Gemma Poke
Impact in
- Neurology top 10%
- Neurofibromatosis and Schwannoma Cases
-
- Glioma Diagnosis and Treatment
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
Papers in
-
- Mitochondrial Function and Pathology 3
- Chromatin Remodeling and Cancer 3
- Genetics 9
- Neurogenetic and Muscular Disorders Research 4
- Genomics and Rare Diseases 3
- Genetics and Neurodevelopmental Disorders 2
- Co-authors
- Miriam J. Smith (2 shared papers)Saba Sharif (2 shared papers)Daniel Rawluk (2 shared papers)Diana Eccles (2 shared papers)D. Gareth Evans (2 shared papers)Sanjeev S. Bhaskar (2 shared papers)David Fitzpatrick (2 shared papers)Kristen D. Hadfield (2 shared papers)
- Journals
- Neuromuscular Disorders (3 papers)Neuroepidemiology (1 paper)Neurology (1 paper)Stem Cell Research (1 paper)Journal of Medical Genetics (1 paper)
- Partner nations
- New ZealandAustraliaUnited Kingdom
In The Last Decade
Gemma Poke
24 papers receiving 436 citations
Peers
Comparison fields: 5 of 52
- Neurology 93
- Genetics 58
- Epidemiology 118
- Genetics 79
- Pathology and Forensic Medicine 46
Countries citing papers authored by Gemma Poke
This map shows the geographic impact of Gemma Poke'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 Gemma Poke with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Gemma Poke more than expected).
Fields of papers citing papers by Gemma Poke
This network shows the impact of papers produced by Gemma Poke. 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 Gemma Poke. The network helps show where Gemma Poke may publish in the future.
Co-authors
The 25 scholars most cited alongside Gemma Poke, 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 24 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2013 | 184 | |
| 2 | 2022 | 49 | |
| 3 | 2016 | 42 | |
| 4 | 2018 | 33 | |
| 5 | 2019 | 30 | |
| 6 | 2012 | 19 | |
| 7 | 2016 | 13 | |
| 8 | 2022 | 12 | |
| 9 | 2019 | 12 | |
| 10 | 2012 | 11 | |
| 11 | 2019 | 7 | |
| 12 | 2021 | 6 | |
| 13 | 2019 | 5 | |
| 14 | 2021 | 4 | |
| 15 | Perry syndrome: a case of atypical parkinsonism with confirmed DCTN1 mutation. | 2020 | 2 |
| 16 | 2023 | 2 | |
| 17 | 2024 | 2 | |
| 18 | 2019 | 2 | |
| 19 | 2018 | 1 | |
| 20 | 2024 | 1 |
About Gemma Poke
Gemma Poke is a scholar working on Molecular Biology, Genetics, Genetics, Cellular and Molecular Neuroscience and Neurology, having authored 24 papers that have together received 441 indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (4 papers), Neurogenetic and Muscular Disorders Research (4 papers), Genomics and Rare Diseases (3 papers), Mitochondrial Function and Pathology (3 papers), Chromatin Remodeling and Cancer (3 papers), Genetics and Neurodevelopmental Disorders (2 papers), Amyotrophic Lateral Sclerosis Research (2 papers) and Neurofibromatosis and Schwannoma Cases (2 papers). The work is most often cited by research in Neurology (93 citations), Genetics (58 citations), Epidemiology (118 citations), Genetics (79 citations) and Pathology and Forensic Medicine (46 citations). Gemma Poke has collaborated with scholars based in New Zealand, Australia and United Kingdom. Frequent co-authors include Miriam J. Smith, Saba Sharif, Daniel Rawluk, Diana Eccles, D. Gareth Evans, Sanjeev S. Bhaskar, David Fitzpatrick, Kristen D. Hadfield, James O’Sullivan and Daniel du Plessis. Their work appears in journals such as Neuromuscular Disorders, Neuroepidemiology, Neurology, Stem Cell Research and Journal of Medical Genetics.
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.