B Dębniak

599 total citations
11 papers, 229 citations indexed

About

B Dębniak is a scholar working on Genetics, Molecular Biology and Cancer Research. According to data from OpenAlex, B Dębniak has authored 11 papers receiving a total of 229 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 4 papers in Molecular Biology and 3 papers in Cancer Research. Recurrent topics in B Dębniak's work include BRCA gene mutations in cancer (5 papers), Cancer Genomics and Diagnostics (3 papers) and DNA Repair Mechanisms (2 papers). B Dębniak is often cited by papers focused on BRCA gene mutations in cancer (5 papers), Cancer Genomics and Diagnostics (3 papers) and DNA Repair Mechanisms (2 papers). B Dębniak collaborates with scholars based in Poland, Australia and Sweden. B Dębniak's co-authors include Bohdan Górski, Jan Lubiński, Cezary Cybulski, Rodney J. Scott, Romuald Maleszka, Józef Kładny, Tomasz Byrski, Grzegorz Kurzawski, Tadeusz Dębniak and Tomasz Huzarski and has published in prestigious journals such as Cancer Research, International Journal of Cancer and European Journal of Cancer.

In The Last Decade

B Dębniak

11 papers receiving 224 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
B Dębniak Poland 9 103 87 76 52 40 11 229
Susana Bizarro Portugal 12 63 0.6× 165 1.9× 58 0.8× 66 1.3× 13 0.3× 29 335
Nicholas Hearle United Kingdom 7 84 0.8× 48 0.6× 59 0.8× 35 0.7× 7 0.2× 8 206
Pi‐Lin Sung Taiwan 12 82 0.8× 113 1.3× 42 0.6× 56 1.1× 12 0.3× 16 340
Josep Maria de Anta Spain 10 139 1.3× 172 2.0× 33 0.4× 98 1.9× 20 0.5× 24 329
Phuong Vu Norway 7 139 1.3× 107 1.2× 19 0.3× 106 2.0× 13 0.3× 12 258
Attila Mokánszki Hungary 9 49 0.5× 70 0.8× 52 0.7× 50 1.0× 13 0.3× 37 291
Renée Perrier Canada 7 29 0.3× 57 0.7× 61 0.8× 24 0.5× 7 0.2× 19 192
Steffen Hirsch Germany 7 134 1.3× 267 3.1× 120 1.6× 39 0.8× 16 0.4× 17 394
Diana Nariţa Romania 10 110 1.1× 80 0.9× 41 0.5× 62 1.2× 5 0.1× 15 236
Petra Kjellman Sweden 9 71 0.7× 62 0.7× 37 0.5× 8 0.2× 12 0.3× 9 285

Countries citing papers authored by B Dębniak

Since Specialization
Citations

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

Fields of papers citing papers by B Dębniak

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of B Dębniak

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

All Works

11 of 11 papers shown
1.
Gromowski, Tomasz, Bartłomiej Masojć, Rodney J. Scott, et al.. (2014). Prevalence of the E318K and V320I MITF germline mutations in Polish cancer patients and multiorgan cancer risk-a population-based study. Cancer Genetics. 207(4). 128–132. 15 indexed citations
2.
Dębniak, Tadeusz, Rodney J. Scott, Bohdan Górski, et al.. (2007). Common variants of DNA repair genes and malignant melanoma. European Journal of Cancer. 44(1). 110–114. 30 indexed citations
3.
Szymańska-Pasternak, Jolanta, Anna Szymańska, Krzysztof Mędrek, et al.. (2006). CHEK2 variants predispose to benign, borderline and low-grade invasive ovarian tumors. Gynecologic Oncology. 102(3). 429–431. 47 indexed citations
4.
Dębniak, Tadeusz, Rodney J. Scott, Bartłomiej Masojć, et al.. (2006). MC1R common variants, CDKN2A and their association with melanoma and breast cancer risk. International Journal of Cancer. 119(11). 2597–2602. 32 indexed citations
5.
Dębniak, Tadeusz, Rodney J. Scott, Tomasz Huzarski, et al.. (2005). CDKN2A Common Variants and Their Association with Melanoma Risk: A Population-Based Study. Cancer Research. 65(3). 835–839. 47 indexed citations
6.
Dębniak, Tadeusz, Grzegorz Kurzawski, Tomasz Huzarski, et al.. (2005). NOD2 variants and the risk of malignant melanoma. European Journal of Cancer Prevention. 14(2). 143–146. 13 indexed citations
7.
Dębniak, Tadeusz, Bohdan Górski, Rodney J. Scott, et al.. (2004). Germline mutation and large deletion analysis of the CDKN2A and ARF genes in families with multiple melanoma or an aggregation of malignant melanoma and breast cancer. International Journal of Cancer. 110(4). 558–562. 17 indexed citations
8.
Dębniak, Tadeusz, Bohdan Górski, Cezary Cybulski, et al.. (2003). Increased risk of breast cancer in relatives of malignant melanoma patients from families with strong cancer familial aggregation. European Journal of Cancer Prevention. 12(3). 241–245. 8 indexed citations
9.
Dubiel, Mariusz, et al.. (1999). Fetal and placental power Doppler imaging in normal and high-risk pregnancy. European Journal of Ultrasound. 9(3). 223–230. 18 indexed citations
10.
Piorunek, Tomasz, et al.. (1997). [Meigs syndrome--diagnostic difficulties].. PubMed. 98(7). 53–8. 1 indexed citations
11.
Strehl, Cindy, et al.. (1977). [Hodgkin's disease in pregnancy].. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 30(13). 1057–9. 1 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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