Christopher M. Watson
Impact in
- Genetics top 10%
- Genomics and Rare Diseases
- Genetic and Kidney Cyst Diseases
- Genomic variations and chromosomal abnormalities
-
- Ubiquitin and proteasome pathways
- RNA modifications and cancer
- Genomics and Phylogenetic Studies
- Retinal Development and Disorders
Papers in
-
- Retinal Development and Disorders 5
- Genomics and Phylogenetic Studies 5
- Ubiquitin and proteasome pathways 4
- Genetics 22
- Genomics and Rare Diseases 9
- Genomic variations and chromosomal abnormalities 8
- Genetic and Kidney Cyst Diseases 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)Gillian A. Wallis (2 shared papers)Alexander F. Markham (10 shared papers)
- Journals
- Human Mutation (7 papers)Journal of Medical Genetics (7 papers)Laboratory Investigation (4 papers)PLoS ONE (3 papers)Molecular Diagnosis & Therapy (3 papers)
- Partner nations
- United KingdomUnited StatesGermany
In The Last Decade
Christopher M. Watson
54 papers receiving 724 citations
Peers
Comparison fields: 5 of 91
- Genetics 265
- Molecular Biology 393
- Aging 9
- Cancer Research 68
- Cell Biology 55
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 59 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2016 | 61 | |
| 2 | 2011 | 56 | |
| 3 | 2015 | 55 | |
| 4 | 2013 | 43 | |
| 5 | 2017 | 31 | |
| 6 | 2019 | 31 | |
| 7 | 2014 | 31 | |
| 8 | 2013 | 28 | |
| 9 | 2017 | 25 | |
| 10 | 2014 | 24 | |
| 11 | 2015 | 24 | |
| 12 | 2015 | 24 | |
| 13 | 2019 | 20 | |
| 14 | 2015 | 19 | |
| 15 | 2000 | 19 | |
| 16 | 2022 | 18 | |
| 17 | 2016 | 17 | |
| 18 | 2014 | 17 | |
| 19 | 2021 | 16 | |
| 20 | 2015 | 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 59 papers that have together received 746 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (9 papers), Genomic variations and chromosomal abnormalities (8 papers), Genetic and Kidney Cyst Diseases (5 papers), Cancer Genomics and Diagnostics (5 papers), Retinal Development and Disorders (5 papers), Genomics and Phylogenetic Studies (5 papers), Ubiquitin and proteasome pathways (4 papers) and Bone and Dental Protein Studies (4 papers). The work is most often cited by research in Genetics (265 citations), Molecular Biology (393 citations), Aging (9 citations), Cancer Research (68 citations) and Cell Biology (55 citations). Christopher M. Watson has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Laura A. Crinnion, David T. Bonthron, Ian Carr, Sally M. Harrison, Agne Antanaviciute, Eamonn Sheridan, Gillian A. Wallis, Alexander F. Markham, Ruth Charlton and Chris F. Inglehearn. Their work appears in journals such as Human Mutation, Journal of Medical Genetics, Laboratory Investigation, PLoS ONE and Molecular Diagnosis & Therapy.
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.