Christopher M. Watson
Impact in
- Genetics top 10%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetic and Kidney Cyst Diseases
- Genetics and Neurodevelopmental Disorders
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- RNA modifications and cancer
- Ubiquitin and proteasome pathways
- Genomics and Phylogenetic Studies
Papers in
-
- Genomics and Phylogenetic Studies 8
- Genetics 24
- Genomics and Rare Diseases 9
- Genomic variations and chromosomal abnormalities 8
- Genetic and Kidney Cyst Diseases 7
- Genetic Syndromes and Imprinting 5
- Co-authors
- Laura A. Crinnion (26 shared papers)David T. Bonthron (24 shared papers)Ian Carr (21 shared papers)Sally M. Harrison (10 shared papers)Agne Antanaviciute (9 shared papers)Eamonn Sheridan (8 shared papers)Alexander F. Markham (10 shared papers)Gillian A. Wallis (2 shared papers)
- Journals
- Journal of Medical Genetics (7 papers)Human Mutation (7 papers)Laboratory Investigation (4 papers)PLoS ONE (3 papers)Bioinformatics (2 papers)
- Partner nations
- United KingdomUnited StatesNetherlands
In The Last Decade
Christopher M. Watson
52 papers receiving 695 citations
Peers
Comparison fields: 5 of 94
- Genetics 301
- Molecular Biology 443
- Cancer Research 80
- Aging 9
- Cell Biology 61
Countries citing papers authored by Christopher M. Watson
This map shows the geographic impact of Christopher M. Watson'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 Christopher M. Watson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Christopher M. Watson more than expected).
Fields of papers citing papers by Christopher M. Watson
This network shows the impact of papers produced by Christopher M. Watson. 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 Christopher M. Watson. The network helps show where Christopher M. Watson may publish in the future.
Co-authors
The 25 scholars most cited alongside Christopher M. Watson, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 56 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2016 | 59 | |
| 2 | 2011 | 54 | |
| 3 | 2015 | 53 | |
| 4 | 2013 | 43 | |
| 5 | 2017 | 31 | |
| 6 | 2019 | 31 | |
| 7 | 2014 | 31 | |
| 8 | 2013 | 28 | |
| 9 | 2014 | 24 | |
| 10 | 2015 | 24 | |
| 11 | 2015 | 24 | |
| 12 | 2017 | 23 | |
| 13 | 2019 | 20 | |
| 14 | 2015 | 19 | |
| 15 | 2000 | 19 | |
| 16 | 2022 | 17 | |
| 17 | 2016 | 17 | |
| 18 | 2014 | 17 | |
| 19 | 2015 | 15 | |
| 20 | 2021 | 15 |
About Christopher M. Watson
Christopher M. Watson is a scholar working on Molecular Biology, Genetics, Cancer Research, Pathology and Forensic Medicine and Rheumatology, having authored 56 papers that have together received 720 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (9 papers), Genomics and Phylogenetic Studies (8 papers), Genomic variations and chromosomal abnormalities (8 papers), Genetic and Kidney Cyst Diseases (7 papers), Cancer Genomics and Diagnostics (6 papers), Genetic Syndromes and Imprinting (5 papers), Chromosomal and Genetic Variations (5 papers) and Genetic factors in colorectal cancer (4 papers). The work is most often cited by research in Genetics (301 citations), Molecular Biology (443 citations), Cancer Research (80 citations), Aging (9 citations) and Cell Biology (61 citations). Christopher M. Watson has collaborated with scholars based in United Kingdom, United States and Netherlands. Frequent co-authors include Laura A. Crinnion, David T. Bonthron, Ian Carr, Sally M. Harrison, Agne Antanaviciute, Eamonn Sheridan, Alexander F. Markham, Gillian A. Wallis, Ruth Charlton and Sarah Hewitt. Their work appears in journals such as Journal of Medical Genetics, Human Mutation, Laboratory Investigation, PLoS ONE and Bioinformatics.
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.