Y Aurran
- Genetics top 10%
- Pediatrics, Perinatology and Child Health top 5%
- Molecular Biology
- Sociology and Political Science
- Public Health, Environmental and Occupational Health
- Co-authors
- Claire Julian‐ReynierSégolène AyméF GiraudMarie‐Geneviève MattéiF ChabalHagay SobolFrançois EisingerCatherine Noguès
- Topics
- BRCA gene mutations in cancer (6 papers)Family Support in Illness (6 papers)Prenatal Screening and Diagnostics (5 papers)
- Journals
- European Journal of CancerJournal of Epidemiology & Community HealthJournal of Medical Genetics
- Partner nations
- France
In The Last Decade
Y Aurran
17 papers receiving 448 citations
Peers
Comparison fields: 5 of 60
- Genetics 269
- Pediatrics, Perinatology and Child Health 195
- Molecular Biology 84
- Sociology and Political Science 74
- Public Health, Environmental and Occupational Health 65
Countries citing papers authored by Y Aurran
This map shows the geographic impact of Y Aurran'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 Y Aurran with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Y Aurran more than expected).
Fields of papers citing papers by Y Aurran
This network shows the impact of papers produced by Y Aurran. 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 Y Aurran. The network helps show where Y Aurran may publish in the future.
Co-authorship network of co-authors of Y Aurran
This figure shows the co-authorship network connecting the top 25 collaborators of Y Aurran. A scholar is included among the top collaborators of Y Aurran 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 Y Aurran. Y Aurran is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 18 | |
| 2 | 38 | |
| 3 | 13 | |
| 4 | [Measurement of anxiety state in women: a short-form scale]. | 11 |
| 5 | Attitudes about breast cancer genetics and preventive strategies: a national survey of French medical and surgical gynecologists. | 2 |
| 6 | 32 | |
| 7 | 90 | |
| 8 | 37 | |
| 9 | 34 | |
| 10 | [Prenatal diagnosis: perceptions of women concerning their pregnancies]. | 7 |
| 11 | 42 | |
| 12 | 32 | |
| 13 | [Evaluation of trisomy 21 risk by serial determination of chorionic gonadotrophin hormone and alpha-fetoprotein: results of a national pilot study]. | 2 |
| 14 | 3 | |
| 15 | 10 | |
| 16 | 63 | |
| 17 | 61 |
About Y Aurran
Y Aurran is a scholar working on Developmental Biology, Genetics and Pediatrics, Perinatology and Child Health, having authored 17 papers that have together received 495 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (6 papers), Family Support in Illness (6 papers) and Prenatal Screening and Diagnostics (5 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (195 citations), Genetics (269 citations) and Medical Terminology (1 citation). Y Aurran has collaborated with scholars based in France. Frequent co-authors include Claire Julian‐Reynier, Ségolène Aymé, F Giraud, Marie‐Geneviève Mattéi, F Chabal, Hagay Sobol, François Eisinger, Catherine Noguès, Philippe Vennin and J. F. Mattéi. Their work appears in journals such as European Journal of Cancer, Journal of Epidemiology & Community Health and Journal of Medical 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.