Simone C. Yendle
Impact in
- Psychiatry and Mental health top 5%
- Epilepsy research and treatment
- Genetics top 10%
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 6
- Genetics and Neurodevelopmental Disorders 6
- Genomic variations and chromosomal abnormalities 3
- Genomics and Rare Diseases 2
-
- Chromatin Remodeling and Cancer 1
- Ion Transport and Channel Regulation 1
- RNA regulation and disease 1
- Co-authors
- Ingrid E. Scheffer (6 shared papers)Samuel F. Berkovic (4 shared papers)Jacinta M. McMahon (3 shared papers)Mark T. Mackay (2 shared papers)Jeremy L. Freeman (2 shared papers)Heather C. Mefford (2 shared papers)Peter De Jonghe (2 shared papers)Arvid Suls (2 shared papers)
- Journals
- Neurology (3 papers)Annals of Neurology (1 paper)Twin Research and Human Genetics (1 paper)Epilepsia (1 paper)
- Partner nations
- AustraliaUnited StatesSweden
In The Last Decade
Simone C. Yendle
6 papers receiving 421 citations
Peers
Comparison fields: 5 of 40
- Psychiatry and Mental health 200
- Genetics 308
- Clinical Biochemistry 28
- Cellular and Molecular Neuroscience 62
- Cell Biology 50
Countries citing papers authored by Simone C. Yendle
This map shows the geographic impact of Simone C. Yendle'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 Simone C. Yendle with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Simone C. Yendle more than expected).
Fields of papers citing papers by Simone C. Yendle
This network shows the impact of papers produced by Simone C. Yendle. 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 Simone C. Yendle. The network helps show where Simone C. Yendle may publish in the future.
Co-authors
The 25 scholars most cited alongside Simone C. Yendle, 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 | 2011 | 150 | |
| 2 | 2010 | 122 | |
| 3 | 2011 | 83 | |
| 4 | 2011 | 33 | |
| 5 | 2010 | 27 | |
| 6 | 2013 | 11 |
About Simone C. Yendle
Simone C. Yendle is a scholar working on Genetics, Molecular Biology, Psychiatry and Mental health, Oncology and Cell Biology, having authored 6 papers that have together received 426 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (6 papers), Genomic variations and chromosomal abnormalities (3 papers), Genomics and Rare Diseases (2 papers), Epilepsy research and treatment (2 papers), Chromatin Remodeling and Cancer (1 paper), Cellular transport and secretion (1 paper), Ion Transport and Channel Regulation (1 paper) and RNA regulation and disease (1 paper). The work is most often cited by research in Psychiatry and Mental health (200 citations), Genetics (308 citations), Clinical Biochemistry (28 citations), Cellular and Molecular Neuroscience (62 citations) and Cell Biology (50 citations). Simone C. Yendle has collaborated with scholars based in Australia, United States and Sweden. Frequent co-authors include Ingrid E. Scheffer, Samuel F. Berkovic, Jacinta M. McMahon, Mark T. Mackay, Jeremy L. Freeman, Heather C. Mefford, Peter De Jonghe, Arvid Suls, Thierry Bienvenu and Orvar Eeg‐Olofsson. Their work appears in journals such as Neurology, Annals of Neurology, Twin Research and Human Genetics and Epilepsia.
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.