Mark F. Bennett
Impact in
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- Genetic Neurodegenerative Diseases
- Genetics top 10%
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
Papers in
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- RNA Research and Splicing 3
- Mitochondrial Function and Pathology 3
- RNA modifications and cancer 3
- Genetics 8
- Genetics and Neurodevelopmental Disorders 7
- Genomics and Rare Diseases 3
- Co-authors
- Melanie Bahlo (17 shared papers)Samuel F. Berkovic (13 shared papers)Ingrid E. Scheffer (13 shared papers)Karen Oliver (3 shared papers)Bronwyn E. Grinton (3 shared papers)A. Melatos (3 shared papers)Martin B. Delatycki (1 shared paper)Paul J. Lockhart (1 shared paper)
- Journals
- Epilepsia (4 papers)European Journal of Human Genetics (3 papers)Epilepsia Open (2 papers)The American Journal of Human Genetics (2 papers)Neurology (1 paper)
- Partner nations
- AustraliaUnited StatesCanada
In The Last Decade
Mark F. Bennett
24 papers receiving 430 citations
Peers
Comparison fields: 5 of 49
- Cellular and Molecular Neuroscience 142
- Genetics 166
- Psychiatry and Mental health 52
- Molecular Biology 183
- Neurology 36
Countries citing papers authored by Mark F. Bennett
This map shows the geographic impact of Mark F. Bennett'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 F. Bennett with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mark F. Bennett more than expected).
Fields of papers citing papers by Mark F. Bennett
This network shows the impact of papers produced by Mark F. Bennett. 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 F. Bennett. The network helps show where Mark F. Bennett may publish in the future.
Co-authors
The 25 scholars most cited alongside Mark F. Bennett, 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 28 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2020 | 98 | |
| 2 | 2023 | 73 | |
| 3 | 2018 | 68 | |
| 4 | 2013 | 29 | |
| 5 | 2020 | 22 | |
| 6 | 2017 | 21 | |
| 7 | 2022 | 21 | |
| 8 | 2020 | 15 | |
| 9 | 2017 | 15 | |
| 10 | 2021 | 9 | |
| 11 | 2022 | 9 | |
| 12 | 2021 | 7 | |
| 13 | 2022 | 7 | |
| 14 | 2023 | 6 | |
| 15 | 2021 | 6 | |
| 16 | 2020 | 5 | |
| 17 | 2017 | 4 | |
| 18 | 2022 | 4 | |
| 19 | 4 Stochastic microhertz gravitational radiation from stellar convection | 2016 | 4 |
| 20 | 2013 | 3 |
About Mark F. Bennett
Mark F. Bennett is a scholar working on Molecular Biology, Genetics, Cellular and Molecular Neuroscience, Psychiatry and Mental health and Astronomy and Astrophysics, having authored 28 papers that have together received 431 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (7 papers), Epilepsy research and treatment (5 papers), Genetic Neurodegenerative Diseases (4 papers), RNA Research and Splicing (3 papers), Genomics and Rare Diseases (3 papers), Mitochondrial Function and Pathology (3 papers), RNA modifications and cancer (3 papers) and Pulsars and Gravitational Waves Research (3 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (142 citations), Genetics (166 citations), Psychiatry and Mental health (52 citations), Molecular Biology (183 citations) and Neurology (36 citations). Mark F. Bennett has collaborated with scholars based in Australia, United States and Canada. Frequent co-authors include Melanie Bahlo, Samuel F. Berkovic, Ingrid E. Scheffer, Karen Oliver, Bronwyn E. Grinton, A. Melatos, Martin B. Delatycki, Paul J. Lockhart, Rick M. Tankard and P. D. Lasky. Their work appears in journals such as Epilepsia, European Journal of Human Genetics, Epilepsia Open, The American Journal of Human Genetics and Neurology.
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.