Christopher Mark Watson
Impact in
- Genetics top 5%
- Genetic and Kidney Cyst Diseases
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Rheumatology top 10%
- Osteoarthritis Treatment and Mechanisms
Papers in
- Genetics 29
- Genomics and Rare Diseases 11
- Genomic variations and chromosomal abnormalities 9
- Genetic and Kidney Cyst Diseases 8
-
- Genomics and Phylogenetic Studies 6
- Retinal Development and Disorders 6
- Ubiquitin and proteasome pathways 4
- Co-authors
- Laura A. Crinnion (28 shared papers)David T. Bonthron (25 shared papers)Ian Carr (22 shared papers)Sally M. Harrison (10 shared papers)Agne Antanaviciute (9 shared papers)Eamonn G. Sheridan (8 shared papers)Alexander F. Markham (10 shared papers)Gillian A. Wallis (2 shared papers)
- Journals
- Journal of Medical Genetics (8 papers)Human Mutation (7 papers)Laboratory Investigation (4 papers)PLoS ONE (4 papers)The American Journal of Human Genetics (3 papers)
- Partner nations
- United KingdomUnited StatesNetherlands
In The Last Decade
Christopher Mark Watson
66 papers receiving 1.5k citations
Peers
Comparison fields: 5 of 112
- Genetics 553
- Rheumatology 152
- Molecular Biology 681
- Pulmonary and Respiratory Medicine 236
- Cancer Research 103
Countries citing papers authored by Christopher Mark Watson
This map shows the geographic impact of Christopher Mark 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 Mark 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 Mark Watson more than expected).
Fields of papers citing papers by Christopher Mark Watson
This network shows the impact of papers produced by Christopher Mark 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 Mark Watson. The network helps show where Christopher Mark Watson may publish in the future.
Co-authors
The 25 scholars most cited alongside Christopher Mark 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 73 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2009 | 163 | |
| 2 | 2014 | 136 | |
| 3 | 2017 | 73 | |
| 4 | 2016 | 72 | |
| 5 | 2016 | 65 | |
| 6 | 2019 | 64 | |
| 7 | 2011 | 60 | |
| 8 | 2015 | 58 | |
| 9 | 2018 | 54 | |
| 10 | 2013 | 48 | |
| 11 | 2010 | 46 | |
| 12 | 2014 | 38 | |
| 13 | 2017 | 34 | |
| 14 | 2013 | 34 | |
| 15 | 2019 | 33 | |
| 16 | 2017 | 28 | |
| 17 | 2017 | 28 | |
| 18 | 2014 | 27 | |
| 19 | 2000 | 25 | |
| 20 | 2015 | 25 |
About Christopher Mark Watson
Christopher Mark Watson is a scholar working on Genetics, Molecular Biology, Cancer Research, Rheumatology and Pathology and Forensic Medicine, having authored 73 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (11 papers), Genomic variations and chromosomal abnormalities (9 papers), Genetic and Kidney Cyst Diseases (8 papers), Cancer Genomics and Diagnostics (6 papers), Genomics and Phylogenetic Studies (6 papers), Retinal Development and Disorders (6 papers), Genetic factors in colorectal cancer (4 papers) and Ubiquitin and proteasome pathways (4 papers). The work is most often cited by research in Genetics (553 citations), Rheumatology (152 citations), Molecular Biology (681 citations), Pulmonary and Respiratory Medicine (236 citations) and Cancer Research (103 citations). Christopher Mark 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 G. Sheridan, Alexander F. Markham, Gillian A. Wallis, Chris F. Inglehearn and Ruth S. Charlton. Their work appears in journals such as Journal of Medical Genetics, Human Mutation, Laboratory Investigation, PLoS ONE and The American Journal of Human 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.