Izabela Brożek

1.1k total citations
23 papers, 583 citations indexed

About

Izabela Brożek is a scholar working on Genetics, Molecular Biology and Reproductive Medicine. According to data from OpenAlex, Izabela Brożek has authored 23 papers receiving a total of 583 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 12 papers in Molecular Biology and 9 papers in Reproductive Medicine. Recurrent topics in Izabela Brożek's work include BRCA gene mutations in cancer (14 papers), Ovarian cancer diagnosis and treatment (9 papers) and DNA Repair Mechanisms (7 papers). Izabela Brożek is often cited by papers focused on BRCA gene mutations in cancer (14 papers), Ovarian cancer diagnosis and treatment (9 papers) and DNA Repair Mechanisms (7 papers). Izabela Brożek collaborates with scholars based in Poland, Sweden and Switzerland. Izabela Brożek's co-authors include Janusz Limon, Magdalena Ratajska, Åke Borg, Jarosław Dębniak, Wojciech Biernat, Maciej Stukan, Jacek Jassem, Anna Piskorz, Janusz Emerich and Christian Spangenberg and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Scientific Reports and European Journal of Cancer.

In The Last Decade

Izabela Brożek

22 papers receiving 569 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Izabela Brożek Poland 15 429 353 108 97 95 23 583
Deborah M. Ketterer United States 6 242 0.6× 294 0.8× 120 1.1× 111 1.1× 90 0.9× 6 585
Beike Leegte Netherlands 11 428 1.0× 189 0.5× 91 0.8× 58 0.6× 63 0.7× 15 531
Valeria Pensotti Italy 13 200 0.5× 155 0.4× 111 1.0× 153 1.6× 138 1.5× 30 451
Therese Sandberg Sweden 7 167 0.4× 189 0.5× 70 0.6× 81 0.8× 46 0.5× 9 382
Paraskevi Apostolou Greece 10 300 0.7× 211 0.6× 130 1.2× 91 0.9× 95 1.0× 22 449
Markéta Janatová Czechia 12 259 0.6× 268 0.8× 133 1.2× 127 1.3× 100 1.1× 35 483
Stefan Furgyik Sweden 9 131 0.3× 114 0.3× 144 1.3× 68 0.7× 73 0.8× 13 364
F. H. Menko Netherlands 8 137 0.3× 116 0.3× 131 1.2× 135 1.4× 250 2.6× 12 396
Tadeusz Dębniak Poland 13 374 0.9× 265 0.8× 189 1.8× 151 1.6× 175 1.8× 18 580
S. Gayther United Kingdom 7 291 0.7× 185 0.5× 133 1.2× 116 1.2× 96 1.0× 7 474

