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
- Genetics 3
- Genomics and Rare Diseases 1
- Genetic and rare skin diseases. 1
- Digestive system and related health 1
- BRCA gene mutations in cancer 1
- Co-authors
- William G. Newman (4 shared papers)D. Gareth Evans (3 shared papers)Helen Byers (2 shared papers)Miriam J. Smith (2 shared papers)Naomi L. Bowers (2 shared papers)J. Ealing (1 shared paper)Elaine F. Harkness (1 shared paper)SM Huson (1 shared paper)
- Journals
- Familial Cancer (1 paper)Reproductive BioMedicine Online (1 paper)Clinical and Experimental Dermatology (1 paper)Human Mutation (1 paper)EBioMedicine (1 paper)
- Partner nations
- United KingdomUnited StatesNetherlands
In The Last Decade
Emma Miles
5 papers receiving 141 citations
Peers
Comparison fields: 5 of 27
- Neurology 41
- Genetics 49
- Cancer Research 19
- Pathology and Forensic Medicine 21
- Rheumatology 16
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 | 8 |
About Emma Miles
Emma Miles is a scholar working on Molecular Biology, Genetics, Dermatology, Neurology and Endocrinology, Diabetes and Metabolism, having authored 5 papers that have together received 143 indexed citations. Recurring topics across this work include Hedgehog Signaling Pathway Studies (2 papers), Cancer and Skin Lesions (1 paper), Genomics and Rare Diseases (1 paper), Genetic and rare skin diseases. (1 paper), Digestive system and related health (1 paper), Oral and Maxillofacial Pathology (1 paper), Neurofibromatosis and Schwannoma Cases (1 paper) and BRCA gene mutations in cancer (1 paper). The work is most often cited by research in Neurology (41 citations), Genetics (49 citations), Cancer Research (19 citations), Pathology and Forensic Medicine (21 citations) and Rheumatology (16 citations). Emma Miles has collaborated with scholars based in United Kingdom, United States and Netherlands. Frequent co-authors include William G. Newman, D. Gareth Evans, Helen Byers, Miriam J. Smith, Naomi L. Bowers, J. Ealing, Elaine F. Harkness, SM Huson, Michael Bulman and Emma Burkitt‐Wright. Their work appears in journals such as Familial Cancer, Reproductive BioMedicine Online, Clinical and Experimental Dermatology, Human Mutation and EBioMedicine.
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.