Mark I. Rees
Impact in
-
- Neuroscience and Neuropharmacology Research
- Genetic Neurodegenerative Diseases
- Developmental Neuroscience top 2%
- Neurogenesis and neuroplasticity mechanisms
Papers in
-
- Ion channel regulation and function 13
- Mitochondrial Function and Pathology 7
- Genetics 28
- Genetics and Neurodevelopmental Disorders 16
- Genomics and Rare Diseases 14
- Genetic Associations and Epidemiology 6
- Co-authors
- Richard L. M. Faull (13 shared papers)Kristin Baer (13 shared papers)Seo‐Kyung Chung (25 shared papers)Kirsten Harvey (6 shared papers)Henry J. Waldvogel (10 shared papers)Michael J. Owen (5 shared papers)Maurice A. Curtis (3 shared papers)Rhys H. Thomas (20 shared papers)
- Journals
- Journal of Neurology Neurosurgery & Psychiatry (9 papers)Human Molecular Genetics (6 papers)Epilepsy & Behavior (5 papers)Seizure (5 papers)Heart Rhythm (5 papers)
- Partner nations
- United KingdomAustraliaNew Zealand
In The Last Decade
Mark I. Rees
118 papers receiving 4.6k citations
Peers
Comparison fields: 5 of 134
- Cellular and Molecular Neuroscience 1.5k
- Developmental Neuroscience 262
- Psychiatry and Mental health 725
- Neurology 288
- Cell Biology 493
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 121 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2004 | 212 | |
| 2 | 2006 | 190 | |
| 3 | 2008 | 165 | |
| 4 | 2012 | 159 | |
| 5 | 2010 | 153 | |
| 6 | 2006 | 152 | |
| 7 | 2010 | 146 | |
| 8 | 2002 | 144 | |
| 9 | 1997 | 137 | |
| 10 | 1994 | 122 | |
| 11 | 1999 | 111 | |
| 12 | 2013 | 110 | |
| 13 | 2018 | 109 | |
| 14 | 2016 | 107 | |
| 15 | 2003 | 102 | |
| 16 | 2018 | 99 | |
| 17 | 2009 | 98 | |
| 18 | 2014 | 86 | |
| 19 | 2008 | 79 | |
| 20 | Linkage analysis of idiopathic generalized epilepsy (IGE) and marker loci on chromosome 6p in families of patients with juvenile myoclonic epilepsy: no evidence for an epilepsy locus in the HLA region. | 1993 | 76 |
About Mark I. Rees
Mark I. Rees is a scholar working on Molecular Biology, Genetics, Psychiatry and Mental health, Cellular and Molecular Neuroscience and Pediatrics, Perinatology and Child Health, having authored 121 papers that have together received 4.8k indexed citations. Recurring topics across this work include Epilepsy research and treatment (19 papers), Neuroscience and Neuropharmacology Research (17 papers), Genetics and Neurodevelopmental Disorders (16 papers), Genomics and Rare Diseases (14 papers), Ion channel regulation and function (13 papers), Mitochondrial Function and Pathology (7 papers), Cardiac electrophysiology and arrhythmias (6 papers) and Genetic Associations and Epidemiology (6 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (1.5k citations), Developmental Neuroscience (262 citations), Psychiatry and Mental health (725 citations), Neurology (288 citations) and Cell Biology (493 citations). Mark I. Rees has collaborated with scholars based in United Kingdom, Australia and New Zealand. Frequent co-authors include Richard L. M. Faull, Kristin Baer, Seo‐Kyung Chung, Kirsten Harvey, Henry J. Waldvogel, Michael J. Owen, Maurice A. Curtis, Rhys H. Thomas, Maya Topf and Jonathan R. Skinner. Their work appears in journals such as Journal of Neurology Neurosurgery & Psychiatry, Human Molecular Genetics, Epilepsy & Behavior, Seizure and Heart Rhythm.
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.