Caroline F. Wright
Impact in
- Genetics top 0.5%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- BRCA gene mutations in cancer
- Genetic Associations and Epidemiology
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 54
- Genomics and Rare Diseases 41
- Genomic variations and chromosomal abnormalities 21
- Genetics and Neurodevelopmental Disorders 9
- BRCA gene mutations in cancer 8
- Genetic Associations and Epidemiology 8
- Co-authors
- Helen V. Firth (25 shared papers)David Fitzpatrick (11 shared papers)Jane Clarke (4 shared papers)Matthew E. Hurles (17 shared papers)H. Burton (2 shared papers)Christopher M. Dobson (2 shared papers)Sarah A. Teichmann (1 shared paper)Eugene Bragin (5 shared papers)
- Journals
- Genetics in Medicine (10 papers)The American Journal of Human Genetics (6 papers)Journal of Medical Genetics (5 papers)Genome Medicine (4 papers)Human Molecular Genetics (3 papers)
- Partner nations
- United KingdomUnited StatesAustralia
In The Last Decade
Caroline F. Wright
74 papers receiving 3.3k citations
Caroline F. Wright's Hit Papers
Peers
Comparison fields: 5 of 140
- Genetics 1.7k
- Pediatrics, Perinatology and Child Health 405
- Molecular Biology 1.3k
- Cancer Research 247
- Clinical Biochemistry 62
Countries citing papers authored by Caroline F. Wright
This map shows the geographic impact of Caroline F. Wright'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 Caroline F. Wright with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Caroline F. Wright more than expected).
Fields of papers citing papers by Caroline F. Wright
This network shows the impact of papers produced by Caroline F. Wright. 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 Caroline F. Wright. The network helps show where Caroline F. Wright may publish in the future.
Co-authors
The 25 scholars most cited alongside Caroline F. Wright, 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 78 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Paediatric genomics: diagnosing rare disease in children Hit paper breakdown → | 2018 | 355 |
| 2 | 2005 | 270 | |
| 3 | 2018 | 200 | |
| 4 | 2018 | 193 | |
| 5 | 2008 | 175 | |
| 6 | 2015 | 143 | |
| 7 | 2013 | 143 | |
| 8 | 2003 | 134 | |
| 9 | 2018 | 132 | |
| 10 | 2022 | 116 | |
| 11 | 2019 | 113 | |
| 12 | 2011 | 104 | |
| 13 | 2020 | 76 | |
| 14 | 2019 | 58 | |
| 15 | 2018 | 55 | |
| 16 | 2019 | 54 | |
| 17 | 2012 | 54 | |
| 18 | 2011 | 50 | |
| 19 | 2012 | 46 | |
| 20 | 2010 | 45 |
About Caroline F. Wright
Caroline F. Wright is a scholar working on Genetics, Molecular Biology, Public Health, Environmental and Occupational Health, Pediatrics, Perinatology and Child Health and Cancer Research, having authored 78 papers that have together received 3.4k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (41 papers), Genomic variations and chromosomal abnormalities (21 papers), Cancer Genomics and Diagnostics (10 papers), Genetics and Neurodevelopmental Disorders (9 papers), Prenatal Screening and Diagnostics (9 papers), BRCA gene mutations in cancer (8 papers), Ethics in Clinical Research (8 papers) and Genetic Associations and Epidemiology (8 papers). The work is most often cited by research in Genetics (1.7k citations), Pediatrics, Perinatology and Child Health (405 citations), Molecular Biology (1.3k citations), Cancer Research (247 citations) and Clinical Biochemistry (62 citations). Caroline F. Wright has collaborated with scholars based in United Kingdom, United States and Australia. Frequent co-authors include Helen V. Firth, David Fitzpatrick, Jane Clarke, Matthew E. Hurles, H. Burton, Christopher M. Dobson, Sarah A. Teichmann, Eugene Bragin, Jeremy F. McRae and Alison Hall. Their work appears in journals such as Genetics in Medicine, The American Journal of Human Genetics, Journal of Medical Genetics, Genome Medicine and Human Molecular 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.