Olivia Knox
Impact in
-
- Genetics and Neurodevelopmental Disorders
- Genetic Syndromes and Imprinting
- Genetic Associations and Epidemiology
- Diabetes and associated disorders
Papers in
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- Epigenetics and DNA Methylation 2
- Congenital heart defects research 1
- Genetics 3
- Genetic Syndromes and Imprinting 3
- Genetic Associations and Epidemiology 1
- Co-authors
- Eilís Hannon (3 shared papers)Jonathan Mill (3 shared papers)Joe Burrage (2 shared papers)Avshalom Caspi (1 shared paper)Chloe C. Y. Wong (1 shared paper)Terrie E. Moffitt (1 shared paper)David L. Corcoran (1 shared paper)Karen Sugden (1 shared paper)
- Journals
- Scientific Reports (1 paper)Diabetes (1 paper)PLoS Genetics (1 paper)Human Molecular Genetics (1 paper)
- Partner nations
- United KingdomAustraliaCanada
In The Last Decade
Olivia Knox
4 papers receiving 254 citations
Peers
Comparison fields: 5 of 63
- Biological Psychiatry 15
- Genetics 115
- Molecular Biology 176
- Developmental Neuroscience 9
- Critical Care and Intensive Care Medicine 9
Countries citing papers authored by Olivia Knox
This map shows the geographic impact of Olivia Knox'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 Olivia Knox with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Olivia Knox more than expected).
Fields of papers citing papers by Olivia Knox
This network shows the impact of papers produced by Olivia Knox. 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 Olivia Knox. The network helps show where Olivia Knox may publish in the future.
Co-authors
The 25 scholars most cited alongside Olivia Knox, 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 | 2018 | 117 | |
| 2 | 2016 | 73 | |
| 3 | 2022 | 35 | |
| 4 | 2020 | 30 |
About Olivia Knox
Olivia Knox is a scholar working on Molecular Biology, Genetics, Surgery, Critical Care and Intensive Care Medicine and Pediatrics, Perinatology and Child Health, having authored 4 papers that have together received 255 indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (3 papers), Epigenetics and DNA Methylation (2 papers), Birth, Development, and Health (1 paper), Pancreatic function and diabetes (1 paper), Congenital heart defects research (1 paper), Anesthesia and Neurotoxicity Research (1 paper), Genetic Associations and Epidemiology (1 paper) and Enhanced Recovery After Surgery (1 paper). The work is most often cited by research in Biological Psychiatry (15 citations), Genetics (115 citations), Molecular Biology (176 citations), Developmental Neuroscience (9 citations) and Critical Care and Intensive Care Medicine (9 citations). Olivia Knox has collaborated with scholars based in United Kingdom, Australia and Canada. Frequent co-authors include Eilís Hannon, Jonathan Mill, Joe Burrage, Avshalom Caspi, Chloe C. Y. Wong, Terrie E. Moffitt, David L. Corcoran, Karen Sugden, Louise Arseneault and Daniel W. Belsky. Their work appears in journals such as Scientific Reports, Diabetes, PLoS Genetics 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.