Una Maye
Impact in
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Psychiatry and Mental health top 10%
- Epilepsy research and treatment
Papers in
- Genetics 12
- Genomic variations and chromosomal abnormalities 8
- Genomics and Rare Diseases 5
- Genetics and Neurodevelopmental Disorders 5
-
- Genomics and Chromatin Dynamics 2
- Advanced biosensing and bioanalysis techniques 2
- RNA modifications and cancer 1
- Co-authors
- Peter Howard (1 shared paper)Sahar Mansour (1 shared paper)May Tassabehji (1 shared paper)Jill Clayton‐Smith (1 shared paper)Shehla N. Mohammed (1 shared paper)Richard Osborne Day (1 shared paper)Bronwyn A. Kerr (1 shared paper)Shane A McKee (1 shared paper)
- Journals
- The American Journal of Human Genetics (5 papers)Investigative Ophthalmology & Visual Science (1 paper)Neurology (1 paper)Clinical Genetics (1 paper)Nature Communications (1 paper)
- Partner nations
- United KingdomUnited StatesFrance
In The Last Decade
Una Maye
13 papers receiving 752 citations
Peers
Comparison fields: 5 of 64
- Genetics 465
- Psychiatry and Mental health 90
- Molecular Biology 399
- Cognitive Neuroscience 77
- Pediatrics, Perinatology and Child Health 57
Countries citing papers authored by Una Maye
This map shows the geographic impact of Una Maye'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 Una Maye with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Una Maye more than expected).
Fields of papers citing papers by Una Maye
This network shows the impact of papers produced by Una Maye. 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 Una Maye. The network helps show where Una Maye may publish in the future.
Co-authors
The 25 scholars most cited alongside Una Maye, 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 | 2017 | 207 | |
| 2 | 2013 | 139 | |
| 3 | 2017 | 111 | |
| 4 | 2018 | 91 | |
| 5 | 2010 | 67 | |
| 6 | 2019 | 62 | |
| 7 | 2019 | 50 | |
| 8 | 2008 | 23 | |
| 9 | 2015 | 18 | |
| 10 | 2019 | 7 | |
| 11 | 2004 | 3 | |
| 12 | 2006 | 2 | |
| 13 | Quality Assessment Of Multiplex Ligation-dependent Probe Amplification (mlpa) In Uveal Melanoma By Comparison With Array Comparative Genomic Hybridization (acgh) And Microsatellite Analysis (msa) | 2012 | 1 |
About Una Maye
Una Maye is a scholar working on Genetics, Molecular Biology, Developmental Biology, Ophthalmology and Psychiatry and Mental health, having authored 13 papers that have together received 781 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (8 papers), Genomics and Rare Diseases (5 papers), Genetics and Neurodevelopmental Disorders (5 papers), Chromosomal and Genetic Variations (2 papers), Genomics and Chromatin Dynamics (2 papers), Advanced biosensing and bioanalysis techniques (2 papers), RNA modifications and cancer (1 paper) and Congenital limb and hand anomalies (1 paper). The work is most often cited by research in Genetics (465 citations), Psychiatry and Mental health (90 citations), Molecular Biology (399 citations), Cognitive Neuroscience (77 citations) and Pediatrics, Perinatology and Child Health (57 citations). Una Maye has collaborated with scholars based in United Kingdom, United States and France. Frequent co-authors include Peter Howard, Sahar Mansour, May Tassabehji, Jill Clayton‐Smith, Shehla N. Mohammed, Richard Osborne Day, Bronwyn A. Kerr, Shane A McKee, Alan E Fryer and Elizabeth M. Sweeney. Their work appears in journals such as The American Journal of Human Genetics, Investigative Ophthalmology & Visual Science, Neurology, Clinical Genetics and Nature Communications.
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.