Emma Miles

961 total citations
5 papers, 142 citations indexed

About

Emma Miles is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Emma Miles has authored 5 papers receiving a total of 142 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 3 papers in Genetics and 1 paper in Cellular and Molecular Neuroscience. Recurrent topics in Emma Miles's work include Hedgehog Signaling Pathway Studies (2 papers), Genomics and Rare Diseases (1 paper) and Digestive system and related health (1 paper). Emma Miles is often cited by papers focused on Hedgehog Signaling Pathway Studies (2 papers), Genomics and Rare Diseases (1 paper) and Digestive system and related health (1 paper). Emma Miles collaborates with scholars based in United Kingdom, Netherlands and United States. Emma Miles's co-authors include William G. Newman, D. Gareth Evans, Miriam J. Smith, Helen Byers, Naomi L. Bowers, J. Ealing, Elaine F. Harkness, Jill Urquhart, Elizabeth Howard and Shruti Garg and has published in prestigious journals such as Human Mutation, EBioMedicine and Reproductive BioMedicine Online.

In The Last Decade

Emma Miles

5 papers receiving 140 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Emma Miles United Kingdom 5 61 59 42 25 24 5 142
Mette Jorgensen United Kingdom 5 45 0.7× 23 0.4× 20 0.5× 29 1.2× 17 0.7× 7 100
Mitchell W. Dillon United States 5 127 2.1× 81 1.4× 16 0.4× 15 0.6× 18 0.8× 7 202
JAMILE DE OLIVEIRA SÁ Brazil 9 51 0.8× 100 1.7× 19 0.5× 73 2.9× 6 0.3× 26 215
Gabriele Lorenzo Capone Italy 7 92 1.5× 37 0.6× 77 1.8× 29 1.2× 7 0.3× 7 174
Ivan Bobyr Italy 9 26 0.4× 53 0.9× 48 1.1× 20 0.8× 5 0.2× 20 241
Lara Rodríguez‐Laguna Spain 8 52 0.9× 59 1.0× 23 0.5× 34 1.4× 12 0.5× 19 154
Eugenia García‐Fernández Spain 7 41 0.7× 12 0.2× 24 0.6× 13 0.5× 14 0.6× 24 132
Zsolt Nagy Hungary 5 32 0.5× 23 0.4× 14 0.3× 31 1.2× 13 0.5× 15 85
Attila Mokánszki Hungary 9 70 1.1× 52 0.9× 12 0.3× 27 1.1× 50 2.1× 37 291
Melitta Kitzwoegerer Austria 6 38 0.6× 9 0.2× 40 1.0× 14 0.6× 12 0.5× 6 119

Countries citing papers authored by Emma Miles

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Emma Miles

This figure shows the co-authorship network connecting the top 25 collaborators of Emma Miles. A scholar is included among the top collaborators of Emma Miles based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Emma Miles. Emma Miles is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

5 of 5 papers shown
1.
Demain, Leigh, Emma Miles, Cheryl T. Fitzgerald, et al.. (2021). Biallelic loss of function variants in STAG3 result in primary ovarian insufficiency. Reproductive BioMedicine Online. 43(5). 899–902. 7 indexed citations
2.
3.
Shaw, N., et al.. (2016). MosaicNRASQ61R mutation in a child with giant congenital melanocytic naevus, epidermal naevus syndrome and hypophosphataemic rickets. Clinical and Experimental Dermatology. 42(1). 75–79. 13 indexed citations
4.
Smith, Miriam J., Jill Urquhart, Elaine F. Harkness, et al.. (2015). The Contribution of Whole Gene Deletions and Large Rearrangements to the Mutation Spectrum in Inherited Tumor Predisposing Syndromes. Human Mutation. 37(3). 250–256. 48 indexed citations
5.
Smith, Miriam J., et al.. (2014). Intronic splicing mutations in PTCH1 cause Gorlin syndrome. Familial Cancer. 13(3). 477–480. 24 indexed citations

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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Mette Jorgensen Breakdown of academic impact, for papers by Mitchell W. Dillon Breakdown of academic impact, for papers by JAMILE DE OLIVEIRA SÁ Breakdown of academic impact, for papers by Gabriele Lorenzo Capone Breakdown of academic impact, for papers by Ivan Bobyr Breakdown of academic impact, for papers by Lara Rodríguez‐Laguna Breakdown of academic impact, for papers by Eugenia García‐Fernández Breakdown of academic impact, for papers by Zsolt Nagy Breakdown of academic impact, for papers by Attila Mokánszki Breakdown of academic impact, for papers by Melitta Kitzwoegerer
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2026