Lucy Raymond
Impact in
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- Neurofibromatosis and Schwannoma Cases
- Vascular Malformations Diagnosis and Treatment
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- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 7
- Genetics and Neurodevelopmental Disorders 5
- Genomics and Rare Diseases 3
- Genomic variations and chromosomal abnormalities 2
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- RNA modifications and cancer 2
- Mitochondrial Function and Pathology 2
- Co-authors
- Alba Sanchis‐Juan (2 shared papers)Patrick Axon (1 shared paper)Miriam J. Smith (1 shared paper)D. Gareth Evans (1 shared paper)Andrew T. King (1 shared paper)Jan M. Friedman (1 shared paper)Amy Taylor (1 shared paper)Andrew J. Wallace (1 shared paper)
- Journals
- Journal of Medical Genetics (2 papers)Scientific Reports (1 paper)Human Molecular Genetics (1 paper)Ophthalmic Genetics (1 paper)Genetics in Medicine (1 paper)
- Partner nations
- United KingdomUnited StatesAustralia
In The Last Decade
Lucy Raymond
10 papers receiving 212 citations
Peers
Comparison fields: 5 of 42
- Neurology 63
- Genetics 95
- Molecular Biology 117
- Clinical Biochemistry 11
- Cognitive Neuroscience 24
Countries citing papers authored by Lucy Raymond
This map shows the geographic impact of Lucy Raymond'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 Lucy Raymond with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Lucy Raymond more than expected).
Fields of papers citing papers by Lucy Raymond
This network shows the impact of papers produced by Lucy Raymond. 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 Lucy Raymond. The network helps show where Lucy Raymond may publish in the future.
Co-authors
The 25 scholars most cited alongside Lucy Raymond, 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 | 2015 | 63 | |
| 2 | 2016 | 41 | |
| 3 | 2021 | 22 | |
| 4 | 2015 | 20 | |
| 5 | 2021 | 18 | |
| 6 | 2019 | 14 | |
| 7 | 2021 | 13 | |
| 8 | 2018 | 12 | |
| 9 | 2019 | 10 | |
| 10 | 2019 | 2 |
About Lucy Raymond
Lucy Raymond is a scholar working on Genetics, Molecular Biology, Cellular and Molecular Neuroscience, Neurology and General Health Professions, having authored 10 papers that have together received 215 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (5 papers), Genomics and Rare Diseases (3 papers), RNA modifications and cancer (2 papers), Mitochondrial Function and Pathology (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Metabolism and Genetic Disorders (1 paper), Meningioma and schwannoma management (1 paper) and Health Literacy and Information Accessibility (1 paper). The work is most often cited by research in Neurology (63 citations), Genetics (95 citations), Molecular Biology (117 citations), Clinical Biochemistry (11 citations) and Cognitive Neuroscience (24 citations). Lucy Raymond has collaborated with scholars based in United Kingdom, United States and Australia. Frequent co-authors include Alba Sanchis‐Juan, Patrick Axon, Miriam J. Smith, D. Gareth Evans, Andrew T. King, Jan M. Friedman, Amy Taylor, Andrew J. Wallace, Allyson Parry and Harry Joe. Their work appears in journals such as Journal of Medical Genetics, Scientific Reports, Human Molecular Genetics, Ophthalmic Genetics and Genetics in Medicine.
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.