Una Maye
Impact in
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- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
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- Prenatal Screening and Diagnostics
Papers in
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- Advanced biosensing and bioanalysis techniques 2
- RNA modifications and cancer 1
- Genomics and Chromatin Dynamics 1
- Genetics 3
- Genomic variations and chromosomal abnormalities 3
- Genomics and Rare Diseases 1
- Co-authors
- Alan Fryer (2 shared papers)Nicola Foulds (1 shared paper)Peter Howard (1 shared paper)Joris Andrieux (1 shared paper)Damien Sanlaville (1 shared paper)Shehla Mohammed (1 shared paper)Michèle Mathieu‐Dramard (1 shared paper)Guillaume Jedraszak (1 shared paper)
- Journals
- Investigative Ophthalmology & Visual Science (1 paper)Clinical Genetics (1 paper)American Journal of Medical Genetics Part A (1 paper)Clinical Dysmorphology (1 paper)
- Partner nations
- United KingdomAustraliaNetherlands
In The Last Decade
Una Maye
4 papers receiving 26 citations
Peers
Comparison fields: 5 of 18
- Genetics 27
- Pediatrics, Perinatology and Child Health 10
- Developmental Biology 1
- Genetics 3
- Occupational Therapy 1
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 | 2015 | 17 | |
| 2 | 2008 | 17 | |
| 3 | 2004 | 3 | |
| 4 | 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 Molecular Biology, Genetics, Pulmonary and Respiratory Medicine, Ophthalmology and Oncology, having authored 4 papers that have together received 38 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (3 papers), Advanced biosensing and bioanalysis techniques (2 papers), Ear and Head Tumors (1 paper), RNA modifications and cancer (1 paper), Genomics and Rare Diseases (1 paper), Medical Imaging and Pathology Studies (1 paper), Chromosomal and Genetic Variations (1 paper) and Genomics and Chromatin Dynamics (1 paper). The work is most often cited by research in Genetics (27 citations), Pediatrics, Perinatology and Child Health (10 citations), Developmental Biology (1 citation), Genetics (3 citations) and Occupational Therapy (1 citation). Una Maye has collaborated with scholars based in United Kingdom, Australia and Netherlands. Frequent co-authors include Alan Fryer, Nicola Foulds, Peter Howard, Joris Andrieux, Damien Sanlaville, Shehla Mohammed, Michèle Mathieu‐Dramard, Guillaume Jedraszak, Richard O. Day and Jill Clayton‐Smith. Their work appears in journals such as Investigative Ophthalmology & Visual Science, Clinical Genetics, American Journal of Medical Genetics Part A and Clinical Dysmorphology.
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.