Emmanuelle Ginglinger
Impact in
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- Genetic Neurodegenerative Diseases
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- Neurological diseases and metabolism
Papers in
- Genetics 3
- Genomic variations and chromosomal abnormalities 3
- Genomics and Rare Diseases 1
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- Prenatal Screening and Diagnostics 2
- Co-authors
- B. Monga (1 shared paper)Denys Chaigne (1 shared paper)G. Rodier (1 shared paper)Nathalie Drouot (1 shared paper)Christine Tranchant (1 shared paper)Jean‐Pierre Delaunoy (1 shared paper)Sylvie Courtois (1 shared paper)Marie‐Céline Fleury (1 shared paper)
- Journals
- Neurogenetics (1 paper)Pediatric Neurology (1 paper)American Journal of Medical Genetics Part A (2 papers)Annales de Dermatologie et de Vénéréologie (1 paper)
- Partner nations
- FranceDemocratic Republic of the CongoAustralia
In The Last Decade
Emmanuelle Ginglinger
5 papers receiving 130 citations
Peers
Comparison fields: 5 of 29
- Cellular and Molecular Neuroscience 90
- Neurology 22
- Molecular Biology 108
- Genetics 39
- Neurology 18
Countries citing papers authored by Emmanuelle Ginglinger
This map shows the geographic impact of Emmanuelle Ginglinger'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 Emmanuelle Ginglinger with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Emmanuelle Ginglinger more than expected).
Fields of papers citing papers by Emmanuelle Ginglinger
This network shows the impact of papers produced by Emmanuelle Ginglinger. 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 Emmanuelle Ginglinger. The network helps show where Emmanuelle Ginglinger may publish in the future.
Co-authors
The 25 scholars most cited alongside Emmanuelle Ginglinger, 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 | 2009 | 103 | |
| 2 | 2003 | 25 | |
| 3 | 2005 | 13 | |
| 4 | 2018 | 1 | |
| 5 | 2024 | 1 |
About Emmanuelle Ginglinger
Emmanuelle Ginglinger is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Cellular and Molecular Neuroscience and Hematology, having authored 5 papers that have together received 143 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (3 papers), Prenatal Screening and Diagnostics (2 papers), Neurological diseases and metabolism (1 paper), Cancer Genomics and Diagnostics (1 paper), Lysosomal Storage Disorders Research (1 paper), Genomics and Rare Diseases (1 paper), Epilepsy research and treatment (1 paper) and Chromosomal and Genetic Variations (1 paper). The work is most often cited by research in Cellular and Molecular Neuroscience (90 citations), Neurology (22 citations), Molecular Biology (108 citations), Genetics (39 citations) and Neurology (18 citations). Emmanuelle Ginglinger has collaborated with scholars based in France, Democratic Republic of the Congo and Australia. Frequent co-authors include B. Monga, Denys Chaigne, G. Rodier, Nathalie Drouot, Christine Tranchant, Jean‐Pierre Delaunoy, Sylvie Courtois, Marie‐Céline Fleury, Mathieu Anheim and Dominique Stoppa‐Lyonnet. Their work appears in journals such as Neurogenetics, Pediatric Neurology, American Journal of Medical Genetics Part A and Annales de Dermatologie et de Vénéréologie.
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.