Clesson Turner
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- BRCA gene mutations in cancer
- Genetics and Neurodevelopmental Disorders
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- Cancer Genomics and Diagnostics
Papers in
- Genetics 29
- BRCA gene mutations in cancer 14
- Genomics and Rare Diseases 7
- Genetics and Neurodevelopmental Disorders 7
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 5
- Genomic variations and chromosomal abnormalities 4
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- Pharmacogenetics and Drug Metabolism 4
- Co-authors
- Rachel E. Ellsworth (9 shared papers)Leslie G. Biesecker (4 shared papers)Nichola R. Dennis (2 shared papers)P. A. Jacobs (2 shared papers)Darrell L. Ellsworth (2 shared papers)Craig D. Shriver (9 shared papers)Mauricio J. De Castro (6 shared papers)Nick S. T. Thomas (1 shared paper)
- Journals
- Human Genetics (4 papers)The American Journal of Human Genetics (3 papers)Annals of Human Genetics (2 papers)Genetics in Medicine (2 papers)Journal of Oncology (1 paper)
- Partner nations
- United StatesUnited KingdomNetherlands
In The Last Decade
Clesson Turner
49 papers receiving 988 citations
Peers
Comparison fields: 5 of 97
- Genetics 398
- Cancer Research 94
- Molecular Biology 448
- Aging 9
- Oncology 98
Countries citing papers authored by Clesson Turner
This map shows the geographic impact of Clesson Turner'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 Clesson Turner with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Clesson Turner more than expected).
Fields of papers citing papers by Clesson Turner
This network shows the impact of papers produced by Clesson Turner. 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 Clesson Turner. The network helps show where Clesson Turner may publish in the future.
Co-authors
The 25 scholars most cited alongside Clesson Turner, 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 51 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2003 | 110 | |
| 2 | 2016 | 81 | |
| 3 | 2017 | 66 | |
| 4 | 2017 | 65 | |
| 5 | 2000 | 58 | |
| 6 | 2019 | 52 | |
| 7 | 2021 | 51 | |
| 8 | 2022 | 50 | |
| 9 | 2023 | 49 | |
| 10 | 2011 | 41 | |
| 11 | 2015 | 37 | |
| 12 | 2015 | 37 | |
| 13 | 2019 | 33 | |
| 14 | 2000 | 31 | |
| 15 | 2016 | 25 | |
| 16 | 2016 | 24 | |
| 17 | 2019 | 24 | |
| 18 | 2000 | 19 | |
| 19 | 2001 | 18 | |
| 20 | 2018 | 18 |
About Clesson Turner
Clesson Turner is a scholar working on Genetics, Pharmacology, Molecular Biology, Cancer Research and Clinical Biochemistry, having authored 51 papers that have together received 1.0k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (14 papers), Genomics and Rare Diseases (7 papers), Genetics and Neurodevelopmental Disorders (7 papers), Cancer Genomics and Diagnostics (5 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), RNA modifications and cancer (5 papers), Genomic variations and chromosomal abnormalities (4 papers) and Pharmacogenetics and Drug Metabolism (4 papers). The work is most often cited by research in Genetics (398 citations), Cancer Research (94 citations), Molecular Biology (448 citations), Aging (9 citations) and Oncology (98 citations). Clesson Turner has collaborated with scholars based in United States, United Kingdom and Netherlands. Frequent co-authors include Rachel E. Ellsworth, Leslie G. Biesecker, Nichola R. Dennis, P. A. Jacobs, Darrell L. Ellsworth, Craig D. Shriver, Mauricio J. De Castro, Nick S. T. Thomas, Marjorie J. Rosenberg and Yelena M. Kemel. Their work appears in journals such as Human Genetics, The American Journal of Human Genetics, Annals of Human Genetics, Genetics in Medicine and Journal of Oncology.
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.