Anouck Schneider
- Co-authors
- Jacques PuechbertyFranck PellestorVincent GâtinoisDominique GaillardDavid GenevièveMartine Doco‐FenzyEmilie LandaisB. Hédon
- Topics
- Genomic variations and chromosomal abnormalities (11 papers)Prenatal Screening and Diagnostics (4 papers)Genetics and Neurodevelopmental Disorders (4 papers)
- Partner nations
- FranceUnited StatesUnited Kingdom
In The Last Decade
Anouck Schneider
19 papers receiving 341 citations
Peers
Comparison fields: 5 of 51
- Genetics 199
- Molecular Biology 134
- Oncology 63
- Pediatrics, Perinatology and Child Health 62
- Plant Science 52
Countries citing papers authored by Anouck Schneider
This map shows the geographic impact of Anouck Schneider'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 Anouck Schneider with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Anouck Schneider more than expected).
Fields of papers citing papers by Anouck Schneider
This network shows the impact of papers produced by Anouck Schneider. 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 Anouck Schneider. The network helps show where Anouck Schneider may publish in the future.
Co-authorship network of co-authors of Anouck Schneider
This figure shows the co-authorship network connecting the top 25 collaborators of Anouck Schneider. A scholar is included among the top collaborators of Anouck Schneider based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Anouck Schneider. Anouck Schneider is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 0 | |
| 2 | 47 | |
| 3 | 0 | |
| 4 | 8 | |
| 5 | 5 | |
| 6 | 19 | |
| 7 | 8 | |
| 8 | 13 | |
| 9 | 20 | |
| 10 | 2 | |
| 11 | 30 | |
| 12 | 13 | |
| 13 | 16 | |
| 14 | 43 | |
| 15 | 2 | |
| 16 | 8 | |
| 17 | 21 | |
| 18 | 11 | |
| 19 | 28 | |
| 20 | 55 |
About Anouck Schneider
Anouck Schneider is a scholar working on Genetics, Developmental Biology and Genetics, having authored 21 papers that have together received 355 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (11 papers), Prenatal Screening and Diagnostics (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). The work is most often cited by research in Genetics (199 citations), Pediatrics, Perinatology and Child Health (62 citations) and Pathology and Forensic Medicine (50 citations). Anouck Schneider has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Jacques Puechberty, Franck Pellestor, Vincent Gâtinois, Dominique Gaillard, David Geneviève, Martine Doco‐Fenzy, Emilie Landais, B. Hédon, T. Anahory and Jacques Motté. Their work appears in journals such as Human Reproduction, Fertility and Sterility and Transplantation.
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.