David C. Wedge

62.9k citations
72 papers · 5.0k indexed · 3 hit papers · h-index 29

Impact in

    • Cancer Genomics and Diagnostics
    • Epigenetics and DNA Methylation
    • Metabolomics and Mass Spectrometry Studies
    • DNA Repair Mechanisms
    • Single-cell and spatial transcriptomics
    • CRISPR and Genetic Engineering

Papers in

David C. Wedge

70 papers receiving 4.9k citations

Hit Papers

Clock-like mutational processes in human somatic cells 2015 · 569 citations
56920132026201720212505007501000

Peers

David C. Wedge
Comparison fields: 5 of 161
  • Cancer Research 2.0k
  • Molecular Biology 2.7k
  • Oncology 984
  • Pathology and Forensic Medicine 570
  • Genetics 737
Replace Ludmil B. Alexandrov with:
Ludmil B. Alexandrov United States
Serena Nik‐Zainal United Kingdom
Venkatraman Seshan United States
Graham Ball United Kingdom
François Radvanyi France
Andra R. Frost United States
George Vasmatzis United States
Trond Stokke Norway
Chai Yin Kok United Kingdom
Garret M. Hampton United States
David C. Wedge relative to Ludmil B. Alexandrov United States Ludmil B. Alexandrov's profile →
Citations per field
00.5×1.5×
Ludmil B. Alexandrov · 1×
Citations per year

Countries citing papers authored by David C. Wedge

Since Specialization
Citations

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

Fields of papers citing papers by David C. Wedge

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David C. Wedge. 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 David C. Wedge. The network helps show where David C. Wedge may publish in the future.

Co-authorship network

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

All Works

20 of 20 papers shown
#Work
1 20252
2 202423
3 202311
4 20234
5 20231
6 202233
7 202211
8 20218
9 20217
10 202113
11 202077
12 202042
13 202080
14 20207
15 201627
16
High burden and pervasive positive selection of somatic mutations in normal human skin
Hit paper breakdown →
20151123
17
Clock-like mutational processes in human somatic cells
Hit paper breakdown →
2015569
18 20113
19 201115
20 20072

About David C. Wedge

David C. Wedge is a scholar working on Cancer Research, Genetics, Molecular Biology, Hematology and Spectroscopy, having authored 72 papers that have together received 5.0k indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (29 papers), Metabolomics and Mass Spectrometry Studies (7 papers), Evolution and Genetic Dynamics (7 papers), RNA and protein synthesis mechanisms (5 papers), Epigenetics and DNA Methylation (5 papers), Advanced Chemical Sensor Technologies (5 papers), Single-cell and spatial transcriptomics (4 papers) and Advanced Proteomics Techniques and Applications (4 papers). The work is most often cited by research in Cancer Research (2.0k citations), Molecular Biology (2.7k citations), Oncology (984 citations), Pathology and Forensic Medicine (570 citations) and Genetics (737 citations). David C. Wedge has collaborated with scholars based in United Kingdom, United States and Norway. Frequent co-authors include Peter J. Campbell, Michael R. Stratton, Ludmil B. Alexandrov, Serena Nik‐Zainal, Philip H. Jones, Peter Van Loo, Julian E. Sale, José M. C. Tubío, Andrew Menzies and Iñigo Martincorena. Their work appears in journals such as Bioinformatics, Nature Communications, European Journal of Cancer, 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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