Britta Blümcke

628 total citations
7 papers, 25 citations indexed

About

Britta Blümcke is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Britta Blümcke has authored 7 papers receiving a total of 25 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 5 papers in Genetics and 2 papers in Pathology and Forensic Medicine. Recurrent topics in Britta Blümcke's work include BRCA gene mutations in cancer (5 papers), DNA Repair Mechanisms (3 papers) and Nutrition, Genetics, and Disease (2 papers). Britta Blümcke is often cited by papers focused on BRCA gene mutations in cancer (5 papers), DNA Repair Mechanisms (3 papers) and Nutrition, Genetics, and Disease (2 papers). Britta Blümcke collaborates with scholars based in Germany, Poland and United Kingdom. Britta Blümcke's co-authors include Eric Hahnen, Jan Hauke, Rita K. Schmutzler, Björn Lampe, Corinna Ernst, Philipp Harter, Kerstin Rhiem, Beyhan Ataseven, Julika Borde and Piotr Kozłowski and has published in prestigious journals such as Cancers, Cancer Medicine and European Journal of Cancer Prevention.

In The Last Decade

Britta Blümcke

6 papers receiving 24 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Britta Blümcke Germany 3 16 12 9 7 3 7 25
Megan Manion United States 3 16 1.0× 16 1.3× 6 0.7× 9 1.3× 5 34
John‐Paul Plazzer Australia 2 23 1.4× 15 1.3× 7 0.8× 4 0.6× 3 31
Jordi Corominas Galbany Netherlands 2 20 1.3× 11 0.9× 5 0.6× 6 0.9× 5 33
Neethu Shah United States 1 16 1.0× 12 1.0× 3 0.3× 7 1.0× 2 25
Anastasios Papakonstantinou United Kingdom 2 16 1.0× 8 0.7× 5 0.6× 3 0.4× 2 21
Emeline Davoine Switzerland 4 9 0.6× 18 1.5× 5 0.6× 5 0.7× 4 32
Vickie Hsuan United States 2 22 1.4× 15 1.3× 9 1.0× 11 1.6× 2 29
Nicholas A. Vulpescu United States 3 20 1.3× 25 2.1× 4 0.4× 11 1.6× 3 39
Heather Zimmermann United States 2 7 0.4× 14 1.2× 6 0.7× 5 0.7× 5 21
Cezary Cybulski Poland 3 18 1.1× 21 1.8× 6 0.7× 3 0.4× 2 0.7× 3 30

Countries citing papers authored by Britta Blümcke

Since Specialization
Citations

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

Fields of papers citing papers by Britta Blümcke

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Britta Blümcke

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

All Works

7 of 7 papers shown
1.
Rhiem, Kerstin, Clara Breidenbach, Anke Waha, et al.. (2025). Online Training to Increase Genetic and Risk Literacy in Physicians Counseling Breast and Ovarian Cancer Patients for Genetic Testing. Breast Care. 20(5). 305–313.
2.
3.
Herold, N, Corinna Ernst, Beyhan Ataseven, et al.. (2023). Pathogenic germline variants in SMARCA4 and further cancer predisposition genes in early onset ovarian cancer. Cancer Medicine. 12(14). 15256–15260. 8 indexed citations
4.
Blümcke, Britta, et al.. (2022). Long‑term survival of a BRCA2 mutation carrier following second ovarian cancer relapse using PARPi therapy: A case report. Molecular and Clinical Oncology. 17(3). 137–137. 1 indexed citations
5.
6.
Weber‐Lassalle, Nana, Julika Borde, Konstantin Weber‐Lassalle, et al.. (2018). Germline loss-of-function variants in the BARD1 gene are associated with familial breast cancer. Senologie - Zeitschrift für Mammadiagnostik und -therapie. 2 indexed citations
7.
Neidhardt, Guido, Alexandra Becker, Jan Hauke, et al.. (2016). The RAD51C exonic splice-site mutations c.404G>C and c.404G>T are associated with familial breast and ovarian cancer. European Journal of Cancer Prevention. 26(2). 165–169. 7 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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2026