Sandra Chantot‐Bastaraud
- Genetics top 2%
- Molecular Biology top 10%
- Pediatrics, Perinatology and Child Health top 2%
- Reproductive Medicine top 2%
- Plant Science
- Co-authors
- Célia RavelKen McElreaveyJean‐Pierre SiffroiIrène NetchineJacqueline MandelbaumSalah AzziJean Pierre SiffroiBrahim El Houate
- Topics
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (21 papers)Genomic variations and chromosomal abnormalities (20 papers)Prenatal Screening and Diagnostics (16 papers)
- Partner nations
- FranceUnited StatesUnited Kingdom
In The Last Decade
Sandra Chantot‐Bastaraud
67 papers receiving 1.2k citations
Peers
Comparison fields: 5 of 72
- Genetics 939
- Molecular Biology 759
- Pediatrics, Perinatology and Child Health 404
- Reproductive Medicine 304
- Plant Science 152
Countries citing papers authored by Sandra Chantot‐Bastaraud
This map shows the geographic impact of Sandra Chantot‐Bastaraud'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 Sandra Chantot‐Bastaraud with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sandra Chantot‐Bastaraud more than expected).
Fields of papers citing papers by Sandra Chantot‐Bastaraud
This network shows the impact of papers produced by Sandra Chantot‐Bastaraud. 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 Sandra Chantot‐Bastaraud. The network helps show where Sandra Chantot‐Bastaraud may publish in the future.
Co-authorship network of co-authors of Sandra Chantot‐Bastaraud
This figure shows the co-authorship network connecting the top 25 collaborators of Sandra Chantot‐Bastaraud. A scholar is included among the top collaborators of Sandra Chantot‐Bastaraud 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 Sandra Chantot‐Bastaraud. Sandra Chantot‐Bastaraud is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 1 | |
| 2 | 4 | |
| 3 | 4 | |
| 4 | 1 | |
| 5 | 8 | |
| 6 | 6 | |
| 7 | 34 | |
| 8 | 20 | |
| 9 | 21 | |
| 10 | 28 | |
| 11 | 51 | |
| 12 | 8 | |
| 13 | 35 | |
| 14 | 34 | |
| 15 | 2 | |
| 16 | 5 | |
| 17 | 1 | |
| 18 | 6 | |
| 19 | 59 | |
| 20 | Génétique des anomalies du tractus génital humain | 2 |
About Sandra Chantot‐Bastaraud
Sandra Chantot‐Bastaraud is a scholar working on Genetics, Reproductive Medicine and Pediatrics, Perinatology and Child Health, having authored 67 papers that have together received 1.4k indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (21 papers), Genomic variations and chromosomal abnormalities (20 papers) and Prenatal Screening and Diagnostics (16 papers). The work is most often cited by research in Reproductive Medicine (304 citations), Genetics (939 citations) and Pediatrics, Perinatology and Child Health (404 citations). Sandra Chantot‐Bastaraud has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Célia Ravel, Ken McElreavey, Jean‐Pierre Siffroi, Irène Netchine, Jacqueline Mandelbaum, Salah Azzi, Jean Pierre Siffroi, Brahim El Houate, Madeleine D. Harbison and Nathalie Thibaud. Their work appears in journals such as PLoS ONE, The Journal of Clinical Endocrinology & Metabolism and Neurology.
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.