Stuart D. Edmonds

15.0k citations
29 papers · 9.4k · 7 hit papers · h-index 26

Impact in

    • Cancer Genomics and Diagnostics
    • Cancer-related molecular mechanisms research
    • RNA modifications and cancer
    • Epigenetics and DNA Methylation
    • DNA Repair Mechanisms
    • Genomics and Chromatin Dynamics
    • CRISPR and Genetic Engineering

Papers in

Stuart D. Edmonds

29 papers receiving 9.3k citations

Stuart D. Edmonds's Hit Papers

Analyses of non-coding somatic drivers in 2,658 cancer whole genomes 2020 · 419 citations
4190+2+4Years since publication50010001.5k2.0k

Peers

Stuart D. Edmonds
Comparison fields: 5 of 168
  • Cancer Research 4.1k
  • Molecular Biology 5.0k
  • Oncology 1.8k
  • Pathology and Forensic Medicine 1.0k
  • Genetics 1.3k
Replace Hana Sušak with:
Hana Sušak Germany
Dai‐Ying Wu United States
Seung Jun Shin South Korea
Jeffrey A. Wintersinger Canada
Liis Uusküla-Reimand Canada
Michelle T. Dow United States
Christopher J. Yoon United States
Jonathan D.S. Kay United Kingdom
Duncan Beardsmore United Kingdom
Husen Muhammad Umer Canada
Stuart D. Edmonds relative to Hana Sušak Germany Hana Sušak's profile →
Citations per field
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Citations per year

Countries citing papers authored by Stuart D. Edmonds

Since Specialization
Citations

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

Fields of papers citing papers by Stuart D. Edmonds

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Stuart D. Edmonds. 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 Stuart D. Edmonds. The network helps show where Stuart D. Edmonds may publish in the future.

Co-authors

The 12 scholars most cited alongside Stuart D. Edmonds, 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 Stuart D. Edmonds Line = papers co-authored together Stuart D. Edmonds links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 29 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
Hit paper breakdown →
20202109
3
The evolutionary history of 2,658 cancers
Hit paper breakdown →
2020705
4
Patterns of somatic structural variation in human cancer genomes
Hit paper breakdown →
2020550
5
Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing
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2020476
6
Analyses of non-coding somatic drivers in 2,658 cancer whole genomes
Hit paper breakdown →
2020419
7 2020317
8
Pan-cancer analysis of whole genomes identifies driver rearrangements promoted by LINE-1 retrotransposition
Hit paper breakdown →
2020309
9 2020301
10 2020293
11 2020184
12 2020160
13 2020159
14 2020152
15 1999125
16 2010110
17 2020104
18 202092
19 202083
20 202077

About Stuart D. Edmonds

Stuart D. Edmonds is a scholar working on Cancer Research, Pathology and Forensic Medicine, Molecular Biology, Genetics and Genetics, having authored 29 papers that have together received 9.4k indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (15 papers), Genetic factors in colorectal cancer (8 papers), Genomics and Chromatin Dynamics (4 papers), RNA modifications and cancer (4 papers), RNA Research and Splicing (4 papers), Genomics and Phylogenetic Studies (3 papers), Genomics and Rare Diseases (3 papers) and Coagulation, Bradykinin, Polyphosphates, and Angioedema (2 papers). The work is most often cited by research in Cancer Research (4.1k citations), Molecular Biology (5.0k citations), Oncology (1.8k citations), Pathology and Forensic Medicine (1.0k citations) and Genetics (1.3k citations). Stuart D. Edmonds has collaborated with scholars based in Canada, United Kingdom and Germany. Frequent co-authors include Hanne L. Ostergaard, Rashida Anwar, Louise Gallivan, Alexander F. Markham, Benoît Macaluso, Vincent Larivière, Éric Archambault, Grégoire Côté, David A. Campbell and Justin Chun. Their work appears in journals such as Nature Communications, Nature, Nature Genetics, Blood and American Journal of Evaluation.

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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