869 citations indexed

About

Verena Steinke is a scholar working on Pathology and Forensic Medicine, Oncology and Cancer Research. According to data from OpenAlex, Verena Steinke has authored 22 papers receiving a total of 869 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Pathology and Forensic Medicine, 16 papers in Oncology and 11 papers in Cancer Research. Recurrent topics in Verena Steinke's work include Genetic factors in colorectal cancer (21 papers), Cancer Genomics and Diagnostics (11 papers) and Colorectal Cancer Screening and Detection (11 papers). Verena Steinke is often cited by papers focused on Genetic factors in colorectal cancer (21 papers), Cancer Genomics and Diagnostics (11 papers) and Colorectal Cancer Screening and Detection (11 papers). Verena Steinke collaborates with scholars based in Germany, Switzerland and Netherlands. Verena Steinke's co-authors include Nils Rahner, Peter Propping, Christoph Engel, Stefan Aretz, Stefanie Vogt, Hans F. A. Vasen, Natalie Jones, Maartje Nielsen, Julian R. Sampson and Astrid Kaufmann and has published in prestigious journals such as Journal of Clinical Oncology, Gastroenterology and International Journal of Cancer.

In The Last Decade

Verena Steinke

22 papers receiving 849 citations

Peers

Verena Steinke

PFM

ONCOL

GENET

Nils Rahner Germany

Monique Goossens Netherlands

T Aoki Japan

Mirjam Tariverdian Germany

Pardeep Kaurah Canada

Michelle Landon United States

A Scarselli Italy

Margot G F van Lier Netherlands

Ingrid Marino United States

Erin Salo‐Mullen United States

Nils Rahner Germany

Verena Steinke

658 ×1.0

PFM

445 ×1.1

ONCOL

331 ×1.0

310 ×1.4

230 ×1.3

GENET

Citations per year, relative to Verena Steinke Verena Steinke (= 1×) peers Nils Rahner

Countries citing papers authored by Verena Steinke

Since Specialization

Citations

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

Fields of papers citing papers by Verena Steinke

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Verena Steinke

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

Hinrichsen, Inga, Dieter Schäfer, David Langer, et al.. (2014). Functional testing strategy for coding genetic variants of unclear significance in MLH1 in Lynch syndrome diagnosis. Carcinogenesis. 36(2). 202–211. 9 indexed citations

Hinrichsen, Inga, Benjamin Philipp Ernst, Dieter Schäfer, et al.. (2014). Reduced migration of MLH1 deficient colon cancer cells depends on SPTAN1. Molecular Cancer. 13(1). 11–11. 29 indexed citations

Spier, Isabel, Stefanie Holzapfel, Janine Altmüller, et al.. (2014). 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. 137(2). 320–331. 103 indexed citations

Steinke, Verena, Stefanie Holzapfel, Markus Loeffler, et al.. (2013). Evaluating the performance of clinical criteria for predicting mismatch repair gene mutations in Lynch syndrome: A comprehensive analysis of 3,671 families. International Journal of Cancer. 135(1). 69–77. 19 indexed citations

Steinke, Verena, Christoph Engel, Reinhard Büttner, et al.. (2013). Hereditary Nonpolyposis Colorectal Cancer (HNPCC)/Lynch Syndrome. Deutsches Ärzteblatt international. 110(3). 32–8. 53 indexed citations

Schulmann, Karsten, Christoph Engel, Verena Steinke, et al.. (2012). Adjuvant chemotherapy (ACT) in stage II colon cancer (CC) in patients with Lynch syndrome.. Journal of Clinical Oncology. 30(15_suppl). 3550–3550. 1 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

Morak, Monika, Udo Koehler, Hans K. Schackert, et al.. (2011). Biallelic MLH1 SNP cDNA expression or constitutional promoter methylation can hide genomic rearrangements causing Lynch syndrome. Journal of Medical Genetics. 48(8). 513–519. 54 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.

Hardt, Karin, Beate Betz, Timm O. Goecke, et al.. (2011). Missense variants in hMLH1 identified in patients from the German HNPCC consortium and functional studies. Familial Cancer. 10(2). 273–284. 22 indexed citations

12.

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

13.

Vogt, Stefanie, Natalie Jones, Christoph Engel, et al.. (2009). Expanded Extracolonic Tumor Spectrum in MUTYH-Associated Polyposis. Gastroenterology. 137(6). 1976–1985.e10. 229 indexed citations

14.

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

15.

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

16.

Rahner, Nils & Verena Steinke. (2008). Hereditary Cancer Syndromes. Deutsches Ärzteblatt international. 105(41). 706–14. 68 indexed citations

17.

Steinke, Verena, Nils Rahner, Monika Morak, et al.. (2008). No association between MUTYH and MSH6 germline mutations in 64 HNPCC patients. European Journal of Human Genetics. 16(5). 587–592. 15 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.

Rahner, Nils, Nicolaus Friedrichs, Maria Wehner, et al.. (2007). Nine novel pathogenic germline mutations inMLH1,MSH2,MSH6andPMS2in families with Lynch syndrome. Acta Oncologica. 46(6). 763–769. 12 indexed citations

20.

Steinke, Verena, Jobst Meyer, Yana V. Syagailo, et al.. (2003). The genomic organization of the murine Mlc1 ( Wkl1 , KIAA0027 ) gene. Journal of Neural Transmission. 110(4). 333–343. 5 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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