Catherine Fourneau
Impact in
-
- Genomic variations and chromosomal abnormalities
- Craniofacial Disorders and Treatments
Papers in
- Co-authors
- Y. Gillerot (7 shared papers)Lionel Van Maldergem (6 shared papers)Alain Verloès (2 shared papers)Marjo Kestilä (1 shared paper)Maximilian Muenke (1 shared paper)LL Wang (1 shared paper)H. Annika Siitonen (1 shared paper)Éliane Chouery (1 shared paper)
- Journals
- Journal of Medical Genetics (2 papers)European Journal of Pediatrics (1 paper)Clinical Genetics (1 paper)European Radiology (1 paper)Prenatal Diagnosis (1 paper)
- Partner nations
- BelgiumFranceNetherlands
In The Last Decade
Catherine Fourneau
12 papers receiving 387 citations
Peers
Comparison fields: 5 of 48
- Developmental Biology 12
- Genetics 119
- Pediatrics, Perinatology and Child Health 66
- Cancer Research 45
- Genetics 26
Countries citing papers authored by Catherine Fourneau
This map shows the geographic impact of Catherine Fourneau'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 Catherine Fourneau with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Catherine Fourneau more than expected).
Fields of papers citing papers by Catherine Fourneau
This network shows the impact of papers produced by Catherine Fourneau. 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 Catherine Fourneau. The network helps show where Catherine Fourneau may publish in the future.
Co-authors
The 25 scholars most cited alongside Catherine Fourneau, 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 | 2005 | 163 | |
| 2 | 1992 | 40 | |
| 3 | 2017 | 38 | |
| 4 | 1990 | 30 | |
| 5 | 1991 | 29 | |
| 6 | 2015 | 24 | |
| 7 | 1993 | 22 | |
| 8 | 2005 | 22 | |
| 9 | 1992 | 21 | |
| 10 | 1997 | 13 | |
| 11 | 2000 | 5 | |
| 12 | 1993 | 1 |
About Catherine Fourneau
Catherine Fourneau is a scholar working on Genetics, Surgery, Genetics, Pediatrics, Perinatology and Child Health and Urology, having authored 12 papers that have together received 408 indexed citations. Recurring topics across this work include Congenital Anomalies and Fetal Surgery (3 papers), Neurogenetic and Muscular Disorders Research (2 papers), Urological Disorders and Treatments (2 papers), Cleft Lip and Palate Research (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Craniofacial Disorders and Treatments (2 papers), Ultrasound and Hyperthermia Applications (1 paper) and Fetal and Pediatric Neurological Disorders (1 paper). The work is most often cited by research in Developmental Biology (12 citations), Genetics (119 citations), Pediatrics, Perinatology and Child Health (66 citations), Cancer Research (45 citations) and Genetics (26 citations). Catherine Fourneau has collaborated with scholars based in Belgium, France and Netherlands. Frequent co-authors include Y. Gillerot, Lionel Van Maldergem, Alain Verloès, Marjo Kestilä, Maximilian Muenke, LL Wang, H. Annika Siitonen, Éliane Chouery, Ethylin Wang Jabs and Nadine Jalkh. Their work appears in journals such as Journal of Medical Genetics, European Journal of Pediatrics, Clinical Genetics, European Radiology and Prenatal Diagnosis.
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.