Sian Corrin
Impact in
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- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
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- Metabolism and Genetic Disorders
Papers in
- Genetics 4
- Genomics and Rare Diseases 3
- Genomic variations and chromosomal abnormalities 2
- Neurogenetic and Muscular Disorders Research 1
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- Gene expression and cancer classification 1
- Co-authors
- Sarah J. Beal (1 shared paper)Sarah E. Anderson (1 shared paper)Morag N. Collinson (1 shared paper)Jennifer Evans (2 shared papers)Francis H. Sansbury (1 shared paper)Siân Morgan (1 shared paper)Hywel Williams (1 shared paper)Jennifer M. Gardner (1 shared paper)
- Journals
- npj Genomic Medicine (1 paper)Archives of Disease in Childhood (1 paper)Human Genetics (1 paper)Abstracts (1 paper)
- Partner nations
- United Kingdom
In The Last Decade
Sian Corrin
3 papers receiving 7 citations
Peers
Comparison fields: 5 of 10
- Genetics 6
- Clinical Biochemistry 1
- Cancer Research 2
- Hematology 1
- Pathology and Forensic Medicine 1
Countries citing papers authored by Sian Corrin
This map shows the geographic impact of Sian Corrin'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 Sian Corrin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sian Corrin more than expected).
Fields of papers citing papers by Sian Corrin
This network shows the impact of papers produced by Sian Corrin. 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 Sian Corrin. The network helps show where Sian Corrin may publish in the future.
Co-authors
The 11 scholars most cited alongside Sian Corrin, 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 | 2021 | 3 | |
| 2 | 2020 | 2 | |
| 3 | 2024 | 2 | |
| 4 | 2018 | 0 |
About Sian Corrin
Sian Corrin is a scholar working on Genetics, Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health and Clinical Biochemistry, having authored 4 papers that have together received 7 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (3 papers), Genomic variations and chromosomal abnormalities (2 papers), Gene expression and cancer classification (1 paper), Neurogenetic and Muscular Disorders Research (1 paper), Prenatal Screening and Diagnostics (1 paper) and Metabolism and Genetic Disorders (1 paper). The work is most often cited by research in Genetics (6 citations), Clinical Biochemistry (1 citation), Cancer Research (2 citations), Hematology (1 citation) and Pathology and Forensic Medicine (1 citation). Sian Corrin has collaborated with scholars based in United Kingdom. Frequent co-authors include Sarah J. Beal, Sarah E. Anderson, Morag N. Collinson, Jennifer Evans, Francis H. Sansbury, Siân Morgan, Hywel Williams, Jennifer M. Gardner, Caroline Pottinger and Oliver Murch. Their work appears in journals such as npj Genomic Medicine, Archives of Disease in Childhood, Human Genetics and Abstracts.
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.