Cecilia Compton
Impact in
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- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
- Ethics and Legal Issues in Pediatric Healthcare
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- Cystic Fibrosis Research Advances
Papers in
- Genetics 2
- Hemoglobinopathies and Related Disorders 1
- Genomics and Rare Diseases 1
- Genomic variations and chromosomal abnormalities 1
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- Mitochondrial Function and Pathology 1
- Co-authors
- Celine Lewis (1 shared paper)Lyn S. Chitty (1 shared paper)Melissa Hill (1 shared paper)Roger Brown (1 shared paper)Philip M. Farrell (1 shared paper)Audrey Tluczek (1 shared paper)Mark Strong (1 shared paper)Oliver Quarrell (1 shared paper)
- Journals
- American Journal of Medical Genetics Part B Neuropsychiatric Genetics (1 paper)Journal of Genetic Counseling (2 papers)
- Partner nations
- United KingdomNetherlandsChina
In The Last Decade
Cecilia Compton
3 papers receiving 69 citations
Peers
Comparison fields: 5 of 24
- Pediatrics, Perinatology and Child Health 34
- Pulmonary and Respiratory Medicine 25
- Genetics 6
- Clinical Biochemistry 3
- Reproductive Medicine 3
Countries citing papers authored by Cecilia Compton
This map shows the geographic impact of Cecilia Compton'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 Cecilia Compton with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Cecilia Compton more than expected).
Fields of papers citing papers by Cecilia Compton
This network shows the impact of papers produced by Cecilia Compton. 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 Cecilia Compton. The network helps show where Cecilia Compton may publish in the future.
Co-authors
The 20 scholars most cited alongside Cecilia Compton, 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 | 2014 | 39 | |
| 2 | 2010 | 31 | |
| 3 | 2017 | 1 |
About Cecilia Compton
Cecilia Compton is a scholar working on Genetics, Molecular Biology, Genetics, Cellular and Molecular Neuroscience and Pediatrics, Perinatology and Child Health, having authored 3 papers that have together received 71 indexed citations. Recurring topics across this work include Hemoglobinopathies and Related Disorders (1 paper), Genomics and Rare Diseases (1 paper), Genomic variations and chromosomal abnormalities (1 paper), Genetic Neurodegenerative Diseases (1 paper), Cystic Fibrosis Research Advances (1 paper), Prenatal Screening and Diagnostics (1 paper) and Mitochondrial Function and Pathology (1 paper). The work is most often cited by research in Pediatrics, Perinatology and Child Health (34 citations), Pulmonary and Respiratory Medicine (25 citations), Genetics (6 citations), Clinical Biochemistry (3 citations) and Reproductive Medicine (3 citations). Cecilia Compton has collaborated with scholars based in United Kingdom, Netherlands and China. Frequent co-authors include Celine Lewis, Lyn S. Chitty, Melissa Hill, Roger Brown, Philip M. Farrell, Audrey Tluczek, Mark Strong, Oliver Quarrell, Mary O’Driscoll and Corien C. Verschuuren‐Bemelmans. Their work appears in journals such as American Journal of Medical Genetics Part B Neuropsychiatric Genetics and Journal of Genetic Counseling.
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.