Peter O’Donovan

2.5k citations
68 papers · 1.7k · 2 hit papers · h-index 25

Impact in

    • Cancer Genomics and Diagnostics
  • Genetics top 5%
    • Genomics and Rare Diseases
    • Genetic and Kidney Cyst Diseases

Papers in

    • Genomics and Rare Diseases 13
    • Genetics and Neurodevelopmental Disorders 6
    • Genetic and Kidney Cyst Diseases 5
    • Lung Cancer Diagnosis and Treatment 5
    • Medical Imaging and Pathology Studies 4
    • Pleural and Pulmonary Diseases 3

Peter O’Donovan

66 papers receiving 1.7k citations

Peter O’Donovan's Hit Papers

Origins and impact of extrachromosomal DNA 2024 · 82 citations
820+1+2Years since publication50100150

Peers

Peter O’Donovan
Comparison fields: 5 of 96
  • Cancer Research 209
  • Genetics 393
  • Pulmonary and Respiratory Medicine 291
  • Genetics 66
  • Molecular Biology 344
Replace Chiara Bacchelli with:
Chiara Bacchelli United Kingdom
Maria Soller Sweden
Ellen R. A. Thomas United Kingdom
Catherine E. Cottrell United States
TERRI L. BEATY United States
Arjan C. Houweling Netherlands
Kaanan P. Shah United States
Sri V. V. Deevi United Kingdom
Lea Lahnstein United Kingdom
Anna‐Lena Volckmar Germany
Peter O’Donovan relative to Chiara Bacchelli United Kingdom Chiara Bacchelli's profile →
Citations per field
00.5×1.5×2.0×
Chiara Bacchelli · 1×
Citations per year

Countries citing papers authored by Peter O’Donovan

Since Specialization
Citations

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

Fields of papers citing papers by Peter O’Donovan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Peter O’Donovan. 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 Peter O’Donovan. The network helps show where Peter O’Donovan may publish in the future.

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 68 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Substitution mutational signatures in whole-genome–sequenced cancers in the UK population
Hit paper breakdown →
2022195
2 1999129
3
Origins and impact of extrachromosomal DNA
Hit paper breakdown →
202482
4 202155
5 202254
6 202248
7 202247
8 198446
9 202144
10 202344
11 200843
12 199341
13 202038
14 202238
15 198437
16 199837
17 202237
18 202235
19 202331
20 202230

About Peter O’Donovan

Peter O’Donovan is a scholar working on Genetics, Pulmonary and Respiratory Medicine, Cancer Research, Surgery and Radiology, Nuclear Medicine and Imaging, having authored 68 papers that have together received 1.7k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (13 papers), Genetics and Neurodevelopmental Disorders (6 papers), Genetic and Kidney Cyst Diseases (5 papers), Lung Cancer Diagnosis and Treatment (5 papers), Cancer Genomics and Diagnostics (5 papers), Medical Imaging and Pathology Studies (4 papers), Pleural and Pulmonary Diseases (3 papers) and Advanced MRI Techniques and Applications (3 papers). The work is most often cited by research in Cancer Research (209 citations), Genetics (393 citations), Pulmonary and Respiratory Medicine (291 citations), Genetics (66 citations) and Molecular Biology (344 citations). Peter O’Donovan has collaborated with scholars based in United States, United Kingdom and Ireland. Frequent co-authors include Atul C. Mehta, Saeed Uz Zaman Khan, Michael A. Matthay, Edward J. Mascha, Alejandro C. Arroliga, Gregory P. Borkowski, Joseph A. Golish, James K. Stoller, P. Eng and Edwin G. Beven. Their work appears in journals such as CHEST Journal, Genetics in Medicine, Nature Communications, British Journal of Cancer and Scientific Reports.

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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