Katrin Rapakko

1.3k total citations
17 papers, 358 citations indexed

About

Katrin Rapakko is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Katrin Rapakko has authored 17 papers receiving a total of 358 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 9 papers in Genetics and 7 papers in Oncology. Recurrent topics in Katrin Rapakko's work include DNA Repair Mechanisms (10 papers), BRCA gene mutations in cancer (8 papers) and Cancer-related Molecular Pathways (6 papers). Katrin Rapakko is often cited by papers focused on DNA Repair Mechanisms (10 papers), BRCA gene mutations in cancer (8 papers) and Cancer-related Molecular Pathways (6 papers). Katrin Rapakko collaborates with scholars based in Finland, Germany and Sweden. Katrin Rapakko's co-authors include Robert Winqvist, Sanna‐Maria Karppinen, Katri Heikkinen, Hannele Erkko, Pentti Nieminen, Katri Pylkäs, Heli Nevanlinna, Minna Allinen, Helmut Pospiech and Hannaleena Kokkonen and has published in prestigious journals such as Nature Communications, Scientific Reports and Human Molecular Genetics.

In The Last Decade

Katrin Rapakko

16 papers receiving 331 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Katrin Rapakko Finland 13 271 188 105 80 72 17 358
Katharina Eirich Germany 6 313 1.2× 145 0.8× 65 0.6× 83 1.0× 34 0.5× 8 389
Alison M. Hosey United Kingdom 6 279 1.0× 138 0.7× 117 1.1× 87 1.1× 23 0.3× 7 384
Eva Macháčková Czechia 11 229 0.8× 279 1.5× 70 0.7× 81 1.0× 87 1.2× 31 423
Man Wang China 9 234 0.9× 133 0.7× 91 0.9× 123 1.5× 29 0.4× 12 347
Pauline C. Ng Singapore 6 207 0.8× 160 0.9× 55 0.5× 107 1.3× 76 1.1× 11 390
Dominique Stoppa-Lyonnet France 6 185 0.7× 217 1.2× 65 0.6× 58 0.7× 40 0.6× 6 350
Sabine Pagès France 7 313 1.2× 380 2.0× 45 0.4× 96 1.2× 74 1.0× 7 528
Irina Kholodnyuk Sweden 10 195 0.7× 83 0.4× 64 0.6× 60 0.8× 46 0.6× 18 278
Ian Kesterton United Kingdom 6 352 1.3× 137 0.7× 100 1.0× 128 1.6× 38 0.5× 8 444
Eva Hilgenfeld Germany 10 194 0.7× 92 0.5× 66 0.6× 44 0.6× 34 0.5× 13 318

Countries citing papers authored by Katrin Rapakko

Since Specialization
Citations

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

Fields of papers citing papers by Katrin Rapakko

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Katrin Rapakko

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

All Works

17 of 17 papers shown
1.
Τσιλιμιδός, Γεράσιμος, et al.. (2023). Refined cytogenetic IPSS‐R evaluation by the use of SNP array in a cohort of 290 MDS patients. Genes Chromosomes and Cancer. 62(12). 721–731. 2 indexed citations
2.
Parplys, Ann Christin, Jonas Willmann, Marco Groth, et al.. (2019). BRCA1 mislocalization leads to aberrant DNA damage response in heterozygous ABRAXAS1 mutation carrier cells. Human Molecular Genetics. 28(24). 4148–4160. 6 indexed citations
3.
Pedersen, Mette Ølgod, Tuomo Mantere, Peter Nørgaard, et al.. (2018). Mutation of TP53, translocation analysis and immunohistochemical expression of MYC, BCL-2 and BCL-6 in patients with DLBCL treated with R-CHOP. Scientific Reports. 8(1). 14814–14814. 23 indexed citations
4.
Mantere, Tuomo, Robert Winqvist, Saila Kauppila, et al.. (2016). Targeted Next-Generation Sequencing Identifies a Recurrent Mutation in MCPH1 Associating with Hereditary Breast Cancer Susceptibility. PLoS Genetics. 12(1). e1005816–e1005816. 18 indexed citations
5.
Nikkilä, Jenni, Ann Christin Parplys, Katri Pylkäs, et al.. (2013). Heterozygous mutations in PALB2 cause DNA replication and damage response defects. Nature Communications. 4(1). 2578–2578. 50 indexed citations
6.
Sólyom, Szilvia, Robert Winqvist, Jenni Nikkilä, et al.. (2011). Screening for large genomic rearrangements in the FANCA gene reveals extensive deletion in a Finnish breast cancer family. Cancer Letters. 302(2). 113–118. 17 indexed citations
7.
Rapakko, Katrin, et al.. (2007). Clinical first-trimester routine screening for Down syndrome in singleton pregnancies in northern Finland. American Journal of Obstetrics and Gynecology. 196(3). 278.e1–278.e5. 6 indexed citations
8.
Rapakko, Katrin. (2007). Hereditary predisposition to breast cancer—evaluation of candidate genes. 3 indexed citations
9.
Rapakko, Katrin, Katri Heikkinen, Sanna‐Maria Karppinen, Hannele Erkko, & Robert Winqvist. (2006). Germline alterations in the 53BP1 gene in breast and ovarian cancer families. Cancer Letters. 245(1-2). 337–340. 12 indexed citations
10.
Pylkäs, Katri, Johanna Tommiska, Kirsi Syrjäkoski, et al.. (2006). Evaluation of the role of Finnish ataxia-telangiectasia mutations in hereditary predisposition to breast cancer. Carcinogenesis. 28(5). 1040–1045. 23 indexed citations
11.
Karppinen, Sanna‐Maria, Hannele Erkko, Kaarina Reini, et al.. (2006). Identification of a common polymorphism in the TopBP1 gene associated with hereditary susceptibility to breast and ovarian cancer. European Journal of Cancer. 42(15). 2647–2652. 32 indexed citations
12.
Rapakko, Katrin, Katri Heikkinen, Sanna‐Maria Karppinen, & Robert Winqvist. (2005). Screening for RAD51 and BRCA2 BRC repeat mutations in breast and ovarian cancer families. Cancer Letters. 236(1). 142–147. 12 indexed citations
13.
Heikkinen, Katri, et al.. (2005). Mutation analysis of the ATRgene in breast and ovarian cancer families. Breast Cancer Research. 7(4). R495–501. 26 indexed citations
14.
Heikkinen, Katri, Katrin Rapakko, Sanna‐Maria Karppinen, et al.. (2005). Association of common ATM polymorphism with bilateral breast cancer. International Journal of Cancer. 116(1). 69–72. 38 indexed citations
15.
Rapakko, Katrin, Hannaleena Kokkonen, & Jaakko Leisti. (2003). UBE3A gene mutations in finnish Angelman syndrome patients detected by conformation sensitive gel electrophoresis. American Journal of Medical Genetics Part A. 126A(3). 248–252. 13 indexed citations
16.
Rapakko, Katrin, Minna Allinen, Kirsi Syrjäkoski, et al.. (2001). Germline TP53 alterations in Finnish breast cancer families are rare and occur at conserved mutation-prone sites. British Journal of Cancer. 84(1). 116–119. 36 indexed citations
17.
Lahti‐Domenici, Jaana, Katrin Rapakko, Kati Pääkkönen, et al.. (2001). Exclusion of large deletions and other rearrangements in BRCA1 and BRCA2 in Finnish breast and ovarian cancer families. Cancer Genetics and Cytogenetics. 129(2). 120–123. 41 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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