C. Mattocks
Impact in
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- Cancer Genomics and Diagnostics
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- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- BRCA gene mutations in cancer
Papers in
- Genetics 7
- Genomics and Rare Diseases 7
- Genomic variations and chromosomal abnormalities 2
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- Genomics and Phylogenetic Studies 2
- Connexins and lens biology 1
- Co-authors
- Reuben J. Pengelly (5 shared papers)Gert Matthijs (3 shared papers)Elfriede Swinnen (1 shared paper)Michael A. Morris (1 shared paper)Elisabeth Dequeker (1 shared paper)Clemens Müller (1 shared paper)Andrew J. Wallace (1 shared paper)Sarah Ennis (5 shared papers)
- Journals
- Scientific Reports (3 papers)Human Mutation (2 papers)Clinical Chemistry (1 paper)European Journal of Human Genetics (1 paper)Bioinformatics (1 paper)
- Partner nations
- United KingdomUnited StatesNetherlands
In The Last Decade
C. Mattocks
11 papers receiving 342 citations
Peers
Comparison fields: 5 of 67
- Cancer Research 74
- Genetics 122
- Immunology 67
- Cell Biology 38
- Pathology and Forensic Medicine 40
Countries citing papers authored by C. Mattocks
This map shows the geographic impact of C. Mattocks'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 C. Mattocks with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites C. Mattocks more than expected).
Fields of papers citing papers by C. Mattocks
This network shows the impact of papers produced by C. Mattocks. 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 C. Mattocks. The network helps show where C. Mattocks may publish in the future.
Co-authors
The 25 scholars most cited alongside C. Mattocks, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2010 | 141 | |
| 2 | 2017 | 46 | |
| 3 | 2017 | 45 | |
| 4 | 2013 | 44 | |
| 5 | 2000 | 17 | |
| 6 | 2017 | 15 | |
| 7 | 2010 | 10 | |
| 8 | 2020 | 9 | |
| 9 | 2019 | 9 | |
| 10 | 2007 | 8 | |
| 11 | 2017 | 4 |
About C. Mattocks
C. Mattocks is a scholar working on Genetics, Molecular Biology, Cancer Research, Cell Biology and Immunology, having authored 11 papers that have together received 348 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (7 papers), Cancer Genomics and Diagnostics (3 papers), Genomics and Phylogenetic Studies (2 papers), melanin and skin pigmentation (2 papers), Immunodeficiency and Autoimmune Disorders (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Metabolism and Genetic Disorders (1 paper) and Connexins and lens biology (1 paper). The work is most often cited by research in Cancer Research (74 citations), Genetics (122 citations), Immunology (67 citations), Cell Biology (38 citations) and Pathology and Forensic Medicine (40 citations). C. Mattocks has collaborated with scholars based in United Kingdom, United States and Netherlands. Frequent co-authors include Reuben J. Pengelly, Gert Matthijs, Elfriede Swinnen, Michael A. Morris, Elisabeth Dequeker, Clemens Müller, Andrew J. Wallace, Sarah Ennis, Anniek Corveleyn and Victoria M. Pratt. Their work appears in journals such as Scientific Reports, Human Mutation, Clinical Chemistry, European Journal of Human Genetics 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.