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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- Hemoglobinopathies and Related Disorders
- Genomics and Rare Diseases
Papers in
- Genetics 2
- Genomics and Rare Diseases 1
- Hemoglobinopathies and Related Disorders 1
- Genomic variations and chromosomal abnormalities 1
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- Mitochondrial Function and Pathology 1
- Co-authors
- Lyn S. Chitty (1 shared paper)Melissa Hill (1 shared paper)Celine Lewis (1 shared paper)Audrey Tluczek (1 shared paper)Roger Brown (1 shared paper)Philip M. Farrell (1 shared paper)Sascha Vermeer (1 shared paper)Alan Fryer (1 shared paper)
- Journals
- American Journal of Medical Genetics Part B Neuropsychiatric Genetics (1 paper)Journal of Genetic Counseling (2 papers)
- Partner nations
- United KingdomNetherlandsBangladesh
In The Last Decade
Cecilia Compton
3 papers receiving 69 citations
Peers
Comparison fields: 5 of 24
- Pediatrics, Perinatology and Child Health 47
- Genetics 10
- Pulmonary and Respiratory Medicine 27
- Genetics 16
- Clinical Biochemistry 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 | 38 | |
| 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 70 indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (1 paper), Cystic Fibrosis Research Advances (1 paper), Mitochondrial Function and Pathology (1 paper), Genomics and Rare Diseases (1 paper), Hemoglobinopathies and Related Disorders (1 paper), Prenatal Screening and Diagnostics (1 paper) and Genomic variations and chromosomal abnormalities (1 paper). The work is most often cited by research in Pediatrics, Perinatology and Child Health (47 citations), Genetics (10 citations), Pulmonary and Respiratory Medicine (27 citations), Genetics (16 citations) and Clinical Biochemistry (3 citations). Cecilia Compton has collaborated with scholars based in United Kingdom, Netherlands and Bangladesh. Frequent co-authors include Lyn S. Chitty, Melissa Hill, Celine Lewis, Audrey Tluczek, Roger Brown, Philip M. Farrell, Sascha Vermeer, Alan Fryer, Angus Clarke and Nayana Lahiri. 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.