Una Maye

1.1k total citations
4 papers, 38 citations indexed

About

Una Maye is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Una Maye has authored 4 papers receiving a total of 38 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 3 papers in Genetics and 1 paper in Pulmonary and Respiratory Medicine. Recurrent topics in Una Maye's work include Genomic variations and chromosomal abnormalities (3 papers), Advanced biosensing and bioanalysis techniques (2 papers) and Medical Imaging and Pathology Studies (1 paper). Una Maye is often cited by papers focused on Genomic variations and chromosomal abnormalities (3 papers), Advanced biosensing and bioanalysis techniques (2 papers) and Medical Imaging and Pathology Studies (1 paper). Una Maye collaborates with scholars based in United Kingdom, Netherlands and Australia. Una Maye's co-authors include Alan Fryer, Meredith Wilson, Lisa Ewans, Nicola Foulds, Gilles Morin, Jed Hawe, Shane McKee, Aline Receveur, Henri Copin and David Pilling and has published in prestigious journals such as Investigative Ophthalmology & Visual Science, Clinical Genetics and American Journal of Medical Genetics Part A.

In The Last Decade

Una Maye

4 papers receiving 26 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Una Maye United Kingdom	3	27	16	10	7	4	4	38
M. Teresa Darnaude Spain	4	21 0.8×	14 0.9×	15 1.5×	7 1.0×	5 1.3×	7	36
Stephen Hellens United Kingdom	3	21 0.8×	10 0.6×	5 0.5×	6 0.9×	3 0.8×	4	32
Dagmar Huhle Germany	4	22 0.8×	22 1.4×	26 2.6×	5 0.7×	3 0.8×	5	48
Arveen Kamath United Kingdom	3	22 0.8×	18 1.1×	7 0.7×	5 0.7×	7 1.8×	4	33
Francesca Inzana Italy	3	27 1.0×	18 1.1×	8 0.8×	5 0.7×	2 0.5×	3	39
Karol Rubin United States	3	24 0.9×	21 1.3×	11 1.1×	5 0.7×	2 0.5×	3	36
Andrea Seeley United States	5	31 1.1×	17 1.1×	13 1.3×	4 0.6×	5 1.3×	8	57
Marie‐Line Jacquemont France	2	17 0.6×	13 0.8×	5 0.5×	3 0.4×	8 2.0×	2	29
Jayson Rodriguez United States	3	39 1.4×	25 1.6×	10 1.0×	7 1.0×	2 0.5×	4	52
Naomi Yachelevich United States	5	20 0.7×	19 1.2×	4 0.4×	4 0.6×	2 0.5×	6	33

Countries citing papers authored by Una Maye

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Una Maye

This figure shows the co-authorship network connecting the top 25 collaborators of Una Maye. A scholar is included among the top collaborators of Una Maye 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 Una Maye. Una Maye is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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4 of 4 papers shown

1.

Jedraszak, Guillaume, Bénédicte Demeer, Michèle Mathieu‐Dramard, et al.. (2015). Clinical and molecular characterization of the 20q11.2 microdeletion syndrome: Six new patients. American Journal of Medical Genetics Part A. 167(3). 504–511. 17 indexed citations

2.

Coupland, Sarah E., et al.. (2012). Quality Assessment Of Multiplex Ligation-dependent Probe Amplification (mlpa) In Uveal Melanoma By Comparison With Array Comparative Genomic Hybridization (acgh) And Microsatellite Analysis (msa). Investigative Ophthalmology & Visual Science. 53(14). 5252–5252. 1 indexed citations

3.

Day, Richard O., Dian Donnai, Alan Fryer, et al.. (2008). A clinical and genetic study of the Say/Barber/Biesecker/Young‐Simpson type of Ohdo syndrome. Clinical Genetics. 74(5). 434–444. 17 indexed citations

4.

Fryer, Alan, et al.. (2004). Isochromosome 20p associated with multiple congenital abnormalities. Clinical Dysmorphology. 14(1). 49–50. 3 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.

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