Countries citing papers authored by Izabela Brożek

Since Specialization
Citations

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

Fields of papers citing papers by Izabela Brożek

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Izabela Brożek

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

All Works

20 of 20 papers shown
1.
Brożek, Izabela, Magdalena Ratajska, Magdalena Koczkowska, et al.. (2018). ovarian cancer in a family with coexistence of germline nf1 and brca1 mutations case report. 1 indexed citations
2.
Koczkowska, Magdalena, Maciej Stukan, Izabela Brożek, et al.. (2018). Spectrum and Prevalence of Pathogenic Variants in Ovarian Cancer Susceptibility Genes in a Group of 333 Patients. Cancers. 10(11). 442–442. 31 indexed citations
3.
Klonowska, Katarzyna, Magdalena Ratajska, Izabela Brożek, et al.. (2015). Analysis of large mutations in BARD1 in patients with breast and/or ovarian cancer: the Polish population as an example. Scientific Reports. 5(1). 10424–10424. 24 indexed citations
4.
Ratajska, Magdalena, Magdalena Matusiak, Bartosz Wasąg, et al.. (2015). Cancer predisposing BARD1 mutations affect exon skipping and are associated with overexpression of specific BARD1 isoforms. Oncology Reports. 34(5). 2609–2617. 15 indexed citations
5.
Ratajska, Magdalena, Maciej Stukan, Magdalena Koczkowska, et al.. (2014). Mutational analysis of BRCA1/2 in a group of 134 consecutive ovarian cancer patients. Novel and recurrent BRCA1/2 alterations detected by next generation sequencing. Journal of Applied Genetics. 56(2). 193–198. 18 indexed citations
6.
Senkus, Elżbieta, Jolanta Szade, Anna J. Żaczek, et al.. (2013). Are bilateral breast cancers different from breast cancers coexisting with ovarian cancer? An immunohistochemical analysis aimed at intrinsic tumor phenotype. The Breast. 22(4). 425–430. 1 indexed citations
7.
Brożek, Izabela, Magdalena Ratajska, Magdalena Piątkowska, et al.. (2012). Limited significance of family history for presence of BRCA1 gene mutation in Polish breast and ovarian cancer cases. Familial Cancer. 11(3). 351–354. 20 indexed citations
8.
Ratajska, Magdalena, Magdalena Matusiak, Izabela Brożek, et al.. (2012). Cancer predisposing BARD1 mutations in breast-ovarian cancer families. Hereditary Cancer in Clinical Practice. 10(Suppl 4). A10–A10. 4 indexed citations
9.
Ratajska, Magdalena, Anna Piskorz, Izabela Brożek, et al.. (2011). Cancer predisposing BARD1 mutations in breast–ovarian cancer families. Breast Cancer Research and Treatment. 131(1). 89–97. 71 indexed citations
10.
Brożek, Izabela, Jarosław Dębniak, Magdalena Ratajska, et al.. (2009). Loss of heterozygosity atBRCA1/2 loci in hereditary and sporadic ovarian cancers. Journal of Applied Genetics. 50(4). 379–384. 7 indexed citations
11.
Brożek, Izabela, et al.. (2007). Germline NBS1 mutations in families with aggregation of Breast and/or ovarian cancer from north-east Poland.. PubMed. 27(4C). 3015–8. 17 indexed citations
12.
Brożek, Izabela, Jarosław Dębniak, Magdalena Ratajska, et al.. (2007). High frequency of BRCA1/2 germline mutations in consecutive ovarian cancer patients in Poland. Gynecologic Oncology. 108(2). 433–437. 44 indexed citations
13.
Brożek, Izabela, Jarosław Dębniak, Maciej Stukan, et al.. (2006). HER2 Amplification Has no Prognostic Value in Sporadic and Hereditary Ovarian Tumours. Hereditary Cancer in Clinical Practice. 4(1). 39–42. 3 indexed citations
14.
Prawitt, Dirk, Thorsten Enklaar, Christian Spangenberg, et al.. (2005). Microdeletion of target sites for insulator protein CTCF in a chromosome 11p15 imprinting center in Beckwith–Wiedemann syndrome and Wilms' tumor. Proceedings of the National Academy of Sciences. 102(11). 4085–4090. 107 indexed citations
15.
Bock, Geertruida H. de, Izabela Brożek, Jarosław Dębniak, et al.. (2004). Prevalence and clinical correlations of BRCA1/BRCA2 unclassified variant carriers among unselected primary ovarian cancer cases – preliminary report. European Journal of Cancer. 41(1). 143–150. 21 indexed citations
16.
Brożek, Izabela, Karin Haraldsson, Therese Sandberg, et al.. (2003). BRCA1 and BRCA2 mutation analysis in breast-ovarian cancer families from northeastern Poland. Human Mutation. 21(5). 553–554. 31 indexed citations
17.
Brożek, Izabela, Małgorzata Babińska, Agnieszka Woźniak, et al.. (2003). Cytogenetic analysis and clinical significance of chromosome 7 aberrations in acute leukaemia.. PubMed. 44(3). 401–12. 13 indexed citations
18.
Stankiewicz, Paweł, Izabela Brożek, Zofia Hélias‐Rodzewicz, et al.. (2001). Clinical and molecular‐cytogenetic studies in seven patients with ring chromosome 18. American Journal of Medical Genetics. 101(3). 226–239. 42 indexed citations
19.
Brożek, Izabela, et al.. (2000). Founder BRCA1 mutations and two novel germline BRCA2 mutations in breast and/or ovarian cancer families from North-Eastern Poland. Human Mutation. 15(5). 480–481. 27 indexed citations
20.
Limon, Janusz, Bogusław Nedoszytko, Izabela Brożek, et al.. (1995). Chromosome aberrations, spontaneous SCE, and growth kinetics in PHA-stimulated lymphocytes of five cases with Sézary syndrome. Cancer Genetics and Cytogenetics. 83(1). 75–81. 27 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Deborah M. Ketterer Breakdown of academic impact, for papers by Beike Leegte Breakdown of academic impact, for papers by Valeria Pensotti Breakdown of academic impact, for papers by Therese Sandberg Breakdown of academic impact, for papers by Paraskevi Apostolou Breakdown of academic impact, for papers by Markéta Janatová Breakdown of academic impact, for papers by Stefan Furgyik Breakdown of academic impact, for papers by F. H. Menko Breakdown of academic impact, for papers by Tadeusz Dębniak Breakdown of academic impact, for papers by S. Gayther
Rankless by CCL
2026