Sylvia Redon
Impact in
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- Genetic and Kidney Cyst Diseases
- Genetic Syndromes and Imprinting
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
Papers in
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- Congenital heart defects research 2
- Melanoma and MAPK Pathways 2
- Ubiquitin and proteasome pathways 1
- Genetics 5
- Genomic variations and chromosomal abnormalities 3
- Genetics and Neurodevelopmental Disorders 1
- Co-authors
- Claude Férec (7 shared papers)Caroline Bénech (5 shared papers)Jian‐Min Chen (2 shared papers)Émilie Cornec-Le Gall (1 shared paper)I. Quéré (1 shared paper)Yannick Le Meur (1 shared paper)Marie‐Pierre Audrézet (1 shared paper)Arnaud Uguen (3 shared papers)
In The Last Decade
Sylvia Redon
11 papers receiving 220 citations
Peers
Comparison fields: 5 of 43
- Genetics 156
- Genetics 17
- Nephrology 11
- Developmental Neuroscience 6
- Molecular Biology 102
Countries citing papers authored by Sylvia Redon
This map shows the geographic impact of Sylvia Redon'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 Sylvia Redon with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sylvia Redon more than expected).
Fields of papers citing papers by Sylvia Redon
This network shows the impact of papers produced by Sylvia Redon. 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 Sylvia Redon. The network helps show where Sylvia Redon may publish in the future.
Co-authors
The 25 scholars most cited alongside Sylvia Redon, 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 | 2012 | 125 | |
| 2 | 2011 | 29 | |
| 3 | 2017 | 17 | |
| 4 | 2013 | 17 | |
| 5 | 2011 | 11 | |
| 6 | 2019 | 11 | |
| 7 | 2012 | 9 | |
| 8 | 2013 | 8 | |
| 9 | 2019 | 2 | |
| 10 | S. Cerevisiae Est1/H. sapiens SMG6 protein family members function in telomere metabolism | 2005 | 1 |
| 11 | 2015 | 1 | |
| 12 | 2024 | 0 |
About Sylvia Redon
Sylvia Redon is a scholar working on Molecular Biology, Genetics, Oncology, Genetics and Physiology, having authored 12 papers that have together received 231 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (3 papers), Cutaneous Melanoma Detection and Management (2 papers), Congenital heart defects research (2 papers), Melanoma and MAPK Pathways (2 papers), Vitamin K Research Studies (1 paper), Genetics and Neurodevelopmental Disorders (1 paper), Cancer Genomics and Diagnostics (1 paper) and Ubiquitin and proteasome pathways (1 paper). The work is most often cited by research in Genetics (156 citations), Genetics (17 citations), Nephrology (11 citations), Developmental Neuroscience (6 citations) and Molecular Biology (102 citations). Sylvia Redon has collaborated with scholars based in France and Monaco. Frequent co-authors include Claude Férec, Caroline Bénech, Jian‐Min Chen, Émilie Cornec-Le Gall, I. Quéré, Yannick Le Meur, Marie‐Pierre Audrézet, Arnaud Uguen, Pascale Marcorelles and Gaëlle Friocourt. Their work appears in journals such as European Journal of Medical Genetics, Prenatal Diagnosis, Applied immunohistochemistry & molecular morphology, PLoS ONE and Journal of Neuro-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.