Mark I. Rees
Impact in
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- Neuroscience and Neuropharmacology Research
- Psychiatry and Mental health top 1%
- Epilepsy research and treatment
Papers in
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- Epilepsy research and treatment 27
- Genetics 45
- Genetics and Neurodevelopmental Disorders 30
- Genomics and Rare Diseases 22
- Genomic variations and chromosomal abnormalities 13
- Genetic Associations and Epidemiology 8
- Co-authors
- Richard L. M. Faull (13 shared papers)Seo‐Kyung Chung (26 shared papers)Kristin Baer (13 shared papers)Michael Owen (13 shared papers)Kirsten Harvey (6 shared papers)Henry John Waldvogel (10 shared papers)Rhys Huw Thomas (18 shared papers)Maurice A. Curtis (3 shared papers)
- Journals
- The American Journal of Human Genetics (9 papers)Journal of Neurology Neurosurgery & Psychiatry (8 papers)Human Molecular Genetics (7 papers)Brain (6 papers)Epilepsy & Behavior (5 papers)
- Partner nations
- United KingdomAustraliaNew Zealand
In The Last Decade
Mark I. Rees
149 papers receiving 6.5k citations
Mark I. Rees's Hit Papers
Peers
Comparison fields: 5 of 147
- Cellular and Molecular Neuroscience 1.9k
- Psychiatry and Mental health 1.1k
- Developmental Neuroscience 279
- Genetics 1.4k
- Neurology 321
Countries citing papers authored by Mark I. Rees
This map shows the geographic impact of Mark I. Rees'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 Mark I. Rees with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mark I. Rees more than expected).
Fields of papers citing papers by Mark I. Rees
This network shows the impact of papers produced by Mark I. Rees. 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 Mark I. Rees. The network helps show where Mark I. Rees may publish in the future.
Co-authors
The 25 scholars most cited alongside Mark I. Rees, 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 152 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2004 | 222 | |
| 2 | 2019 | 218 | |
| 3 | 2006 | 195 | |
| 4 | 2017 | 173 | |
| 5 | 2008 | 170 | |
| 6 | 2010 | 169 | |
| 7 | 2012 | 169 | |
| 8 | 1996 | 166 | |
| 9 | 2006 | 163 | |
| 10 | 2010 | 155 | |
| 11 | 2002 | 148 | |
| 12 | 1997 | 138 | |
| 13 | 1994 | 125 | |
| 14 | GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture Hit paper breakdown → | 2023 | 124 |
| 15 | 2013 | 123 | |
| 16 | 1999 | 119 | |
| 17 | 2018 | 115 | |
| 18 | 2016 | 115 | |
| 19 | 2019 | 113 | |
| 20 | 2010 | 112 |
About Mark I. Rees
Mark I. Rees is a scholar working on Psychiatry and Mental health, Genetics, Cellular and Molecular Neuroscience, Molecular Biology and Pediatrics, Perinatology and Child Health, having authored 152 papers that have together received 6.8k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (30 papers), Epilepsy research and treatment (27 papers), Genomics and Rare Diseases (22 papers), Neuroscience and Neuropharmacology Research (22 papers), Ion channel regulation and function (15 papers), Genomic variations and chromosomal abnormalities (13 papers), Mitochondrial Function and Pathology (8 papers) and Genetic Associations and Epidemiology (8 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (1.9k citations), Psychiatry and Mental health (1.1k citations), Developmental Neuroscience (279 citations), Genetics (1.4k citations) and Neurology (321 citations). Mark I. Rees has collaborated with scholars based in United Kingdom, Australia and New Zealand. Frequent co-authors include Richard L. M. Faull, Seo‐Kyung Chung, Kristin Baer, Michael Owen, Kirsten Harvey, Henry John Waldvogel, Rhys Huw Thomas, Maurice A. Curtis, Maya Topf and Jonathan Robert Skinner. Their work appears in journals such as The American Journal of Human Genetics, Journal of Neurology Neurosurgery & Psychiatry, Human Molecular Genetics, Brain and Epilepsy & Behavior.
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.