Katrin Rapakko

1.3k citations
17 papers · 361 · h-index 13

Impact in

  • Genetics top 10%
    • BRCA gene mutations in cancer
    • Genomic variations and chromosomal abnormalities
    • Cancer Genomics and Diagnostics

Papers in

Katrin Rapakko

16 papers receiving 334 citations

Peers

Katrin Rapakko
Comparison fields: 5 of 36
  • Genetics 176
  • Cancer Research 62
  • Pathology and Forensic Medicine 63
  • Oncology 96
  • Molecular Biology 235
Replace Lesley McGuffog with:
Lesley McGuffog United Kingdom
Chris Leo United States
Dominique Stoppa-Lyonnet France
Katharina Eirich Germany
Daniela Endt Germany
Rebecca A. Hinshelwood Australia
Alison M. Hosey United Kingdom
Sandra Barral United States
Ian Kesterton United Kingdom
Françoise Dorion-Bonnet France
Katrin Rapakko relative to Lesley McGuffog United Kingdom Lesley McGuffog's profile →
Citations per field
00.5×1.5×2.1×
Lesley McGuffog · 1×
Citations per year

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-authors

The 25 scholars most cited alongside Katrin Rapakko, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Katrin Rapakko Line = papers co-authored together Katrin Rapakko links everyone, so they are left out of the graph.

All Works

17 of 17 papers shown
#Work
1 201351
2 200141
3 200538
4 200135
5 200632
6 200526
7 200624
8 201824
9 201619
10 201117
11 200313
12 200512
13 200612
14 20076
15 20196
16
Hereditary predisposition to breast cancer—evaluation of candidate genes
20073
17 20232

About Katrin Rapakko

Katrin Rapakko is a scholar working on Molecular Biology, Genetics, Oncology, Pathology and Forensic Medicine and Cancer Research, having authored 17 papers that have together received 361 indexed citations. Recurring topics across this work include DNA Repair Mechanisms (10 papers), BRCA gene mutations in cancer (8 papers), Cancer-related Molecular Pathways (5 papers), Cancer Genomics and Diagnostics (3 papers), Lymphoma Diagnosis and Treatment (2 papers), Genomics and Chromatin Dynamics (2 papers), Prenatal Screening and Diagnostics (2 papers) and Genetic factors in colorectal cancer (2 papers). The work is most often cited by research in Genetics (176 citations), Cancer Research (62 citations), Pathology and Forensic Medicine (63 citations), Oncology (96 citations) and Molecular Biology (235 citations). Katrin Rapakko has collaborated with scholars based in Finland, Germany and Switzerland. Frequent co-authors include Robert Winqvist, Sanna‐Maria Karppinen, Katri Heikkinen, Hannele Erkko, Katri Pylkäs, Pentti Nieminen, Minna Allinen, Heli Nevanlinna, Helmut Pospiech and Pia Huusko. Their work appears in journals such as Cancer Letters, Nature Communications, Carcinogenesis, Genes Chromosomes and Cancer and PLoS Genetics.

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