F Chabal
Impact in
- Genetics top 10%
- BRCA gene mutations in cancer
- Genomics and Rare Diseases
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- Prenatal Screening and Diagnostics
- Ethics and Legal Issues in Pediatric Healthcare
- Childhood Cancer Survivors' Quality of Life
Papers in
- Genetics 6
- BRCA gene mutations in cancer 6
- Genomics and Rare Diseases 1
- Nutrition, Genetics, and Disease 1
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- Prenatal Screening and Diagnostics 4
- Co-authors
- Claire Julian‐Reynier (8 shared papers)Y Aurran (9 shared papers)François Eisinger (6 shared papers)Philippe Vennin (5 shared papers)Hagay Sobol (6 shared papers)Catherine Noguès (4 shared papers)Christine Lasset (1 shared paper)Dominique Stoppa‐Lyonnet (1 shared paper)
- Journals
- European Journal of Cancer (2 papers)Journal of Medical Genetics (2 papers)Journal of Epidemiology & Community Health (1 paper)Oncology Reports (1 paper)American Journal of Medical Genetics (1 paper)
- Partner nations
- France
In The Last Decade
F Chabal
10 papers receiving 325 citations
Peers
Comparison fields: 5 of 43
- Genetics 250
- Pediatrics, Perinatology and Child Health 112
- Pathology and Forensic Medicine 37
- Public Health, Environmental and Occupational Health 41
- Sociology and Political Science 74
Countries citing papers authored by F Chabal
This map shows the geographic impact of F Chabal'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 F Chabal with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites F Chabal more than expected).
Fields of papers citing papers by F Chabal
This network shows the impact of papers produced by F Chabal. 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 F Chabal. The network helps show where F Chabal may publish in the future.
Co-authors
The 22 scholars most cited alongside F Chabal, 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 | 2000 | 97 | |
| 2 | 1996 | 94 | |
| 3 | 1995 | 40 | |
| 4 | 1998 | 38 | |
| 5 | 1994 | 34 | |
| 6 | 1996 | 32 | |
| 7 | 1998 | 13 | |
| 8 | [Prenatal diagnosis: perceptions of women concerning their pregnancies]. | 1994 | 7 |
| 9 | [Evaluation of trisomy 21 risk by serial determination of chorionic gonadotrophin hormone and alpha-fetoprotein: results of a national pilot study]. | 1993 | 2 |
| 10 | Attitudes about breast cancer genetics and preventive strategies: a national survey of French medical and surgical gynecologists. | 1997 | 2 |
About F Chabal
F Chabal is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Sociology and Political Science, Oncology and General Health Professions, having authored 10 papers that have together received 359 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (6 papers), Prenatal Screening and Diagnostics (4 papers), Family Support in Illness (3 papers), Global Cancer Incidence and Screening (2 papers), Genomics and Rare Diseases (1 paper), Cancer Genomics and Diagnostics (1 paper), Nutrition, Genetics, and Disease (1 paper) and Patient-Provider Communication in Healthcare (1 paper). The work is most often cited by research in Genetics (250 citations), Pediatrics, Perinatology and Child Health (112 citations), Pathology and Forensic Medicine (37 citations), Public Health, Environmental and Occupational Health (41 citations) and Sociology and Political Science (74 citations). F Chabal has collaborated with scholars based in France. Frequent co-authors include Claire Julian‐Reynier, Y Aurran, François Eisinger, Philippe Vennin, Hagay Sobol, Catherine Noguès, Christine Lasset, Dominique Stoppa‐Lyonnet, Ségolène Aymé and D. Serin. Their work appears in journals such as European Journal of Cancer, Journal of Medical Genetics, Journal of Epidemiology & Community Health, Oncology Reports and American 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.