Mark Greenslade
Impact in
- Genetics top 10%
- Glioma Diagnosis and Treatment
- Neurogenetic and Muscular Disorders Research
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- Hereditary Neurological Disorders
Papers in
-
- Retinal Development and Disorders 1
- Genetics 3
- Glioma Diagnosis and Treatment 2
- Genomics and Rare Diseases 1
- Co-authors
- Hayley Ellis (2 shared papers)Kathreena M. Kurian (2 shared papers)Andrea Sottoriva (1 shared paper)Inmaculada Spiteri (1 shared paper)Alan Fryer (1 shared paper)Claire Bailey (1 shared paper)Rita Horváth (2 shared papers)Roger G. Whittaker (1 shared paper)
- Journals
- European Journal of Medical Genetics (1 paper)npj Genomic Medicine (1 paper)The Medical Journal of Australia (1 paper)Frontiers in Oncology (1 paper)Neurology (1 paper)
- Partner nations
- United KingdomNew ZealandAustralia
In The Last Decade
Mark Greenslade
10 papers receiving 252 citations
Peers
Comparison fields: 5 of 47
- Genetics 82
- Cellular and Molecular Neuroscience 61
- Neurology 38
- Neurology 17
- Cancer Research 28
Countries citing papers authored by Mark Greenslade
This map shows the geographic impact of Mark Greenslade'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 Greenslade with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mark Greenslade more than expected).
Fields of papers citing papers by Mark Greenslade
This network shows the impact of papers produced by Mark Greenslade. 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 Greenslade. The network helps show where Mark Greenslade may publish in the future.
Co-authors
The 25 scholars most cited alongside Mark Greenslade, 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 | 2015 | 81 | |
| 2 | 2017 | 69 | |
| 3 | 2015 | 44 | |
| 4 | 2015 | 28 | |
| 5 | 2021 | 14 | |
| 6 | 2020 | 12 | |
| 7 | 2024 | 9 | |
| 8 | 2023 | 6 | |
| 9 | 2025 | 2 | |
| 10 | 2016 | 1 |
About Mark Greenslade
Mark Greenslade is a scholar working on Molecular Biology, Genetics, Surgery, Cellular and Molecular Neuroscience and Cancer Research, having authored 10 papers that have together received 266 indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (2 papers), Hereditary Neurological Disorders (2 papers), Glioma Diagnosis and Treatment (2 papers), Genomics and Rare Diseases (1 paper), Mathematical Biology Tumor Growth (1 paper), Microtubule and mitosis dynamics (1 paper), Retinal Development and Disorders (1 paper) and Lymphoma Diagnosis and Treatment (1 paper). The work is most often cited by research in Genetics (82 citations), Cellular and Molecular Neuroscience (61 citations), Neurology (38 citations), Neurology (17 citations) and Cancer Research (28 citations). Mark Greenslade has collaborated with scholars based in United Kingdom, New Zealand and Australia. Frequent co-authors include Hayley Ellis, Kathreena M. Kurian, Andrea Sottoriva, Inmaculada Spiteri, Alan Fryer, Claire Bailey, Rita Horváth, Roger G. Whittaker, Jennifer Duff and Angela Pyle. Their work appears in journals such as European Journal of Medical Genetics, npj Genomic Medicine, The Medical Journal of Australia, Frontiers in Oncology 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.