Y Aurran
Impact in
-
- Prenatal Screening and Diagnostics
- Ethics and Legal Issues in Pediatric Healthcare
- Childhood Cancer Survivors' Quality of Life
- Genetics top 10%
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 10
- BRCA gene mutations in cancer 6
- Genomics and Rare Diseases 2
- Genomic variations and chromosomal abnormalities 2
-
- Prenatal Screening and Diagnostics 5
- Co-authors
- Claire Julian‐Reynier (11 shared papers)Ségolène Aymé (9 shared papers)F Giraud (5 shared papers)Marie‐Geneviève Mattéi (3 shared papers)F Chabal (9 shared papers)Hagay Sobol (6 shared papers)François Eisinger (6 shared papers)Catherine Noguès (5 shared papers)
- Journals
- European Journal of Cancer (2 papers)Journal of Medical Genetics (2 papers)Prenatal Diagnosis (2 papers)Psychology and Health (1 paper)Oncology Reports (1 paper)
- Partner nations
- France
In The Last Decade
Y Aurran
17 papers receiving 448 citations
Peers
Comparison fields: 5 of 60
- Pediatrics, Perinatology and Child Health 195
- Genetics 269
- Medical Terminology 1
- Developmental Biology 7
- Pathology and Forensic Medicine 51
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-authors
The 25 scholars most cited alongside Y Aurran, 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 | 1996 | 90 | |
| 2 | 1979 | 63 | |
| 3 | 1976 | 61 | |
| 4 | 1994 | 42 | |
| 5 | 1998 | 38 | |
| 6 | 1995 | 37 | |
| 7 | 1994 | 34 | |
| 8 | 1996 | 32 | |
| 9 | 1993 | 32 | |
| 10 | 1999 | 18 | |
| 11 | 1998 | 13 | |
| 12 | [Measurement of anxiety state in women: a short-form scale]. | 1998 | 11 |
| 13 | 1979 | 10 | |
| 14 | [Prenatal diagnosis: perceptions of women concerning their pregnancies]. | 1994 | 7 |
| 15 | 1982 | 3 | |
| 16 | Attitudes about breast cancer genetics and preventive strategies: a national survey of French medical and surgical gynecologists. | 1997 | 2 |
| 17 | [Evaluation of trisomy 21 risk by serial determination of chorionic gonadotrophin hormone and alpha-fetoprotein: results of a national pilot study]. | 1993 | 2 |
About Y Aurran
Y Aurran is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Sociology and Political Science, General Health Professions and Molecular Biology, having authored 17 papers that have together received 495 indexed citations. Recurring topics across this work include Family Support in Illness (6 papers), BRCA gene mutations in cancer (6 papers), Prenatal Screening and Diagnostics (5 papers), Genomics and Rare Diseases (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Metabolism and Genetic Disorders (1 paper), Cancer Genomics and Diagnostics (1 paper) and Cytomegalovirus and herpesvirus research (1 paper). The work is most often cited by research in Pediatrics, Perinatology and Child Health (195 citations), Genetics (269 citations), Medical Terminology (1 citation), Developmental Biology (7 citations) and Pathology and Forensic Medicine (51 citations). 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 Medical Genetics, Prenatal Diagnosis, Psychology and Health and Oncology Reports.
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.