Simon Sadedin
Impact in
- Genetics top 10%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 11
- Genomics and Rare Diseases 9
- Genomic variations and chromosomal abnormalities 6
- Genetics and Neurodevelopmental Disorders 2
-
- Genomics and Phylogenetic Studies 3
- RNA and protein synthesis mechanisms 3
- RNA modifications and cancer 2
- RNA Research and Splicing 2
- Co-authors
- Alicia Oshlack (6 shared papers)Bernard J. Pope (1 shared paper)Zornitza Stark (7 shared papers)Harriet Dashnow (4 shared papers)Andreas Halman (2 shared papers)Sebastian Lunke (7 shared papers)Susan M. White (4 shared papers)Phillipa J. Lamont (1 shared paper)
- Journals
- European Journal of Human Genetics (3 papers)Genome biology (2 papers)Genetics in Medicine (1 paper)Epigenomics (1 paper)Human Mutation (1 paper)
- Partner nations
- AustraliaUnited StatesUnited Kingdom
In The Last Decade
Simon Sadedin
17 papers receiving 465 citations
Peers
Comparison fields: 5 of 57
- Genetics 177
- Information Systems and Management 33
- Molecular Biology 253
- Cellular and Molecular Neuroscience 50
- Cancer Research 38
Countries citing papers authored by Simon Sadedin
This map shows the geographic impact of Simon Sadedin'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 Simon Sadedin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Simon Sadedin more than expected).
Fields of papers citing papers by Simon Sadedin
This network shows the impact of papers produced by Simon Sadedin. 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 Simon Sadedin. The network helps show where Simon Sadedin may publish in the future.
Co-authors
The 25 scholars most cited alongside Simon Sadedin, 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 | 2012 | 94 | |
| 2 | 2018 | 83 | |
| 3 | 2015 | 55 | |
| 4 | 2019 | 37 | |
| 5 | 2019 | 37 | |
| 6 | 2020 | 34 | |
| 7 | 2017 | 31 | |
| 8 | 2019 | 22 | |
| 9 | 2018 | 19 | |
| 10 | 2019 | 15 | |
| 11 | 2017 | 13 | |
| 12 | 2021 | 11 | |
| 13 | 2023 | 8 | |
| 14 | 2024 | 3 | |
| 15 | 2024 | 3 | |
| 16 | 2023 | 2 | |
| 17 | 2018 | 1 |
About Simon Sadedin
Simon Sadedin is a scholar working on Genetics, Molecular Biology, Cancer Research, Genetics and Pathology and Forensic Medicine, having authored 17 papers that have together received 468 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (9 papers), Genomic variations and chromosomal abnormalities (6 papers), Genomics and Phylogenetic Studies (3 papers), RNA and protein synthesis mechanisms (3 papers), Genetics and Neurodevelopmental Disorders (2 papers), Cancer Genomics and Diagnostics (2 papers), RNA modifications and cancer (2 papers) and RNA Research and Splicing (2 papers). The work is most often cited by research in Genetics (177 citations), Information Systems and Management (33 citations), Molecular Biology (253 citations), Cellular and Molecular Neuroscience (50 citations) and Cancer Research (38 citations). Simon Sadedin has collaborated with scholars based in Australia, United States and United Kingdom. Frequent co-authors include Alicia Oshlack, Bernard J. Pope, Zornitza Stark, Harriet Dashnow, Andreas Halman, Sebastian Lunke, Susan M. White, Phillipa J. Lamont, Belinda Phipson and Monkol Lek. Their work appears in journals such as European Journal of Human Genetics, Genome biology, Genetics in Medicine, Epigenomics and Human Mutation.
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.