Joe Rainger
Impact in
- Genetics top 10%
- Ocular Disorders and Treatments
- Congenital Ear and Nasal Anomalies
- Ophthalmology top 10%
- Glaucoma and retinal disorders
Papers in
-
- Hedgehog Signaling Pathway Studies 4
- Developmental Biology and Gene Regulation 4
- Wnt/β-catenin signaling in development and cancer 3
- Retinal Development and Disorders 3
- Genetics 11
- Ocular Disorders and Treatments 6
- Congenital Ear and Nasal Anomalies 2
- Co-authors
- David Fitzpatrick (7 shared papers)Kathleen A. Williamson (5 shared papers)Veronica van Heyningen (4 shared papers)Mario Messina (2 shared papers)Freddie H. Sharkey (2 shared papers)Judy Fantes (2 shared papers)Peter D. Turnpenny (2 shared papers)Ann Hever (2 shared papers)
- Journals
- Human Molecular Genetics (4 papers)Scientific Reports (2 papers)PLoS Genetics (2 papers)Human Mutation (1 paper)The American Journal of Human Genetics (1 paper)
- Partner nations
- United KingdomUnited StatesAustralia
In The Last Decade
Joe Rainger
18 papers receiving 491 citations
Peers
Comparison fields: 5 of 58
- Genetics 251
- Genetics 71
- Ophthalmology 55
- Molecular Biology 289
- Cell Biology 65
Countries citing papers authored by Joe Rainger
This map shows the geographic impact of Joe Rainger'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 Joe Rainger with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Joe Rainger more than expected).
Fields of papers citing papers by Joe Rainger
This network shows the impact of papers produced by Joe Rainger. 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 Joe Rainger. The network helps show where Joe Rainger may publish in the future.
Co-authors
The 25 scholars most cited alongside Joe Rainger, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2006 | 158 | |
| 2 | 2014 | 77 | |
| 3 | 2013 | 46 | |
| 4 | 2020 | 33 | |
| 5 | 2019 | 32 | |
| 6 | 2016 | 32 | |
| 7 | 2014 | 23 | |
| 8 | 2018 | 21 | |
| 9 | 2017 | 20 | |
| 10 | 2019 | 12 | |
| 11 | 2018 | 10 | |
| 12 | 2021 | 10 | |
| 13 | 2013 | 9 | |
| 14 | 2006 | 7 | |
| 15 | 2023 | 4 | |
| 16 | 2023 | 3 | |
| 17 | 2025 | 1 | |
| 18 | 2025 | 1 |
About Joe Rainger
Joe Rainger is a scholar working on Molecular Biology, Genetics, Radiology, Nuclear Medicine and Imaging, Surgery and Genetics, having authored 18 papers that have together received 499 indexed citations. Recurring topics across this work include Ocular Disorders and Treatments (6 papers), Hedgehog Signaling Pathway Studies (4 papers), Developmental Biology and Gene Regulation (4 papers), Wnt/β-catenin signaling in development and cancer (3 papers), Retinal Development and Disorders (3 papers), Congenital Ear and Nasal Anomalies (2 papers), Glaucoma and retinal disorders (2 papers) and Corneal Surgery and Treatments (2 papers). The work is most often cited by research in Genetics (251 citations), Genetics (71 citations), Ophthalmology (55 citations), Molecular Biology (289 citations) and Cell Biology (65 citations). Joe Rainger has collaborated with scholars based in United Kingdom, United States and Australia. Frequent co-authors include David Fitzpatrick, Kathleen A. Williamson, Veronica van Heyningen, Mario Messina, Freddie H. Sharkey, Judy Fantes, Peter D. Turnpenny, Ann Hever, Adele Schneider and Niolette I. McGill. Their work appears in journals such as Human Molecular Genetics, Scientific Reports, PLoS Genetics, Human Mutation and The American Journal of Human 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.