Fiona Richards
Impact in
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- Genetic Neurodegenerative Diseases
- Neurology top 10%
- Neurological disorders and treatments
Papers in
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- Genetic Neurodegenerative Diseases 7
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- Mitochondrial Function and Pathology 4
- DNA Repair Mechanisms 2
- Co-authors
- Michael R. Hayden (3 shared papers)Alicia Semaka (2 shared papers)Chris Kay (2 shared papers)Emilia K. Bijlsma (2 shared papers)Jennifer A. Collins (2 shared papers)Y. Paul Goldberg (2 shared papers)Katrina Williams (1 shared paper)David Sillence (2 shared papers)
- Journals
- International Journal for Educational Integrity (1 paper)European Journal of Human Genetics (1 paper)Human Molecular Genetics (1 paper)Journal of Medical Genetics (1 paper)The American Journal of Human Genetics (1 paper)
- Partner nations
- AustraliaUnited StatesCanada
In The Last Decade
Fiona Richards
9 papers receiving 397 citations
Peers
Comparison fields: 5 of 53
- Cellular and Molecular Neuroscience 306
- Neurology 101
- Molecular Biology 233
- Genetics 61
- Clinical Biochemistry 13
Countries citing papers authored by Fiona Richards
This map shows the geographic impact of Fiona Richards'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 Fiona Richards with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Fiona Richards more than expected).
Fields of papers citing papers by Fiona Richards
This network shows the impact of papers produced by Fiona Richards. 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 Fiona Richards. The network helps show where Fiona Richards may publish in the future.
Co-authors
The 25 scholars most cited alongside Fiona Richards, 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 | 2019 | 130 | |
| 2 | 1997 | 92 | |
| 3 | 2013 | 57 | |
| 4 | 2003 | 30 | |
| 5 | Delay in the diagnosis of testicular tumours - changes over the past 18 years. | 2004 | 30 |
| 6 | 2023 | 22 | |
| 7 | 2003 | 20 | |
| 8 | 2000 | 15 | |
| 9 | 1997 | 11 | |
| 10 | 2024 | 0 |
About Fiona Richards
Fiona Richards is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology, Neurology, Pediatrics, Perinatology and Child Health and Clinical Biochemistry, having authored 10 papers that have together received 407 indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (7 papers), Mitochondrial Function and Pathology (4 papers), DNA Repair Mechanisms (2 papers), Genomics and Rare Diseases (1 paper), Neurological disorders and treatments (1 paper), Higher Education Practises and Engagement (1 paper), Higher Education Learning Practices (1 paper) and Prenatal Screening and Diagnostics (1 paper). The work is most often cited by research in Cellular and Molecular Neuroscience (306 citations), Neurology (101 citations), Molecular Biology (233 citations), Genetics (61 citations) and Clinical Biochemistry (13 citations). Fiona Richards has collaborated with scholars based in Australia, United States and Canada. Frequent co-authors include Michael R. Hayden, Alicia Semaka, Chris Kay, Emilia K. Bijlsma, Jennifer A. Collins, Y. Paul Goldberg, Katrina Williams, David Sillence, Galen E.B. Wright and Kristina Bečanović. Their work appears in journals such as International Journal for Educational Integrity, European Journal of Human Genetics, Human Molecular Genetics, Journal of Medical Genetics 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.