Colin Ellis
Impact in
- Psychiatry and Mental health top 2%
- Epilepsy research and treatment
- Genetics top 5%
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genetic Associations and Epidemiology
Papers in
-
- Epilepsy research and treatment 19
- Genetics 18
- Genomics and Rare Diseases 15
- Genetics and Neurodevelopmental Disorders 13
- Genomic variations and chromosomal abnormalities 5
- Co-authors
- Samuel Frank Berkovic (10 shared papers)Slavé Petrovski (1 shared paper)Ingo Helbig (8 shared papers)Brian Litt (13 shared papers)Chloé E. Hill (6 shared papers)John Whyte (3 shared papers)Jennifer S. Myers (1 shared paper)Nathaniel H. Mayer (1 shared paper)
- Journals
- Epilepsia (10 papers)Brain (5 papers)The American Journal of Human Genetics (4 papers)Annals of Neurology (4 papers)EBioMedicine (4 papers)
- Partner nations
- United StatesAustraliaUnited Kingdom
In The Last Decade
Colin Ellis
62 papers receiving 1.4k citations
Colin Ellis's Hit Papers
Peers
Comparison fields: 5 of 85
- Psychiatry and Mental health 488
- Genetics 473
- Health Informatics 15
- Cellular and Molecular Neuroscience 151
- Neurology 101
Countries citing papers authored by Colin Ellis
This map shows the geographic impact of Colin Ellis'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 Colin Ellis with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Colin Ellis more than expected).
Fields of papers citing papers by Colin Ellis
This network shows the impact of papers produced by Colin Ellis. 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 Colin Ellis. The network helps show where Colin Ellis may publish in the future.
Co-authors
The 25 scholars most cited alongside Colin Ellis, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 65 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2019 | 218 | |
| 2 | GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture Hit paper breakdown → | 2023 | 124 |
| 3 | 2019 | 106 | |
| 4 | 2017 | 79 | |
| 5 | 2021 | 79 | |
| 6 | 2020 | 56 | |
| 7 | 2008 | 47 | |
| 8 | 2020 | 41 | |
| 9 | 2022 | 41 | |
| 10 | 2021 | 39 | |
| 11 | 2022 | 36 | |
| 12 | 2023 | 32 | |
| 13 | 2022 | 31 | |
| 14 | 2024 | 30 | |
| 15 | 2020 | 29 | |
| 16 | 2022 | 26 | |
| 17 | 2021 | 25 | |
| 18 | 2018 | 20 | |
| 19 | 2021 | 20 | |
| 20 | 2008 | 18 |
About Colin Ellis
Colin Ellis is a scholar working on Psychiatry and Mental health, Genetics, Neurology, Genetics and Rheumatology, having authored 65 papers that have together received 1.4k indexed citations. Recurring topics across this work include Epilepsy research and treatment (19 papers), Genomics and Rare Diseases (15 papers), Genetics and Neurodevelopmental Disorders (13 papers), Genomic variations and chromosomal abnormalities (5 papers), Traumatic Brain Injury Research (3 papers), Neurological disorders and treatments (3 papers), Topic Modeling (3 papers) and Glycogen Storage Diseases and Myoclonus (2 papers). The work is most often cited by research in Psychiatry and Mental health (488 citations), Genetics (473 citations), Health Informatics (15 citations), Cellular and Molecular Neuroscience (151 citations) and Neurology (101 citations). Colin Ellis has collaborated with scholars based in United States, Australia and United Kingdom. Frequent co-authors include Samuel Frank Berkovic, Slavé Petrovski, Ingo Helbig, Brian Litt, Chloé E. Hill, John Whyte, Jennifer S. Myers, Nathaniel H. Mayer, Tessa Hart and David J. Lewis-Smith. Their work appears in journals such as Epilepsia, Brain, The American Journal of Human Genetics, Annals of Neurology and EBioMedicine.
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.