Sandy Goodburn
Impact in
- Genetics top 10%
- Genetic diversity and population structure
- Connective tissue disorders research
- Genetic Mapping and Diversity in Plants and Animals
- Genetics and Neurodevelopmental Disorders
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- Genetic Neurodegenerative Diseases
Papers in
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- Genetic Neurodegenerative Diseases 6
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- Mitochondrial Function and Pathology 3
- Fungal and yeast genetics research 1
- Co-authors
- David C. Rubinsztein (7 shared papers)Jayne Leggo (6 shared papers)William Amos (2 shared papers)M.A. Ferguson‐Smith (5 shared papers)Sanjeev Jain (3 shared papers)Christopher A. Ross (2 shared papers)Russell L. Margolis (1 shared paper)David Barton (3 shared papers)
- Journals
- Prenatal Diagnosis (3 papers)Nature Genetics (2 papers)Ophthalmology (1 paper)Journal of Cataract & Refractive Surgery (1 paper)Human Molecular Genetics (1 paper)
- Partner nations
- United KingdomUnited StatesIndia
In The Last Decade
Sandy Goodburn
12 papers receiving 613 citations
Peers
Comparison fields: 5 of 89
- Genetics 275
- Cellular and Molecular Neuroscience 178
- Neurology 61
- Molecular Biology 266
- Ophthalmology 28
Countries citing papers authored by Sandy Goodburn
This map shows the geographic impact of Sandy Goodburn'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 Sandy Goodburn with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sandy Goodburn more than expected).
Fields of papers citing papers by Sandy Goodburn
This network shows the impact of papers produced by Sandy Goodburn. 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 Sandy Goodburn. The network helps show where Sandy Goodburn may publish in the future.
Co-authors
The 25 scholars most cited alongside Sandy Goodburn, 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 | 1995 | 248 | |
| 2 | 1994 | 108 | |
| 3 | 2007 | 87 | |
| 4 | 1994 | 60 | |
| 5 | 2000 | 57 | |
| 6 | 1995 | 36 | |
| 7 | 1996 | 21 | |
| 8 | 2003 | 16 | |
| 9 | 2010 | 9 | |
| 10 | 2018 | 4 | |
| 11 | 1995 | 3 | |
| 12 | 1996 | 2 |
About Sandy Goodburn
Sandy Goodburn is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health and Infectious Diseases, having authored 12 papers that have together received 651 indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (6 papers), Genetics and Neurodevelopmental Disorders (3 papers), Mitochondrial Function and Pathology (3 papers), Prenatal Screening and Diagnostics (3 papers), Disability Rights and Representation (1 paper), Neurological disorders and treatments (1 paper), Childhood Cancer Survivors' Quality of Life (1 paper) and Fungal and yeast genetics research (1 paper). The work is most often cited by research in Genetics (275 citations), Cellular and Molecular Neuroscience (178 citations), Neurology (61 citations), Molecular Biology (266 citations) and Ophthalmology (28 citations). Sandy Goodburn has collaborated with scholars based in United Kingdom, United States and India. Frequent co-authors include David C. Rubinsztein, Jayne Leggo, William Amos, M.A. Ferguson‐Smith, Sanjeev Jain, Christopher A. Ross, Russell L. Margolis, David Barton, Martin P. Snead and Arabella Poulson. Their work appears in journals such as Prenatal Diagnosis, Nature Genetics, Ophthalmology, Journal of Cataract & Refractive Surgery and Human Molecular 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.