Emma Miles
Impact in
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- Neurofibromatosis and Schwannoma Cases
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- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
- Genetic and rare skin diseases.
Papers in
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- Hedgehog Signaling Pathway Studies 2
- RNA regulation and disease 1
- Chromatin Remodeling and Cancer 1
- Genetics 3
- Genomic variations and chromosomal abnormalities 1
- BRCA gene mutations in cancer 1
- Genomics and Rare Diseases 1
- Digestive system and related health 1
- Co-authors
- William G. Newman (4 shared papers)D. Gareth Evans (3 shared papers)Naomi L. Bowers (2 shared papers)Helen Byers (2 shared papers)Miriam J. Smith (2 shared papers)Emma Burkitt‐Wright (1 shared paper)Shruti Garg (1 shared paper)SM Huson (1 shared paper)
- Journals
- Human Mutation (1 paper)Reproductive BioMedicine Online (1 paper)Familial Cancer (1 paper)EBioMedicine (1 paper)Clinical and Experimental Dermatology (1 paper)
- Partner nations
- United KingdomNetherlandsUnited States
In The Last Decade
Emma Miles
5 papers receiving 140 citations
Peers
Comparison fields: 5 of 28
- Neurology 42
- Genetics 59
- Cancer Research 24
- Rheumatology 21
- Pathology and Forensic Medicine 25
Countries citing papers authored by Emma Miles
This map shows the geographic impact of Emma Miles'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 Emma Miles with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Emma Miles more than expected).
Fields of papers citing papers by Emma Miles
This network shows the impact of papers produced by Emma Miles. 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 Emma Miles. The network helps show where Emma Miles may publish in the future.
Co-authors
The 24 scholars most cited alongside Emma Miles, 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 | 2016 | 50 | |
| 2 | 2015 | 48 | |
| 3 | 2014 | 24 | |
| 4 | 2016 | 13 | |
| 5 | 2021 | 7 |
About Emma Miles
Emma Miles is a scholar working on Molecular Biology, Genetics, Cellular and Molecular Neuroscience, Dermatology and Neurology, having authored 5 papers that have together received 142 indexed citations. Recurring topics across this work include Hedgehog Signaling Pathway Studies (2 papers), RNA regulation and disease (1 paper), Hereditary Neurological Disorders (1 paper), Genomic variations and chromosomal abnormalities (1 paper), BRCA gene mutations in cancer (1 paper), Genomics and Rare Diseases (1 paper), Digestive system and related health (1 paper) and Chromatin Remodeling and Cancer (1 paper). The work is most often cited by research in Neurology (42 citations), Genetics (59 citations), Cancer Research (24 citations), Rheumatology (21 citations) and Pathology and Forensic Medicine (25 citations). Emma Miles has collaborated with scholars based in United Kingdom, Netherlands and United States. Frequent co-authors include William G. Newman, D. Gareth Evans, Naomi L. Bowers, Helen Byers, Miriam J. Smith, Emma Burkitt‐Wright, Shruti Garg, SM Huson, Angus Dobbie and Elizabeth Howard. Their work appears in journals such as Human Mutation, Reproductive BioMedicine Online, Familial Cancer, EBioMedicine and Clinical and Experimental Dermatology.
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.