Christopher Mattocks
Impact in
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- Myeloproliferative Neoplasms: Diagnosis and Treatment
- Genomics and Rare Diseases
- BRCA gene mutations in cancer
- Genetic Syndromes and Imprinting
- Neurology top 10%
- Neurofibromatosis and Schwannoma Cases
Papers in
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- Neurofibromatosis and Schwannoma Cases 3
- Genetics 4
- Genomics and Rare Diseases 2
- BRCA gene mutations in cancer 1
- Genetic Syndromes and Imprinting 1
- Myeloproliferative Neoplasms: Diagnosis and Treatment 1
- Co-authors
- Charles ffrench‐Constant (3 shared papers)Diana Baralle (3 shared papers)Caroline Fiona Wright (1 shared paper)Sowmiya A. Moorthie (1 shared paper)Patrick S. Tarpey (2 shared papers)Francisco Ernesto Baralle (1 shared paper)Marco Baralle (1 shared paper)Kamini Kalidas (1 shared paper)
- Journals
- Journal of Medical Genetics (2 papers)Clinical Microbiology and Infection (1 paper)Leukemia Research (1 paper)Human Mutation (1 paper)Diabetologia (1 paper)
- Partner nations
- United KingdomGermanyItaly
In The Last Decade
Christopher Mattocks
11 papers receiving 458 citations
Peers
Comparison fields: 5 of 55
- Genetics 58
- Neurology 90
- Genetics 111
- Molecular Biology 115
- Infectious Diseases 32
Countries citing papers authored by Christopher Mattocks
This map shows the geographic impact of Christopher 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 Christopher Mattocks with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Christopher Mattocks more than expected).
Fields of papers citing papers by Christopher Mattocks
This network shows the impact of papers produced by Christopher 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 Christopher Mattocks. The network helps show where Christopher Mattocks may publish in the future.
Co-authors
The 25 scholars most cited alongside Christopher 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 | 2003 | 72 | |
| 2 | 2010 | 68 | |
| 3 | 2011 | 66 | |
| 4 | 2003 | 57 | |
| 5 | 2004 | 55 | |
| 6 | 2014 | 55 | |
| 7 | 2021 | 38 | |
| 8 | 2010 | 28 | |
| 9 | 2009 | 20 | |
| 10 | 2004 | 15 | |
| 11 | 2006 | 4 |
About Christopher Mattocks
Christopher Mattocks is a scholar working on Neurology, Genetics, Genetics, Pathology and Forensic Medicine and Infectious Diseases, having authored 11 papers that have together received 478 indexed citations. Recurring topics across this work include Neurofibromatosis and Schwannoma Cases (3 papers), Genomics and Rare Diseases (2 papers), Genomics and Phylogenetic Studies (2 papers), BRCA gene mutations in cancer (1 paper), SARS-CoV-2 detection and testing (1 paper), Genetic Syndromes and Imprinting (1 paper), Myeloproliferative Neoplasms: Diagnosis and Treatment (1 paper) and Genetic factors in colorectal cancer (1 paper). The work is most often cited by research in Genetics (58 citations), Neurology (90 citations), Genetics (111 citations), Molecular Biology (115 citations) and Infectious Diseases (32 citations). Christopher Mattocks has collaborated with scholars based in United Kingdom, Germany and Italy. Frequent co-authors include Charles ffrench‐Constant, Diana Baralle, Caroline Fiona Wright, Sowmiya A. Moorthie, Patrick S. Tarpey, Francisco Ernesto Baralle, Marco Baralle, Kamini Kalidas, Ian Carr and Alexander F. Markham. Their work appears in journals such as Journal of Medical Genetics, Clinical Microbiology and Infection, Leukemia Research, Human Mutation and Diabetologia.
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.