Anna O’Grady

489 total citations
10 papers, 383 citations indexed

About

Anna O’Grady is a scholar working on Molecular Biology, Ophthalmology and Genetics. According to data from OpenAlex, Anna O’Grady has authored 10 papers receiving a total of 383 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 5 papers in Ophthalmology and 3 papers in Genetics. Recurrent topics in Anna O’Grady's work include Retinal Development and Disorders (6 papers), Retinal Diseases and Treatments (5 papers) and Retinoids in leukemia and cellular processes (2 papers). Anna O’Grady is often cited by papers focused on Retinal Development and Disorders (6 papers), Retinal Diseases and Treatments (5 papers) and Retinoids in leukemia and cellular processes (2 papers). Anna O’Grady collaborates with scholars based in United Kingdom, Ireland and Czechia. Anna O’Grady's co-authors include Simon Ramsden, Graeme C. Black, Niki Hart‐Holden, Alison Jones, Georgina Hall, Alan F. Wright, Xinhua Shu, James O’Sullivan, Andrew R. Webster and Jonathan E. Dickerson and has published in prestigious journals such as British Journal of Haematology, Age and Ageing and Journal of Medical Genetics.

In The Last Decade

Anna O’Grady

10 papers receiving 376 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Anna O’Grady United Kingdom	9	290	163	133	36	34	10	383
Jean-Louis Dufier France	7	173 0.6×	85 0.5×	61 0.5×	8 0.2×	37 1.1×	8	288
Anand Saggar United Kingdom	8	280 1.0×	22 0.1×	231 1.7×	14 0.4×	7 0.2×	15	415
Kathy H. C. Wu Australia	7	132 0.5×	168 1.0×	24 0.2×	4 0.1×	82 2.4×	23	309
Irene Marcos Spain	11	212 0.7×	53 0.3×	85 0.6×	3 0.1×	8 0.2×	21	290
M. A. D. Tilanus Netherlands	7	306 1.1×	137 0.8×	71 0.5×	8 0.2×	132 3.9×	12	470
Lvzhen Huang China	13	258 0.9×	234 1.4×	18 0.1×	10 0.3×	127 3.7×	43	460
Francesco Benedicenti Italy	10	165 0.6×	27 0.2×	123 0.9×	4 0.1×	9 0.3×	21	417
Sarah Meredith United Kingdom	9	102 0.4×	148 0.9×	162 1.2×	14 0.4×	149 4.4×	11	345
D. B. van Dorp Netherlands	13	248 0.9×	62 0.4×	149 1.1×	19 0.5×	24 0.7×	21	409
Sara Moore Canada	8	95 0.3×	102 0.6×	119 0.9×	3 0.1×	46 1.4×	10	338

Countries citing papers authored by Anna O’Grady

Since Specialization

Citations

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

Fields of papers citing papers by Anna O’Grady

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Anna O’Grady. 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 Anna O’Grady. The network helps show where Anna O’Grady may publish in the future.

Co-authorship network of co-authors of Anna O’Grady

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

All Works

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10 of 10 papers shown

Kousal, Bohdan, et al.. (2014). Severe retinal degeneration in females with c.2543del mutation in the RPGR gene. Acta Ophthalmologica. 92(s253). 0–0. 2 indexed citations

Kousal, Bohdan, Pavlína Skalická, Tracy Fletcher, et al.. (2014). Severe retinal degeneration in women with a c.2543del mutation in ORF15 of the RPGR gene.. PubMed. 20. 1307–17. 12 indexed citations

Ramsden, Simon, Anna O’Grady, Tracy Fletcher, et al.. (2013). A clinical molecular genetic service for United Kingdom families with choroideraemia. European Journal of Medical Genetics. 56(8). 432–438. 16 indexed citations

O’Sullivan, James, Sanjeev S. Bhaskar, Jonathan E. Dickerson, et al.. (2012). A paradigm shift in the delivery of services for diagnosis of inherited retinal disease. Journal of Medical Genetics. 49(5). 322–326. 124 indexed citations

Boyle, Jennifer, Malcolm Hawkins, David Barton, et al.. (2011). Establishment of the first WHO international genetic reference panel for Prader Willi and Angelman syndromes. European Journal of Human Genetics. 19(8). 857–864. 12 indexed citations

Hawkins, Malcolm, Jennifer Boyle, Rob Elles, et al.. (2010). Preparation and validation of the first WHO international genetic reference panel for Fragile X syndrome. European Journal of Human Genetics. 19(1). 10–17. 20 indexed citations

O’Grady, Anna, et al.. (2009). Phenotypic progression in X-linked retinitis pigmentosa secondary to a novel mutation in the RPGR gene. Eye. 23(3). 519–521. 19 indexed citations

Horgan, Frances, et al.. (2008). The effects of usual footwear on balance amongst elderly women attending a day hospital. Age and Ageing. 38(1). 62–67. 21 indexed citations

Shu, Xinhua, Graeme C. Black, Niki Hart‐Holden, et al.. (2006). RPGRmutation analysis and disease: an update. Human Mutation. 28(4). 322–328. 117 indexed citations

10.

Ashton, Fern, et al.. (2004). Mutations within the protein Z‐dependent protease inhibitor gene are associated with venous thromboembolic disease: a new form of thrombophilia. British Journal of Haematology. 127(2). 190–194. 40 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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