Agnès Choiset
- Co-authors
- F. ThépotSylvie GirardMarguerite PrieurJ BouéPatrice EydouxJean‐François VielSylvie RamondE Gautier
- Topics
- Prenatal Screening and Diagnostics (14 papers)Genomic variations and chromosomal abnormalities (10 papers)Congenital Anomalies and Fetal Surgery (8 papers)
In The Last Decade
Agnès Choiset
20 papers receiving 353 citations
Peers
Comparison fields: 5 of 46
- Pediatrics, Perinatology and Child Health 181
- Genetics 150
- Surgery 113
- Molecular Biology 96
- Physiology 44
Countries citing papers authored by Agnès Choiset
This map shows the geographic impact of Agnès Choiset'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 Agnès Choiset with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Agnès Choiset more than expected).
Fields of papers citing papers by Agnès Choiset
This network shows the impact of papers produced by Agnès Choiset. 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 Agnès Choiset. The network helps show where Agnès Choiset may publish in the future.
Co-authorship network of co-authors of Agnès Choiset
This figure shows the co-authorship network connecting the top 25 collaborators of Agnès Choiset. A scholar is included among the top collaborators of Agnès Choiset 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 Agnès Choiset. Agnès Choiset is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 12 | |
| 2 | 15 | |
| 3 | 4 | |
| 4 | 15 | |
| 5 | 19 | |
| 6 | 8 | |
| 7 | 15 | |
| 8 | 31 | |
| 9 | 79 | |
| 10 | Prenatal diagnosis of Niemann-Pick type C disease: current strategy from an experience of 37 pregnancies at risk. | 45 |
| 11 | [The placenta and trisomies 13, 18, 21]. | 9 |
| 12 | 81 | |
| 13 | [Chorionic villi sampling. Results with the first 500 samples]. | 1 |
| 14 | 5 | |
| 15 | Interstitial dup(1p) and severe intrauterine growth retardation. | 11 |
| 16 | 10 | |
| 17 | De novo inv del(4) in an infant with the Wolf-Hirschhorn syndrome. | 1 |
| 18 | 10 | |
| 19 | [Sampling, culturing and karyotyping of chorionic villi]. | 1 |
| 20 | 18 |
About Agnès Choiset
Agnès Choiset is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Surgery, having authored 20 papers that have together received 390 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (14 papers), Genomic variations and chromosomal abnormalities (10 papers) and Congenital Anomalies and Fetal Surgery (8 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (181 citations), Genetics (150 citations) and Obstetrics and Gynecology (42 citations). Agnès Choiset has collaborated with scholars based in France and Japan. Frequent co-authors include F. Thépot, Sylvie Girard, Marguerite Prieur, J Boué, Patrice Eydoux, Jean‐François Viel, Sylvie Ramond, E Gautier, Nicole Morichon and Marianne Till. Their work appears in journals such as The American Journal of Human Genetics, Human Reproduction and Human Genetics.
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.