Deirdre E. Donnelly

466 total citations
8 papers, 63 citations indexed

About

Deirdre E. Donnelly is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Deirdre E. Donnelly has authored 8 papers receiving a total of 63 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 2 papers in Molecular Biology and 1 paper in Surgery. Recurrent topics in Deirdre E. Donnelly's work include Connective tissue disorders research (3 papers), Genetic Syndromes and Imprinting (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Deirdre E. Donnelly is often cited by papers focused on Connective tissue disorders research (3 papers), Genetic Syndromes and Imprinting (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Deirdre E. Donnelly collaborates with scholars based in United Kingdom, United States and Australia. Deirdre E. Donnelly's co-authors include Vivienne McConnell, Patrick J. Morrison, Pradeep Vasudevan, Josh Willoughby, Simon Sadedin, Kate Chandler, Zornitza Stark, Anne Paterson, Peter D. Turnpenny and Jeffrey Baron and has published in prestigious journals such as European Journal of Human Genetics, Clinical Genetics and American Journal of Medical Genetics Part A.

In The Last Decade

Deirdre E. Donnelly

7 papers receiving 62 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Deirdre E. Donnelly United Kingdom	4	41	39	9	6	3	8	63
María Eugenia Rocha Germany	5	32 0.8×	34 0.9×	11 1.2×	5 0.8×	3 1.0×	8	70
Jin Fang Chai China	5	32 0.8×	27 0.7×	7 0.8×	5 0.8×	3 1.0×	13	72
Theresia Herget Germany	4	29 0.7×	22 0.6×	7 0.8×	5 0.8×	2 0.7×	6	54
Melissa A Dempsey United States	5	63 1.5×	47 1.2×	11 1.2×	5 0.8×	1 0.3×	8	86
Julian Delanne France	5	29 0.7×	29 0.7×	6 0.7×	4 0.7×	6 2.0×	8	57
Ozvan Bocher France	5	29 0.7×	42 1.1×	8 0.9×	3 0.5×		16	63
Valerie Banks United States	3	56 1.4×	56 1.4×	10 1.1×	4 0.7×	6 2.0×	3	77
Andrey N. Smirnov United States	4	25 0.6×	39 1.0×	6 0.7×	4 0.7×	2 0.7×	5	57
Ikeoluwa Osei‐Owusu United States	2	28 0.7×	32 0.8×	11 1.2×	3 0.5×	5 1.7×	4	57
Anna Lehman Canada	4	32 0.8×	30 0.8×	6 0.7×	5 0.8×		8	66

Countries citing papers authored by Deirdre E. Donnelly

Since Specialization

Citations

This map shows the geographic impact of Deirdre E. 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 E. 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 E. Donnelly more than expected).

Fields of papers citing papers by Deirdre E. Donnelly

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Deirdre E. Donnelly

This figure shows the co-authorship network connecting the top 25 collaborators of Deirdre E. Donnelly. A scholar is included among the top collaborators of Deirdre E. 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 E. Donnelly. Deirdre E. 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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8 of 8 papers shown

1.

Albaba, Shadi, Glenda Sobey, Jessica Bowen, et al.. (2025). Vascular Ehlers Danlos Syndrome and Chromosome 2q32 Microdeletion Syndrome. European Journal of Human Genetics. 33(10). 1309–1315.

2.

Lui, Julian C., Youn Hee Jee, Audrey Lee, et al.. (2018). QRICH1 mutations cause a chondrodysplasia with developmental delay. Clinical Genetics. 95(1). 160–164. 8 indexed citations

3.

Vasudevan, Pradeep, Kate Chandler, Deirdre E. Donnelly, et al.. (2017). De novo mutations in HNRNPU result in a neurodevelopmental syndrome. American Journal of Medical Genetics Part A. 173(11). 3003–3012. 30 indexed citations

4.

O’Byrne, James J., et al.. (2017). Incidence of Fragile X syndrome in Ireland. American Journal of Medical Genetics Part A. 173(3). 678–683. 2 indexed citations

5.

Donnelly, Deirdre E. & Patrick J. Morrison. (2014). Hereditary Gigantism-the biblical giant Goliath and his brothers.. PubMed. 83(2). 86–8. 3 indexed citations

6.

Donnelly, Deirdre E., Peter D. Turnpenny, & Vivienne McConnell. (2011). Phenotypic variability in a three-generation Northern Irish family with Sotos syndrome. Clinical Dysmorphology. 20(4). 175–181. 5 indexed citations

7.

Donnelly, Deirdre E., et al.. (2011). Growth retardation, developmental delay and dysmorphic features in a girl with a partial duplication of Xq. Clinical Dysmorphology. 20(2). 82–85. 2 indexed citations

8.

Donnelly, Deirdre E., Vivienne McConnell, Anne Paterson, & Patrick J. Morrison. (2010). The prevalence of thanatophoric dysplasia and lethal osteogenesis imperfecta type II in Northern Ireland - a complete population study.. PubMed. 79(3). 114–8. 13 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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