Johan Staaf

199 papers receiving 18.8k citations

Johan Staaf's Hit Papers

Pan-cancer analysis of whole genomes identifies driver rearrangements promoted by LINE-1 retrotransposition 2020 · 309 citations
3090+3+6Years since publication50010001.5k2.0k

Peers

Johan Staaf
Comparison fields: 5 of 168
  • Cancer Research 7.3k
  • Oncology 4.7k
  • Molecular Biology 9.7k
  • Genetics 3.2k
  • Pathology and Forensic Medicine 1.8k
Replace Abel González-Pérez with:
Abel González-Pérez Spain
Aquila Fatima United States
Mingming Jia United Kingdom
Peter T. Simpson Australia
Dilip D. Giri United States
Colin A. Purdie United Kingdom
Steven Van Laere Belgium
Dariush Etemadmoghadam Australia
Joshy George United States
Anita Langerød United States
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Citations per field
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Citations per year

Countries citing papers authored by Johan Staaf

Since Specialization
Citations

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

Fields of papers citing papers by Johan Staaf

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Johan Staaf, 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 Johan Staaf Line = papers co-authored together Johan Staaf links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 203 papers — load more, or switch the sort, to bring in the rest.

#Work
1
The repertoire of mutational signatures in human cancer
Hit paper breakdown →
20202339
2
Pan-cancer analysis of whole genomes
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20202109
3
Landscape of somatic mutations in 560 breast cancer whole-genome sequences
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20161649
4
HRDetect is a predictor of BRCA1 and BRCA2 deficiency based on mutational signatures
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2017780
5
The evolutionary history of 2,658 cancers
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2020705
6
Patterns of somatic structural variation in human cancer genomes
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2020550
7
Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing
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2020476
8
Analyses of non-coding somatic drivers in 2,658 cancer whole genomes
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2020419
9 2011345
10 2020317
11
Pan-cancer analysis of whole genomes identifies driver rearrangements promoted by LINE-1 retrotransposition
Hit paper breakdown →
2020309
12 2020301
13 2007300
14 2020293
15 2010253
16 2019213
17 2016202
18 2008192
19 2020184
20 2012175

About Johan Staaf

Johan Staaf is a scholar working on Cancer Research, Oncology, Genetics, Molecular Biology and Pathology and Forensic Medicine, having authored 203 papers that have together received 19.1k indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (59 papers), Genomic variations and chromosomal abnormalities (31 papers), Genetic factors in colorectal cancer (23 papers), Epigenetics and DNA Methylation (21 papers), RNA modifications and cancer (20 papers), Lung Cancer Treatments and Mutations (17 papers), Breast Cancer Treatment Studies (13 papers) and Genomics and Chromatin Dynamics (13 papers). The work is most often cited by research in Cancer Research (7.3k citations), Oncology (4.7k citations), Molecular Biology (9.7k citations), Genetics (3.2k citations) and Pathology and Forensic Medicine (1.8k citations). Johan Staaf has collaborated with scholars based in Sweden, United States and United Kingdom. Frequent co-authors include Åke Borg, Markus Ringnér, Johan Vallon‐Christersson, Goran B Jönsson, Mattias Höglund, Jari Häkkinen, Erik Fredlund, Hakan Lars Olsson, Goran G. Jonsson and Martin Lauss. Their work appears in journals such as Nature Communications, Breast Cancer Research, Molecular Oncology, Clinical Cancer Research and Nature 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.

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