Joanna Kennedy
- Co-authors
- David FitzpatrickGraham E. HolderAnthony T. MooreKathleen A. WilliamsonAnthony G. RobsonVeronica van HeyningenAndrew R. WebsterRobert Henderson
- Topics
- Retinal Development and Disorders (2 papers)Genetics and Neurodevelopmental Disorders (2 papers)Genomics and Rare Diseases (1 paper)
- Cited by
- OphthalmologyGenetics
- Partner nations
- United KingdomUnited States
In The Last Decade
Joanna Kennedy
4 papers receiving 68 citations
Peers
Comparison fields: 5 of 22
- Molecular Biology 48
- Genetics 34
- Ophthalmology 17
- Endocrinology, Diabetes and Metabolism 10
- Genetics 8
Countries citing papers authored by Joanna Kennedy
This map shows the geographic impact of Joanna Kennedy'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 Joanna Kennedy with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Joanna Kennedy more than expected).
Fields of papers citing papers by Joanna Kennedy
This network shows the impact of papers produced by Joanna Kennedy. 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 Joanna Kennedy. The network helps show where Joanna Kennedy may publish in the future.
Co-authorship network of co-authors of Joanna Kennedy
This figure shows the co-authorship network connecting the top 25 collaborators of Joanna Kennedy. A scholar is included among the top collaborators of Joanna Kennedy 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 Joanna Kennedy. Joanna Kennedy is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 0 | |
| 2 | 6 | |
| 3 | 6 | |
| 4 | 6 | |
| 5 | A rare de novo nonsense mutation in OTX2 causes early onset retinal dystrophy and pituitary dysfunction. | 51 |
About Joanna Kennedy
Joanna Kennedy is a scholar working on Ophthalmology, Genetics and Molecular Biology, having authored 5 papers that have together received 69 indexed citations. Recurring topics across this work include Retinal Development and Disorders (2 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Genomics and Rare Diseases (1 paper). The work is most often cited by research in Ophthalmology (17 citations), Genetics (34 citations) and Genetics (8 citations). Joanna Kennedy has collaborated with scholars based in United Kingdom and United States. Frequent co-authors include David Fitzpatrick, Graham E. Holder, Anthony T. Moore, Kathleen A. Williamson, Anthony G. Robson, Veronica van Heyningen, Andrew R. Webster, Robert Henderson, Ruth Newbury‐Ecob and Ling Zhi Heng. Their work appears in journals such as PLoS Genetics, European Journal of Human Genetics and Clinical Genetics.
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.