Anna O’Grady

493 citations
10 papers · 385 · h-index 9

Impact in

    • Retinal Diseases and Treatments
    • Retinal Development and Disorders
    • CRISPR and Genetic Engineering
    • Advanced biosensing and bioanalysis techniques

Papers in

    • Retinal Development and Disorders 5
    • Epigenetics and DNA Methylation 1
    • Retinoids in leukemia and cellular processes 1
    • Genomics and Rare Diseases 2
    • Genetic Syndromes and Imprinting 1
    • Genetics and Neurodevelopmental Disorders 1

Anna O’Grady

10 papers receiving 379 citations

Peers

Anna O’Grady
Comparison fields: 5 of 50
  • Ophthalmology 88
  • Molecular Biology 262
  • Genetics 102
  • Physical Therapy, Sports Therapy and Rehabilitation 14
  • Hematology 34
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Citations per field
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Citations per year

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-authors

The 25 scholars most cited alongside Anna O’Grady, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Anna O’Grady Line = papers co-authored together Anna O’Grady links everyone, so they are left out of the graph.

All Works

10 of 10 papers shown
#Work
1 2012125
2 2006118
3 200440
4 200821
5 201020
6 200919
7 201316
8 201112
9
Severe retinal degeneration in women with a c.2543del mutation in ORF15 of the RPGR gene.
201412
10 20142

About Anna O’Grady

Anna O’Grady is a scholar working on Molecular Biology, Genetics, Ophthalmology, Pediatrics, Perinatology and Child Health and Internal Medicine, having authored 10 papers that have together received 385 indexed citations. Recurring topics across this work include Retinal Development and Disorders (5 papers), Genomics and Rare Diseases (2 papers), Retinal Diseases and Treatments (2 papers), Epigenetics and DNA Methylation (1 paper), Venous Thromboembolism Diagnosis and Management (1 paper), Genetic Syndromes and Imprinting (1 paper), Genetics and Neurodevelopmental Disorders (1 paper) and Retinoids in leukemia and cellular processes (1 paper). The work is most often cited by research in Ophthalmology (88 citations), Molecular Biology (262 citations), Genetics (102 citations), Physical Therapy, Sports Therapy and Rehabilitation (14 citations) and Hematology (34 citations). Anna O’Grady has collaborated with scholars based in United Kingdom, Ireland and Czechia. Frequent co-authors include Simon Ramsden, Graeme C. Black, Niki Hart‐Holden, Alan F. Wright, Xinhua Shu, Georgina Hall, James O’Sullivan, Andrew R. Webster, Alison Jones and Sanjeev S. Bhaskar. Their work appears in journals such as European Journal of Human Genetics, Human Mutation, European Journal of Medical Genetics, Eye and Age and Ageing.

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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