Deirdre Donnelly

1.6k total citations
4 papers, 38 citations indexed

About

Deirdre Donnelly is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Deirdre Donnelly has authored 4 papers receiving a total of 38 indexed citations (citations by other indexed papers that have themselves been cited), including 2 papers in Molecular Biology, 2 papers in Genetics and 1 paper in Oncology. Recurrent topics in Deirdre Donnelly's work include RNA modifications and cancer (2 papers), Genomics and Rare Diseases (2 papers) and Radiomics and Machine Learning in Medical Imaging (1 paper). Deirdre Donnelly is often cited by papers focused on RNA modifications and cancer (2 papers), Genomics and Rare Diseases (2 papers) and Radiomics and Machine Learning in Medical Imaging (1 paper). Deirdre Donnelly collaborates with scholars based in United Kingdom, Ireland and Poland. Deirdre Donnelly's co-authors include Graeme C. Black, Jill Urquhart, Helen Mundy, Sarah Waller, Mark T. Handley, David Fitzpatrick, Rachel L. Taylor, Jamie M. Ellingford, Charu Deshpande and Gisela Wilcox and has published in prestigious journals such as Investigative Ophthalmology & Visual Science, Journal of Thoracic Oncology and European Journal of Human Genetics.

In The Last Decade

Deirdre Donnelly

4 papers receiving 37 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Deirdre Donnelly United Kingdom	3	27	7	4	4	3	4	38
Kirsti Kvaløy Norway	2	17 0.6×	5 0.7×	6 1.5×	4 1.0×	3 1.0×	3	38
Erh‐Chan Yeh Taiwan	2	24 0.9×	12 1.7×	6 1.5×	2 0.5×	6 2.0×	3	38
Hannah J. Perrin United States	2	18 0.7×	8 1.1×	2 0.5×	4 1.0×	6 2.0×	3	27
Cecilia Rivas United States	3	31 1.1×	6 0.9×	2 0.5×	4 1.0×	2 0.7×	3	40
Sadegheh Haghshenas Canada	4	33 1.2×	16 2.3×	2 0.5×	3 0.8×	4 1.3×	9	45
Clément Chatelain France	4	11 0.4×	13 1.9×	3 0.8×	2 0.5×	2 0.7×	6	35
Friedhelm Hildebrandt United States	3	23 0.9×	18 2.6×	3 0.8×	2 0.5×	4 1.3×	4	29
Milena Jakimovska North Macedonia	4	19 0.7×	10 1.4×	4 1.0×	1 0.3×	5 1.7×	7	36
Tara Akhtarkhavari Iran	3	20 0.7×	4 0.6×	4 1.0×	3 0.8×	13 4.3×	5	35
Daria Rukina Switzerland	1	25 0.9×	6 0.9×	1 0.3×	9 2.3×	3 1.0×	2	36

Countries citing papers authored by Deirdre Donnelly

Since Specialization

Citations

This map shows the geographic impact of Deirdre Donnelly'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 Deirdre Donnelly with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Deirdre Donnelly more than expected).

Fields of papers citing papers by Deirdre Donnelly

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Deirdre Donnelly. 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 Deirdre Donnelly. The network helps show where Deirdre Donnelly may publish in the future.

Co-authorship network of co-authors of Deirdre Donnelly

This figure shows the co-authorship network connecting the top 25 collaborators of Deirdre Donnelly. A scholar is included among the top collaborators of Deirdre Donnelly 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 Deirdre Donnelly. Deirdre Donnelly 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.

Ochoa, Eguzkine, Magdalena Badura‐Stronka, Deirdre Donnelly, et al.. (2023). Germline pathogenic variants in HNRNPU are associated with alterations in blood methylome. European Journal of Human Genetics. 31(9). 1040–1047. 5 indexed citations

2.

McVeigh, Terri, Deirdre Donnelly, Elizabeth A. Jones, et al.. (2019). Towards establishing consistency in triage in a tertiary specialty. European Journal of Human Genetics. 27(4). 547–555. 8 indexed citations

3.

Taylor, Rachel L., Mark T. Handley, Sarah Waller, et al.. (2017). Novel PEX11B Mutations Extend the Peroxisome Biogenesis Disorder 14B Phenotypic Spectrum and Underscore Congenital Cataract as an Early Feature. Investigative Ophthalmology & Visual Science. 58(1). 594–594. 24 indexed citations

4.

Niemeijer, Anna-Larissa N., Egbert F. Smit, Guus A.M.S. van Dongen, et al.. (2017). MA 05.07 Whole Body PD-1 and PD-L1 PET in Pts with NSCLC. Journal of Thoracic Oncology. 12(11). S1817–S1817. 1 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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