Florence Démurger
Impact in
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- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetic and Kidney Cyst Diseases
- Genetic Syndromes and Imprinting
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- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
Papers in
- Genetics 6
- Genomic variations and chromosomal abnormalities 5
- Genetic and Kidney Cyst Diseases 1
- Genetics and Neurodevelopmental Disorders 1
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- Congenital heart defects research 2
- Protein Tyrosine Phosphatases 1
- Renal and related cancers 1
- Co-authors
- Sylvie Odent (6 shared papers)Laurent Pasquier (5 shared papers)Chloé Quēlin (4 shared papers)Mélanie Fradin (4 shared papers)Sylvie Jaillard (5 shared papers)Dominique Martin‐Coignard (2 shared papers)Marc‐Antoine Belaud‐Rotureau (3 shared papers)Estelle Colin (1 shared paper)
- Journals
- European Journal of Medical Genetics (3 papers)Clinical Genetics (1 paper)American Journal of Medical Genetics Part A (2 papers)Molecular Syndromology (1 paper)
- Partner nations
- France
In The Last Decade
Florence Démurger
7 papers receiving 66 citations
Peers
Comparison fields: 5 of 27
- Genetics 50
- Pediatrics, Perinatology and Child Health 33
- Molecular Biology 40
- Developmental Biology 1
- Plant Science 8
Countries citing papers authored by Florence Démurger
This map shows the geographic impact of Florence Démurger'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 Florence Démurger with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Florence Démurger more than expected).
Fields of papers citing papers by Florence Démurger
This network shows the impact of papers produced by Florence Démurger. 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 Florence Démurger. The network helps show where Florence Démurger may publish in the future.
Co-authors
The 25 scholars most cited alongside Florence Démurger, 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 | 2015 | 31 | |
| 2 | 2019 | 12 | |
| 3 | 2018 | 11 | |
| 4 | 2013 | 11 | |
| 5 | 2022 | 7 | |
| 6 | 2021 | 4 | |
| 7 | 2010 | 2 |
About Florence Démurger
Florence Démurger is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Epidemiology and Plant Science, having authored 7 papers that have together received 78 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (5 papers), Prenatal Screening and Diagnostics (2 papers), Congenital heart defects research (2 papers), Genetic and Kidney Cyst Diseases (1 paper), Protein Tyrosine Phosphatases (1 paper), Renal and related cancers (1 paper), Genetics and Neurodevelopmental Disorders (1 paper) and Fetal and Pediatric Neurological Disorders (1 paper). The work is most often cited by research in Genetics (50 citations), Pediatrics, Perinatology and Child Health (33 citations), Molecular Biology (40 citations), Developmental Biology (1 citation) and Plant Science (8 citations). Florence Démurger has collaborated with scholars based in France. Frequent co-authors include Sylvie Odent, Laurent Pasquier, Chloé Quēlin, Mélanie Fradin, Sylvie Jaillard, Dominique Martin‐Coignard, Marc‐Antoine Belaud‐Rotureau, Estelle Colin, Philippe Loget and Linda Akloul. Their work appears in journals such as European Journal of Medical Genetics, Clinical Genetics, American Journal of Medical Genetics Part A and Molecular Syndromology.
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.