Charlotte Rodwell
- Genetics top 5%
- Genomics and Rare Diseases 6
- Genetic Syndromes and Imprinting 1
- Dermatological and Skeletal Disorders 1
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- Genomics and Rare Diseases 6
- Genetic Syndromes and Imprinting 1
- Dermatological and Skeletal Disorders 1
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- CRISPR and Genetic Engineering 1
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- Cystic Fibrosis Research Advances 2
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- Oral and gingival health research 1
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- Neurological diseases and metabolism 1
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- Genetic factors in colorectal cancer 1
- Co-authors
- Valérie Serrière-LanneauAnnie OlryAna RathDaniel N. MurphyStéphanie Nguengang WakapDeborah M. LambertYann Le CamSégolène Aymé
- Cited by
- GeneticsHealth Informatics
- Journals
- Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease (1 paper)European Journal of Human Genetics (1 paper)Orphanet Journal of Rare Diseases (3 papers)
- Partner nations
- FranceAustraliaUnited Kingdom
In The Last Decade
Charlotte Rodwell
7 papers receiving 893 citations
Hit Papers
Peers
Comparison fields: 5 of 104
- Genetics 551
- Genetics 78
- Health Informatics 9
- Aging 8
- Molecular Biology 302
Countries citing papers authored by Charlotte Rodwell
This map shows the geographic impact of Charlotte Rodwell'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 Charlotte Rodwell with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Charlotte Rodwell more than expected).
Fields of papers citing papers by Charlotte Rodwell
This network shows the impact of papers produced by Charlotte Rodwell. 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 Charlotte Rodwell. The network helps show where Charlotte Rodwell may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Charlotte Rodwell, 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 | 2024 | 6 | |
| 2 | Estimating cumulative point prevalence of rare diseases: analysis of the Orphanet databasebreakdown → | 2019 | 833 |
| 3 | 2018 | 16 | |
| 4 | 2015 | 57 | |
| 5 | 2014 | 6 | |
| 6 | 2012 | 1 | |
| 7 | 2011 Report on the State of the Art of Rare Disease Activities in Europe of the European Union Committee of Experts on Rare Diseases - Part I: Overview of Rare Disease Activities in Europe and Key Developments in 2010 (United Kingdom) | 2011 | 1 |
About Charlotte Rodwell
Charlotte Rodwell is a scholar working on Genetics, Pharmacy and Neurology, having authored 7 papers that have together received 920 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (6 papers), Cystic Fibrosis Research Advances (2 papers), Oral and gingival health research (1 paper), Genetic Syndromes and Imprinting (1 paper), Neurological diseases and metabolism (1 paper), CRISPR and Genetic Engineering (1 paper), Dermatological and Skeletal Disorders (1 paper) and Genetic factors in colorectal cancer (1 paper). The work is most often cited by research in Genetics (551 citations), Genetics (78 citations) and Health Informatics (9 citations). Charlotte Rodwell has collaborated with scholars based in France, Australia and United Kingdom. Frequent co-authors include Valérie Serrière-Lanneau, Annie Olry, Ana Rath, Daniel N. Murphy, Stéphanie Nguengang Wakap, Deborah M. Lambert, Yann Le Cam, Ségolène Aymé, Peter N. Robinson and Tudor Groza. Their work appears in journals such as Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, European Journal of Human Genetics and Orphanet Journal of Rare Diseases.
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.